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Anand Swaroop

Showing results (241-250 of 338) with videos related to

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Eneuro|September 30, 2022
Frmpd1 Facilitates Trafficking of G-Protein Transducin and Modulates Synaptic Function in Rod Photoreceptors of Mammalian RetinaChristie K Campla, Ulisse Bocchero, Ryan Strickland, et al.
Iscience|May 8, 2023
Ultra-rare complement factor 8 coding variants in families with age-related macular degenerationLina Zelinger, Tammy M Martin, Jayshree Advani, et al.
Cell Reports|April 23, 2020
Genome-wide Profiling Identifies DNA Methylation Signatures of Aging in Rod Photoreceptors Associated with Alterations in Energy MetabolismXimena Corso-Díaz, James Gentry, Ryan Rebernick, et al.
Plos One|May 8, 2012
Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15Debra A Thompson, Naheed W Khan, Mohammad I Othman, et al.
Human Mutation|June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosisArtur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
Investigative Ophthalmology & Visual Science|August 28, 2014
Deletion of aryl hydrocarbon receptor AHR in mice leads to subretinal accumulation of microglia and RPE atrophySoo-Young Kim, Hyun-Jin Yang, Yi-Sheng Chang, et al.
Genetics|March 26, 2017
Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk ScoresYing Ding, Yi Liu, Qi Yan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2012
Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retinaJerome E Roger, Keerthi Ranganath, Lian Zhao, et al.
Frontiers in Cell and Developmental Biology|November 1, 2021
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 PatientsAvigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, et al.
JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Pageof 34

Showing results (241-250 of 338) with videos related to

Sort By:
Pageof 34
Eneuro|September 30, 2022
Frmpd1 Facilitates Trafficking of G-Protein Transducin and Modulates Synaptic Function in Rod Photoreceptors of Mammalian RetinaChristie K Campla, Ulisse Bocchero, Ryan Strickland, et al.
Iscience|May 8, 2023
Ultra-rare complement factor 8 coding variants in families with age-related macular degenerationLina Zelinger, Tammy M Martin, Jayshree Advani, et al.
Cell Reports|April 23, 2020
Genome-wide Profiling Identifies DNA Methylation Signatures of Aging in Rod Photoreceptors Associated with Alterations in Energy MetabolismXimena Corso-Díaz, James Gentry, Ryan Rebernick, et al.
Plos One|May 8, 2012
Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15Debra A Thompson, Naheed W Khan, Mohammad I Othman, et al.
Human Mutation|June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosisArtur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
Investigative Ophthalmology & Visual Science|August 28, 2014
Deletion of aryl hydrocarbon receptor AHR in mice leads to subretinal accumulation of microglia and RPE atrophySoo-Young Kim, Hyun-Jin Yang, Yi-Sheng Chang, et al.
Genetics|March 26, 2017
Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk ScoresYing Ding, Yi Liu, Qi Yan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2012
Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retinaJerome E Roger, Keerthi Ranganath, Lian Zhao, et al.
Frontiers in Cell and Developmental Biology|November 1, 2021
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 PatientsAvigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, et al.
JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Pageof 34