Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy-Reference-Cited by-同舟云学术

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Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy

Published:2018-12-10 Issue:3 Volume:12 Page:257-267
ISSN:1937-5387
Container-title:Journal of Cardiovascular Translational Research
language:en
Short-container-title:J. of Cardiovasc. Trans. Res.

Author:

Xu Ying-Jia,Wang Zhang-Sheng,Yang Chen-Xi,Di Ruo-Min,Qiao Qi,Li Xiu-Mei,Gu Jia-Ning,Guo Xiao-Juan,Yang Yi-Qing

Funder

National Natural Science Foundation of China

Shanghai Municipal Population and Family Planning Commission

the Fifth People′s Hospital of Shanghai

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Cardiology and Cardiovascular Medicine,Pharmaceutical Science,Genetics,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12265-018-9851-8.pdf

Reference57 articles.

1. Merlo, M., Cannatà, A., Gobbo, M., Stolfo, D., Elliott, P. M., & Sinagra, G. (2018). Evolving concepts in dilated cardiomyopathy. European Journal of Heart Failure, 20, 228–239.

2. Tabish, A. M., Azzimato, V., Alexiadis, A., Buyandelger, B., & Knöll, R. (2017). Genetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy. Biophysical Reviews, 9, 207–223.

3. Halliday, B. P., Gulati, A., Ali, A., Guha, K., Newsome, S., Arzanauskaite, M., et al. (2017). Association between midwall late gadolinium enhancement and sudden cardiac death in patients with dilated cardiomyopathy and mild and moderate left ventricular systolic dysfunction. Circulation, 135, 2106–2115.

4. Halliday, B. P., Cleland, J. G. F., Goldberger, J. J., & Prasad, S. K. (2017). Personalizing risk stratification for sudden death in dilated cardiomyopathy: the past, present, and future. Circulation, 136, 215–231.

5. Stolfo, D., Ceschia, N., Zecchin, M., De Luca, A., Gobbo, M., Barbati, G., et al. (2018). Arrhythmic risk stratification in patients with idiopathic dilated cardiomyopathy. The American Journal of Cardiology, 121, 1601–1609.

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2. Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis;Biomolecules;2023-02-13

3. Identification of a novel missense mutation in the TPM1 gene via exome sequencing in a Chinese family with dilated cardiomyopathy;Medicine;2022-01-14

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