Single allele mutations at the heart of congenital disease
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference10 articles.
1. NK-2Homeobox Genes and Heart Development
2. Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner
3. Tinman Function Is Essential for Vertebrate Heart Development: Elimination of Cardiac Differentiation by Dominant Inhibitory Mutants of thetinman-Related Genes,XNkx2-3andXNkx2-5
4. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
5. Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5
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1. Single amino acid polymorphism in aldehyde dehydrogenase gene superfamily;Frontiers in Bioscience;2015
2. ALDH1A2 (RALDH2) genetic variation in human congenital heart disease;BMC Medical Genetics;2009-11-03
3. Double outlet right ventricle: aetiologies and associations;Journal of Medical Genetics;2008-05-02
4. The Transcriptional Coactivator CAMTA2 Stimulates Cardiac Growth by Opposing Class II Histone Deacetylases;Cell;2006-05
5. Transgenic analysis of the atrialnatriuretic factor (ANF) promoter: Nkx2-5 and GATA-4 binding sites are required for atrial specific expression of ANF;Developmental Biology;2003-09
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