Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects-Reference-Cited by-同舟云学术

Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects

Published:2013-07-11 Issue:9 Volume:34 Page:1226-1230
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Chang Sheng-Wei¹,Mislankar Mona¹,Misra Chaitali¹,Huang Nianyuan¹,DaJusta Daniel G.²,Harrison Steven M.²,McBride Kim L.¹³,Baker Linda A.²⁴,Garg Vidu¹³⁵

Affiliation:

1. Center for Cardiovascular and Pulmonary Research and The Heart Center; Nationwide Children's Hospital; Columbus Ohio

2. Department of Urology; University of Texas Southwestern Medical Center; Dallas Texas

3. Department of Pediatrics; The Ohio State University; Columbus Ohio

4. McDermott Center for Human Growth and Development/Center for Human Genetics; University of Texas Southwestern Medical Center; Dallas Texas

5. Department of Molecular Genetics; The Ohio State University; Columbus Ohio

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22366/fullpdf

Reference28 articles.

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2. HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte;Claycomb;Proc Natl Acad Sci USA,1998

3. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome;Elliott;J Am Coll Cardiol,2003

4. Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group;Ferencz;J Am Coll Cardiol,1989

5. Enhancement of the recycling and activation of beta-adrenergic receptor by Rab4 GTPase in cardiac myocytes;Filipeanu;J Biol Chem,2006

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