Sustaining Cardiac Claudin-5 Levels Prevents Functional Hallmarks of Cardiomyopathy in a Muscular Dystrophy Mouse Model-Reference-Cited by-同舟云学术

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Sustaining Cardiac Claudin-5 Levels Prevents Functional Hallmarks of Cardiomyopathy in a Muscular Dystrophy Mouse Model

Published:2012-07 Issue:7 Volume:20 Page:1378-1383
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Delfín Dawn A,Xu Ying,Schill Kevin E,Mays Tessily A,Canan Benjamin D,Zang Kara E,Barnum Jamie A,Janssen Paul ML,Rafael-Fortney Jill A

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference29 articles.

1. Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy;Kaspar;J Am Acad Nurse Pract,2009

2. Hereditary muscular dystrophies and the heart;Hermans;Neuromuscul Disord,2010

3. Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy;Duan;Hum Mol Genet,2006

4. Emergent dilated cardiomyopathy caused by targeted repair of dystrophic skeletal muscle;Townsend;Mol Ther,2008

5. Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice;Rafael;Nat Genet,1998

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1. A novel function of claudin-5 in maintaining the structural integrity of the heart and its implications in cardiac pathology;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-08

2. CLDN5: From structure and regulation to roles in tumors and other diseases beyond CNS disorders;Pharmacological Research;2024-02

3. Atrial fibrillation is associated with decreased claudin-5 in cardiomyocyte;2023-07-13

4. Hypoxia-induced vascular remodeling responses in the brain are much more robust than other organs;Microvascular Research;2023-07

5. Micro-dystrophin gene therapy demonstrates long-term cardiac efficacy in a severe Duchenne muscular dystrophy model;Molecular Therapy - Methods & Clinical Development;2023-03

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