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J Pittler

Showing results (61-70 of 69) with videos related to

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Investigative Ophthalmology & Visual Science|September 9, 2008
Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutationNalinee Tuntivanich, Steven J Pittler, Andy J Fischer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit geneM L Suber, S J Pittler, N Qin, et al.
The Journal of Biological Chemistry|February 20, 2016
The B3 Subunit of the Cone Cyclic Nucleotide-gated Channel Regulates the Light Responses of Cones and Contributes to the Channel Structural FlexibilityXi-Qin Ding, Arjun Thapa, Hongwei Ma, et al.
Cell Death & Disease|March 24, 2026
Dysfunction of α2δ4 leads to photoreceptor degeneration through disrupted synaptic mitochondria and calcium crosstalkChoice I Amieghemen, Trong Thuan Ung, Gillian N Huskin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
Iscience|June 12, 2020
Retinal Degeneration Caused by Rod-Specific Dhdds Ablation Occurs without Concomitant Inhibition of Protein N-GlycosylationSriganesh Ramachandra Rao, Lara A Skelton, Fuguo Wu, et al.
Cell Death & Disease|July 13, 2023
A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmissionMai N Nguyen, Dibyendu Chakraborty, Sriganesh Ramachandra Rao, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy successSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Investigative Ophthalmology & Visual Science|September 9, 2008
Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutationNalinee Tuntivanich, Steven J Pittler, Andy J Fischer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit geneM L Suber, S J Pittler, N Qin, et al.
The Journal of Biological Chemistry|February 20, 2016
The B3 Subunit of the Cone Cyclic Nucleotide-gated Channel Regulates the Light Responses of Cones and Contributes to the Channel Structural FlexibilityXi-Qin Ding, Arjun Thapa, Hongwei Ma, et al.
Cell Death & Disease|March 24, 2026
Dysfunction of α2δ4 leads to photoreceptor degeneration through disrupted synaptic mitochondria and calcium crosstalkChoice I Amieghemen, Trong Thuan Ung, Gillian N Huskin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
Iscience|June 12, 2020
Retinal Degeneration Caused by Rod-Specific Dhdds Ablation Occurs without Concomitant Inhibition of Protein N-GlycosylationSriganesh Ramachandra Rao, Lara A Skelton, Fuguo Wu, et al.
Cell Death & Disease|July 13, 2023
A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmissionMai N Nguyen, Dibyendu Chakraborty, Sriganesh Ramachandra Rao, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy successSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Pageof 7