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Podosomal proteins as causes of human syndromes: a role in craniofacial development?

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

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The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function Genetic disruption of the sh3pxd2a gene reveals an essential role in mouse development and the existence of a novel isoform of tks5 Macrophage mesenchymal migration requires podosome stabilization by filamin A Cell migration and invasion in human disease: the Tks adaptor proteins Regulation of invadopodia by the tumor microenvironment.Control of macrophage 3D migration: a therapeutic challenge to limit tissue infiltration.Tks adaptor proteins at a glance.

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Podosomal proteins as causes of human syndromes: a role in craniofacial development?

http://www.wikidata.org/entity/Q37843989

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on April 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

@en

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

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type

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Podosomal proteins as causes of human syndromes: a role in craniofacial development?

@en

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

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prefLabel

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

@en

Podosomal proteins as causes of human syndromes: a role in craniofacial development?

@nl

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Podosomal proteins as causes of human syndromes: a role in craniofacial development?

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Pilar Cejudo-Martin

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

Sara A Courtneidge

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P2860

Dynamics of alpha-actinin in focal adhesions and stress fibers visualized with alpha-actinin-green fluorescent protein

FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner

Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome

The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor

A new method for isolating tyrosine kinase substrates used to identify fish, an SH3 and PX domain-containing protein, and Src substrate.

The novel adaptor protein Tks4 (SH3PXD2B) is required for functional podosome formation

Faciogenital dysplasia protein (FGD1) regulates export of cargo proteins from the golgi complex via Cdc42 activation.

Wiskott-Aldrich syndrome protein regulates podosomes in primary human macrophages

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209-221

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scholarly article

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10.1002/DVG.20732

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4

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49

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2011-04-01T00:00:00Z

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49843061

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21328520

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