Pituitary adenomas

[1]. Andrew V Uzilov, et al. Identification of a novel RASD1 somatic mutation in a USP8-mutated corticotroph adenoma. Cold Spring Harb Mol Case Stud. 2017 May;3(3):a001602. [Content Brief]

[2]. E A Williamson, et al. G-protein mutations in human pituitary adrenocorticotrophic hormone-secreting adenomas. Eur J Clin Invest. 1995 Feb;25(2):128-31. [Content Brief]

[3]. Francisca Caimari, et al. Novel Genetic Causes of Pituitary Adenomas. Clin Cancer Res. 2016 Oct 15;22(20):5030-5042. [Content Brief]

[4]. Giampaolo Trivellin, et al. Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation. N Engl J Med. 2014 Dec 18;371(25):2363-74. [Content Brief]

[5]. L S Kirschner, et al. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet. 2000 Sep;26(1):89-92. [Content Brief]

[6]. M A Tichomirowa, et al. Familial pituitary adenomas. J Intern Med. 2009 Jul;266(1):5-18. [Content Brief]

[7]. Martin Reincke, et al. Mutations in the deubiquitinase gene USP8 cause Cushing's disease. Nat Genet. 2015 Jan;47(1):31-8. [Content Brief]

[8]. Natalia S Pellegata, et al. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci U S A. 2006 Oct 17;103(42):15558-63. [Content Brief]

[9]. Outi Vierimaa, et al. Pituitary adenoma predisposition caused by germline mutations in the AIP gene. Science. 2006 May 26;312(5777):1228-30. [Content Brief]

[10]. Qi Xiong, et al. Gene mutations in Cushing's disease. Biomed Rep. 2016 Sep;5(3):277-282. [Content Brief]

[11]. Qilin Zhang, et al. Germline Mutations in CDH23, Encoding Cadherin-Related 23, Are Associated with Both Familial and Sporadic Pituitary Adenomas. Am J Hum Genet. 2017 May 4;100(5):817-823. [Content Brief]

[12]. S C Chandrasekharappa, et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science. 1997 Apr 18;276(5311):404-7. [Content Brief]