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dc.contributor.authorHay, Colin
dc.contributor.authorShanley, Lynne
dc.contributor.authorDavidson, Scott
dc.contributor.authorCowie, Philip
dc.contributor.authorLear, Marissa
dc.contributor.authorMcGuffin, Peter
dc.contributor.authorRiedel, Gernot
dc.contributor.authorMcEwan, Iain J
dc.contributor.authorMacKenzie, Alasdair
dc.date.accessioned2014-09-10T08:57:01Z
dc.date.available2014-09-10T08:57:01Z
dc.date.issued2014-09
dc.identifier36828125
dc.identifier1927b944-14c8-4f58-bd0c-df48c6713e86
dc.identifier84903700487
dc.identifier.citationHay , C , Shanley , L , Davidson , S , Cowie , P , Lear , M , McGuffin , P , Riedel , G , McEwan , I J & MacKenzie , A 2014 , ' Functional effects of polymorphisms on glucocorticoid receptor modulation of human anxiogenic substance-P gene promoter activity in primary amygdala neurones ' , Psychoneuroendocrinology , vol. 47 , pp. 43-55 . https://doi.org/10.1016/j.psyneuen.2014.04.017en
dc.identifier.issn0306-4530
dc.identifier.urihttp://hdl.handle.net/2164/3470
dc.descriptionThis work was funded by The BBSRC (BB/D004659/1) the Wellcome Trust (080980/Z/06/Z) and the Medical Research Council (G0701003). Colin Hay was funded by the Chief Scientist Office, Scotland. Scott Davidson was funded by a BBSRC strategic studentship (BBS/S/2005/12001). Philip Cowie was funded by the Scottish Universities Life Sciences Alliance (SULCA).en
dc.format.extent13
dc.format.extent2329769
dc.language.isoeng
dc.relation.ispartofPsychoneuroendocrinologyen
dc.subjectTAC1 promoteren
dc.subjectglucocorticoid receptoren
dc.subjectgene regulationen
dc.subjectsingle nucleotide polymorphismen
dc.subjectstress and anxietyen
dc.subjectRC0321 Neuroscience. Biological psychiatry. Neuropsychiatryen
dc.subjectBiotechnology and Biological Sciences Research Council (BBSRC)en
dc.subjectBB/D004659/1en
dc.subjectBBS/S/2005/12001en
dc.subjectWellcome Trusten
dc.subject080980/Z/06/Zen
dc.subjectMedical Research Council (MRC)en
dc.subjectG0701003en
dc.subject.lccRC0321en
dc.titleFunctional effects of polymorphisms on glucocorticoid receptor modulation of human anxiogenic substance-P gene promoter activity in primary amygdala neuronesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.description.statusPeer revieweden
dc.identifier.doi10.1016/j.psyneuen.2014.04.017


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