Viral vectors for gene therapy of hematopoietic cells (Q41473032)

1 October 2017

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title

Viral vectors for gene therapy of hematopoietic cells (English)

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1 October 2017

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Medin JA

1

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1 October 2017

Karlsson S

series ordinal

2

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1 October 2017

publication date

1 March 1997

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Immunotechnology : an international journal of immunological engineering

1 October 2017

published in

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1 October 2017

volume

3

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1 October 2017

issue

1

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1 October 2017

page(s)

3-19

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Overexpression of HOXB4 in hematopoietic cells causes the selective expansion of more primitive populations in vitro and in vivo

1 October 2017

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Cord blood transplantation and the potential for gene therapy. Gene transduction using a recombinant adeno-associated viral vector.

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A Human Parvovirus, Adeno-Associated Virus, as a Eucaryotic Vector: Transient Expression and Encapsidation of the Procaryotic Gene for Chloramphenicol Acetyltransferase

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Adeno-associated virus 2-mediated high efficiency gene transfer into immature and mature subsets of hematopoietic progenitor cells in human umbilical cord blood

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Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector

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7 January 2021

Productive persistent infection of hematopoietic cells by human foamy virus

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7 January 2021

Analysis of the determinants of neurotropism and neurotoxicity of HFV in transgenic mice

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7 January 2021

Targeted and highly efficient gene transfer into CD4+ cells by a recombinant human immunodeficiency virus retroviral vector

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7 January 2021

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector

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7 January 2021

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7 January 2021

A latent, nonpathogenic HSV-1-derived vector stably expresses beta-galactosidase in mouse neurons

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7 January 2021

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7 January 2021

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7 January 2021

Gene therapy using adenovirus vectors.

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7 January 2021

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7 January 2021

Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses

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7 January 2021

Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis.

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7 January 2021

Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung.

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7 January 2021

Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis

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7 January 2021

Non-viral gene therapy

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7 January 2021

10.1016/S1380-2933(96)00059-0

Identifiers

DOI

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1 October 2017

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