Publications by authors named "Vivian Haffner"

Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy and is caused by mutations in the dystrophin gene. Dystrophin deficiency is associated with structural and functional changes of the muscle cell sarcolemma and/or stretch-induced ion channel activation. In this investigation, we use mice with transgenic cardiomyocyte-specific expression of the GCaMP6f Ca indicator to test the hypothesis that dystrophin deficiency leads to cardiomyocyte Ca handling abnormalities following preload challenge.

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