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  6. The exercise of recombinant enolase was assessed by measuring the transformation of NADHH to NAD as explained elsewhere‏‎ (19:09, 4 лютого 2017)
  7. Representative fluorescent traces of cytosolic Ca2 in pancreatic primary b cells transfected with either siNCLX or siControl loaded with Fura 2 AM and stimulated with high glucose following the same experimental paradigm described‏‎ (19:16, 4 лютого 2017)
  8. To increase accessibility, the epitope was flanked with fragments from the extracellular D12 loop of the ClC-five chloride channel‏‎ (19:28, 4 лютого 2017)
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  10. Here, we show that the lysine analogue ACA and recombinant enolase substantially inhibited L. interrogans-‏‎ (19:30, 4 лютого 2017)
  11. Below, we show that the lysine analogue ACA and recombinant enolase drastically inhibited L. interrogans-‏‎ (19:33, 4 лютого 2017)
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  18. Our results indicate that NCLX activity is critical for clearance of mitochondrial Ca2 and is therefore a rate limiting player in the mitochondrial Ca2 response induced by glucose‏‎ (19:49, 4 лютого 2017)
  19. All experiments were performed with approval of the ethical committee of the Katholieke Universiteit Leuven‏‎ (19:58, 4 лютого 2017)
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  21. Colocalization of C/EBPb or c-Jun with CREB figure out genes which expression and induction upon differentiation is dependent on C/EBPb and c-Jun features‏‎ (20:09, 4 лютого 2017)
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  27. This evaluation implies that combinatorial sited and combination of consensus transcription factor binding internet sites direct to particular‏‎ (20:33, 4 лютого 2017)
  28. This examination implies that combinatorial sited and mix of consensus transcription element binding websites direct to specific‏‎ (20:37, 4 лютого 2017)
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  33. Promonocytes were identified based on an increased nuclear/ cytoplasmic ratio, and granulocyes were identified based on their specific nuclear morphology‏‎ (20:44, 4 лютого 2017)
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  39. Several Nmyristoylated proteins enjoy important roles in regulating mobile construction and operate‏‎ (21:09, 4 лютого 2017)
  40. Briefly, a set of four proofreading PCR reactions with mutagenized primers was carried out using the psiCHECK2-Nf1 39-UTR vector as a template‏‎ (21:10, 4 лютого 2017)
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  45. Additionally, the injected human apoA-I facilitated HDL development as evidenced by its existence in lipoprotein fractions attained by FPLC‏‎ (21:18, 4 лютого 2017)
  46. Additionally, the injected human apoA-I facilitated HDL development as evidenced by its presence in lipoprotein fractions received by FPLC‏‎ (21:21, 4 лютого 2017)
  47. Affinity purification of FLAG-tagged protein was carried out as described beforehand‏‎ (21:34, 4 лютого 2017)
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  50. The mRNAs encoding the cDNAs were well prepared employing an AmpliScribe T7 Substantial Yield Transcription Kit in accordance with manufacturer's directions‏‎ (21:41, 4 лютого 2017)

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