(Q46940069)

English

Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration.

scientific article published on 22 October 2007

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scholarly article

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9 January 2020

Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration (English)

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9 January 2020

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9 January 2020

author name string

Ji-jing Pang

1

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9 January 2020

Amanda Lauramore

2

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9 January 2020

Qiuhong Li

4

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9 January 2020

Thomas J Doyle

5

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9 January 2020

Vince Chiodo

6

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9 January 2020

Jie Li

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9 January 2020

William W Hauswirth

8

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9 January 2020

publication date

22 October 2007

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9 January 2020

Vision Research

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9 January 2020

48

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9 January 2020

3

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9 January 2020

377-385

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9 January 2020

Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness

1 reference

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Restoration of cone vision in a mouse model of achromatopsia

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Gene transfer into the mouse retina mediated by an adeno-associated viral vector

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Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model

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Pseudotyped AAV vectors for constitutive and regulated gene expression in the eye.

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Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina

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Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina

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Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system.

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7 January 2021

Adeno-associated virus-mediated expression of vascular endothelial growth factor peptides inhibits retinal neovascularization in a mouse model of oxygen-induced retinopathy

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7 January 2021

Adeno-associated virus-vectored gene therapy for retinal disease

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Persistent transgene product in retina, optic nerve and brain after intraocular injection of rAAV.

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Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus

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7 January 2021

Adeno-associated virus: a ubiquitous commensal of mammals

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7 January 2021

Clades of Adeno-associated viruses are widely disseminated in human tissues.

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7 January 2021

Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy

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7 January 2021

Reporter expression persists 1 year after adeno-associated virus-mediated gene transfer to the optic nerve

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7 January 2021

Light-driven cone arrestin translocation in cones of postnatal guanylate cyclase-1 knockout mouse retina treated with AAV-GC1.

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7 January 2021

Retrovirus-mediated gene transfer to retinal explants

1 reference

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7 January 2021

AAV-mediated intravitreal gene therapy reduces lysosomal storage in the retinal pigmented epithelium and improves retinal function in adult MPS VII mice.

1 reference

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7 January 2021

Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8.

1 reference

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7 January 2021

AAV-mediated expression of CNTF promotes long-term survival and regeneration of adult rat retinal ganglion cells

1 reference

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7 January 2021

Gene delivery to the eye using adeno-associated viral vectors

1 reference

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7 January 2021

Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis

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7 January 2021

Two novel adeno-associated viruses from cynomolgus monkey: pseudotyping characterization of capsid protein

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7 January 2021

A reliable method for organ culture of neonatal mouse retina with long-term survival

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7 January 2021

Adenoviral-mediated gene transfer to retinal explants during development and degeneration

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7 January 2021

Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis

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7 January 2021

Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.

1 reference

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7 January 2021

Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity

1 reference

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7 January 2021

Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

1 reference

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7 January 2021

Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors

1 reference

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7 January 2021

Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transduction

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7 January 2021

Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal delivery

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7 January 2021

Virus-mediated transduction of murine retina with adeno-associated virus: effects of viral capsid and genome size.

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Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors

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A "humanized" green fluorescent protein cDNA adapted for high-level expression in mammalian cells

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Effect of deletions in adenovirus early region 1 genes upon replication of adeno-associated virus

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Müller cell transduction by AAV2 in normal and degenerative retinas

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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