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Prospects for lentiviral vector mediated prostaglandin F synthase gene delivery in monkey eyes in vivoAdvancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano SymposiumIn vitro-in vivo correlation for complex non-oral drug products: Where do we stand?Viral and nonviral delivery systems for gene deliveryBone marrow mesenchymal stem cells protect against retinal ganglion cell loss in aged rats with glaucoma.Development of gene therapy for treatment of age-related macular degeneration.Gene therapy using stem cellsCapsid Mutated Adeno-Associated Virus Delivered to the Anterior Chamber Results in Efficient Transduction of Trabecular Meshwork in Mouse and RatGene therapy of inherited retinopathies: a long and successful road from viral vectors to patients.Transduction of photoreceptors with equine infectious anemia virus lentiviral vectors: safety and biodistribution of StarGen for Stargardt diseasePrimate neural retina upregulates IL-6 and IL-10 in response to a herpes simplex vector suggesting the presence of a pro-/anti-inflammatory axis.Enhancing titres of therapeutic viral vectors using the transgene repression in vector production (TRiP) system.Gene therapy for noninfectious uveitis.Convergence of Human Genetics and Animal Studies: Gene Therapy for X-Linked Retinoschisis.Taking Stock of Retinal Gene Therapy: Looking Back and Moving Forward.Production of Retrovirus-Based Vectors in Mildly Acidic pH Conditions.Viral Vectors: The Road to Reducing Genotoxicity.Lentivirus-mediated shRNA targeting Nanog inhibits cell proliferation and attenuates cancer stem cell activities in breast cancer.Gene Therapy and Stem Cell Transplantation in Retinal Disease: The New Frontier.[Developments in gene delivery vectors for ocular gene therapy].Adenovirus-Mediated Gene Delivery: Potential Applications for Gene and Cell-Based Therapies in the New Era of Personalized Medicine.CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype.Ocular gene therapy: introduction to the special issue.In Vivo Knockout of the Vegfa Gene by Lentiviral Delivery of CRISPR/Cas9 in Mouse Retinal Pigment Epithelium Cells.Potential of Gene Editing and Induced Pluripotent Stem Cells (iPSCs) in Treatment of Retinal Diseases.Late neuroprogenitors contribute to normal retinal vascular development in a Hif2a-dependent manner.In Vivo Genome Editing as a Therapeutic Approach
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Ocular gene delivery using lentiviral vectors.
@en
Ocular gene delivery using lentiviral vectors.
@nl
type
label
Ocular gene delivery using lentiviral vectors.
@en
Ocular gene delivery using lentiviral vectors.
@nl
prefLabel
Ocular gene delivery using lentiviral vectors.
@en
Ocular gene delivery using lentiviral vectors.
@nl
P2860
P356
P1433
P1476
Ocular gene delivery using lentiviral vectors.
@en
P2093
P2860
P2888
P304
P356
10.1038/GT.2011.153
P577
2011-11-03T00:00:00Z