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Multi-omics and imaging mass cytometry characterization of human kidneys to identify pathways and phenotypes associated with impaired kidney function.

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dc.contributor.authorAsowata, Evans O.
dc.contributor.authorRomoli, Simone
dc.contributor.authorSargeant, Rebecca
dc.contributor.authorTan, Jennifer Y.
dc.contributor.authorHoffmann, Scott
dc.contributor.authorHuang, Margaret M.
dc.contributor.authorMahbubani, Krishnaa T
dc.contributor.authorKrause, Fynn N.
dc.contributor.authorJachimowicz, Daniel
dc.contributor.authorAgren, Rasmus
dc.contributor.authorKoulman, Albert
dc.contributor.authorJenkins, Benjamin J
dc.contributor.authorMusial, Barbara
dc.contributor.authorGriffin, Jules
dc.contributor.authorSoderberg, Magnus
dc.contributor.authorLing, Stephanie
dc.contributor.authorHansen, Pernille B.L.
dc.contributor.authorSaeb-Parsy, Kourosh
dc.contributor.authorWoollard, Kevin J.
dc.contributor.institutionUniversity of Aberdeen.Rowett Instituteen
dc.date.accessioned2024-07-16T13:28:00Z
dc.date.available2024-07-16T13:28:00Z
dc.date.issued2024-07-01
dc.descriptionWe are grateful to the donors, donor families, and NHS Blood and Transplant service and the Cambridge Biorepository for Translational Medicine (CBTM) for access to human samples; Karolina Nilsson (Medicinal Chemistry, AstraZeneca) for providing the cytosolic phospholipase A2 inhibitor; and Julia Lindgren (Discovery Sciences, AstraZenca) for coordinating the RNA-sequencing workflow.en
dc.description.statusPeer revieweden
dc.format.extent13
dc.format.extent5150328
dc.identifier289141512
dc.identifierd5289c80-f66e-4cc7-8c96-4cd6fcd9d2f2
dc.identifier85191300325
dc.identifier.citationAsowata, E O, Romoli, S, Sargeant, R, Tan, J Y, Hoffmann, S, Huang, M M, Mahbubani, K T, Krause, F N, Jachimowicz, D, Agren, R, Koulman, A, Jenkins, B J, Musial, B, Griffin, J, Soderberg, M, Ling, S, Hansen, P B L, Saeb-Parsy, K & Woollard, K J 2024, 'Multi-omics and imaging mass cytometry characterization of human kidneys to identify pathways and phenotypes associated with impaired kidney function.', Kidney International, vol. 106, no. 1, pp. 85-97. https://doi.org/10.1016/j.kint.2024.01.041en
dc.identifier.doi10.1016/j.kint.2024.01.041
dc.identifier.iss1en
dc.identifier.issn0085-2538
dc.identifier.otherORCID: /0000-0003-1336-7744/work/160390224
dc.identifier.urihttps://hdl.handle.net/2164/23825
dc.identifier.vol106en
dc.language.isoeng
dc.relation.ispartofKidney Internationalen
dc.subjectarachidonic aciden
dc.subjectkidney damageen
dc.subjectkidney inflammationen
dc.subjectimaging mass cytometryen
dc.subjectlipidomicsen
dc.subjectmetabolic pathwaysen
dc.subjectR Medicine (General)en
dc.subjectSupplementary Informationen
dc.subjecthttps://ars.els-cdn.com/content/image/1-s2.0-S0085253824001686-mmc1.pdfen
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dc.subjecthttps://doi.org/10.1016/j.kint.2024.01.041en
dc.subject.lccR1en
dc.titleMulti-omics and imaging mass cytometry characterization of human kidneys to identify pathways and phenotypes associated with impaired kidney function.en
dc.typeJournal articleen

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