Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity.
about
Biology of adeno-associated viral vectors in the central nervous systemPackaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps.The atomic structure of adeno-associated virus (AAV-2), a vector for human gene therapy.Efficient transduction of vascular endothelial cells with recombinant adeno-associated virus serotype 1 and 5 vectorsAdeno-associated virus type 2 VP2 capsid protein is nonessential and can tolerate large peptide insertions at its N terminusCross-dressing the virion: the transcapsidation of adeno-associated virus serotypes functionally defines subgroupsSelf-complementary AAVs induce more potent transgene product-specific immune responses compared to a single-stranded genomeRecombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65-/- knockout mouse eye results in limited rescueAntiangiogenic gene therapy of cancer: recent developmentsProgresses towards safe and efficient gene therapy vectorsAdeno-associated Virus as a Mammalian DNA VectorAdeno-associated virus for cystic fibrosis gene therapyParvovirus glycan interactionsAdeno-associated virus at 50: a golden anniversary of discovery, research, and gene therapy success--a personal perspectiveGene delivery to adipose tissue using transcriptionally targeted rAAV8 vectorsStructure of Adeno-Associated Virus Serotype 8, a Gene Therapy VectorThe structure of adeno-associated virus serotype 3B (AAV-3B): Insights into receptor binding and immune evasionStructure–function analysis of receptor-binding in adeno-associated virus serotype 6 (AAV-6)Structural Insight into the Unique Properties of Adeno-Associated Virus Serotype 9Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophyAAV-mediated overexpression of human α7 integrin leads to histological and functional improvement in dystrophic miceRecombinant adeno-associated viral (rAAV) vectors mediate efficient gene transduction in cultured neonatal and adult microgliaStructure of neurotropic adeno-associated virus AAVrh.8.Rapid, long-term labeling of cells in the developing and adult rodent visual cortex using double-stranded adeno-associated viral vectors.Rescue of bilirubin-induced neonatal lethality in a mouse model of Crigler-Najjar syndrome type I by AAV9-mediated gene transferOptimization of scAAVIL-1ra In Vitro and In Vivo to Deliver High Levels of Therapeutic Protein for Treatment of Osteoarthritis.Comparative analysis of adeno-associated virus capsid stability and dynamicsThe potential of gene transfer into primary B-CLL cells using recombinant virus vectors.SCHEMA computational design of virus capsid chimeras: calibrating how genome packaging, protection, and transduction correlate with calculated structural disruption.Directed evolution of adeno-associated virus yields enhanced gene delivery vectors.Engineering and selection of shuffled AAV genomes: a new strategy for producing targeted biological nanoparticles.Different tropism of adenoviruses and adeno-associated viruses to corneal cells: implications for corneal gene therapyGeneration of novel AAV variants by directed evolution for improved CFTR delivery to human ciliated airway epithelium.Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brainsGene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutationsComplete correction of hyperphenylalaninemia following liver-directed, recombinant AAV2/8 vector-mediated gene therapy in murine phenylketonuria.Cationic lipid formulations alter the in vivo tropism of AAV2/9 vector in lungMicroRNA-29 overexpression by adeno-associated virus suppresses fibrosis and restores muscle function in combination with micro-dystrophinAn adeno-associated viral vector transduces the rat hypothalamus and amygdala more efficient than a lentiviral vectorRecombinant adeno-associated virus: efficient transduction of the rat VMH and clearance from blood.
P2860
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P2860
Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Cross-packaging of a single ad ...... uction with broad specificity.
@en
Cross-packaging of a single adeno-associated virus
@nl
type
label
Cross-packaging of a single ad ...... uction with broad specificity.
@en
Cross-packaging of a single adeno-associated virus
@nl
prefLabel
Cross-packaging of a single ad ...... uction with broad specificity.
@en
Cross-packaging of a single adeno-associated virus
@nl
P2093
P2860
P1433
P1476
Cross-packaging of a single ad ...... uction with broad specificity.
@en
P2093
Chengwen Li
Fabienne Rolling
Hervè Conrath
Joseph E Rabinowitz
R Jude Samulski
Weidong Xiao
P2860
P304
P356
10.1128/JVI.76.2.791-801.2002
P407
P577
2002-01-01T00:00:00Z