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Isabelle Richard

Showing results (111-120 of 182) with videos related to

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Investigative Ophthalmology & Visual Science|May 26, 2007
Age-related cataracts in alpha3Cx46-knockout mice are dependent on a calpain 3 isoformYajun Tang, Xiangyang Liu, Rebecca K Zoltoski, et al.
Human Gene Therapy. Clinical Development|June 1, 2013
The phenotype of dysferlin-deficient mice is not rescued by adeno-associated virus-mediated transfer of anoctamin 5François Monjaret, Laurence Suel-Petat, Nathalie Bourg-Alibert, et al.
British Journal of Pharmacology|March 20, 2025
High-throughput screening identifies bazedoxifene as a potential therapeutic for dysferlin-deficient limb girdle muscular dystrophyCeline Bruge, Nathalie Bourg, Emilie Pellier, et al.
Biochimica Et Biophysica Acta|September 29, 2009
Calcium-dependent plasma membrane repair requires m- or mu-calpain, but not calpain-3, the proteasome, or caspasesRonald L Mellgren, Katsuya Miyake, Irina Kramerova, et al.
The Spine Journal : Official Journal of the North American Spine Society|July 17, 2013
Biomechanical constraints remain major risk factors for low back pain. Results from a prospective cohort study in French male employeesAline Ramond-Roquin, Julie Bodin, Céline Serazin, et al.
Science Advances|June 19, 2024
Late Neolithic collective burial reveals admixture dynamics during the third millennium BCE and the shaping of the European genomeOğuzhan Parasayan, Christophe Laurelut, Christine Bôle, et al.
American Journal of Human Genetics|July 30, 2002
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titinPeter Hackman, Anna Vihola, Henna Haravuori, et al.
Molecular Therapy. Methods & Clinical Development|September 2, 2025
FAP-CAR-T cells reduce dystrophic muscle fibrosis, improving adeno-associated virus gene transfer efficacyMaxime Ferrand, Céline J Rocca, Guillaume Corre, et al.
Human Molecular Genetics|February 7, 2008
Mannosidase I inhibition rescues the human alpha-sarcoglycan R77C recurrent mutationMarc Bartoli, Evelyne Gicquel, Laetitia Barrault, et al.
Presse Medicale (Paris, France : 1983)|February 17, 2012
[Assessment of scientific production after initial medical education at the Faculty of Medicine of Angers from 2002 to 2008]Christophe Baufreton, Jean-Marie Chrétien, Florence Moreau-Cordier, et al.
Pageof 19

Showing results (111-120 of 182) with videos related to

Sort By:
Pageof 19
Investigative Ophthalmology & Visual Science|May 26, 2007
Age-related cataracts in alpha3Cx46-knockout mice are dependent on a calpain 3 isoformYajun Tang, Xiangyang Liu, Rebecca K Zoltoski, et al.
Human Gene Therapy. Clinical Development|June 1, 2013
The phenotype of dysferlin-deficient mice is not rescued by adeno-associated virus-mediated transfer of anoctamin 5François Monjaret, Laurence Suel-Petat, Nathalie Bourg-Alibert, et al.
British Journal of Pharmacology|March 20, 2025
High-throughput screening identifies bazedoxifene as a potential therapeutic for dysferlin-deficient limb girdle muscular dystrophyCeline Bruge, Nathalie Bourg, Emilie Pellier, et al.
Biochimica Et Biophysica Acta|September 29, 2009
Calcium-dependent plasma membrane repair requires m- or mu-calpain, but not calpain-3, the proteasome, or caspasesRonald L Mellgren, Katsuya Miyake, Irina Kramerova, et al.
The Spine Journal : Official Journal of the North American Spine Society|July 17, 2013
Biomechanical constraints remain major risk factors for low back pain. Results from a prospective cohort study in French male employeesAline Ramond-Roquin, Julie Bodin, Céline Serazin, et al.
Science Advances|June 19, 2024
Late Neolithic collective burial reveals admixture dynamics during the third millennium BCE and the shaping of the European genomeOğuzhan Parasayan, Christophe Laurelut, Christine Bôle, et al.
American Journal of Human Genetics|July 30, 2002
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titinPeter Hackman, Anna Vihola, Henna Haravuori, et al.
Molecular Therapy. Methods & Clinical Development|September 2, 2025
FAP-CAR-T cells reduce dystrophic muscle fibrosis, improving adeno-associated virus gene transfer efficacyMaxime Ferrand, Céline J Rocca, Guillaume Corre, et al.
Human Molecular Genetics|February 7, 2008
Mannosidase I inhibition rescues the human alpha-sarcoglycan R77C recurrent mutationMarc Bartoli, Evelyne Gicquel, Laetitia Barrault, et al.
Presse Medicale (Paris, France : 1983)|February 17, 2012
[Assessment of scientific production after initial medical education at the Faculty of Medicine of Angers from 2002 to 2008]Christophe Baufreton, Jean-Marie Chrétien, Florence Moreau-Cordier, et al.
Pageof 19