(Q58413953)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16979943%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

title

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

1 reference

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30 December 2019

1 reference

3

1 reference

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30 December 2019

Luciano Domenici

6

1 reference

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30 December 2019

Alberto Auricchio

8

1 reference

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30 December 2019

4

Mariacarmela Allocca

1 reference

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30 December 2019

author name string

Alessandra Tessitore

1

1 reference

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30 December 2019

Fabiana Parisi

2

1 reference

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30 December 2019

Umberto Di Vicino

5

1 reference

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30 December 2019

Irene Bozzoni

7

1 reference

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30 December 2019

publication date

18 September 2006

1 reference

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30 December 2019

1 reference

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30 December 2019

volume

14

1 reference

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30 December 2019

issue

5

1 reference

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30 December 2019

page(s)

692-699

1 reference

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Gene mutations in retinitis pigmentosa and their clinical implications

30 December 2019

cites work

1 reference

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

7 January 2021

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Focus on molecules: rhodopsin

7 January 2021

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

7 January 2021

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Retinopathy induced in mice by targeted disruption of the rhodopsin gene

7 January 2021

1 reference

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A rare homozygous rhodopsin splice-site mutation: the issue of when and whether to offer presymptomatic testing.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Ribozymes, DNAzymes and small interfering RNAs as therapeutics

7 January 2021

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Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa.

7 January 2021

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Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy.

7 January 2021

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Small RNA asymmetry in RNAi: function in RISC assembly and gene regulation.

7 January 2021

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Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interference

7 January 2021

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Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach

7 January 2021

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Effects on RNA interference in gene expression (RNAi) in cultured mammalian cells of mismatches and the introduction of chemical modifications at the 3'-ends of siRNAs

7 January 2021

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Allele-specific RNA interference for neurological disease

7 January 2021

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Stable suppression of tumorigenicity by virus-mediated RNA interference

7 January 2021

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A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA interference

7 January 2021

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RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.

7 January 2021

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Approaches for chemically synthesized siRNA and vector-mediated RNAi

7 January 2021

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Adeno-associated viral vectors for retinal gene transfer and treatment of retinal diseases

7 January 2021

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Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model

7 January 2021

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Virus-mediated transduction of murine retina with adeno-associated virus: effects of viral capsid and genome size.

7 January 2021

1 reference

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

A new vector, based on the PolII promoter of the U1 snRNA gene, for the expression of siRNAs in mammalian cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Body-wide gene therapy of Duchenne muscular dystrophy in the mdx mouse model.

7 January 2021

1 reference

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Involvement of the intracellular ion channel CLIC1 in microglia-mediated beta-amyloid-induced neurotoxicity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Phenotypic alteration of eukaryotic cells using randomized libraries of artificial transcription factors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Purification of recombinant adeno-associated virus vectors by column chromatography and its performance in vivo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Nerve growth factor prevents the amblyopic effects of monocular deprivation

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.07.008

Functionally rodless mice: transgenic models for the investigation of cone function in retinal disease and therapy

7 January 2021

1 reference

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10.1016/J.YMTHE.2006.07.008

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16979943%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

1 reference