Mutations in Cardiac T-Box Factor Gene TBX20 Are Associated with Diverse Cardiac Pathologies, Including Defects of Septation and Valvulogenesis and Cardiomyopathy
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- 1 August 2007
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 81 (2) , 280-291
- https://doi.org/10.1086/519530
Abstract
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This publication has 46 references indexed in Scilit:
- An Nkx2-5/Bmp2/Smad1 Negative Feedback Loop Controls Heart Progenitor Specification and ProliferationCell, 2007
- Tbx20 regulation of endocardial cushion cell proliferation and extracellular matrix gene expressionDevelopmental Biology, 2006
- T-Box Genes in Vertebrate DevelopmentAnnual Review of Genetics, 2005
- T-box transcription factors and their roles in regulatory hierarchies in the developing heartDevelopment, 2005
- Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing lossNature Genetics, 2005
- GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5Nature, 2003
- Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathwaysJournal of Clinical Investigation, 1999
- Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNature Genetics, 1997
- Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeNature Genetics, 1997
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyNature Genetics, 1997