Related references
Note: Only part of the references are listed.Congenital Heart Disease in the Older Adult A Scientific Statement From the American Heart Association
Ami B. Bhatt et al.
CIRCULATION (2015)
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
Romaric Bouveret et al.
ELIFE (2015)
Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease
Stella Marie Reamon-Buettner et al.
PLOS ONE (2013)
Integration of Nodal and BMP Signals in the Heart Requires FoxH1 to Create Left-Right Differences in Cell Migration Rates That Direct Cardiac Asymmetry
Kari F. Lenhart et al.
PLOS GENETICS (2013)
Gene Regulatory Networks in Cardiac Conduction System Development
Nikhil V. Munshi
CIRCULATION RESEARCH (2012)
Endocardial and Epicardial Epithelial to Mesenchymal Transitions in Heart Development and Disease
Alexander von Gise et al.
CIRCULATION RESEARCH (2012)
Coordinating Tissue Interactions: Notch Signaling in Cardiac Development and Disease
Jose Luis de la Pompa et al.
DEVELOPMENTAL CELL (2012)
Genetic and Functional Analysis of the NKX2-5 Gene Promoter in Patients With Ventricular Septal Defects
Shuchao Pang et al.
PEDIATRIC CARDIOLOGY (2012)
Novel NKX2-5 Mutations in Patients With Familial Atrial Septal Defects
Xing-Yuan Liu et al.
PEDIATRIC CARDIOLOGY (2011)
Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: Introduction
Ariane Marelli et al.
CANADIAN JOURNAL OF CARDIOLOGY (2010)
Mortality Resulting From Congenital Heart Disease Among Children and Adults in the United States, 1999 to 2006
Suzanne M. Gilboa et al.
CIRCULATION (2010)
Consanguinity Mapping of Congenital Heart Disease in a South Indian Population
Tracy L. McGregor et al.
PLOS ONE (2010)
Congenital Cardiovascular Disease in Turner Syndrome
Carolyn A. Bondy
Congenital Heart Disease (2010)
Importance of gene-environment interactions in the etiology of selected birth defects
H. Zhu et al.
CLINICAL GENETICS (2009)
Overview of Developmental Heart Defects by Dioxins, PCBs, and Pesticides
PHILLIP G. KOPF et al.
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART C-ENVIRONMENTAL CARCINOGENESIS & ECOTOXICOLOGY REVIEWS (2009)
Investigation of somatic NKX2-5 mutations in congenital heart disease
J. M. Draus et al.
JOURNAL OF MEDICAL GENETICS (2009)
A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomaldominant inherited congenital heart disease
S. Pabst et al.
CLINICAL RESEARCH IN CARDIOLOGY (2008)
GATA4 sequence variants in patients with congenital heart disease
A. Tomita-Mitchell et al.
JOURNAL OF MEDICAL GENETICS (2007)
Genetic basis for congenital heart defects: Current knowledge - A scientific statement from the American heart association congenital cardiac defects committee, council on cardiovascular disease in the young
Mary Ella Pierpont et al.
CIRCULATION (2007)
Atrial septal defects in the adult - Recent progress and overview
Gary Webb et al.
CIRCULATION (2006)
The prevalence of cardiovascular malformations in offspring of diabetic mothers
C. Cavalli et al.
PEDIATRIC CARDIOLOGY (2006)
Congenital malformations among liveborn infants with trisomies 18 and 13
Stephen J. Pont et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Phenotypes with GATA4 or NKX2.5 mutations in familial artrial septal defect
K Hirayama-Yamada et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors
A Sarkozy et al.
JOURNAL OF MEDICAL GENETICS (2005)
Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease
SM Reamon-Buettner et al.
JOURNAL OF MEDICAL GENETICS (2004)
Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects
SM Ware et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
NKX2.5 mutations in patients with congenital heart disease
DB McElhinney et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease -: Associations with atrial septal defect and hypoplastic left heart syndrome
DA Elliott et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD
Y Watanabe et al.
JOURNAL OF MEDICAL GENETICS (2002)
NKX2.5 mutations in patients with tetralogy of Fallot
E Goldmuntz et al.
CIRCULATION (2001)
Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease
WD Zhu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
