HuGE Literature Finder
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| Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism. Endocrine 2022 9 79 (1): 125-134. Li Liangshan, Li Xiaole, Wang Xiaoyu, Han Mengmeng, Zhao Dehua, Wang Fang, Liu Shig |
| Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. Journal of endocrinological investigation 2021 Nov . Acar S, Gürsoy S, Arslan G, Nalbanto?lu Ö, Hazan F, Köprülü Ö, Özkaya B, Özkan |
| Moderating Role of TSHR and PTPN22 Gene Polymorphisms in Effects of Excessive Fluoride on Thyroid: a School-Based Cross-Sectional Study. Biological trace element research 2021 May . Wang Yang, Cui Yushan, Zhang Dandan, Chen Chen, Hou Changchun, Cao Lich |
| Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort. Frontiers in endocrinology 2021 9 12 705773. Long Wei, Guo Fang, Yao Ruen, Wang Ying, Wang Huaiyan, Yu Bin, Xue Pe |
| Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis. Frontiers in endocrinology 2021 7 12 657913. Oliver-Petit Isabelle, Edouard Thomas, Jacques Virginie, Bournez Marie, Cartault Audrey, Grunenwald Solange, Savagner Frédériq |
| Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism. Molecular biology reports 2020 Sep . Kollati Yedukondalu, Akella Radha Rama Devi, Naushad Shaik Mohammad, Borkar Divya, Thalla Maunika, Nagalingam Swapna, Lingappa Lokesh, Patel Rajesh K, Reddy G Bhanuprakash, Dirisala Vijaya |
| 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 |
| Is the TSHR D727E polymorphism a genetic predisposition for multinodular goiter in the Turkish population? Genetics and molecular research : GMR 2016 15 (3): . Gözü H I, Özçelik S, Alo?lu M, ?ahin A, Temiz S, Dayan A, Cengiz H, Tütüncü Y, Bircan |
| The association between development and progression of multinodular goiter and thyroid-stimulating hormone receptor gene D727E and P52T polymorphisms. Genetic testing and molecular biomarkers 2013 Feb 17 (2): 109-14. Bayram Banu, Sonmez Resit, Bozari Sedat, Onlu Harun, Turkoglu Züleyha, Mutlu Fezan Sah |
| The Impact of the D727E Polymorphism has no Significant Role in Multi Nodular Goiter. Balkan journal of medical genetics : BJMG 2012 Dec 15 (2): 67-72. Tug E, Sengül N, Aydin H, Yilmaz |
| Study on the relationship between TSHR gene and thyroid diseases. Cell biochemistry and biophysics 2011 Nov 61 (2): 377-82. Shao Li, Jiang Hua, Liang Jun, Niu Xianping, Teng Lili, Zhang H |
| Mutations of GNAS and TSHR genes in subclinical toxic multinodular goiter. The Annals of otology, rhinology, and laryngology 2010 Feb 119 (2): 118-24. Liu Chunbo, Wu Changjun, Wang Fengjun, Zhou M |
| United detection GNAS and TSHR mutations in subclinical toxic multinodular goiter. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2010 Feb 267 (2): 281-7. Liu Chunbo, Yang Jingyuan, Wang Fengjun, Wu Changjun, Zhou M |
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