Dystrophin deficiency impairs vascular structure and function in the canine model of Duchenne muscular dystrophy

Author:

Kodippili Kasun1ORCID,Thorne Pamela K2,Laughlin M Harold2,Duan Dongsheng1234ORCID

Affiliation:

1. Department of Molecular Microbiology and Immunology University of Missouri Columbia MO USA

2. Department of Biomedical Sciences College of Veterinary Medicine, University of Missouri Columbia MO USA

3. Department of Neurology School of Medicine, University of Missouri Columbia MO USA

4. Department of Biomedical, Biological & Chemical Engineering College of Engineering, University of Missouri Columbia MO USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Pathology and Forensic Medicine

Reference60 articles.

1. 2004 William Allan Award address. Cloning of the DMD gene;Kunkel LM;Am J Hum Genet,2005

2. Duchenne muscular dystrophin;Duan D;Nat Rev Dis Primers,2021

3. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig M;Cell,1987

4. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman EP;Cell,1987

5. On the pathogenesis of Duchenne muscular dystrophy;Fenichel GM;Dev Med Child Neurol,1975

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