Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-010-0927-z.pdf
Reference20 articles.
1. Calado J, Soto K, Clemente C, Correia P, Rueff J (2004) Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. Hum Genet 114:314–316
2. Calado J, Loeffler J, Sakallioglu O, Gok F, Lhotta K, Barata J, Rueff J (2006) Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting. Kidney Int 69:852–855
3. Calado J, Sznajer Y, Metzger D, Rita A, Hogan MC, Kattamis A, Scharf M, Tasic V, Greil J, Brinkert F, Kemper MJ, Santer R (2008) Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Nephrol Dial Transplant 23:3874–3879
4. Chazotte B (2008) Labeling the components of the plasma membrane with fluorescent dyes for imaging. Cold Spring Harb Protoc. doi: 10.1101/pdb.prot4930
5. Francis J, Zhang J, Farhi A, Carey H, Geller DS (2004) A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria. Nephrol Dial Transpl 19:2893–2895
Cited by 41 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. The Impact of Genetic Polymorphisms on the Anti-Hyperglycemic Effect of Dapagliflozin;Diabetes, Metabolic Syndrome and Obesity;2024-07
2. Role of SLC5A2 polymorphisms and effects of genetic polymorphism on sodium glucose cotransporter 2 inhibitorsinhibitor response;Molecular Biology Reports;2023-10-11
3. Review on Molecular Mechanism of Hypertensive Nephropathy;Current Pharmaceutical Design;2023-09
4. Excretion of glucose analogue with SGLT2 affinity predicts response effectiveness to sodium glucose transporter 2 inhibitors in patients with type 2 diabetes mellitus;European Journal of Nuclear Medicine and Molecular Imaging;2023-05-17
5. Associations of SGLT2 genetic polymorphisms with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults;Hypertension Research;2023-05-09
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