Williams M - Search Results

1

[3H]CGS 21680, a selective A2 adenosine receptor agonist directly labels A2 receptors in rat brain.

Jarvis MF, Schulz R, Hutchison AJ, Do UH, Sills MA, Williams M. Jarvis MF, et al. Among authors: williams m. J Pharmacol Exp Ther. 1989 Dec;251(3):888-93. J Pharmacol Exp Ther. 1989. PMID: 2600819

2

[3H]CGP 39653: a new N-methyl-D-aspartate antagonist radioligand with low nanomolar affinity in rat brain.

Sills MA, Fagg G, Pozza M, Angst C, Brundish DE, Hurt SD, Wilusz EJ, Williams M. Sills MA, et al. Among authors: williams m. Eur J Pharmacol. 1991 Jan 3;192(1):19-24. doi: 10.1016/0014-2999(91)90063-v. Eur J Pharmacol. 1991. PMID: 1674916

3

Characterization of the binding of a novel nonxanthine adenosine antagonist radioligand, [3H]CGS 15943, to multiple affinity states of the adenosine A1 receptor in the rat cortex.

Jarvis MF, Williams M, Do UH, Sills MA. Jarvis MF, et al. Among authors: williams m. Mol Pharmacol. 1991 Jan;39(1):49-54. Mol Pharmacol. 1991. PMID: 1987452

4

2-(Arylalkylamino)adenosin-5'-uronamides: a new class of highly selective adenosine A2 receptor ligands.

Hutchison AJ, Williams M, de Jesus R, Yokoyama R, Oei HH, Ghai GR, Webb RL, Zoganas HC, Stone GA, Jarvis MF. Hutchison AJ, et al. Among authors: williams m. J Med Chem. 1990 Jul;33(7):1919-24. doi: 10.1021/jm00169a015. J Med Chem. 1990. PMID: 2362269

5

Direct autoradiographic localization of adenosine A2 receptors in the rat brain using the A2-selective agonist, [3H]CGS 21680.

Jarvis MF, Williams M. Jarvis MF, et al. Among authors: williams m. Eur J Pharmacol. 1989 Sep 13;168(2):243-6. doi: 10.1016/0014-2999(89)90571-2. Eur J Pharmacol. 1989. PMID: 2558026

6

Autoradiographic characterization of high-affinity adenosine A2 receptors in the rat brain.

Jarvis MF, Jackson RH, Williams M. Jarvis MF, et al. Among authors: williams m. Brain Res. 1989 Apr 10;484(1-2):111-8. doi: 10.1016/0006-8993(89)90353-3. Brain Res. 1989. PMID: 2713675

7

CGS 21680C, an A2 selective adenosine receptor agonist with preferential hypotensive activity.

Hutchison AJ, Webb RL, Oei HH, Ghai GR, Zimmerman MB, Williams M. Hutchison AJ, et al. Among authors: williams m. J Pharmacol Exp Ther. 1989 Oct;251(1):47-55. J Pharmacol Exp Ther. 1989. PMID: 2795469

8

Quantitative autoradiographic localization of NMDA receptors in rat brain using [3H]CPP: comparison with [3H]TCP binding sites.

Jarvis MF, Murphy DE, Williams M. Jarvis MF, et al. Among authors: williams m. Eur J Pharmacol. 1987 Sep 2;141(1):149-52. doi: 10.1016/0014-2999(87)90423-7. Eur J Pharmacol. 1987. PMID: 2822443

9

Characterization of the binding of [3H]-CGS 19755: a novel N-methyl-D-aspartate antagonist with nanomolar affinity in rat brain.

Murphy DE, Hutchison AJ, Hurt SD, Williams M, Sills MA. Murphy DE, et al. Among authors: williams m. Br J Pharmacol. 1988 Nov;95(3):932-8. doi: 10.1111/j.1476-5381.1988.tb11723.x. Br J Pharmacol. 1988. PMID: 2850065 Free PMC article.

10

The NMDA antagonists, CPP and CGS 19755, lack affinity for central benzodiazepine receptors.

Williams M, Loo PS, Sills MA. Williams M, et al. Eur J Pharmacol. 1988 Oct 11;155(1-2):185-7. doi: 10.1016/0014-2999(88)90421-9. Eur J Pharmacol. 1988. PMID: 2854072

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