C-terminal Tail of FGF19 Determines Its Specificity toward Klotho Co-receptors
Open Access
- 28 November 2008
- journal article
- Published by Elsevier BV
- Vol. 283 (48), 33304-33309
- https://doi.org/10.1074/jbc.m803319200
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Co-receptor Requirements for Fibroblast Growth Factor-19 SignalingJournal of Biological Chemistry, 2007
- Tissue-specific Expression of βKlotho and Fibroblast Growth Factor (FGF) Receptor Isoforms Determines Metabolic Activity of FGF19 and FGF21Journal of Biological Chemistry, 2007
- Endocrine Regulation of the Fasting Response by PPARα-Mediated Induction of Fibroblast Growth Factor 21Cell Metabolism, 2007
- Molecular Insights into the Klotho-Dependent, Endocrine Mode of Action of Fibroblast Growth Factor 19 Subfamily MembersMolecular and Cellular Biology, 2007
- βKlotho is required for metabolic activity of fibroblast growth factor 21Proceedings of the National Academy of Sciences, 2007
- Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasisCell Metabolism, 2005
- Impaired negative feedback suppression of bile acid synthesis in mice lacking βKlothoJCI Insight, 2005
- FGF-21 as a novel metabolic regulatorJCI Insight, 2005
- Transgenic Mice Expressing Human Fibroblast Growth Factor-19 Display Increased Metabolic Rate and Decreased AdiposityEndocrinology, 2002
- Mediation of Unusually High Concentrations of 1,25-Dihydroxyvitamin D in Homozygous klotho Mutant Mice by Increased Expression of Renal 1 -Hydroxylase GeneEndocrinology, 2002