(Q45876424)

17 December 2017

title

In vivo transduction of hematopoietic stem cells after neonatal intravenous injection of an amphotropic retroviral vector in mice (English)

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17 December 2017

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Lingfei Xu

1

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17 December 2017

Tom O'Malley

2

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17 December 2017

Mark S Sands

3

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17 December 2017

Bin Wang

4

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17 December 2017

Todd Meyerrose

5

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17 December 2017

Mark E Haskins

6

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17 December 2017

Katherine Parker Ponder

7

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17 December 2017

publication date

1 July 2004

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17 December 2017

published in

Molecular Therapy

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17 December 2017

volume

10

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17 December 2017

issue

1

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17 December 2017

page(s)

37-44

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17 December 2017

Development of gene therapy for blood disorders by gene transfer into haematopoietic stem cells

cites work

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Changes in integrin expression are associated with altered homing properties of Lin(-/lo)Thy1.1(lo)Sca-1(+)c-kit(+) hematopoietic stem cells following mobilization by cyclophosphamide/granulocyte colony-stimulating factor

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Donor chimerism and stem cell function in a murine congenic transplantation model after low-dose radiation conditioning: effects of a retroviral-mediated gene transfer protocol and implications for gene therapy

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Quantitative analysis reveals expansion of human hematopoietic repopulating cells after short-term ex vivo culture

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Interleukin 3 or interleukin 1 abrogates the reconstituting ability of hematopoietic stem cells

7 January 2021

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CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens

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In vivo retrovirus-mediated gene transfer into multiple hematopoietic lineages in rabbits without preconditioning

7 January 2021

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Rapid myeloerythroid repopulation after intrafemoral transplantation of NOD-SCID mice reveals a new class of human stem cells

7 January 2021

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In vivo retroviral gene transfer by direct intrafemoral injection results in correction of the SCID phenotype in Jak3 knock-out animals

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Biodistribution and toxicity studies of VSVG-pseudotyped lentiviral vector after intravenous administration in mice with the observation of in vivo transduction of bone marrow

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Neonatal or hepatocyte growth factor-potentiated adult gene therapy with a retroviral vector results in therapeutic levels of canine factor IX for hemophilia B.

7 January 2021

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Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient mice

7 January 2021

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Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo

7 January 2021

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Superior transduction of mouse hematopoietic stem cells with 10A1 and VSV-G pseudotyped retrovirus vectors.

7 January 2021

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The level of mRNA encoding the amphotropic retrovirus receptor in mouse and human hematopoietic stem cells is low and correlates with the efficiency of retrovirus transduction

7 January 2021

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

7 January 2021

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LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

7 January 2021

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Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency

7 January 2021

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7 January 2021

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

7 January 2021

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10.1016/J.YMTHE.2004.04.010

7 January 2021

Identifiers

DOI

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17 December 2017

PubMed ID

15233940

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17 December 2017