Human Genome Epidemiology Literature Finder
|
Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and DIO2[original query] |
|---|
| The association of polymorphisms in the type 1 and 2 deiodinase genes with circulating thyroid hormone parameters and atrophy of the medial temporal lobe. The Journal of clinical endocrinology and metabolism 2007 Feb 92 (2): 636-40. de Jong Frank Jan, Peeters Robin P, den Heijer Tom, van der Deure Wendy M, Hofman Albert, Uitterlinden André G, Visser Theo J, Breteler Monique M |
| Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis. Human molecular genetics 2008 Jun 17 (12): 1867-75. Meulenbelt Ingrid, Min Josine L, Bos Steffan, Riyazi Naghmeh, Houwing-Duistermaat Jeanine J, van der Wijk Henk-Jan, Kroon Herman M, Nakajima Masahiro, Ikegawa Shiro, Uitterlinden André G, van Meurs Joyce B J, van der Deure Wendy M, Visser Theo J, Seymour Albert B, Lakenberg Nico, van der Breggen Ruud, Kremer Dennis, van Duijn Cornelia M, Kloppenburg Margreet, Loughlin John, Slagboom P Eli |
| Association study between polymorphisms in selenoprotein genes and susceptibility to Kashin-Beck disease. Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2010 Jun 18 (6): 817-24. Xiong Y M, Mo X Y, Zou X Z, Song R X, Sun W Y, Lu W, Chen Q, Yu Y X, Zang W |
| Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan population. PloS one 2013 8 (8): e71411. Huang Lulin, Shi Yi, Lu Fang, Zheng Hong, Liu Xiaoqi, Gong Bo, Yang Jiyun, Lin Ying, Cheng Jing, Ma Shi, Lin He, Yang Zhengl |
| [DIO2, TPO, CYP1A1 AND CYP1A2 gene polymorphism in women with thyroid disease]. Gigiena i sanitariia 0 (3): 52-6. Kochetova O V, Gaynullina M K, Viktorova T |
| Association of the DIO2 gene single nucleotide polymorphisms with recurrent depressive disorder. Acta biochimica Polonica 2015 62 (2): 297-302. Ga?ecka El?bieta, Talarowska Monika, Orzechowska Agata, Górski Pawe?, Bie?kiewicz Ma?gorzata, Szemraj Janu |
| Field synopsis and meta-analyses of genetic epidemiological evidence for Kashin-Beck disease, an endemic osteoarthropathy in China. Molecular genetics and genomics : MGG 2016 Jun . Yang Lei, Zhao Guang-Hui, Liu Huan, Wang Xi, Guo Xiong, Lammi Mikko |
| Polymorphisms of iodothyronine deiodinases (DIO1, DIO3) genes are not associated with recurrent depressive disorder. Pharmacological reports : PR 2016 Oct 68 (5): 913-7. Ga?ecka El?bieta, Talarowska Monika, Maes Michael, Su Kuan-Pin, Górski Pawe?, Szemraj Janu |
Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes.
Human molecular genetics 2018 May . Aponte Jennifer L, Chiano Mathias N, Yerges-Armstrong Laura M, Hinds David A, Tian Chao, Gupta Akansha, Guo Cong, Fraser Dana J, Freudenberg Johannes M, Rajpal Deepak K, Ehm Margaret G, Waterworth Dawn |
| Deiodinases, Organic Anion Transporter Polypeptide Polymorphisms, and Thyroid Hormones in Patients with Myocardial Infarction. Genetic testing and molecular biomarkers 2018 Mar . Brozaitiene Julija, Skiriute Daina, Burkauskas Julius, Podlipskyte Aurelija, Jankauskiene Edita, Serretti Alessandro, Mickuviene Narse |
| A Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans. The Journal of clinical endocrinology and metabolism 2018 Feb . McAninch Elizabeth A, Rajan Kumar B, Evans Denis A, Jo Sungro, Chaker Layal, Peeters Robin P, Bennett David A, Mash Deborah C, Bianco Antonio |
| Study of Deiodinase Type 2 Polymorphisms in Graves' Disease and Ophthalmopathy in a Swedish Population. European thyroid journal 2018 Nov 7 (6): 289-293. Shahida Bushra, Planck Tereza, Åsman Peter, Lantz Mika |
| A study of the role of DIO1 and DIO2 polymorphism in thyroid cancer and drug response to therapy in the Saudi population. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society 2019 9 27 (6): 841-845. AlRasheed Maha M, AlAnzi Ashwaq, AlShalhoub Rawan, Abanmy Norah, Bakheet Da |
| Association between DIO2 polymorphism and the risk of Kashin-Beck disease in the Tibetan population. The journal of gene medicine 2019 Aug e3123. Jin Tianbo, Wang Li, He Xue, Liu Ming, Bai Mei, Rong Hao, He Yongjun, Yuan Dong |
| The polymorphic inheritance of DIO2 rs225014 may predict body weight variation after Graves' disease treatment. Archives of endocrinology and metabolism 2020 Oct . Comarella Ana Paula, Vilagellin Danilo, Bufalo Natassia Elena, Euflauzino Jessica Ferreira, de Souza Teixeira Elisangela, Miklos Ana Beatriz Pinotti Pedro, Dos Santos Roberto Bernardo, Romaldini João H, Ward Laura |
| Meta-analysis of Association Studies of Selenoprotein Gene Polymorphism and Kashin-Beck Disease: an Updated Systematic Review. Biological trace element research 2021 Apr . Yu Fang-Fang, Sun Lei, Zhou Guo-Yu, Ping Zhi-Guang, Guo Xiong, Ba Y |
| Age Worsens the Cognitive Phenotype in Mice Carrying the Thr92Ala-DIO2 Polymorphism. Metabolites 2022 7 12 (7): . Lorena Fernanda B, Sato Juliana M, Coviello Beatriz Martin, Arnold Alexandre J T, Batistuzzo Alice, Yamanouchi Laís M, Dias Junior Eduardo, do Nascimento Bruna P P, Fonseca Tatiana de L, Bianco Antonio C, Ribeiro Miriam |
| Type 2 Deiodinase Thr92Ala Polymorphism Is Not Associated with Cognitive Impairment in Older Adults: A Cross-Sectional Study. Metabolites 2022 Apr 12 (5): . Schwengber Wallace Klein, Silveira Vitor Bock, Hetzel Guilherme Moreira, Robaina Amanda, Ceolin Lucieli, Camelier Marli Teresinha, Goemann Iuri, Dalla Corte Roberta Rigo, Scheffel Rafael Selbach, de Mello Renato Gorga Bandeira, Maia Ana Luiza, Dora José Migu |
| Crosstalk between CpG Methylation and Polymorphisms (CpG-SNPs) in the Promotor Region of DIO2 in Kashin-Beck Disease. Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih 2022 3 37 (1): 52-59. Zhang Rong-Qiang, Zhang Dan-Dan, Zhang Di, Yang Xiao-Li, Li Qiang, Wang Chen, Yang Xue-Na, Xiong Yong-M |
| Thyroid function, pernicious anemia and erythropoiesis: a two-sample Mendelian randomization study. Human molecular genetics 2022 Feb . Kjaergaard Alisa D, Teumer Alexander, Marouli Eirini, Deloukas Panos, Ku? Aleksander, Sterenborg Rosalie, Åsvold Bjørn O, Medici Marco, Ellervik Christi |
| Polymorphisms within DIO2 and GADD45A genes increase the risk of liver disease progression in chronic hepatitis b carriers. Scientific reports 2023 4 13 (1): 6124. Rybicka Magda, Verrier Eloi R, Baumert Thomas F, Bielawski Krzysztof Pio |
| Thr92Ala-DIO2 heterozygosity is associated with skeletal muscle mass and myosteatosis in patients with COVID-19. European thyroid journal 2024 6 . Fabyan Esberard de Lima Beltrão, Daniele Carvalhal de Almeida Beltrão, Giulia Carvalhal, Fabyanna Lethicia de Lima Beltrão, Jocyel de Brito Oliveira, Hatilla Dos Santos Silva, Helena Mariana Pitangueira Teixeira, Juliana Lopes Rodrigues, Camila Alexandrina Viana de Figueiredo, Ryan Dos Santos Costa, Fabio Hecht, Giciane Carvalho Vieira, Maria da Conceição Rodrigues Gonçalves, Antonio Bianco, Helton Estrela Ram |
- Page last reviewed:Feb 1, 2024
- Content source: