Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SLC26A2[original query] |
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Identification of sequence polymorphisms in two sulfation-related genes, PAPSS2 and SLC26A2, and an association analysis with knee osteoarthritis. Journal of human genetics 2001 46 (9): 538-43. Ikeda T, Mabuchi A, Fukuda A, Hiraoka H, Kawakami A, Yamamoto S, Machida H, Takatori Y, Kawaguchi H, Nakamura K, Ikegawa |
Positive association of SLC26A2 gene polymorphisms with susceptibility to systemic-onset juvenile idiopathic arthritis. Arthritis and rheumatism 2007 Apr 56 (4): 1286-91. Lamb Rebecca, Thomson Wendy, , Ogilvie Emma M, Donn Rachel |
The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis. Bone 2009 Aug 45 (2): 289-94. Huang Qing-Yang, Li Gloria H Y, Kung Annie W |
Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns. International journal of pediatric otorhinolaryngology 2011 Apr 75 (4): 535-42. Wang Qiu-Ju, Zhao Ya-Li, Rao Shao-Qi, Guo Yu-Fen, He Yao, Lan Lan, Yang Wei-Yan, Zheng Qing-Yin, Ruben Robert J, Han Dong-Yi, Shen Y |
Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome. Gut 2014 Jul 63 (7): 1103-11. Wouters Mira M, Lambrechts Diether, Knapp Michael, Cleynen Isabelle, Whorwell Peter, Agréus Lars, Dlugosz Aldona, Schmidt Peter Thelin, Halfvarson Jonas, Simrén Magnus, Ohlsson Bodil, Karling Pontus, Van Wanrooy Sander, Mondelaers Stéphanie, Vermeire Severine, Lindberg Greger, Spiller Robin, Dukes George, D'Amato Mauro, Boeckxstaens G |
B-RAF mutation and accumulated gene methylation in aberrant crypt foci (ACF), sessile serrated adenoma/polyp (SSA/P) and cancer in SSA/P. British journal of cancer 2015 Jan 112 (2): 403-12. Inoue A, Okamoto K, Fujino Y, Nakagawa T, Muguruma N, Sannomiya K, Mitsui Y, Takaoka T, Kitamura S, Miyamoto H, Okahisa T, Fujimori T, Imoto I, Takayama |
Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene. Proceedings of the National Academy of Sciences of the United States of America 2015 Jun 112 (26): 8064-9. Cai Tao, Yang Liu, Cai Wanshi, Guo Sen, Yu Ping, Li Jinchen, Hu Xueyu, Yan Ming, Shao Qianzhi, Jin Yan, Sun Zhong Sheng, Luo Zhuo-Ji |
Exome sequencing reveals a novel COL2A1 mutation implicated in multiple epiphyseal dysplasia. American journal of medical genetics. Part A 2019 2 179 (4): 534-541. Dasa Vinod, Eastwood James R B, Podgorski Michal, Park Heewon, Blackstock Christopher, Antoshchenko Tetyana, Rogala Piotr, Bieganski Tadeusz, Jazwinski S Michal, Czarny-Ratajczak Malwi |
Anatomical characteristics and potential gene mutation sites of a familial recurrent patellar dislocation. BMC medical genomics 2022 8 15 (1): 176. Zhang Qi-Hao, Zhang Yan, He Rui-Xuan, Guo Han-Ming, Wang Xin-Gua |
Genetic screening of hypertensive patients with aldosterone hypersecretion under conditions of stress. Hormones (Athens, Greece) 2022 Aug . Mourtzi Niki, Sertedaki Amalia, Markou Athina, Piaditis George P, Katsanis Nicholas, Traeger-Synodinos Joanne, Tsigos Constantine, Charmandari Evangel |
Genom-wide analysis identifies single nucleotide polymorphism variations and altered pathways associated with poor semen quality in breeding bulls. Reproduction in domestic animals = Zuchthygiene 2022 Jun . Ebenezer Samuel King John Peter, Kumaresan Arumugam, Talluri Thirumala Rao, Sinha Manish Kumar, Raval Kathan, Nag Pradeep, Karuthadurai Thirumalaisamy, Aranganathan Veerama |
Identification of recurrent pathogenic alleles using exome sequencing data: Proof-of-concept study of Russian subjects. European journal of medical genetics 2022 1 65 (2): 104426. Orlov Igor E, Laidus Tatiana A, Tumakova Anastasia V, Yanus Grigoriy A, Iyevleva Aglaya G, Sokolenko Anna P, Bizin Ilya V, Imyanitov Evgeny N, Suspitsin Evgeny |
SLC26A2/DTDST Spectrum: A Cohort of 12 Patients Associated with a Comprehensive Review of the Genotype-Phenotype Correlation. Molecular syndromology 2023 1 13 (6): 485-495. Silveira Cynthia, da Costa Silveira Karina, Lacarrubba-Flores Maria D, Sakata Maurício T, Carbognani Silvia N, Llerena Juan, Moreno Carolina A, Cavalcanti Denise |
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- Page last updated:Apr 22, 2024
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