(Q43730527)

26 November 2017

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Hepatic gene therapy using lentiviral vectors: has safety been established? (English)

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26 November 2017

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David Dismuke

1

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26 November 2017

R Jude Samulski

series ordinal

2

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26 November 2017

language of work or name

English

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publication date

1 July 2013

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26 November 2017

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26 November 2017

volume

58

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26 November 2017

issue

1

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26 November 2017

page(s)

13-14

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Potential of AAV vectors in the treatment of metabolic disease

26 November 2017

cites work

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Adenovirus-associated virus vector-mediated gene transfer in hemophilia B

21 January 2018

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Helper-dependent adenoviral vectors for liver-directed gene therapy.

21 January 2018

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Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

21 January 2018

1 reference

Efficacy of gene therapy for X-linked severe combined immunodeficiency

21 January 2018

1 reference

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

21 January 2018

1 reference

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

21 January 2018

1 reference

T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 years.

21 January 2018

1 reference

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

21 January 2018

1 reference

Retroviral DNA integration: ASLV, HIV, and MLV show distinct target site preferences

21 January 2018

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Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

21 January 2018

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

21 January 2018

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Unique risk factors for insertional mutagenesis in a mouse model of XSCID gene therapy

21 January 2018

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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

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Oncogenesis following delivery of a nonprimate lentiviral gene therapy vector to fetal and neonatal mice

21 January 2018

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Transcription start regions in the human genome are favored targets for MLV integration

21 January 2018

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Distribution of lentiviral vector integration sites in mice following therapeutic gene transfer to treat β-thalassemia

21 January 2018

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Biosafety features of lentiviral vectors

21 January 2018

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Hepatic lentiviral gene transfer is associated with clonal selection, but not with tumor formation in serially transplanted rodents.

21 January 2018

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Unaltered repopulation properties of mouse hematopoietic stem cells transduced with lentiviral vectors.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/HEP.26460

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release_k6lf3d74nffbvkjv7jnqycnsw4

26 November 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/k6lf3d74nffbvkjv7jnqycnsw4

mapped directly with Wikidata item

24 November 2022

based on heuristic

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