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Arthritis Research & Therapy
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December 17, 2011
Regenerative potential of human muscle stem cells in chronic inflammation
Bouke J Duijnisveld, Anne Bigot, Karel G M Beenakker, et al.
Medcomm
|
January 16, 2026
Obestatin Treatment Counteracts Muscle Wasting by Reactivation of Autophagy in Duchenne Muscular Dystrophy
Icía Santos-Zas, Silvia Costas-Abalde, Andrea C Lodeiro, et al.
Plos One
|
June 15, 2007
Human muscle satellite cells as targets of Chikungunya virus infection
Simona Ozden, Michel Huerre, Jean-Pierre Riviere, et al.
Plos One
|
March 22, 2014
Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy
Claudia Langhans, Steffen Weber-Carstens, Franziska Schmidt, et al.
Nature Communications
|
April 16, 2024
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus
Tayma Handal, Sarah Juster, Manar Abu Diab, et al.
Acta Neuropathologica
|
October 5, 2022
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy
Fanny Roth, Jamila Dhiab, Alexis Boulinguiez, et al.
Brain : a Journal of Neurology
|
May 10, 2018
JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis
Leandro Ladislau, Xavier Suárez-Calvet, Ségolène Toquet, et al.
Skeletal Muscle
|
November 2, 2011
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders
Kamel Mamchaoui, Capucine Trollet, Anne Bigot, et al.
Human Molecular Genetics
|
March 9, 2010
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres
Capucine Trollet, Seyed Yahya Anvar, Andrea Venema, et al.
Iscience
|
December 30, 2024
Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity
Judit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 187) with videos related to
Sort By:
Page
of 19
Arthritis Research & Therapy
|
December 17, 2011
Regenerative potential of human muscle stem cells in chronic inflammation
Bouke J Duijnisveld, Anne Bigot, Karel G M Beenakker, et al.
Medcomm
|
January 16, 2026
Obestatin Treatment Counteracts Muscle Wasting by Reactivation of Autophagy in Duchenne Muscular Dystrophy
Icía Santos-Zas, Silvia Costas-Abalde, Andrea C Lodeiro, et al.
Plos One
|
June 15, 2007
Human muscle satellite cells as targets of Chikungunya virus infection
Simona Ozden, Michel Huerre, Jean-Pierre Riviere, et al.
Plos One
|
March 22, 2014
Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy
Claudia Langhans, Steffen Weber-Carstens, Franziska Schmidt, et al.
Nature Communications
|
April 16, 2024
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus
Tayma Handal, Sarah Juster, Manar Abu Diab, et al.
Acta Neuropathologica
|
October 5, 2022
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy
Fanny Roth, Jamila Dhiab, Alexis Boulinguiez, et al.
Brain : a Journal of Neurology
|
May 10, 2018
JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis
Leandro Ladislau, Xavier Suárez-Calvet, Ségolène Toquet, et al.
Skeletal Muscle
|
November 2, 2011
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders
Kamel Mamchaoui, Capucine Trollet, Anne Bigot, et al.
Human Molecular Genetics
|
March 9, 2010
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres
Capucine Trollet, Seyed Yahya Anvar, Andrea Venema, et al.
Iscience
|
December 30, 2024
Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity
Judit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Page
of 19