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Publications by Alison Schwein

AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa

Human Gene Therapy

English

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159. Long-Term Rescue by AAV-Delivered Therapy in Autosomal Dominant Retinitis Pigmentosa (ADRP) Mice

English

Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.

Journal of Medical Genetics

Genetics

1982

English

Mutations in Known Genes Account for 58% of Autosomal Dominant Retinitis Pigmentosa (adRP)

Advances in Experimental Medicine and Biology

English

Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N

Current Eye Research

Molecular Neuroscience

English

Retinal Transplantation–Induced Recovery of Retinotectal Visual Function in a Rodent Model of Retinitis Pigmentosa

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

PLoS ONE

Multidisciplinary

2016

English

Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

A Rhodopsin Gene Mutation Responsible for Autosomal Dominant Retinitis Pigmentosa Results in a Protein That Is Defective in Localization to the Photoreceptor Outer Segment

Journal of Neuroscience

Neuroscience

1994

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Alison Schwein

AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa

Related publications

159. Long-Term Rescue by AAV-Delivered Therapy in Autosomal Dominant Retinitis Pigmentosa (ADRP) Mice

Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa

Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.

Mutations in Known Genes Account for 58% of Autosomal Dominant Retinitis Pigmentosa (adRP)

Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N

Retinal Transplantation–Induced Recovery of Retinotectal Visual Function in a Rodent Model of Retinitis Pigmentosa

De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)

A Rhodopsin Gene Mutation Responsible for Autosomal Dominant Retinitis Pigmentosa Results in a Protein That Is Defective in Localization to the Photoreceptor Outer Segment