Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 148 Records) |
Query Trace: TPO[original query] |
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Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease. Oxidative medicine and cellular longevity 2021 2021 2531062. Roumeliotis Athanasios, Roumeliotis Stefanos, Tsetsos Fotis, Georgitsi Marianthi, Georgianos Panagiotis I, Stamou Aikaterini, Vasilakou Anna, Kotsa Kalliopi, Tsekmekidou Xanthippi, Paschou Peristera, Panagoutsos Stylianos, Liakopoulos Vassili |
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 |
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 |
A recurrent somatic missense mutation in GNAS gene identified in familial thyroid follicular cell carcinomas in German longhaired pointer dogs. BMC genomics 2022 Sep 23 (1): 669. Yu Yun, Manders Freek, Grinwis Guy C M, Groenen Martien A M, Crooijmans Richard P M |
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 |
Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1? Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory. Genetic testing and molecular biomarkers 2022 6 26 (6): 324-330. Singsanan Sanita, Yamsri Supawadee, Pangjit Kanjana, Saenwang Phairo, Karnpean Rossarin, Fucharoen Sup |
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 |
Longitudinal study of 2 patients with cyclic thrombocytopenia, STAT3 and MPL mutations. Blood advances 2022 4 7 (1): 190-194. Zhang Haiyu, Chien May, Hou Yu, Shomali William, Brar Rondeep S, Ho Chandler, Han Panpan, Xu Danfei, Zhang Bing M, Guo Xiangqian, Tolentino Lorna L, Wu Nancy C, Tsai Albert G, Jin Jing, Witteles Wesley H, Chen Zhenping, Abidi Parveen, Jangam Diwash, Krieger Madison S, Craig Morgan, Bussel James B, Gotlib Jason R, Zehnder James |
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 |
IgE and IgG Anti-Thyroid Autoantibodies in Chinese Patients With Chronic Spontaneous Urticaria and a Literature Review. Allergy, asthma & immunology research 2022 1 14 (1): 131-142. Zhang Liming, Qiu Li, Wu Jian, Qi Yumeng, Wang Hexiao, Qi Ruiqun, Yao Xu, Zhu Hong, Li Yuzhen, Hao Siyu, Lu Qianjin, Long Hai, Lian Shi, Zhang Haiping, Zhu Wei, Lai Wei, Su Xiangyang, Lu Rongbiao, Guo Zaipei, Li Jingyi, Li Mengmeng, Liu Quanzhong, Wang Huiping, He Li, Nong Xiang, Li Fuqiu, Li Yang, Yao Chunli, Xu Jinhua, Tang Hui, Wang Duoqin, Li Zhenlu, Yu Huiqian, Xiao Shengxiang, An Jingang, Pu Xiongming, Yu Shirong, Zhang Jianzhong, Chen Xue, Gao Xinghua, Chen Hongduo, Xiao Ti |
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 |
Association of thyroid peroxidase antibody with the RNF213 p.R4810K variant in ischemic stroke/transient ischemic attack. Atherosclerosis 2023 9 382 117281. Takeshi Yoshimoto, Hiroyuki Ishiyama, Yorito Hattori, Kunihiro Nishimura, Yoko Okada, Hideaki Watanabe, Yasumasa Ohyagi, Yasuhisa Akaiwa, Tomoyuki Miyamoto, Michi Kawamoto, Masahiko Ichijo, Hiroyasu Inoue, Noriyuki Matsukawa, Toshiki Mizuno, Hirofumi Matsuyama, Hidekazu Tomimoto, Daisuke Kawakami, Kazunori Toyoda, Masatoshi Koga, Masafumi Iha |
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 |
Anti-TPO IgG/Total IgE Ratio: Biomarker for Omalizumab Response Prediction in Chronic Spontaneous Urticaria. International archives of allergy and immunology 2023 8 1-4. Rita Brás, Leonor Esteves Caldeira, Ana Bernardino, Célia Cos |
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 |
THE STUDY OF VDR FOKI RS2228570 SNP IN AUTOIMMUNE THYROIDITIS. Georgian medical news 2023 6 (337): 99-103. S Glonti, N Kedelidze, I Kalandadze, M Inaishvili, N Tchelidze, R Khurana, A Shaikh, D Baratashvili, G Tsetskhladze, D Dzneladze, I Nakashid |
Secondary Prevention of Diabetes Type 1 with Oral Calcitriol and Analogs, the PRECAL Study. Children (Basel, Switzerland) 2023 5 10 (5): . Dimitrios T Papadimitriou, Eleni Dermitzaki, Panagiotis Christopoulos, Maria Papagianni, Kleanthis Kleanthous, Chrysanthi Marakaki, Anastasios Papadimitriou, George Mastorak |
Unexpected high frequency of anti-thyroid peroxidase (anti-TPO) antibodies in Golestan province, Iran. Caspian journal of internal medicine 2023 5 14 (2): 371-375. Hadise Heidarpour, Farnaz Hooshmand, Fazel Isapanah Amlashi, Behnaz Khodabakhshi, Mahsa Mahmoudi, Taghi Amiriani, Sima Beshar |
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 |
Longitudinal Associations Between TPO Gene Variants and Thyroid Peroxidase Antibody Seroconversion in a Population-Based Study: Tehran Thyroid Study. Genetic testing and molecular biomarkers 2023 3 27 (3): 65-73. Ghanooni Amir Hossein, Zadeh-Vakili Azita, Rezvankhah Boshra, Jafari Nodushan Somayeh, Akbarzadeh Mahdi, Amouzegar Atieh, Daneshpour Maryam S, Khalili Davood, Mehrabi Yadollah, Ebadi Seyed Alireza, Azizi Fereido |
[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 |
Variants in TPO rs2048722, PTCSC2 rs925489 and SEMA4G rs4919510 affect thyroid carcinoma susceptibility risk. BMC medical genomics 2023 2 16 (1): 19. Shen Zhen, Sun Yingjun, Niu Guoh |
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 |
Differences between adult and pediatric chronic spontaneous urticaria from a cohort of 751 patients: Clinical features, associated conditions and indicators of treatment response. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2023 2 34 (2): e13925. Özçeker Deniz, Can Pelin Kuteyla, Terzi Özlem, Ornek Sinem Ay?e, De?irmentepe Ece Nur, K?z?ltac Kübra, Sarac Esra, Kocatürk Em |
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 |
High-resolution melt curve analysis: An approach for variant detection in the TPO gene of congenital hypothyroid patients in Bangladesh. PloS one 2024 4 19 (4): e0293570. Mst Noorjahan Begum, Rumana Mahtarin, Md Tarikul Islam, Nusrat Jahan Antora, Suprovath Kumar Sarker, Nusrat Sultana, Abu A Sajib, Abul B M M K Islam, Hurjahan Banu, M A Hasanat, Kohinoor Jahan Shyamaly, Suraiya Begum, Tasnia Kawsar Konika, Shahinur Haque, Mizanul Hasan, Sadia Sultana, Taufiqur Rahman Bhuiyan, Kaiissar Mannoor, Firdausi Qadri, Sharif Akhteruzzam |
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- Page last updated:Apr 16, 2024
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