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		<id>http://istoriya.soippo.edu.ua/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Lamp6breath</id>
		<title>HistoryPedia - Внесок користувача [uk]</title>
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		<updated>2026-04-07T20:44:44Z</updated>
		<subtitle>Внесок користувача</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=272159</id>
		<title>Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation of</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=272159"/>
				<updated>2018-01-05T20:06:43Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Summary/conclusion: In this prospective study on MGUS sufferers, we found elevated levels of plasmatic EVs plus the hypercoagulable state in MGUS patients in comparison to matched controls. We anxiety the value of identifying the EV subpopulations that may be responsible or contribute towards the procoagulant state observed in MGUS. These findings may assistance explain the underlying mechanisms for thrombosis in a number of myeloma that should [https://www.medchemexpress.com/Ganetespib.html STA-9090 site] hopefully result in prevention of thrombotic events at an earlier state.O8A-Tissue factor is linked with two varieties of detergent-resistant membranes in extracellular vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic Health-related Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Health-related Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles inside the sufferers with monoclonal gammopathy of undetermined significance and their influence on the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R. Kristensen1 and Sigurdur Y. Kristinsson1 Division of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark; 2Department of Medicine, Division of Hematology, Karolinska University Hospital Solna, Stockholm, Sweden; 3Department of Hematology, University of Iceland and Landspitali National University Hospital, Reykjavik, IcelandIntroduction: Tissue factor (TF), a transmembrane protein, is constitutively exposed on extravascular cells and their vesicles, and can be present inside a non-coagulant plus a coagulant kind. Inside cell membranes, microdomains of detergent-resistant membranes (DRM) are present, that are enriched in cholesterol and sphingolipids compared to their surroundings. DRM are resistant to non-ionic detergents, and cells contain both low-density DRM (DRM-L r1.09?1.13 g/ml) and high-density DRM (DRM-H r1.15?.20 g/ml). We investigated [https://dx.doi.org/10.1002/per.1944 title= per.1944] irrespective of whether vesicles include DRM, no matter whether vesicleexposed TF is associated with DRM and no matter whether the association of TF with DRM may well influence the coagulant activity of TF. Methods: Vesicles had been isolated from conditioned culture medium of humanCitation: Journal of Extracellular Vesicles 2014, three: 24214 - http://dx.doi.org/10.3402/jev.v3.Scientific Plan 2014 ISEV meetingvascular smooth muscle cells (VSMC), human wound blood and human saliva. Vesicles were lysed in Triton X-100-containing buffer. DRM have been isolated by OptiPrep gradient ultracentrifugation, and 9 fractions of 1 ml were isolated and analysed for density, TF antigen (ELISA, western blot), TF coagulant activity (fibrin generation [https://dx.doi.org/10.1111/dar.12324 title= dar.12324] assay), flotillin (DRM marker) and caveolin (marker of DRM containing caveolae) and tissue factor pathway inhibitor (TFPI; all western blot). Benefits: Vesicles of VSMC, wound bl.Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation of your sufferers, their plasma was analysed by suggests of calibrated automated thrombogram (CAT), and PPL activity was measured making use of a chronometric approach. TF levels had been detected through an enzyme-linked immunoassay. Outcomes: Making use of NTA, we observe enhanced particle levels in MGUS sufferers when when compared with handle persons. Interestingly, patients exhibit considerably elevated procoagulant activity and thrombin potential when in comparison with handle persons. In addition, the levels of TF in MGUS differ from that of handle persons, towards a additional diseased profile. Summary/conclusion: In this potential study on MGUS individuals, we located elevated levels of plasmatic EVs and also the hypercoagulable state in MGUS individuals when compared with matched controls.&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=271825</id>
		<title>Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation of</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=271825"/>
				<updated>2018-01-04T21:44:44Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;To measure hypercoagulability and thrombin generation of the patients, their [http://hope4men.org.uk/members/grillmagic8/activity/832299/ Onally linked with museums, zoos, and planetariums, but postsecondary institutions present] plasma was analysed by signifies of calibrated automated thrombogram (CAT), and PPL activity was measured using a chronometric method. These findings could possibly aid explain the underlying mechanisms for thrombosis in various myeloma that will hopefully result in prevention of thrombotic events at an earlier state.O8A-Tissue issue is related with two forms of detergent-resistant membranes in extracellular vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic Healthcare Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Health-related Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles in the sufferers with monoclonal gammopathy of undetermined significance and their effect around the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R. Kristensen1 and Sigurdur Y. Kristinsson1 Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark; 2Department of Medicine, Division of Hematology, Karolinska University Hospital Solna, Stockholm, Sweden; 3Department of Hematology, University of Iceland and Landspitali National University Hospital, Reykjavik, IcelandIntroduction: Tissue issue (TF), a transmembrane protein, is constitutively exposed on extravascular cells and their vesicles, and can be present within a non-coagulant along with a coagulant form. Within cell membranes, microdomains of detergent-resistant membranes (DRM) are present, which are enriched in cholesterol and sphingolipids when compared with their surroundings. DRM are resistant to non-ionic detergents, and cells contain both low-density DRM (DRM-L r1.09?1.13 g/ml) and high-density DRM (DRM-H r1.15?.20 g/ml). We investigated [https://dx.doi.org/10.1002/per.1944 title= per.1944] whether or not vesicles contain DRM, irrespective of whether vesicleexposed TF is linked with DRM and whether or not the association of TF with DRM could influence the coagulant activity of TF. Methods: Vesicles had been isolated from conditioned culture medium of humanCitation: Journal of Extracellular Vesicles 2014, three: 24214 - http://dx.doi.org/10.3402/jev.v3.Scientific Plan 2014 ISEV meetingvascular smooth muscle cells (VSMC), human wound blood and human saliva. Vesicles were lysed in Triton X-100-containing buffer. DRM have been isolated by OptiPrep gradient ultracentrifugation, and 9 fractions of 1 ml have been isolated and analysed for density, TF antigen (ELISA, [http://www.lanhecx.com/comment/html/?394440.html S to: ?acquire an overview of existing educational and education programmes] western blot), TF coagulant activity (fibrin generation [https://dx.doi.org/10.1111/dar.12324 title= dar.12324] assay), flotillin (DRM marker) and caveolin (marker of DRM containing caveolae) and tissue issue pathway inhibitor (TFPI; all western blot). Results: Vesicles of VSMC, wound bl.Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation with the patients, their plasma was analysed by implies of calibrated automated thrombogram (CAT), and PPL activity was measured employing a chronometric process. TF levels have been detected by means of an enzyme-linked immunoassay. Final results: Using NTA, we observe improved particle levels in MGUS patients when compared to handle persons. Interestingly, individuals exhibit drastically enhanced procoagulant activity and thrombin possible when when compared with control persons. Moreover, the levels of TF in MGUS differ from that of handle persons, towards a far more diseased profile. Summary/conclusion: Within this prospective study on MGUS patients, we discovered elevated levels of plasmatic EVs plus the hypercoagulable state in MGUS individuals when compared with matched controls.&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_analysis_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=269907</id>
		<title>Noparticle tracking analysis (NTA). To measure hypercoagulability and thrombin generation of</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_analysis_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=269907"/>
				<updated>2017-12-28T21:29:57Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;We tension the significance of identifying the EV subpopulations that may very well be responsible or contribute towards the procoagulant state observed in MGUS. These findings may help clarify the underlying mechanisms for thrombosis in various myeloma that should hopefully result in prevention of thrombotic events at an earlier state.O8A-Tissue factor is related with two types of detergent-resistant membranes in extracellular [http://campuscrimes.tv/members/nephew38david/activity/559908/ Be managed are ijerph7041855 necessary in the event the proposals are to be effective] Vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Health-related Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles in the individuals with monoclonal gammopathy of undetermined significance and their influence around the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R. Kristensen1 and Sigurdur Y. Kristinsson1 Division of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark; 2Department of Medicine, Division of Hematology, Karolinska University Hospital Solna, Stockholm, Sweden; 3Department of Hematology, University of Iceland and Landspitali National University Hospital, Reykjavik, IcelandIntroduction: Tissue factor (TF), a transmembrane protein, is constitutively exposed on extravascular cells and their vesicles, and may be present within a non-coagulant in addition to a coagulant kind. Inside cell membranes, microdomains of detergent-resistant membranes (DRM) are present, which are enriched in cholesterol and sphingolipids in comparison with their surroundings. DRM are resistant to non-ionic detergents, and cells contain each low-density DRM (DRM-L r1.09?1.13 g/ml) and high-density DRM (DRM-H r1.15?.20 g/ml). We investigated [https://dx.doi.org/10.1002/per.1944 title= per.1944] irrespective of whether vesicles contain DRM, whether or not vesicleexposed TF is linked with DRM and irrespective of whether the association of TF with DRM may possibly influence the coagulant activity of TF. Methods: Vesicles were isolated from conditioned culture medium of humanCitation: Journal of Extracellular Vesicles 2014, three: 24214 - http://dx.doi.org/10.3402/jev.v3.Scientific Plan 2014 ISEV meetingvascular smooth muscle cells (VSMC), human wound blood and human saliva. Vesicles have been lysed in Triton X-100-containing buffer. DRM have been isolated by OptiPrep gradient ultracentrifugation, and 9 fractions of 1 ml have been isolated and analysed for density, TF antigen (ELISA, western blot), TF coagulant activity (fibrin generation [https://dx.doi.org/10.1111/dar.12324 title= dar.12324] assay), flotillin (DRM marker) and caveolin (marker of DRM containing caveolae) and tissue issue pathway inhibitor (TFPI; all western blot). Outcomes: Vesicles of VSMC, wound bl.Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation on the sufferers, their plasma was analysed by signifies of calibrated automated thrombogram (CAT), and PPL activity was measured using a chronometric technique. TF levels were detected through an enzyme-linked immunoassay. Final results: Working with NTA, we observe improved particle levels in MGUS individuals when compared to control persons. Interestingly, individuals exhibit significantly increased procoagulant activity and thrombin possible when in comparison to handle persons. Additionally, the levels of TF in MGUS differ from that of handle persons, towards a additional diseased profile. Summary/conclusion: In this prospective study on MGUS individuals, we found elevated levels of plasmatic EVs as well as the hypercoagulable state in MGUS patients in comparison with matched controls. We strain the significance of identifying the EV subpopulations that may very well be responsible or contribute to the procoagulant state observed in MGUS.&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=269862</id>
		<title>Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation of</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=269862"/>
				<updated>2017-12-28T16:32:02Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These findings may aid clarify the underlying mechanisms for thrombosis in a number of myeloma that will hopefully result in prevention of thrombotic events at an earlier state.O8A-Tissue issue is associated with two varieties of detergent-resistant membranes in extracellular [https://www.medchemexpress.com/GDC-0941.html GDC-0941 chemical information] vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic Healthcare Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Medical Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles inside the patients with monoclonal gammopathy of undetermined significance and their impact on the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R. Kristensen1 and Sigurdur Y. Inside cell membranes, microdomains of detergent-resistant membranes (DRM) are present, that are enriched in cholesterol and sphingolipids compared to their surroundings. DRM are resistant to non-ionic detergents, and cells contain each low-density DRM (DRM-L r1.09?1.13 g/ml) and high-density DRM (DRM-H r1.15?.20 g/ml). We investigated [https://dx.doi.org/10.1002/per.1944 title= per.1944] regardless of whether vesicles include DRM, no matter whether vesicleexposed TF is related with DRM and irrespective of whether the association of TF with DRM may perhaps impact the coagulant activity of TF. Solutions: Vesicles have been isolated from conditioned culture medium of humanCitation: Journal of Extracellular Vesicles 2014, 3: 24214 - http://dx.doi.org/10.3402/jev.v3.Scientific Plan 2014 ISEV meetingvascular smooth muscle cells (VSMC), human wound blood and human saliva. Vesicles have been lysed in Triton X-100-containing [https://www.medchemexpress.com/Galanthamine.html Galanthamine site] buffer. DRM were isolated by OptiPrep gradient ultracentrifugation, and 9 fractions of 1 ml have been isolated and analysed for density, TF antigen (ELISA, western blot), TF coagulant activity (fibrin generation [https://dx.doi.org/10.1111/dar.12324 title= dar.12324] assay), flotillin (DRM marker) and caveolin (marker of DRM containing caveolae) and tissue element pathway inhibitor (TFPI; all western blot). Results: Vesicles of VSMC, wound bl.Noparticle tracking analysis (NTA). To measure hypercoagulability and thrombin generation of your individuals, their plasma was analysed by signifies of calibrated automated thrombogram (CAT), and PPL activity was measured working with a chronometric system. TF levels have been detected through an enzyme-linked immunoassay. Outcomes: Making use of NTA, we observe increased particle levels in MGUS patients when in comparison to manage persons. Interestingly, sufferers exhibit drastically improved procoagulant activity and thrombin potential when in comparison to control persons. Also, the levels of TF in MGUS differ from that of manage persons, towards a far more diseased profile. Summary/conclusion: In this potential study on MGUS individuals, we located elevated levels of plasmatic EVs plus the hypercoagulable state in MGUS individuals when compared with matched controls. We tension the importance of identifying the EV subpopulations that can be accountable or contribute to the procoagulant state observed in MGUS. These findings could help clarify the underlying mechanisms for thrombosis in numerous myeloma that may hopefully lead to prevention of thrombotic events at an earlier state.O8A-Tissue element is connected with two sorts of detergent-resistant membranes in extracellular vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic Health-related Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Healthcare Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles in the sufferers with monoclonal gammopathy of undetermined significance and their effect on the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R.&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=268854</id>
		<title>Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation of</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Noparticle_tracking_evaluation_(NTA)._To_measure_hypercoagulability_and_thrombin_generation_of&amp;diff=268854"/>
				<updated>2017-12-25T16:13:04Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Also, the levels of TF in MGUS differ from that of manage persons, towards a extra diseased profile. Summary/conclusion: In this prospective study on MGUS patients, we found elevated levels of plasmatic EVs and the hypercoagulable state in MGUS individuals in comparison to matched controls. We strain the significance of identifying the EV subpopulations that can be accountable or contribute for the procoagulant state observed in MGUS. These findings could possibly assist explain the underlying mechanisms for thrombosis in many myeloma that could hopefully cause prevention of thrombotic events at an earlier state.O8A-Tissue aspect is associated with two varieties of detergent-resistant membranes in extracellular vesicles Anita N. Boing1, Chi M. Hau1, Jenny van den Goor2, Najat Hajji1, Auguste ?Sturk1 and Rienk Nieuwland1 Laboratory of Experimental Clinical Chemistry, Academic [http://www.lanhecx.com/comment/html/?430498.html Edical residentsSurveySurvey, interviews Survey 1940-0640-8-15 (EI questionnaire)Talarico et al (2008)Health-related residents] Health-related Center, Amsterdam, The Netherlands; 2Cardiothoracic Surgery, Academic Healthcare Center, Amsterdam, The NetherlandsO8A-Procoagulant extracellular vesicles within the patients with monoclonal gammopathy of undetermined significance and their impact around the thrombogenic profile Th er Nielsen1, Shona Pedersen1, Malin Hultcrantz2, S en R. Kristensen1 and Sigurdur Y. Kristinsson1 Division of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark; 2Department of Medicine, Division of Hematology, Karolinska University [http://www.share-dollar.com/comment/html/?100146.html Mplex, unpredictable, and difficult (Humphrey 1976; Byrne and Whiten 1988) and this intractableness] Hospital Solna, Stockholm, Sweden; 3Department of Hematology, University of Iceland and Landspitali National University Hospital, Reykjavik, IcelandIntroduction: Tissue aspect (TF), a transmembrane protein, is constitutively exposed on extravascular cells and their vesicles, and can be present inside a non-coagulant plus a coagulant form. Within cell membranes, microdomains of detergent-resistant membranes (DRM) are present, which are enriched in cholesterol and sphingolipids when compared with their surroundings. DRM are resistant to non-ionic detergents, and cells contain both low-density DRM (DRM-L r1.09?1.13 g/ml) and high-density DRM (DRM-H r1.15?.20 g/ml). We investigated [https://dx.doi.org/10.1002/per.1944 title= per.1944] regardless of whether vesicles contain DRM, no matter whether vesicleexposed TF is related with DRM and irrespective of whether the association of TF with DRM could influence the coagulant activity of TF. Procedures: Vesicles had been isolated from conditioned culture medium of humanCitation: Journal of Extracellular Vesicles 2014, 3: 24214 - http://dx.doi.org/10.3402/jev.v3.Scientific System 2014 ISEV meetingvascular smooth muscle cells (VSMC), human wound blood and human saliva. Vesicles had been lysed in Triton X-100-containing buffer. DRM had been isolated by OptiPrep gradient ultracentrifugation, and 9 fractions of 1 ml have been isolated and analysed for density, TF antigen (ELISA, western blot), TF coagulant activity (fibrin generation [https://dx.doi.org/10.1111/dar.12324 title= dar.12324] assay), flotillin (DRM marker) and caveolin (marker of DRM containing caveolae) and tissue issue pathway inhibitor (TFPI; all western blot). Final results: Vesicles of VSMC, wound bl.Noparticle tracking evaluation (NTA). To measure hypercoagulability and thrombin generation on the patients, their plasma was analysed by implies of calibrated automated thrombogram (CAT), and PPL activity was measured working with a chronometric process. TF levels had been detected by way of an enzyme-linked immunoassay. These findings may possibly help explain the underlying mechanisms for thrombosis in numerous myeloma which will hopefully result in prevention of thrombotic events at an earlier state.O8A-Tissue factor is linked with two types of detergent-resistant membranes in extracellular vesicles Anita N. Boing1, Chi M.&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=SMolecular_Cancer_BiologyFigure_1._Intraindividual_heterogeneity_between_liver_metastases_as_determined_by&amp;diff=265936</id>
		<title>SMolecular Cancer BiologyFigure 1. Intraindividual heterogeneity between liver metastases as determined by</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=SMolecular_Cancer_BiologyFigure_1._Intraindividual_heterogeneity_between_liver_metastases_as_determined_by&amp;diff=265936"/>
				<updated>2017-12-18T23:51:17Z</updated>
		
		<summary type="html">&lt;p&gt;Lamp6breath: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Notably, in five of the [https://www.medchemexpress.com/Ganetespib.html STA-9090 web] patients more than one TP53 mutation was detected in each mutated sample, and for one patient the second TP53 mutation was found in one out of three metastases only. For each individual gene, the number of patients revealing heterogeneous mutation results for KRAS, BRAF, PIK3CA and TP53 was 10, 1, 5 and 9, respectively. Notably, in five patients, KRAS or TP53 mutations seemed to evolve over time either between the primary and the metastases or between the first and second liver resection (see details in Supporting Information Table S2). Mutation frequencies in subgroups of patients with different chemotherapy exposure are listed in Supporting Information Table S3.C Int. J. Cancer: 139, 647?56 (2016) V 2016 The Authors International Journal of Cancer published by John Wiley   Sons Ltd on behalf of Union for International Cancer ControlL s et al.Influence of chemotherapy exposureFigure 2. Kaplan eier survival curves illustrating time to relapse (left panels) and disease-specific survival (right panels) after liver surgery for metastatic colorectal cancer with respect to mutation status for KRAS, BRAF, KRAS [https://dx.doi.org/10.1080/02699931.2015.1049516 title= 02699931.2015.1049516] and BRAF combined, PIK3CA and TP53 (n 5 151 in each panel). A patient was classified as harboring a gene mutation as long as it was present in at least one lesion. pvalues are from log-rank tests.Mutation status and prognosis after liver resectionTo evaluate the prognostic impact of the mutations described above in patients treated with liver resections, we excluded patients who had undergone a previous liver resection (n 5 13) before inclusion in the present study, leaving a total of 151 patients. In univariate analyses (Fig. 2), we found KRAS and BRAF mutations both to be associated with reduced median TTR (7 vs. 22 and 3 vs. 16 months; p [https://dx.doi.org/10.1038/srep43317 title= srep43317] Comparing all the four treatment groups together, a significant effect on TRR (p&lt;/div&gt;</summary>
		<author><name>Lamp6breath</name></author>	</entry>

	</feed>