Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver. - Wikidata - awgldk - TriplyDB

Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

http://www.wikidata.org/entity/Q33737640

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Gene therapy for haemophilia Gene therapy for haemophilia DNA ligase III and DNA ligase IV carry out genetically distinct forms of end joining in human somatic cells Adeno-associated virus vector integration A transposon and transposase system for human application Adeno-associated Virus as a Mammalian DNA Vector Perinatal systemic gene delivery using adeno-associated viral vectors Selection of target sites for mobile DNA integration in the human genome High-resolution genome-wide mapping of transposon integration in mammals.Gene expression omnibus: microarray data storage, submission, retrieval, and analysis.Designer gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transfer Characterization of genome integrity for oversized recombinant AAV vector.Progress towards gene therapy for haemophilia B.A NEW RECOMBINANT ADENO-ASSOCIATED VIRUS (AAV)-BASED RANDOM PEPTIDE DISPLAY LIBRARY SYSTEM: INFECTION-DEFECTIVE AAV1.9-3 AS A NOVEL DETARGETED PLATFORM FOR VECTOR EVOLUTION.Large-scale analysis of adeno-associated virus vector integration sites in normal human cells.AAV-mediated liver-directed gene therapy.Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors Scavenger receptors and their potential as therapeutic targets in the treatment of cardiovascular disease Liver transduction with recombinant adeno-associated virus is primarily restricted by capsid serotype not vector genotype.rAAV-mediated tumorigenesis: still unresolved after an AAV assault Intranasal vaccination with recombinant adeno-associated virus type 5 against human papillomavirus type 16 L1 Assessing the potential for AAV vector genotoxicity in a murine model.Long-term safety and efficacy following systemic administration of a self-complementary AAV vector encoding human FIX pseudotyped with serotype 5 and 8 capsid proteins.Hybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells.Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo.The mechanism of gene targeting in human somatic cells Long-term sex-biased correction of circulating propionic acidemia disease markers by adeno-associated virus vectors.Existence of transient functional double-stranded DNA intermediates during recombinant AAV transduction AAV-mediated gene targeting is significantly enhanced by transient inhibition of nonhomologous end joining or the proteasome in vivo DNA palindromes with a modest arm length of greater, similar 20 base pairs are a significant target for recombinant adeno-associated virus vector integration in the liver, muscles, and heart in mice.The role of DNA-PKcs and artemis in opening viral DNA hairpin termini in various tissues in mice.Targeting site-specific chromosome integration.The threefold protrusions of adeno-associated virus type 8 are involved in cell surface targeting as well as postattachment processing.Predicting preferential DNA vector insertion sites: implications for functional genomics and gene therapy.AAV vectors containing rDNA homology display increased chromosomal integration and transgene persistence.Ribosomal DNA integrating rAAV-rDNA vectors allow for stable transgene expression.AAV vectors for the nucleolus Precise hit: adeno-associated virus in gene targeting.Gene therapy progress and prospects--vectorology: design and production of expression cassettes in AAV vectors.Patterns of scAAV vector insertion associated with oncogenic events in a mouse model for genotoxicity

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Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

http://www.wikidata.org/entity/Q33737640

description

2005 nî lūn-bûn

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2005 թուականի Մարտին հրատարակուած գիտական յօդուած

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2005 թվականի մարտին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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JVI.79.6.3606-3614.2005

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Journal of Virology

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Large-scale molecular characte ...... or integration in mouse liver.

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P2093

David Munroe

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Eugenio Montini

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Hiroyuki Nakai

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Mark A Kay

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Markus Grompe

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Sally Fuess

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Shawn M Burgess

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Theresa A Storm

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Xiaolin Wu

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P2860

Circular intermediates of recombinant adeno-associated virus have defined structural characteristics responsible for long-term episomal persistence in muscle tissue.

Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy

A gene atlas of the mouse and human protein-encoding transcriptomes

Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors

Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

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

Transcription start regions in the human genome are favored targets for MLV integration

HIV-1 integration in the human genome favors active genes and local hotspots

Genetic fate of recombinant adeno-associated virus vector genomes in muscle

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3606-3614

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scholarly article

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10.1128/JVI.79.6.3606-3614.2005

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6

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79

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2005-03-01T00:00:00Z

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15731255

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vector-borne disease

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1075691

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