High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells.
about
Altering the tropism of lentiviral vectors through pseudotyping.A single amino acid substitution in human APOBEC3G antiretroviral enzyme confers resistance to HIV-1 virion infectivity factor-induced depletionP body-associated protein Mov10 inhibits HIV-1 replication at multiple stagesVisualization of targeted transduction by engineered lentiviral vectorsA novel mammalian expression system derived from components coordinating nicotine degradation in arthrobacter nicotinovorans pAO1.Improved tagging strategy for protein identification in mammalian cellsTherapeutic protein transduction of mammalian cells and mice by nucleic acid-free lentiviral nanoparticles.Renal epithelial cells produce and spread HIV-1 via T-cell contactA lentivirus packaging system based on alternative RNA transport mechanisms to express helper and gene transfer vector RNAs and its use to study the requirement of accessory proteins for particle formation and gene delivery.In vivo delivery of recombinant viruses to the fetal murine cochlea: transduction characteristics and long-term effects on auditory function.Identification of a novel proliferation-inducing determinant using lentiviral expression cloning.Rab11-FIP1C and Rab14 direct plasma membrane sorting and particle incorporation of the HIV-1 envelope glycoprotein complex.Small-molecule screening using a human primary cell model of HIV latency identifies compounds that reverse latency without cellular activationIntegration-defective lentiviral vector mediates efficient gene editing through homology-directed repair in human embryonic stem cellsMucosal immunization with integrase-defective lentiviral vectors protects against influenza virus challenge in miceViral RNA is required for the association of APOBEC3G with human immunodeficiency virus type 1 nucleoprotein complexes.Development of multigene and regulated lentivirus vectors.Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cellsA murine leukemia virus (MuLV) long terminal repeat derived from rhesus macaques in the context of a lentivirus vector and MuLV gag sequence results in high-level gene expression in human T lymphocytesNovel Tat-encoding bicistronic human immunodeficiency virus type 1-based gene transfer vectors for high-level transgene expression.Sequences in the cytoplasmic tail of the gibbon ape leukemia virus envelope protein that prevent its incorporation into lentivirus vectorsInhibition of human immunodeficiency virus type 1 (HIV-1) replication by HIV-1-based lentivirus vectors expressing transdominant RevHuman immunodeficiency virus type 1 Vif protein is packaged into the nucleoprotein complex through an interaction with viral genomic RNA.Design of an HIV-1 lentiviral-based gene-trap vector to detect developmentally regulated genes in mammalian cells.Optimization of mucosal responses after intramuscular immunization with integrase defective lentiviral vectorCorrect mRNA processing at a mutant TT splice donor in FANCC ameliorates the clinical phenotype in patients and is enhanced by delivery of suppressor U1 snRNAs.Site-specific gene insertion mediated by a Cre-loxP-carrying lentiviral vector.Fibroblast growth factor signaling potentiates VE-cadherin stability at adherens junctions by regulating SHP2In vivo assessment of gene delivery to keratinocytes by lentiviral vectorsAdvanced modular self-inactivating lentiviral expression vectors for multigene interventions in mammalian cells and in vivo transduction.Cytopathic killing of peripheral blood CD4(+) T lymphocytes by human immunodeficiency virus type 1 appears necrotic rather than apoptotic and does not require env.Potential of mesenchymal stem cells in gene therapy approaches for inherited and acquired diseases.Optimized lentiviral transduction of mouse bone marrow-derived mesenchymal stem cellsHIV-1 tat promotes integrin-mediated HIV transmission to dendritic cells by binding Env spikes and competes neutralization by anti-HIV antibodiesMind-controlled transgene expression by a wireless-powered optogenetic designer cell implant.Pseudotype-dependent lentiviral transduction of astrocytes or neurons in the rat substantia nigra.Foamy virus for efficient gene transfer in regeneration studiesPoly(ADP-ribose) polymerase-1 is required for efficient HIV-1 integrationOverexpression of cdk4 and cyclinD1 triggers greater expansion of neural stem cells in the adult mouse brainHighly efficient retrograde gene transfer into motor neurons by a lentiviral vector pseudotyped with fusion glycoprotein.
P2860
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P2860
High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells.
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
High-titer human immunodeficie ...... livery into nondividing cells.
@ast
High-titer human immunodeficie ...... livery into nondividing cells.
@en
type
label
High-titer human immunodeficie ...... livery into nondividing cells.
@ast
High-titer human immunodeficie ...... livery into nondividing cells.
@en
prefLabel
High-titer human immunodeficie ...... livery into nondividing cells.
@ast
High-titer human immunodeficie ...... livery into nondividing cells.
@en
P2093
P2860
P1433
P1476
High-titer human immunodeficie ...... elivery into nondividing cells
@en
P2093
P2860
P304
P577
1998-11-01T00:00:00Z