Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Hyperthyroidism and TSHR[original query] |
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| Shared sporadic and somatic thyrotropin receptor mutations display more active in vitro activities than familial thyrotropin receptor mutations. Thyroid : official journal of the American Thyroid Association 2010 12 21 (3): 221-9. Lueblinghoff Julia, Eszlinger Markus, Jaeschke Holger, Mueller Sandra, Bircan Rifat, Gozu Hulya, Sancak Seda, Akalin Sema, Paschke Ra |
A genome-wide association study identifies two new risk loci for Graves' disease.
Nature genetics 2011 Sep 43 (9): 897-901. Chu Xun, Pan Chun-Ming, Zhao Shuang-Xia, Liang Jun, Gao Guan-Qi, Zhang Xiao-Mei, Yuan Guo-Yue, Li Chang-Gui, Xue Li-Qiong, Shen Min, Liu Wei, Xie Fang, Yang Shao-Ying, Wang Hai-Feng, Shi Jing-Yi, Sun Wei-Wei, Du Wen-Hua, Zuo Chun-Lin, Shi Jin-Xiu, Liu Bing-Li, Guo Cui-Cui, Zhan Ming, Gu Zhao-Hui, Zhang Xiao-Na, Sun Fei, Wang Zhi-Quan, Song Zhi-Yi, Zou Cai-Yan, Sun Wei-Hua, Guo Ting, Cao Huang-Ming, Ma Jun-Hua, Han Bing, Li Ping, Jiang He, Huang Qiu-Hua, Liang Liming, Liu Li-Bin, Chen Gang, Su Qing, Peng Yong-De, Zhao Jia-Jun, Ning Guang, Chen Zhu, Chen Jia-Lun, Chen Sai-Juan, Huang Wei, Song Huai-Dong, |
| Association between polymorphisms in the TSHR gene and Graves' orbitopathy. PloS one 2014 9 (7): e102653. Jurecka-Lubieniecka Beata, Ploski Rafal, Kula Dorota, Szymanski Konrad, Bednarczuk Tomasz, Ambroziak Urszula, Hasse-Lazar Kornelia, Hyla-Klekot Lidia, Tukiendorf Andrzej, Kolosza Zofia, Jarzab Barba |
| Association of Human Leukocyte Antigens Class I and II with Graves' Disease in Iranian Population. Iranian journal of immunology : IJI 2017 Sep 14 (3): 223-230. Mehraji Zahra, Farazmand Ali, Esteghamati Alireza, Noshad Sina, Sadr Maryam, Amirzargar Somayeh, Yekaninejad Mir Saeed, Amirzargar Aliakb |
| Cancer risk and clinicopathological characteristics of thyroid nodules harboring thyroid-stimulating hormone receptor gene mutations. Diagnostic cytopathology 2018 Mar . Mon Sann Y, Riedlinger Gregory, Abbott Collette E, Seethala Raja, Ohori N Paul, Nikiforova Marina N, Nikiforov Yuri E, Hodak Steven |
| Utility of systematic TSHR gene testing in adults with hyperthyroidism lacking overt autoimmunity and diffuse uptake on thyroid scintigraphy. Clinical endocrinology 2019 Feb 90 (2): 328-333. Patel Kashyap A, Knight Bridget, Aziz Aftab, Babiker Tarig, Tamar Avades, Findlay Joanna, Cox Sue, Dimitropoulos Ioannis, Tysoe Carolyn, Panicker Vijay, Vaidya Bij |
| Clinical Significance of Thyroid-Stimulating Hormone Receptor Gene Mutations and/or Sodium-Iodine Symporter Gene Overexpression in Indeterminate Thyroid Fine Needle Biopsies. Frontiers in endocrinology 2018 10 9 566. Guan Haixia, Matonis Danielle, Toraldo Gianluca, Lee Stephanie |
| Association of TSHR gene single nucleotide intronic polymorphism with the risk of hypothyroid and hyperthyroid disorders in Yazd province. Scientific reports 2022 9 12 (1): 15745. Naghibi Fahime Sadat, Miresmaeili Seyed Mohsen, Javid Aman |
| Transcriptomic analysis reveals a critical role for activating G? mutations in spontaneous feline hyperthyroidism. Scientific reports 2024 11 14 (1): 28749. Thomas K Hiron, Joana Aguiar, Jonathan M Williams, Sara Falcone, Paul A Norman, Jonathan Elliott, Robert C Fowkes, Harriet M Syme, Lucy J Davis |
| Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T knock-in model. JCI insight 2024 1 . Kristiina Makkonen, Meeri Jännäri, Luís Crisóstomo, Matilda Kuusi, Konrad Patyra, Vladyslav Melnyk, Veli M Linnossuo, Johanna O Ojala, Rowmika Ravi, Christoffer Löf, Juho-Antti Mäkelä, Päivi J Miettinen, Saila Laakso, Marja Ojaniemi, Jarmo Jääskeläinen, Markku Laakso, Filip Bossowski, Beata Sawicka, Karolina Sto?ek, Artur Bossowski, Gunnar Kleinau, Patrick Scheerer, Finngen Finngen, Mary Pat Reeve, Jukka Ke |
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