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dc.contributor.authorCondliffe, Daniel
dc.contributor.authorWong, A
dc.contributor.authorTroakes, C
dc.contributor.authorProitsi, P
dc.contributor.authorPatel, Y
dc.contributor.authorChouliaras, L
dc.contributor.authorFernandes, C
dc.contributor.authorCooper, J
dc.contributor.authorLovestone, Simon
dc.contributor.authorSchalkwyk, Leonard
dc.contributor.authorMill, J
dc.contributor.authorLunnon, Katie
dc.date.accessioned2016-02-11T09:54:47Z
dc.date.issued2014-02-06
dc.description.abstractEpigenetic processes play a key role in the central nervous system and altered levels of 5-methylcytosine have been associated with a number of neurologic phenotypes, including Alzheimer's disease (AD). Recently, 3 additional cytosine modifications have been identified (5-hydroxymethylcytosine, 5-formylcytosine, and 5-carboxylcytosine), which are thought to be intermediate steps in the demethylation of 5-methylcytosine to unmodified cytosine. Little is known about the frequency of these modifications in the human brain during health or disease. In this study, we used immunofluorescence to confirm the presence of each modification in human brain and investigate their cross-tissue abundance in AD patients and elderly control samples. We identify a significant AD-associated decrease in global 5-hydroxymethylcytosine in entorhinal cortex and cerebellum, and differences in 5-formylcytosine levels between brain regions. Our study further implicates a role for epigenetic alterations in AD.en_GB
dc.description.sponsorshipUS National Institutes of Health (NIH)en_GB
dc.identifier.citationNeurobiology of Aging, 2014, Vol. 35, Issue 8, pp. 1850 - 1854en_GB
dc.identifier.doi10.1016/j.neurobiolaging.2014.02.002
dc.identifier.grantnumberAG036039en_GB
dc.identifier.otherS0197-4580(14)00175-4
dc.identifier.urihttp://hdl.handle.net/10871/19697
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/24679604en_GB
dc.rights© 2014. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dc.subject5-caCen_GB
dc.subject5-carboxylcytosineen_GB
dc.subject5-fCen_GB
dc.subject5-formylcytosineen_GB
dc.subject5-hmCen_GB
dc.subject5-hydroxymethylcytosineen_GB
dc.subject5-mCen_GB
dc.subject5-methylcytosineen_GB
dc.subjectAlzheimer's diseaseen_GB
dc.subjectBrainen_GB
dc.subjectDNA methylationen_GB
dc.subjectEpigeneticsen_GB
dc.subjectAgeden_GB
dc.subjectAged, 80 and overen_GB
dc.subjectAlzheimer Diseaseen_GB
dc.subjectBrainen_GB
dc.subjectCytosineen_GB
dc.subjectEpigenesis, Geneticen_GB
dc.subjectFemaleen_GB
dc.subjectFluorescent Antibody Techniqueen_GB
dc.subjectHumansen_GB
dc.subjectIvermectinen_GB
dc.subjectMaleen_GB
dc.subjectMethylationen_GB
dc.titleCross-region reduction in 5-hydroxymethylcytosine in Alzheimer's disease brain.en_GB
dc.typeArticleen_GB
dc.date.available2016-02-11T09:54:47Z
dc.identifier.issn0197-4580
exeter.place-of-publicationUnited States
dc.descriptionPublisheden_GB
dc.descriptionJournal Articleen_GB
dc.descriptionResearch Support, N.I.H., Extramuralen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.identifier.journalNeurobiology of Agingen_GB


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