Wilk S - Search Results

1

Crystal structures of DPP-IV (CD26) from rat kidney exhibit flexible accommodation of peptidase-selective inhibitors.

Longenecker KL, Stewart KD, Madar DJ, Jakob CG, Fry EH, Wilk S, Lin CW, Ballaron SJ, Stashko MA, Lubben TH, Yong H, Pireh D, Pei Z, Basha F, Wiedeman PE, von Geldern TW, Trevillyan JM, Stoll VS. Longenecker KL, et al. Among authors: wilk s. Biochemistry. 2006 Jun 20;45(24):7474-82. doi: 10.1021/bi060184f. Biochemistry. 2006. PMID: 16768443

2

A comparison of the effect of substituted benzamides in radioreceptor binding assays with their effects on brain dopaminergic systems in vivo.

Lin CW, Wilk S. Lin CW, et al. Among authors: wilk s. Adv Biochem Psychopharmacol. 1982;35:51-60. Adv Biochem Psychopharmacol. 1982. PMID: 6183929 No abstract available.

3

Aminoacylpyrrolidine-2-nitriles: potent and stable inhibitors of dipeptidyl-peptidase IV (CD 26).

Li J, Wilk E, Wilk S. Li J, et al. Among authors: wilk e, wilk s. Arch Biochem Biophys. 1995 Oct 20;323(1):148-54. doi: 10.1006/abbi.1995.0020. Arch Biochem Biophys. 1995. PMID: 7487060

4

[3H]dihydroergocryptine binding to bovine striatal membranes defined by a low d-butaclamol concentration: antagonism by substituted benzamides.

Lin CW, Maayani S, Wilk S. Lin CW, et al. Among authors: wilk s. Biochem Pharmacol. 1981 Jun 1;30(11):1305-14. doi: 10.1016/0006-2952(81)90314-2. Biochem Pharmacol. 1981. PMID: 6168265 No abstract available.

5

The effect of typical and atypical neuroleptics on binding of [3H]spiroperidol in calf caudate.

Lin CW, Maayani S, Wilk S. Lin CW, et al. Among authors: wilk s. J Pharmacol Exp Ther. 1980 Mar;212(3):462-8. J Pharmacol Exp Ther. 1980. PMID: 6102144

6

5-Oxoprolinal: transition-state aldehyde inhibitor of pyroglutamyl-peptide hydrolase.

Friedman TC, Kline TB, Wilk S. Friedman TC, et al. Among authors: wilk s. Biochemistry. 1985 Jul 16;24(15):3907-13. doi: 10.1021/bi00336a015. Biochemistry. 1985. PMID: 2864952

7

Purification and specificity of a membrane-bound metalloendopeptidase from bovine pituitaries.

Orlowski M, Wilk S. Orlowski M, et al. Among authors: wilk s. Biochemistry. 1981 Aug 18;20(17):4942-50. doi: 10.1021/bi00520a021. Biochemistry. 1981. PMID: 7028098

8

Production and properties of a recombinant soluble form of aminopeptidase A.

Vazeux G, Wilk S, Wilk E, Corvol P, Llorens-Cortès C. Vazeux G, et al. Among authors: wilk e, wilk s. Eur J Biochem. 1998 Jun 15;254(3):671-8. doi: 10.1046/j.1432-1327.1998.2540671.x. Eur J Biochem. 1998. PMID: 9688281 Free article.

9

Inhibition of human immunodeficiency virus type 1 infection in a T-cell line (CEM) by new dipeptidyl-peptidase IV (CD26) inhibitors.

Jiang JD, Wilk S, Li J, Zhang H, Bekesi JG. Jiang JD, et al. Among authors: wilk s. Res Virol. 1997 Jul-Aug;148(4):255-66. doi: 10.1016/s0923-2516(97)88362-8. Res Virol. 1997. PMID: 9272576

10

Inhibition of prolyl oligopeptidase by Fmoc-aminoacylpyrrolidine-2-nitriles.

Li J, Wilk E, Wilk S. Li J, et al. Among authors: wilk e, wilk s. J Neurochem. 1996 May;66(5):2105-12. doi: 10.1046/j.1471-4159.1996.66052105.x. J Neurochem. 1996. PMID: 8780042

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