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Investigative Ophthalmology & Visual Science
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February 22, 2013
Visual signal pathway reorganization in the Cacna1f mutant rat model
Ye Tao, Tao Chen, Bei Liu, et al.
Vision Research
|
October 24, 2007
Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration
Ji-jing Pang, Amanda Lauramore, Wen-tao Deng, et al.
Journal of Ophthalmology
|
February 8, 2017
The Degeneration and Apoptosis Patterns of Cone Photoreceptors in <i>rd11</i> Mice
Hua Zhang, Xia Li, Xufeng Dai, et al.
Experimental Eye Research
|
February 9, 2010
Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse
Fansheng Kong, Wensheng Li, Xia Li, et al.
Investigative Ophthalmology & Visual Science
|
September 28, 2007
SOD2 knockdown mouse model of early AMD
Verline Justilien, Ji-Jing Pang, Kutralanathan Renganathan, et al.
Investigative Ophthalmology & Visual Science
|
February 22, 2014
AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice
Xufeng Dai, Juanjuan Han, Yan Qi, et al.
Investigative Ophthalmology & Visual Science
|
December 21, 2010
Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis
Xia Li, Wensheng Li, Xufeng Dai, et al.
Molecular Vision
|
October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis
Alejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 11, 2008
High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Neurobiology of Aging
|
March 15, 2011
AAV5-mediated sFLT01 gene therapy arrests retinal lesions in Ccl2(-/-)/Cx3cr1(-/-) mice
Jingsheng Tuo, Ji-Jing Pang, Xiaoguang Cao, et al.
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Search research articles
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Showing results (11-20 of 37) with videos related to
Sort By:
Page
of 4
Investigative Ophthalmology & Visual Science
|
February 22, 2013
Visual signal pathway reorganization in the Cacna1f mutant rat model
Ye Tao, Tao Chen, Bei Liu, et al.
Vision Research
|
October 24, 2007
Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration
Ji-jing Pang, Amanda Lauramore, Wen-tao Deng, et al.
Journal of Ophthalmology
|
February 8, 2017
The Degeneration and Apoptosis Patterns of Cone Photoreceptors in <i>rd11</i> Mice
Hua Zhang, Xia Li, Xufeng Dai, et al.
Experimental Eye Research
|
February 9, 2010
Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse
Fansheng Kong, Wensheng Li, Xia Li, et al.
Investigative Ophthalmology & Visual Science
|
September 28, 2007
SOD2 knockdown mouse model of early AMD
Verline Justilien, Ji-Jing Pang, Kutralanathan Renganathan, et al.
Investigative Ophthalmology & Visual Science
|
February 22, 2014
AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice
Xufeng Dai, Juanjuan Han, Yan Qi, et al.
Investigative Ophthalmology & Visual Science
|
December 21, 2010
Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis
Xia Li, Wensheng Li, Xufeng Dai, et al.
Molecular Vision
|
October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis
Alejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 11, 2008
High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectors
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Neurobiology of Aging
|
March 15, 2011
AAV5-mediated sFLT01 gene therapy arrests retinal lesions in Ccl2(-/-)/Cx3cr1(-/-) mice
Jingsheng Tuo, Ji-Jing Pang, Xiaoguang Cao, et al.
Page
of 4