about
Combinatorial RNA-based gene therapy for the treatment of HIV/AIDSAssessment of multifunctional contrast agent probes in neuroimaging: Implications of nanopharmaceutical therapeutic interventionsPromising and delivering gene therapies for vision lossAdeno-associated virus vector mediated gene transfer to pancreatic beta cells.Effective in vivo and ex vivo gene transfer to intestinal mucosa by VSV-G-pseudotyped lentiviral vectorsGene delivery to the spinal cord: comparison between lentiviral, adenoviral, and retroviral vector delivery systemsGene therapy for Parkinson's disease: review and update.Conformation, independent of charge, in the R domain affects cystic fibrosis transmembrane conductance regulator channel openingsLentivirus and foamy virus vectors: novel gene therapy tools.Cell Therapy From Bench to Bedside Translation in CNS Neurorestoratology Era.Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo.Imaging adenoviral-directed reporter gene expression in living animals with positron emission tomography.Selection of RNAi-based inhibitors for anti-HIV gene therapyEffective gene expression in the rat dorsal root ganglia with a non-viral vector delivered via spinal nerve injection.Using viral vectors as gene transfer tools (Cell Biology and Toxicology Special Issue: ETCS-UK 1 day meeting on genetic manipulation of cells).Destination Brain: the Past, Present, and Future of Therapeutic Gene Delivery.Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations.Tropism, intracerebral distribution, and transduction efficiency of HIV- and SIV-based lentiviral vectors after injection into the mouse brain: a qualitative and quantitative in vivo study.Cotransduction of nondividing cells using lentiviral vectors.Reconstitution of a metabolic pathway with triple-cistronic IRES-containing retroviral vectors for correction of tetrahydrobiopterin deficiency.Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon.Modulation of neuronal survival and axonal growth in vivo by tetracycline-regulated neurotrophin expression.NRSF causes cAMP-sensitive suppression of sodium current in cultured hippocampal neurons.Gene transfer into the CNS using recombinant adeno-associated virus: analysis of vector DNA forms resulting in sustained expression.Syngeneic central nervous system transplantation of genetically transduced mature, adult astrocytes.Adenoviral vector-directed expression of neurotrophin-3 in rat dorsal root ganglion explants results in a robust neurite outgrowth response.Gene therapy for Rett syndrome: prospects and challenges
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Applications of gene therapy to the CNS.
@en
type
label
Applications of gene therapy to the CNS.
@en
prefLabel
Applications of gene therapy to the CNS.
@en
P2093
P2860
P1476
Applications of gene therapy to the CNS.
@en
P2093
P2860
P304
P356
10.1093/HMG/5.SUPPLEMENT_1.1397
P478
P577
1996-01-01T00:00:00Z