Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome and IL2RA[original query] |
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Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Human immunology 2012 Jul 73 (7): 740-6. Fourati Hajer, Bouzid Dorra, Abida Olfa, Kharrat Najla, Mnif Fatma, Haddouk Samy, Fesel Constantin, Costa João, Ben Ayed Mourad, Abid Mohamed, Rebai Ahmed, Penha-Gonçalves Carlos, Masmoudi Hat |
Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome. Gut 2014 Jul 63 (7): 1103-11. Wouters Mira M, Lambrechts Diether, Knapp Michael, Cleynen Isabelle, Whorwell Peter, Agréus Lars, Dlugosz Aldona, Schmidt Peter Thelin, Halfvarson Jonas, Simrén Magnus, Ohlsson Bodil, Karling Pontus, Van Wanrooy Sander, Mondelaers Stéphanie, Vermeire Severine, Lindberg Greger, Spiller Robin, Dukes George, D'Amato Mauro, Boeckxstaens G |
Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182. Journal of molecular medicine (Berlin, Germany) 2014 Sep 92 (9): 961-7. Yu Hongsong, Liu Yunjia, Bai Lin, Kijlstra Aize, Yang Peize |
Chromosomal Numerical Aberrations and Rare Copy Number Variation in Patients with Inflammatory Bowel Disease. Journal of Crohn's & colitis 2022 Jul . Dirvanskyte Paulina, Gurram Bhaskar, Bolton Chrissy, Warner Neil, Jones Kelsey D J, Griffin Helen R, , Park Jason Y, Keller Klaus-Michael, Gilmour Kimberly C, Hambleton Sophie, Muise Aleixo M, Wysocki Christian, Uhlig Holm |
Prediction of Tacrolimus Dose/Weight-Adjusted Trough Concentration in Pediatric Refractory Nephrotic Syndrome: A Machine Learning Approach. Pharmacogenomics and personalized medicine 2022 3 15 143-155. Mo Xiaolan, Chen Xiujuan, Wang Xianggui, Zhong Xiaoli, Liang Huiying, Wei Yuanyi, Deng Houliang, Hu Rong, Zhang Tao, Chen Yilu, Gao Xia, Huang Min, Li Jia |
An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population. BMC medical genomics 2022 Oct 15 (1): 208. Qiao Yimeng, Wang Yangong, Xu Yiran, Zhang Jin, Su Yu, Cheng Ye, Bi Dan, Song Juan, Xia Lei, Li Ming, Zhang Xiaoli, Zhu Dengna, Wang Ting, Ding Jian, Wang Xiaoyang, Zhu Changlian, Xing Qing |
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