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Journal of Cachexia, Sarcopenia and Muscle
|
March 9, 2021
Obestatin signalling counteracts glucocorticoid-induced skeletal muscle atrophy via NEDD4/KLF15 axis
Tania Cid-Díaz, Saúl Leal-López, Fátima Fernández-Barreiro, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 18, 2021
Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies
Xavier Suárez-Calvet, Esther Fernández-Simón, Patricia Piñol-Jurado, et al.
Science Advances
|
May 29, 2024
DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis
Eden Engal, Aveksha Sharma, Uria Aviel, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
March 23, 2022
A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis
Mona Bensalah, Laura Muraine, Alexis Boulinguiez, et al.
Frontiers in Genetics
|
August 19, 2021
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle
Olivier Boyer, Gillian Butler-Browne, Hector Chinoy, et al.
The Journal of Biological Chemistry
|
June 19, 2008
Inhibition of Chikungunya virus infection in cultured human muscle cells by furin inhibitors: impairment of the maturation of the E2 surface glycoprotein
Simona Ozden, Marianne Lucas-Hourani, Pierre-Emmanuel Ceccaldi, et al.
EMBO Molecular Medicine
|
September 6, 2024
Author Correction: Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
Francesco Galli, Laricia Bragg, Maira Rossi, et al.
EMBO Molecular Medicine
|
March 4, 2024
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
Francesco Galli, Laricia Bragg, Maira Rossi, et al.
Plos Genetics
|
March 28, 2015
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis
Aymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Human Molecular Genetics
|
January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy
Alberto Malerba, Fanny Roth, Pradeep Harish, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 187) with videos related to
Sort By:
Page
of 19
Journal of Cachexia, Sarcopenia and Muscle
|
March 9, 2021
Obestatin signalling counteracts glucocorticoid-induced skeletal muscle atrophy via NEDD4/KLF15 axis
Tania Cid-Díaz, Saúl Leal-López, Fátima Fernández-Barreiro, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 18, 2021
Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies
Xavier Suárez-Calvet, Esther Fernández-Simón, Patricia Piñol-Jurado, et al.
Science Advances
|
May 29, 2024
DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis
Eden Engal, Aveksha Sharma, Uria Aviel, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
March 23, 2022
A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis
Mona Bensalah, Laura Muraine, Alexis Boulinguiez, et al.
Frontiers in Genetics
|
August 19, 2021
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle
Olivier Boyer, Gillian Butler-Browne, Hector Chinoy, et al.
The Journal of Biological Chemistry
|
June 19, 2008
Inhibition of Chikungunya virus infection in cultured human muscle cells by furin inhibitors: impairment of the maturation of the E2 surface glycoprotein
Simona Ozden, Marianne Lucas-Hourani, Pierre-Emmanuel Ceccaldi, et al.
EMBO Molecular Medicine
|
September 6, 2024
Author Correction: Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
Francesco Galli, Laricia Bragg, Maira Rossi, et al.
EMBO Molecular Medicine
|
March 4, 2024
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
Francesco Galli, Laricia Bragg, Maira Rossi, et al.
Plos Genetics
|
March 28, 2015
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis
Aymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Human Molecular Genetics
|
January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy
Alberto Malerba, Fanny Roth, Pradeep Harish, et al.
Page
of 19