Cardiovascular phenotype of the


Journal

Disease models & mechanisms
ISSN: 1754-8411
Titre abrégé: Dis Model Mech
Pays: England
ID NLM: 101483332

Informations de publication

Date de publication:
22 02 2021
Historique:
received: 08 10 2020
accepted: 23 12 2020
entrez: 23 2 2021
pubmed: 24 2 2021
medline: 19 1 2022
Statut: epublish

Résumé

Besides skeletal muscle abnormalities, Duchenne muscular dystrophy (DMD) patients present with dilated cardiomyopathy development, which considerably contributes to morbidity and mortality. Because the mechanisms responsible for the cardiac complications in the context of DMD are largely unknown, evidence-based therapy approaches are still lacking. This has increased the need for basic research efforts into animal models for DMD. Here, we characterized in detail the cardiovascular abnormalities of

Identifiants

pubmed: 33619211
pii: 14/2/dmm047704
doi: 10.1242/dmm.047704
pmc: PMC7927653
pii:
doi:

Substances chimiques

CACNA1C protein, human 0
Calcium Channels, L-Type 0
DMD protein, human 0
Dmd protein, rat 0
Dystrophin 0
Peptidyl-Dipeptidase A EC 3.4.15.1
Calcium SY7Q814VUP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Austrian Science Fund FWF
ID : P 30234
Pays : Austria

Informations de copyright

© 2021. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing or financial interests.

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Auteurs

Petra Lujza Szabó (PL)

Ludwig Boltzmann Institute for Cardiovascular Research at Center for Biomedical Research, Medical University of Vienna, Vienna 1090, Austria.

Janine Ebner (J)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

Xaver Koenig (X)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

Ouafa Hamza (O)

Ludwig Boltzmann Institute for Cardiovascular Research at Center for Biomedical Research, Medical University of Vienna, Vienna 1090, Austria.

Simon Watzinger (S)

Ludwig Boltzmann Institute for Cardiovascular Research at Center for Biomedical Research, Medical University of Vienna, Vienna 1090, Austria.

Sandra Trojanek (S)

Center for Anatomy and Cell Biology, Medical University of Vienna, Vienna 1090, Austria.

Dietmar Abraham (D)

Center for Anatomy and Cell Biology, Medical University of Vienna, Vienna 1090, Austria.

Hannes Todt (H)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

Helmut Kubista (H)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

Klaus Schicker (K)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

Séverine Remy (S)

INSERM, Center for Research in Transplantation and Immunology, UMR 1064, Nantes Université, F-44000 Nantes, France.

Ignacio Anegon (I)

INSERM, Center for Research in Transplantation and Immunology, UMR 1064, Nantes Université, F-44000 Nantes, France.

Attila Kiss (A)

Ludwig Boltzmann Institute for Cardiovascular Research at Center for Biomedical Research, Medical University of Vienna, Vienna 1090, Austria attila.kiss@meduniwien.ac.at.

Bruno K Podesser (BK)

Ludwig Boltzmann Institute for Cardiovascular Research at Center for Biomedical Research, Medical University of Vienna, Vienna 1090, Austria.

Karlheinz Hilber (K)

Department of Neurophysiology and Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna 1090, Austria.

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Classifications MeSH