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Investigative Ophthalmology & Visual Science
|
January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype
Sharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Plos Medicine
|
June 28, 2007
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation
Geoffrey K Aguirre, András M Komáromy, Artur V Cideciyan, 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.
Cell Reports
|
July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations
Hiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, 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.
American Journal of Human Genetics
|
November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
M D Weston, P M Kelley, L D Overbeck, et al.
Human Gene Therapy
|
July 8, 2010
Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel
Eyal Banin, Dikla Bandah-Rozenfeld, Alexey Obolensky, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 5, 2004
In utero gene therapy rescues vision in a murine model of congenital blindness
Nadine S Dejneka, Enrico M Surace, Tomas S Aleman, 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.
International Journal of Epidemiology
|
June 22, 2023
Cohort Profile Update: The US Millennium Cohort Study-evaluating the impact of military experiences on service members and veteran health
Sheila F Castañeda, Jennifer N Belding, Claire A Kolaja, et al.
Page
of 68
Search research articles
Search
Showing results (591-600 of 677) with videos related to
Sort By:
Page
of 68
Investigative Ophthalmology & Visual Science
|
January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype
Sharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Plos Medicine
|
June 28, 2007
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation
Geoffrey K Aguirre, András M Komáromy, Artur V Cideciyan, 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.
Cell Reports
|
July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations
Hiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, 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.
American Journal of Human Genetics
|
November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
M D Weston, P M Kelley, L D Overbeck, et al.
Human Gene Therapy
|
July 8, 2010
Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel
Eyal Banin, Dikla Bandah-Rozenfeld, Alexey Obolensky, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 5, 2004
In utero gene therapy rescues vision in a murine model of congenital blindness
Nadine S Dejneka, Enrico M Surace, Tomas S Aleman, 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.
International Journal of Epidemiology
|
June 22, 2023
Cohort Profile Update: The US Millennium Cohort Study-evaluating the impact of military experiences on service members and veteran health
Sheila F Castañeda, Jennifer N Belding, Claire A Kolaja, et al.
Page
of 68