Sodium modulation of ³H-agonist and ³H-antagonist binding to α₂-adrenoceptor subtypesMACKINNON, A. C; SPEDDING, M; BROWN, C. M et al.British journal of pharmacology. 1993, Vol 109, Num 2, pp 371-378, issn 0007-1188Article

[Arg⁶, D-Trp^7,9, N^mePhe⁸]-substance P (6-11) activates JNK and induces apoptosis in small cell lung cancer cells via an oxidant-dependent mechanismMACKINNON, A. C; ARMSTRONG, R. A; WATERS, C. M et al.British journal of cancer. 1999, Vol 80, Num 7, pp 1026-1034, issn 0007-0920Article

Non-α₂-adrenoceptor idazoxan binding sites ; a new target for drug development : 640th meeting Heriot-Watt, Edinburgh, 4-6 September 1991KILPATRICK, A. T; BROWN, C. C; MACKINNON, A. C et al.Biochemical Society transactions. 1992, Vol 20, Num 1, pp 113-118, issn 0300-5127Conference Paper

Structure-affinity relationship of 12-sulfonyl derivatives of 8,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at α-adrenoceptorsCLARK, R. D; REPKE, D. B; BERGER, J et al.Journal of medicinal chemistry (Print). 1991, Vol 34, Num 2, pp 705-717, issn 0022-2623, 13 p.Article

Increased gastrin-releasing peptide (GRP) receptor expression in tumour cells confers sensitivity to [Arg⁶, D-Trp^7,9, N^meOhe⁸]-substance P (6-11)-induced growth inhibitionWATERS, C. M; MACKINNON, A. C; CUMMINGS, J et al.British journal of cancer. 2003, Vol 88, Num 11, pp 1808-1816, issn 0007-0920, 9 p.Article

[³H]-lifarizine, a high affinity probe for inactivated sodium channelsMACKINNON, A. C; WYATT, K. M; MCGIVERN, J. G et al.British journal of pharmacology. 1995, Vol 115, Num 6, pp 1103-1109, issn 0007-1188Article

The α₂-adrenoceptor antagonist SK&F 104078 has high affinity for 5-HT_1A and 5-HT₂ receptorsKILPATRICK, A. T; BROWN, C. M; MACKINNON, A. C et al.European journal of pharmacology. 1989, Vol 166, Num 2, pp 315-318, issn 0014-2999Article

Expression of V_IA and GRP receptors leads to cellular transformation and increased sensitivity to substance-P analogue-induced growth inhibitionMACKINNON, A. C; TUFAIL-HANIF, U; LUCAS, C. D et al.British journal of cancer. 2005, Vol 92, Num 3, pp 522-531, issn 0007-0920, 10 p.Article

[³H]-RS-45041-190 : a selective high-affinity radioligand for I₂ imidazoline receptorsMACKINNON, A. C; REDFERN, W. S; BROWN, C. M et al.British journal of pharmacology. 1995, Vol 116, Num 2, pp 1729-1736, issn 0007-1188Article

Affinity of 2-(tetrahydroisoquinolin-2-ylmethyl)- and 2-(isoindolin-2-ylmethyl)imidazolines for α-adrenoceptors. Differential affinity of imidazolines for the [³H]idazoxan-labeled α₂-adrenoceptor vs the [³H]yohimbine-labeled siteCLARK, R. D; BERGER, J; GARG, P et al.Journal of medicinal chemistry (Print). 1990, Vol 33, Num 2, pp 596-600, issn 0022-2623Article

Heterogeneity of α₂-adrenoceptors in rat cortex but not human platelets can be defined by 8-OH-DPAT, RU 24969 and methysergideBROWN, C. M; MACKINNON, A. C; MCGRATH, J. C et al.British journal of pharmacology. 1990, Vol 99, Num 3, pp 481-486, issn 0007-1188Article

[³H]-idazoxan binds with high affinity to two sites on hamster adipocytes: an α₂-adrenoceptor and a non-adrenoceptor siteMACKINNON, A. C; BROWN, C. M; SPEDDING, M et al.British journal of pharmacology. 1989, Vol 98, Num 4, pp 1143-1150, issn 0007-1188Article

(8aα,12aα,13aα)-5,8,8a,9,10,11,12,12a,13,13a-Decahydro-3-methoxy-12-(methylsulfonyl)-6H-isoquino[2,1-g][1,6]naphthyridine, a potent and highly selective α₂-adrenoceptor antagonistCLARK, R. D; REPKE, D. B; KILPATRICK, A. T et al.Journal of medicinal chemistry (Print). 1989, Vol 32, Num 9, pp 2034-2036, issn 0022-2623, 3 p.Article