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Jacques P Tremblay

Showing results (111-120 of 139) with videos related to

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The CRISPR Journal|July 21, 2022
Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9Mbarka Bchetnia, Rebecca Dionne Gagné, Julie Powell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 28, 2007
Stem and progenitor cells in skeletal muscle development, maintenance, and therapyBruno Péault, Michael Rudnicki, Yvan Torrente, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|October 28, 2009
Percutaneous versus surgical delivery of autologous myoblasts after chronic myocardial infarction: an in vivo cardiovascular magnetic resonance studyEric Larose, Guy Proulx, Pierre Voisine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 20, 2007
Autologous transplantation of muscle precursor cells modified with a lentivirus for muscular dystrophy: human cells and primate modelsSimon P Quenneville, Pierre Chapdelaine, Daniel Skuk, et al.
Genes|August 26, 2023
Finding an Appropriate Mouse Model to Study the Impact of a Treatment for Friedreich Ataxia on the Behavioral PhenotypeCamille Bouchard, Catherine Gérard, Solange Gni-Fiene Yanyabé, et al.
Plos One|October 12, 2012
Macrophages improve survival, proliferation and migration of engrafted myogenic precursor cells into MDX skeletal musclePierre-François Lesault, Marine Theret, Mélanie Magnan, et al.
Frontiers in Medicine|June 12, 2023
Prime editing strategies to mediate exon skipping in <i>DMD</i> geneCedric Happi Mbakam, Jeanne Roustant, Joel Rousseau, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 10, 2018
CRISPR-Induced Deletion with SaCas9 Restores Dystrophin Expression in Dystrophic Models In Vitro and In VivoBenjamin L Duchêne, Khadija Cherif, Jean-Paul Iyombe-Engembe, et al.
Molecular Therapy. Methods & Clinical Development|May 28, 2015
An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse modelsCatherine Gérard, Xiao Xiao, Mohammed Filali, et al.
Stem Cells Translational Medicine|September 4, 2020
Myogenic progenitor cells derived from human induced pluripotent stem cell are immune-tolerated in humanized miceBasma Benabdallah, Cynthia Désaulniers-Langevin, Marie-Lyn Goyer, et al.
Pageof 14

Showing results (111-120 of 139) with videos related to

Sort By:
Pageof 14
The CRISPR Journal|July 21, 2022
Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9Mbarka Bchetnia, Rebecca Dionne Gagné, Julie Powell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 28, 2007
Stem and progenitor cells in skeletal muscle development, maintenance, and therapyBruno Péault, Michael Rudnicki, Yvan Torrente, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|October 28, 2009
Percutaneous versus surgical delivery of autologous myoblasts after chronic myocardial infarction: an in vivo cardiovascular magnetic resonance studyEric Larose, Guy Proulx, Pierre Voisine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 20, 2007
Autologous transplantation of muscle precursor cells modified with a lentivirus for muscular dystrophy: human cells and primate modelsSimon P Quenneville, Pierre Chapdelaine, Daniel Skuk, et al.
Genes|August 26, 2023
Finding an Appropriate Mouse Model to Study the Impact of a Treatment for Friedreich Ataxia on the Behavioral PhenotypeCamille Bouchard, Catherine Gérard, Solange Gni-Fiene Yanyabé, et al.
Plos One|October 12, 2012
Macrophages improve survival, proliferation and migration of engrafted myogenic precursor cells into MDX skeletal musclePierre-François Lesault, Marine Theret, Mélanie Magnan, et al.
Frontiers in Medicine|June 12, 2023
Prime editing strategies to mediate exon skipping in <i>DMD</i> geneCedric Happi Mbakam, Jeanne Roustant, Joel Rousseau, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 10, 2018
CRISPR-Induced Deletion with SaCas9 Restores Dystrophin Expression in Dystrophic Models In Vitro and In VivoBenjamin L Duchêne, Khadija Cherif, Jean-Paul Iyombe-Engembe, et al.
Molecular Therapy. Methods & Clinical Development|May 28, 2015
An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse modelsCatherine Gérard, Xiao Xiao, Mohammed Filali, et al.
Stem Cells Translational Medicine|September 4, 2020
Myogenic progenitor cells derived from human induced pluripotent stem cell are immune-tolerated in humanized miceBasma Benabdallah, Cynthia Désaulniers-Langevin, Marie-Lyn Goyer, et al.
Pageof 14