35 results on '"Hamasaki, Takayuki"'
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2. Synthesis and evaluation of novel 3-(3,5-dimethylbenzyl)uracil analogs as potential anti-HIV-1 agents
3. Synthesis and anti-HIV-1 evaluation of phosphonates which mimic the 5′-monophosphate of 4′-branched 2′,3′-didehydro-2′,3′-dideoxy nucleosides
4. Highly potent and selective inhibition of bovine viral diarrhea virus replication by γ-carboline derivatives
5. Modulation of innate and adaptive immunity by biodegradable nanoparticles
6. Synthesis of (±)-4′-ethynyl-5′,5′-difluoro-2′,3′-dehydro-3′-deoxy- carbocyclic thymidine: a difluoromethylidene analogue of promising anti-HIV agent Ed4T
7. Synthesis of (±)-9-[ c-4, t-5-bis(hydroxymethyl)cyclopent-2-en- r-1-yl]-9 H-adenine (BCA) derivatives branched at the 4′-position based on intramolecular S H2′ cyclization
8. A novel tetramethylnaphthalene derivative synergistically inhibits HTLV-1-infected cell proliferation in combination with cepharanthine
9. Human Anti–Human IL-18 Antibody Recognizing the IL-18–Binding Site 3 with IL-18 Signaling Blocking Activity
10. Potent and selective inhibition of hepatitis C virus replication by novel phenanthridinone derivatives
11. Identification of Novel Inhibitors of Human Immunodeficiency Virus Type 1 Replication by In Silico Screening Targeting Cyclin T1/Tat Interaction
12. From the Chemistry of Epoxy-Sugar Nucleosides to the Discovery of Anti-HIV Agent 4'-ethynylstavudine-Festinavir
13. Anti-Human Immunodeficiency Virus Type 1 Activity of Novel 6-Substituted 1-Benzyl-3-(3,5-Dimethylbenzyl)Uracil Derivatives
14. Synthesis of 1-benzyl-3-(3,5-dimethylbenzyl)Uracil Derivatives with Potential Anti-HIV Activity
15. Synthesis of 4′-Ethynyl-2′-deoxy-4′-thioribonucleosides and Discovery of a Highly Potent and Less Toxic NRTI
16. A novel tetramethylnaphthalene derivative synergistically inhibits HTLV-1-infected cell proliferation in combination with cepharanthine
17. In silico Screening of Compounds Targeting Human Cyclin T1 and In vitro Evaluation of their Anti-HIV-1 Activity
18. Differential Expression of Host Cellular Factors upon HIV-1 Reactivation
19. Synthesis and Anti-human Immunodeficiency Virus Activity of the Skeleton Isomers of 3',4'-Di-(O)-(-)-camphanoyl-(+)-khellactone
20. Modulation of Gene Expression Related to Toll-Like Receptor Signaling in Dendritic Cells by Poly(γ-Glutamic Acid) Nanoparticles
21. Impact of Novel Human Immunodeficiency Virus Type 1 Reverse Transcriptase Mutations P119S and T165A on 4′-Ethynylthymidine Analog Resistance Profile
22. Discovery of tetrahydrotetramethylnaphthalene analogs as adult T-cell leukemia cell-selective proliferation inhibitors in a small chemical library constructed based on multi-template hypothesis
23. In Silico Screening for Anti-HIV-1 Compounds Targeting to Human Cyclin T1
24. Synthesis and Anti-HIV Activity of 4′-Substituted 4′-Thiothymidines: A New Entry Based on Nucleophilic Substitution of the 4′-Acetoxy Group
25. Highly Enhanced Expression of CD70 on Human T-Lymphotropic Virus Type 1-Carrying T-Cell Lines and Adult T-Cell Leukemia Cells
26. Synthesis of (±)-9-[c-4, t-5-bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine (BCA) derivatives branched at the 4′-position based on intramolecular SH2′ cyclization
27. Biopanning of Antibody-Phage Clones Using Immunoplates Coated with Gel Slices of Electrophoresis: Immunogel-Biopanning
28. Information Security and Cryptography. Recent Security Techniques in Satellite Broadcasting.
29. Identification of Novel Inhibitors of Human Immunodeficiency Virus Type 1 Replication by In SilicoScreening Targeting Cyclin T1/Tat Interaction
30. Launch, Tracking and Control
31. Synthesis and anti-HIV activity of 4'-C-ethynyl-2'-deoxy-4'-thio-nucleosides
32. Synthesis and antiviral evaluation of ()-4'-ethynyl-5'-difluorocarbocyclic-d4T analogue
33. Synergistic inhibition of HTLV-1-infected cell proliferation by combination of cepharanthine and a tetramethylnaphthalene derivative.
34. Selective inhibition of HTLV-1-infected cell proliferation by a novel tetramethylnaphthalene derivative.
35. Synthesis and antiviral evaluation of (+/-)-4'-ethynyl-5'-difluorocarbocyclic-d4T analogue.
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