Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and NR3C2[original query] |
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| Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1. European journal of endocrinology / European Federation of Endocrine Societies 2007 Feb 156 (2): 249-56. Balsamo Antonio, Cicognani Alessandro, Gennari Monia, Sippell Wolfgang G, Menabò Soara, Baronio Federico, Riepe Felix |
| NTM and NR3C2 polymorphisms influencing intelligence: family-based association studies. Progress in neuro-psychopharmacology & biological psychiatry 2011 Jan 35 (1): 154-60. Pan Yue, Wang Ke-Sheng, Aragam Nage |
| SNPs in microRNA binding sites in 3'-UTRs of RAAS genes influence arterial blood pressure and risk of myocardial infarction. American journal of hypertension 2011 Sep 24 (9): 999-1006. Nossent A Yaël, Hansen Jakob L, Doggen Carine, Quax Paul H A, Sheikh Søren P, Rosendaal Frits |
| Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation research 2012 Nov . Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freeman BI, Coresh J, Kao LW, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A |
| Intermediary quantitative traits--an alternative in the identification of disease genes in asthma? Genes and immunity 2014 Jan 15 (1): 1-7. Sargurupremraj M, Pukelsheim K, Hofer T, Wjst |
| Hidden risk genes with high-order intragenic epistasis in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2014 41 (4): 1039-56. Sun Jiya, Song Fuhai, Wang Jiajia, Han Guangchun, Bai Zhouxian, Xie Bin, Feng Xuemei, Jia Jianping, Duan Yong, Lei Hongxi |
| Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies. Journal of human hypertension 2017 Apr . Ji L-D, Li J-Y, Yao B-B, Cai X-B, Shen Q-J, Xu |
| Association of a Haplotype in the NR3C2 Gene, Encoding the Mineralocorticoid Receptor, With Chronic Central Serous Chorioretinopathy. JAMA ophthalmology 2017 Mar . van Dijk Elon H C, Schellevis Rosa L, van Bergen Maaike G J M, Breukink Myrte B, Altay Lebriz, Scholz Paula, Fauser Sascha, Meijer Onno C, Hoyng Carel B, den Hollander Anneke I, Boon Camiel J F, de Jong Eiko |
| A Dynamic Transcription Factor Signature Along the Colorectal Adenoma-Carcinoma Sequence in Patients With Co-Occurrent Adenoma and Carcinoma. Frontiers in oncology 2021 6 11 597447. Pan Zongfu, He Ying, Zhu Wenjuan, Xu Tong, Hu Xiaoping, Huang Pi |
| Associations of Single-Nucleotide Polymorphisms in Slovenian Patients with Acute Central Serous Chorioretinopathy. Genes 2021 12 13 (1): . Kiraly Peter, Zupan Andrej, Matjaši? Alenka, Mekjavi? Polona Ja |
| The expression of glucocorticoid and mineralocorticoid receptors in pituitary tumors causing Cushing's disease and silent corticotroph tumors. Frontiers in endocrinology 2023 4 14 1124646. Kober Paulina, Rusetska Natalia, Mossakowska Beata J, Maksymowicz Maria, P?kul Monika, Zieli?ski Grzegorz, Styk Andrzej, Kunicki Jacek, Dzia?ach ?ukasz, Witek Przemys?aw, Bujko Mateu |
| Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases. Scientific reports 2023 10 13 (1): 16769. Ishani Mhatre, Habiba Abdelhalim, William Degroat, Shreya Ashok, Bruce T Liang, Zeeshan Ahm |
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