Diminished Replicative Fitness of Primary Human Immunodeficiency Virus Type 1 Isolates Harboring the K65R Mutation
Author:
Affiliation:
1. Department of Molecular Genetics, Section Virology, Lerner Research Institute, Cleveland Clinic Foundation
2. Gilead Sciences, Inc., Foster City, California
3. Center for AIDS Research, Case Western Reserve University, Cleveland, Ohio
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.43.3.1395-1400.2005
Reference31 articles.
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3. Deeks, S. G. 2001. Durable HIV treatment benefit despite low-level viremia: reassessing definitions of success or failure. JAMA286:224-226.
4. Deval, J., K. L. White, M. D. Miller, N. T. Parkin, J. Courcambeck, P. Halfon, B. Selmi, J. Boretto, and B. Canard. 2004. Mechanistic basis for reduced viral and enzymatic fitness of HIV-1 reverse transcriptase containing both K65R and M184V mutations. J. Biol. Chem.279:509-516.
5. Gallant, J. E., P. Z. Gerondelis, M. A. Wainberg, N. S. Shulman, R. H. Haubrich, M. St. Clair, E. R. Lanier, N. S. Hellmann, and D. D. Richman. 2003. Nucleoside and nucleotide analogue reverse transcriptase inhibitors: a clinical review of antiretroviral resistance. Antivir. Ther.8:489-506.
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