Showing results (41-50 of 111) with videos related to
Sort By:
Pageof 12
Heart & Lung : the Journal of Critical Care|October 25, 2011
Novel c.367_369del LMNA mutation manifesting as severe arrhythmias, dilated cardiomyopathy, and myopathyHans Keller, Josef Finsterer, Christine Steger, et al.Circulation|June 3, 2004
Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15Sabine Sasse-Klaassen, Susanne Probst, Brenda Gerull, et al.Frontiers in Bioscience (Landmark Edition)|April 3, 2023
The Consideration of Pseudoxanthoma Elasticum as a Progeria SyndromeJanina Tiemann, Christopher Lindenkamp, Thomas Wagner, et al.Journal of Clinical Medicine|July 15, 2020
New Insights on Genetic Diagnostics in Cardiomyopathy and Arrhythmia Patients Gained by Stepwise Exome Data AnalysisKonstantinos Kolokotronis, Natalie Pluta, Eva Klopocki, et al.Journal of Molecular Medicine (Berlin, Germany)|May 31, 2006
Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathyBrenda Gerull, John Atherton, Anke Geupel, et al.Stem Cell Research|February 28, 2021
CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM)Anna Janz, Miriam Zink, Alexandra Cirnu, et al.Human Mutation|March 30, 2019
Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotypeKonstantinos Kolokotronis, Jirko Kühnisch, Eva Klopocki, et al.Stem Cell Research|June 11, 2020
Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutationAnna Janz, Ruping Chen, Martina Regensburger, et al.Cardiovascular Research|February 4, 2021
Immuno-metabolic interfaces in cardiac disease and failureEdoardo Bertero, Jan Dudek, Clement Cochain, et al.The American Journal of Cardiology|April 6, 2012
A novel titin mutation in adult-onset familial dilated cardiomyopathyGuy Yoskovitz, Yael Peled, Michael Gramlich, et al.Pageof 12