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The N-terminal domains of cyclin-dependent kinase inhibitory proteins block the phosphorylation of cdk2/Cyclin E by the CDK-activating kinase.
Rank KB, Evans DB, Sharma SK. Rank KB, et al. Biochem Biophys Res Commun. 2000 May 10;271(2):469-73. doi: 10.1006/bbrc.2000.2648. Biochem Biophys Res Commun. 2000. PMID: 10799321
A scintillation proximity assay for studying inhibitors of human tau protein kinase II/cdk5 using a 96-well format.
Evans DB, Rank KB, Sharma SK. Evans DB, et al. Among authors: rank kb. J Biochem Biophys Methods. 2002 Jan 4;50(2-3):151-61. doi: 10.1016/s0165-022x(01)00184-1. J Biochem Biophys Methods. 2002. PMID: 11741704
Direct interaction of soluble human recombinant tau protein with Abeta 1-42 results in tau aggregation and hyperphosphorylation by tau protein kinase II.
Rank KB, Pauley AM, Bhattacharya K, Wang Z, Evans DB, Fleck TJ, Johnston JA, Sharma SK. Rank KB, et al. FEBS Lett. 2002 Mar 13;514(2-3):263-8. doi: 10.1016/s0014-5793(02)02376-1. FEBS Lett. 2002. PMID: 11943163 Free article.
Role of cysteine-291 and cysteine-322 in the polymerization of human tau into Alzheimer-like filaments.
Bhattacharya K, Rank KB, Evans DB, Sharma SK. Bhattacharya K, et al. Among authors: rank kb. Biochem Biophys Res Commun. 2001 Jul 6;285(1):20-6. doi: 10.1006/bbrc.2001.5116. Biochem Biophys Res Commun. 2001. PMID: 11437366
Tau phosphorylation at serine 396 and serine 404 by human recombinant tau protein kinase II inhibits tau's ability to promote microtubule assembly.
Evans DB, Rank KB, Bhattacharya K, Thomsen DR, Gurney ME, Sharma SK. Evans DB, et al. Among authors: rank kb. J Biol Chem. 2000 Aug 11;275(32):24977-83. doi: 10.1074/jbc.M000808200. J Biol Chem. 2000. PMID: 10818091 Free article.
A rapid and quantitative assay for inhibition of 3' cleavage activity of HIV-1 integrase.
Rank KB, Fan N, Sharma SK. Rank KB, et al. Antiviral Res. 1997 Sep;36(1):27-33. doi: 10.1016/s0166-3542(97)00033-8. Antiviral Res. 1997. PMID: 9330758
Simultaneous mutations at Tyr-181 and Tyr-188 in HIV-1 reverse transcriptase prevents inhibition of RNA-dependent DNA polymerase activity by the bisheteroarylpiperazine (BHAP) U-90152s.
Fan N, Rank KB, Evans DB, Thomas RC, Tarpley WG, Sharma SK. Fan N, et al. Among authors: rank kb. FEBS Lett. 1995 Aug 14;370(1-2):59-62. doi: 10.1016/0014-5793(95)00793-9. FEBS Lett. 1995. PMID: 7544302
(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes.
Olmsted RA, Slade DE, Kopta LA, Poppe SM, Poel TJ, Newport SW, Rank KB, Biles C, Morge RA, Dueweke TJ, Yagi Y, Romero DL, Thomas RC, Sharma SK, Tarpley WG. Olmsted RA, et al. Among authors: rank kb. J Virol. 1996 Jun;70(6):3698-705. doi: 10.1128/JVI.70.6.3698-3705.1996. J Virol. 1996. PMID: 8648704 Free PMC article.
Mechanism of resistance to U-90152S and sensitization to L-697,661 by a proline to leucine change at residue 236 of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase.
Fan N, Evans DB, Rank KB, Thomas RC, Tarpley WG, Sharma SK. Fan N, et al. Among authors: rank kb. FEBS Lett. 1995 Feb 13;359(2-3):233-8. doi: 10.1016/0014-5793(95)00051-a. FEBS Lett. 1995. PMID: 7532595
[W206R]-procaspase 3: an inactivatable substrate for caspase 8.
Rank KB, Mildner AM, Leone JW, Koeplinger KA, Chou KC, Tomasselli AG, Heinrikson RL, Sharma SK. Rank KB, et al. Protein Expr Purif. 2001 Jul;22(2):258-66. doi: 10.1006/prep.2001.1433. Protein Expr Purif. 2001. PMID: 11437602
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