Phosphorylation-dependent paxillin-ERK association mediates hepatocyte growth factor-stimulated epithelial morphogenesis (Q28587743)

31 January 2017

title

Phosphorylation-dependent paxillin-ERK association mediates hepatocyte growth factor-stimulated epithelial morphogenesis (English)

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phosphotyrosine residue binding

31 January 2017

0 references

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Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0001784

V-crk avian sarcoma virus CT10 oncogene homolog

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Rous sarcoma oncogene

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Paxillin

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Mitogen-activated protein kinase 3

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Mitogen-activated protein kinase 1

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Shuta Ishibe

1

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31 January 2017

Dominique Joly

series ordinal

2

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31 January 2017

Xiaolei Zhu

series ordinal

3

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31 January 2017

Lloyd G. Cantley

series ordinal

4

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31 January 2017

publication date

1 November 2003

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31 January 2017

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31 January 2017

volume

12

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31 January 2017

issue

5

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31 January 2017

page(s)

1275–1285

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Architectural patterns in branching morphogenesis in the kidney.

31 January 2017

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HGF promotes adhesion of ATP-depleted renal tubular epithelial cells in a MAPK-dependent manner

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Hepatocyte growth factor induces ERK-dependent paxillin phosphorylation and regulates paxillin-focal adhesion kinase association

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Identification of a fibroblast-derived epithelial morphogen as hepatocyte growth factor

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Hepatocyte growth factor enables enhanced integrin-cytoskeleton linkage by affecting integrin expression in subconfluent epithelial cells

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Phosphorylation of tyrosine residues 31 and 118 on paxillin regulates cell migration through an association with CRK in NBT-II cells

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KSR is a scaffold required for activation of the ERK/MAPK module

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In vitro branching tubulogenesis: implications for developmental and cystic disorders, nephron number, renal repair, and nephron engineering

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Localized suppression of RhoA activity by Tyr31/118-phosphorylated paxillin in cell adhesion and migration

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7 January 2021

Paxillin and focal adhesion signalling

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