A novel mutation of GATA4 in a familial atrial septal defect-Reference-Cited by-同舟云学术

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A novel mutation of GATA4 in a familial atrial septal defect

Published:2010-11 Issue:21-22 Volume:411 Page:1741-1745
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Chen Ying,Mao Jun,Sun Ying,Zhang Qiang,Cheng Hong-Bo,Yan Wen-Hua,Choy Kwong Wai,Li Hong

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference9 articles.

1. Congenital heart disease in adolescents and adults. Natural and postoperative history across age groups;Kaplan;Cardiol Clin,1993

2. GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease;Pehlivan;Am J Med Genet,1999

3. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency;Law;BJOG,2009

4. Detection of large-scale variation in the human genome;Iafrate;Nat Genet,2004

5. Human non-synonymous SNPs: server and survey;Ramensky;Nucleic Acids Res,2002

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1. High throughput mutation screening of cardiac transcription factor GATA4 among Tanzania children with congenital heart diseases;The Nucleus;2023-01-04

2. Utilization of induced pluripotent stem cells to model the molecular network regulating congenital heart disease;Cardiovascular Research;2021-12-31

3. In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease;Journal of Cardiovascular and Thoracic Research;2021-11-01

4. Patient-specific iPSC-derived cardiomyocytes reveal abnormal regulation of FGF16 in a familial atrial septal defect;Cardiovascular Research;2021-05-06

5. Establishment and characterization of a human embryonic stem cell line carrying a heterozygous GATA4T280M mutation;Stem Cell Research;2021-05

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