Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle. - Wikidata - wikimedia - TriplyDB

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

http://www.wikidata.org/entity/Q36845715

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Adeno-associated virus-mediated microRNA delivery and therapeutics Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates Terminal differentiation of cardiac and skeletal myocytes induces permissivity to AAV transduction by relieving inhibition imposed by DNA damage response proteins Adeno-associated viral vector-mediated transgene expression is independent of DNA methylation in primate liver and skeletal muscle Massively parallel cis-regulatory analysis in the mammalian central nervous system Integration preferences of wildtype AAV-2 for consensus rep-binding sites at numerous loci in the human genome.Role of cyclic AMP-dependent kinase response element-binding protein in recombinant adeno-associated virus-mediated transduction of heart muscle cells.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.IL-2 protects lupus-prone mice from multiple end-organ damage by limiting CD4-CD8- IL-17-producing T cells PCR-based detection of gene transfer vectors: application to gene doping surveillance.Linear amplification mediated PCR--localization of genetic elements and characterization of unknown flanking DNA.MAR-mediated integration of plasmid vectors for in vivo gene transfer and regulation Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.CpG distribution and methylation pattern in porcine parvovirus.Stable human FIX expression after 0.9G intrauterine gene transfer of self-complementary adeno-associated viral vector 5 and 8 in macaques A 10 patient case report on the impact of plasmapheresis upon neutralizing factors against adeno-associated virus (AAV) types 1, 2, 6, and 8.Cystic Fibrosis Gene Therapy in the UK and Elsewhere.Short-lived recombinant adeno-associated virus transgene expression in dystrophic muscle is associated with oxidative damage to transgene mRNA.A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration Integration frequency and intermolecular recombination of rAAV vectors in non-human primate skeletal muscle and liver.Human galectin 3 binding protein interacts with recombinant adeno-associated virus type 6 Bulk regional viral injection in neonatal mice enables structural and functional interrogation of defined neuronal populations throughout targeted brain areas.Infectious molecular clones of adeno-associated virus isolated directly from human tissues.Adeno-associated virus-2 and its primary cellular receptor--Cryo-EM structure of a heparin complex.Suppression of experimental uveitis by a recombinant adeno-associated virus vector encoding interleukin-1 receptor antagonist Vector-mediated gene transfer engenders long-lived neutralizing activity and protection against SIV infection in monkeys Therapeutic expression of hairpins targeting apolipoprotein B100 induces phenotypic and transcriptome changes in murine liver.Radioiodinated Capsids Facilitate In Vivo Non-Invasive Tracking of Adeno-Associated Gene Transfer Vectors.AAV-directed muscular dystrophy gene therapy.Recombinant Adeno-Associated Virus Vector Genomes Take the Form of Long-Lived, Transcriptionally Competent Episomes in Human Muscle.Gene-based therapies of neuromuscular disorders: an update and the pivotal role of patient organizations in their discovery and implementation.Safety profile of recombinant adeno-associated viral vectors: focus on alipogene tiparvovec (Glybera®).Adeno-associated virus delivery of broadly neutralizing antibodies Molecular basis of intervertebral disc degeneration and herniations: what are the important translational questions?Delivery of Adeno-Associated Virus Gene Therapy by Intravascular Limb Infusion Methods.Gene Targeting in Neuroendocrinology.New and improved AAVenues: current status of hemophilia B gene therapy.Systemic gene delivery transduces the enteric nervous system of guinea pigs and cynomolgus macaques.Engineering broadly neutralizing antibodies for HIV prevention and therapy.Promoter-Targeted Histone Acetylation of Chromatinized Parvoviral Genome Is Essential for the Progress of Infection.

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P2860

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

http://www.wikidata.org/entity/Q36845715

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

@en

type

label

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

@en

prefLabel

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

@en

P1433

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P1433

Journal of Virology

P1476

Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle.

@en

P2093

Ali Nowrouzi

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

Alice Toromanoff

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

Caroline Le Guiner

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

Fabienne Rolling

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

Manfred Schmidt

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

Philippe Moullier

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

Pierre Chenuaud

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

Richard O Snyder

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

Yan Chérel

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

P2860

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

Exploring the sequence space for tetracycline-dependent transcriptional activators: novel mutations yield expanded range and sensitivity

A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage

Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate

Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patients

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

Histone deacetylase inhibitors.

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

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

Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver.

P304

7875-7885

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P31

scholarly article

P356

10.1128/JVI.00649-08

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P407

P433

16

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

P478

82

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

P50

Christof von Kalle

Fabienne Rolling

Magalie Penaud-Budloo

Magalie Penaud-Budloo

P577

2008-06-04T00:00:00Z

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

P698

18524821

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

P921

vector-borne disease

P932

2519600

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