2023 - Research.com Microbiology in Canada Leader Award
2022 - Research.com Microbiology in Canada Leader Award
2011 - Fellow of the American Association for the Advancement of Science (AAAS)
2000 - Fellow of the Royal Society of Canada Academy of Science
Mark A. Wainberg mainly investigates Virology, Reverse transcriptase, Virus, Molecular biology and Drug resistance. His research in Virology is mostly concerned with Viral replication. His work carried out in the field of Reverse transcriptase brings together such families of science as Nucleotidyltransferase, Mutant, Zidovudine and Primer.
His study focuses on the intersection of Virus and fields such as Amino acid with connections in the field of Capsid. The various areas that Mark A. Wainberg examines in his Molecular biology study include Cell culture, Transfection, RNA, DNA synthesis and Transcription. His Drug resistance research includes themes of Acquired immunodeficiency syndrome, Lentivirus, Viral load, Immunology and Genotype.
Virology, Reverse transcriptase, Virus, Molecular biology and Drug resistance are his primary areas of study. His research on Virology focuses in particular on Viral replication. His study explores the link between Reverse transcriptase and topics such as Nevirapine that cross with problems in Efavirenz.
His Virus research includes elements of Cell culture and In vitro. The concepts of his Molecular biology study are interwoven with issues in RNA, Mutant, DNA, Enzyme and Primer binding site. His study in Drug resistance is interdisciplinary in nature, drawing from both Transmission, Viral load and Pharmacology, Drug.
His main research concerns Virology, Dolutegravir, Integrase, Drug resistance and Raltegravir. His Virology research integrates issues from Mutation, Genetics and Reverse transcriptase. His research in Reverse transcriptase intersects with topics in Nevirapine, Molecular biology, Lamivudine and Rilpivirine.
His Dolutegravir study deals with Elvitegravir intersecting with Cabotegravir. The Integrase study combines topics in areas such as Integrase inhibitor and Resistance mutation. Within one scientific family, he focuses on topics pertaining to Viral load under Raltegravir, and may sometimes address concerns connected to Acquired immunodeficiency syndrome.
Mark A. Wainberg focuses on Virology, Dolutegravir, Integrase, Drug resistance and Raltegravir. His Virology research is multidisciplinary, relying on both Mutation, Genetics and Resistance mutation. His Dolutegravir research incorporates themes from Integrase inhibitor, HIV drug resistance, Elvitegravir and Pharmacology.
His Integrase study incorporates themes from Reverse transcriptase and Binding site. Mark A. Wainberg has researched Drug resistance in several fields, including Regimen and Drug. He combines subjects such as Molecular biology, Antibody and In vivo with his study of Viral replication.
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A randomized, double-blind trial comparing combinations of nevirapine, didanosine, and zidovudine for HIV-infected patients: the INCAS Trial. Italy, The Netherlands, Canada and Australia Study.
Julio S. G. Montaner;Peter Reiss;David Cooper;Stefano Vella.
JAMA (1998)
High Rates of Forward Transmission Events after Acute/Early HIV-1 Infection
Bluma G Brenner;Michel Roger;Jean-Pierre Routy;Daniela Moisi.
The Journal of Infectious Diseases (2007)
Public health implications of antiretroviral therapy and HIV drug resistance.
Mark A. Wainberg;Gerald Friedland.
JAMA (1998)
High-level resistance to (-) enantiomeric 2'-deoxy-3'-thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase.
C. A. B. Boucher;N. Cammack;P. Schipper;R. Schuurman.
Antimicrobial Agents and Chemotherapy (1993)
Enhanced fidelity of 3TC-selected mutant HIV-1 reverse transcriptase.
Mark A. Wainberg;William C. Drosopoulos;Horacio Salomon;Mayla Hsu.
Science (1996)
Efficacy, safety, and effect on sexual behaviour of on-demand pre-exposure prophylaxis for HIV in men who have sex with men: an observational cohort study
Jean-Michel Molina;Jean-Michel Molina;Isabelle Charreau;Bruno Spire;Laurent Cotte.
The Lancet HIV (2017)
A V106M mutation in HIV-1 clade C viruses exposed to efavirenz confers cross-resistance to non-nucleoside reverse transcriptase inhibitors.
Bluma Brenner;Dan Turner;Maureen Oliveira;Daniela Moisi.
AIDS (2003)
In vitro selection and characterization of HIV-1 with reduced susceptibility to PMPA.
Mark A Wainberg;Michael D Miller;Yudong Quan;Horacio Salomon.
Antiviral Therapy (1999)
The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2',3'-dideoxyinosine and 2',3'-dideoxycytidine confers high-level resistance to the (-) enantiomer of 2',3'-dideoxy-3'-thiacytidine.
Qing Gao;Zhengxian Gu;M. A. Parniak;J. Cameron.
Antimicrobial Agents and Chemotherapy (1993)
Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2'-deoxy-3'-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog.
H. Soudeyns;Xiao-Jian Yao;Qing Gao;B. Belleau.
Antimicrobial Agents and Chemotherapy (1991)
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