Showing results (51-60 of 64) with videos related to
Sort By:
Pageof 7
Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.Journal of Muscle Research and Cell Motility|November 5, 2017
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathyJudith Montag, Mandy Syring, Julia Rose, et al.Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.Journal of Molecular and Cellular Cardiology|September 25, 2017
Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytesKatrin Streckfuss-Bömeke, Malte Tiburcy, Andrey Fomin, et al.Journal of Medical Genetics|September 19, 2009
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defectsMaximilian G Posch, Michael Gramlich, Margaret Sunde, et al.Frontiers in Physiology|April 25, 2018
Burst-Like Transcription of Mutant and Wildtype <i>MYH7</i>-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic CardiomyopathyJudith Montag, Kathrin Kowalski, Mirza Makul, et al.Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.Journal of the American College of Cardiology|January 28, 2012
Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort studyIngrid A W van Rijsingen, Eloisa Arbustini, Perry M Elliott, et al.European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.European Journal of Heart Failure|November 28, 2012
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriersIngrid A W van Rijsingen, Eline A Nannenberg, Eloisa Arbustini, et al.Pageof 7