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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2013
Autologous myoblast transplantation for oculopharyngeal muscular dystrophy: a phase I/IIa clinical study
Sophie Périé, Capucine Trollet, Vincent Mouly, et al.
ACS Omega
|
January 8, 2026
Human Laminin-111-Derived AG73 Increases Proliferation, Migration, and Differentiation of Human Myoblasts: A Promising Candidate in Regenerative Medicine
Samuel Iwao Maia Horita, Mona Bensalah, Anne Bigot, et al.
BMC Neurology
|
July 3, 2013
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophy
Vered Raz, Ellen Sterrenburg, Samantha Routledge, et al.
Nucleic Acids Research
|
July 10, 2012
Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation
Eleonora de Klerk, Andrea Venema, S Yahya Anvar, et al.
Molecular Therapy. Nucleic Acids
|
March 19, 2021
BB-301: a silence and replace AAV-based vector for the treatment of oculopharyngeal muscular dystrophy
Vanessa Strings-Ufombah, Alberto Malerba, Shih-Chu Kao, et al.
EMBO Reports
|
July 1, 2026
Publisher Correction: Collagen VI is a fibrosis-associated signal disrupting muscle regeneration across distinct human myopathies
Laura Muraine, Mona Bensalah, Stephen Gargan, et al.
EMBO Reports
|
June 19, 2026
Collagen VI is a fibrosis-associated signal disrupting muscle regeneration across distinct human myopathies
Laura Muraine, Mona Bensalah, Stephen Gargan, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 3, 2021
Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation
Aline Bamia, Maha Sinane, Rima Naït-Saïdi, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling
Pascale Richard, Capucine Trollet, Teresa Gidaro, et al.
Cell Death & Disease
|
May 9, 2026
EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne muscular dystrophy
Maeva Zamperoni, Laura Muraine, Minh-Y Tran, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2013
Autologous myoblast transplantation for oculopharyngeal muscular dystrophy: a phase I/IIa clinical study
Sophie Périé, Capucine Trollet, Vincent Mouly, et al.
ACS Omega
|
January 8, 2026
Human Laminin-111-Derived AG73 Increases Proliferation, Migration, and Differentiation of Human Myoblasts: A Promising Candidate in Regenerative Medicine
Samuel Iwao Maia Horita, Mona Bensalah, Anne Bigot, et al.
BMC Neurology
|
July 3, 2013
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophy
Vered Raz, Ellen Sterrenburg, Samantha Routledge, et al.
Nucleic Acids Research
|
July 10, 2012
Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation
Eleonora de Klerk, Andrea Venema, S Yahya Anvar, et al.
Molecular Therapy. Nucleic Acids
|
March 19, 2021
BB-301: a silence and replace AAV-based vector for the treatment of oculopharyngeal muscular dystrophy
Vanessa Strings-Ufombah, Alberto Malerba, Shih-Chu Kao, et al.
EMBO Reports
|
July 1, 2026
Publisher Correction: Collagen VI is a fibrosis-associated signal disrupting muscle regeneration across distinct human myopathies
Laura Muraine, Mona Bensalah, Stephen Gargan, et al.
EMBO Reports
|
June 19, 2026
Collagen VI is a fibrosis-associated signal disrupting muscle regeneration across distinct human myopathies
Laura Muraine, Mona Bensalah, Stephen Gargan, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 3, 2021
Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation
Aline Bamia, Maha Sinane, Rima Naït-Saïdi, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling
Pascale Richard, Capucine Trollet, Teresa Gidaro, et al.
Cell Death & Disease
|
May 9, 2026
EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne muscular dystrophy
Maeva Zamperoni, Laura Muraine, Minh-Y Tran, et al.
Page
of 7