Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis - Wikidata - thesis-toulmin - TriplyDB

Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis

Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis

http://www.wikidata.org/entity/Q28213353

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Hematopoietic- and neurologic-expressed sequence 1 (Hn1) depletion in B16.F10 melanoma cells promotes a differentiated phenotype that includes increased melanogenesis and cell cycle arrest Self-complementary AAVs induce more potent transgene product-specific immune responses compared to a single-stranded genome Hematopoietic- and neurologic-expressed sequence 1 expression in the murine GL261 and high-grade human gliomas Therapeutic application of RNAi: is mRNA targeting finally ready for prime time?The recombinant adeno-associated virus vector (rAAV2)-mediated apolipoprotein B mRNA-specific hammerhead ribozyme: a self-complementary AAV2 vector improves the gene expression Intrathecal long-term gene expression by self-complementary adeno-associated virus type 1 suitable for chronic pain studies in rats MicroRNA-regulated viral vectors for gene therapy Gene therapy: progress and predictions Neuroanatomy goes viral!Developments in the treatment of hemophilia B: focus on emerging gene therapy The gene therapy journey for hemophilia: are we there yet?Adeno-associated virus at 50: a golden anniversary of discovery, research, and gene therapy success--a personal perspective Animal models of hemophilia Adeno-associated virus-mediated cancer gene therapy: current status Implantation of rAAV5-IGF-I transduced autologous chondrocytes improves cartilage repair in full-thickness defects in the equine model.A large animal model of spinal muscular atrophy and correction of phenotype.Adeno-associated virus: from defective virus to effective vector Gene therapy for hemophilia Gene therapy in an era of emerging treatment options for hemophilia B Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy Central Mechanisms Mediating Thrombospondin-4-induced Pain States.Rapid, long-term labeling of cells in the developing and adult rodent visual cortex using double-stranded adeno-associated viral vectors.Quantitative 3D tracing of gene-delivery viral vectors in human cells and animal tissues.Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping Cytoplasmic trafficking, endosomal escape, and perinuclear accumulation of adeno-associated virus type 2 particles are facilitated by microtubule network.Optimization of scAAVIL-1ra In Vitro and In Vivo to Deliver High Levels of Therapeutic Protein for Treatment of Osteoarthritis.Selective forelimb impairment in rats expressing a pathological TDP-43 25 kDa C-terminal fragment to mimic amyotrophic lateral sclerosis.Indexing TNF-alpha gene expression using a gene-targeted reporter cell line LIGHT induces distinct signals to clear an AAV-expressed persistent antigen in the mouse liver and to induce liver inflammation.Retrograde gene delivery to hypoglossal motoneurons using adeno-associated virus serotype 9.Sustained Inhibition of HBV Replication In Vivo after Systemic Injection of AAVs Encoding Artificial Antiviral Primary MicroRNAs.AAV's anatomy: roadmap for optimizing vectors for translational success In vivo dynamics of AAV-mediated gene delivery to sensory neurons of the trigeminal ganglia Evidence for the failure of adeno-associated virus serotype 5 to package a viral genome > or = 8.2 kb.Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.Optimized adeno-associated virus (AAV)-protein phosphatase-5 helper viruses for efficient liver transduction by single-stranded AAV vectors: therapeutic expression of factor IX at reduced vector doses.Self-complementary AAV virus (scAAV) safe and long-term gene transfer in the trabecular meshwork of living rats and monkeys.VHL and PTEN loss coordinate to promote mouse liver vascular lesions.Hoechst increases adeno-associated virus-mediated transgene expression in airway epithelia by inducing the cytomegalovirus promoter Intra-articular gene delivery and expression of interleukin-1Ra mediated by self-complementary adeno-associated virus

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Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis

http://www.wikidata.org/entity/Q28213353

description

2001 nî lūn-bûn

@nan

2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի օգոստոսին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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type

label

Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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Self-complementary recombinant ...... independently of DNA synthesis

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D M McCarty

http://www.w3.org/2001/XMLSchema#string

P E Monahan

http://www.w3.org/2001/XMLSchema#string

R J Samulski

http://www.w3.org/2001/XMLSchema#string

P2860

Nonrandom transduction of recombinant adeno-associated virus vectors in mouse hepatocytes in vivo: cell cycling does not influence hepatocyte transduction.

Design and packaging of adeno-associated virus gene targeting vectors

Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo.

DNA synthesis and topoisomerase inhibitors increase transduction by adeno-associated virus vectors

Concatemers of alternating plus and minus strands are intermediates in adenovirus-associated virus DNA synthesis.

Evidence for a single-stranded adenovirus-associated virus genome: formation of a DNA density hybrid on release of viral DNA

Effects of gamma irradiation on the transduction of dividing and nondividing cells in brain and muscle of rats by adeno-associated virus vectors.

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors.

Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield.

Quantitative analysis of the packaging capacity of recombinant adeno-associated virus.

P2888

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1248-54

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scholarly article

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584555

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10.1038/SJ.GT.3301514

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16

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8

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11835352

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11509958

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vector-borne disease