Heterozygous Mutations in MAP3K7 , Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome-Reference-Cited by-同舟云学术

Heterozygous Mutations in MAP3K7 , Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome

Published:2016-08 Issue:2 Volume:99 Page:407-413
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Le Goff Carine,Rogers Curtis,Le Goff Wilfried,Pinto Graziella,Bonnet Damien,Chrabieh Maya,Alibeu Olivier,Nistchke Patrick,Munnich Arnold,Picard Capucine,Cormier-Daire Valérie

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference17 articles.

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2. Identification of a member of the MAPKKK family as a potential mediator of TGF-beta signal transduction;Yamaguchi;Science,1995

3. TAB2, a novel adaptor protein, mediates activation of TAK1 MAPKKK by linking TAK1 to TRAF6 in the IL-1 signal transduction pathway;Takaesu;Mol. Cell,2000

4. Autoactivation of transforming growth factor beta-activated kinase 1 is a sequential bimolecular process;Scholz;J. Biol. Chem.,2010

5. TGF-beta activated kinase-1: new insights into the diverse roles of TAK1 in development and immunity;Delaney;Cell Cycle,2006

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