Recombinant AAV-mediated BEST1 transfer to the retinal pigment epithelium: analysis of serotype-dependent retinal effects. (Q35021596)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24143172%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

Recombinant AAV-mediated BEST1 transfer to the retinal pigment epithelium: analysis of serotype-dependent retinal effects (English)

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28 February 2020

7

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28 February 2020

Gustavo D Aguirre

9

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28 February 2020

author name string

Karina E Guziewicz

1

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28 February 2020

Barbara Zangerl

2

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28 February 2020

András M Komáromy

3

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28 February 2020

Simone Iwabe

4

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28 February 2020

Vincent A Chiodo

5

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28 February 2020

Sanford L Boye

6

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28 February 2020

William A Beltran

8

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28 February 2020

language of work or name

English

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publication date

15 October 2013

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28 February 2020

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28 February 2020

volume

8

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28 February 2020

issue

10

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28 February 2020

page(s)

e75666

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Creative Commons Attribution 4.0 International

28 February 2020

copyright license

start time

15 October 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Interaction of bestrophin-1 and Ca2+ channel β-subunits: identification of new binding domains on the bestrophin-1 C-terminus

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Molecular consequences of BEST1 gene mutations in canine multifocal retinopathy predict functional implications for human bestrophinopathies.

8 July 2018

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Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3).

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The spectrum of ocular phenotypes caused by mutations in the BEST1 gene

8 July 2018

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Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

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Effect of gene therapy on visual function in Leber's congenital amaurosis

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Molecular physiology of bestrophins: multifunctional membrane proteins linked to best disease and other retinopathies

8 July 2018

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Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease

8 July 2018

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Suppression of mouse rhodopsin expression in vivo by AAV mediated siRNA delivery

8 July 2018

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Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells

8 July 2018

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8 July 2018

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Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium

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21 January 2018

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21 January 2018

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Gene therapy restores vision in a canine model of childhood blindness

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AUTOSOMAL RECESSIVE VITELLIFORM MACULAR DYSTROPHY IN A LARGE COHORT OF VITELLIFORM MACULAR DYSTROPHY PATIENTS

25 October 2018

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10.1371/JOURNAL.PONE.0075666

21 January 2018

Identifiers

DOI

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28 February 2020

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mapped directly with Wikidata item

24 November 2022

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28 February 2020

PubMed publication ID

24143172

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