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Genes|April 3, 2021
Special Issue "Cardiovascular Genetics"Andreas Brodehl, Hendrik Milting, Brenda GerullFrontiers in Physiology|July 17, 2020
Genetic Animal Models for Arrhythmogenic CardiomyopathyBrenda Gerull, Andreas BrodehlCurrent Heart Failure Reports|September 3, 2021
Insights Into Genetics and Pathophysiology of Arrhythmogenic CardiomyopathyBrenda Gerull, Andreas BrodehlJournal of Clinical Medicine|April 23, 2022
Genetic Insights into Primary Restrictive CardiomyopathyAndreas Brodehl, Brenda GerullBiophysical Reviews|June 22, 2018
Molecular insights into cardiomyopathies associated with desmin (DES) mutationsAndreas Brodehl, Anna Gaertner-Rommel, Hendrik MiltingCells|December 11, 2022
The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic <i>DES</i> Mutations Affecting Filament AssemblyAndreas Brodehl, Stephanie Holler, Jan Gummert, et al.Genes|November 14, 2019
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (<i>DES</i>) Mutation p.Y122H Leading to a Severe Filament Assembly DefectAndreas Brodehl, Seyed Ahmad Pour Hakimi, Caroline Stanasiuk, et al.FEBS Open Bio|April 4, 2019
Incorporation of desmocollin-2 into the plasma membrane requires N-glycosylation at multiple sitesAndreas Brodehl, Caroline Stanasiuk, Dario Anselmetti, et al.STAR Protocols|April 11, 2022
A detailed protocol for expression, purification, and activity determination of recombinant SaCas9Franziska Flottmann, Greta Marie Pohl, Jan Gummert, et al.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.Pageof 23