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

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

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

http://www.wikidata.org/entity/Q24310282

about

Cloning of a novel signaling molecule, AMSH-2, that potentiates transforming growth factor beta signaling Transforming growth factor beta -inducible independent binding of SMAD to the Smad7 promoter Type III TGF-beta receptor-independent signalling of TGF-beta2 via TbetaRII-B, an alternatively spliced TGF-beta type II receptor Smad proteins function as co-modulators for MEF2 transcriptional regulatory proteins Transforming growth factor-beta receptor-associated protein 1 is a Smad4 chaperone The adaptor molecule Disabled-2 links the transforming growth factor beta receptors to the Smad pathway.Functional proteomics mapping of a human signaling pathway Nuclear targeting of transforming growth factor-beta-activated Smad complexes Sumoylated SnoN represses transcription in a promoter-specific manner Smad3 allostery links TGF-beta receptor kinase activation to transcriptional control Epicardial-myocardial signaling directing coronary vasculogenesis Smad inhibition by the Ste20 kinase Misshapen Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes Potentiation of Smad-mediated transcriptional activation by the RNA-binding protein RBPMS TGF-beta receptor-mediated signalling through Smad2, Smad3 and Smad4 Identification of PCTA, a TGIF antagonist that promotes PML function in TGF-beta signalling Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor Vascular MADs: two novel MAD-related genes selectively inducible by flow in human vascular endothelium TAZ controls Smad nucleocytoplasmic shuttling and regulates human embryonic stem-cell self-renewal A novel protein distinguishes between quiescent and activated forms of the type I transforming growth factor beta receptor Identification of novel Smad2 and Smad3 associated proteins in response to TGF-beta1 Hgs (Hrs), a FYVE domain protein, is involved in Smad signaling through cooperation with SARA.STRAP and Smad7 synergize in the inhibition of transforming growth factor beta signaling TLP, a novel modulator of TGF-beta signaling, has opposite effects on Smad2- and Smad3-dependent signaling Synergistic cooperation of TFE3 and smad proteins in TGF-beta-induced transcription of the plasminogen activator inhibitor-1 gene A mechanism of suppression of TGF-beta/SMAD signaling by NF-kappa B/RelA Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and -independent pathways Homeoprotein DLX-1 interacts with Smad4 and blocks a signaling pathway from activin A in hematopoietic cells Transforming growth factor beta-mediated transcriptional repression of c-myc is dependent on direct binding of Smad3 to a novel repressive Smad binding element Review of the activation of TGF-beta in immunity Association of Smads with lymphoid enhancer binding factor 1/T cell-specific factor mediates cooperative signaling by the transforming growth factor-beta and wnt pathways Interaction of the PA2G4 (EBP1) protein with ErbB-3 and regulation of this binding by heregulin Specificity in transforming growth factor beta-induced transcription of the plasminogen activator inhibitor-1 gene: interactions of promoter DNA, transcription factor muE3, and Smad proteins Transforming growth factor beta-induced phosphorylation of Smad3 is required for growth inhibition and transcriptional induction in epithelial cells Inhibition of transforming growth factor-beta1-induced signaling and epithelial-to-mesenchymal transition by the Smad-binding peptide aptamer Trx-SARA Glucocorticoid receptor inhibits transforming growth factor-beta signaling by directly targeting the transcriptional activation function of Smad3 Loss of p12CDK2-AP1 expression in human oral squamous cell carcinoma with disrupted transforming growth factor-beta-Smad signaling pathway Smads bind directly to the Jun family of AP-1 transcription factors TGF-beta expression during rat pregnancy and activity on decidual cell survival Targeting TGF-β signaling in cancer

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

http://www.wikidata.org/entity/Q24310282

description

1996 nî lūn-bûn

@nan

1996 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年论文

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name

MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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type

label

MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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prefLabel

MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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MADR2 is a substrate of the TG ...... ear accumulation and signaling

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J L Wrana

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L Attisano

http://www.w3.org/2001/XMLSchema#string

M Macías-Silva

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P A Hoodless

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R Pirone

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S Abdollah

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scholarly article

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10.1016/S0092-8674(00)81817-6

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type I transforming growth factor beta receptor binding

phosphorylation

SMAD family member 2

Transforming growth factor beta receptor 1