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ZAP-70 restoration in mice by in vivo thymic electroporationIn vivo correction of ZAP-70 immunodeficiency by intrathymic gene transferIntrathymic injection of hematopoietic progenitor cells establishes functional T cell development in a mouse model of severe combined immunodeficiency.Intrathymic administration of hematopoietic progenitor cells enhances T cell reconstitution in ZAP-70 severe combined immunodeficiency.In vivo reversion to normal of inherited mutations in humans.Incorporation of DOPE into Lipoplexes formed from a Ferrocenyl Lipid leads to Inverse Hexagonal Nanostructures that allow Redox-Based Control of Transfection in High Serum.Stable gene transfer and expression in human primary T cells by the Sleeping Beauty transposon system.Theory and praxis of cloning via nuclear transfer: ;Never say never' or ;mission impossible'?
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description
article
@en
im August 2002 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в серпні 2002
@uk
ലേഖനം
@ml
name
Gene therapy of severe combined immunodeficiencies
@en
Gene therapy of severe combined immunodeficiencies
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type
label
Gene therapy of severe combined immunodeficiencies
@en
Gene therapy of severe combined immunodeficiencies
@nl
prefLabel
Gene therapy of severe combined immunodeficiencies
@en
Gene therapy of severe combined immunodeficiencies
@nl
P2860
P356
P1476
Gene therapy of severe combined immunodeficiencies
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P2093
Alain Fischer
Salima Hacein-Bey
P2860
P304
P356
10.1038/NRI859
P577
2002-08-01T00:00:00Z