24 results on '"Jin, Lixia"'
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2. TRIM21-mediated ubiquitination of PLIN2 regulates neuronal lipid droplet accumulation after acute spinal cord injury
3. Preparation of g-C3N4/NS-CQDs composites and their application in the detection of hydrogen peroxide and glucose
4. Characteristics and influences of urban shrinkage in the exo-urbanization area of the Pearl River Delta, China
5. Identifying the determinants of housing prices in China using spatial regression and the geographical detector technique
6. Enantiomeric separation of organophosphorus pesticides by high-performance liquid chromatography, gas chromatography and capillary electrophoresis and their applications to environmental fate and toxicity assays
7. Prediction of protein structural classes by a new measure of information discrepancy
8. Methyl-substitution of an iminohydantoin spiropiperidine β-secretase (BACE-1) inhibitor has a profound effect on its potency
9. Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8-hydroxy-[1,6]-naphthyridine-7-carboxamide inhibitors of HIV-1 integrase
10. Dihydroxypyridopyrazine-1,6-dione HIV-1 integrase inhibitors
11. A potent and orally active HIV-1 integrase inhibitor
12. BACE-1 inhibition by a series of ψ[CH 2NH] reduced amide isosteres
13. A series of 5-aminosubstituted 4-fluorobenzyl-8-hydroxy-[1,6]naphthyridine-7-carboxamide HIV-1 integrase inhibitors
14. Orally bioavailable highly potent HIV protease inhibitors against PI-resistant virus
15. A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells
16. Novel HIV-1 protease inhibitors active against multiple PI-Resistant viral strains: coadministration with indinavir
17. HIV-1 protease inhibitors with picomolar potency against PI-resistant HIV-1 by modification of the P 1′ substituent
18. The design, synthesis and evaluation of novel HIV-1 protease inhibitors with high potency against PI-resistant viral strains
19. HIV protease inhibitors with picomolar potency against PI-Resistant HIV-1 by extension of the P 3 substituent
20. Design and synthesis of highly potent HIV protease inhibitors with activity against resistant virus
21. Synthesis and activity of novel HIV protease inhibitors with improved potency against multiple PI-resistant viral strains
22. Indinavir analogues with blocked metabolism sites as HIV protease inhibitors with improved pharmacological profiles and high potency against PI-Resistant viral strains
23. A Combinatorial Library of Indinavir Analogues and Its In Vitro and In Vivo Studies
24. On “A comment on ‘Prediction of protein structural classes by a new measure of information discrepancy”’
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