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Annals of Epidemiology|December 15, 2021
The Millennium Cohort Study: The first 20 years of research dedicated to understanding the long-term health of US Service Members and VeteransJennifer N Belding, Sheila F Castañeda, Isabel G Jacobson, et al.American Journal of Human Genetics|February 18, 2004
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage diseaseGonçalo R Abecasis, Beverly M Yashar, Yu Zhao, et al.Human Molecular Genetics|April 4, 2017
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survivalShobi Veleri, Jacob Nellissery, Bibhudatta Mishra, et al.Proceedings of the National Academy of Sciences of the United States of America|September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kineticsArtur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosaWilliam A Beltran, Artur V Cideciyan, Alfred S Lewin, et al.Human Mutation|February 24, 2011
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definitionCatherine Deveault, Gail Billingsley, Jacque L Duncan, et al.Environmental Monitoring and Assessment|December 21, 2006
Watershed nitrogen and mercury geochemical fluxes integrate landscape factors in long-term research watersheds at Acadia National Park, Maine, USAJ S Kahl, S J Nelson, I Fernandez, et al.Human Gene Therapy|January 8, 2020
Toxicity and Efficacy Evaluation of an Adeno-Associated Virus Vector Expressing Codon-Optimized RPGR Delivered by Subretinal Injection in a Canine Model of X-linked Retinitis PigmentosaValérie L Dufour, Artur V Cideciyan, Guo-Jie Ye, et al.Human Gene Therapy|September 1, 2006
Safety in nonhuman primates of ocular AAV2-RPE65, a candidate treatment for blindness in Leber congenital amaurosisSamuel G Jacobson, Sanford L Boye, Tomas S Aleman, et al.American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.Pageof 57