Human cord blood cells as targets for gene transfer: potential use in genetic therapies of severe combined immunodeficiency disease.
about
Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapyHigh-efficiency gene transfer into normal and adenosine deaminase-deficient T lymphocytes is mediated by transduction on recombinant fibronectin fragments.Bone marrow extracellular matrix molecules improve gene transfer into human hematopoietic cells via retroviral vectors.Long-term culture system for selective growth of human B-cell progenitors.Intracellular immunization of human fetal cord blood stem/progenitor cells with a ribozyme against human immunodeficiency virus type 1.Establishment of an adherent cell feeder layer from human umbilical cord blood for support of long-term hematopoietic progenitor cell growth.Genetic engineering: moral aspects and control of practiceHigh efficiency retroviral mediated gene transduction into single isolated immature and replatable CD34(3+) hematopoietic stem/progenitor cells from human umbilical cord blood.Adeno-associated virus 2-mediated high efficiency gene transfer into immature and mature subsets of hematopoietic progenitor cells in human umbilical cord blood.Improved engraftment of human hematopoietic cells in severe combined immunodeficient (SCID) mice carrying human cytokine transgenes.Differences amid bone marrow and cord blood hematopoietic stem/progenitor cell division kinetics.Heparin inhibits retrovirus binding to fibronectin as well as retrovirus gene transfer on fibronectin fragments.Growth factors and cord blood stem and progenitor cells.Hematopoietic stem cells: "form--method--characteristics".Transplantation of transduced nonhuman primate CD34+ cells using a gibbon ape leukemia virus vector: restricted expression of the gibbon ape leukemia virus receptor to a subset of CD34+ cells.Human umbilical cord blood for hematopoietic progenitor cells transplantation.Amphotropic retrovirus transduction of hematopoietic stem cells.Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells.Efficiency of transgenic T cell generation from gene-marked cultured human CD34+ cord blood cells is determined by their maturity and the cytokines present in the culture medium.Cord blood transplantation and the potential for gene therapy. Gene transduction using a recombinant adeno-associated viral vector.Resistance to cytarabine and gemcitabine and in vitro selection of transduced cells after retroviral expression of cytidine deaminase in human hematopoietic progenitor cells.Early proliferation of umbilical cord blood cells from premature neonates.Retrovirus-mediated transfer of the multidrug resistance gene into human haemopoietic progenitor cells.
P2860
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P2860
Human cord blood cells as targets for gene transfer: potential use in genetic therapies of severe combined immunodeficiency disease.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Human cord blood cells as targ ...... ined immunodeficiency disease.
@ast
Human cord blood cells as targ ...... ined immunodeficiency disease.
@en
type
label
Human cord blood cells as targ ...... ined immunodeficiency disease.
@ast
Human cord blood cells as targ ...... ined immunodeficiency disease.
@en
prefLabel
Human cord blood cells as targ ...... ined immunodeficiency disease.
@ast
Human cord blood cells as targ ...... ined immunodeficiency disease.
@en
P2093
P2860
P356
P1476
Human cord blood cells as targ ...... ined immunodeficiency disease.
@en
P2093
D A Williams
D C Keller
P2860
P304
P356
10.1084/JEM.178.2.529
P407
P577
1993-08-01T00:00:00Z