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Journal of Molecular and Cellular Cardiology|January 3, 2016
Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defectAndreas Brodehl, Mareike Dieding, Niklas Biere, et al.
Human Mutation|December 16, 2015
Mutations in FLNC are Associated with Familial Restrictive CardiomyopathyAndreas Brodehl, Raechel A Ferrier, Sara J Hamilton, et al.
Trends in Molecular Medicine|September 6, 2025
Targeting pathological ERK1/2 signaling in cancer and beyondConstanze Schanbacher, Maria-Elisabeth Goebeler, Brenda Gerull, et al.
Heart & Lung : the Journal of Critical Care|September 20, 2014
Congenital long QT syndrome: severe torsades de pointes provoked by epinephrine in a digenic mutation carrierVern Hsen Tan, Henry Duff, Vikas Kuriachan, et al.
Biophysical Reviews|June 22, 2018
Molecular insights into cardiomyopathies associated with desmin (DES) mutationsAndreas Brodehl, Anna Gaertner-Rommel, Hendrik Milting
Journal of Molecular and Cellular Cardiology|March 24, 2020
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomyAndreas Brodehl, Jürgen Weiss, Jana Davina Debus, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 19, 2004
Titin isoform-dependent effect of calcium on passive myocardial tensionHideaki Fujita, Dietmar Labeit, Brenda Gerull, et al.
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