Physical and functional interaction between GATA-3 and Smad3 allows TGF-beta regulation of GATA target genes (Q40757292)

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scientific article published on January 2002

Language	Label	Description	Also known as
English	Physical and functional interaction between GATA-3 and Smad3 allows TGF-beta regulation of GATA target genes	scientific article published on January 2002

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Physical and functional interaction between GATA-3 and Smad3 allows TGF-beta regulation of GATA target genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

author name string

Andries Blokzijl

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Peter ten Dijke

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Carlos F Ibáñez

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

0 references

publication date

1 January 2002

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Current Biology

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

35-45

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Transcriptional regulation of T lymphocyte development and function

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Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

1 reference

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7 January 2021

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Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system

1 reference

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Transcription factor GATA-3 is required for development of the T-cell lineage

1 reference

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The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells

1 reference

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Transcription factor GATA-3 is differentially expressed in murine Th1 and Th2 cells and controls Th2-specific expression of the interleukin-5 gene

1 reference

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Regulation of Smad signalling by protein associations and signalling crosstalk

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TGF-beta1: immunosuppressant and viability factor for T lymphocytes

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Regulation of immune responses by TGF-beta

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Targeted disruption of SMAD3 results in impaired mucosal immunity and diminished T cell responsiveness to TGF-beta

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Targeted disruption of Smad3 reveals an essential role in transforming growth factor beta-mediated signal transduction

1 reference

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Direct binding of Smad3 and Smad4 to critical TGF beta-inducible elements in the promoter of human plasminogen activator inhibitor-type 1 gene

1 reference

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Human Smad3 and Smad4 are sequence-specific transcription activators

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Crystal structure of a Smad MH1 domain bound to DNA: insights on DNA binding in TGF-beta signaling

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Functional consequences of tumorigenic missense mutations in the amino-terminal domain of Smad4

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A single missense mutant of Smad3 inhibits activation of both Smad2 and Smad3, and has a dominant negative effect on TGF-beta signals

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Identification of Smad7, a TGFbeta-inducible antagonist of TGF-beta signalling

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Protein loop grafting to construct a variant of tissue-type plasminogen activator that binds platelet integrin alpha IIb beta 3.

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Acetylation of GATA-3 affects T-cell survival and homing to secondary lymphoid organs

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Inhibition of allergic inflammation in a murine model of asthma by expression of a dominant-negative mutant of GATA-3

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Structural and functional characterization of the transforming growth factor-beta -induced Smad3/c-Jun transcriptional cooperativity.

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Role of Smad proteins and transcription factor Sp1 in p21(Waf1/Cip1) regulation by transforming growth factor-beta.

1 reference

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

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ATF-2 is a common nuclear target of Smad and TAK1 pathways in transforming growth factor-beta signaling

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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

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

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Smad2, Smad3 and Smad4 cooperate with Sp1 to induce p15(Ink4B) transcription in response to TGF-beta

1 reference

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Functional analysis of the transforming growth factor beta responsive elements in the WAF1/Cip1/p21 promoter

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TGF-beta 1 differentially regulates IL-2 expression and [3H]-thymidine incorporation in CD3 epsilon mAb- and CD28 mAb-activated splenocytes and thymocytes

1 reference

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Transforming growth factor-beta1, a strong costimulator of rat T-cell activation promoting a shift towards a Th2-like cytokine profile

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Tumor-associated transforming growth factor-beta and interleukin-10 contribute to a systemic Th2 immune phenotype in pancreatic carcinoma patients

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Transforming growth factor beta (TGF-beta)-dependent inhibition of T helper cell 2 (Th2)-induced autoimmunity by self-major histocompatibility complex (MHC) class II-specific, regulatory CD4(+) T cell lines.

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TGF-β1 down-regulates Th2 development and results in decreased IL-4-induced STAT6 activation and GATA-3 expression

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The tumor suppressor Smad4/DPC4 and transcriptional adaptor CBP/p300 are coactivators for smad3 in TGF-beta-induced transcriptional activation

1 reference

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TGF-beta-stimulated cooperation of smad proteins with the coactivators CBP/p300

1 reference

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A Smad transcriptional corepressor

1 reference

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Cooperative binding of Smad proteins to two adjacent DNA elements in the plasminogen activator inhibitor-1 promoter mediates transforming growth factor beta-induced smad-dependent transcriptional activation

1 reference

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7 January 2021

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1 reference

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1 reference

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Definition of cis-regulatory elements of the mouse interleukin-5 gene promoter. Involvement of nuclear factor of activated T cell-related factors in interleukin-5 expression

1 reference

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1 reference

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Identifiers

10.1016/S0960-9822(01)00623-6

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

ResearchGate publication ID

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