STAT5b, a Mediator of Synergism between c-Src and the Epidermal Growth Factor Receptor (Q30310214)

16 June 2017

title

STAT5b, a Mediator of Synergism between c-Src and the Epidermal Growth Factor Receptor (English)

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16 June 2017

Michael T Kloth

1

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16 June 2017

Kristen K Laughlin

2

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Jacqueline S Biscardi

3

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16 June 2017

Julie L Boerner

4

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16 June 2017

Sarah J Parsons

5

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16 June 2017

Corinne M Silva

6

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16 June 2017

language of work or name

English

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publication date

11 November 2002

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Journal of Biological Chemistry

16 June 2017

published in

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16 June 2017

volume

278

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issue

3

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16 June 2017

page(s)

1671-1679

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Presence of epidermal growth factor receptor as an indicator of poor prognosis in patients with breast cancer

16 June 2017

cites work

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Involvement of pp60c-src with two major signaling pathways in human breast cancer

21 January 2018

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Augmented mitogenic responsiveness to epidermal growth factor in murine fibroblasts that overexpress pp60c-src

21 January 2018

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DNA synthesis induced by some but not all growth factors requires Src family protein tyrosine kinases.

21 January 2018

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pp60c-src tyrosine kinase, myristylation, and modulatory domains are required for enhanced mitogenic responsiveness to epidermal growth factor seen in cells overexpressing c-src

21 January 2018

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Tyrosine kinase signalling in breast cancer: epidermal growth factor receptor and c-Src interactions in breast cancer

21 January 2018

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Characterization of human epidermal growth factor receptor and c-Src interactions in human breast tumor cells

21 January 2018

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Potentiation of epidermal growth factor receptor-mediated oncogenesis by c-Src: implications for the etiology of multiple human cancers

21 January 2018

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c-Src-mediated phosphorylation of the epidermal growth factor receptor on Tyr845 and Tyr1101 is associated with modulation of receptor function

21 January 2018

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Mechanism of biological synergy between cellular Src and epidermal growth factor receptor

21 January 2018

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Signaling through the hematopoietic cytokine receptors.

21 January 2018

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Transcriptional responses to polypeptide ligands: the JAK-STAT pathway

21 January 2018

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JAK/STAT signaling by cytokine receptors

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Jaks and STATs: biological implications

21 January 2018

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Elevated levels of members of the STAT family of transcription factors in breast carcinoma nuclear extracts

21 January 2018

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Stat3 activation is required for cellular transformation by v-src

21 January 2018

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Stat3 activation by Src induces specific gene regulation and is required for cell transformation

21 January 2018

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Novel activation of STAT5b in response to epidermal growth factor

21 January 2018

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Stat5a and Stat5b proteins have essential and nonessential, or redundant, roles in cytokine responses

21 January 2018

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

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Characterization and cloning of STAT5 from IM-9 cells and its activation by growth hormone

21 January 2018

1 reference

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Deletion of the carboxyl-terminal transactivation domain of MGF-Stat5 results in sustained DNA binding and a dominant negative phenotype.

21 January 2018

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STAT activation by epidermal growth factor (EGF) and amphiregulin. Requirement for the EGF receptor kinase but not for tyrosine phosphorylation sites or JAK1.

21 January 2018

1 reference

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Phosphorylation and Activation of the DNA Binding Activity of Purified Stat1 by the Janus Protein-tyrosine Kinases and the Epidermal Growth Factor Receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207289200

ErbB receptor-induced activation of stat transcription factors is mediated by Src tyrosine kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207289200

Constitutive activation of Stat3 by the Src and JAK tyrosine kinases participates in growth regulation of human breast carcinoma cells

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M207289200

Loss of Stat5a delays mammary cancer progression in a mouse model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207289200

21 January 2018

Identifiers

DOI

10.1074/JBC.M207289200

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16 June 2017

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