Abstract
In end-stage heart failure, several molecular, biochemical and functional alterations have been described to occur at the cellular level [11, 32]. Evidence indicates that disturbed excitation-contraction coupling processes may underlie disturbed myocardial function in various animal models and human conditions [3, 34]. Specifically, Ca2+ uptake and release by the sarcoplasmic reticulum (SR) have been shown to be altered, and the ratio of phospholamban/SR Ca2+ ATPase has been suggested to play a key role in the pathophysiology of heart failure [10]. Thus, it becomes important to dissect the molecular mechanisms governing the highly regulated excitation-contraction coupling process and their alterations in heart failure in order to develop new therapeutic approaches for this disease.
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Schmidt, A.G., Kranias, E.G. (2000). Genetic approaches to elucidate the regulatory role of phospholamban in the heart. In: Hasenfuss, G., Marbán, E. (eds) Molecular Approaches to Heart Failure Therapy. Steinkopff, Heidelberg. https://doi.org/10.1007/978-3-642-57710-9_4
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DOI: https://doi.org/10.1007/978-3-642-57710-9_4
Publisher Name: Steinkopff, Heidelberg
Print ISBN: 978-3-642-63332-4
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