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Vincent Mouly

Showing results (151-160 of 187) with videos related to

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Journal of Cachexia, Sarcopenia and Muscle|March 9, 2021
Obestatin signalling counteracts glucocorticoid-induced skeletal muscle atrophy via NEDD4/KLF15 axisTania 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 biopsiesXavier 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 pathogenesisEden 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 fibrosisMona Bensalah, Laura Muraine, Alexis Boulinguiez, et al.
Frontiers in Genetics|August 19, 2021
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal MuscleOlivier 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 glycoproteinSimona 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 DystrophyFrancesco 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 DystrophyFrancesco 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 pathogenesisAymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Human Molecular Genetics|January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophyAlberto Malerba, Fanny Roth, Pradeep Harish, et al.
Pageof 19

Showing results (151-160 of 187) with videos related to

Sort By:
Pageof 19
Journal of Cachexia, Sarcopenia and Muscle|March 9, 2021
Obestatin signalling counteracts glucocorticoid-induced skeletal muscle atrophy via NEDD4/KLF15 axisTania 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 biopsiesXavier 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 pathogenesisEden 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 fibrosisMona Bensalah, Laura Muraine, Alexis Boulinguiez, et al.
Frontiers in Genetics|August 19, 2021
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal MuscleOlivier 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 glycoproteinSimona 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 DystrophyFrancesco 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 DystrophyFrancesco 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 pathogenesisAymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Human Molecular Genetics|January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophyAlberto Malerba, Fanny Roth, Pradeep Harish, et al.
Pageof 19