Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model (Q58413953)

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30 December 2019

title

Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model (English)

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30 December 2019

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30 December 2019

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30 December 2019

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30 December 2019

Mariacarmela Allocca

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30 December 2019

Alessandra Tessitore

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30 December 2019

Fabiana Parisi

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30 December 2019

Umberto Di Vicino

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30 December 2019

Irene Bozzoni

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publication date

18 September 2006

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30 December 2019

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volume

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issue

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30 December 2019

page(s)

692-699

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Gene mutations in retinitis pigmentosa and their clinical implications

30 December 2019

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The nature of dominant mutations of rhodopsin and implications for gene therapy

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Focus on molecules: rhodopsin

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A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

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Retinopathy induced in mice by targeted disruption of the rhodopsin gene

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Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

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A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

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Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene

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Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa

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Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

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30 December 2019

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