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Publications by Cuthbert D. Martyr
C-5-Modified Tetrahydropyrano-Tetrahydofuran-Derived Protease Inhibitors (PIs) Exert Potent Inhibition of the Replication of HIV-1 Variants Highly Resistant to Various PIs, Including Darunavir
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Novel Central Nervous System (CNS)-Targeting Protease Inhibitors for Drug-Resistant HIV Infection and HIV-Associated CNS Complications
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology
Related publications
Novel Protease Inhibitors Containing C-5-Modified Bis-THF and Aminobenzothiazole as P2 and P2′ Ligands That Exert Potent Antiviral Activity Against Highly Multidrug-Resistant HIV-1 With High Genetic Barrier Against the Emergence of Drug Resistance.
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology
Investigating PIs
Nature Chemical Biology
Cell Biology
Molecular Biology
Assessment of in Vitro Bioactivities of Pis v 1 (2S Albumin) and Pis v 2.0101 (11S Globulin) Proteins Derived From Pistachio (Pistacia Vera L.)
Journal of Food Measurement and Characterization
Industrial
Risk
Food Science
Manufacturing Engineering
Reliability
Safety
Chemical Engineering
Quality
HIV-1 Protease Inhibitors From Inverse Design in the Substrate Envelope Exhibit Subnanomolar Binding to Drug-Resistant Variants
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
PIS Forn-Coupled Nonlinear Systems
International Journal of Mathematics and Mathematical Sciences
Mathematics
STKE: PIs as Ligands?
Science
Multidisciplinary
Philosophy of Science
History
Intracellular Expression of Human Immunodeficiency Virus Type 1 (HIV-1) Protease Variants Inhibits Replication of Wild-Type and Protease Inhibitor-Resistant HIV-1 Strains in Human T-Cell Lines.
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Amino Acid Insertions Near Gag Cleavage Sites Restore the Otherwise Compromised Replication of Human Immunodeficiency Virus Type 1 Variants Resistant to Protease Inhibitors
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Halogen Bond Interactions of Novel HIV-1 Protease Inhibitors (PI)(GRL-001-15 and GRL-003-15) With the Flap of Protease Are Critical for Their Potent Activity Against Wild-Type and Multi-Pi-Resistant HIV-1 Variants
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology