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G Jacobson

Showing results (621-630 of 677) with videos related to

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Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 23, 2006
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degenerationJames S Friedman, Bo Chang, Chitra Kannabiran, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.
Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Investigative Ophthalmology & Visual Science|August 25, 2011
Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosaManir Ali, Paul M Hocking, Martin McKibbin, et al.
Iscience|May 17, 2021
Safety and improved efficacy signals following gene therapy in childhood blindness caused by <i>GUCY2D</i> mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Iscience|October 24, 2022
Night vision restored in days after decades of congenital blindnessSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|July 16, 2011
Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse modelTomas S Aleman, Artur V Cideciyan, Geoffrey K Aguirre, et al.
Pageof 68

Showing results (621-630 of 677) with videos related to

Sort By:
Pageof 68
Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 23, 2006
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degenerationJames S Friedman, Bo Chang, Chitra Kannabiran, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.
Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Investigative Ophthalmology & Visual Science|August 25, 2011
Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosaManir Ali, Paul M Hocking, Martin McKibbin, et al.
Iscience|May 17, 2021
Safety and improved efficacy signals following gene therapy in childhood blindness caused by <i>GUCY2D</i> mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Iscience|October 24, 2022
Night vision restored in days after decades of congenital blindnessSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|July 16, 2011
Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse modelTomas S Aleman, Artur V Cideciyan, Geoffrey K Aguirre, et al.
Pageof 68