Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: SLC17A1[original query] |
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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 |
A genome-wide association study of red blood cell traits using the electronic medical record.
PloS one 2010 5 (9): 9. Kullo Iftikhar J, Ding Keyue, Jouni Hayan, Smith Carin Y, Chute Christopher |
Pathway analysis of genome-wide association studies on uric acid concentrations. Human immunology 2012 Aug 73 (8): 805-10. Lee Young Ho, Song Gwan G |
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 |
Genetic variability related to serum uric acid concentration and risk of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2013 Oct 28 (12): 1737-40. González-Aramburu Isabel, Sánchez-Juan Pascual, Jesús Silvia, Gorostidi Ana, Fernández-Juan Eduardo, Carrillo Fátima, Sierra María, Gómez-Garre Pilar, Cáceres-Redondo María T, Berciano José, Ruiz-Martínez Javier, Combarros Onofre, Mir Pablo, Infante J |
A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.
Obesity (Silver Spring, Md.) 2013 Jan . Li WD, Jiao H, Wang K, Zhang CK, Glessner JT, Grant SF, Zhao H, Hakonarson H, Arlen Price R |
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 |
Serum uric acid and risk of dementia in Parkinson's disease. Parkinsonism & related disorders 2014 Jun 20 (6): 637-9. González-Aramburu Isabel, Sánchez-Juan Pascual, Sierra María, Fernández-Juan Eduardo, Sánchez-Quintana Coro, Berciano José, Combarros Onofre, Infante J |
Serum uric acid levels are associated with polymorphisms in the SLC2A9, SF1, and GCKR genes in a Chinese population. Acta pharmacologica Sinica 2014 Nov 35 (11): 1421-7. Sun Xue, Jiang Feng, Zhang Rong, Tang Shan-shan, Chen Miao, Peng Dan-feng, Yan Jing, Wang Tao, Wang Shi-yun, Bao Yu-qian, Hu Cheng, Jia Wei-pi |
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 |
Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.
Pharmacogenetics and genomics 2015 Sep 25 (9): 450-61. Wanga Valentine, Venuto Charles, Morse Gene D, Acosta Edward P, Daar Eric S, Haas David W, Li Chun, Shepherd Bryan |
[Polymorphisms of SLC17A1 gene and their interaction with alcohol drinking among Uygur patients with hyperuricemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Dec 32 (6): 881-5. Wang Tingting, Su Yinxia, Wang Zhiqiang, Ma Qi, Yao H |
Genetic variants of SLC17A1 are associated with cholesterol homeostasis and hyperhomocysteinaemia in Japanese men. Scientific reports 2015 5 15888. Koyama Teruhide, Matsui Daisuke, Kuriyama Nagato, Ozaki Etsuko, Tanaka Keitaro, Oze Isao, Hamajima Nobuyuki, Wakai Kenji, Okada Rieko, Arisawa Kokichi, Mikami Haruo, Shimatani Keiichi, Hirata Akie, Takashima Naoyuki, Suzuki Sadao, Nagata Chisato, Kubo Michiaki, Tanaka Hid |
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 |
Common variants related to serum uric acid concentrations are associated with glucose metabolism and insulin secretion in a Chinese population. PloS one 2015 10 (1): e0116714. Sun Xue, Zhang Rong, Jiang Feng, Tang Shanshan, Chen Miao, Peng Danfeng, Yan Jing, Wang Tao, Wang Shiyun, Bao Yuqian, Hu Cheng, Jia Weipi |
Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling. Clinical kidney journal 2016 Jun 9 (3): 444-53. Bhatnagar Vibha, Richard Erin L, Wu Wei, Nievergelt Caroline M, Lipkowitz Michael S, Jeff Janina, Maihofer Adam X, Nigam Sanjay |
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 |
A mendelian randomization analysis: The causal association between serum uric acid and atrial fibrillation. European journal of clinical investigation 2020 May e13300. Hong Myunghee, Park Je-Wook, Yang Pil-Sung, Hwang Inseok, Kim Tae-Hoon, Yu Hee Tae, Uhm Jae-Sun, Joung Boyoung, Lee Moon-Hyoung, Jee Sun Ha, Pak Hui-N |
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. International journal of molecular sciences 2020 1 21 (2): . Gianesello Lisa, Ceol Monica, Bertoldi Loris, Terrin Liliana, Priante Giovanna, Murer Luisa, Peruzzi Licia, Giordano Mario, Paglialonga Fabio, Cantaluppi Vincenzo, Musetti Claudio, Valle Giorgio, Del Prete Dorella, Anglani Franca, Network Dent Disease Itali |
Causal Associations of Urate With Cardiovascular Risk Factors: Two-Sample Mendelian Randomization. Frontiers in genetics 2021 12 687279. Lukkunaprasit Thitiya, Rattanasiri Sasivimol, Ongphiphadhanakul Boonsong, McKay Gareth J, Attia John, Thakkinstian Ammar |
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 |
A genome-wide association study of 24-hour urinary excretion of endocrine disrupting chemicals. Environment international 2023 12 183 108396. Xueling Lu, Thomas P van der Meer, Zoha Kamali, Martijn van Faassen, Ido P Kema, André P van Beek, Xijin Xu, Xia Huo, Alireza Ani, , Ilja M Nolte, Bruce H R Wolffenbuttel, Jana V van Vliet-Ostaptchouk, Harold Snied |
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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