Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.
about
AAV-mediated gene therapy in mouse models of recessive retinal degenerationCorneal gene therapy: basic science and translational perspectiveReview: the history and role of naturally occurring mouse models with Pde6b mutationsGene Delivery by Subconjunctival Injection of Adenovirus in Rats: A Study of Local Distribution, Transgene Duration and SafetyAAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsiaIn vivo gene knockdown in rat dorsal root ganglia mediated by self-complementary adeno-associated virus serotype 5 following intrathecal delivery.Vector platforms for gene therapy of inherited retinopathies.Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration.Subretinal gene delivery using helper-dependent adenoviral vectors.Self-complementary adeno-associated viral vectors for gene therapy of hemophilia B: progress and challengesGene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosisVitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsiaTrans-Corneal Subretinal Injection in Mice and Its Effect on the Function and Morphology of the Retina.Nanoparticle-mediated gene transfer specific to retinal pigment epithelial cells.Gene therapy of inherited retinopathies: a long and successful road from viral vectors to patients.Long-term rescue of cone photoreceptor degeneration in retinitis pigmentosa 2 (RP2)-knockout mice by gene replacement therapy.Impact of Heparan Sulfate Binding on Transduction of Retina by Recombinant Adeno-Associated Virus VectorsTransient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia.Heparan Sulfate Binding Promotes Accumulation of Intravitreally Delivered Adeno-associated Viral Vectors at the Retina for Enhanced Transduction but Weakly Influences Tropism.Retinal detachment model in rodents by subretinal injection of sodium hyaluronateThe Degeneration and Apoptosis Patterns of Cone Photoreceptors in rd11 Mice.AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice.Gene therapy in animal models of autosomal dominant retinitis pigmentosaGene-based Therapy in a Mouse Model of Blue Cone Monochromacy.Delivery of CR2-fH Using AAV Vector Therapy as Treatment Strategy in the Mouse Model of Choroidal Neovascularization.AAV-mediated gene delivery of the calreticulin anti-angiogenic domain inhibits ocular neovascularization.
P2860
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P2860
Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@ast
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@en
type
label
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@ast
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@en
prefLabel
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@ast
Self-complementary AAV5 vector ...... thelial cells of normal mouse.
@en
P2093
P2860
P1476
Self-complementary AAV5 vector ...... ithelial cells of normal mouse
@en
P2093
Fansheng Kong
Ji-jing Pang
Qinxiang Zheng
Sanford L Boye
Wensheng Li
Xiangtian Zhou
Xufeng Dai
P2860
P304
P356
10.1016/J.EXER.2010.01.011
P577
2010-02-04T00:00:00Z