Brown NA - Search Results

1

Salicylidene salicylhydrazide, a selective inhibitor of beta 1-containing GABAA receptors.

Thompson SA, Wheat L, Brown NA, Wingrove PB, Pillai GV, Whiting PJ, Adkins C, Woodward CH, Smith AJ, Simpson PB, Collins I, Wafford KA. Thompson SA, et al. Among authors: brown na. Br J Pharmacol. 2004 May;142(1):97-106. doi: 10.1038/sj.bjp.0705689. Epub 2004 Apr 20. Br J Pharmacol. 2004. PMID: 15100159 Free PMC article.

2

Pharmacological characterization of a novel cell line expressing human alpha(4)beta(3)delta GABA(A) receptors.

Brown N, Kerby J, Bonnert TP, Whiting PJ, Wafford KA. Brown N, et al. Br J Pharmacol. 2002 Aug;136(7):965-74. doi: 10.1038/sj.bjp.0704795. Br J Pharmacol. 2002. PMID: 12145096 Free PMC article.

3

theta, a novel gamma-aminobutyric acid type A receptor subunit.

Bonnert TP, McKernan RM, Farrar S, le Bourdellès B, Heavens RP, Smith DW, Hewson L, Rigby MR, Sirinathsinghji DJ, Brown N, Wafford KA, Whiting PJ. Bonnert TP, et al. Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9891-6. doi: 10.1073/pnas.96.17.9891. Proc Natl Acad Sci U S A. 1999. PMID: 10449790 Free PMC article.

4

Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A) receptor alpha1 subtype.

McKernan RM, Rosahl TW, Reynolds DS, Sur C, Wafford KA, Atack JR, Farrar S, Myers J, Cook G, Ferris P, Garrett L, Bristow L, Marshall G, Macaulay A, Brown N, Howell O, Moore KW, Carling RW, Street LJ, Castro JL, Ragan CI, Dawson GR, Whiting PJ. McKernan RM, et al. Nat Neurosci. 2000 Jun;3(6):587-92. doi: 10.1038/75761. Nat Neurosci. 2000. PMID: 10816315

5

Imidazo[1,2-a]pyrimidines as functionally selective and orally bioavailable GABA(A)alpha2/alpha3 binding site agonists for the treatment of anxiety disorders.

Goodacre SC, Street LJ, Hallett DJ, Crawforth JM, Kelly S, Owens AP, Blackaby WP, Lewis RT, Stanley J, Smith AJ, Ferris P, Sohal B, Cook SM, Pike A, Brown N, Wafford KA, Marshall G, Castro JL, Atack JR. Goodacre SC, et al. J Med Chem. 2006 Jan 12;49(1):35-8. doi: 10.1021/jm051065l. J Med Chem. 2006. PMID: 16392789

6

Human D2 and D4 dopamine receptors couple through betagamma G-protein subunits to inwardly rectifying K+ channels (GIRK1) in a Xenopus oocyte expression system: selective antagonism by L-741,626 and L-745,870 respectively.

Pillai G, Brown NA, McAllister G, Milligan G, Seabrook GR. Pillai G, et al. Among authors: brown na. Neuropharmacology. 1998 Aug;37(8):983-7. doi: 10.1016/s0028-3908(98)00092-6. Neuropharmacology. 1998. PMID: 9833627

7

Involvement of G-protein alpha il subunits in activation of G-protein gated inward rectifying K+ channels (GIRK1) by human NPY1 receptors.

Brown NA, McAllister G, Weinberg D, Milligan G, Seabrook GR. Brown NA, et al. Br J Pharmacol. 1995 Nov;116(5):2346-8. doi: 10.1111/j.1476-5381.1995.tb15077.x. Br J Pharmacol. 1995. PMID: 8581266 Free PMC article.

8

Phosphorylation- and voltage-dependent inhibition of neuronal calcium currents by activation of human D2(short) dopamine receptors.

Brown NA, Seabrook GR. Brown NA, et al. Br J Pharmacol. 1995 Jun;115(3):459-66. doi: 10.1111/j.1476-5381.1995.tb16355.x. Br J Pharmacol. 1995. PMID: 7582457 Free PMC article.

9

Pharmacology of high-threshold calcium currents in GH4C1 pituitary cells and their regulation by activation of human D2 and D4 dopamine receptors.

Seabrook GR, Knowles M, Brown N, Myers J, Sinclair H, Patel S, Freedman SB, McAllister G. Seabrook GR, et al. Br J Pharmacol. 1994 Jul;112(3):728-34. doi: 10.1111/j.1476-5381.1994.tb13138.x. Br J Pharmacol. 1994. PMID: 7921596 Free PMC article.

10

Block of human voltage-sensitive Na+ currents in differentiated SH-SY5Y cells by lifarizine.

Brown NA, Kemp JA, Seabrook GR. Brown NA, et al. Br J Pharmacol. 1994 Oct;113(2):600-6. doi: 10.1111/j.1476-5381.1994.tb17032.x. Br J Pharmacol. 1994. PMID: 7834213 Free PMC article.

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