Surface engineering of lentiviral vectors for gene transfer into gene therapy target cells-Reference-Cited by-同舟云学术

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Surface engineering of lentiviral vectors for gene transfer into gene therapy target cells

Published:2015-10 Issue: Volume:24 Page:79-85
ISSN:1471-4892
Container-title:Current Opinion in Pharmacology
language:en
Short-container-title:Current Opinion in Pharmacology

Author:

Lévy Camille,Verhoeyen Els,Cosset François-Loïc

Funder

‘Agence Nationale pour la Recherche contre le SIDA et les Hépatites Virales’ (ANRS)

‘Agence Nationale de la Recherche’ (ANR)

European Research Council

European Community

LabEx Ecofect

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology

Reference55 articles.

1. Gene delivery by lentivirus vectors;Cockrell;Mol Biotechnol,2007

2. Medicine. A comeback for gene therapy;Naldini;Science,2009

3. Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector;Naldini;Proc Natl Acad Sci U S A,1996

4. Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor;Amirache;Blood,2014

5. LDL receptor and its family members serve as the cellular receptors for vesicular stomatitis virus;Finkelshtein;Proc Natl Acad Sci U S A,2013

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1. Envelope protein-specific B cell receptors direct lentiviral vector tropism in vivo;Molecular Therapy;2024-05

2. Current Status and Prospects of Viral Vector-Based Gene Therapy to Treat Kidney Diseases;Human Gene Therapy;2024-03-01

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