Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina. - Wikidata - awgldk - TriplyDB

Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina.

Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina.

http://www.wikidata.org/entity/Q37500297

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A novel mutation in the RPE65 gene causing Leber congenital amaurosis and its transcriptional expression in vitro

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P2860

Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina.

http://www.wikidata.org/entity/Q37500297

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 21 January 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Immuno-histochemical analysis ...... or and superior canine retina.

@en

Immuno-histochemical analysis ...... or and superior canine retina.

@nl

type

label

Immuno-histochemical analysis ...... or and superior canine retina.

@en

Immuno-histochemical analysis ...... or and superior canine retina.

@nl

prefLabel

Immuno-histochemical analysis ...... or and superior canine retina.

@en

Immuno-histochemical analysis ...... or and superior canine retina.

@nl

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JOURNAL.PONE.0086304

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Immuno-histochemical analysis ...... or and superior canine retina.

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Alexandra Mendes-Madeira

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Birgit Lorenz

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Daniela Klein

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Fabienne Rolling

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Patrice Schlegel

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Silke Haverkamp

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P2860

RPE65 is the isomerohydrolase in the retinoid visual cycle

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

Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration

Safety and efficacy of gene transfer for Leber's congenital amaurosis

Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year

RPE65 is present in human green/red cones and promotes photopigment regeneration in an in vitro cone cell model

Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium

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

Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.

Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65.

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e86304

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scholarly article

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10.1371/JOURNAL.PONE.0086304

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1

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Fabienne Rolling

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2014-01-21T00:00:00Z

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