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Publications by Samuel G. Jacobson

The Genomic, Biochemical, and Cellular Responses of the Retina in Inherited Photoreceptor Degenerations and Prospects for the Treatment of These Disorders

Annual Review of Neuroscience

Neuroscience

2010

English

A Gly86Arg Mutation in the Calcium-Sensor Protein GCAP1 Alters Regulation of Retinal Guanylyl Cyclase and Causes Dominant Cone-Rod Degeneration

Journal of Biological Chemistry

English

Human Retinal Disease fromAIPL1Gene Mutations: Foveal Cone Loss With Minimal Macular Photoreceptors and Rod Function Remaining

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, With Homoallelism for Mutations in RPE65 or MERTK, Respectively

American Journal of Human Genetics

Genetics

2002

English

Analysis of the RPGRGene in 11 Pedigrees With the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families

American Journal of Human Genetics

Genetics

1997

English

Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

American Journal of Human Genetics

Genetics

2002

English

Macular Pigment and Lutein Supplementation inABCA4-Associated Retinal Degenerations

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

ABCA4-Associated Retinal Degenerations Spare Structure and Function of the Human Parapapillary Retina

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

Treatment of Leber Congenital Amaurosis Due toRPE65Mutations by Ocular Subretinal Injection of Adeno-Associated Virus Gene Vector: Short-Term Results of a Phase I Trial

English

Reduced-Illuminance Autofluorescence Imaging in ABCA4-associated Retinal Degenerations

Journal of the Optical Society of America A: Optics and Image Science, and Vision

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Samuel G. Jacobson

The Genomic, Biochemical, and Cellular Responses of the Retina in Inherited Photoreceptor Degenerations and Prospects for the Treatment of These Disorders

A Gly86Arg Mutation in the Calcium-Sensor Protein GCAP1 Alters Regulation of Retinal Guanylyl Cyclase and Causes Dominant Cone-Rod Degeneration

Human Retinal Disease fromAIPL1Gene Mutations: Foveal Cone Loss With Minimal Macular Photoreceptors and Rod Function Remaining

Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, With Homoallelism for Mutations in RPE65 or MERTK, Respectively

Analysis of the RPGRGene in 11 Pedigrees With the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families

Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

Macular Pigment and Lutein Supplementation inABCA4-Associated Retinal Degenerations

ABCA4-Associated Retinal Degenerations Spare Structure and Function of the Human Parapapillary Retina

Treatment of Leber Congenital Amaurosis Due toRPE65Mutations by Ocular Subretinal Injection of Adeno-Associated Virus Gene Vector: Short-Term Results of a Phase I Trial

Reduced-Illuminance Autofluorescence Imaging in ABCA4-associated Retinal Degenerations