Systematic Determination of the Packaging Limit of Lentiviral Vectors-Reference-Cited by-同舟云学术

Systematic Determination of the Packaging Limit of Lentiviral Vectors

Published:2001-10-10 Issue:15 Volume:12 Page:1893-1905
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Kumar Mukesh¹,Keller Brian²,Makalou Ndeye³,Sutton Richard E.²

Affiliation:

1. LCMB, NICHD, National Institutes of Health, Bethesda, MD 20852

2. Departments of Molecular Virology & Microbiology, Medicine, and the Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030

3. M.D. Anderson Cancer Research Center, Houston, TX 77030

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/104303401753153947

Reference16 articles.

1. High-efficiency gene transfer into CD34+ cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G

2. Mutations of RNA and protein sequences involved in human immunodeficiency virus type 1 packaging result in production of noninfectious virus

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

4. A mutant of human immunodeficiency virus with reduced RNA packaging and abnormal particle morphology

5. HIV-1 infection of nondividing cells through the recognition of integrase by the importin/karyopherin pathway

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