Bankowski K - Search Results

1

Oxytocin and vasopressin agonists and antagonists as research tools and potential therapeutics.

Manning M, Misicka A, Olma A, Bankowski K, Stoev S, Chini B, Durroux T, Mouillac B, Corbani M, Guillon G. Manning M, et al. Among authors: bankowski k. J Neuroendocrinol. 2012 Apr;24(4):609-28. doi: 10.1111/j.1365-2826.2012.02303.x. J Neuroendocrinol. 2012. PMID: 22375852 Free PMC article. Review.

2

Synthesis and some pharmacological properties of potent and selective antagonists of the vasopressor (V1-receptor) response to arginine-vasopressin.

Manning M, Stoev S, Bankowski K, Misicka A, Lammek B, Wo NC, Sawyer WH. Manning M, et al. Among authors: bankowski k. J Med Chem. 1992 Jan 24;35(2):382-8. doi: 10.1021/jm00080a027. J Med Chem. 1992. PMID: 1531076

3

Advances in the design of selective antagonists, potential tocolytics, and radioiodinated ligands for oxytocin receptors.

Manning M, Cheng LL, Klis WA, Stoev S, Przybylski J, Bankowski K, Sawyer WH, Barberis C, Chan WY. Manning M, et al. Among authors: bankowski k. Adv Exp Med Biol. 1995;395:559-83. Adv Exp Med Biol. 1995. PMID: 8714021 Review.

4

Novel approach to the design of synthetic radioiodinated linear V1A receptor antagonists of vasopressin.

Manning M, Bankowski K, Barberis C, Jard S, Elands J, Chan WY. Manning M, et al. Among authors: bankowski k. Int J Pept Protein Res. 1992 Sep-Oct;40(3-4):261-7. doi: 10.1111/j.1399-3011.1992.tb00300.x. Int J Pept Protein Res. 1992. PMID: 1478783

5

2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists.

Lammek B, Bankowski K, Misicka A, Manning M, Seto J, Sawyer WH. Lammek B, et al. Among authors: bankowski k. J Med Chem. 1989 Jan;32(1):244-7. doi: 10.1021/jm00121a043. J Med Chem. 1989. PMID: 2909737

6

Solid-phase synthesis of 16 potent (selective and nonselective) in vivo antagonists of oxytocin.

Manning M, Kruszynski M, Bankowski K, Olma A, Lammek B, Cheng LL, Klis WA, Seto J, Haldar J, Sawyer WH. Manning M, et al. Among authors: bankowski k. J Med Chem. 1989 Feb;32(2):382-91. doi: 10.1021/jm00122a016. J Med Chem. 1989. PMID: 2913298

7

C-terminal deletions in agonistic and antagonistic analogues of vasopressin that improve their specificities for antidiuretic (V2) and vasopressor (V1) receptors.

Manning M, Misicka A, Olma A, Klis WA, Bankowski K, Nawrocka E, Kruszynski M, Kolodziejczyk A, Cheng LL, Seto J, et al. Manning M, et al. Among authors: bankowski k. J Med Chem. 1987 Dec;30(12):2245-52. doi: 10.1021/jm00395a012. J Med Chem. 1987. PMID: 2960812

8

Potent V2 vasopressin antagonists with structural changes at their C-terminals.

Sawyer WH, Bankowski K, Misicka A, Nawrocka E, Kruszynski M, Stoev S, Klis WA, Przybylski JP, Manning M. Sawyer WH, et al. Among authors: bankowski k. Peptides. 1988 Jan-Feb;9(1):157-63. doi: 10.1016/0196-9781(88)90022-8. Peptides. 1988. PMID: 3362743

9

An exploration of the effects of L- and D-tetrahydroisoquinoline-3-carboxylic acid substitutions at positions 2, 3 and 7 in cyclic and linear antagonists of vasopressin and oxytocin and at position 3 in arginine vasopressin.

Manning M, Cheng LL, Stoev S, Bankowski K, Przybyiski J, Klis WA, Sawyer WH, Wo NC, Chan WY. Manning M, et al. Among authors: bankowski k. J Pept Sci. 1995 Jan-Feb;1(1):66-79. doi: 10.1002/psc.310010109. J Pept Sci. 1995. PMID: 9222985

10

Characterization of a novel, linear radioiodinated vasopressin antagonist: an excellent radioligand for vasopressin V1a receptors.

Barbeis C, Balestre MN, Jard S, Tribollet E, Arsenijevic Y, Dreifuss JJ, Bankowski K, Manning M, Chan WY, Schlosser SS, et al. Barbeis C, et al. Among authors: bankowski k. Neuroendocrinology. 1995 Aug;62(2):135-46. doi: 10.1159/000126998. Neuroendocrinology. 1995. PMID: 8584113

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