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133 related items for PubMed ID: 1894448
21. Distinct requirements for activation at CCK-A and CCK-B/gastrin receptors: studies with a C-terminal hydrazide analogue of cholecystokinin tetrapeptide (30-33). Lin CW, Holladay MW, Barrett RW, Wolfram CA, Miller TR, Witte D, Kerwin JF, Wagenaar F, Nadzan AM. Mol Pharmacol; 1989 Dec; 36(6):881-6. PubMed ID: 2601685 [Abstract] [Full Text] [Related]
30. Synthesis and solution characterization of a porphyrin-CCK8 conjugate. De Luca S, Tesauro D, Di Lello P, Fattorusso R, Saviano M, Pedone C, Morelli G. J Pept Sci; 2001 Jul 01; 7(7):386-94. PubMed ID: 11495499 [Abstract] [Full Text] [Related]
31. Synthesis of potent heptapeptide analogues of cholecystokinin. Penke B, Hajnal F, Lonovics J, Holzinger G, Kadar T, Telegdy G, Rivier J. J Med Chem; 1984 Jul 01; 27(7):845-9. PubMed ID: 6737428 [Abstract] [Full Text] [Related]
32. Synthesis and some pharmacological properties of Z-Tyr(SO3H)-Met-Gly-Trp-Met-Asp(Phe-NH2)-OH, a 32-beta-aspartyl analogue of cholecystokinin (pancreozymin) 27-33. Martinez J, Winternitz F, Bodanszky M, Gardner JD, Walker MD, Mutt V. J Med Chem; 1982 May 01; 25(5):589-93. PubMed ID: 6177857 [Abstract] [Full Text] [Related]
33. Synthesis of O-phosphotyrosine-containing peptides. Perich JW. Methods Enzymol; 1991 May 01; 201():234-45. PubMed ID: 1719342 [Abstract] [Full Text] [Related]
37. Conformational analysis of CCK-B agonists using 1H-NMR and restrained molecular dynamics: comparison of biologically active Boc-Trp-(N-Me) Nle-Asp-Phe-NH2 and inactive Boc-Trp-(N-Me)Phe-Asp-Phe-NH2. Goudreau N, Weng JH, Roques BP. Biopolymers; 1994 Feb 01; 34(2):155-69. PubMed ID: 8142585 [Abstract] [Full Text] [Related]
39. Modifications to the N-terminus but not the C-terminus of calcitonin gene-related peptide(8-37) produce antagonists with increased affinity. Smith DD, Saha S, Fang G, Schaffert C, Waugh DJ, Zeng W, Toth G, Hulce M, Abel PW. J Med Chem; 2003 Jun 05; 46(12):2427-35. PubMed ID: 12773046 [Abstract] [Full Text] [Related]