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Tiansen Li

Showing results (91-100 of 105) with videos related to

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BMC Medical Genetics|February 8, 2008
DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversityBao Jian Fan, Louis Pasquale, Cynthia L Grosskreutz, 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.
Investigative Ophthalmology & Visual Science|February 26, 2008
Increased choroidal neovascularization following laser induction in mice lacking lysyl oxidase-like 1Hyeong Gon Yu, Xiaoqing Liu, Szilard Kiss, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2017
Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouseJianguo Fan, Li Jia, Yan Li, et al.
Nature Communications|June 21, 2014
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesisShobi Veleri, Souparnika H Manjunath, Robert N Fariss, et al.
Investigative Ophthalmology & Visual Science|September 11, 2023
RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3'-end of ORF15Matthew D Benson, Souvick Mukherjee, Aime R Agather, et al.
Cell Reports|October 27, 2016
Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the RetinaHelen L May-Simera, Jessica D Gumerson, Chun Gao, et al.
The EMBO Journal|December 20, 2003
Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial functionAlexander G Marneros, Douglas R Keene, Uwe Hansen, et al.
Human Molecular Genetics|April 11, 2015
CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathiesRivka A Rachel, Erin A Yamamoto, Mrinal K Dewanjee, et al.
Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
BMC Medical Genetics|February 8, 2008
DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversityBao Jian Fan, Louis Pasquale, Cynthia L Grosskreutz, 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.
Investigative Ophthalmology & Visual Science|February 26, 2008
Increased choroidal neovascularization following laser induction in mice lacking lysyl oxidase-like 1Hyeong Gon Yu, Xiaoqing Liu, Szilard Kiss, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2017
Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouseJianguo Fan, Li Jia, Yan Li, et al.
Nature Communications|June 21, 2014
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesisShobi Veleri, Souparnika H Manjunath, Robert N Fariss, et al.
Investigative Ophthalmology & Visual Science|September 11, 2023
RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3'-end of ORF15Matthew D Benson, Souvick Mukherjee, Aime R Agather, et al.
Cell Reports|October 27, 2016
Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the RetinaHelen L May-Simera, Jessica D Gumerson, Chun Gao, et al.
The EMBO Journal|December 20, 2003
Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial functionAlexander G Marneros, Douglas R Keene, Uwe Hansen, et al.
Human Molecular Genetics|April 11, 2015
CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathiesRivka A Rachel, Erin A Yamamoto, Mrinal K Dewanjee, et al.
Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Pageof 11