Lentiviral vector gene therapy: effective and safe? (Q24630888)

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English	Lentiviral vector gene therapy: effective and safe?	scientific article

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instance of

scholarly article

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editorial

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title

Lentiviral vector gene therapy: effective and safe? (English)

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Derek A Persons

1

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language of work or name

English

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publication date

May 2010

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published in

Molecular Therapy

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volume

18

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page(s)

861-2

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issue

5

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cites work

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

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PubMed Central

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7 April 2017

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

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PubMed Central

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7 April 2017

Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration

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PubMed Central

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7 April 2017

Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

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PubMed Central

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27 September 2017

Ten years of gene therapy for primary immune deficiencies.

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27 September 2017

Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy

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PubMed Central

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27 September 2017

The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy

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PubMed Central

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27 September 2017

Transcription factor binding sites are genetic determinants of retroviral integration in the human genome

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PubMed Central

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27 September 2017

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

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PubMed Central

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27 September 2017

Physiological promoters reduce the genotoxic risk of integrating gene vectors

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PubMed Central

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27 September 2017

Identification and characterization of cell type-specific and ubiquitous chromatin regulatory structures in the human genome

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27 September 2017

Gammaretrovirus-mediated correction of SCID-X1 is associated with skewed vector integration site distribution in vivo

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27 September 2017

Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy

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PubMed Central

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27 September 2017

Overcoming promoter competition in packaging cells improves production of self-inactivating retroviral vectors

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27 September 2017

Assessing the risk of T-cell malignancies in mouse models of SCID-X1.

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PubMed Central

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27 September 2017

Gene therapy. Beta-thalassemia treatment succeeds, with a caveat

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PubMed Central

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30 May 2018

Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning

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PubMed Central

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retrieved

28 November 2018

Identifiers

DOI

10.1038/MT.2010.70

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3903769

OpenCitations bibliographic resource ID

3903769

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3903769

ResearchGate publication ID

43535448

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Lentiviral vector gene therapy: effective and safe? (Q24630888)

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Lentiviral vector gene therapy: effective and safe? (Q24630888)

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