檢索結果 - Brenda Gerull

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  1. 1
    Genetic Animal Models for Arrhythmogenic Cardiomyopathy

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

    出版 2020
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  2. 2
    Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy

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

    出版 2021
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  3. 3
    Genetic Insights into Primary Restrictive Cardiomyopathy

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

    出版 2022
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  4. 4
    Novel Gene Locus for Autosomal Dominant Left Ventricular Noncompaction Maps to Chromosome 11p15

    Novel Gene Locus for Autosomal Dominant Left Ventricular Noncompaction Maps to Chromosome 11p15 由 Sabine Klaassen, Susanne Probst, Brenda Gerull, Erwin Oechslin, Peter Nürnberg, Arnd Heuser, Rolf Jenni, Hans Christian Hennies, Ludwig Thierfelder

    出版 2004
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  5. 5
    Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations

    Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations 由 Florian Kirchner, A. Schuetz, Leif‐Hendrik Boldt, Kristina Martens, Gunnar Dittmar, Wilhelm Haverkamp, Ludwig Thierfelder, Udo Heinemann, Brenda Gerull

    出版 2012
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  6. 6
    Homozygous Founder Mutation in Desmocollin-2 ( <i>DSC2</i> ) Causes Arrhythmogenic Cardiomyopathy in the Hutterite Population

    Homozygous Founder Mutation in Desmocollin-2 ( <i>DSC2</i> ) Causes Arrhythmogenic Cardiomyopathy in the Hutterite Population 由 Brenda Gerull, Florian Kirchner, Jessica X. Chong, Julia Tagoe, Kumaran Chandrasekharan, Oliver Strohm, Darrel Waggoner, Carole Ober, Henry J. Duff

    出版 2013
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  7. 7
    Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect

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

    出版 2019
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  8. 8
    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 由 Andreas Brodehl, Darrell D. Belke, Lauren Garnett, Kristina Martens, Nelly Abdelfatah, M. Rodriguez, Catherine Diao, Yong-Xiang Chen, Paul M. K. Gordon, Anders Nygren, Brenda Gerull

    出版 2017
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  9. 9
    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy

    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy 由 Arnd Heuser, Eva Plovie, Patrick T. Ellinor, Katja S. Grossmann, Jordan T. Shin, Thomas Wichter, Craig T. Basson, Bruce B. Lerman, Sabine Klaassen, Ludwig Thierfelder, Calum A. MacRae, Brenda Gerull

    出版 2006
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  10. 10
    Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease

    Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease 由 Michael Gramlich, Beate Michely, Christian Krohne, Arnd Heuser, Bettina Erdmann, Sabine Klaassen, Bryan D. Hudson, Manuela Magarin, Florian Kirchner, Mihail Todiraş, Henk Granzier, Siegfried Labeit, Ludwig Thierfelder, Brenda Gerull

    出版 2009
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  11. 11
    Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2

    Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2 由 Nelly Abdelfatah, Ruping Chen, Henry J. Duff, Colette Seifer, Ilan Buffo, Cathleen Huculak, Stéphanie Clarke, Robin Clegg, Davinder S. Jassal, Paul M. K. Gordon, Carole Ober, Patrick Frosk, Brenda Gerull

    出版 2019
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  12. 12
    Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy

    Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy 由 Ruping Chen, Simone Buchmann, Amos Kroth, Paula Arias-Loza, Michael Kohlhaas, Nicole Wagner, Gianna Grüner, Alexander Nickel, Alexandra Cirnu, Tatjana Williams, Christoph Maack, Süleyman Ergün, Stefan Frantz, Brenda Gerull

    出版 2023
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  13. 13
    Mutations in<i>FLNC</i>are Associated with Familial Restrictive Cardiomyopathy

    Mutations in<i>FLNC</i>are Associated with Familial Restrictive Cardiomyopathy 由 Andreas Brodehl, Raechel A. Ferrier, Sara Hamilton, Steven C. Greenway, Marie‐Anne Bründler, Weiming Yu, William T. Gibson, Margaret L. McKinnon, Barbara McGillivray, Nanette Alvarez, Michael Giuffre, Jeremy Schwartzentruber, Brenda Gerull

    出版 2015
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  14. 14
    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction 由 Sabine Klaassen, Susanne Probst, Erwin Oechslin, Brenda Gerull, Gregor Krings, Pia Schuler, Matthias Greutmann, David Hürlimann, M. Yegitbasi, Lucía Pons, Michael Gramlich, Jörg‐Detlef Drenckhahn, Arnd Heuser, Felix Berger, Rolf Jenni, Ludwig Thierfelder

    出版 2008
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  15. 15
    A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy

    A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy 由 Andreas Brodehl, Jürgen Weiß, Jana Davina Debus, Caroline Stanasiuk, Bärbel Klauke, Marcus André Deutsch, Henrik Fox, Jördis Bax, Hans Ebbinghaus, Anna Gärtner, Jens Tiesmeier, T. Laser, Andreas Peterschröder, Brenda Gerull, Jan Gummert, Lech Paluszkiewicz, Hendrik Milting

    出版 2020
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  16. 16
    Meeting report – Desmosome dysfunction and disease: Alpine desmosome disease meeting

    Meeting report – Desmosome dysfunction and disease: Alpine desmosome disease meeting 由 Volker Spindler, Brenda Gerull, Kathleen J. Green, Andrew P. Kowalczyk, Rudolf E. Leube, Ali J. Marian, Hendrik Milting, Eliane J. Müller, Carien M. Niessen, Aimee Payne, Nicolas Schlegel, Enno Schmidt, Pavel Strnad, Ritva Tikkanen, Franziska Vielmuth, Jens Waschke

    出版 2023
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  17. 17
    Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy

    Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy 由 Andreas Brodehl, Saman Rezazadeh, Tatjana Williams, Nicole Munsie, Daniel Liedtke, Tracey Oh, Raechel A. Ferrier, Yaoqing Shen, Steven J.M. Jones, Amy L. Stiegler, Titus J. Boggon, Henry J. Duff, Jan M. Friedman, William T. Gibson, Sarah J. Childs, Brenda Gerull

    出版 2019
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  18. 18
    Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

    Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy 由 Brenda Gerull, Arnd Heuser, Thomas Wichter, Matthias Paul, Craig T. Basson, Deborah A. McDermott, Bruce B. Lerman, Steve Markowitz, Patrick T. Ellinor, Calum A. MacRae, Stefan Peters, Katja S. Grossmann, Beate Michely, Sabine Klaassen, Walter Birchmeier, Rainer Dietz, Günter Breithardt, Eric Schulze‐Bahr, Ludwig Thierfelder

    出版 2004
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  19. 19
    Epinephrine Infusion in the Evaluation of Unexplained Cardiac Arrest and Familial Sudden Death

    Epinephrine Infusion in the Evaluation of Unexplained Cardiac Arrest and Familial Sudden Death 由 Andrew D. Krahn, Jeff S. Healey, Vijay S. Chauhan, David H. Birnie, Jean Champagne, Shubhayan Sanatani, Kamran Ahmad, Emily Ballantyne, Brenda Gerull, Raymond Yee, Allan C. Skanes, Lorne J. Gula, Peter Leong‐Sit, George J. Klein, Michael H. Gollob, Christopher S. Simpson, Mario Talajic, Martin J. Gardner

    出版 2012
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  20. 20
    Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims

    Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims 由 Christian Steinberg, Gareth J. Padfield, Jean Champagne, Shubhayan Sanatani, Paul Angaran, Jason G. Andrade, Jason D. Roberts, Jeff S. Healey, Vijay S. Chauhan, David H. Birnie, Mikyla Janzen, Brenda Gerull, George J. Klein, Richard Leather, Christopher S. Simpson, Colette Seifer, Mario Talajic, Martin J. Gardner, Andrew D. Krahn

    出版 2016
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