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Molecular Genetics & Genomic Medicine
|
February 24, 2025
Unveiling the Genetic and Phenotypic Landscape of a Chinese Cohort With Retinitis Pigmentosa
He-Nan Sun, Kai-Li Du, Yan Sun, et al.
Human Molecular Genetics
|
April 10, 2015
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia
Wei Du, Ye Tao, Wen-Tao Deng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 4, 2010
Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Human Gene Therapy. Clinical Development
|
May 23, 2013
Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa
Thomas J Conlon, Wen-Tao Deng, Kirsten Erger, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 15, 2005
Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis
Ji-jing Pang, Bo Chang, Ashok Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
September 14, 2011
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years
Samuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, et al.
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of 4
Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Molecular Genetics & Genomic Medicine
|
February 24, 2025
Unveiling the Genetic and Phenotypic Landscape of a Chinese Cohort With Retinitis Pigmentosa
He-Nan Sun, Kai-Li Du, Yan Sun, et al.
Human Molecular Genetics
|
April 10, 2015
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia
Wei Du, Ye Tao, Wen-Tao Deng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 4, 2010
Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina
Hilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Human Gene Therapy. Clinical Development
|
May 23, 2013
Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa
Thomas J Conlon, Wen-Tao Deng, Kirsten Erger, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 15, 2005
Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis
Ji-jing Pang, Bo Chang, Ashok Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
September 14, 2011
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years
Samuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, et al.
Page
of 4