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Neurology
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December 25, 2016
Correlation between PABPN1 genotype and disease severity in oculopharyngeal muscular dystrophy
Pascale Richard, Capucine Trollet, Tanya Stojkovic, et al.
Current Opinion in Pharmacology
|
December 25, 2022
Update on anti-fibrotic pharmacotherapies in skeletal muscle disease
Laura Muraine, Mona Bensalah, Gillian Butler-Browne, et al.
The American Journal of Pathology
|
September 16, 2022
Dystrophin Restoration after Adeno-Associated Virus U7-Mediated Dmd Exon Skipping Is Modulated by Muscular Exercise in the Severe D2-Mdx Duchenne Muscular Dystrophy Murine Model
Alexandra Monceau, Dylan Moutachi, Mégane Lemaitre, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 28, 2010
Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice
Julie Dumonceaux, Solenne Marie, Cyriaque Beley, et al.
Human Vaccines & Immunotherapeutics
|
July 24, 2013
DNA electroporation in rabbits as a method for generation of high-titer neutralizing antisera: examples of the botulinum toxins types A, B, and E
Aurore Burgain, Alice Rochard, Capucine Trollet, et al.
Human Molecular Genetics
|
May 31, 2008
RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology
Mohammad M Ghahramani Seno, Ian R Graham, Takis Athanasopoulos, et al.
Frontiers in Cell and Developmental Biology
|
October 6, 2022
Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their "virtual" secretome
Elisa Negroni, Maria Kondili, Laura Muraine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 4, 2008
Codon and mRNA sequence optimization of microdystrophin transgenes improves expression and physiological outcome in dystrophic mdx mice following AAV2/8 gene transfer
Helen Foster, Paul S Sharp, Takis Athanasopoulos, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
May 9, 2019
Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD)
Pradeep Harish, Alberto Malerba, Ngoc Lu-Nguyen, et al.
Human Gene Therapy
|
April 2, 2011
Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx mice
Taeyoung Koo, Alberto Malerba, Takis Athanasopoulos, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 61) with videos related to
Sort By:
Page
of 7
Neurology
|
December 25, 2016
Correlation between PABPN1 genotype and disease severity in oculopharyngeal muscular dystrophy
Pascale Richard, Capucine Trollet, Tanya Stojkovic, et al.
Current Opinion in Pharmacology
|
December 25, 2022
Update on anti-fibrotic pharmacotherapies in skeletal muscle disease
Laura Muraine, Mona Bensalah, Gillian Butler-Browne, et al.
The American Journal of Pathology
|
September 16, 2022
Dystrophin Restoration after Adeno-Associated Virus U7-Mediated Dmd Exon Skipping Is Modulated by Muscular Exercise in the Severe D2-Mdx Duchenne Muscular Dystrophy Murine Model
Alexandra Monceau, Dylan Moutachi, Mégane Lemaitre, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 28, 2010
Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice
Julie Dumonceaux, Solenne Marie, Cyriaque Beley, et al.
Human Vaccines & Immunotherapeutics
|
July 24, 2013
DNA electroporation in rabbits as a method for generation of high-titer neutralizing antisera: examples of the botulinum toxins types A, B, and E
Aurore Burgain, Alice Rochard, Capucine Trollet, et al.
Human Molecular Genetics
|
May 31, 2008
RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology
Mohammad M Ghahramani Seno, Ian R Graham, Takis Athanasopoulos, et al.
Frontiers in Cell and Developmental Biology
|
October 6, 2022
Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their "virtual" secretome
Elisa Negroni, Maria Kondili, Laura Muraine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 4, 2008
Codon and mRNA sequence optimization of microdystrophin transgenes improves expression and physiological outcome in dystrophic mdx mice following AAV2/8 gene transfer
Helen Foster, Paul S Sharp, Takis Athanasopoulos, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
May 9, 2019
Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD)
Pradeep Harish, Alberto Malerba, Ngoc Lu-Nguyen, et al.
Human Gene Therapy
|
April 2, 2011
Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx mice
Taeyoung Koo, Alberto Malerba, Takis Athanasopoulos, et al.
Page
of 7