Smad4 dependency defines two classes of transforming growth factor {beta} (TGF-{beta}) target genes and distinguishes TGF-{beta}-induced epithelial-mesenchymal transition from its antiproliferative and migratory responses (Q30476201)

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English	Smad4 dependency defines two classes of transforming growth factor {beta} (TGF-{beta}) target genes and distinguishes TGF-{beta}-induced epithelial-mesenchymal transition from its antiproliferative and migratory responses	scientific article

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scholarly article

1 reference

Europe PubMed Central

13 October 2017

Smad4 dependency defines two classes of transforming growth factor {beta} (TGF-{beta}) target genes and distinguishes TGF-{beta}-induced epithelial-mesenchymal transition from its antiproliferative and migratory responses (English)

1 reference

Europe PubMed Central

13 October 2017

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Caroline S. Hill

2

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Europe PubMed Central

13 October 2017

author name string

Laurence Levy

1

1 reference

Europe PubMed Central

13 October 2017

language of work or name

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publication date

1 September 2005

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Europe PubMed Central

13 October 2017

Molecular and Cellular Biology

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Europe PubMed Central

13 October 2017

25

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Europe PubMed Central

13 October 2017

18

1 reference

Europe PubMed Central

13 October 2017

8108-8125

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Europe PubMed Central

13 October 2017

describes a project that uses

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Type I transforming growth factor beta receptor binds to and activates phosphatidylinositol 3-kinase.

1 reference

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1 reference

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Smad4 deficiency in cervical carcinoma cells.

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Differential requirements for Smad4 in TGFbeta-dependent patterning of the early mouse embryo

1 reference

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1 reference

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New insights into TGF-beta-Smad signalling

1 reference

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1 reference

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1 reference

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Smad4-independent regulation of p21/WAF1 by transforming growth factor-beta

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Expression profiling reveals off-target gene regulation by RNAi

1 reference

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A self-enabling TGFbeta response coupled to stress signaling: Smad engages stress response factor ATF3 for Id1 repression in epithelial cells.

1 reference

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Pancreatic cancer biology and genetics

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Restoration of transforming growth factor Beta signaling by functional expression of smad4 induces anoikis

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Genetic programs of epithelial cell plasticity directed by transforming growth factor-beta

1 reference

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Transforming growth factor beta-independent shuttling of Smad4 between the cytoplasm and nucleus.

1 reference

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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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Smad4/DPC4-mediated tumor suppression through suppression of angiogenesis

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

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based on heuristic

inferred from PubMed ID database lookup

High levels of transforming growth factor beta 1 in patients with colorectal cancer: association with disease progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of growth factors, growth-inhibiting factors, and their receptors in invasive breast cancer. II: Correlations with proliferation and angiogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16135802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.25.18.8108-8125.2005

1 reference

Europe PubMed Central

13 October 2017

1 reference

Europe PubMed Central

13 October 2017

1 reference

Europe PubMed Central

13 October 2017

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