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Lipofuscin Accumulation, Abnormal Electrophysiology, and Photoreceptor Degeneration in Mutant ELOVL4 Transgenic Mice: A Model for Macular Degeneration

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (11), p.4164-4169

2005

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Psychophysical assessment of low visual function in patients with retinal degenerative diseases (RDDs) with the Diagnosys full-field stimulus threshold (D-FST)

Documenta ophthalmologica, 2009-12, Vol.119 (3), p.217-224

2009

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Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants

Pediatric research, 1998-08, Vol.44 (2), p.201-209

1998

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Delayed Dark-Adaptation and Lipofuscin Accumulation in abcr+/- Mice: Implications for Involvement of ABCR in Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2001-07, Vol.42 (8), p.1685-1690

2001

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Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy

Ophthalmology (Rochester, Minn.), 1999-02, Vol.106 (2), p.258-268

1999

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Dietary essential fatty acid supply and visual acuity development

Investigative ophthalmology & visual science, 1992-10, Vol.33 (11), p.3242-3253

1992

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Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave

Investigative ophthalmology & visual science, 1994-06, Vol.35 (7), p.2948-2961

1994

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The Very Large G-Protein-Coupled Receptor VLGR1: A Component of the Ankle Link Complex Required for the Normal Development of Auditory Hair Bundles

The Journal of neuroscience, 2006-06, Vol.26 (24), p.6543-6553

2006

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Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids

Investigative ophthalmology & visual science, 1992-07, Vol.33 (8), p.2365-2376

1992

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Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis

Nature genetics, 2000-05, Vol.25 (1), p.67-73

2000

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Essential fatty acids in visual and brain development

Lipids, 2001-09, Vol.36 (9), p.885-895

2001

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A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants

Developmental medicine and child neurology, 2000-03, Vol.42 (3), p.174-181, Article S0012162200000311

2000

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Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23- his mutation

Investigative ophthalmology & visual science, 1995-07, Vol.36 (8), p.1603-1614

1995

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Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice

Cell, 1999-07, Vol.98 (1), p.13-23

1999

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Interocular amplitude differences of the full field electroretinogram in normal subjects

British journal of ophthalmology, 2003-10, Vol.87 (10), p.1268-1271

2003

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Mutations in the RP1 Gene Causing Autosomal Dominant Retinitis Pigmentosa

Human molecular genetics, 1999-10, Vol.8 (11), p.2121-2128

1999

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Docosahexaenoic acid in red blood cells of patients with X-linked retinitis pigmentosa

Investigative ophthalmology & visual science, 1995-05, Vol.36 (6), p.1009-1018

1995

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Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors

Investigative ophthalmology & visual science, 1997-02, Vol.38 (2), p.498-509

1997

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Control of Late Off-Center Cone Bipolar Cell Differentiation and Visual Signaling by the Homeobox Gene Vsx1

Proceedings of the National Academy of Sciences - PNAS, 2004-02, Vol.101 (6), p.1754-1759

2004

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Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

American journal of human genetics, 1997-12, Vol.61 (6), p.1287-1292

1997

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Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Nature genetics, 2000-11, Vol.26 (3), p.319-323

2000

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Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity

Vision research (Oxford), 1993-08, Vol.33 (12), p.1605-1618

1993

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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

Human molecular genetics, 2002-03, Vol.11 (5), p.559-568

2002

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Safety and efficacy of omega-3 fatty acids in the nutrition of very low birth weight infants: Soy oil and marine oil supplementation of formula

The Journal of pediatrics, 1994-04, Vol.124 (4), p.612-620

1994

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Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

Human mutation, 2001, Vol.17 (1), p.42-51

2001

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Lipofuscin Accumulation, Abnormal Electrophysiology, and Photoreceptor Degeneration in Mutant ELOVL4 Transgenic Mice: A Model for Macular Degeneration

Psychophysical assessment of low visual function in patients with retinal degenerative diseases (RDDs) with the Diagnosys full-field stimulus threshold (D-FST)

Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants

Delayed Dark-Adaptation and Lipofuscin Accumulation in abcr+/- Mice: Implications for Involvement of ABCR in Age-Related Macular Degeneration

Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy

Dietary essential fatty acid supply and visual acuity development

Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave

The Very Large G-Protein-Coupled Receptor VLGR1: A Component of the Ankle Link Complex Required for the Normal Development of Auditory Hair Bundles

Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis

Essential fatty acids in visual and brain development

A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants

Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23- his mutation

Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice

Interocular amplitude differences of the full field electroretinogram in normal subjects

Mutations in the RP1 Gene Causing Autosomal Dominant Retinitis Pigmentosa

Docosahexaenoic acid in red blood cells of patients with X-linked retinitis pigmentosa

Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors

Control of Late Off-Center Cone Bipolar Cell Differentiation and Visual Signaling by the Homeobox Gene Vsx1

Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

Safety and efficacy of omega-3 fatty acids in the nutrition of very low birth weight infants: Soy oil and marine oil supplementation of formula

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

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