Zinc Finger Protein Designed to Target 2-Long Terminal Repeat Junctions Interferes with Human Immunodeficiency Virus Integration-Reference-Cited by-同舟云学术

Zinc Finger Protein Designed to Target 2-Long Terminal Repeat Junctions Interferes with Human Immunodeficiency Virus Integration

Published:2012-09 Issue:9 Volume:23 Page:932-942
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Sakkhachornphop Supachai¹²,Barbas Carlos F.³,Keawvichit Rassamee²,Wongworapat Kanlaya²,Tayapiwatana Chatchai¹⁴

Affiliation:

1. Division of Clinical Immunology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

2. Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

3. Skaggs Institute for Chemical Biology, and Departments of Molecular Biology and Chemistry, Scripps Research Institute, La Jolla, CA 92037.

4. Biomedical Technology Research Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2011.124

Reference63 articles.

1. HIV-1 integrates into resting CD4+ T cells even at low inoculums as demonstrated with an improved assay for HIV-1 integration

2. Functional identification of nucleotides conferring substrate specificity to retroviral integrase reactions

3. Kinetic Analysis of HIV-1 Early Replicative Steps in a Coculture System

4. A small circular TAR RNA decoy specifically inhibits Tat-activated HIV- 1 transcription

5. Dynamic, Thermodynamic, and Kinetic Basis for Recognition and Transformation of DNA by Human Immunodeficiency Virus Type 1 Integrase

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