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Viral vectors for gene therapy of hematopoietic cells
scientific article published on March 1997
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
review article
1 reference
stated in
Europe PubMed Central
title
Viral vectors for gene therapy of hematopoietic cells
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
main subject
gene therapy
0 references
author name string
Medin JA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
Karlsson S
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
publication date
1 March 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
published in
Immunotechnology : an international journal of immunological engineering
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
volume
3
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
issue
1
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stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
page(s)
3-19
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
cites work
Overexpression of HOXB4 in hematopoietic cells causes the selective expansion of more primitive populations in vitro and in vivo
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An early haematopoietic defect in mice lacking the transcription factor GATA-2
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A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis
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T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 years.
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Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients
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Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus
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Biochemistry of multidrug resistance mediated by the multidrug transporter
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Adeno-associated virus vectors
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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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Strategies for efficient gene transfer into hematopoietic cells. The use of adeno-associated virus vectors in gene therapy
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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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Expression of the human multidrug resistance and glucocerebrosidase cDNAs from adeno-associated vectors: efficient promoter activity of AAV sequences and in vivo delivery via liposomes
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Identifiers
DOI
10.1016/S1380-2933(96)00059-0
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
PubMed ID
9154464
1 reference
stated in
Europe PubMed Central
PubMed ID
9154464
retrieved
1 October 2017
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