A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease-Reference-Cited by-同舟云学术

A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

Published:2001-09 Issue:6 Volume:106 Page:709-721
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Bruneau Benoit G.,Nemer Georges,Schmitt Joachim P.,Charron Frédéric,Robitaille Lynda,Caron Sophie,Conner David A.,Gessler Manfred,Nemer Mona,Seidman Christine E.,Seidman J.G.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference45 articles.

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4. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome;Basson;Nat. Genet.,1997

5. Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations;Basson;Proc. Natl. Acad. Sci. USA,1999

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