Hasil Pencarian - Andreas Brodehl

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  1. 1
    Genetic Animal Models for Arrhythmogenic Cardiomyopathy

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

    Diterbitkan 2020-06-01
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  2. 2
    Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene?

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

    Diterbitkan 2018-11-01
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  3. 3
    The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic <i>DES</i> Mutations Affecting Filament Assembly

    The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic <i>DES</i> Mutations Affecting Filament Assembly oleh Andreas Brodehl, Stephanie Holler, Jan Gummert, Hendrik Milting

    Diterbitkan 2022-12-01
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  4. 4
    RBM20 mutations in left ventricular non‐compaction cardiomyopathy

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

    Diterbitkan 2020-03-01
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  5. 5
    Incorporation of desmocollin‐2 into the plasma membrane requires N‐glycosylation at multiple sites

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

    Diterbitkan 2019-05-01
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  6. 6
    A detailed protocol for expression, purification, and activity determination of recombinant SaCas9

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

    Diterbitkan 2022-06-01
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  7. 7
    Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies

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

    Diterbitkan 2019-09-01
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  8. 8
    Apertureless scanning near-field optical microscopy of sparsely labeled tobacco mosaic viruses and the intermediate filament desmin

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

    Diterbitkan 2013-09-01
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  9. 9
    Altered Expression of <i>TMEM43</i> Causes Abnormal Cardiac Structure and Function in Zebrafish

    Altered Expression of <i>TMEM43</i> Causes Abnormal Cardiac Structure and Function in Zebrafish oleh Miriam Zink, Anne Seewald, Mareike Rohrbach, Andreas Brodehl, Daniel Liedtke, Tatjana Williams, Sarah J. Childs, Brenda Gerull

    Diterbitkan 2022-08-01
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  10. 10
    The Consideration of Pseudoxanthoma Elasticum as a Progeria Syndrome

    The Consideration of Pseudoxanthoma Elasticum as a Progeria Syndrome oleh Janina Tiemann, Christopher Lindenkamp, Thomas Wagner, Andreas Brodehl, Ricarda Plümers, Isabel Faust-Hinse, Cornelius Knabbe, Doris Hendig

    Diterbitkan 2023-03-01
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  11. 11
    Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing

    Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing oleh Greta Marie Pohl, Manuel Göz, Anna Gaertner, Andreas Brodehl, Tolga Cimen, Ardan M. Saguner, Eric Schulze-Bahr, Volker Walhorn, Dario Anselmetti, Hendrik Milting

    Diterbitkan 2023-05-01
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  12. 12
    Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

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

    Diterbitkan 2022-06-01
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  13. 13
    The Desmin Mutation <i>DES</i>-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3

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

    Diterbitkan 2021-10-01
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  14. 14
    Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling.

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

    Diterbitkan 2017-01-01
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  15. 15
    The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report

    The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report oleh Roman Myasnikov, Andreas Brodehl, Alexey Meshkov, Olga Kulikova, Anna Kiseleva, Greta Marie Pohl, Evgeniia Sotnikova, Mikhail Divashuk, Marina Klimushina, Anastasia Zharikova, Maria Pokrovskaya, Sergey Koretskiy, Maria Kharlap, Elena Mershina, Valentin Sinitsyn, Elena Basargina, Leila Gandaeva, Vladimir Barskiy, Sergey Boytsov, Hendrik Milting, Oxana Drapkina

    Diterbitkan 2021-06-01
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  16. 16
    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset

    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset oleh Andreas Brodehl, Alexey Meshkov, Roman Myasnikov, Anna Kiseleva, Olga Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail Divashuk, Greta Marie Pohl, Maria Kudryavtseva, Karin Klingel, Brenda Gerull, Anastasia Zharikova, Jan Gummert, Sergey Koretskiy, Stephan Schubert, Elena Mershina, Anna Gärtner, Polina Pilus, Kai Thorsten Laser, Valentin Sinitsyn, Sergey Boytsov, Oxana Drapkina, Hendrik Milting

    Diterbitkan 2021-04-01
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