Perturbed Length–Dependent Activation in Human Hypertrophic Cardiomyopathy With Missense Sarcomeric Gene Mutations

RATIONALE: High-myofilament Ca(2+)-sensitivity has been proposed as trigger of disease pathogenesis in familial hypertrophic cardiomyopathy (HCM) based on in vitro and transgenic mice studies. However, myofilament Ca(2+)-sensitivity depends on protein phosphorylation and muscle length, and at presen...

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Bibliografski detalji
Glavni autori: Sequeira, Vasco, Wijnker, Paul J.M., Nijenkamp, Louise L.A.M., Kuster, Diederik W.D., Najafi, Aref, Witjas-Paalberends, E. Rosalie, Regan, Jessica A., Boontje, Nicky, ten Cate, Folkert J., Germans, Tjeerd, Carrier, Lucie, Sadayappan, Sakthivel, van Slegtenhorst, Marjon A., Zaremba, Ruud, Foster, D. Brian, Murphy, Anne M., Poggesi, Corrado, dos Remedios, Cris, Stienen, Ger J.M., Ho, Carolyn Y., Michels, Michelle, van der Velden, Jolanda
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3675884/
https://ncbi.nlm.nih.gov/pubmed/23508784
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.111.300436
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