Effective gene therapy with nonintegrating lentiviral vectors.
about
Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosisReconstitution of an infectious human endogenous retrovirusCorrection of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapyLentiviral vectors in gene therapy: their current status and future potentialGenetic manipulation for inherited neurodegenerative diseases: myth or reality?State-of-the-art human gene therapy: part I. Gene delivery technologiesGene therapy on the moveHematopoietic-stem-cell-based gene therapy for HIV diseaseLentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessCortical overexpression of neuronal calcium sensor-1 induces functional plasticity in spinal cord following unilateral pyramidal tract injury in ratProtective Antiviral Immunity Conferred by a Nonintegrative Lentiviral Vector-Based VaccineGene therapy for hemophiliaBiology and therapy of inherited retinal degenerative disease: insights from mouse modelsIdentification of key residues determining isomerohydrolase activity of human RPE65GABAergic circuits mediate the reinforcement-related signals of striatal cholinergic interneuronsPotential therapeutic approaches for modulating expression and accumulation of defective lamin A in laminopathies and age-related diseasesNon-integrative lentivirus drives high-frequency cre-mediated cassette exchange in human cellsDriving DNA transposition by lentiviral protein transductionRetinal degeneration progression changes lentiviral vector cell targeting in the retinaHuman immunodeficiency virus type 1 Vpu and cellular TASK proteins suppress transcription of unintegrated HIV-1 DNA.Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice.Immunologic and Virologic Mechanisms for Partial Protection from Intravenous Challenge by an Integration-Defective SIV Vaccine.Molecular engineering of viral gene delivery vehiclesGenomic insertion of lentiviral DNA circles directed by the yeast Flp recombinase.Nonintegrating lentiviral vectors can effectively deliver ovalbumin antigen for induction of antitumor immunity.Lentiviral-vector-mediated expression of murine IL-1 receptor antagonist or IL-10 reduces the severity of endotoxin-induced uveitisLong-term episomal transgene expression from mitotically stable integration-deficient lentiviral vectors.Integrase-Deficient Lentiviral Vector as an All-in-One Platform for Highly Efficient CRISPR/Cas9-Mediated Gene EditingLentiviral vectors can be used for full-length dystrophin gene therapySleeping beauty transposition from nonintegrating lentivirus.Hybrid lentivirus-transposon vectors with a random integration profile in human cells.Mechanism of reduction in titers from lentivirus vectors carrying large inserts in the 3'LTR.Puromycin-resistant lentiviral control shRNA vector, pLKO.1 induces unexpected cellular differentiation of P19 embryonic stem cells.Hybrid lentivirus-phiC31-int-NLS vector allows site-specific recombination in murine and human cells but induces DNA damage.Protein transduction from retroviral Gag precursorsGene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects.Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon systemTransgenic expression of human glial cell line-derived neurotrophic factor from integration-deficient lentiviral vectors is neuroprotective in a rodent model of Parkinson's disease.Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapyOptimization of mucosal responses after intramuscular immunization with integrase defective lentiviral vector
P2860
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P2860
Effective gene therapy with nonintegrating lentiviral vectors.
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին 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
Effective gene therapy with nonintegrating lentiviral vectors.
@ast
Effective gene therapy with nonintegrating lentiviral vectors.
@en
Effective gene therapy with nonintegrating lentiviral vectors.
@nl
type
label
Effective gene therapy with nonintegrating lentiviral vectors.
@ast
Effective gene therapy with nonintegrating lentiviral vectors.
@en
Effective gene therapy with nonintegrating lentiviral vectors.
@nl
prefLabel
Effective gene therapy with nonintegrating lentiviral vectors.
@ast
Effective gene therapy with nonintegrating lentiviral vectors.
@en
Effective gene therapy with nonintegrating lentiviral vectors.
@nl
P2093
P2860
P50
P356
P1433
P1476
Effective gene therapy with nonintegrating lentiviral vectors.
@en
P2093
Alexander J Smith
Angus MacNeil
Christine Kinnon
Cynthia Bartholomae
John R Heckenlively
Kamaljit S Balaggan
Manfred Schmidt
Patrick N Anderson
Prateek Buch
Rafael J Yáñez-Muñoz
P2860
P2888
P304
P356
10.1038/NM1365
P407
P577
2006-02-19T00:00:00Z