(Q47353883)

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Efficient marking of murine long-term repopulating stem cells targeting unseparated marrow cells at low lentiviral vector particle concentration

scientific article published in June 2004

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scholarly article

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Efficient marking of murine long-term repopulating stem cells targeting unseparated marrow cells at low lentiviral vector particle concentration (English)

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Hans-Peter Kiem

5

object named as

Hans-Peter Kiem

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

author name string

Peter Kurre

1

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Ponni Anandakumar

2

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Michael A Harkey

3

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Bobbie Thomasson

4

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Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

publication date

1 June 2004

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Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Molecular Therapy

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14 January 2018

http://europepmc.org/abstract/MED/15194058

9

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Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

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14 January 2018

http://europepmc.org/abstract/MED/15194058

914-922

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Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors

1 reference

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Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles

1 reference

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MDR1 gene expression in NOD/SCID repopulating cells after retroviral gene transfer under clinically relevant conditions.

1 reference

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7 January 2021

Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection

1 reference

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7 January 2021

Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells

1 reference

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7 January 2021

Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis

1 reference

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7 January 2021

Lentiviral transduction of P140K MGMT into human CD34(+) hematopoietic progenitors at low multiplicity of infection confers significant resistance to BG/BCNU and allows selection in vitro

1 reference

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Avoidance of stimulation improves engraftment of cultured and retrovirally transduced hematopoietic cells in primates

1 reference

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Lentiviral vector-mediated transduction of murine CD34(-) hematopoietic stem cells

1 reference

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Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectors.

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Development of gene therapy for hematopoietic stem cells using lentiviral vectors

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Distinct classes of factor-independent mutants can be isolated after retroviral mutagenesis of a human myeloid stem cell line

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Murine leukemia induced by retroviral gene marking

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Insertion mutagenesis of embryonal carcinoma cells by retroviruses

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Activation of a cellular onc gene by promoter insertion in ALV-induced lymphoid leukosis

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A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency

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Dose finding with retroviral vectors: correlation of retroviral vector copy numbers in single cells with gene transfer efficiency in a cell population

1 reference

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Predictable and efficient retroviral gene transfer into murine bone marrow repopulating cells using a defined vector dose

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Influence of multiplicity of infection and protein stability on retroviral vector-mediated gene expression in hematopoietic cells

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Lentivirus vectors incorporating the immunoglobulin heavy chain enhancer and matrix attachment regions provide position-independent expression in B lymphocytes

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7 January 2021

Lack of expression from a retroviral vector after transduction of murine hematopoietic stem cells is associated with methylation in vivo

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Kinetics of fluorescence expression in nonhuman primates transplanted with GFP retrovirus-modified CD34 cells

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In vivo selection of MGMT(P140K) lentivirus–transduced human NOD/SCID repopulating cells without pretransplant irradiation conditioning

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Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C.

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Cytokines, including stem cell factor alone, enhance lentiviral transduction in nondividing human LTCIC and NOD/SCID repopulating cells.

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Comparison of gene transfer efficiencies and gene expression levels achieved with equine infectious anemia virus- and human immunodeficiency virus type 1-derived lentivirus vectors

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Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice

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Clinical gene therapy in hematology: past and future

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Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

1 reference

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Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo

1 reference

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Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells

1 reference

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7 January 2021

Polyclonal long-term repopulating stem cell clones in a primate model

1 reference

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7 January 2021

Identifiers

10.1016/J.YMTHE.2004.03.008

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

1 reference

Europe PubMed Central

14 January 2018

http://europepmc.org/abstract/MED/15194058

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