Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Adenoma and CYP11B1[original query] |
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Polymorphic differences from normal in the aldosterone synthase gene (CYP11B2) in patients with primary hyperaldosteronism and adrenal tumour (Conn's syndrome). Clinical endocrinology 2001 Jun 54 (6): 725-30. Inglis G C, Plouin P F, Friel E C, Davies E, Fraser R, Connell J |
Polymorphisms in CYP11B2 and CYP11B1 genes associated with primary hyperaldosteronism. Hypertension research : official journal of the Japanese Society of Hypertension 2010 May 33 (5): 478-84. Zhang Guo-xi, Wang Bao-jun, Ouyang Jin-zhi, Deng Xi-yuan, Ma Xin, Li Hong-zhao, Wu Zhun, Liu Shuang-lin, Xu Hua, Zhang |
Somatic mutations in the KCNJ5 gene raise the lateralization index: implications for the diagnosis of primary aldosteronism by adrenal vein sampling. The Journal of clinical endocrinology and metabolism 2012 Dec 97 (12): E2307-13. Seccia Teresa M, Mantero Franco, Letizia Claudio, Kuppusamy Maniselvan, Caroccia Brasilina, Barisa Marlena, Cicala Maria Verena, Miotto Diego, Rossi Gian Pao |
A polymorphism in the CYP17A1 gene influences the therapeutic response to steroidogenesis inhibitors in Cushing's syndrome. Clinical endocrinology 2017 Jun . Valassi Elena, Aulinas Anna, Glad Camilla Am, Johannsson Gudmundur, Ragnarsson Oskar, Webb Susan |
Aldosterone Suppression by Dexamethasone in Patients With KCNJ5-Mutated Aldosterone-Producing Adenoma. The Journal of clinical endocrinology and metabolism 2018 7 103 (9): 3477-3485. Inoue Kosuke, Yamazaki Yuto, Kitamoto Takumi, Hirose Rei, Saito Jun, Omura Masao, Sasano Hironobu, Nishikawa Tets |
Exploration of KCNJ5 Somatic Mutation and CYP11B1/CYP11B2 Staining in Multiple Nodules in Primary Aldosteronism. Frontiers in medicine 2022 9 823065. Xie Jing, Zhang Cui, Wang Xuefeng, Jiang Yiran, Wu Luming, Ye Lei, Wang Xuan, Xie Wen, Xu Haimin, Wang Weiqi |
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- Page last updated:Apr 16, 2024
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