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Tiansen Li

Showing results (81-90 of 105) with videos related to

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Investigative Ophthalmology & Visual Science|January 16, 2014
Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking lysyl oxidase-like 1 (LOXL1)Janey L Wiggs, Basil Pawlyk, Edward Connolly, et al.
Journal of Microbiology (Seoul, Korea)|July 5, 2014
A potent Brucella abortus 2308 Δery live vaccine allows for the differentiation between natural and vaccinated infectionJunbo Zhang, Shuanghong Yin, Fei Guo, et al.
Human Molecular Genetics|November 12, 2024
Loss of paired immunoglobin-like type 2 receptor B gene associated with age-related macular degeneration impairs photoreceptor function in mouse retinaPartha Narayan Dey, Nivedita Singh, Lina Zelinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2004
AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesteraseXiaoqing Liu, Oleg V Bulgakov, Xiao-Hong Wen, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoterShahrokh C Khani, Basil S Pawlyk, Oleg V Bulgakov, et al.
Bioengineering (Basel, Switzerland)|May 25, 2024
OCT Intensity of the Region between Outer Retina Band 2 and Band 3 as a Biomarker for Retinal Degeneration and TherapyYong Zeng, Shasha Gao, Yichao Li, et al.
Plos Genetics|December 28, 2020
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degenerationPassley Hargrove-Grimes, Anupam K Mondal, Jessica Gumerson, et al.
Molecular Therapy. Advances|May 15, 2026
Gene therapy induces pigmentation in induced pluripotent stem cell-derived retinal pigment epithelium of OCA1A patients and albino rat eyeAman George, Arnold Leigh, Evan Selzer, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Investigative Ophthalmology & Visual Science|November 5, 2024
Progressive Optic Neuropathy in Hydrocephalic Ccdc13 Mutant Mice Caused by Impaired Axoplasmic Transport at the Optic Nerve HeadMingjuan Wu, Xinyi Zhao, Shanzhen Peng, et al.
Pageof 11

Showing results (81-90 of 105) with videos related to

Sort By:
Pageof 11
Investigative Ophthalmology & Visual Science|January 16, 2014
Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking lysyl oxidase-like 1 (LOXL1)Janey L Wiggs, Basil Pawlyk, Edward Connolly, et al.
Journal of Microbiology (Seoul, Korea)|July 5, 2014
A potent Brucella abortus 2308 Δery live vaccine allows for the differentiation between natural and vaccinated infectionJunbo Zhang, Shuanghong Yin, Fei Guo, et al.
Human Molecular Genetics|November 12, 2024
Loss of paired immunoglobin-like type 2 receptor B gene associated with age-related macular degeneration impairs photoreceptor function in mouse retinaPartha Narayan Dey, Nivedita Singh, Lina Zelinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2004
AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesteraseXiaoqing Liu, Oleg V Bulgakov, Xiao-Hong Wen, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoterShahrokh C Khani, Basil S Pawlyk, Oleg V Bulgakov, et al.
Bioengineering (Basel, Switzerland)|May 25, 2024
OCT Intensity of the Region between Outer Retina Band 2 and Band 3 as a Biomarker for Retinal Degeneration and TherapyYong Zeng, Shasha Gao, Yichao Li, et al.
Plos Genetics|December 28, 2020
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degenerationPassley Hargrove-Grimes, Anupam K Mondal, Jessica Gumerson, et al.
Molecular Therapy. Advances|May 15, 2026
Gene therapy induces pigmentation in induced pluripotent stem cell-derived retinal pigment epithelium of OCA1A patients and albino rat eyeAman George, Arnold Leigh, Evan Selzer, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Investigative Ophthalmology & Visual Science|November 5, 2024
Progressive Optic Neuropathy in Hydrocephalic Ccdc13 Mutant Mice Caused by Impaired Axoplasmic Transport at the Optic Nerve HeadMingjuan Wu, Xinyi Zhao, Shanzhen Peng, et al.
Pageof 11