[HTML][HTML] Clinical development of new drug–radiotherapy combinations

…, MD Forster, J Golec, RM Hagan… - Nature reviews Clinical …, 2016 - nature.com
In countries with the best cancer outcomes, approximately 60% of patients receive radiotherapy
as part of their treatment, which is one of the most cost-effective cancer treatments. …

Lamotrigine inhibits monoamine uptake in vitro and modulates 5-hydroxytryptamine uptake in rats

E Southam, D Kirkby, GA Higgins, RM Hagan - European journal of …, 1998 - Elsevier
Lamotrigine is a novel anticonvulsant drug which also stabilises mood in bipolar illness via
an unknown mechanism. We report the concentration-dependent inhibition of 5-…

Effects of lamotrigine and levetiracetam on seizure development in a rat amygdala kindling model

SC Stratton, CH Large, B Cox, G Davies, RM Hagan - Epilepsy research, 2003 - Elsevier
In kindling models of epilepsy, the period during which repeated stimulation evokes intensifying
seizures is attributed to an underlying epileptogenic process, and the point at which …

GR196429: a nonindolic agonist at high-affinity melatonin receptors

…, PC North, ML Dubocovich, RM Hagan - … of Pharmacology and …, 1998 - ASPET
N-[2-[2,3,7,8-tetrahydro-1H-furo(2,3-g)indol-1-yl]ethyl]acetamide (GR196429) is a novel,
nonindolic melatonin receptor agonist. GR196429 had high affinity for human mt 1 (pK i 9.9) …

5-HT3 and 5-HT4 receptors in terminal regions of the mesolimbic system

GJ Kilpatrick, RM Hagan, JD Gale - Behavioural brain research, 1995 - Elsevier
In this brief review, we present the evidence for the regulation of the mesolimbic dopamine
system by 5-HT 3 and 5-HT 4 receptors. A range of studies show good evidence that 5-HT 3 …

Highly potent and selective heptapeptide antagonists of the neurokinin NK-2 receptor

…, SP Clegg, MJ Deal, GB Ewan, RM Hagan… - Journal of medicinal …, 1992 - ACS Publications
Incorporation of D-Pro9 into substance P related peptides is known to enhance neurokinin
NK-2 receptor agonist potency and selectivity with respect to other neurokinin receptors. We …

GR159897, a potent non-peptide antagonist at tachykinin NK2 receptors

…, AB Hawcock, RA Coleman, RM Hagan… - European journal of …, 1995 - Elsevier
GR159897 ((R)-1-[2-(5-fluoro-1H-indol-3-yl)ethyl]-4-methoxy-4-[(phenylsulfinyl)methyl]piperidine)
is a novel, highly potent and selective non-peptide antagonist at tachykinin NK 2 …

Conformationally constrained tachykinin analogs: potent and highly selective neurokinin NK-2 receptor agonists

MJ Deal, RM Hagan, SJ Ireland… - Journal of medicinal …, 1992 - ACS Publications
The design and synthesis of potent and selective neurokinin NK-2 receptor agonists 12 (GR64349)
and 31 are described, together with structure-activity relationships for related …

Neurokinin agonists differentially affect A9 and A10 dopamine cells in the rat

P Overton, PJ Elliott, RM Hagan, D Clark - European journal of …, 1992 - Elsevier
The effect of selective neurokinin (NK) receptor agonists on the activity of A9 and A10 dopamine
cells was assessed using extracellular recording. A higher proportion of A10 cells which …

Development of tolerance in mice to the sedative effects of the neuroactive steroid minaxolone following chronic exposure

…, E Ford, SP Worton, NR Oakley, RM Hagan - Pharmacology …, 1997 - Elsevier
Minaxolone is a potent ligand for the neurosteroid binding site of the GABA A receptor. In
radioligand binding studies to rat brain membranes, minaxolone caused a 69% increase in [ 3 …