Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Gout and SLC17A1[original query] |
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Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.
PLoS genetics 2009 Jun 5 (6): e1000504. Kolz Melanie, Johnson Toby, Sanna Serena, Teumer Alexander, Vitart Veronique, Perola Markus, Mangino Massimo, Albrecht Eva, Wallace Chris, Farrall Martin, Johansson Asa, Nyholt Dale R, Aulchenko Yurii, Beckmann Jacques S, Bergmann Sven, Bochud Murielle, Brown Morris, Campbell Harry, , Connell John, Dominiczak Anna, Homuth Georg, Lamina Claudia, McCarthy Mark I, , Meitinger Thomas, Mooser Vincent, Munroe Patricia, Nauck Matthias, Peden John, Prokisch Holger, Salo Perttu, Salomaa Veikko, Samani Nilesh J, Schlessinger David, Uda Manuela, Völker Uwe, Waeber Gérard, Waterworth Dawn, Wang-Sattler Rui, Wright Alan F, Adamski Jerzy, Whitfield John B, Gyllensten Ulf, Wilson James F, Rudan Igor, Pramstaller Peter, Watkins Hugh, , Doering Angela, Wichmann H-Erich, , Spector Tim D, Peltonen Leena, Völzke Henry, Nagaraja Ramaiah, Vollenweider Peter, Caulfield Mark, , Illig Thomas, Gieger Christi |
| Sodium-dependent phosphate cotransporter type 1 sequence polymorphisms in male patients with gout. Annals of the rheumatic diseases 2010 Jun 69 (6): 1232-4. Urano Wako, Taniguchi Atsuo, Anzai Naohiko, Inoue Eisuke, Kanai Yoshikatsu, Yamanaka Mariko, Endou Hitoshi, Kamatani Naoyuki, Yamanaka Hisas |
| Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease. PloS one 2009 4 (11): e7729. Stark Klaus, Reinhard Wibke, Grassl Martina, Erdmann Jeanette, Schunkert Heribert, Illig Thomas, Hengstenberg Christi |
| Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.
Circulation. Cardiovascular genetics 2010 Dec 3 (6): 523-30. Yang Qiong, Köttgen Anna, Dehghan Abbas, Smith Albert V, Glazer Nicole L, Chen Ming-Huei, Chasman Daniel I, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Launer Lenore, Nalls Michael, Hernandez Dena, Arking Dan E, Boerwinkle Eric, Grove Megan L, Li Man, Linda Kao W H, Chonchol Michel, Haritunians Talin, Li Guo, Lumley Thomas, Psaty Bruce M, Shlipak Michael, Hwang Shih-Jen, Larson Martin G, O'Donnell Christopher J, Upadhyay Ashish, van Duijn Cornelia M, Hofman Albert, Rivadeneira Fernando, Stricker Bruno, Uitterlinden Andre G, Paré Guillaume, Parker Alex N, Ridker Paul M, Siscovick David S, Gudnason Vilmundur, Witteman Jacqueline C, Fox Caroline S, Coresh Jos |
| The renal urate transporter SLC17A1 locus: confirmation of association with gout. Arthritis research & therapy 2012 14 (2): R92. Hollis-Moffatt Jade E, Phipps-Green Amanda J, Chapman Brett, Jones Gregory T, van Rij Andre, Gow Peter J, Harrison Andrew A, Highton John, Jones Peter B, Montgomery Grant W, Stamp Lisa K, Dalbeth Nicola, Merriman Tony |
| NPT1/SLC17A1 is a renal urate exporter in humans and its common gain-of-function variant decreases the risk of renal underexcretion gout. Arthritis & rheumatology (Hoboken, N.J.) 2015 Jan 67 (1): 281-7. Chiba Toshinori, Matsuo Hirotaka, Kawamura Yusuke, Nagamori Shushi, Nishiyama Takashi, Wei Ling, Nakayama Akiyoshi, Nakamura Takahiro, Sakiyama Masayuki, Takada Tappei, Taketani Yutaka, Suma Shino, Naito Mariko, Oda Takashi, Kumagai Hiroo, Moriyama Yoshinori, Ichida Kimiyoshi, Shimizu Toru, Kanai Yoshikatsu, Shinomiya Nariyos |
| Tubular urate transporter gene polymorphisms differentiate patients with gout who have normal and decreased urinary uric acid excretion. The Journal of rheumatology 2014 Sep 41 (9): 1863-70. Torres Rosa J, de Miguel Eugenio, Bailén Rebeca, Banegas José R, Puig Juan |
| Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study. BMC medical genetics 2015 16 (1): 66. Zhou Zhao-Wei, Cui Ling-Ling, Han Lin, Wang Can, Song Zhi-Jian, Shen Jia-Wei, Li Zhi-Qiang, Chen Jian-Hua, Wen Zu-Jia, Wang Xiao-Min, Shi Yong-Yong, Li Chang-G |
| Erratum to: Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study. BMC medical genetics 2015 16 (1): 99. Zhou Zhao-Wei, Cui Ling-Ling, Han Lin, Wang Can, Song Zhi-Jian, Shen Jia-Wei, Li Zhi-Qiang, Chen Jian-Hua, Wen Zu-Jia, Wang Xiao-Min, Shi Yong-Yong, Li Chang-G |
| GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
Annals of the rheumatic diseases 2016 Nov . Nakayama Akiyoshi, Nakaoka Hirofumi, Yamamoto Ken, Sakiyama Masayuki, Shaukat Amara, Toyoda Yu, Okada Yukinori, Kamatani Yoichiro, Nakamura Takahiro, Takada Tappei, Inoue Katsuhisa, Yasujima Tomoya, Yuasa Hiroaki, Shirahama Yuko, Nakashima Hiroshi, Shimizu Seiko, Higashino Toshihide, Kawamura Yusuke, Ogata Hiraku, Kawaguchi Makoto, Ohkawa Yasuyuki, Danjoh Inaho, Tokumasu Atsumi, Ooyama Keiko, Ito Toshimitsu, Kondo Takaaki, Wakai Kenji, Stiburkova Blanka, Pavelka Karel, Stamp Lisa K, Dalbeth Nicola, , Sakurai Yutaka, Suzuki Hiroshi, Hosoyamada Makoto, Fujimori Shin, Yokoo Takashi, Hosoya Tatsuo, Inoue Ituro, Takahashi Atsushi, Kubo Michiaki, Ooyama Hiroshi, Shimizu Toru, Ichida Kimiyoshi, Shinomiya Nariyoshi, Merriman Tony R, Matsuo Hirota |
| Assessment of genetic polymorphisms associated with hyperuricemia or gout in the Hmong. Personalized medicine 2016 Sep 13 (5): 429-440. Roman Youssef M, Culhane-Pera Kathleen A, Menk Jeremiah, Straka Robert |
| Effects of multiple genetic loci on the pathogenesis from serum urate to gout. Scientific reports 2017 Mar 7 43614. Dong Zheng, Zhou Jingru, Jiang Shuai, Li Yuan, Zhao Dongbao, Yang Chengde, Ma Yanyun, Wang Yi, He Hongjun, Ji Hengdong, Yang Yajun, Wang Xiaofeng, Xu Xia, Pang Yafei, Zou Hejian, Jin Li, Wang Jiuc |
| The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database Analysis. Journal of personalized medicine 2021 4 11 (3): . Butler Faven, Alghubayshi Ali, Roman Youss |
| Examining an Association of Single Nucleotide Polymorphisms with Hyperuricemia in Chinese Flight Attendants. Pharmacogenomics and personalized medicine 2022 15 589-602. Ye Jianpin, Zeng Zhiwei, Chen Yuxian, Wu Zhenkun, Yang Qingwei, Sun T |
| The impact of genetic variability in urate transporters on oxypurinol pharmacokinetics. Clinical and translational science 2022 11 . Hishe Hailemichael Z, Stocker Sophie L, Stamp Lisa K, Dalbeth Nicola, Merriman Tony R, Phipps-Green Amanda, Wright Daniel F |
| Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families. Scientific reports 2023 9 13 (1): 14978. Prashantha Hebbar, Rasheeba Nizam, Sumi Elsa John, Dinu Antony, Mohammad Dashti, Arshad Channanath, Azza Shaltout, Hessa Al-Khandari, Heikki A Koistinen, Jaakko Tuomilehto, Osama Alsmadi, Thangavel Alphonse Thanaraj, Fahd Al-Mul |
| GLUT9 as a potential drug target for chronic kidney disease: Drug target validation by a Mendelian randomization study. Journal of human genetics 2023 6 . Masatoshi Ueda, Kenji Fukui, Naoyuki Kamatani, Shigeo Kamitsuji, Akira Matsuo, Tomohiko Sasase, Jun Nishiu, Mutsuyoshi Matsushi |
| Association of rare and common genetic variants in MOCOS with inadequate response to allopurinol. Rheumatology (Oxford, England) 2024 8 . Niamh C Fanning, Murray Cadzow, Ruth K Topless, Chris Frampton, Nicola Dalbeth, Tony R Merriman, Lisa K Sta |
| Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 1 2024 5930566. Ji?í Vávra, Kate?ina Pavelcová, Jana Mašínová, Lenka Hasíková, Eliška Bubeníková, Aneta Urbanová, Andrea Man?íková, Blanka Stib?rko |
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