Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and NR3C2[original query] |
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Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008 Jun 51 (6): 1658-64. Tobin Martin D, Tomaszewski Maciej, Braund Peter S, Hajat Cother, Raleigh Stuart M, Palmer Thomas M, Caulfield Mark, Burton Paul R, Samani Nilesh |
Inefficient arterial hypertension control in patients with metabolic syndrome and its link to renin-angiotensin-aldosterone system polymorphisms. Hypertension research : official journal of the Japanese Society of Hypertension 2011 Jun 34 (6): 758-66. Morales-Suárez-Varela Maria M, Mansego Maria L, Vicedo-Cabrera Ana M, Pineda-Alonso Monica, Llopis-González Aqustin, Martin-Moreno Jose M, Martín-Escudero Juan C, Chaves F |
Common genetic variants in the glucocorticoid receptor and the 11ß-hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing's syndrome in remission. The Journal of clinical endocrinology and metabolism 2014 Sep 99 (9): E1803-7. Ragnarsson Oskar, Glad Camilla A M, Berglund Peter, Bergthorsdottir Ragnhildur, Eder Derek N, Johannsson Gudmund |
Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients. Journal of hypertension 2017 Sep . Liu Kai, Qin Fang, Sun Xiaolu, Zhang Yang, Wang Jizheng, Wu Yajie, Ma Wenjun, Wang Wei, Wu Xueyi, Qin Ying, Zhang Huimin, Zhou Xianliang, Wu Haiying, Hui Rutai, Zou Yubao, Jiang Xiongjing, Song L |
The mineralocorticoid receptor gene (NR3C2) is linked to and associated with polycystic ovarian syndrome in Italian families. European review for medical and pharmacological sciences 2023 2 27 (3): 942-948. Amin M, Perrelli M, Wu R, Gragnoli |
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