Absence of Association Between Length Variation of an Intronic Region in the NFATC1 Gene and Congenital Heart Defects in a Han Chinese Population-Reference-Cited by-同舟云学术

Absence of Association Between Length Variation of an Intronic Region in the NFATC1 Gene and Congenital Heart Defects in a Han Chinese Population

Published:2012-01 Issue:1 Volume:31 Page:88-91
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Liu Hanmin¹²³,Dai Li²³⁴,Mao Meng²³⁵,Wang Xiaoshuang¹²³,Hua Yimin¹²³,Xie Liang¹²³

Affiliation:

1. The Pulmonary Vascular Remodeling Research Unit, West China Institute of Women and Children's Health, West China Second University Hospital, Sichuan University, Chengdu, China.

2. Department of Pediatric, West China Second University Hospital, Sichuan University, Chengdu, China.

3. Key Laboratory of Obstetric and Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, China.

4. National Center for Birth Defect Monitoring, West China Second University Hospital, Sichuan University, Chengdu, China.

5. Laboratory of Early Development Injury and Repair, West China Institute of Women and Children's Health, West China Second University Hospital, Sichuan University, Chengdu, China.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/dna.2011.1286

Reference17 articles.

1. The developmental genetics of congenital heart disease

2. Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

3. A Field of Myocardial-Endocardial NFAT Signaling Underlies Heart Valve Morphogenesis

4. VEGF and RANKL Regulation of NFATc1 in Heart Valve Development

5. Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease;American Journal of Medical Genetics Part A;2013-09-24

2. Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot;DNA and Cell Biology;2012-11

3. An Excess of Deleterious Variants in VEGF-A Pathway Genes in Down-Syndrome-Associated Atrioventricular Septal Defects;The American Journal of Human Genetics;2012-10