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Investigative Ophthalmology & Visual Science
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December 17, 2009
Paracrine modulation of CXCR4 by IGF-1 and VEGF: implications for choroidal neovascularization
Nilanjana Sengupta, Aqeela Afzal, Sergio Caballero, et al.
Nature Medicine
|
May 23, 2007
Restoration of cone vision in a mouse model of achromatopsia
John J Alexander, Yumiko Umino, Drew Everhart, et al.
Molecular Vision
|
February 5, 2009
Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye
Wensheng Li, Fansheng Kong, Xia Li, et al.
Scientific Reports
|
July 29, 2017
Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy
Yuxin Zhang, Wen-Tao Deng, Wei Du, et al.
Scientific Reports
|
March 16, 2018
Publisher Correction: Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy
Yuxin Zhang, Wen-Tao Deng, Wei Du, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2008
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation
Ji-Jing Pang, Sanford L Boye, Ashok Kumar, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 9, 2010
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa
Ji-jing Pang, Xufeng Dai, Shannon E Boye, et al.
Molecular Vision
|
March 15, 2005
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)
Ji-Jing Pang, Bo Chang, Norman L Hawes, et al.
Human Gene Therapy
|
July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year
Artur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Plos One
|
April 18, 2012
AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia
Ji-jing Pang, Wen-Tao Deng, Xufeng Dai, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Investigative Ophthalmology & Visual Science
|
December 17, 2009
Paracrine modulation of CXCR4 by IGF-1 and VEGF: implications for choroidal neovascularization
Nilanjana Sengupta, Aqeela Afzal, Sergio Caballero, et al.
Nature Medicine
|
May 23, 2007
Restoration of cone vision in a mouse model of achromatopsia
John J Alexander, Yumiko Umino, Drew Everhart, et al.
Molecular Vision
|
February 5, 2009
Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye
Wensheng Li, Fansheng Kong, Xia Li, et al.
Scientific Reports
|
July 29, 2017
Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy
Yuxin Zhang, Wen-Tao Deng, Wei Du, et al.
Scientific Reports
|
March 16, 2018
Publisher Correction: Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy
Yuxin Zhang, Wen-Tao Deng, Wei Du, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2008
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation
Ji-Jing Pang, Sanford L Boye, Ashok Kumar, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 9, 2010
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa
Ji-jing Pang, Xufeng Dai, Shannon E Boye, et al.
Molecular Vision
|
March 15, 2005
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)
Ji-Jing Pang, Bo Chang, Norman L Hawes, et al.
Human Gene Therapy
|
July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year
Artur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Plos One
|
April 18, 2012
AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia
Ji-jing Pang, Wen-Tao Deng, Xufeng Dai, et al.
Page
of 4