勘误：肥胖与合并症：同时靶向内源性分泌型晚期糖基化终产物受体（esRAGE）和可溶性晚期糖基化终产物受体（sRAGE）会是万灵药吗？
Corrigendum: Obesity and Comorbidity: Could Simultaneous Targeting of esRAGE and sRAGE Be the Panacea?
作者信息
Eleazu Chinedum, Omar Norsuhana, Lim Oon Zhi, Yeoh Boon Seng, Nik Hussain Nik Hazlina, Mohamed Mahaneem
机构信息
Department of Physiology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Malaysia.
Department of Chemistry/Biochemistry/Molecular Biology, Alex Ekwueme Federal University, Ndufu-Alike, Ikwo, Nigeria.
出版信息
Front Physiol. 2019 Aug 7;10:1017. doi: 10.3389/fphys.2019.01017. eCollection 2019.
Abstract
[This corrects the article DOI: 10.3389/fphys.2019.00787.].
摘要
[本文更正了文章DOI：10.3389/fphys.2019.00787。]
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Corrigendum: Obesity and Comorbidity: Could Simultaneous Targeting of esRAGE and sRAGE Be the Panacea?勘误：肥胖与合并症：同时靶向内源性分泌型晚期糖基化终产物受体（esRAGE）和可溶性晚期糖基化终产物受体（sRAGE）会是万灵药吗？
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本文引用的文献
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Serum levels of advanced glycation end-products (AGEs) and the decoy soluble receptor for AGEs (sRAGE) can identify non-alcoholic fatty liver disease in age-, sex- and BMI-matched normo-glycemic adults.血清中晚期糖基化终产物（AGEs）和 AGEs 的诱饵可溶性受体（sRAGE）的水平可以在年龄、性别和 BMI 匹配的血糖正常成年人中识别非酒精性脂肪性肝病。
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Circulating soluble RAGE isoforms are attenuated in obese, impaired-glucose-tolerant individuals and are associated with the development of type 2 diabetes.循环可溶性RAGE异构体在肥胖、糖耐量受损个体中减少，并与2型糖尿病的发生有关。
Am J Physiol Endocrinol Metab. 2017 Dec 1;313(6):E631-E640. doi: 10.1152/ajpendo.00146.2017. Epub 2017 Aug 15.
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