Liver transduction with recombinant adeno-associated virus is primarily restricted by capsid serotype not vector genotype.
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Adeno-associated virus vector integrationSystemic Delivery of scAAV8-Encoded MiR-29a Ameliorates Hepatic Fibrosis in Carbon Tetrachloride-Treated MiceArgonaute proteins are key determinants of RNAi efficacy, toxicity, and persistence in the adult mouse liverGene transfer in skeletal and cardiac muscle using recombinant adeno-associated virusDesigner gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transferIn vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses.Creating a novel origin of replication through modulating DNA-protein interfaces.Sustained Inhibition of HBV Replication In Vivo after Systemic Injection of AAVs Encoding Artificial Antiviral Primary MicroRNAs.AAV2/8-mediated correction of OTC deficiency is robust in adult but not neonatal Spf(ash) mice.Sexually dimorphic patterns of episomal rAAV genome persistence in the adult mouse liver and correlation with hepatocellular proliferationBiochemical and Physiological Improvement in a Mouse Model of Smith-Lemli-Opitz Syndrome (SLOS) Following Gene Transfer with AAV Vectors.RH10 provides superior transgene expression in mice when compared with natural AAV serotypes for neonatal gene therapy.Promoterless gene targeting without nucleases ameliorates haemophilia B in mice.Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo.Targeting adipose tissue via systemic gene therapyComparison of efficacy of the disease-specific LOX1- and constitutive cytomegalovirus-promoters in expressing interleukin 10 through adeno-associated virus 2/8 delivery in atherosclerotic mice.A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degenerationDevelopment and rescue of human familial hypercholesterolaemia in a xenograft mouse modelAAV-based neonatal gene therapy for hemophilia A: long-term correction and avoidance of immune responses in miceHybrid adeno-associated virus bearing nonhomologous inverted terminal repeats enhances dual-vector reconstruction of minigenes in vivo.Structural Insights into the Assembly of the Adeno-associated Virus Type 2 Rep68 Protein on the Integration Site AAVS1Gene transfer in the lung using recombinant adeno-associated virusAdeno-associated virus vector genomes persist as episomal chromatin in primate muscle.Gene transfer of apolipoprotein A-V improves the hypertriglyceridemic phenotype of apoa5 (-/-) mice.Strategies to generate high-titer, high-potency recombinant AAV3 serotype vectorsLiver-specific microRNA-122 target sequences incorporated in AAV vectors efficiently inhibits transgene expression in the liver.Recombinant adeno-associated virus transduction and integration.Potential of AAV vectors in the treatment of metabolic disease.Chimeric adeno-associated virus and bacteriophage: a potential targeted gene therapy vector for malignant glioma.miR-181a mediates TGF-β-induced hepatocyte EMT and is dysregulated in cirrhosis and hepatocellular cancer.Seek and destroy: targeted adeno-associated viruses for gene delivery to hepatocellular carcinoma.CRISPR/Cas9: at the cutting edge of hepatology.Apolipoprotein B knockdown by AAV-delivered shRNA lowers plasma cholesterol in mice.Reducing the risk of adeno-associated virus (AAV) vector mobilization with AAV type 5 vectors.Relevance of assembly-activating protein for Adeno-associated virus vector production and capsid protein stability in mammalian and insect cells.Immunoadhesins containing pre-S domains of hepatitis B virus large envelope protein are secreted and inhibit virus infection.Plasmodium berghei EXP-1 interacts with host Apolipoprotein H during Plasmodium liver-stage development.Efficient Gene Delivery and Expression in Pancreas and Pancreatic Tumors by Capsid-Optimized AAV8 Vectors.Long-term glycemic control with hepatic insulin gene therapy in streptozotocin-diabetic mice.
P2860
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P2860
Liver transduction with recombinant adeno-associated virus is primarily restricted by capsid serotype not vector genotype.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին հրատարակված գիտական հոդված
@hy
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
name
Liver transduction with recomb ...... serotype not vector genotype.
@ast
Liver transduction with recomb ...... serotype not vector genotype.
@en
Liver transduction with recomb ...... serotype not vector genotype.
@nl
type
label
Liver transduction with recomb ...... serotype not vector genotype.
@ast
Liver transduction with recomb ...... serotype not vector genotype.
@en
Liver transduction with recomb ...... serotype not vector genotype.
@nl
prefLabel
Liver transduction with recomb ...... serotype not vector genotype.
@ast
Liver transduction with recomb ...... serotype not vector genotype.
@en
Liver transduction with recomb ...... serotype not vector genotype.
@nl
P2093
P2860
P1433
P1476
Liver transduction with recomb ...... serotype not vector genotype.
@en
P2093
Dirk Grimm
Hiroyuki Nakai
Kusum Pandey
Mark A Kay
Theresa A Storm
P2860
P304
P356
10.1128/JVI.80.1.426-439.2006
P407
P577
2006-01-01T00:00:00Z