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  39. We demonstrate that, although broad access to ART remains an elusive goal of low and middle income countries‏‎ (2 версії)
  40. We did not observe changes in cell viability or proliferative fraction in the presence of up to 300 mM menthol or 10 mM icilin in any cell line‏‎ (2 версії)
  41. We did not prospectively collect peripheral blood on these patients so it is unknown if these changes in tissue metabolic substrates correlate with peripheral abnormalities‏‎ (2 версії)
  42. We have not observed subcutaneous tumors in our sDll4-Fc treated mice or Dll4 mutant mice for the duration of the experiments‏‎ (2 версії)
  43. We have shown previously that WA ROS production was measured by flow cytometry or immunofluorescence microscopy following staining with MitoSOX Red and EPR‏‎ (2 версії)
  44. We included consecutive patients discharged from the general internal medicine service at St‏‎ (2 версії)
  45. We observed a WFA dose- and time-dependent lower in pAKT levels, but not total AKT levels, in STS cells‏‎ (2 версії)
  46. We observed significantly reduced tolerance in DFgABC3 strains for the triazoles tebuconazole, prothioconazole and epoxyconazole‏‎ (2 версії)
  47. We performed in vitro studies to determine the level of cytotoxicity induced by TQ in human glioblastoma cells‏‎ (2 версії)
  48. We reasoned that these schistosome peptidases besides being likely vaccine targets may also, because of their intrinsic proteolytic activity‏‎ (2 версії)
  49. We selected a number of genes that had roles in transcriptional regulation, development and signal transduction and tested the expression level of these genes using quantitative RT-PCR‏‎ (2 версії)
  50. We therefore employed a diverse method to swiftly assess achievable interference with the specifically‏‎ (2 версії)

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