Author
Listed:
- Jae Myoung Suh
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Johan W. Jonker
(Center for Liver, Digestive and Metabolic Diseases, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands)
- Maryam Ahmadian
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Regina Goetz
(New York University School of Medicine)
- Denise Lackey
(University of California at San Diego)
- Olivia Osborn
(University of California at San Diego)
- Zhifeng Huang
(New York University School of Medicine
Present address: School of Pharmacy, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.)
- Weilin Liu
(Center for Liver, Digestive and Metabolic Diseases, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands)
- Eiji Yoshihara
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Theo H. van Dijk
(Center for Liver, Digestive and Metabolic Diseases, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands)
- Rick Havinga
(Center for Liver, Digestive and Metabolic Diseases, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands)
- Weiwei Fan
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Yun-Qiang Yin
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Ruth T. Yu
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Christopher Liddle
(The Storr Liver Unit, Westmead Millennium Institute and University of Sydney, Westmead Hospital)
- Annette R. Atkins
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Jerrold M. Olefsky
(University of California at San Diego)
- Moosa Mohammadi
(New York University School of Medicine)
- Michael Downes
(Gene Expression Laboratory, Salk Institute for Biological Studies)
- Ronald M. Evans
(Gene Expression Laboratory, Salk Institute for Biological Studies
Howard Hughes Medical Institute, Salk Institute for Biological Studies)
Abstract
Pharmacological fibroblast growth factor 1 (FGF1) normalizes blood glucose in diabetic mice by means of an FGF receptor signalling pathway that is independent of its mitogenic activity.
Suggested Citation
Jae Myoung Suh & Johan W. Jonker & Maryam Ahmadian & Regina Goetz & Denise Lackey & Olivia Osborn & Zhifeng Huang & Weilin Liu & Eiji Yoshihara & Theo H. van Dijk & Rick Havinga & Weiwei Fan & Yun-Qia, 2014.
"Endocrinization of FGF1 produces a neomorphic and potent insulin sensitizer,"
Nature, Nature, vol. 513(7518), pages 436-439, September.
Handle:
RePEc:nat:nature:v:513:y:2014:i:7518:d:10.1038_nature13540
DOI: 10.1038/nature13540
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Cited by:
- Lei Ying & Luyao Wang & Kaiwen Guo & Yushu Hou & Na Li & Shuyi Wang & Xingfeng Liu & Qijin Zhao & Jie Zhou & Longwei Zhao & Jianlou Niu & Chuchu Chen & Lintao Song & Shaocong Hou & Lijuan Kong & Xiaok, 2021.
"Paracrine FGFs target skeletal muscle to exert potent anti-hyperglycemic effects,"
Nature Communications, Nature, vol. 12(1), pages 1-14, December.
- Fei Pei & Li Ma & Junjun Jing & Jifan Feng & Yuan Yuan & Tingwei Guo & Xia Han & Thach-Vu Ho & Jie Lei & Jinzhi He & Mingyi Zhang & Jian-Fu Chen & Yang Chai, 2023.
"Sensory nerve niche regulates mesenchymal stem cell homeostasis via FGF/mTOR/autophagy axis,"
Nature Communications, Nature, vol. 14(1), pages 1-18, December.
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