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Vincent Mouly

Showing results (91-100 of 187) with videos related to

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Frontiers in Cellular and Infection Microbiology|December 13, 2019
<i>Toxoplasma gondii</i> Impairs Myogenesis <i>in vitro</i>, With Changes in Myogenic Regulatory Factors, Altered Host Cell Proliferation and Secretory ProfilePaloma de Carvalho Vieira, Mariana Caldas Waghabi, Daniela Gois Beghini, et al.
Frontiers in Cell and Developmental Biology|March 21, 2022
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 MutationsJaione Lasa-Elgarresta, Laura Mosqueira-Martín, Klaudia González-Imaz, et al.
Human Mutation|December 3, 2009
Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skippingNicolas Wein, Aurélie Avril, Marc Bartoli, et al.
Medicine and Science in Sports and Exercise|September 16, 2003
Athletes with exercise-associated fatigue have abnormally short muscle DNA telomeresMalcolm Collins, Valerie Renault, Liesl A Grobler, et al.
Aging Cell|June 15, 2007
Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophiesChun-Hong Zhu, Vincent Mouly, Racquel N Cooper, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 5, 2013
Reading frame correction by targeted genome editing restores dystrophin expression in cells from Duchenne muscular dystrophy patientsDavid G Ousterout, Pablo Perez-Pinera, Pratiksha I Thakore, et al.
Disease Models & Mechanisms|September 28, 2014
Predictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophyInès Barthélémy, Fernanda Pinto-Mariz, Erica Yada, et al.
Stem Cells and Cloning : Advances and Applications|December 7, 2018
A functional human motor unit platform engineered from human embryonic stem cells and immortalized skeletal myoblastsMarwah Abd Al Samid, Jamie S McPhee, Jasdeep Saini, et al.
Annals of Neurology|February 23, 2017
Pathogenic role of anti-signal recognition protein and anti-3-Hydroxy-3-methylglutaryl-CoA reductase antibodies in necrotizing myopathies: Myofiber atrophy and impairment of muscle regeneration in necrotizing autoimmune myopathiesLouiza Arouche-Delaperche, Yves Allenbach, Damien Amelin, et al.
Pageof 19

Showing results (91-100 of 187) with videos related to

Sort By:
Pageof 19
Frontiers in Cellular and Infection Microbiology|December 13, 2019
<i>Toxoplasma gondii</i> Impairs Myogenesis <i>in vitro</i>, With Changes in Myogenic Regulatory Factors, Altered Host Cell Proliferation and Secretory ProfilePaloma de Carvalho Vieira, Mariana Caldas Waghabi, Daniela Gois Beghini, et al.
Frontiers in Cell and Developmental Biology|March 21, 2022
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 MutationsJaione Lasa-Elgarresta, Laura Mosqueira-Martín, Klaudia González-Imaz, et al.
Human Mutation|December 3, 2009
Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skippingNicolas Wein, Aurélie Avril, Marc Bartoli, et al.
Medicine and Science in Sports and Exercise|September 16, 2003
Athletes with exercise-associated fatigue have abnormally short muscle DNA telomeresMalcolm Collins, Valerie Renault, Liesl A Grobler, et al.
Aging Cell|June 15, 2007
Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophiesChun-Hong Zhu, Vincent Mouly, Racquel N Cooper, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 5, 2013
Reading frame correction by targeted genome editing restores dystrophin expression in cells from Duchenne muscular dystrophy patientsDavid G Ousterout, Pablo Perez-Pinera, Pratiksha I Thakore, et al.
Disease Models & Mechanisms|September 28, 2014
Predictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophyInès Barthélémy, Fernanda Pinto-Mariz, Erica Yada, et al.
Stem Cells and Cloning : Advances and Applications|December 7, 2018
A functional human motor unit platform engineered from human embryonic stem cells and immortalized skeletal myoblastsMarwah Abd Al Samid, Jamie S McPhee, Jasdeep Saini, et al.
Annals of Neurology|February 23, 2017
Pathogenic role of anti-signal recognition protein and anti-3-Hydroxy-3-methylglutaryl-CoA reductase antibodies in necrotizing myopathies: Myofiber atrophy and impairment of muscle regeneration in necrotizing autoimmune myopathiesLouiza Arouche-Delaperche, Yves Allenbach, Damien Amelin, et al.
Pageof 19