24 results on '"Chung, Suhman"'
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2. Synthesis and high-throughput evaluation of triskelion uracil libraries for inhibition of human dUTPase and UNG2
3. Crystal structures of the reverse transcriptase- associated ribonuclease H domain of xenotropic murine leukemia-virus related virus: 138
4. Mimicking damaged DNA with a small molecule inhibitor of human UNG2
5. Detection of protein–DNA interaction with a DNA probe: distinction between single-strand and double-strand DNA–protein interaction
6. Engineering of a thermostable viral polymerase using metagenome-derived diversity for highly sensitive and specific RT-PCR
7. Stereochemistry in enzyme inhibition: synthesis and evaluation of enantiomerically pure 2-benzyl-3-formylpropanoic acids as inhibitors of carboxypeptidase A
8. N-Substituted Quinolinonyl Diketo Acid Derivatives as HIV Integrase Strand Transfer Inhibitors and Their Activity against RNase H Function of Reverse Transcriptase
9. Synergistic effect between metal coordination and hydrogen bonding in phosphate halide recognition
10. Abasic Phosphorothioate Oligomers Inhibit HIV-1 Reverse Transcription and Block Virus Transmission across Polarized Ectocervical Organ Cultures
11. Basic Quinolinonyl Diketo Acid Derivatives as Inhibitors of HIV Integrase and their Activity against RNase H Function of Reverse Transcriptase
12. Exploiting Drug-Resistant Enzymes as Tools To Identify Thienopyrimidinone Inhibitors of Human Immunodeficiency Virus Reverse Transcriptase-Associated Ribonuclease H
13. Examining the Role of the HIV-1 Reverse Transcriptase p51 Subunit in Positioning and Hydrolysis of RNA/DNA Hybrids
14. Crystal structures of the reverse transcriptase-associated ribonuclease H domain of xenotropic murine leukemia-virus related virus
15. Mutagenesis of Human Immunodeficiency Virus Reverse Transcriptase p51 Subunit Defines Residues Contributing to Vinylogous Urea Inhibition of Ribonuclease H Activity
16. Synthesis, Activity, and Structural Analysis of Novel α-Hydroxytropolone Inhibitors of Human Immunodeficiency Virus Reverse Transcriptase-Associated Ribonuclease H
17. Structure-Activity Analysis of Vinylogous Urea Inhibitors of Human Immunodeficiency Virus-Encoded Ribonuclease H
18. Impact of linker strain and flexibility in the design of a fragment-based inhibitor
19. Synergistic Effect between Metal Coordination and Hydrogen Bonding in Phosphate and Halide Recognition
20. Mechanistic Insight into the Inactivation of Carboxypeptidase A by α-Benzyl-2-oxo-1,3-oxazolidine-4-acetic Acid, a Novel Type of Irreversible Inhibitor for Carboxypeptidase A with No Stereospecificity
21. Basic Quinolinonyl DiketoAcid Derivatives as Inhibitorsof HIV Integrase andtheir Activity against RNase H Function of Reverse Transcriptase.
22. ExploitingDrug-Resistant Enzymes as Tools To Identify Thienopyrimidinone Inhibitorsof Human Immunodeficiency Virus Reverse Transcriptase-Associated RibonucleaseH.
23. Synthesis, Activity, and Structural Analysis of Novel α-Hydroxytropolone Inhibitors of Human Immunodeficiency Virus Reverse Transcriptase-Associated Ribonuclease H.
24. N‑substituted quinolinonyl diketo acid derivatives as HIV integrase strand transfer inhibitors and their activity against RNase H function of reverse transcriptase
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