标题
AAV9 Targets Cone Photoreceptors in the Nonhuman Primate Retina
作者
关键词
-
出版物
PLoS One
Volume 8, Issue 1, Pages e53463
出版商
Public Library of Science (PLoS)
发表日期
2013-01-31
DOI
10.1371/journal.pone.0053463
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The Human Rhodopsin Kinase Promoter in an AAV5 Vector Confers Rod- and Cone-Specific Expression in the Primate Retina
- (2012) Shannon E. Boye et al. HUMAN GENE THERAPY
- AAV-mediated photoreceptor transduction of the pig cone-enriched retina
- (2011) C Mussolino et al. GENE THERAPY
- TerminalN-Linked Galactose Is the Primary Receptor for Adeno-associated Virus 9
- (2011) Shen Shen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The AAV9 receptor and its modification to improve in vivo lung gene transfer in mice
- (2011) Christie L. Bell et al. JOURNAL OF CLINICAL INVESTIGATION
- rAAV2/5 gene-targeting to rods:dose-dependent efficiency and complications associated with different promoters
- (2010) W A Beltran et al. GENE THERAPY
- Efficient Serotype-Dependent Release of Functional Vector into the Culture Medium During Adeno-Associated Virus Manufacturing
- (2010) Luk H. Vandenberghe et al. HUMAN GENE THERAPY
- Gene therapy rescues cone function in congenital achromatopsia
- (2010) András M. Komáromy et al. HUMAN MOLECULAR GENETICS
- Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies
- (2010) Anneke I. den Hollander et al. JOURNAL OF CLINICAL INVESTIGATION
- Treatment Possibilities for Retinitis Pigmentosa
- (2010) Samuel G. Jacobson et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
- (2010) V. Busskamp et al. SCIENCE
- Naturally occurring singleton residues in AAV capsid impact vector performance and illustrate structural constraints
- (2009) L H Vandenberghe et al. GENE THERAPY
- Gene therapy for red–green colour blindness in adult primates
- (2009) Katherine Mancuso et al. NATURE
- 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
- (2008) William W. Hauswirth et al. HUMAN GENE THERAPY
- Novel AAV serotypes for improved ocular gene transfer
- (2008) Corinna Lebherz et al. JOURNAL OF GENE MEDICINE
- Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain
- (2008) Knut Stieger et al. MOLECULAR THERAPY
- Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis
- (2008) Albert M. Maguire et al. NEW ENGLAND JOURNAL OF MEDICINE
- Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
- (2008) James W.B. Bainbridge et al. NEW ENGLAND JOURNAL OF MEDICINE
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