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Human Gene Therapy
|
November 22, 2017
Assessment of Adeno-Associated Virus Serotype Tropism in Human Retinal Explants
Luke A Wiley, Erin R Burnight, Emily E Kaalberg, et al.
Human Molecular Genetics
|
October 5, 2012
Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants
Samuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, et al.
Ophthalmology Science
|
September 6, 2023
Genetic Association between <i>MMP9</i> and Choroidal Neovascularization in Age-Related Macular Degeneration
Elliott H Sohn, Ian C Han, Benjamin R Roos, et al.
American Journal of Ophthalmology
|
November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
Wallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
The British Journal of Ophthalmology
|
September 17, 2024
Progressive inner retinal neurodegeneration in non-proliferative macular telangiectasia type 2
Alec L Amram, S Scott Whitmore, Cheryl Wang, et al.
American Journal of Medical Genetics. Part A
|
December 25, 2009
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
Colleen A Campbell, Charley C Della Santina, Nicole C Meyer, et al.
Plos One
|
March 28, 2014
Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy
Shannon E Boye, Wei-Chieh Huang, Alejandro J Roman, et al.
Human Gene Therapy
|
September 19, 2020
Retinal Tropism and Transduction of Adeno-Associated Virus Varies by Serotype and Route of Delivery (Intravitreal, Subretinal, or Suprachoroidal) in Rats
Ian C Han, Justine L Cheng, Erin R Burnight, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Progress in Retinal and Eye Research
|
March 27, 2018
CRISPR-Cas9 genome engineering: Treating inherited retinal degeneration
Erin R Burnight, Joseph C Giacalone, Jessica A Cooke, et al.
Page
of 39
Search research articles
Search
Showing results (331-340 of 384) with videos related to
Sort By:
Page
of 39
Human Gene Therapy
|
November 22, 2017
Assessment of Adeno-Associated Virus Serotype Tropism in Human Retinal Explants
Luke A Wiley, Erin R Burnight, Emily E Kaalberg, et al.
Human Molecular Genetics
|
October 5, 2012
Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants
Samuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, et al.
Ophthalmology Science
|
September 6, 2023
Genetic Association between <i>MMP9</i> and Choroidal Neovascularization in Age-Related Macular Degeneration
Elliott H Sohn, Ian C Han, Benjamin R Roos, et al.
American Journal of Ophthalmology
|
November 5, 2003
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
Wallace L M Alward, Young H Kwon, Kazuhide Kawase, et al.
The British Journal of Ophthalmology
|
September 17, 2024
Progressive inner retinal neurodegeneration in non-proliferative macular telangiectasia type 2
Alec L Amram, S Scott Whitmore, Cheryl Wang, et al.
American Journal of Medical Genetics. Part A
|
December 25, 2009
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
Colleen A Campbell, Charley C Della Santina, Nicole C Meyer, et al.
Plos One
|
March 28, 2014
Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy
Shannon E Boye, Wei-Chieh Huang, Alejandro J Roman, et al.
Human Gene Therapy
|
September 19, 2020
Retinal Tropism and Transduction of Adeno-Associated Virus Varies by Serotype and Route of Delivery (Intravitreal, Subretinal, or Suprachoroidal) in Rats
Ian C Han, Justine L Cheng, Erin R Burnight, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Progress in Retinal and Eye Research
|
March 27, 2018
CRISPR-Cas9 genome engineering: Treating inherited retinal degeneration
Erin R Burnight, Joseph C Giacalone, Jessica A Cooke, et al.
Page
of 39