Witte DG - Search Results

1

Characterization of cloned human dopamine D1 receptor-mediated calcium release in 293 cells.

Lin CW, Miller TR, Witte DG, Bianchi BR, Stashko M, Manelli AM, Frail DE. Lin CW, et al. Among authors: witte dg. Mol Pharmacol. 1995 Jan;47(1):131-9. Mol Pharmacol. 1995. PMID: 7838121

2

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 Jr, Wagenaar F, Nadzan AM. Lin CW, et al. Mol Pharmacol. 1989 Dec;36(6):881-6. Mol Pharmacol. 1989. PMID: 2601685

3

ABT-431: the diacetyl prodrug of A-86929, a potent and selective dopamine D1 receptor agonist: in vitro characterization and effects in animal models of Parkinson's disease.

Shiosaki K, Jenner P, Asin KE, Britton DR, Lin CW, Michaelides M, Smith L, Bianchi B, Didomenico S, Hodges L, Hong Y, Mahan L, Mikusa J, Miller T, Nikkel A, Stashko M, Witte D, Williams M. Shiosaki K, et al. J Pharmacol Exp Ther. 1996 Jan;276(1):150-60. J Pharmacol Exp Ther. 1996. PMID: 8558425

4

Characterization of two novel cholecystokinin tetrapeptide (30-33) analogues, A-71623 and A-70874, that exhibit high potency and selectivity for cholecystokinin-A receptors.

Lin CW, Shiosaki K, Miller TR, Witte DG, Bianchi BR, Wolfram CA, Kopecka H, Craig R, Wagenaar F, Nadzan AM. Lin CW, et al. Among authors: witte dg. Mol Pharmacol. 1991 Mar;39(3):346-51. Mol Pharmacol. 1991. PMID: 1706470

5

Cloning and characterization of a truncated dopamine D1 receptor from goldfish retina: stimulation of cyclic AMP production and calcium mobilization.

Frail DE, Manelli AM, Witte DG, Lin CW, Steffey ME, Mackenzie RG. Frail DE, et al. Among authors: witte dg. Mol Pharmacol. 1993 Dec;44(6):1113-8. Mol Pharmacol. 1993. PMID: 8264547

6

Identification and characterization of type A endothelin receptors in MMQ cells.

Wu-Wong JR, Chiou W, Magnuson SR, Witte DG, Lin CW. Wu-Wong JR, et al. Among authors: witte dg. Mol Pharmacol. 1993 Aug;44(2):285-91. Mol Pharmacol. 1993. PMID: 8355666

7

Cloning and characterization of the monkey histamine H3 receptor isoforms.

Strakhova MI, Fox GB, Carr TL, Witte DG, Vortherms TA, Manelli AM, Miller TR, Yao BB, Brioni JD, Esbenshade TA. Strakhova MI, et al. Among authors: witte dg. Eur J Pharmacol. 2008 Dec 28;601(1-3):8-15. doi: 10.1016/j.ejphar.2008.10.026. Epub 2008 Oct 21. Eur J Pharmacol. 2008. PMID: 18977214

8

Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N epsilon)-amide residues.

Shiosaki K, Lin CW, Kopecka H, Craig RA, Bianchi BR, Miller TR, Witte DG, Stashko M, Nadzan AM. Shiosaki K, et al. Among authors: witte dg. J Med Chem. 1992 May 29;35(11):2007-14. doi: 10.1021/jm00089a010. J Med Chem. 1992. PMID: 1375964

9

Both CCK-A and CCK-B/gastrin receptors mediate pepsinogen release in guinea pig gastric glands.

Lin CW, Bianchi BR, Miller TR, Witte DG, Wolfram CA. Lin CW, et al. Among authors: witte dg. Am J Physiol. 1992 Jun;262(6 Pt 1):G1113-20. doi: 10.1152/ajpgi.1992.262.6.G1113. Am J Physiol. 1992. PMID: 1616041

10

Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-a receptor agonists.

Shiosaki K, Lin CW, Kopecka H, Tufano MD, Bianchi BR, Miller TR, Witte DG, Nadzan AM. Shiosaki K, et al. Among authors: witte dg. J Med Chem. 1991 Sep;34(9):2837-42. doi: 10.1021/jm00113a023. J Med Chem. 1991. PMID: 1716682

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