Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes - Wikidata - awgldk - TriplyDB

Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes

Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes

http://www.wikidata.org/entity/Q24310852

about

The MSG1 non-DNA-binding transactivator binds to the p300/CBP coactivators, enhancing their functional link to the Smad transcription factors Transforming growth factor beta -inducible independent binding of SMAD to the Smad7 promoter Identification of a functional binding site for activin on the type I receptor ALK4 Dual roles of Cripto as a ligand and coreceptor in the nodal signaling pathway.Nuclear targeting of transforming growth factor-beta-activated Smad complexes Smad7 antagonizes transforming growth factor beta signaling in the nucleus by interfering with functional Smad-DNA complex formation Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor TAZ controls Smad nucleocytoplasmic shuttling and regulates human embryonic stem-cell self-renewal Transcriptional activating activity of Smad4: roles of SMAD hetero-oligomerization and enhancement by an associating transactivator XIAP, a cellular member of the inhibitor of apoptosis protein family, links the receptors to TAB1-TAK1 in the BMP signaling pathway BF-1 interferes with transforming growth factor beta signaling by associating with Smad partners STRAP and Smad7 synergize in the inhibition of transforming growth factor beta signaling FAST-2 is a mammalian winged-helix protein which mediates transforming growth factor beta signals Synergistic cooperation of TFE3 and smad proteins in TGF-beta-induced transcription of the plasminogen activator inhibitor-1 gene Smad3 recruits the anaphase-promoting complex for ubiquitination and degradation of SnoN CHIP mediates degradation of Smad proteins and potentially regulates Smad-induced transcription Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and -independent pathways Transforming growth factor beta-mediated transcriptional repression of c-myc is dependent on direct binding of Smad3 to a novel repressive Smad binding element Activation of Smad transcriptional activity by protein inhibitor of activated STAT3 (PIAS3)Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease Effect of interleukin-1beta on osteogenic protein 1-induced signaling in adult human articular chondrocytes FoxL2 and Smad3 coordinately regulate follistatin gene transcription Mutant p53 attenuates the SMAD-dependent transforming growth factor beta1 (TGF-beta1) signaling pathway by repressing the expression of TGF-beta receptor type II Smads bind directly to the Jun family of AP-1 transcription factors Targeting TGF-β signaling in cancer Switching Roles of TGF-β in Cancer Development: Implications for Therapeutic Target and Biomarker Studies Importin beta mediates nuclear translocation of Smad 3 Smad6 as a transcriptional corepressor TGIF2 interacts with histone deacetylase 1 and represses transcription Crossing Smads A Smad-binding element in intron 1 participates in activin-dependent regulation of the follistatin gene TGFβ signalling in context Transforming growth factor beta1 induces nuclear export of inhibitory Smad7 Functional association of TGF-beta receptor II with cyclin B Gatifloxacin induces S and G2-phase cell cycle arrest in pancreatic cancer cells via p21/p27/p53 BMP canonical Smad signaling through Smad1 and Smad5 is required for endochondral bone formation Galectin-9-CD44 interaction enhances stability and function of adaptive regulatory T cells Master transcription factors determine cell-type-specific responses to TGF-β signaling Targeted disruption of SMAD3 results in impaired mucosal immunity and diminished T cell responsiveness to TGF-beta The role of FAST-1 and Smads in transcriptional regulation by activin during early Xenopus embryogenesis

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Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes

http://www.wikidata.org/entity/Q24310852

description

1997 nî lūn-bûn

@nan

1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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Dual role of the Smad4/DPC4 tu ...... ible transcriptional complexes

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C Pouponnot

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F Liu

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P2860

MADR2 is a substrate of the TGFbeta receptor and its phosphorylation is required for nuclear accumulation and signaling

Heteromeric and homomeric interactions correlate with signaling activity and functional cooperativity of Smad3 and Smad4/DPC4

TGF-beta receptor-mediated signalling through Smad2, Smad3 and Smad4

MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

MADR1, a MAD-related protein that functions in BMP2 signaling pathways

Receptor-associated Mad homologues synergize as effectors of the TGF-beta response

p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

Serine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1

Vascular MADs: two novel MAD-related genes selectively inducible by flow in human vascular endothelium

Mad-related genes in the human

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3157-3167

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scholarly article

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2157121

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10.1101/GAD.11.23.3157

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23

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11

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Joan Massagué Solé

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1997-12-01T00:00:00Z

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13839722

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9389648

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BMP signaling pathway

Transforming growth factor beta 1

Forkhead box H1

SMAD2-SMAD3 protein complex

Bone morphogenetic protein receptor type 1A

SMAD family member 4

SMAD family member 2

SMAD family member 1

Bone morphogenetic protein 4

Transforming growth factor beta receptor 1

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316747

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