Gene transfer by adeno-associated virus vectors into the central nervous system.
about
Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirusLatent adeno-associated virus infection elicits humoral but not cell-mediated immune responses in a nonhuman primate modelEfficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectorsStructure of adeno-associated virus-2 in complex with neutralizing monoclonal antibody A20Adenoviral and adeno-associated viral transfer of genes to the peripheral nervous systemMethods, potentials, and limitations of gene delivery to regenerate central nervous system cellsGene therapy for metachromatic leukodystrophy.Targeted delivery of brain-derived neurotrophic factor for the treatment of blindness and deafness.Long-distance axonal transport of AAV9 is driven by dynein and kinesin-2 and is trafficked in a highly motile Rab7-positive compartment.Recombinant adeno-associated virus vector expressing angiostatin inhibits preretinal neovascularization in adult rats.Long-term safety of GDNF gene delivery in the retina.Designer gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transferDisease-inducible transgene expression from a recombinant adeno-associated virus vector in a rat arthritis model.Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates.Two-photon imaging of calcium in virally transfected striate cortical neurons of behaving monkeyPhosphatidylserine immobilization of lentivirus for localized gene transfer.Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy.A chimeric protein containing the N terminus of the adeno-associated virus Rep protein recognizes its target site in an in vivo assay.Repeated delivery of adeno-associated virus vectors to the rabbit airway.Overexpression of cyclin A inhibits augmentation of recombinant adeno-associated virus transduction by the adenovirus E4orf6 protein.Involvement of cellular double-stranded DNA break binding proteins in processing of the recombinant adeno-associated virus genome.Formation of AAV single stranded DNA genome from a circular plasmid in Saccharomyces cerevisiaeAdeno-associated virus serotypes 1, 8, and 9 share conserved mechanisms for anterograde and retrograde axonal transport.Inhibitory RNA in epilepsy: research tools and therapeutic perspectivesIntrathecal delivery of a mutant micro-opioid receptor activated by naloxone as a possible antinociceptive paradigm.Recombinant adeno-associated virus vector: use for transgene expression and anterograde tract tracing in the CNSInsight into the mechanism of inhibition of adeno-associated virus by the Mre11/Rad50/Nbs1 complexEnhancement of recombinant adeno-associated virus type 2-mediated transgene expression in a lung epithelial cell line by inhibition of the epidermal growth factor receptorImmunity to adenovirus and adeno-associated viral vectors: implications for gene therapy.Targeting neurons of rat nucleus tractus solitarii with the gene transfer vector adeno-associated virus type 2 to up-regulate neuronal nitric oxide synthase.Molecular basis of Canavan's disease: from human to mouse.FGF2 gene transfer restores hippocampal functions in mouse models of Alzheimer's disease and has therapeutic implications for neurocognitive disordersA Single Vector Platform for High-Level Gene Transduction of Central Neurons: Adeno-Associated Virus Vector Equipped with the Tet-Off System.The assessment of adeno-associated vectors as potential intrinsic treatments for brainstem axon regeneration.Use of Adeno-Associated and Herpes Simplex Viral Vectors for In Vivo Neuronal Expression in Mice.Recombinant Semliki Forest virus and Sindbis virus efficiently infect neurons in hippocampal slice culturesTropism and toxicity of adeno-associated viral vector serotypes 1, 2, 5, 6, 7, 8, and 9 in rat neurons and glia in vitro.Gene therapy in the treatment of heart failure.AAV1/2-mediated CNS gene delivery of dominant-negative CCL2 mutant suppresses gliosis, beta-amyloidosis, and learning impairment of APP/PS1 mice.Large animal models of neurological disorders for gene therapy.
P2860
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P2860
Gene transfer by adeno-associated virus vectors into the central nervous system.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Gene transfer by adeno-associated virus vectors into the central nervous system.
@en
type
label
Gene transfer by adeno-associated virus vectors into the central nervous system.
@en
prefLabel
Gene transfer by adeno-associated virus vectors into the central nervous system.
@en
P2093
P356
P1476
Gene transfer by adeno-associated virus vectors into the central nervous system.
@en
P2093
P304
P356
10.1006/EXNR.1996.6396
P407
P577
1997-03-01T00:00:00Z