HuGE Literature Finder
Records 1 - 13
| 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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