Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anne Galy

Showing results (61-70 of 108) with videos related to

Pageof 11
Sort By:
Plos One|November 13, 2012
Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modificationsYoshiaki Yamagata, Véronique Parietti, Daniel Stockholm, et al.
Current Gene Therapy|September 30, 2015
Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCsF Javier Molina-Estevez, Ali Nowrouzi, M Luz Lozano, et al.
Molecular Therapy. Methods & Clinical Development|May 9, 2017
Vectofusin-1 Promotes RD114-TR-Pseudotyped Lentiviral Vector Transduction of Human HSPCs and T LymphocytesClaudia Piovan, Virna Marin, Cinzia Scavullo, et al.
The Journal of Biological Chemistry|September 21, 2017
Peptides derived from evolutionarily conserved domains in Beclin-1 and Beclin-2 enhance the entry of lentiviral vectors into human cellsSaliha Majdoul, Jeremie Cosette, Ababacar K Seye, et al.
Developmental Biology|March 6, 2003
Transcriptional regulation of glial cell specificationGianluca Ragone, Véronique Van De Bor, Sandro Sorrentino, 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.
Molecular Therapy. Methods & Clinical Development|September 10, 2019
Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene TransferSylvie Da Rocha, Jérémy Bigot, Fanny Onodi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 31, 2012
MyD88 signaling in B cells regulates the production of Th1-dependent antibodies to AAVMuriel Sudres, Séverine Ciré, Virginie Vasseur, et al.
JAMA Ophthalmology|February 8, 2019
Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical TrialCéline Bouquet, Catherine Vignal Clermont, Anne Galy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 13, 2009
Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectorsUte Modlich, Susana Navarro, Daniela Zychlinski, et al.
Pageof 11

Showing results (61-70 of 108) with videos related to

Sort By:
Pageof 11
Plos One|November 13, 2012
Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modificationsYoshiaki Yamagata, Véronique Parietti, Daniel Stockholm, et al.
Current Gene Therapy|September 30, 2015
Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCsF Javier Molina-Estevez, Ali Nowrouzi, M Luz Lozano, et al.
Molecular Therapy. Methods & Clinical Development|May 9, 2017
Vectofusin-1 Promotes RD114-TR-Pseudotyped Lentiviral Vector Transduction of Human HSPCs and T LymphocytesClaudia Piovan, Virna Marin, Cinzia Scavullo, et al.
The Journal of Biological Chemistry|September 21, 2017
Peptides derived from evolutionarily conserved domains in Beclin-1 and Beclin-2 enhance the entry of lentiviral vectors into human cellsSaliha Majdoul, Jeremie Cosette, Ababacar K Seye, et al.
Developmental Biology|March 6, 2003
Transcriptional regulation of glial cell specificationGianluca Ragone, Véronique Van De Bor, Sandro Sorrentino, 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.
Molecular Therapy. Methods & Clinical Development|September 10, 2019
Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene TransferSylvie Da Rocha, Jérémy Bigot, Fanny Onodi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 31, 2012
MyD88 signaling in B cells regulates the production of Th1-dependent antibodies to AAVMuriel Sudres, Séverine Ciré, Virginie Vasseur, et al.
JAMA Ophthalmology|February 8, 2019
Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical TrialCéline Bouquet, Catherine Vignal Clermont, Anne Galy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 13, 2009
Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectorsUte Modlich, Susana Navarro, Daniela Zychlinski, et al.
Pageof 11