Britton DR - Search Results

1

Site and event specific increase of striatal adenosine release by adenosine kinase inhibition in rats.

Britton DR, Mikusa J, Lee CH, Jarvis MF, Williams M, Kowaluk EA. Britton DR, et al. Neurosci Lett. 1999 May 7;266(2):93-6. doi: 10.1016/s0304-3940(99)00280-3. Neurosci Lett. 1999. PMID: 10353335

2

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. Among authors: britton dr. J Pharmacol Exp Ther. 1996 Jan;276(1):150-60. J Pharmacol Exp Ther. 1996. PMID: 8558425

3

Hyperactivity and behavioral seizures in rodents following treatment with the dopamine D1 receptor agonists A-86929 and ABT-431.

Shiosaki K, Asin KE, Britton DR, Giardina WJ, Bednarz L, Mahan L, Mikusa J, Nikkel A, Wismer C. Shiosaki K, et al. Among authors: britton dr. Eur J Pharmacol. 1996 Dec 19;317(2-3):183-90. doi: 10.1016/s0014-2999(96)00718-2. Eur J Pharmacol. 1996. PMID: 8997599

4

A-77636: a potent and selective dopamine D1 receptor agonist with antiparkinsonian activity in marmosets.

Kebabian JW, Britton DR, DeNinno MP, Perner R, Smith L, Jenner P, Schoenleber R, Williams M. Kebabian JW, et al. Among authors: britton dr. Eur J Pharmacol. 1992 Dec 15;229(2-3):203-9. doi: 10.1016/0014-2999(92)90556-j. Eur J Pharmacol. 1992. PMID: 1362704

5

(5aR,11bS)-4,5,5a,6,7,11b-hexahydro-2-propyl-3-thia-5-azacyclopent-1- ena[c]-phenanthrene-9,10-diol (A-86929): a potent and selective dopamine D1 agonist that maintains behavioral efficacy following repeated administration and characterization of its diacetyl prodrug (ABT-431).

Michaelides MR, Hong Y, DiDomenico S Jr, Asin KE, Britton DR, Lin CW, Williams M, Shiosaki K. Michaelides MR, et al. Among authors: britton dr. J Med Chem. 1995 Sep 1;38(18):3445-7. doi: 10.1021/jm00018a002. J Med Chem. 1995. PMID: 7658429 No abstract available.

6

Evidence for involvement of both D1 and D2 receptors in maintaining cocaine self-administration.

Britton DR, Curzon P, Mackenzie RG, Kebabian JW, Williams JE, Kerkman D. Britton DR, et al. Pharmacol Biochem Behav. 1991 Aug;39(4):911-5. doi: 10.1016/0091-3057(91)90052-4. Pharmacol Biochem Behav. 1991. PMID: 1684870

7

Persistent activation of the dopamine D1 receptor contributes to prolonged receptor desensitization: studies with A-77636.

Lin CW, Bianchi BR, Miller TR, Stashko MA, Wang SS, Curzon P, Bednarz L, Asin KE, Britton DR. Lin CW, et al. Among authors: britton dr. J Pharmacol Exp Ther. 1996 Mar;276(3):1022-9. J Pharmacol Exp Ther. 1996. PMID: 8786531

8

A68930: a potent and specific agonist for the D-1 dopamine receptor.

Kebabian JW, Briggs C, Britton DR, Asin K, DeNinno M, MacKenzie RG, McKelvy JF, Schoenleber R. Kebabian JW, et al. Among authors: britton dr. Am J Hypertens. 1990 Jun;3(6 Pt 2):40S-42S. doi: 10.1093/ajh/3.6.40s. Am J Hypertens. 1990. PMID: 2143387 Review.

9

Substituted hexahydrobenzo[f]thieno[c]quinolines as dopamine D1-selective agonists: synthesis and biological evaluation in vitro and in vivo.

Michaelides MR, Hong Y, DiDomenico S Jr, Bayburt EK, Asin KE, Britton DR, Lin CW, Shiosaki K. Michaelides MR, et al. Among authors: britton dr. J Med Chem. 1997 May 23;40(11):1585-99. doi: 10.1021/jm970038v. J Med Chem. 1997. PMID: 9171869

10

Evaluation of a stable CCK agonist (A68552) in conditioned avoidance responding in mice, rats, and primates: comparison with typical and atypical antipsychotics.

Britton DR, Curzon P, Yahiro L, Buckley M, Tufano M, Nadzan A. Britton DR, et al. Pharmacol Biochem Behav. 1992 Oct;43(2):369-76. doi: 10.1016/0091-3057(92)90164-b. Pharmacol Biochem Behav. 1992. PMID: 1359571

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