(Q34613525)

3 August 2017

title

Medicine. A comeback for gene therapy (English)

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3 August 2017

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1

Luigi Naldini

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language of work or name

English

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publication date

1 November 2009

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3 August 2017

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3 August 2017

volume

326

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3 August 2017

issue

5954

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3 August 2017

page(s)

805-806

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Gene therapy for immunodeficiency due to adenosine deaminase deficiency.

3 August 2017

cites work

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https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Gene therapy of inherited diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Preliminary results of gene therapy for retinal degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Lentivector-mediated clonal tracking reveals intrinsic heterogeneity in the human hematopoietic stem cell compartment and culture-induced stem cell impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Efficient transduction of pigtailed macaque hematopoietic repopulating cells with HIV-based lentiviral vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Sustained high-level polyclonal hematopoietic marking and transgene expression 4 years after autologous transplantation of rhesus macaques with SIV lentiviral vector-transduced CD34+ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Genome-wide analysis of retroviral DNA integration

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Hot spots of retroviral integration in human CD34+ hematopoietic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1181937

21 January 2018

Identifiers

DOI

10.1126/SCIENCE.1181937

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3 August 2017

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