Viral serotype and the transgene sequence influence overlapping adeno-associated viral (AAV) vector-mediated gene transfer in skeletal muscle.
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Transduction efficiency of AAV 2/6, 2/8 and 2/9 vectors for delivering genes in human corneal fibroblastsEvidence for the failure of adeno-associated virus serotype 5 to package a viral genome > or = 8.2 kb.Full-length dystrophin reconstitution with adeno-associated viral vectorsGene and cell-mediated therapies for muscular dystrophy.Efficacious and safe tissue-selective controlled gene therapy approaches for the cornea.The potential of adeno-associated viral vectors for gene delivery to muscle tissue.AAV serotype influences gene transfer in corneal stroma in vivo.Efficient production of dual recombinant adeno-associated viral vectors for factor VIII deliveryGene therapy of mdx mice with large truncated dystrophins generated by recombination using rAAV6.Efficient transgene reconstitution with hybrid dual AAV vectors carrying the minimized bridging sequencesGene therapy progress and prospects: Duchenne muscular dystrophy.Gene therapy using adeno-associated virus vectorsAn AAV vector-mediated gene delivery approach facilitates reconstitution of functional human CD8+ T cells in miceCombination therapy utilizing shRNA knockdown and an optimized resistant transgene for rescue of diseases caused by misfolded proteins.Novel mini-dystrophin gene dual adeno-associated virus vectors restore neuronal nitric oxide synthase expression at the sarcolemmaA simplified immune suppression scheme leads to persistent micro-dystrophin expression in Duchenne muscular dystrophy dogsViral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advancesControlled and localized genetic manipulation in the brain.Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice.Expressing Transgenes That Exceed the Packaging Capacity of Adeno-Associated Virus Capsids.AAV-mediated gene transfer for retinal diseases.Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus.C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout miceGene delivery in the equine cornea: a novel therapeutic strategy.Expanding adeno-associated viral vector capacity: a tale of two vectors.Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophyMolecular-targeted therapy for Duchenne muscular dystrophy: progress and potential.Designing heart performance by gene transfer.Effective delivery of large genes to the retina by dual AAV vectors.Gene therapy for retinal diseaseGene therapy to rescue retinal degeneration caused by mutations in rhodopsin.A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequencePseudotyped adeno-associated viral vectors for gene transfer in dermal fibroblasts: implications for wound-healing applications.Soluble TNF-α receptor secretion from healthy or dystrophic mice after AAV6-mediated muscle gene transfer.Adeno-associated Virus (AAV) Dual Vector Strategies for Gene Therapy Encoding Large Transgenes.
P2860
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P2860
Viral serotype and the transgene sequence influence overlapping adeno-associated viral (AAV) vector-mediated gene transfer in skeletal muscle.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Viral serotype and the transge ...... e transfer in skeletal muscle.
@en
type
label
Viral serotype and the transge ...... e transfer in skeletal muscle.
@en
prefLabel
Viral serotype and the transge ...... e transfer in skeletal muscle.
@en
P2093
P2860
P356
P1476
Viral serotype and the transge ...... e transfer in skeletal muscle.
@en
P2093
Arkasubhra Ghosh
Dongsheng Duan
Yongping Yue
P2860
P304
P356
10.1002/JGM.835
P577
2006-03-01T00:00:00Z