Mechanism of a transcriptional cross talk between transforming growth factor-beta-regulated Smad3 and Smad4 proteins and orphan nuclear receptor hepatocyte nuclear factor-4
about
Crosstalk of HNF4α with extracellular and intracellular signaling pathways in the regulation of hepatic metabolism of drugs and lipidsIdentification of glucocorticoid receptor domains involved in transrepression of transforming growth factor-beta actionTransforming growth factor-beta-mediated signaling via the p38 MAP kinase pathway activates Smad-dependent transcription through SUMO-1 modification of Smad4Cx43 mediates TGF-beta signaling through competitive Smads binding to microtubules.An integrative ChIP-chip and gene expression profiling to model SMAD regulatory modules.Mutations in protein-binding hot-spots on the hub protein Smad3 differentially affect its protein interactions and Smad3-regulated gene expressionGlobal gene expression responses to low- or high-dose radiation in a human three-dimensional tissue model.Differential effects of continuous and intermittent 17beta-estradiol replacement and tamoxifen therapy on the prevention of glomerulosclerosis: modulation of the mesangial cell phenotype in vivo.Fn14, a Downstream Target of the TGF-β Signaling Pathway, Regulates Fibroblast Activation.Prediction and Validation of Transcription Factors Modulating the Expression of Sestrin3 Gene Using an Integrated Computational and Experimental Approach.Nuclear receptors in the cross-talk of drug metabolism and inflammation.Cell type-specific target selection by combinatorial binding of Smad2/3 proteins and hepatocyte nuclear factor 4alpha in HepG2 cellsCritical role of charged residues in helix 7 of the ligand binding domain in Hepatocyte Nuclear Factor 4alpha dimerisation and transcriptional activity.Inhibition of hepatocyte nuclear factor 4 transcriptional activity by the nuclear factor kappaB pathway.Critical role of residues defining the ligand binding pocket in hepatocyte nuclear factor-4alpha.Mice exclusively expressing the short isoform of Smad2 develop normally and are viable and fertile.Expression of the alpha7 isoform of hepatocyte nuclear factor (HNF) 4 is activated by HNF6/OC-2 and HNF1 and repressed by HNF4alpha1 in the liver.Hepatocyte Nuclear Factor 4 Alpha Promotes Definitive Endoderm Differentiation from Human Induced Pluripotent Stem Cells.Orphan nuclear receptor small heterodimer partner inhibits transforming growth factor-beta signaling by repressing SMAD3 transactivation.Fatty Acid Regulation of Gene Transcription
P2860
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P2860
Mechanism of a transcriptional cross talk between transforming growth factor-beta-regulated Smad3 and Smad4 proteins and orphan nuclear receptor hepatocyte nuclear factor-4
description
2003 nî lūn-bûn
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2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
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name
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@ast
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@en
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@nl
type
label
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@ast
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@en
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@nl
prefLabel
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@ast
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@en
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@nl
P2093
P2860
P356
P1476
Mechanism of a transcriptional ...... or hepatocyte nuclear factor-4
@en
P2093
Aristidis Moustakas
Dimitris Kardassis
Keiko Shiraishi
Margarita Hadzopoulou-Cladaras
Ulrich Valcourt
Vassiliki Prokova
Vassilis I Zannis
Wan-Chih Chou
P2860
P304
P356
10.1091/MBC.E02-07-0375
P577
2003-03-01T00:00:00Z