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dc.contributor.authorSchroth, Jen_US
dc.contributor.authorHenson, SMen_US
dc.date.accessioned2020-11-11T08:30:20Z
dc.date.available2020-10-14en_US
dc.date.issued2020-10-16en_US
dc.identifier.issn2084-6835en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68158
dc.description.abstractWe review here the seminal findings of Desdin-Mico et al. showing that T cells with dysfunctional mitochondria induce multimorbity and premature senescence, due to mitochondrial transcription factor A (TFAM). They add further weight to the idea that targeting immunometabolism could be beneficial in combating the detrimental effects of age-related disease.en_US
dc.format.extente200035 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofImmunometabolismen_US
dc.subjectT cellen_US
dc.subjectageingen_US
dc.subjectmetabolismen_US
dc.subjectmitochondriaen_US
dc.subjectsenescenceen_US
dc.titleMitochondrial Dysfunction Accelerates Ageing.en_US
dc.typeArticle
dc.identifier.doi10.20900/immunometab20200035en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33101729en_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume2en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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