Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation-Reference-Cited by-同舟云学术

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Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation

Published:2017-04-03 Issue:1 Volume:15 Page:
ISSN:1479-5876
Container-title:Journal of Translational Medicine
language:en
Short-container-title:J Transl Med

Author:

Qian Yanyan,Xiao Deyong,Guo Xiao,Chen Hongbo,Hao Lili,Ma Xiaojing,Huang Guoying,Ma Duan,Wang Huijun

Funder

National Natural Science Foundation of China

National Key Research and Development Program

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12967-017-1173-0.pdf

Reference47 articles.

1. Pierpont ME, Basson CT, Benson DW Jr, Gelb BD, Giglia TM, Goldmuntz E, McGee G, Sable CA, Srivastava D, Webb CL. American Heart Association Congenital Cardiac Defects Committee CoCDitY: 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: endorsed by the American Academy of Pediatrics. Circulation. 2007;115:3015–38.

2. Zhao QM, Ma XJ, Jia B, Huang GY. Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening. Acta Paediatr. 2013;102:397–402.

3. Grunert M, Dorn C, Schueler M, Dunkel I, Schlesinger J, Mebus S, Alexi-Meskishvili V, Perrot A, Wassilew K, Timmermann B, et al. Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot. Hum Mol Genet. 2014;23:3115–28.

4. McCulley DJ, Black BL. Transcription factor pathways and congenital heart disease. Curr Top Dev Biol. 2012;100:253–77.

5. Ruiz-Villalba A, Hoppler S, van den Hoff MJ. Wnt signaling in the heart fields: variations on a common theme. Dev Dyn. 2016;245:294–306.

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3. Familial congenital heart disease caused by a frameshift variant in glyoxylate reductase 1 homolog (GLYR1);QJM: An International Journal of Medicine;2023-12-09

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