Research Topics
| Ron KaganSummaryAffiliation: Quest Diagnostics Country: USA Publications
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Detail Information
Publications
Additional HIV-1 mutation patterns associated with reduced phenotypic susceptibility to etravirine in clinical samplesRon M Kagan
Department of Infectious Diseases, Quest Diagnostics Nichols Institute, San Juan Capistrano, California 92675, USA
AIDS 23:1602-5. 2009..Although the effect of K103S is unclear, additional position 138 substitutions seem important for etravirine susceptibility...
HIV type 1 genotypic resistance in a clinical database correlates with antiretroviral utilizationRon Kagan
Department of Infectious Diseases, Quest Diagnostics Nichols Institute, San Juan Capistrano, California 92690, USA
AIDS Res Hum Retroviruses 20:1-9. 2004..Continued monitoring of ARV resistance prevalence, patterns, and utilization trends in clinical databases provides insight into the evolving relationship between clinical practice and ARV resistance...
Structural analysis of an HIV-1 protease I47A mutant resistant to the protease inhibitor lopinavirRon M Kagan
Department of Infectious Diseases, Quest Diagnostics Inc, San Juan Capistrano, CA 92675, USA
Protein Sci 14:1870-8. 2005..The emergence of mutations at PR residue 47 strongly correlates with increasing prescriptions of LPV (Spearman correlation r(s) = 0.96, P < .0001)...
Ninety-nine is not enough: molecular characterization of inhibitor-resistant human immunodeficiency virus type 1 protease mutants with insertions in the flap regionMilan Kozísek
Gilead Sciences and IOCB Research Center, Institute of Organic Chemistry and Biochemistry of the Academy of Sciences of the Czech Republic, v v i, Flemingovo 2, 166 10 Praha 6, Czech Republic
J Virol 82:5869-78. 2008..Amino acid insertions in the vicinity of the binding cleft therefore represent a novel mechanism of HIV resistance development...
Identification of a novel resistance (E40F) and compensatory (K43E) substitution in HIV-1 reverse transcriptaseMarleen C D G Huigen
Department of Medical Microbiology, University Medical Center Utrecht, The Netherlands
Retrovirology 5:20. 2008..To unravel the role of two of these newly identified changes, E40F and K43E, we investigated their effect on viral drug susceptibility and replicative capacity...
The probable source of both the primary multidrug-resistant (MDR) HIV-1 strain found in a patient with rapid progression to AIDS and a second recombinant MDR strain found in a chronically HIV-1-infected patientGary Blick
Circle Medical LLC, Norwalk, CT 06851, USA
J Infect Dis 195:1250-9. 2007..The probable source of this HIV-1 (hereafter referred to as "CT01") and the development of a recombinant MDR HIV-1 in the source's partner (hereafter referred to as "CT02") are described...
New two-amino acid insertion near codon 70 of the HIV type 1 protease geneMark A Winters
Division of Infectious Diseases, Stanford University Medical Center, Stanford, California 94305, USA
AIDS Res Hum Retroviruses 21:311-3. 2005..Susceptibility of this strain to protease inhibitors was similar to that of non-insert-containing strains with comparable resistance mutations and one or more other major PI mutations...
Rare one and two amino acid inserts adjacent to codon 103 of the HIV-1 reverse transcriptase (RT) affect susceptibility to non-nucleoside RT inhibitorsMark A Winters
Center for AIDS Research, Stanford University, Stanford, CA, USA
Antivir Ther 10:363-6. 2005..These results suggest that inserts in the NNRTI-binding pocket contribute to NNRTI resistance, but are tolerated only under specific genetic conditions...
Increasing prevalence of HIV-1 reverse transcriptase mutation K65R correlates with tenofovir utilizationRon M Kagan
Antivir Ther 9:827-8. 2004
Structure-based phenotyping predicts HIV-1 protease inhibitor resistanceMark D Shenderovich
Cengent Therapeutics Inc, 10929 Technology Place, San Diego, CA 92127, USA
Protein Sci 12:1706-18. 2003..666) with PhenoSense and Antivirogram phenotypes, respectively. The structural phenotyping predicted drug resistance of clinical HIV-1 PR variants with an accuracy approaching that of frequently used cell-based phenotypic assays...
