Signaling via PINCH: Functions, binding partners and implications in human diseases.

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High PINCH1 Expression in Human Laryngeal Carcinoma Associates with Poor Prognosis.Novel functions for integrin-associated proteins revealed by analysis of myofibril attachment in

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Signaling via PINCH: Functions, binding partners and implications in human diseases.

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http://www.wikidata.org/entity/Q38945219

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-my

2016年学术文章

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2016年學術文章

@yue

2016年學術文章

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2016年學術文章

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Signaling via PINCH: Functions, binding partners and implications in human diseases.

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Signaling via PINCH: Functions, binding partners and implications in human diseases.

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Signaling via PINCH: Functions, binding partners and implications in human diseases.

@en

P1476

Signaling via PINCH: Functions, binding partners and implications in human diseases.

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Guozhi Xiao

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

Huamin Xu

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

Huiling Cao

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

P2860

Integrin-linked kinase is localized to cell-matrix focal adhesions but not cell-cell adhesion sites and the focal adhesion localization of integrin-linked kinase is regulated by the PINCH-binding ANK repeats

Parvin, a 42 kDa focal adhesion protein, related to the alpha-actinin superfamily

Structure of an ultraweak protein-protein complex and its crucial role in regulation of cell morphology and motility

PINCH1 is transcriptional regulator in podocytes that interacts with WT1 and represses podocalyxin expression

A new LIM protein containing an autoepitope homologous to "senescent cell antigen"

Regulation of cell adhesion and anchorage-dependent growth by a new beta 1-integrin-linked protein kinase

Assembly of the PINCH-ILK-CH-ILKBP complex precedes and is essential for localization of each component to cell-matrix adhesion sites

The LIM-only protein PINCH directly interacts with integrin-linked kinase and is recruited to integrin-rich sites in spreading cells

Increased expression of the Ras suppressor Rsu-1 enhances Erk-2 activation and inhibits Jun kinase activation

Nck-2, a novel Src homology2/3-containing adaptor protein that interacts with the LIM-only protein PINCH and components of growth factor receptor kinase-signaling pathways

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10-15

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

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scholarly article

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10.1016/J.GENE.2016.08.039

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

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English

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

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594

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

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2016-08-30T00:00:00Z

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

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27590440

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P932

5056850

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Signaling via PINCH: Functions, binding partners and implications in human diseases.

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P2860

P2860

Signaling via PINCH: Functions, binding partners and implications in human diseases.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932