(Q45883369)

17 December 2017

title

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

1 reference

17 December 2017

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1 reference

Cashman SM

1

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17 December 2017

Binkley EA

series ordinal

2

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17 December 2017

Kumar-Singh R

series ordinal

3

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17 December 2017

publication date

1 August 2005

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17 December 2017

published in

Gene Therapy

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17 December 2017

volume

12

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17 December 2017

page(s)

1223-1228

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17 December 2017

issue

15

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.gt.3302512

exact match

0 references

cites work

How photons start vision

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Inhibition of fibrillin 1 expression using U1 snRNA as a vehicle for the presentation of antisense targeting sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

A system for stable expression of short interfering RNAs in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

siRNA-mediated gene silencing in vitro and in vivo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Characterization of 911: a new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Structure and function in rhodopsin: correct folding and misfolding in two point mutants in the intradiscal domain of rhodopsin identified in retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Rapid and efficient site-directed mutagenesis by single-tube 'megaprimer' PCR method

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

inferred from DOI database lookup

7 January 2021

based on heuristic

Strategems in vitro for gene therapies directed to dominant mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

inferred from DOI database lookup

7 January 2021

based on heuristic

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302512

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.GT.3302512

1 reference

17 December 2017

Dimensions Publication ID

0 references

1 reference

17 December 2017