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Michelle E McClements

Showing results (61-70 of 65) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|May 28, 2017
Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis PigmentosaM Dominik Fischer, Michelle E McClements, Cristina Martinez-Fernandez de la Camara, et al.
Ophthalmic Genetics|June 22, 2017
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalitiesValentina Cipriani, Ambreen Kalhoro, Gavin Arno, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Scientific Reports|June 10, 2022
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell modelsJiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 5, 2017
Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapySamantha R De Silva, Alun R Barnard, Steven Hughes, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 28, 2017
Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis PigmentosaM Dominik Fischer, Michelle E McClements, Cristina Martinez-Fernandez de la Camara, et al.
Ophthalmic Genetics|June 22, 2017
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalitiesValentina Cipriani, Ambreen Kalhoro, Gavin Arno, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Scientific Reports|June 10, 2022
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell modelsJiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 5, 2017
Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapySamantha R De Silva, Alun R Barnard, Steven Hughes, et al.
Pageof 7