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dc.contributor.authorChapple, J. Paul
dc.contributor.authorMetherell, Louise A.
dc.contributor.authorBanerjee, Ritwik
dc.contributor.authorKing, Peter J.
dc.contributor.authorClark, Adrian J. L.
dc.contributor.authorSaka, H. Nurcin
dc.contributor.authorMeimaridou, Eirini
dc.contributor.authorKowalczyk, Julia
dc.contributor.authorGuasti, Leonardo
dc.contributor.authorHughes, Claire R.
dc.contributor.authorWagner, Florian
dc.contributor.authorFrommolt, Peter
dc.contributor.authorNuernberg, Peter
dc.contributor.authorMann, Nicholas P.
dc.date.accessioned2021-03-03T17:44:11Z
dc.date.available2021-03-03T17:44:11Z
dc.date.issued2012
dc.identifier.citationMeimaridou E., Kowalczyk J., Guasti L., Hughes C. R. , Wagner F., Frommolt P., Nuernberg P., Mann N. P. , Banerjee R., Saka H. N. , et al., "Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency", NATURE GENETICS, cilt.44, sa.7, ss.740-742, 2012
dc.identifier.issn1061-4036
dc.identifier.othervv_1032021
dc.identifier.otherav_4b27fc33-7194-454d-ac5b-32e22e3faef0
dc.identifier.urihttp://hdl.handle.net/20.500.12627/53982
dc.identifier.urihttps://doi.org/10.1038/ng.2299
dc.description.abstractUsing targeted exome sequencing, we identified mutations in NNT, an antioxidant defense gene, in individuals with familial glucocorticoid deficiency. In mice with Nnt loss, higher levels of adrenocortical cell apoptosis and impaired glucocorticoid production were observed. NNT knockdown in a human adrenocortical cell line resulted in impaired redox potential and increased reactive oxygen species (ROS) levels. Our results suggest that NNT may have a role in ROS detoxification in human adrenal glands.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectYaşam Bilimleri
dc.titleMutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency
dc.typeMakale
dc.relation.journalNATURE GENETICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume44
dc.identifier.issue7
dc.identifier.startpage740
dc.identifier.endpage742
dc.contributor.firstauthorID204991


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