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Patsy M Nishina

Showing results (11-20 of 80) with videos related to

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Human Molecular Genetics|October 14, 2008
New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a geneKenji Sakamoto, Michael McCluskey, Theodore G Wensel, et al.
Annual Review of Neuroscience|October 7, 2003
Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerationsLaura R Pacione, Michael J Szego, Sakae Ikeda, et al.
Investigative Ophthalmology & Visual Science|October 30, 2018
Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 AlleleBo Chang, Bernard FitzMaurice, Jieping Wang, et al.
Investigative Ophthalmology & Visual Science|March 16, 2016
Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θXiaojie Ji, Ye Liu, Ron Hurd, et al.
Human Molecular Genetics|October 31, 2012
Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosaKatherine J Wert, Richard J Davis, Javier Sancho-Pelluz, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
Translational vision research models programJungyeon Won, Lan Ying Shi, Wanda Hicks, et al.
Journal of Cell Science|September 21, 2023
Epithelial mechanics are maintained by inhibiting cell fusion with age in DrosophilaAri S Dehn, Levi Duhaime, Navdeep Gogna, et al.
Human Molecular Genetics|July 26, 2002
Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6Shuhei Kameya, Norman L Hawes, Bo Chang, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Current Views on Chr10q26 Contribution to Age-Related Macular DegenerationNavdeep Gogna, Lillian F Hyde, Gayle B Collin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 22, 2026
Polyunsaturated fatty acid metabolism in the retinal pigment epithelium and its association with outer retinal diseaseNaga Pradeep Rayana, Navdeep Gogna, Mark P Krebs, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|October 14, 2008
New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a geneKenji Sakamoto, Michael McCluskey, Theodore G Wensel, et al.
Annual Review of Neuroscience|October 7, 2003
Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerationsLaura R Pacione, Michael J Szego, Sakae Ikeda, et al.
Investigative Ophthalmology & Visual Science|October 30, 2018
Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 AlleleBo Chang, Bernard FitzMaurice, Jieping Wang, et al.
Investigative Ophthalmology & Visual Science|March 16, 2016
Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θXiaojie Ji, Ye Liu, Ron Hurd, et al.
Human Molecular Genetics|October 31, 2012
Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosaKatherine J Wert, Richard J Davis, Javier Sancho-Pelluz, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
Translational vision research models programJungyeon Won, Lan Ying Shi, Wanda Hicks, et al.
Journal of Cell Science|September 21, 2023
Epithelial mechanics are maintained by inhibiting cell fusion with age in DrosophilaAri S Dehn, Levi Duhaime, Navdeep Gogna, et al.
Human Molecular Genetics|July 26, 2002
Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6Shuhei Kameya, Norman L Hawes, Bo Chang, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Current Views on Chr10q26 Contribution to Age-Related Macular DegenerationNavdeep Gogna, Lillian F Hyde, Gayle B Collin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 22, 2026
Polyunsaturated fatty acid metabolism in the retinal pigment epithelium and its association with outer retinal diseaseNaga Pradeep Rayana, Navdeep Gogna, Mark P Krebs, et al.
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