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Cu, Fe, and Zn isotope ratios in murine Alzheimer's disease models suggest specific signatures of amyloidogenesis and tauopathy

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dc.contributor.authorSolovyev, Nikolay
dc.contributor.authorEl-Khatib, Ahmed H.
dc.contributor.authorCostas Rodríguez, Marta
dc.contributor.authorSchwab, Karima
dc.contributor.authorGriffin, Elizabeth
dc.contributor.authorRaab, Andrea
dc.contributor.authorRiedel, Bettina
dc.contributor.authorTheuring, Franz
dc.contributor.authorVogl, Jochen
dc.contributor.authorVanhaecke, Frank
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.contributor.institutionUniversity of Aberdeen.Chemistryen
dc.contributor.institutionUniversity of Aberdeen.Neuroscienceen
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.date.accessioned2021-03-31T11:55:01Z
dc.date.available2021-03-31T11:55:01Z
dc.date.issued2021-01
dc.descriptionAcknowledgments—A.H.E-K thanks Maren Koenig and Dorit Becker for their support in sample preparation. The authors thank Prof. Gernot Riedel, Dr Silke Frahm, and Mandy Magbagbeolu for help with mouse perfusion and harvesting of the brain tissues. Funding and additional information—This work was carried out in the context of the EMPIR research project 15HLT02 (ReMiND). This project has received funding from the EMPIR programme cofinanced by the Participating States and from the European Union’s Horizon 2020 research and innovation program.en
dc.description.statusPeer revieweden
dc.format.extent15
dc.format.extent1687969
dc.identifier185619514
dc.identifier28822e3b-fd4a-409b-b618-ab504c3e2b30
dc.identifier33453282
dc.identifier85102583105
dc.identifier000672866400266
dc.identifier.citationSolovyev, N, El-Khatib, A H, Costas Rodríguez, M, Schwab, K, Griffin, E, Raab, A, Riedel, B, Theuring, F, Vogl, J & Vanhaecke, F 2021, 'Cu, Fe, and Zn isotope ratios in murine Alzheimer's disease models suggest specific signatures of amyloidogenesis and tauopathy', The Journal of Biological Chemistry, vol. 296, 100292. https://doi.org/10.1016/j.jbc.2021.100292en
dc.identifier.doi10.1016/j.jbc.2021.100292
dc.identifier.issn0021-9258
dc.identifier.otherORCID: /0000-0001-7063-7136/work/96308221
dc.identifier.otherORCID: /0000-0002-7852-0749/work/88320832
dc.identifier.otherPubMedCentral: PMC7949056
dc.identifier.otherORCID: /0000-0001-7063-7136/work/96308221
dc.identifier.urihttps://hdl.handle.net/2164/16161
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85102583105&partnerID=8YFLogxKen
dc.identifier.vol296en
dc.language.isoeng
dc.relation.ispartofThe Journal of Biological Chemistryen
dc.subjectAlzheimer's diseaseen
dc.subjecttauen
dc.subjectamyloid betaen
dc.subjectcopperen
dc.subjectironen
dc.subjectzincen
dc.subjectmulticollector inductively coupled plasma-mass spectrometry (ICP-MS)en
dc.subjectbrainen
dc.subjectserumen
dc.subjectisotopic analysisen
dc.subjectQD Chemistryen
dc.subjectR Medicineen
dc.subjectMolecular Biologyen
dc.subjectBiochemistryen
dc.subjectCell Biologyen
dc.subjectEuropean Commissionen
dc.subject15HLT02en
dc.subjectSupplementary Informationen
dc.subject.lccQDen
dc.subject.lccRen
dc.titleCu, Fe, and Zn isotope ratios in murine Alzheimer's disease models suggest specific signatures of amyloidogenesis and tauopathyen
dc.typeJournal articleen

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