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Frontiers in Cellular and Infection Microbiology
|
February 16, 2026
Zika virus infection disturbs development of human muscle progenitor cells
Cássia Rocha, Daniella Arêas Mendes-da-Cruz, Elisa Negroni, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells
Florian Barthélémy, Cédric Blouin, Nicolas Wein, et al.
Nature Communications
|
January 15, 2026
Development of a split-toxin CRISPR screening platform to systematically identify regulators of human myoblast fusion
Haifeng Zhang, Renjie Shang, Zheng Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 17, 2019
Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene
Yusuke Echigoya, Kenji Rowel Q Lim, Dyanna Melo, et al.
The Journal of Gene Medicine
|
December 13, 2007
Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes
Valérie Allamand, Laure Bidou, Masayuki Arakawa, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 17, 2012
Proinflammatory macrophages enhance the regenerative capacity of human myoblasts by modifying their kinetics of proliferation and differentiation
Maximilien Bencze, Elisa Negroni, Denis Vallese, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 27, 2013
The Rag2⁻Il2rb⁻Dmd⁻ mouse: a novel dystrophic and immunodeficient model to assess innovating therapeutic strategies for muscular dystrophies
Denis Vallese, Elisa Negroni, Stéphanie Duguez, et al.
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.
Plos One
|
February 19, 2015
miRNA expression in control and FSHD fetal human muscle biopsies
Débora Morueco Portilho, Marcelo Ribeiro Alves, Gueorgui Kratassiouk, et al.
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of 19
Search research articles
Search
Showing results (111-120 of 187) with videos related to
Sort By:
Page
of 19
Frontiers in Cellular and Infection Microbiology
|
February 16, 2026
Zika virus infection disturbs development of human muscle progenitor cells
Cássia Rocha, Daniella Arêas Mendes-da-Cruz, Elisa Negroni, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells
Florian Barthélémy, Cédric Blouin, Nicolas Wein, et al.
Nature Communications
|
January 15, 2026
Development of a split-toxin CRISPR screening platform to systematically identify regulators of human myoblast fusion
Haifeng Zhang, Renjie Shang, Zheng Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 17, 2019
Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene
Yusuke Echigoya, Kenji Rowel Q Lim, Dyanna Melo, et al.
The Journal of Gene Medicine
|
December 13, 2007
Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes
Valérie Allamand, Laure Bidou, Masayuki Arakawa, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 17, 2012
Proinflammatory macrophages enhance the regenerative capacity of human myoblasts by modifying their kinetics of proliferation and differentiation
Maximilien Bencze, Elisa Negroni, Denis Vallese, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 27, 2013
The Rag2⁻Il2rb⁻Dmd⁻ mouse: a novel dystrophic and immunodeficient model to assess innovating therapeutic strategies for muscular dystrophies
Denis Vallese, Elisa Negroni, Stéphanie Duguez, et al.
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.
Plos One
|
February 19, 2015
miRNA expression in control and FSHD fetal human muscle biopsies
Débora Morueco Portilho, Marcelo Ribeiro Alves, Gueorgui Kratassiouk, et al.
Page
of 19