Retinal degeneration progression changes lentiviral vector cell targeting in the retina

Item

http://www.wikidata.org/entity/Q28741007

description

2011 nî lūn-bûn

@nan

2011 թուականին հրատարակուած գիտական յօդուած

@hyw

2011 թվականին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@ast

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@en

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@nl

type

Item

label

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@ast

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@en

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@nl

prefLabel

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@ast

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@en

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@nl

P1476

Retinal degeneration progression changes lentiviral vector cell targeting in the retina

@en

P2093

Chamsy Sarkis

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Dana Wanner

http://www.w3.org/2001/XMLSchema#string

Karine Schouwey

http://www.w3.org/2001/XMLSchema#string

Maité Cachafeiro

http://www.w3.org/2001/XMLSchema#string

Maritza Calame

http://www.w3.org/2001/XMLSchema#string

Meriem Tekaya

http://www.w3.org/2001/XMLSchema#string

Stéphanie Philippe

http://www.w3.org/2001/XMLSchema#string

Yvan Arsenijevic

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P2860

A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cells

Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis

Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy

A novel and efficient gene transfer strategy reduces glial reactivity and improves neuronal survival and axonal growth in vitro.

GFAP-driven GFP expression in activated mouse Müller glial cells aligning retinal blood vessels following intravitreal injection of AAV2/6 vectors

Development of a self-inactivating lentivirus vector.

Adenovirus vectors targeting distinct cell types in the retina.

Targeted disruption of outer limiting membrane junctional proteins (Crb1 and ZO-1) increases integration of transplanted photoreceptor precursors into the adult wild-type and degenerating retina.

Adeno-associated virus-vectored gene therapy for retinal disease.

Effective gene therapy with nonintegrating lentiviral vectors.

P304

e23782

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P31

scholarly article

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10.1371/JOURNAL.PONE.0023782

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Corinne Kostic

P577

2011-01-01T00:00:00Z

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P5875

51627022

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P698

21901134

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P932

3161995

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