International audienceMuscular dystrophies (MD) are a group of genetically and phenotypically heterogeneous inherited disorders characterized by the progressive degeneration of the skeletal muscle tissue. In the last decade, a tremendous amount of studies were performed to test therapeutic strategies in animal models. Evaluation of such strategies requires the use of criteria predictive of their therapeutic relevance. Here we describe a simple, noninvasive assay to monitor muscle degenerative process. An adeno-associated vector encoding a secreted form of murine embryonic alkaline phosphatase (mSEAP) reporter gene is administrated at the time of treatment. The amount of circulating mSEAP will reflect the level of myofiber survival. We teste...
AbstractMuch progress has been made over the past decade elucidating the molecular basis for a varie...
Duchenne Muscular Dystrophy (DMD) is a X-linked inherited muscle-wasting disease primarily affecting...
To investigate efficacy of synthetic SPc5-12 promoter expression in skeletal and heart muscles and c...
International audienceMuscular dystrophies are a genetically and phenotypically heterogeneous group ...
Thesis (Ph.D.), Molecular Biosciences, Washington State UniversityMuscular dystrophies are a subset ...
Gene therapy is a promising approach for the treatment of Duchenne Muscular Dystrophy (DMD). Adenovi...
International audienceIn preclinical models for Duchenne muscular dystrophy, dystrophin restoration ...
Muscular Dystrophy (MD) is a progressive muscle wasting disease which currently has no cure, and is ...
The objective of this study was to investigate the efficacy of using quantitative magnetic resonance...
<div><p>The objective of this study was to investigate the efficacy of using quantitative magnetic r...
BackgroundDuchenne muscular dystrophy (DMD) is due to mutations in the gene coding for human DMD; DM...
Abstract Intramuscular injection and electroporation of naked plasmid DNA (IMEP) has emerged as a po...
The objective of this project was to evaluate the alleviation of muscle wasting phenotypes by hepati...
International audienceThe adeno-associated virus (AAV) vector is an efficient tool for gene delivery...
AbstractMuch progress has been made over the past decade elucidating the molecular basis for a varie...
Duchenne Muscular Dystrophy (DMD) is a X-linked inherited muscle-wasting disease primarily affecting...
To investigate efficacy of synthetic SPc5-12 promoter expression in skeletal and heart muscles and c...
International audienceMuscular dystrophies are a genetically and phenotypically heterogeneous group ...
Thesis (Ph.D.), Molecular Biosciences, Washington State UniversityMuscular dystrophies are a subset ...
Gene therapy is a promising approach for the treatment of Duchenne Muscular Dystrophy (DMD). Adenovi...
International audienceIn preclinical models for Duchenne muscular dystrophy, dystrophin restoration ...
Muscular Dystrophy (MD) is a progressive muscle wasting disease which currently has no cure, and is ...
The objective of this study was to investigate the efficacy of using quantitative magnetic resonance...
<div><p>The objective of this study was to investigate the efficacy of using quantitative magnetic r...
BackgroundDuchenne muscular dystrophy (DMD) is due to mutations in the gene coding for human DMD; DM...
Abstract Intramuscular injection and electroporation of naked plasmid DNA (IMEP) has emerged as a po...
The objective of this project was to evaluate the alleviation of muscle wasting phenotypes by hepati...
International audienceThe adeno-associated virus (AAV) vector is an efficient tool for gene delivery...
AbstractMuch progress has been made over the past decade elucidating the molecular basis for a varie...
Duchenne Muscular Dystrophy (DMD) is a X-linked inherited muscle-wasting disease primarily affecting...
To investigate efficacy of synthetic SPc5-12 promoter expression in skeletal and heart muscles and c...