High-efficiency gene transfer into normal and adenosine deaminase-deficient T lymphocytes is mediated by transduction on recombinant fibronectin fragments.
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Expression of herpes simplex virus ICP47 and human cytomegalovirus US11 prevents recognition of transgene products by CD8(+) cytotoxic T lymphocytes.Fluorophore-conjugated iron oxide nanoparticle labeling and analysis of engrafting human hematopoietic stem cells.Human CD25+CD4+ T suppressor cell clones produce transforming growth factor beta, but not interleukin 10, and are distinct from type 1 T regulatory cells.Identification of amino acid determinants in CYP4B1 for optimal catalytic processing of 4-ipomeanol.Characterization of an Additional Splice Acceptor Site Introduced into CYP4B1 in Hominoidae during Evolution.Telomere loss, senescence, and genetic instability in CD4+ T lymphocytes overexpressing hTERT.Clinical-scale lentiviral vector transduction of PBL for TCR gene therapy and potential for expression in less-differentiated cells.In vivo selection of CD4(+) T cells transduced with a gamma-retroviral vector expressing a single-chain intrabody targeting HIV-1 tat.Evaluation of engraftment and immunological tolerance after reduced intensity conditioning in a rhesus hematopoietic stem cell gene therapy modelTransduction of an IL-2 gene into human melanoma-reactive lymphocytes results in their continued growth in the absence of exogenous IL-2 and maintenance of specific antitumor activityInterleukin-2-independent proliferation of human melanoma-reactive T lymphocytes transduced with an exogenous IL-2 gene is stimulation dependentRetroviral transduction of murine primary T lymphocytes.Lack of specific gamma-retroviral vector long terminal repeat promoter silencing in patients receiving genetically engineered lymphocytes and activation upon lymphocyte restimulation.Efficient Transduction of Human and Rhesus Macaque Primary T Cells by a Modified Human Immunodeficiency Virus Type 1-Based Lentiviral Vector.An efficient large-scale retroviral transduction method involving preloading the vector into a RetroNectin-coated bag with low-temperature shaking.Simultaneous infection with retroviruses pseudotyped with different envelope proteins bypasses viral receptor interference associated with colocalization of gp70 and target cells on fibronectin CH-296.Retrovirus-associated heparan sulfate mediates immobilization and gene transfer on recombinant fibronectin.Extracellular Matrix Proteins Mediate HIV-1 gp120 Interactions with α4β7.Serial Activation of the Inducible Caspase 9 Safety Switch After Human Stem Cell Transplantation.
P2860
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P2860
High-efficiency gene transfer into normal and adenosine deaminase-deficient T lymphocytes is mediated by transduction on recombinant fibronectin fragments.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին 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-efficiency gene transfer ...... mbinant fibronectin fragments.
@ast
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@en
type
label
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@ast
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@en
prefLabel
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@ast
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@en
P2093
P2860
P1433
P1476
High-efficiency gene transfer ...... mbinant fibronectin fragments.
@en
P2093
D A Williams
H Hanenberg
K E Pollok
T W Noblitt
W L Schroeder
P2860
P304
P577
1998-06-01T00:00:00Z