| First Author | Meimaridou E | Year | 2012 |
| Journal | Nat Genet | Volume | 44 |
| Issue | 7 | Pages | 740-2 |
| PubMed ID | 22634753 | Mgi Jnum | J:185986 |
| Mgi Id | MGI:5430703 | Doi | 10.1038/ng.2299 |
| Citation | Meimaridou E, et al. (2012) Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency. Nat Genet 44(7):740-2 |
| abstractText | Using 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. |
