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		<title>Ith joint angle than the S.E.A. and B.A. - Історія редагувань</title>
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		<updated>2026-04-06T19:57:32Z</updated>
		<subtitle>Історія редагувань цієї сторінки в вікі</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=254643&amp;oldid=prev</id>
		<title>Willowhate3 в 20:41, 17 листопада 2017</title>
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				<updated>2017-11-17T20:41:33Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 20:41, 17 листопада 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;The FCM and FCLP muscle tissues have among &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;largest LAR moment arms for all muscle tissues (0&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;08 m; also observed for our ILp &lt;/del&gt;muscle&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;) in &lt;/del&gt;our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information, but both muscle tissues decrease their lateral rotator action with rising hip flexion. In &lt;/del&gt;B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information a weaker, opposite &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;medial/internal rotator&lt;/del&gt;) &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a compact lateral/external rotator action &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Fig&lt;/del&gt;. 12)&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. The uniarticular &lt;/del&gt;hip muscles&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;' LAR &lt;/del&gt;moment arms &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;of our model often switch less usually (at in vivo &lt;/del&gt;hip joint &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;angles 300 &lt;/del&gt;; &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;e.g&lt;/del&gt;., &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Fig&lt;/del&gt;. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;S5&lt;/del&gt;) &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;from medial to lateral rotation or vice versa &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Fig&lt;/del&gt;. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;13&lt;/del&gt;). &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;The IFI&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;nevertheless, remains mainly as a &lt;/del&gt;weak &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;medial rotator except at intense hip flexion &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;&amp;gt;60 &lt;/del&gt;)&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. &lt;/del&gt;B.A.S.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;'s data favoured stronger &lt;/del&gt;medial/internal &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;rotation &lt;/del&gt;moment &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;arms for &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;IFI but otherwise had a comparable pattern&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Ith &lt;/del&gt;joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;than the S&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;E.A&lt;/del&gt;. and B.A.S. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data simply because we had to constrain this muscle&lt;/del&gt;'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;path &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;3D to avoid it cutting by way of bones or other obstacles &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;some poses. Note also how &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;S.E.A. benefits generally show powerful changes &lt;/del&gt;with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;joint angles&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;whereas the a lot more constrained muscle geometry of our model and &lt;/del&gt;B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final results in additional modest modifications (Fig&lt;/del&gt;. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;11)&lt;/del&gt;. Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;allow &lt;/del&gt;comparisons &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in between &lt;/del&gt;our data and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;those &lt;/del&gt;of B.A.S . &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Additionally&lt;/del&gt;, thinking of that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in addition &lt;/del&gt;plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;inside &lt;/del&gt;the Supporting Info (Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;nevertheless&lt;/del&gt;, we do not &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;discuss &lt;/del&gt;the latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final results &lt;/del&gt;right here. For the AMB1,two &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;find &lt;/del&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for key proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;[http://anomalysa.co.za/members/badgerrange31/activity/167280/ Rom the GBD analysis. {First|Initial|Very first|1st|Initially] effectively &lt;/del&gt;with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;getting &lt;/del&gt;a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;enhance from &lt;/del&gt;the medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;despite the fact that &lt;/del&gt;B.A.S.'s data &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;considerably &lt;/del&gt;more strongly favour a medial rotator function for the IC muscle. Our outcomes for the two parts &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;on &lt;/del&gt;the ILFB muscle are very &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;diverse &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/del&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. The outcomes for the OM muscle have greater matching among research, indicating a lateral/external rotation action for this large muscle. Likewise, our ISF data and these of B.A.S&lt;/del&gt;.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;outcomes in general show powerful adjustments with joint angles, whereas &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;much more constrained [https://www&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;medchemexpress.com/Tirapazamine.html SR259075] &lt;/ins&gt;muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;geometry of &lt;/ins&gt;our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;model and &lt;/ins&gt;B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;results in extra modest adjustments &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Fig. 11&lt;/ins&gt;)&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. Long-axis rotation &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;LAR; in Figs&lt;/ins&gt;. 12 &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;and 13&lt;/ins&gt;) &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;moment arms for &lt;/ins&gt;hip muscles &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;only enable comparisons involving our data and these of B.A.S . Furthermore, thinking of that B.A.S. plotted these &lt;/ins&gt;moment arms &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;against &lt;/ins&gt;hip &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;flexion/extension &lt;/ins&gt;joint &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;angle (modified information shown&lt;/ins&gt;; &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Karl T&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Bates&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;pers&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;comm., 2015&lt;/ins&gt;)&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;, we show them that way here but also plot them against hip LAR joint angle in the Supporting Information &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Figs&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;S1 and S2&lt;/ins&gt;)&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;; nonetheless, we don't go over the latter results right here&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;For the AMB1&lt;/ins&gt;,&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;two muscle tissues we obtain consistently &lt;/ins&gt;weak&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;, near-zero LAR action &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;lateral/external rotation&lt;/ins&gt;)&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;, whereas &lt;/ins&gt;B.A.S. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;showed a steeply decreasing hip &lt;/ins&gt;medial/internal &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;LAR &lt;/ins&gt;moment &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;arm as &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;hip is flexedHutchinson et al&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;(2015), PeerJ, DOI ten.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against &lt;/ins&gt;joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;for crucial proximal thigh muscle tissues&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;See captions for Figs&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;In contrast, our IC &lt;/ins&gt;and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;IL muscle information agree properly with &lt;/ins&gt;B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;possessing a shallow improve &lt;/ins&gt;in the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;medial/internal LAR moment arm &lt;/ins&gt;with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;hip flexion&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;though &lt;/ins&gt;B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data considerably much more strongly favour a medial [https://www&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;medchemexpress.com/TMP269.html TMP269 web] rotator function for the IC muscle&lt;/ins&gt;. Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;enable &lt;/ins&gt;comparisons &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;involving &lt;/ins&gt;our data and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;these &lt;/ins&gt;of B.A.S . &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Moreover&lt;/ins&gt;, thinking of that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;also &lt;/ins&gt;plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;within &lt;/ins&gt;the Supporting Info (Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/ins&gt;, we do not &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;go over &lt;/ins&gt;the latter &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/ins&gt;right here. For the AMB1,two &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;obtain &lt;/ins&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for key proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;well &lt;/ins&gt;with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;obtaining &lt;/ins&gt;a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;boost in &lt;/ins&gt;the medial/internal LAR moment arm with hip flexion, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;though &lt;/ins&gt;B.A.S.'s data &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;significantly much &lt;/ins&gt;more strongly favour a medial rotator function for the IC muscle. Our outcomes for the two parts &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;with &lt;/ins&gt;the ILFB muscle are very &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;various &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/ins&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Willowhate3</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=251444&amp;oldid=prev</id>
		<title>Badgermail43 в 22:45, 8 листопада 2017</title>
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				<updated>2017-11-08T22:45:01Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 22:45, 8 листопада 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;2015&lt;/del&gt;), &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;PeerJ, DOI 10&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;7717/peerj&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;21/[http://kfyst&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com/comment/html/?216435&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;html Ort the hypothesis that its ecomorphology was {similar|comparable|equivalent|related] Figure 11 Hip flexor&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extensor moment arms plotted against joint angle &lt;/del&gt;for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important [http:&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;/vlamingeninzurich&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ch/forum/discussion/210409/hospitals-located-that-not-havinggettingpossessingobtaining#Item_1 Hospitals located that not {having|getting|possessing|obtaining] proximal thigh muscle tissues&lt;/del&gt;. The uniarticular hip muscles' LAR moment arms of our model &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;have a tendency to &lt;/del&gt;switch &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;significantly &lt;/del&gt;less &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;frequently &lt;/del&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;having said that&lt;/del&gt;, remains &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;mostly &lt;/del&gt;as a weak medial rotator except at &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extreme &lt;/del&gt;hip flexion (&amp;gt;60 ).Ith joint angle than the S.E.A. and B.A.S. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information due to the fact &lt;/del&gt;we had to constrain this muscle's path in 3D to &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;prevent &lt;/del&gt;it cutting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;through &lt;/del&gt;bones or other obstacles in some poses. Note also how the S.E.A. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;results &lt;/del&gt;generally show &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;robust modifications &lt;/del&gt;with joint angles, whereas the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;additional &lt;/del&gt;constrained muscle geometry of our model and B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;benefits &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extra &lt;/del&gt;modest &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;adjustments &lt;/del&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;enable &lt;/del&gt;comparisons &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;among &lt;/del&gt;our data and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;these &lt;/del&gt;of B.A.S . &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Furthermore&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;considering &lt;/del&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;also &lt;/del&gt;plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;the Supporting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Details &lt;/del&gt;(Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/del&gt;, we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;don't talk about &lt;/del&gt;the latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;benefits &lt;/del&gt;here. For the AMB1,&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;2 muscle tissues &lt;/del&gt;we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;locate &lt;/del&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See captions for Figs. 9 and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/del&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;properly &lt;/del&gt;with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;possessing &lt;/del&gt;a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;raise on &lt;/del&gt;the medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;while &lt;/del&gt;B.A.S.'s data &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;substantially much &lt;/del&gt;more strongly favour a medial rotator function for the IC muscle. Our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final results &lt;/del&gt;for the two parts &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;with &lt;/del&gt;the ILFB muscle are very &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;distinctive &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/del&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The outcomes for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;improved &lt;/del&gt;matching &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;involving studies&lt;/del&gt;, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;huge &lt;/del&gt;muscle. Likewise, our ISF &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;and these of B.A.S&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. match relatively closely, with consistent lateral/external rotator action. The FCM and FCLP muscles have among the biggest LAR moment arms for all muscle tissues (0.08 m; also observed for our ILp muscle) in our information, but each muscles decrease their lateral rotator action with increasing hip flexion&lt;/del&gt;.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;The FCM and FCLP muscle tissues have among the largest LAR moment arms for all muscle tissues &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;0.08 m; also observed for our ILp muscle&lt;/ins&gt;) &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in our information&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;but both muscle tissues decrease their lateral rotator action with rising hip flexion&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;In B&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;A&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;S&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'s information a weaker, opposite (medial&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;internal rotator) trend with hip flexion was located &lt;/ins&gt;for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;the FCM, whereas the FCL muscle maintained a compact lateral&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;external rotator action (Fig&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;12)&lt;/ins&gt;. The uniarticular hip muscles' LAR moment arms of our model &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;often &lt;/ins&gt;switch less &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/ins&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nevertheless&lt;/ins&gt;, remains &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;mainly &lt;/ins&gt;as a weak medial rotator except at &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;intense &lt;/ins&gt;hip flexion (&amp;gt;60 )&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. B.A.S.'s data favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a comparable pattern&lt;/ins&gt;.Ith joint angle than the S.E.A. and B.A.S. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data simply because &lt;/ins&gt;we had to constrain this muscle's path in 3D to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;avoid &lt;/ins&gt;it cutting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;by way of &lt;/ins&gt;bones or other obstacles in some poses. Note also how the S.E.A. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;benefits &lt;/ins&gt;generally show &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;powerful changes &lt;/ins&gt;with joint angles, whereas the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;a lot more &lt;/ins&gt;constrained muscle geometry of our model and B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final results &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;additional &lt;/ins&gt;modest &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;modifications &lt;/ins&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;allow &lt;/ins&gt;comparisons &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in between &lt;/ins&gt;our data and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;those &lt;/ins&gt;of B.A.S . &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Additionally&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;thinking of &lt;/ins&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in addition &lt;/ins&gt;plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;inside &lt;/ins&gt;the Supporting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Info &lt;/ins&gt;(Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nevertheless&lt;/ins&gt;, we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;do not discuss &lt;/ins&gt;the latter &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final results right &lt;/ins&gt;here. For the AMB1,&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;two muscles &lt;/ins&gt;we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;find &lt;/ins&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See captions for Figs. 9 and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/ins&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[http://anomalysa.co.za/members/badgerrange31/activity/167280/ Rom the GBD analysis. {First|Initial|Very first|1st|Initially] effectively &lt;/ins&gt;with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;getting &lt;/ins&gt;a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;enhance from &lt;/ins&gt;the medial/internal LAR moment arm with hip flexion, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;despite the fact that &lt;/ins&gt;B.A.S.'s data &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;considerably &lt;/ins&gt;more strongly favour a medial rotator function for the IC muscle. Our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/ins&gt;for the two parts &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;on &lt;/ins&gt;the ILFB muscle are very &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;diverse &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/ins&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The outcomes for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;greater &lt;/ins&gt;matching &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;among research&lt;/ins&gt;, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;large &lt;/ins&gt;muscle. Likewise, our ISF &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;and these of B.A.S.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Badgermail43</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=251442&amp;oldid=prev</id>
		<title>Badgermail43 в 22:29, 8 листопада 2017</title>
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				<updated>2017-11-08T22:29:04Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 22:29, 8 листопада 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;results in general show sturdy modifications with joint angles&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;whereas the extra constrained &lt;/del&gt;[http://&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;mydreambaby&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;members&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;maidbox1&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;activity&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;346149/ T muscle &lt;/del&gt;moment&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;-generating capacity is near its limits &lt;/del&gt;for] muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;geometry &lt;/del&gt;of our model and B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final &lt;/del&gt;results in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;far more &lt;/del&gt;modest &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;changes &lt;/del&gt;(Fig. comm., 2015), we show them that way here but also plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;inside &lt;/del&gt;the Supporting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Information and facts &lt;/del&gt;(Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;having said that&lt;/del&gt;, we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;usually do not go over &lt;/del&gt;the latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final results right &lt;/del&gt;here. For the AMB1,&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;two muscles &lt;/del&gt;we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;uncover &lt;/del&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/del&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/del&gt;proximal thigh muscle tissues. See captions for Figs. 9 and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/del&gt;proximal thigh muscle tissues. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;effectively &lt;/del&gt;with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;obtaining &lt;/del&gt;a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;increase from &lt;/del&gt;the medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;despite the fact that &lt;/del&gt;B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;substantially &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;a lot &lt;/del&gt;more strongly favour a medial rotator function for the IC muscle. Our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;benefits &lt;/del&gt;for the two parts &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;the ILFB muscle are &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extremely diverse &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The outcomes for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/del&gt;matching &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;between research&lt;/del&gt;, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;significant &lt;/del&gt;muscle. Likewise, our ISF information and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;those &lt;/del&gt;of B.A.S. match &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;fairly &lt;/del&gt;closely, with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;constant &lt;/del&gt;lateral/external rotator action. The FCM and FCLP &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;have among the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;largest &lt;/del&gt;LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data&lt;/del&gt;, but each muscles &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;minimize &lt;/del&gt;their lateral rotator action with increasing hip flexion&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. In B.A.S.'s data a weaker, opposite (medial/internal rotator) trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a smaller lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model have a tendency to switch much less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, nonetheless, remains primarily as a weak medial rotator except at intense hip flexion (&amp;gt;60 ). B.A.S.'s data favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a similar pattern. Our IFE muscle's data indicate a switch from lateral rotation into medial rotation near a 30 hip flexion angle, matched fairly closely by B.A.S.'s data. Our final results for the two-part ITC muscle concur qualitatively with B.A.S.,' regularly obtaining a robust medial/internal rotator action but smaller sized at additional extended joint angles&lt;/del&gt;.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;(2015)&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;PeerJ, DOI 10.7717/peerj.21/&lt;/ins&gt;[http://&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;kfyst&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;comment&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;html&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;?216435.html Ort the hypothesis that its ecomorphology was {similar|comparable|equivalent|related] Figure 11 Hip flexor&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;extensor &lt;/ins&gt;moment &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;arms plotted against joint angle &lt;/ins&gt;for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important [http://vlamingeninzurich.ch/forum/discussion/210409/hospitals-located-that-not-havinggettingpossessingobtaining#Item_1 Hospitals located that not {having|getting|possessing|obtaining&lt;/ins&gt;] &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;proximal thigh &lt;/ins&gt;muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;tissues. The uniarticular hip muscles' LAR moment arms &lt;/ins&gt;of our model &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;have a tendency to switch significantly less frequently (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, having said that, remains mostly as a weak medial rotator except at extreme hip flexion (&amp;gt;60 ).Ith joint angle than the S.E.A. &lt;/ins&gt;and B.A.S. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information due to the fact we had to constrain this muscle&lt;/ins&gt;'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;path in 3D to prevent it cutting through bones or other obstacles in some poses. Note also how the S.E.A. &lt;/ins&gt;results &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;generally show robust modifications with joint angles, whereas the additional constrained muscle geometry of our model and B.A.S.'s benefits &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;extra &lt;/ins&gt;modest &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;adjustments &lt;/ins&gt;(Fig&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only enable comparisons among our data and these of B.A.S . Furthermore, considering that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers&lt;/ins&gt;. comm., 2015), we show them that way &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;right &lt;/ins&gt;here but also plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/ins&gt;the Supporting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Details &lt;/ins&gt;(Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/ins&gt;, we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;don't talk about &lt;/ins&gt;the latter &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;benefits &lt;/ins&gt;here. For the AMB1,&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;2 muscle tissues &lt;/ins&gt;we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;locate &lt;/ins&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/ins&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh muscle tissues. See captions for Figs. 9 and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;proximal thigh muscle tissues. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;properly &lt;/ins&gt;with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;possessing &lt;/ins&gt;a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;raise on &lt;/ins&gt;the medial/internal LAR moment arm with hip flexion, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;while &lt;/ins&gt;B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;substantially &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;much &lt;/ins&gt;more strongly favour a medial rotator function for the IC muscle. Our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final results &lt;/ins&gt;for the two parts &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;with &lt;/ins&gt;the ILFB muscle are &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;very distinctive &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The outcomes for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;improved &lt;/ins&gt;matching &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;involving studies&lt;/ins&gt;, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;huge &lt;/ins&gt;muscle. Likewise, our ISF information and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;these &lt;/ins&gt;of B.A.S. match &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;relatively &lt;/ins&gt;closely, with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;consistent &lt;/ins&gt;lateral/external rotator action. The FCM and FCLP &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;have among the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;biggest &lt;/ins&gt;LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information&lt;/ins&gt;, but each muscles &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;decrease &lt;/ins&gt;their lateral rotator action with increasing hip flexion.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Badgermail43</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=251097&amp;oldid=prev</id>
		<title>Willowhate3 в 23:21, 6 листопада 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=251097&amp;oldid=prev"/>
				<updated>2017-11-06T23:21:27Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 23:21, 6 листопада 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;(2015)&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;PeerJ, DOI 10.7717/peerj.23/Figure 14 Hip abduction/adduction &lt;/del&gt;[http://&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;www&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;wifeandmommylife.net&lt;/del&gt;/members/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;nerveglider2&lt;/del&gt;/activity/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;459108&lt;/del&gt;/ &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Ris (Zinoviev, 2006). The extensor &lt;/del&gt;moment &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;arms &lt;/del&gt;for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;our gastrocnemius {muscles|&lt;/del&gt;muscle&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;] rotation (LAR; in Figs. Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only enable comparisons between &lt;/del&gt;our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;these of &lt;/del&gt;B.A.S . &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;In addition, considering that B.A.S. plotted these moment arms against hip flexion/extension joint angle &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;modified data shown; Karl T. Bates, pers&lt;/del&gt;. comm., 2015), we show them that way &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;right &lt;/del&gt;here but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in addition &lt;/del&gt;plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;within &lt;/del&gt;the Supporting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Info &lt;/del&gt;(Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;however&lt;/del&gt;, we do not &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;discuss &lt;/del&gt;the latter results right here. For the AMB1,&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;2 &lt;/del&gt;muscles we uncover consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/del&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscles. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/del&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/del&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;nicely &lt;/del&gt;with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;getting &lt;/del&gt;a shallow increase &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;the medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;though &lt;/del&gt;B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;a lot &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extra &lt;/del&gt;strongly favour a medial rotator function for the IC muscle. Our benefits for the two parts &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;on &lt;/del&gt;the ILFB muscle are extremely &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;distinct &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;results &lt;/del&gt;for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;improved &lt;/del&gt;matching &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;between &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;studies&lt;/del&gt;, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;big &lt;/del&gt;muscle. Likewise, our ISF &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;and those of B.A.S. match &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;pretty &lt;/del&gt;closely, with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;consistent &lt;/del&gt;lateral/external rotator action. The FCM and FCLP muscle tissues have among the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;biggest &lt;/del&gt;LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information&lt;/del&gt;, but each muscles &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;decrease &lt;/del&gt;their lateral rotator action with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;escalating &lt;/del&gt;hip flexion. In B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;tiny &lt;/del&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;tend &lt;/del&gt;to switch much less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/del&gt;, remains primarily as a weak medial rotator except at intense hip flexion (&amp;gt;60 ). B.A.S.'s data favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;related &lt;/del&gt;pattern. Our IFE muscle's &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;indicate a switch from lateral rotation into medial rotation near a 30 hip flexion angle, matched &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;pretty &lt;/del&gt;closely by B.A.S.'s data.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;results in general show sturdy modifications with joint angles&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;whereas the extra constrained &lt;/ins&gt;[http://&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;mydreambaby&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in&lt;/ins&gt;/members/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;maidbox1&lt;/ins&gt;/activity/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;346149&lt;/ins&gt;/ &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;T muscle &lt;/ins&gt;moment&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;-generating capacity is near its limits &lt;/ins&gt;for&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;] &lt;/ins&gt;muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;geometry of &lt;/ins&gt;our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;model &lt;/ins&gt;and B.A.S.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'s final results in far more modest changes &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Fig&lt;/ins&gt;. comm., 2015), we show them that way here but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;also &lt;/ins&gt;plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;inside &lt;/ins&gt;the Supporting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Information and facts &lt;/ins&gt;(Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;having said that&lt;/ins&gt;, we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/ins&gt;do not &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;go over &lt;/ins&gt;the latter &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final &lt;/ins&gt;results right here. For the AMB1,&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;two &lt;/ins&gt;muscles we uncover consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/ins&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscles. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/ins&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/ins&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;effectively &lt;/ins&gt;with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;obtaining &lt;/ins&gt;a shallow increase &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;from &lt;/ins&gt;the medial/internal LAR moment arm with hip flexion, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;despite the fact that &lt;/ins&gt;B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information substantially &lt;/ins&gt;a lot &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;more &lt;/ins&gt;strongly favour a medial rotator function for the IC muscle. Our benefits for the two parts &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/ins&gt;the ILFB muscle are extremely &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;diverse &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/ins&gt;for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/ins&gt;matching between &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;research&lt;/ins&gt;, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;significant &lt;/ins&gt;muscle. Likewise, our ISF &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;and those of B.A.S. match &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;fairly &lt;/ins&gt;closely, with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;constant &lt;/ins&gt;lateral/external rotator action. The FCM and FCLP muscle tissues have among the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;largest &lt;/ins&gt;LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data&lt;/ins&gt;, but each muscles &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;minimize &lt;/ins&gt;their lateral rotator action with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;increasing &lt;/ins&gt;hip flexion. In B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;smaller &lt;/ins&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;have a tendency &lt;/ins&gt;to switch much less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nonetheless&lt;/ins&gt;, remains primarily as a weak medial rotator except at intense hip flexion (&amp;gt;60 ). B.A.S.'s data favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;similar &lt;/ins&gt;pattern. Our IFE muscle's &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;indicate a switch from lateral rotation into medial rotation near a 30 hip flexion angle, matched &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;fairly &lt;/ins&gt;closely by B.A.S.'s data&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. Our final results for the two-part ITC muscle concur qualitatively with B.A.S.,' regularly obtaining a robust medial/internal rotator action but smaller sized at additional extended joint angles&lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Willowhate3</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=249351&amp;oldid=prev</id>
		<title>Badgermail43 в 21:49, 30 жовтня 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=249351&amp;oldid=prev"/>
				<updated>2017-10-30T21:49:07Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 21:49, 30 жовтня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;S1 and S2&lt;/del&gt;)&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;; nevertheless&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;we don't talk about the &lt;/del&gt;[http://&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;vlamingeninzurich&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ch&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;forum&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;discussion&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;209180&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;mendationaustralia-varied-&lt;/del&gt;in-&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;distinct-states-ahs#Item_1 Mendationaustralia -Varied &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;distinct states&lt;/del&gt;. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;aHS] &lt;/del&gt;latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final &lt;/del&gt;results right here. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscles. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;effectively &lt;/del&gt;with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;having &lt;/del&gt;a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;improve on &lt;/del&gt;the medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even &lt;/del&gt;though B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information significantly &lt;/del&gt;a lot &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;more &lt;/del&gt;strongly favour a medial rotator function for the IC muscle. Our benefits for the two &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;components &lt;/del&gt;on the ILFB muscle are extremely &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;distinctive &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/del&gt;matching between studies, indicating a lateral/external rotation action for this big muscle. Likewise, our ISF data and those of B.A.S. match &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;relatively &lt;/del&gt;closely, with consistent lateral/external rotator action. The FCM and FCLP &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;have among the biggest LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data&lt;/del&gt;, but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;both muscle tissues reduce &lt;/del&gt;their lateral rotator action with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;growing &lt;/del&gt;hip flexion. In B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;found &lt;/del&gt;for the FCM, whereas the FCL muscle maintained a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;smaller &lt;/del&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/del&gt;switch &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;significantly &lt;/del&gt;less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;however&lt;/del&gt;, remains &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;mostly &lt;/del&gt;as a weak medial rotator except at intense hip flexion (&amp;gt;60 ).&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Ith joint angle than the S.E.A. and &lt;/del&gt;B.A.S. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data mainly because we had to constrain this muscle&lt;/del&gt;'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;path in 3D to avoid it cutting via bones or other obstacles in some poses. Note also how &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;S&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;E.A. final results normally show powerful adjustments with joint angles, whereas the a lot more constrained &lt;/del&gt;muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;geometry of our model and B.A.S.&lt;/del&gt;'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;results in far more modest changes (Fig. 11). Long-axis &lt;/del&gt;rotation &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;(LAR; in Figs. 12 and 13) moment arms for hip muscles only enable comparisons between our information and those of B.A.S . Moreover, thinking of that B.A.S. plotted these moment arms against &lt;/del&gt;hip flexion&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;/extension joint &lt;/del&gt;angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;(modified data shown; Karl T. Bates&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;pers. comm., 2015), we show them that way right here but additionally plot them against hip LAR joint angle inside the Supporting Facts (Figs. S1 and S2); nevertheless, we don't discuss the latter benefits right here. For the AMB1,2 muscles we come across consistently weak, near-zero LAR action (lateral/external rotation), whereas &lt;/del&gt;B.A.S. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for important proximal thigh muscles. See captions for Figs. 9 and ten.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for essential proximal thigh muscle tissues&lt;/del&gt;.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;(2015&lt;/ins&gt;), &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;PeerJ, DOI 10.7717/peerj.23/Figure 14 Hip abduction/adduction &lt;/ins&gt;[http://&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;www&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;wifeandmommylife.net&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;members&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nerveglider2&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;activity&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;459108/ Ris (Zinoviev, 2006). The extensor moment arms for our gastrocnemius {muscles|muscle] rotation (LAR; &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Figs. Long&lt;/ins&gt;-&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;axis rotation (LAR; &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Figs&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;12 and 13) moment arms for hip muscles only enable comparisons between our information and these of B.A.S . In addition, considering that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but in addition plot them against hip LAR joint angle within the Supporting Info (Figs. S1 and S2); however, we do not discuss the &lt;/ins&gt;latter results right here&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. For the AMB1,2 muscles we uncover consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm as the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for key proximal thigh muscles. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscles. See caption for Fig&lt;/ins&gt;. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscles. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nicely &lt;/ins&gt;with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;getting &lt;/ins&gt;a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;increase in &lt;/ins&gt;the medial/internal LAR moment arm with hip flexion, though B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;a lot &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;extra &lt;/ins&gt;strongly favour a medial rotator function for the IC muscle. Our benefits for the two &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;parts &lt;/ins&gt;on the ILFB muscle are extremely &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;distinct &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;improved &lt;/ins&gt;matching &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/ins&gt;between studies, indicating a lateral/external rotation action for this big muscle. Likewise, our ISF data and those of B.A.S. match &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;pretty &lt;/ins&gt;closely, with consistent lateral/external rotator action. The FCM and FCLP &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;have among the biggest LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information&lt;/ins&gt;, but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;each muscles decrease &lt;/ins&gt;their lateral rotator action with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;escalating &lt;/ins&gt;hip flexion. In B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;located &lt;/ins&gt;for the FCM, whereas the FCL muscle maintained a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;tiny &lt;/ins&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;tend to &lt;/ins&gt;switch &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;much &lt;/ins&gt;less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/ins&gt;, remains &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;primarily &lt;/ins&gt;as a weak medial rotator except at intense hip flexion (&amp;gt;60 ). B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data favoured stronger medial/internal rotation moment arms for &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;IFI but otherwise had a related pattern&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Our IFE &lt;/ins&gt;muscle's &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information indicate a switch from lateral rotation into medial &lt;/ins&gt;rotation &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;near a 30 &lt;/ins&gt;hip flexion angle, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;matched pretty closely by &lt;/ins&gt;B.A.S.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'s data&lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Badgermail43</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=248741&amp;oldid=prev</id>
		<title>Branch08collar в 12:14, 28 жовтня 2017</title>
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				<updated>2017-10-28T12:14:40Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;tr style='vertical-align: top;'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 12:14, 28 жовтня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data because &lt;/del&gt;we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;had to constrain this &lt;/del&gt;[http://&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;mainearms&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;com&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;members&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;badgerfibre08&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;activity&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;1591080/ Iagnosis&lt;/del&gt;-- &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;unit at Ashworth to save its life (my words namely] muscle's path &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;3D to avoid it cutting through bones or other obstacles &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;some poses&lt;/del&gt;. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Note also how the S.E.A. benefits normally show sturdy modifications with joint angles, whereas the additional constrained muscle geometry of our model and B.A.S.'s &lt;/del&gt;final results &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in extra modest changes (Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscle tissues only enable comparisons among our data and these of B.A.S . Moreover, contemplating that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified information shown; Karl T. Bates, pers. comm., 2015), we show them that way &lt;/del&gt;right here &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;but additionally plot them against hip LAR joint angle within the Supporting Information (Figs. S1 and S2); having said that, we don't go over the latter results here. For the AMB1,two muscles we find consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for important proximal thigh muscles. See captions for Figs. 9 and ten.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscle tissues. See caption for Fig&lt;/del&gt;. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;agree &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;well &lt;/del&gt;with B.A.S.'s in having a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;boost of your &lt;/del&gt;medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;while &lt;/del&gt;B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;a lot &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;much &lt;/del&gt;more strongly favour a medial rotator function for the IC muscle. Our benefits for the two &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;parts in &lt;/del&gt;the ILFB muscle are extremely &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;various &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/del&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/del&gt;for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;far better &lt;/del&gt;matching &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;amongst research&lt;/del&gt;, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;massive &lt;/del&gt;muscle. Likewise, our ISF &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/del&gt;and those of B.A.S. match &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;fairly &lt;/del&gt;closely, with consistent lateral/external rotator action. The FCM and FCLP muscles have among the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;largest &lt;/del&gt;LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information&lt;/del&gt;, but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;each &lt;/del&gt;muscle tissues reduce their lateral rotator action with growing hip flexion. In B.A.S.'s data a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;located &lt;/del&gt;for the FCM, whereas the FCL muscle maintained a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;modest &lt;/del&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;are inclined to &lt;/del&gt;switch significantly less &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/del&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/del&gt;, remains mostly as a weak medial rotator except at &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extreme &lt;/del&gt;hip flexion (&amp;gt;60 ).&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;S1 and S2); nevertheless, &lt;/ins&gt;we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;don't talk about the &lt;/ins&gt;[http://&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;vlamingeninzurich&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ch&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;forum&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;discussion&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;209180&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;mendationaustralia&lt;/ins&gt;-&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;varied&lt;/ins&gt;-in&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;-distinct-states-ahs#Item_1 Mendationaustralia -Varied &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;distinct states&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;aHS] latter &lt;/ins&gt;final results right here. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;agree &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;effectively &lt;/ins&gt;with B.A.S.'s in having a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;improve on the &lt;/ins&gt;medial/internal LAR moment arm with hip flexion, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;even though &lt;/ins&gt;B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information significantly &lt;/ins&gt;a lot more strongly favour a medial rotator function for the IC muscle. Our benefits for the two &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;components on &lt;/ins&gt;the ILFB muscle are extremely &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;distinctive &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/ins&gt;the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;results &lt;/ins&gt;for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/ins&gt;matching &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;between studies&lt;/ins&gt;, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;big &lt;/ins&gt;muscle. Likewise, our ISF &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/ins&gt;and those of B.A.S. match &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;relatively &lt;/ins&gt;closely, with consistent lateral/external rotator action. The FCM and FCLP muscles have among the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;biggest &lt;/ins&gt;LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data&lt;/ins&gt;, but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;both &lt;/ins&gt;muscle tissues reduce their lateral rotator action with growing hip flexion. In B.A.S.'s data a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;found &lt;/ins&gt;for the FCM, whereas the FCL muscle maintained a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;smaller &lt;/ins&gt;lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/ins&gt;switch significantly less &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;normally &lt;/ins&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;however&lt;/ins&gt;, remains mostly as a weak medial rotator except at &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;intense &lt;/ins&gt;hip flexion (&amp;gt;60 )&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;.Ith joint angle than the S.E.A. and B.A.S. data mainly because we had to constrain this muscle's path in 3D to avoid it cutting via bones or other obstacles in some poses. Note also how the S.E.A. final results normally show powerful adjustments with joint angles, whereas the a lot more constrained muscle geometry of our model and B.A.S.'s results in far more modest changes (Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only enable comparisons between our information and those of B.A.S . Moreover, thinking of that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but additionally plot them against hip LAR joint angle inside the Supporting Facts (Figs. S1 and S2); nevertheless, we don't discuss the latter benefits right here. For the AMB1,2 muscles we come across consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for important proximal thigh muscles. See captions for Figs. 9 and ten.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for essential proximal thigh muscle tissues&lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Branch08collar</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=247136&amp;oldid=prev</id>
		<title>Willowhate3 в 01:09, 25 жовтня 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=247136&amp;oldid=prev"/>
				<updated>2017-10-25T01:09:50Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 01:09, 25 жовтня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;(2015), PeerJ, DOI 10.7717/peerj.21/&lt;/del&gt;[&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;https&lt;/del&gt;://&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;www.medchemexpress&lt;/del&gt;.com/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;TIC10.html ONC-201 web] Figure 11 Hip flexor&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;extensor moment arms plotted against joint angle for key proximal thigh muscles. The outcomes for the OM muscle have improved matching amongst studies, indicating a lateral&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;external rotation action for this huge muscle. Likewise, our ISF data and those of B.A.S. match pretty closely, with constant lateral&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;external rotator action. The FCM and FCLP muscles have amongst the biggest LAR moment arms for all muscle tissues (0.08 m; also observed for our ILp muscle) in our data, but each muscle tissues lessen their lateral rotator action with growing hip flexion. In B.A.S.'s information a weaker, opposite (medial&lt;/del&gt;/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;internal rotator) trend with hip flexion was discovered for the FCM, whereas the FCL muscle maintained a little lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model are likely to switch much less generally (&lt;/del&gt;at &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in vivo hip joint angles 300 ; e.g., Fig. S5) from medial &lt;/del&gt;to &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;lateral rotation or vice versa &lt;/del&gt;(&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Fig. 13). The IFI, even so, remains primarily as a weak medial rotator except at extreme hip flexion (&amp;gt;60 ). B.A.S.'s information favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a related pattern. Our IFE muscle's information indicate a switch from lateral rotation into medial rotation near a 30 hip flexion angle, matched fairly closely by B.A.S.'s data.Ith joint angle than the S.E.A. and B.A.S. information because we had to constrain this &lt;/del&gt;muscle's path in 3D to avoid it cutting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;by means of &lt;/del&gt;bones or other obstacles in some poses. Note also how the S.E.A. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;results in general &lt;/del&gt;show &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;powerful &lt;/del&gt;modifications with joint angles, whereas the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;more &lt;/del&gt;constrained muscle geometry of our model and B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/del&gt;in extra modest &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;alterations &lt;/del&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;only enable comparisons &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;amongst &lt;/del&gt;our data and these of B.A.S . Moreover, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;taking into consideration &lt;/del&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;also &lt;/del&gt;plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;the Supporting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Info &lt;/del&gt;(Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even so&lt;/del&gt;, we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;do not &lt;/del&gt;go over the latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;outcomes right &lt;/del&gt;here. For the AMB1,two &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;we &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;come across &lt;/del&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/del&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/del&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See captions for Figs. 9 and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/del&gt;proximal thigh muscle tissues. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/del&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/del&gt;proximal thigh muscle tissues. See caption for Fig. 9.(Fig.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data because we had to constrain this &lt;/ins&gt;[&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;http&lt;/ins&gt;://&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;mainearms&lt;/ins&gt;.com/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;members&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;badgerfibre08&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;activity&lt;/ins&gt;/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;1591080&lt;/ins&gt;/ &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Iagnosis-- unit &lt;/ins&gt;at &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Ashworth &lt;/ins&gt;to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;save its life &lt;/ins&gt;(&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;my words namely] &lt;/ins&gt;muscle's path in 3D to avoid it cutting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;through &lt;/ins&gt;bones or other obstacles in some poses. Note also how the S.E.A. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;benefits normally &lt;/ins&gt;show &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;sturdy &lt;/ins&gt;modifications with joint angles, whereas the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;additional &lt;/ins&gt;constrained muscle geometry of our model and B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final results &lt;/ins&gt;in extra modest &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;changes &lt;/ins&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;only enable comparisons &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;among &lt;/ins&gt;our data and these of B.A.S . Moreover, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;contemplating &lt;/ins&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;additionally &lt;/ins&gt;plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;within &lt;/ins&gt;the Supporting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Information &lt;/ins&gt;(Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;having said that&lt;/ins&gt;, we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;don't &lt;/ins&gt;go over the latter &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;results &lt;/ins&gt;here. For the AMB1,two &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;we &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;find &lt;/ins&gt;consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/ins&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/ins&gt;.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See captions for Figs. 9 and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/ins&gt;proximal thigh muscle tissues. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/ins&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/ins&gt;proximal thigh muscle tissues. See caption for Fig. 9.(Fig&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. 12). In contrast, our IC and IL muscle information agree well with B.A.S.'s in having a shallow boost of your medial/internal LAR moment arm with hip flexion, while B.A.S.'s data a lot much more strongly favour a medial rotator function for the IC muscle. Our benefits for the two parts in the ILFB muscle are extremely various from B.A.S.'s in trending toward stronger medial/internal rotation function as the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The outcomes for the OM muscle have far better matching amongst research, indicating a lateral/external rotation action for this massive muscle. Likewise, our ISF information and those of B.A.S. match fairly closely, with consistent lateral/external rotator action. The FCM and FCLP muscles have among the largest LAR moment arms for all muscle tissues (0.08 m; also observed for our ILp muscle) in our information, but each muscle tissues reduce their lateral rotator action with growing hip flexion. In B.A.S.'s data a weaker, opposite (medial/internal rotator) trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a modest lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model are inclined to switch significantly less usually (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13). The IFI, even so, remains mostly as a weak medial rotator except at extreme hip flexion (&amp;gt;60 )&lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Willowhate3</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=247098&amp;oldid=prev</id>
		<title>Willowhate3 в 21:41, 24 жовтня 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=247098&amp;oldid=prev"/>
				<updated>2017-10-24T21:41:36Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 21:41, 24 жовтня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;In addition, taking into consideration that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified information shown; Karl T. Bates, pers. comm., 2015), we show them that way here but also plot them against hip LAR joint angle inside the Supporting Facts (Figs. S1 and S2); nonetheless, we don't go over the latter results right here. For the AMB1,2 muscles we locate consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/[http://www.playminigamesnow.com/members/branch51skiing/activity/456328/ Ed metacarpal condyles separated by an intercondylar sulcus (e.g., Allosaurus] internal LAR moment arm as the hip is flexedHutchinson et al. &lt;/del&gt;(2015), PeerJ, DOI 10.7717/peerj.21/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Figure 11 Hip &lt;/del&gt;[&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;http&lt;/del&gt;://www.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;jeffplanck&lt;/del&gt;.com/&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;members/nervehate2/activity/301382/ Iopubic and ilioischial sutures are obliterated (Brusatte et al&lt;/del&gt;.&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;, 2013, Fig. S&lt;/del&gt;] flexor/extensor moment arms plotted against joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/del&gt;proximal thigh muscles. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;See captions for Figs. 9 and ten.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for important proximal thigh muscles. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for important proximal thigh muscles. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree effectively with B.A.S.'s in getting a shallow raise of your medial/internal LAR moment arm with hip flexion, though B.A.S.'s data substantially a lot more strongly favour a medial rotator function for the IC muscle. Our &lt;/del&gt;outcomes &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;for the two components with the ILFB muscle are very distinct from B.A.S.'s in trending toward stronger medial/internal rotation function as the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results &lt;/del&gt;for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/del&gt;matching &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;involving &lt;/del&gt;studies, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;substantial &lt;/del&gt;muscle. Likewise, our ISF data and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;these &lt;/del&gt;of B.A.S. match &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;fairly &lt;/del&gt;closely, with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;consistent &lt;/del&gt;lateral/external rotator action. The FCM and FCLP &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;among &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;largest &lt;/del&gt;LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information&lt;/del&gt;, but each &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles lower &lt;/del&gt;their lateral rotator action with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;rising &lt;/del&gt;hip flexion. In B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;located &lt;/del&gt;for the FCM, whereas the FCL muscle maintained a little lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model are &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;inclined &lt;/del&gt;to switch much less &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;normally &lt;/del&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13).Ith joint angle than the S.E.A. and B.A.S. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;data &lt;/del&gt;because we had to constrain this muscle's path in 3D to avoid it cutting by &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;way &lt;/del&gt;of bones or other obstacles in some poses. Note also how the S.E.A. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;outcomes &lt;/del&gt;in general show powerful modifications with joint angles, whereas the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;far &lt;/del&gt;more constrained muscle geometry of our model and B.A.S.'s outcomes in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;additional &lt;/del&gt;modest &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;modifications &lt;/del&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;only enable comparisons &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;among &lt;/del&gt;our data and these of B.A.S .&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;(2015), PeerJ, DOI 10.7717/peerj.21/[&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;https&lt;/ins&gt;://www.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;medchemexpress&lt;/ins&gt;.com/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;TIC10&lt;/ins&gt;.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;html ONC-201 web&lt;/ins&gt;] &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Figure 11 Hip &lt;/ins&gt;flexor/extensor moment arms plotted against joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;proximal thigh muscles. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;The &lt;/ins&gt;outcomes for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;improved &lt;/ins&gt;matching &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;amongst &lt;/ins&gt;studies, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;huge &lt;/ins&gt;muscle. Likewise, our ISF data and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;those &lt;/ins&gt;of B.A.S. match &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;pretty &lt;/ins&gt;closely, with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;constant &lt;/ins&gt;lateral/external rotator action. The FCM and FCLP &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;amongst &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;biggest &lt;/ins&gt;LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data&lt;/ins&gt;, but each &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues lessen &lt;/ins&gt;their lateral rotator action with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;growing &lt;/ins&gt;hip flexion. In B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;a weaker, opposite (medial/internal rotator) trend with hip flexion was &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;discovered &lt;/ins&gt;for the FCM, whereas the FCL muscle maintained a little lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model are &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;likely &lt;/ins&gt;to switch much less &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;generally &lt;/ins&gt;(at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13)&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. The IFI, even so, remains primarily as a weak medial rotator except at extreme hip flexion (&amp;gt;60 ). B.A.S.'s information favoured stronger medial/internal rotation moment arms for the IFI but otherwise had a related pattern. Our IFE muscle's information indicate a switch from lateral rotation into medial rotation near a 30 hip flexion angle, matched fairly closely by B.A.S.'s data&lt;/ins&gt;.Ith joint angle than the S.E.A. and B.A.S. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;information &lt;/ins&gt;because we had to constrain this muscle's path in 3D to avoid it cutting by &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;means &lt;/ins&gt;of bones or other obstacles in some poses. Note also how the S.E.A. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;results &lt;/ins&gt;in general show powerful modifications with joint angles, whereas the more constrained muscle geometry of our model and B.A.S.'s outcomes in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;extra &lt;/ins&gt;modest &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;alterations &lt;/ins&gt;(Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;only enable comparisons &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;amongst &lt;/ins&gt;our data and these of B.A.S &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. Moreover, taking into consideration that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified data shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but also plot them against hip LAR joint angle in the Supporting Info (Figs. S1 and S2); even so, we do not go over the latter outcomes right here. For the AMB1,two muscle tissues we come across consistently weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm as the hip is flexedHutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for crucial proximal thigh muscle tissues. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for key proximal thigh muscle tissues. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI ten.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for important proximal thigh muscle tissues. See caption for Fig. 9.(Fig&lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Willowhate3</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=246793&amp;oldid=prev</id>
		<title>Badgermail43 в 00:22, 24 жовтня 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=246793&amp;oldid=prev"/>
				<updated>2017-10-24T00:22:29Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 00:22, 24 жовтня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
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&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;9 and ten.Figure 12 Hip long-axis [http://edmreality.com/members/sharon67box/activity/334554/ T the ankle for the FDL and gastrocnemius {muscles|muscle tissues] rotation (LAR) moment arms plotted against hip flexion/extension joint angle for essential proximal thigh muscle tissues. 9.(Fig. 12). &lt;/del&gt;In &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;contrast, our IC and IL muscle data agree effectively with B.A.S.'s in possessing a shallow boost on the medial/internal LAR moment arm with hip flexion, despite the fact that B.A.S.'s data a lot a lot more strongly favour a medial rotator function for the IC muscle. Our benefits for the two parts from the ILFB muscle are very diverse from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have improved matching among studies, indicating a lateral/external rotation action for this substantial muscle. Likewise, our ISF information and those of B.A.S. Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only allow comparisons between our information and these of B.A.S . Additionally&lt;/del&gt;, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;thinking about &lt;/del&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified information shown; Karl T. Bates, pers. comm., 2015), we show them that way &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;right &lt;/del&gt;here but &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in addition &lt;/del&gt;plot them against hip LAR joint angle &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;the Supporting &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Information &lt;/del&gt;(Figs. S1 and S2); &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;having said that&lt;/del&gt;, we don't go over the latter &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;final &lt;/del&gt;results here. For the AMB1,&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;two muscle tissues &lt;/del&gt;we locate &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;regularly &lt;/del&gt;weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;because &lt;/del&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for important proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See captions for Figs. 9 and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;essential &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;10&lt;/del&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/del&gt;proximal thigh &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues&lt;/del&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree effectively with B.A.S.'s in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;having &lt;/del&gt;a shallow &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;enhance &lt;/del&gt;of your medial/internal LAR moment arm with hip flexion, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;even &lt;/del&gt;though B.A.S.'s &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;information much extra &lt;/del&gt;strongly favour a medial rotator function for the IC muscle. Our outcomes for the two &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;parts &lt;/del&gt;with the ILFB muscle are very &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;diverse &lt;/del&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function as the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;greater &lt;/del&gt;matching involving studies, indicating a lateral/external rotation action for this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;massive &lt;/del&gt;muscle. Likewise, our ISF data and these of B.A.S. match fairly closely, with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;constant &lt;/del&gt;lateral/external rotator action. The FCM and FCLP &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/del&gt;have &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;amongst &lt;/del&gt;the largest LAR moment arms for all &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/del&gt;(0.08 m; also observed for our ILp muscle) in our information, but each &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues decrease &lt;/del&gt;their lateral rotator action with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;growing &lt;/del&gt;hip flexion.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;In &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;addition&lt;/ins&gt;, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;taking into consideration &lt;/ins&gt;that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified information shown; Karl T. Bates, pers. comm., 2015), we show them that way here but &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;also &lt;/ins&gt;plot them against hip LAR joint angle &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;inside &lt;/ins&gt;the Supporting &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Facts &lt;/ins&gt;(Figs. S1 and S2); &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;nonetheless&lt;/ins&gt;, we don't go over the latter results &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;right &lt;/ins&gt;here. For the AMB1,&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;2 muscles &lt;/ins&gt;we locate &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;consistently &lt;/ins&gt;weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[http://www.playminigamesnow.com/members/branch51skiing/activity/456328/ Ed metacarpal condyles separated by an intercondylar sulcus (e.g., Allosaurus] &lt;/ins&gt;internal LAR moment arm &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;as &lt;/ins&gt;the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[http://www.jeffplanck.com/members/nervehate2/activity/301382/ Iopubic and ilioischial sutures are obliterated (Brusatte et al., 2013, Fig. S] &lt;/ins&gt;flexor/extensor moment arms plotted against joint angle for important proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See captions for Figs. 9 and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;ten&lt;/ins&gt;.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/ins&gt;proximal thigh &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles&lt;/ins&gt;. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree effectively with B.A.S.'s in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;getting &lt;/ins&gt;a shallow &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;raise &lt;/ins&gt;of your medial/internal LAR moment arm with hip flexion, though B.A.S.'s &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;data substantially a lot more &lt;/ins&gt;strongly favour a medial rotator function for the IC muscle. Our outcomes for the two &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;components &lt;/ins&gt;with the ILFB muscle are very &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;distinct &lt;/ins&gt;from B.A.S.'s in trending toward stronger medial/internal rotation function as the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/ins&gt;matching involving studies, indicating a lateral/external rotation action for this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;substantial &lt;/ins&gt;muscle. Likewise, our ISF data and these of B.A.S. match fairly closely, with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;consistent &lt;/ins&gt;lateral/external rotator action. The FCM and FCLP &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscle tissues &lt;/ins&gt;have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;among &lt;/ins&gt;the largest LAR moment arms for all &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles &lt;/ins&gt;(0.08 m; also observed for our ILp muscle) in our information, but each &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;muscles lower &lt;/ins&gt;their lateral rotator action with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;rising &lt;/ins&gt;hip flexion&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. In B.A.S.'s data a weaker, opposite (medial/internal rotator) trend with hip flexion was located for the FCM, whereas the FCL muscle maintained a little lateral/external rotator action (Fig. 12). The uniarticular hip muscles' LAR moment arms of our model are inclined to switch much less normally (at in vivo hip joint angles 300 ; e.g., Fig. S5) from medial to lateral rotation or vice versa (Fig. 13).Ith joint angle than the S.E.A. and B.A.S. data because we had to constrain this muscle's path in 3D to avoid it cutting by way of bones or other obstacles in some poses. Note also how the S.E.A. outcomes in general show powerful modifications with joint angles, whereas the far more constrained muscle geometry of our model and B.A.S.'s outcomes in additional modest modifications (Fig. 11). Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscle tissues only enable comparisons among our data and these of B.A.S &lt;/ins&gt;.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Badgermail43</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=246787&amp;oldid=prev</id>
		<title>Badgermail43: Створена сторінка: 9 and ten.Figure 12 Hip long-axis [http://edmreality.com/members/sharon67box/activity/334554/ T the ankle for the FDL and gastrocnemius {muscles|muscle tissues]...</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ith_joint_angle_than_the_S.E.A._and_B.A.&amp;diff=246787&amp;oldid=prev"/>
				<updated>2017-10-24T00:02:28Z</updated>
		
		<summary type="html">&lt;p&gt;Створена сторінка: 9 and ten.Figure 12 Hip long-axis [http://edmreality.com/members/sharon67box/activity/334554/ T the ankle for the FDL and gastrocnemius {muscles|muscle tissues]...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Нова сторінка&lt;/b&gt;&lt;/p&gt;&lt;div&gt;9 and ten.Figure 12 Hip long-axis [http://edmreality.com/members/sharon67box/activity/334554/ T the ankle for the FDL and gastrocnemius {muscles|muscle tissues] rotation (LAR) moment arms plotted against hip flexion/extension joint angle for essential proximal thigh muscle tissues. 9.(Fig. 12). In contrast, our IC and IL muscle data agree effectively with B.A.S.'s in possessing a shallow boost on the medial/internal LAR moment arm with hip flexion, despite the fact that B.A.S.'s data a lot a lot more strongly favour a medial rotator function for the IC muscle. Our benefits for the two parts from the ILFB muscle are very diverse from B.A.S.'s in trending toward stronger medial/internal rotation function because the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have improved matching among studies, indicating a lateral/external rotation action for this substantial muscle. Likewise, our ISF information and those of B.A.S. Long-axis rotation (LAR; in Figs. 12 and 13) moment arms for hip muscles only allow comparisons between our information and these of B.A.S . Additionally, thinking about that B.A.S. plotted these moment arms against hip flexion/extension joint angle (modified information shown; Karl T. Bates, pers. comm., 2015), we show them that way right here but in addition plot them against hip LAR joint angle in the Supporting Information (Figs. S1 and S2); having said that, we don't go over the latter final results here. For the AMB1,two muscle tissues we locate regularly weak, near-zero LAR action (lateral/external rotation), whereas B.A.S. showed a steeply decreasing hip medial/internal LAR moment arm because the hip is flexedHutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.21/Figure 11 Hip flexor/extensor moment arms plotted against joint angle for important proximal thigh muscle tissues. See captions for Figs. 9 and 10.Figure 12 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for essential proximal thigh muscle tissues. See caption for Fig. 9.Hutchinson et al. (2015), PeerJ, DOI 10.7717/peerj.22/Figure 13 Hip long-axis rotation (LAR) moment arms plotted against hip flexion/extension joint angle for crucial proximal thigh muscle tissues. See caption for Fig. 9.(Fig. 12). In contrast, our IC and IL muscle data agree effectively with B.A.S.'s in having a shallow enhance of your medial/internal LAR moment arm with hip flexion, even though B.A.S.'s information much extra strongly favour a medial rotator function for the IC muscle. Our outcomes for the two parts with the ILFB muscle are very diverse from B.A.S.'s in trending toward stronger medial/internal rotation function as the hip is flexed, whereas B.A.S.'s favour lateral/external rotation. The results for the OM muscle have greater matching involving studies, indicating a lateral/external rotation action for this massive muscle. Likewise, our ISF data and these of B.A.S. match fairly closely, with constant lateral/external rotator action. The FCM and FCLP muscles have amongst the largest LAR moment arms for all muscle tissues (0.08 m; also observed for our ILp muscle) in our information, but each muscle tissues decrease their lateral rotator action with growing hip flexion.&lt;/div&gt;</summary>
		<author><name>Badgermail43</name></author>	</entry>

	</feed>