about
A Reduced-Amide Inhibitor of Pin1 Binds in a Conformation Resembling a Twisted-Amide Transition StateStereochemical Control in the Still-Wittig Rearrangement Synthesis of Cyclohexyl (Z)-Alkene Inhibitors of Pin1Regulation of cardiac hypertrophic signaling by prolyl isomerase Pin1Molecular basis for an ancient partnership between prolyl isomerase Pin1 and phosphatase inhibitor-2Aberrant regulation of FBW7 in cancer.In silico identification of potential key regulatory factors in smoking-induced lung cancer.Oxidative stress in HPV-driven viral carcinogenesis: redox proteomics analysis of HPV-16 dysplastic and neoplastic tissues.Cyclohexyl ketone inhibitors of Pin1 dock in a trans-diaxial cyclohexane conformation.Investigating Dynamic Interdomain Allostery in Pin1Cross-talk of phosphorylation and prolyl isomerization of the C-terminal domain of RNA Polymerase II.ShaPINg Cell Fate Upon DNA Damage: Role of Pin1 Isomerase in DNA Damage-Induced Cell Death and Repair.Convergent synthesis of alpha-ketoamide inhibitors of Pin1.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Pin1 as an anticancer drug target.
@ast
Pin1 as an anticancer drug target.
@en
Pin1 as an anticancer drug target.
@nl
type
label
Pin1 as an anticancer drug target.
@ast
Pin1 as an anticancer drug target.
@en
Pin1 as an anticancer drug target.
@nl
prefLabel
Pin1 as an anticancer drug target.
@ast
Pin1 as an anticancer drug target.
@en
Pin1 as an anticancer drug target.
@nl
P1476
Pin1 as an anticancer drug target.
@en
P2093
Guoyan G Xu
P304
P356
10.1358/DNP.2009.22.7.1381751
P577
2009-09-01T00:00:00Z