Article
F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers.
The Journal of biological chemistry - 4 Nov 2005
Hernandez Olga M, Szczesna-Cordary Danuta, Knollmann Björn C, Miller Todd, Bell Michael, Zhao Jiaju, Sirenko Syevda G, Diaz Zoraida, Guzman Georgianna, Xu Yuanyuan, Wang Ying, Kerrick W Glenn L, Potter James D
Abstract excerpt
We have studied the physiological effects of the troponin T (TnT) F110I and R278C mutations associated with familial hypertrophic cardiomyopathy (FHC) in humans. Three to four-month-old transgenic (Tg) mice expressing F110I-TnT and R278C-TnT did not develop significant hypertrophy or ventricular fibrosis even after chronic exercise challenge. The F110I mutation impaired acute exercise tolerance, whereas R278C did...
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