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Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy

Data up to Jan 2025

Published1995
Citations153
References20

Total Citations Per Year

Abstract

References (20)

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The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

1991 • 892 citations

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1992 • 489 citations

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

1991 • 486 citations

Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice

1993 • 455 citations

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice.

1991 • 424 citations

Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle

1991 • 368 citations

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1988 • 343 citations

Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice.

1993 • 169 citations

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1989 • 167 citations

Multiple regulatory elements contribute differentially to muscle creatine kinase enhancer activity in skeletal and cardiac muscle.

1993 • 143 citations

Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster

1993 • 127 citations

Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo

1993 • 120 citations

Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice

1992 • 69 citations

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1991 • 44 citations

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Expression of human full-length and minidystrophin in transgenic mdx mice: implications… (1995) – Human Molecular Genetics | Metascience Observatory Explorer