Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy-Reference-Cited by-同舟云学术

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Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy

Published:2020-03 Issue:3 Volume:28 Page:845-854
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Wasala Nalinda B.,Yue Yongping,Lostal William,Wasala Lakmini P.,Niranjan Nandita,Hajjar Roger J.,Babu Gopal J.,Duan Dongsheng

Funder

Parent Project Muscular Dystrophy

National Institutes of Health

Publisher

Elsevier BV

Subject

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

Reference60 articles.

1. Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy;Burr;Cell Death Differ.,2015

2. Dystrophic cardiomyopathy—potential role of calcium in pathogenesis, treatment and novel therapies;Johnstone;Genes (Basel),2017

3. Absence of dystrophin disrupts skeletal muscle signaling: roles of Ca2+, reactive oxygen species, and nitric oxide in the development of muscular dystrophy;Allen;Physiol. Rev.,2016

4. Dysregulation of calcium homeostasis in muscular dystrophies;Vallejo-Illarramendi;Expert Rev. Mol. Med.,2014

5. SERCA pump isoforms: their role in calcium transport and disease;Periasamy;Muscle Nerve,2007

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1. Duchenne muscular dystrophy skeletal muscle cells derived from human induced pluripotent stem cells recapitulate various calcium dysregulation pathways;Cell Calcium;2024-11

2. Pathological mutations in the phospholamban cytoplasmic region affect its topology and dynamics modulating the extent of SERCA inhibition;Biochimica et Biophysica Acta (BBA) - Biomembranes;2024-10

3. Cardiomyopathy in Duchenne Muscular Dystrophy and the Potential for Mitochondrial Therapeutics to Improve Treatment Response;Cells;2024-07-09

4. Systemic Treatment of Body‐Wide Duchenne Muscular Dystrophy Symptoms;Clinical Pharmacology & Therapeutics;2024-07-04

5. Inhibition of miR-25 ameliorates cardiac and skeletal muscle dysfunction in aged mdx/utrn haploinsufficient (+/−) mice;Molecular Therapy - Nucleic Acids;2024-06

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