ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study

Published:2018-02-16 Issue:1 Volume:8 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Chen Chung-Jen,Tseng Chia-Chun,Yen Jeng-Hsien,Chang Jan-Gowth,Chou Wen-Cheng,Chu Hou-Wei,Chang Shun-Jen,Liao Wei-Ting

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-21425-7.pdf

Reference44 articles.

1. Yang, Q. et al. Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart Study. Metabolism 54, 1435–1441, https://doi.org/10.1016/j.metabol.2005.05.007 (2005).

2. Enomoto, A. et al. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 417, 447–452, https://doi.org/10.1038/nature742 (2002).

3. Matsuo, H. et al. Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia. Am J Hum Genet 83, 744–751, https://doi.org/10.1016/j.ajhg.2008.11.001 (2008).

4. Dinour, D. et al. Homozygous SLC2A9 mutations cause severe renal hypouricemia. J Am Soc Nephrol 21, 64–72, https://doi.org/10.1681/ASN.2009040406 (2010).

5. Woodward, O. M. et al. Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Proc Natl Acad Sci USA 106, 10338–10342, https://doi.org/10.1073/pnas.0901249106 (2009).

Cited by 51 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hyperuricemia and its related diseases: mechanisms and advances in therapy;Signal Transduction and Targeted Therapy;2024-08-28

2. Mendelian randomization analysis identified potential genes pleiotropically associated with gout;Frontiers in Genetics;2024-08-05

3. The pathogenesis of gout: molecular insights from genetic, epigenomic and transcriptomic studies;Nature Reviews Rheumatology;2024-07-11

4. Polymorphism rs3733591 of the SLC2A9 gene and metabolic syndrome affect gout risk in Taiwan Biobank subjects;Frontiers in Genetics;2024-04-16

5. Association Between Family History in Patients with Primary Gout and Left Ventricular Diastolic Function: A Cross-Sectional Study;International Journal of General Medicine;2024-04

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3