Combined rod and cone transduction by adeno-associated virus 2/8. - Wikidata - wikimedia - TriplyDB

Combined rod and cone transduction by adeno-associated virus 2/8.

Combined rod and cone transduction by adeno-associated virus 2/8.

http://www.wikidata.org/entity/Q37404344

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Rod Outer Segment Development Influences AAV-Mediated Photoreceptor Transduction After Subretinal Injection.Vector platforms for gene therapy of inherited retinopathies.Gene Therapy Fully Restores Vision to the All-Cone Nrl(-/-) Gucy2e(-/-) Mouse Model of Leber Congenital Amaurosis-1.Improved dual AAV vectors with reduced expression of truncated proteins are safe and effective in the retina of a mouse model of Stargardt disease.AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects Non-viral therapeutic approaches to ocular diseases: An overview and future directions Healthy and diseased corticospinal motor neurons are selectively transduced upon direct AAV2-2 injection into the motor cortex.Let There Be Light: Gene and Cell Therapy for Blindness.Advances in Gene Therapy for Diseases of the Eye.Retinal transduction profiles by high-capacity viral vectors.Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors.Design and Development of AAV-based Gene Supplementation Therapies for Achromatopsia and Retinitis Pigmentosa.Triple Vectors Expand AAV Transfer Capacity in the Retina.ASSESSMENT OF AAV SEROTYPE TROPISM IN HUMAN RETINAL EXPLANTS.

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Combined rod and cone transduction by adeno-associated virus 2/8.

http://www.wikidata.org/entity/Q37404344

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 October 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Combined rod and cone transduction by adeno-associated virus 2/8.

@en

Combined rod and cone transduction by adeno-associated virus 2/8.

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type

label

Combined rod and cone transduction by adeno-associated virus 2/8.

@en

Combined rod and cone transduction by adeno-associated virus 2/8.

@nl

prefLabel

Combined rod and cone transduction by adeno-associated virus 2/8.

@en

Combined rod and cone transduction by adeno-associated virus 2/8.

@nl

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Human Gene Therapy

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Combined rod and cone transduction by adeno-associated virus 2/8.

@en

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Agostina Puppo

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Andrea Sommella

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Anna Manfredi

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Cheryl M Craft

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Elena Marrocco

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Giulia Cesi

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Massimo Giunti

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Settimio Rossi

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P2860

Vision 1 year after gene therapy for Leber's congenital amaurosis

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

The human visual cortex responds to gene therapy-mediated recovery of retinal function

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

Recombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65-/- knockout mouse eye results in limited rescue

Dosage thresholds for AAV2 and AAV8 photoreceptor gene therapy in monkey

MicroRNA-restricted transgene expression in the retina

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial

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982-992

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scholarly article

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10.1089/HUM.2013.154

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12

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24

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Francesca Simonelli

Maria Laura Bacci

Enrico M. Surace

Alberto Auricchio

Michele Della Corte

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2013-10-30T00:00:00Z

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24067103

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3868409

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