Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 70 Records) |
Query Trace: Hypothyroidism and TPO[original query] |
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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 |
Association of Thyroid Peroxidase Gene Polymorphisms and Serum Anti- TPO Levels in Egyptian Patients with Autoimmune Hypothyroidism. Endocrine, metabolic & immune disorders drug targets 2020 Jul . Ahmed Hanan S, Nsrallah Ayman A M, Abdel-Fatah Azza H, Mahmoud Amira A, Fikry Abeer |
Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism. Journal of pediatric endocrinology & metabolism : JPEM 2020 May . Tanaka Tatsushi, Aoyama Kohei, Suzuki Atsushi, Saitoh Shinji, Mizuno Har |
Mutation spectrum analysis of 29 causative genes in 43 Chinese patients with congenital hypothyroidism. Molecular medicine reports 2020 Apr . Wang Huijuan, Kong Xiaohong, Pei Yanrui, Cui Xuemei, Zhu Yijie, He Zixuan, Wang Yanxia, Zhang Lirong, Zhuo Lixia, Chen Chao, Yan Xiao |
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism. Molecular and cellular endocrinology 2020 2 506 110761. Zhang Rui-Jia, Sun Feng, Chen Feng, Fang Ya, Yan Chen-Yan, Zhang Chang-Run, Ying Ying-Xia, Wang Zheng, Zhang Cao-Xu, Wu Feng-Yao, Han Bing, Liang Jun, Zhao Shuang-Xia, Song Huai-Do |
DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients. Endocrine connections 2020 12 9 (11): 1121-1134. Sorapipatcharoen Kinnaree, Tim-Aroon Thipwimol, Mahachoklertwattana Pat, Chantratita Wasun, Iemwimangsa Nareenart, Sensorn Insee, Panthan Bhakbhoom, Jiaranai Poramate, Noojarern Saisuda, Khlairit Patcharin, Pongratanakul Sarunyu, Suprasongsin Chittiwat, Korwutthikulrangsri Manassawee, Sriphrapradang Chutintorn, Poomthavorn Preamrud |
Antithyroid Antibody Status in Non-Pregnant Adult Bangladeshi Patients with Subclinical Hypothyroidism. Mymensingh medical journal : MMJ 2020 1 29 (1): 156-161. Rafiq-Uddin M, Kamrul-Hasan A B, Asaduzzaman M, Aminul-Islam A K, Islam M, Rauniyar B K, Hoque A, Mustari M, Fariduddin M, Hasanat M |
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 |
Long-Term Outcome of Patients with TPO Mutations. Journal of clinical medicine 2021 9 10 (17): . Tobias Leraz, Elias-Assad Ghadir, Khayat Morad, Admoni Osnat, Almashanu Shlomo, Tenenbaum-Rakover Yarde |
Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing. Endocrine journal 2021 7 68 (12): 1411-1419. Watanabe Daisuke, Yagasaki Hideaki, Narusawa Hiromune, Saito Tomohiro, Mitsui Yumiko, Miyake Kunio, Ohta Masanori, Inukai Takes |
Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population. Frontiers in endocrinology 2021 12 695426. Huang Miao, Lu Xiyan, Dong Guoqing, Li Jianxu, Chen Chengcong, Yu Qiuxia, Li Mingzhu, Su Yuey |
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 |
Programmed Cell Death-Ligand 1 (PD-L1) gene Single Nucleotide Polymorphism in Graves' Disease and Hashimoto's Thyroiditis in Korean Patients. Endocrinology and metabolism (Seoul, Korea) 2021 Jun . Yoon Jee Hee, Shin Min-Ho, Kim Hee Nam, Choi Wonsuk, Park Ji Yong, Hong A Ram, Kim Hee Kyung, Kang Ho-Che |
Vitamin D status in Hashimoto's thyroiditis and its association with vitamin D receptor genetic variants. The Journal of steroid biochemistry and molecular biology 2021 5 212 105922. Hanna Hany William Z, Rizzo Cristiano, Abdel Halim Radwa Marawan, El Haddad Hemmat Elewa, Salam Randa, El-Sayed Abou-Youssef Haz |
Genetic Evaluation of Congenital Hypothyroidism with Gland in situ Using Targeted Exome Sequencing. Annals of clinical and laboratory science 2021 Jan 51 (1): 73-81. Shin Jung Hyun, Kim Hye Young, Kim Young Mi, Lee Heirim, Bae Mi Hye, Park Kyung Hee, Lee Sae-Mi, Kwak Min Ju |
BDNF blood serum linkage with BDNF gene polymorphism (rs6265) in thyroid pathology patients in the West-Ukrainian population. Endocrine regulations 2021 12 55 (4): 193-203. Kamyshna Iryna I, Pavlovych Larysa B, Sydorchuk Larysa P, Malyk Igor V, Kamyshnyi Aleksandr |
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 |
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 |
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis. Endocrine 2022 5 77 (1): 86-101. Molina Maricel F, Papendieck Patricia, Sobrero Gabriela, Balbi Viviana A, Belforte Fiorella S, Martínez Elena Bueno, Adrover Ezequiela, Olcese María C, Chiesa Ana, Miras Mirta B, González Verónica G, Pio Mauricio Gomes, González-Sarmiento Rogelio, Targovnik Héctor M, Rivolta Carina |
Association between NMDA gene polymorphism (rs4880213) and GRIN2B blood serum levels in thyroid pathology patients. Journal of medicine and life 2022 Jan 15 (1): 109-116. Kamyshna Iryna Ivanivna, Pavlovych Larysa Borysivna, Kamyshnyi Aleksandr Mychailovi |
Gene mutations in children with permanent congenital hypothyroidism in Yunnan, China. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2022 Jun 51 (3): 306-313. Gong Yanling, Zhang Yinhong, Liu Fan, Zhu Baosheng, Zhou Xiaoyan, Chan Ying, Li Suyun, Li |
Screening and Functional Analysis of TPO Gene Mutations in a Cohort of Chinese Patients With Congenital Hypothyroidism. Frontiers in endocrinology 2022 1 12 774941. Wang Huijjuan, Wang Wenxia, Chen Xi, Shi Hailong, Shi Yinmin, Ding Guife |
Genetic screening and functional analysis of TPO variants in Chinese patients with congenital hypothyroidism. Hormone research in paediatrics 2023 9 . Hai-Yang Zhang, Feng-Yao Wu, Xue-Song Li, Cao-Xu Zhang, Ping-Hui Tu, Rui-Meng Yang, Xiao-Yu Liu, Ren-Jie Cui, Liu Yang, Chen-Yang Wu, Rui-Jia Zhang, Ya Fang, Feng Sun, Jun Liang, Feng Cheng, Huai-Dong Song, Shuang-Xia Zh |
A Case-Control Study of the Relationship Between Genetic Polymorphism and Cretinism in Xinjiang. Pharmacogenomics and personalized medicine 2023 8 16 785-794. Jia Huang, Haiyan Wu, Guiqiang Zhao, Yan Ma, Yunping An, Li Sun, Fuye Li, Shengling Wa |
Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China. Clinica chimica acta; international journal of clinical chemistry 2023 6 547 117459. Ting Zhang, Yaping Shen, Yanhua Xu, Dingwen Wu, Chi Chen, Rulai Ya |
Case Report - Multinodular goiter in a patient with Congenital Hypothyroidism and Bannayan-Riley-Ruvalcaba syndrome: the possible synergic role of TPO and PTEN mutation. Frontiers in endocrinology 2023 6 14 1205785. Gaia Vincenzi, Ilenia Teresa Petralia, Marco Abbate, Giulia Tarantola, Silvia Laura Carla Meroni, Riccardo Maggiore, Gilberto Mari, Maria Grazia Patricelli, Marco Schiavo Lena, Graziano Barera, Maria Cristina Vigo |
Subacute THYROiditis Related to SARS-CoV-2 VAccine and Covid-19 (THYROVAC Study): A Multicenter Nationwide Study. The Journal of clinical endocrinology and metabolism 2023 5 . Adnan Batman, Dilek Yazici, Oguz Dikbas, Kemal Agbaht, Emre Sedar Saygili, Ibrahim Demirci, Nurbanu Bursa, Görkem Ayas, Cüneyd An?l, Mustafa Cesur, Fatma Nur Korkmaz, Adile Begüm Bahçecioglu, Demet Corapc?oglu, Murat Faik Erdogan, Hayri Bostan, Murat Calapkulu, Sema Hepsen, Bekir Ucan, Erman Cakal, Bagdagul Yuksel Guler, Cem Haymana, Suleyman Hilmi Ipekci, Selami Ayd?n, Havva Sezer, Seçil Oz?s?k, Oguzhan Deyneli, Faruk Alagol, Refik Tanakol, Mustafa Eroglu, Ummu Mutlu, Hulya Hacisahinogullari, Ayse Kubat Uzum, Canan Demir, Gonul Koç, Sevde Nur F?rat, Tulay Omma, Nurcan Ince, ?efika Burcak Polat, Oya Topaloglu, Cevdet Ayd?n, Bekir Cak?r, Cigdem Tura Bahad?r, Mehmet Guven, Mehmet Sözen, Alev Selek, Zeynep Canturk, Berrin Cetinarslan, Mustafa Aydemir, Isilay Taskaldiran, Yusuf Bozkus, Özlem Turhan Iyidir, Filiz Eksi Haydardedeoglu, Seda Erem Basmaz, Mehmet Cagri Unal, Tevfik Demir, Ayten Oguz, Ozlem Celik, Merve Yilmaz, Aykut Cimsir, Serdar Kayihan, Ziynet Alphan Uc, Sakin Tekin, Ömercan Topaloglu, Basak Ozgen Saydam, Yasemin Aydogan Unsal, Ozge Ozer, Goknur Yorulmaz, Kader Ugur, Sezin Dogan Cakir, Mehmet Asik, Mustafa Unubol, Selin Genc, Burak Andac, Mine Okur, Ozlem Dogan, Ersen Karakiliç, Gokcen Unal Kocabas, Cem Onur Kirac, Guven Baris Cansu, Meliha Melin Uygur, Zafer Pekkolay, Sadettin Ozturk, Askin Gungunes, Eren Gurkan, Lezzan Keskin, Kenan Caglayan, Yasemin Emur Gunay, Eren ?mre, Selcuk Yusuf Sener, Ahmet Toygar Kalkan, Deniz Engin Gok, Mustafa Sah |
[Genetic mutation profiles for children with congenital hypothyroidism in Fujian province]. Zhonghua yi xue za zhi 2023 2 103 (5): 336-343. Cheng F, Su Y Q, Wang X R, Wu F Y, Sun F, Fang Y, Zhang R J, Zhao S X, Song H |
DUOX1 Gene Missense Mutation Confers Susceptibility on Type 2 Amiodarone-Induced Thyrotoxicosis. International journal of molecular sciences 2023 2 24 (4): . Biakina Olga, Mitina Yulia, Gognieva Daria, Axenova Marina, Ermolaeva Alexandra, Bestavashvili Afina, Fadeev Valentin, Syrkin Abram, Kopylov Phili |
Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with down syndrome and autoimmune thyroid diseases. La Pediatria medica e chirurgica : Medical and surgical pediatrics 2023 2 45 (1): . Faizi Muhammad, Rochmah Nur, Soetjipto Soetjipto, Endaryanto Anang, Basuki Sukmawati, Hisbiyah Yuni, Kurnia Perwitasari Ra |
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- Page last updated:Apr 16, 2024
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