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dc.contributor.authorMartin, H L
dc.contributor.authorMounsey, R B
dc.contributor.authorSathe, K
dc.contributor.authorMustafa, S
dc.contributor.authorNelson, M C
dc.contributor.authorEvans, R M
dc.contributor.authorTeismann, P
dc.date.accessioned2014-09-05T11:29:02Z
dc.date.available2014-09-05T11:29:02Z
dc.date.issued2013-06-14
dc.identifier40156703
dc.identifier2b043bb0-65db-47f0-b829-d9b85c5606e9
dc.identifier23500098
dc.identifier84876383781
dc.identifier.citationMartin , H L , Mounsey , R B , Sathe , K , Mustafa , S , Nelson , M C , Evans , R M & Teismann , P 2013 , ' A peroxisome proliferator-activated receptor-δ agonist provides neuroprotection in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease ' , Neuroscience , vol. 240 , pp. 191-203 . https://doi.org/10.1016/j.neuroscience.2013.02.058en
dc.identifier.issn0306-4522
dc.identifier.urihttp://hdl.handle.net/2164/3441
dc.descriptionCopyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.en
dc.format.extent13
dc.format.extent3160294
dc.language.isoeng
dc.relation.ispartofNeuroscienceen
dc.subject3,4-dihydroxyphenylacetic Aciden
dc.subjectanimalsen
dc.subjectcell counten
dc.subjectcells, cultureden
dc.subjectdisease models, animalen
dc.subjectdopamineen
dc.subjectdose-response relationship, drugen
dc.subjectfemaleen
dc.subjectglial fibrillary acidic proteinen
dc.subjecthumansen
dc.subjectmacrophage-1 antigenen
dc.subjectmaleen
dc.subjectmiceen
dc.subjectmice, inbred C57BLen
dc.subjectmice, transgenicen
dc.subjectneuroprotective agentsen
dc.subjectPPAR deltaen
dc.subjectParkinsonian disordersen
dc.subjectratsen
dc.subjectsulfonesen
dc.subjectthiazolesen
dc.subjectthiophenesen
dc.subjecttyrosine 3-monooxygenaseen
dc.subjectRC0321 Neuroscience. Biological psychiatry. Neuropsychiatryen
dc.subject.lccRC0321en
dc.titleA peroxisome proliferator-activated receptor-δ agonist provides neuroprotection in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's diseaseen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.description.statusPeer revieweden
dc.identifier.doi10.1016/j.neuroscience.2013.02.058


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