Bilaketaren emaitzak - Brodehl, Andreas

Genetic Animal Models for Arrhythmogenic Cardiomyopathy nork Gerull, Brenda, Brodehl, Andreas

Testu osoa Testu osoa Testu osoa

Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy nork Gerull, Brenda, Brodehl, Andreas

Testu osoa Testu osoa Testu osoa

Genetic Insights into Primary Restrictive Cardiomyopathy nork Brodehl, Andreas, Gerull, Brenda

Testu osoa Testu osoa Testu osoa

Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene? nork Gaertner, Anna, Brodehl, Andreas, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Special Issue “Cardiovascular Genetics” nork Brodehl, Andreas, Milting, Hendrik, Gerull, Brenda

Testu osoa Testu osoa Testu osoa

Molecular insights into cardiomyopathies associated with desmin (DES) mutations nork Brodehl, Andreas, Gaertner-Rommel, Anna, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

RBM20 mutations in left ventricular non‐compaction cardiomyopathy nork Gaertner, Anna, Klauke, Bärbel, Brodehl, Andreas, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Incorporation of desmocollin‐2 into the plasma membrane requires N‐glycosylation at multiple sites nork Brodehl, Andreas, Stanasiuk, Caroline, Anselmetti, Dario, Gummert, Jan, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

A detailed protocol for expression, purification, and activity determination of recombinant SaCas9 nork Flottmann, Franziska, Pohl, Greta Marie, Gummert, Jan, Milting, Hendrik, Brodehl, Andreas

Testu osoa Testu osoa Testu osoa

Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies nork Brodehl, Andreas, Ebbinghaus, Hans, Deutsch, Marcus-André, Gummert, Jan, Gärtner, Anna, Ratnavadivel, Sandra, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Functional characterization of desmin mutant p.P419S nork Brodehl, Andreas, Dieding, Mareike, Cakar, Hamdin, Klauke, Bärbel, Walhorn, Volker, Gummert, Jan, Anselmetti, Dario, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Apertureless scanning near-field optical microscopy of sparsely labeled tobacco mosaic viruses and the intermediate filament desmin nork Harder, Alexander, Dieding, Mareike, Walhorn, Volker, Degenhard, Sven, Brodehl, Andreas, Wege, Christina, Milting, Hendrik, Anselmetti, Dario

Testu osoa Testu osoa Testu osoa

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect nork Brodehl, Andreas, Pour Hakimi, Seyed Ahmad, Stanasiuk, Caroline, Ratnavadivel, Sandra, Hendig, Doris, Gaertner, Anna, Gerull, Brenda, Gummert, Jan, Paluszkiewicz, Lech, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy nork Schirmer, Ilona, Dieding, Mareike, Klauke, Bärbel, Brodehl, Andreas, Gaertner‐Rommel, Anna, Walhorn, Volker, Gummert, Jan, Schulz, Uwe, Paluszkiewicz, Lech, Anselmetti, Dario, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Compound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern nork Gaertner, Anna, Burr, Lidia, Klauke, Baerbel, Brodehl, Andreas, Laser, Kai Thorsten, Klingel, Karin, Tiesmeier, Jens, Schulz, Uwe, zu Knyphausen, Edzard, Gummert, Jan, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3 nork Brodehl, Andreas, Hain, Carsten, Flottmann, Franziska, Ratnavadivel, Sandra, Gaertner, Anna, Klauke, Bärbel, Kalinowski, Jörn, Körperich, Hermann, Gummert, Jan, Paluszkiewicz, Lech, Deutsch, Marcus-André, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling nork Brodehl, Andreas, Belke, Darrell D., Garnett, Lauren, Martens, Kristina, Abdelfatah, Nelly, Rodriguez, Marcela, Diao, Catherine, Chen, Yong-Xiang, Gordon, Paul M. K., Nygren, Anders, Gerull, Brenda

Testu osoa Testu osoa Testu osoa

The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy nork Gaertner, Anna, Bloebaum, Julia, Brodehl, Andreas, Klauke, Baerbel, Sielemann, Katharina, Kassner, Astrid, Fox, Henrik, Morshuis, Michiel, Tiesmeier, Jens, Schulz, Uwe, Knoell, Ralph, Gummert, Jan, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Dual Color Photoactivation Localization Microscopy of Cardiomyopathy-associated Desmin Mutants nork Brodehl, Andreas, Hedde, Per Niklas, Dieding, Mareike, Fatima, Azra, Walhorn, Volker, Gayda, Susan, Šarić, Tomo, Klauke, Bärbel, Gummert, Jan, Anselmetti, Dario, Heilemann, Mike, Nienhaus, Gerd Ulrich, Milting, Hendrik

Testu osoa Testu osoa Testu osoa

Distinct Myocardial Transcriptomic Profiles of Cardiomyopathies Stratified by the Mutant Genes nork Sielemann, Katharina, Elbeck, Zaher, Gärtner, Anna, Brodehl, Andreas, Stanasiuk, Caroline, Fox, Henrik, Paluszkiewicz, Lech, Tiesmeier, Jens, Wlost, Stefan, Gummert, Jan, Albaum, Stefan P., Sielemann, Janik, Knöll, Ralph, Milting, Hendrik

Testu osoa Testu osoa Testu osoa