(Q44491759)

3 December 2017

title

Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences (English)

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3 December 2017

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3 December 2017

L Naldini

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3 December 2017

L E Ailles

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3 December 2017

S Bakovic

series ordinal

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3 December 2017

M Geuna

series ordinal

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3 December 2017

language of work or name

English

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publication date

1 June 2000

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3 December 2017

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3 December 2017

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3 December 2017

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3 December 2017

page(s)

217-222

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

3 December 2017

cites work

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7 January 2021

Lentiviruses as gene transfer agents for delivery to non-dividing cells

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7 January 2021

A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells

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7 January 2021

HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator

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7 January 2021

Viral protein R regulates nuclear import of the HIV-1 pre-integration complex

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7 January 2021

HIV-1 Reverse Transcription A Termination Step at the Center of the Genome

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7 January 2021

Identification of a sequence element immediately upstream of the polypurine tract that is essential for replication of simian immunodeficiency virus

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7 January 2021

Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo

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7 January 2021

A third-generation lentivirus vector with a conditional packaging system

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7 January 2021

Human immunodeficiency virus infection of cells arrested in the cell cycle

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7 January 2021

The putative alpha helix 2 of human immunodeficiency virus type 1 Vpr contains a determinant which is responsible for the nuclear translocation of proviral DNA in growth-arrested cells

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7 January 2021

Human immunodeficiency virus type 1 T-lymphotropic strains enter macrophages via a CD4- and CXCR4-mediated pathway: replication is restricted at a postentry level

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7 January 2021

Integration complexes derived from HIV vectors for rapid assays in vitro

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Retrovirus-mediated gene transfer into human CD34+38low primitive cells capable of reconstituting long-term cultures in vitro and nonobese diabetic-severe combined immunodeficiency mice in vivo

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7 January 2021

Gene therapy for the hemophilias

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7 January 2021

Moloney murine leukemia virus-derived retroviral vectors decay intracellularly with a half-life in the range of 5.5 to 7.5 hours

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7 January 2021

Antiviral activity of the proteasome on incoming human immunodeficiency virus type 1.

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7 January 2021

A single-stranded gap in human immunodeficiency virus unintegrated linear DNA defined by a central copy of the polypurine tract.

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7 January 2021

Establishment of a functional human immunodeficiency virus type 1 (HIV-1) reverse transcription complex involves the cytoskeleton

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7 January 2021

Identifiers

DOI

10.1038/76095

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3 December 2017

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