Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta. - Wikidata - awgldk - TriplyDB

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

http://www.wikidata.org/entity/Q34771801

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Response gene to complement 32 interacts with Smad3 to promote epithelial-mesenchymal transition of human renal tubular cells Transcriptional induction of Smurf2 ubiquitin ligase by TGF-beta The SWI/SNF chromatin remodeling complex regulates myocardin-induced smooth muscle-specific gene expression Response gene to complement 32 is essential for fibroblast activation in renal fibrosis Association of the actin-binding protein transgelin with lymph node metastasis in human colorectal cancer Smad2 and myocardin-related transcription factor B cooperatively regulate vascular smooth muscle differentiation from neural crest cells.JunB mediates basal- and TGFβ1-induced smooth muscle cell contractility Targeting the activin type IIB receptor to improve muscle mass and function in the mdx mouse model of Duchenne muscular dystrophy.Role of smooth muscle protein SM22α in glomerular epithelial cell injury.Smad3-mediated myocardin silencing: a novel mechanism governing the initiation of smooth muscle differentiation.Smad2 and PEA3 cooperatively regulate transcription of response gene to complement 32 in TGF-β-induced smooth muscle cell differentiation of neural crest cells.Caffeine and rolipram affect Smad signalling and TGF-β1 stimulated CTGF and transgelin expression in lung epithelial cells.Role played by Prx1-dependent extracellular matrix properties in vascular smooth muscle development in embryonic lungs RhoA modulates Smad signaling during transforming growth factor-beta-induced smooth muscle differentiation.Cell division cycle 7 is a novel regulator of transforming growth factor-β-induced smooth muscle cell differentiation.Transforming growth factor-β and smooth muscle differentiation Vascular smooth muscle cell Smad4 gene is important for mouse vascular development.A novel in vitro model system for smooth muscle differentiation from human embryonic stem cell-derived mesenchymal cells Fibroblast growth factor (FGF) signaling regulates transforming growth factor beta (TGFβ)-dependent smooth muscle cell phenotype modulation.Cell division cycle 7 mediates transforming growth factor-β-induced smooth muscle maturation through activation of myocardin gene transcription.Transgelin is a TGFβ-inducible gene that regulates osteoblastic and adipogenic differentiation of human skeletal stem cells through actin cytoskeleston organization.Signaling mechanisms that regulate smooth muscle cell differentiation.Distinct signaling pathways activated by "extracellular" and "intracellular" serotonin in heart valve development and disease.Transgelins, cytoskeletal proteins implicated in different aspects of cancer development.Cooperation of myocardin and Smad2 in inducing differentiation of mesenchymal stem cells into smooth muscle cells.Transgelin expressing myofibroblasts orchestrate ventral midline closure through TGF-β signalling TGFβ-TAZ/SRF signalling regulates vascular smooth muscle cell differentiation.Response gene to complement 32, a novel regulator for transforming growth factor-beta-induced smooth muscle differentiation of neural crest cells.Gene expression profile in the activation of subperitoneal fibroblasts reflects prognosis of patients with colon cancer.The long non-coding RNA GAS5 regulates transforming growth factor β (TGF-β)-induced smooth muscle cell differentiation via RNA Smad-binding elements.Metastatic potential of melanomas defined by specific gene expression profiles with no BRAF signature.Transforming growth factor-beta1 signaling contributes to development of smooth muscle cells from embryonic stem cells.Fibroblast-specific TGF-β-Smad2/3 signaling underlies cardiac fibrosis.Loss of heme oxygenase-1 accelerates mesodermal gene expressions during embryoid body development from mouse embryonic stem cells.Transgelin mediates transforming growth factor-β1-induced proliferation of human periodontal ligament cells.Pericytes: The Role of Multipotent Stem Cells in Vascular Maintenance and Regenerative Medicine.Abrogation of TGF-beta signalling in TAGLN expressing cells recapitulates Pentalogy of Cantrell in the mouse.TAZ is involved in transcriptional complexes regulating smooth muscle cell differentiation.Brain cytoplasmic RNA 1 suppresses smooth muscle differentiation and vascular development in mice.Inhibition of the methyltranferase EZH2 improves aortic performance in experimental thoracic aortic aneurysm.

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P2860

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

http://www.wikidata.org/entity/Q34771801

description

2003 nî lūn-bûn

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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի փետրվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@ast

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@en

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@nl

type

label

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@ast

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@en

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@nl

prefLabel

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@ast

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@en

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@nl

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P1433

Nucleic Acids Research

P1476

Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.

@en

P2093

Magdalena Kulik

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

Robert J Lechleider

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

Shiyou Chen

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

P2860

Smad3 and Smad4 cooperate with c-Jun/c-Fos to mediate TGF-beta-induced transcription

Alternative neural crest cell fates are instructively promoted by TGFbeta superfamily members

PDGF, TGF-beta, and heterotypic cell-cell interactions mediate endothelial cell-induced recruitment of 10T1/2 cells and their differentiation to a smooth muscle fate

Smads bind directly to the Jun family of AP-1 transcription factors

Tumor necrosis factor-alpha inhibits transforming growth factor-beta /Smad signaling in human dermal fibroblasts via AP-1 activation

The Smad4 activation domain (SAD) is a proline-rich, p300-dependent transcriptional activation domain

Identification and functional characterization of distinct critically important bone morphogenetic protein-specific response elements in the Id1 promoter

Characterization of functional domains within Smad4/DPC4

Human Smad3 and Smad4 are sequence-specific transcription activators

Analysis of SM22alpha-deficient mice reveals unanticipated insights into smooth muscle cell differentiation and function

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1302-1310

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10.1093/NAR/GKG224

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4

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31

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12582250

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150242

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