MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway-Reference-Cited by-同舟云学术

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MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Published:2020-03-17 Issue:9 Volume:63 Page:1347-1362
ISSN:1674-7305
Container-title:Science China Life Sciences
language:en
Short-container-title:Sci. China Life Sci.

Author:

Chen Peng,Li Zongzhe,Nie Jiali,Wang Hong,Yu Bo,Wen Zheng,Sun Yang,Shi Xiaolu,Jin Li,Wang Dao-Wen

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology

Link

https://link.springer.com/content/pdf/10.1007/s11427-019-1627-y.pdf

Reference50 articles.

1. Alfares, A.A., Kelly, M.A., McDermott, G., Funke, B.H., Lebo, M.S., Baxter, S.B., Shen, J., McLaughlin, H.M., Clark, E.H., Babb, L.J., et al. (2015). Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. Genet Med 17, 880–888.

2. Black, B.L., and Olson, E.N. (1998). Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins. Annu Rev Cell Dev Biol 14, 167–196.

3. Braun, A.P., and Schulman, H. (1995). The multifunctional calcium/calmodulin-dependent protein kinase: from form to function. Annu Rev Physiol 57, 417–445.

4. Brito, D., Miltenberger-Miltenyi, G., Vale Pereira, S., Silva, D., Diogo, A. N., and Madeira, H. (2012). Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population. Rev Port Cardiol 31, 577–587.

5. Cingolani, H.E., and Ennis, I.L. (2007). Sodium-hydrogen exchanger, cardiac overload, and myocardial hypertrophy. Circulation 115, 1090–1100.

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