Genetics of Mechanosensation in the Heart-Reference-Cited by-同舟云学术

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Genetics of Mechanosensation in the Heart

Published:2011-03-01 Issue:3 Volume:4 Page:238-244
ISSN:1937-5387
Container-title:Journal of Cardiovascular Translational Research
language:en
Short-container-title:J. of Cardiovasc. Trans. Res.

Author:

Buyandelger Byambajav,Ng Keat-Eng,Miocic Snjezana,Gunkel Sylvia,Piotrowska Izabela,Ku Ching-Hsin,Knöll Ralph

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.springerlink.com/index/pdf/10.1007/s12265-011-9262-6

Reference47 articles.

1. Leal, J., Luengo-Fernandez, R., Gray, A., Petersen, S., & Rayner, M. (2006). Economic burden of cardiovascular diseases in the enlarged European Union. European Heart Journal, 27(13), 1610–1619.

2. Maron, B. J., Towbin, J. A., Thiene, G., Antzelevitch, C., Corrado, D., Arnett, D., et al. (2006). Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation, 113(14), 1807–1816.

3. Carballo, S., Robinson, P., Otway, R., Fatkin, D., Jongbloed, J. D., de Jonge, N., et al. (2009). Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. Circulation Research, 105(4), 375–382. doi: 10.1161/CIRCRESAHA.109.196055 .

4. Watkins, H., Ashrafian, H., & McKenna, W. J. (2008). The genetics of hypertrophic cardiomyopathy: Teare redux. Heart, 94(10), 1264–1268. doi: 10.1136/hrt.2008.154104 .

5. Kimura, A. (2010). Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond. Journal of Human Genetics, 55(2), 81–90. doi: 10.1038/jhg.2009.138 .

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