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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
1999 2
2000 1
2001 2
2004 2
2005 5
2006 5
2007 7
2008 2
2009 9
2010 7
2011 4
2012 4
2013 4
2014 5
2015 5
2016 3
2017 4
2018 8
2019 5
2020 6
2021 8
2022 1
2023 5
2024 2
2025 2

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95 results

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Page 1
Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause.
Zhou J, Azizan EAB, Cabrera CP, Fernandes-Rosa FL, Boulkroun S, Argentesi G, Cottrell E, Amar L, Wu X, O'Toole S, Goodchild E, Marker A, Senanayake R, Garg S, Åkerström T, Backman S, Jordan S, Polubothu S, Berney DM, Gluck A, Lines KE, Thakker RV, Tuthill A, Joyce C, Kaski JP, Karet Frankl FE, Metherell LA, Teo AED, Gurnell M, Parvanta L, Drake WM, Wozniak E, Klinzing D, Kuan JL, Tiang Z, Gomez Sanchez CE, Hellman P, Foo RSY, Mein CA, Kinsler VA, Björklund P, Storr HL, Zennaro MC, Brown MJ. Zhou J, et al. Among authors: metherell la. Nat Genet. 2021 Sep;53(9):1360-1372. doi: 10.1038/s41588-021-00906-y. Epub 2021 Aug 12. Nat Genet. 2021. PMID: 34385710 Free PMC article.
Adrenal Dysfunction in Mitochondrial Diseases.
Corkery-Hayward M, Metherell LA. Corkery-Hayward M, et al. Among authors: metherell la. Int J Mol Sci. 2023 Jan 6;24(2):1126. doi: 10.3390/ijms24021126. Int J Mol Sci. 2023. PMID: 36674647 Free PMC article. Review.
Oxidative stress and adrenocortical insufficiency.
Prasad R, Kowalczyk JC, Meimaridou E, Storr HL, Metherell LA. Prasad R, et al. Among authors: metherell la. J Endocrinol. 2014 Jun;221(3):R63-73. doi: 10.1530/JOE-13-0346. Epub 2014 Mar 12. J Endocrinol. 2014. PMID: 24623797 Free PMC article. Review.
Isolated glucocorticoid deficiency: Genetic causes and animal models.
Maharaj A, Maudhoo A, Chan LF, Novoselova T, Prasad R, Metherell LA, Guasti L. Maharaj A, et al. Among authors: metherell la. J Steroid Biochem Mol Biol. 2019 May;189:73-80. doi: 10.1016/j.jsbmb.2019.02.012. Epub 2019 Feb 25. J Steroid Biochem Mol Biol. 2019. PMID: 30817990 Review.
Reassessing the role of the p.(Arg304Gln) missense AIP variant in pituitary tumorigenesis.
Loughrey PB, Mothojakan NB, Iacovazzo D, Arni A, Aflorei ED, Arnaldi G, Barlier A, Beckers A, Bizzi MF, Chanson P, Dal J, Daly AF, Dang MN, David A, Andrade MO, Else T, Elston MS, Evans A, Ferrau F, Fica S, Flanagan D, Gadelha MR, Grossman AB, Kapur S, Khoo B, Kumar AV, Kumar-Sinha C, Lechan RM, Ludman M, Metherell LA, Miljic D, Mourougavelou V, Musat M, Occhi G, Owens M, Pascanu I, Pinheiro SVB, Radian S, Ribeiro-Oliveira A, Schöfl C, Patel KA, Hernández-Ramírez LC, Korbonits M. Loughrey PB, et al. Among authors: metherell la. Eur J Endocrinol. 2025 Mar 27;192(4):385-397. doi: 10.1093/ejendo/lvaf044. Eur J Endocrinol. 2025. PMID: 40070360 Free PMC article.
ACTH resistance: genes and mechanisms.
Meimaridou E, Hughes CR, Kowalczyk J, Chan LF, Clark AJ, Metherell LA. Meimaridou E, et al. Among authors: metherell la. Endocr Dev. 2013;24:57-66. doi: 10.1159/000342504. Epub 2013 Feb 1. Endocr Dev. 2013. PMID: 23392095 Review.
The genetics of ACTH resistance syndromes.
Metherell LA, Chan LF, Clark AJ. Metherell LA, et al. Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):547-60. doi: 10.1016/j.beem.2006.09.002. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 17161331 Review.
Genetics of ACTH insensitivity syndromes.
Clark JL, Metherell LA, Naville D, Begeot M, Huebner A. Clark JL, et al. Among authors: metherell la. Ann Endocrinol (Paris). 2005 Jun;66(3):247-9. doi: 10.1016/s0003-4266(05)81757-3. Ann Endocrinol (Paris). 2005. PMID: 15988386 Review.
The genetics of familial glucocorticoid deficiency.
Clark AJ, Chan LF, Chung TT, Metherell LA. Clark AJ, et al. Among authors: metherell la. Best Pract Res Clin Endocrinol Metab. 2009 Apr;23(2):159-65. doi: 10.1016/j.beem.2008.09.006. Best Pract Res Clin Endocrinol Metab. 2009. PMID: 19500760 Review.
95 results