A Simplified Immune Suppression Scheme Leads to Persistent Micro-dystrophin Expression in Duchenne Muscular Dystrophy Dogs-Reference-Cited by-同舟云学术

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A Simplified Immune Suppression Scheme Leads to Persistent Micro-dystrophin Expression in Duchenne Muscular Dystrophy Dogs

Published:2012-02 Issue:2 Volume:23 Page:202-209
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Shin Jin-Hong¹,Yue Yongping¹,Srivastava Arun²,Smith Bruce³,Lai Yi¹,Duan Dongsheng¹

Affiliation:

1. Department of Molecular Microbiology and Immunology, University of Missouri, Columbia, Missouri 65212.

2. Departments of Pediatrics and Molecular Genetics & Microbiology, University of Florida Gainesville, Florida 32611.

3. Scott-Ritchey Research Center and the Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, Alabama 36849.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2011.147

Reference42 articles.

1. The Polyproline Site in Hinge 2 Influences the Functional Capacity of Truncated Dystrophins

2. An optimized protocol for detection of E. coli β-galactosidase in lung tissue following gene transfer

3. Gene Therapy Strategies for Duchenne Muscular Dystrophy Utilizing Recombinant Adeno-associated Virus Vectors

4. The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs

5. Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy

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1. SERCA2a overexpression improves muscle function in a canine Duchenne muscular dystrophy model;Molecular Therapy - Methods & Clinical Development;2024-06

2. Immunosuppression reduces rAAV2.5T neutralizing antibodies that limit efficacy following repeat dosing to ferret lungs;Molecular Therapy - Methods & Clinical Development;2023-06

3. Molecular Genetic Therapies in the Muscular Dystrophies;Current Clinical Neurology;2023

4. Rational Use of Immunosuppressive Corticosteroids in Liver-Directed Adeno-Associated Virus Gene Therapy Studies;Human Gene Therapy;2022-02-01

5. Intraosseous transplant of dystrophin expressing chimeric (DEC) cells improves skeletal muscle function in mdx mouse model of Duchenne muscular dystrophy;Advances in Interventional Cardiology;2021

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