Bannon AW - Search Results

1

Broad-spectrum, non-opioid analgesic activity by selective modulation of neuronal nicotinic acetylcholine receptors.

Bannon AW, Decker MW, Holladay MW, Curzon P, Donnelly-Roberts D, Puttfarcken PS, Bitner RS, Diaz A, Dickenson AH, Porsolt RD, Williams M, Arneric SP. Bannon AW, et al. Science. 1998 Jan 2;279(5347):77-81. doi: 10.1126/science.279.5347.77. Science. 1998. PMID: 9417028

2

Cholinergic channel activators: novel opportunities for the treatment of CNS disorders.

Sullivan JP, Decker MW, Donnelly-Roberts D, Brioni JD, Bannon AW, Holladay MW, Anderson DJ, Briggs CA, Williams M, Arneric SP. Sullivan JP, et al. Among authors: bannon aw. Proc West Pharmacol Soc. 1995;38:127-30. Proc West Pharmacol Soc. 1995. PMID: 7480004 Review.

3

The influence of Bay K 8644 treatment on (+/-)-epibatidine-induced analgesia.

Bannon AW, Gunther KL, Decker MW, Arneric SP. Bannon AW, et al. Brain Res. 1995 Apr 24;678(1-2):244-50. doi: 10.1016/0006-8993(95)00189-w. Brain Res. 1995. PMID: 7542542

4

Is epibatidine really analgesic? Dissociation of the activity, temperature, and analgesic effects of (+/-)-epibatidine.

Bannon AW, Gunther KL, Decker MW. Bannon AW, et al. Pharmacol Biochem Behav. 1995 Aug;51(4):693-8. doi: 10.1016/0091-3057(94)00439-p. Pharmacol Biochem Behav. 1995. PMID: 7675845

5

Diversity of neuronal nicotinic acetylcholine receptors: lessons from behavior and implications for CNS therapeutics.

Decker MW, Brioni JD, Bannon AW, Arneric SP. Decker MW, et al. Among authors: bannon aw. Life Sci. 1995;56(8):545-70. doi: 10.1016/0024-3205(94)00488-e. Life Sci. 1995. PMID: 7869835 Review.

6

(+/-)-Epibatidine elicits a diversity of in vitro and in vivo effects mediated by nicotinic acetylcholine receptors.

Sullivan JP, Decker MW, Brioni JD, Donnelly-Roberts D, Anderson DJ, Bannon AW, Kang CH, Adams P, Piattoni-Kaplan M, Buckley MJ, et al. Sullivan JP, et al. Among authors: bannon aw. J Pharmacol Exp Ther. 1994 Nov;271(2):624-31. J Pharmacol Exp Ther. 1994. PMID: 7965777

7

Identification and initial structure-activity relationships of (R)-5-(2-azetidinylmethoxy)-2-chloropyridine (ABT-594), a potent, orally active, non-opiate analgesic agent acting via neuronal nicotinic acetylcholine receptors.

Holladay MW, Wasicak JT, Lin NH, He Y, Ryther KB, Bannon AW, Buckley MJ, Kim DJ, Decker MW, Anderson DJ, Campbell JE, Kuntzweiler TA, Donnelly-Roberts DL, Piattoni-Kaplan M, Briggs CA, Williams M, Arneric SP. Holladay MW, et al. Among authors: bannon aw. J Med Chem. 1998 Feb 12;41(4):407-12. doi: 10.1021/jm9706224. J Med Chem. 1998. PMID: 9484491

8

ABT-594 [(R)-5-(2-azetidinylmethoxy)-2-chloropyridine]: a novel, orally effective antinociceptive agent acting via neuronal nicotinic acetylcholine receptors: II. In vivo characterization.

Bannon AW, Decker MW, Curzon P, Buckley MJ, Kim DJ, Radek RJ, Lynch JK, Wasicak JT, Lin NH, Arnold WH, Holladay MW, Williams M, Arneric SP. Bannon AW, et al. J Pharmacol Exp Ther. 1998 May;285(2):787-94. J Pharmacol Exp Ther. 1998. PMID: 9580627

9

Antinociceptive effects of the novel neuronal nicotinic acetylcholine receptor agonist, ABT-594, in mice.

Decker MW, Bannon AW, Buckley MJ, Kim DJ, Holladay MW, Ryther KB, Lin NH, Wasicak JT, Williams M, Arneric SP. Decker MW, et al. Among authors: bannon aw. Eur J Pharmacol. 1998 Apr 3;346(1):23-33. doi: 10.1016/s0014-2999(98)00042-9. Eur J Pharmacol. 1998. PMID: 9617748

10

Role of the nucleus raphe magnus in antinociception produced by ABT-594: immediate early gene responses possibly linked to neuronal nicotinic acetylcholine receptors on serotonergic neurons.

Bitner RS, Nikkel AL, Curzon P, Arneric SP, Bannon AW, Decker MW. Bitner RS, et al. Among authors: bannon aw. J Neurosci. 1998 Jul 15;18(14):5426-32. doi: 10.1523/JNEUROSCI.18-14-05426.1998. J Neurosci. 1998. PMID: 9651224 Free PMC article.

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