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2 ing reactions for cytokeratins 8 and 19, for glutathione S-transferase pi 7, and for luminal gamma-gl
3 B overexpression increases the expression of glutathione-S-transferase pi and protects from oxidant-i
4 s; DHs are negative or only weakly stain for glutathione-S-transferase-pi and are type IV collagenase
5 protein 27, manganese superoxide dismutase, glutathione S-transferase pi, and protein kinase C inhib
7 rmal endothelium including nuclear ferritin, glutathione S-transferase-pi, and heat shock 70-kDa prot
8 sexually dimorphic cytochrome P 450 Cyp2d9, glutathione S-transferase pi, Cyp2a, Cyp2b, and Cyp3a ge
10 was mechanistically linked to alterations in glutathione S-transferase-pi expression and function.
13 in humans, is a noncompetitive inhibitor of glutathione S-transferase pi (GST pi), but its binding s
14 he purpose is to evaluate the association of glutathione S-transferase pi (GST-pi) amplification and
15 creased expression of the genes encoding for glutathione S-transferase Pi (GST-Pi), multidrug resista
16 ss defense enzymes heme-oxygenase (HO)-1 and glutathione S-transferase-pi (GST-pi) in cultured human
18 s of six markers (p53, thymidylate synthase, glutathione s-transferase pi [GST-pi], Bcl 2, beta tubul
19 glutathione S-transferase (alpha-GST) and Pi-glutathione S-transferase (Pi-GST) are potential noninva
20 nhibitor that was purified and identified as glutathione S-transferase Pi (GSTp) and was characterize
21 y induced associations of Fas with ERp57 and glutathione S-transferase pi (GSTP), a protein disulfide
23 glutathione-S transferase Theta (GSTT1), and glutathione-S transferase Pi (GSTP1) polymorphisms, the
24 hich inversely correlated with the levels of glutathione-S-transferase pi (GSTP1), but not GSTpi(1) a
25 egions of two prostate cancer-related genes: glutathione S-transferase pi (GSTPi) and retinoic acid r
29 is mediated through its association with the glutathione S-transferase pi (GSTpi)-JNK complex, thereb
32 bcl-2 expression, proliferative indices and glutathione S-transferase-pi in predicting response to r
34 the first time, suggested that the levels of glutathione S-transferase Pi may play an important role
35 lar proteins involved in detoxification (eg, glutathione S-transferase pi, metallothioneins, human Mu
36 cell division rate, and number and volume of glutathione-S-transferase pi-positive foci were collecte
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