A Gpr120-selective agonist improves insulin resistance and chronic inflammation in obese mice

被引：0
|
作者：
Da Young Oh
Evelyn Walenta
Taro E Akiyama
William S Lagakos
Denise Lackey
Ariane R Pessentheiner
Roman Sasik
Nasun Hah
Tyler J Chi
Jason M Cox
Mary Ann Powels
Jerry Di Salvo
Christopher Sinz
Steven M Watkins
Aaron M Armando
Heekyung Chung
Ronald M Evans
Oswald Quehenberger
Joanne McNelis
Juliane G Bogner-Strauss
Jerrold M Olefsky
机构：
[1] University of California,Division of Endocrinology and Metabolism, Department of Medicine
[2] San Diego,Department of Pharmacology
[3] Merck Research Laboratories,undefined
[4] Institute of Biochemistry,undefined
[5] Graz University of Technology,undefined
[6] Gene Expression Laboratory,undefined
[7] Salk Institute for Biological Studies,undefined
[8] Lipomics Technologies,undefined
[9] University of California,undefined
[10] San Diego,undefined
[11] Howard Hughes Medical Institute,undefined
[12] Salk Institute for Biological Studies,undefined
来源：
Nature Medicine | 2014年 / 20卷
关键词：
D O I：
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中图分类号：
学科分类号：
摘要：
An orally available, highly selective agonist of Gpr120 is developed and tested.
引用
收藏
页码：942 / 947
页数：5
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