Hybrid vectors based on adeno-associated virus serotypes 2 and 5 for muscle-directed gene transfer.
about
Deciphering the Neuronal Circuitry Controlling Local Blood Flow in the Cerebral Cortex with Optogenetics in PV::Cre Transgenic MiceNovel adeno-associated viruses from rhesus monkeys as vectors for human gene therapyAdeno-associated virus type 2 VP2 capsid protein is nonessential and can tolerate large peptide insertions at its N terminusThe microphthalmia transcription factor (Mitf) controls expression of the ocular albinism type 1 gene: link between melanin synthesis and melanosome biogenesisThe long noncoding RNA Vax2os1 controls the cell cycle progression of photoreceptor progenitors in the mouse retinaAdeno-associated virus for cystic fibrosis gene therapyAAV-mediated gene therapy for heart failure: enhancing contractility and calcium handlingDevelopment of Patient-specific AAV Vectors After Neutralizing Antibody Selection for Enhanced Muscle Gene TransferRestoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor functionIn vivo delivery of recombinant viruses to the fetal murine cochlea: transduction characteristics and long-term effects on auditory function.Designer gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transferDifferent tropism of adenoviruses and adeno-associated viruses to corneal cells: implications for corneal gene therapyAAV's anatomy: roadmap for optimizing vectors for translational successComparative study of anti-hepatitis B virus RNA interference by double-stranded adeno-associated virus serotypes 7, 8, and 9.Adeno-associated virus (AAV) serotype 9 provides global cardiac gene transfer superior to AAV1, AAV6, AAV7, and AAV8 in the mouse and rat.Molecular characterization of adeno-associated viruses infecting childrenSuppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosaIdentification of PDGFR as a receptor for AAV-5 transduction.Successful production of pseudotyped rAAV vectors using a modified baculovirus expression system.Virus-mediated transduction of murine retina with adeno-associated virus: effects of viral capsid and genome size.Bronchoalveolar fluid is not a major hindrance to virus-mediated gene therapy in cystic fibrosis.Pseudotyped AAV vector-mediated gene transfer in a human fetal trachea xenograft model: implications for in utero gene therapy for cystic fibrosis.AAV hybrid serotypes: improved vectors for gene deliveryNoninvasive gene transfer to the lung for systemic delivery of therapeutic proteins.Immunological aspects of recombinant adeno-associated virus delivery to the mammalian brainAlpha2,3 and alpha2,6 N-linked sialic acids facilitate efficient binding and transduction by adeno-associated virus types 1 and 6Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transductionImmune responses to adeno-associated virus and its recombinant vectors.Structurally mapping the diverse phenotype of adeno-associated virus serotype 4.Receptor targeting of adeno-associated virus vectors.Induction of robust immune responses against human immunodeficiency virus is supported by the inherent tropism of adeno-associated virus type 5 for dendritic cells.Advances in AAV-mediated gene transfer for the treatment of inherited disorders.Protection of mice from lethal Escherichia coli infection by chimeric human bactericidal/permeability-increasing protein and immunoglobulin G1 Fc gene deliveryIntravenous AAV8 Encoding Urocortin-2 Increases Function of the Failing Heart in Mice.Methods for gene transfer to the central nervous system.Immune responses to gene therapy vectors: influence on vector function and effector mechanisms.Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD).Gene therapy for obesity.Single amino acid modification of adeno-associated virus capsid changes transduction and humoral immune profiles.New vectors and strategies for cardiovascular gene therapy.
P2860
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P2860
Hybrid vectors based on adeno-associated virus serotypes 2 and 5 for muscle-directed gene transfer.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@en
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@nl
type
label
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@en
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@nl
prefLabel
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@en
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@nl
P2093
P2860
P1433
P1476
Hybrid vectors based on adeno- ...... muscle-directed gene transfer.
@en
P2093
P2860
P304
P356
10.1128/JVI.75.13.6199-6203.2001
P407
P577
2001-07-01T00:00:00Z