FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
about
Promotion of liver regeneration/repair by farnesoid X receptor in both liver and intestine in miceEndocrine fibroblast growth factors 15/19 and 21: from feast to famineNovel bile acid therapeutics for the treatment of chronic liver diseasesFibroblast Growth Factor Signaling in Metabolic RegulationEndocrine FGFs: Evolution, Physiology, Pathophysiology, and PharmacotherapyFibroblast Growth Factor 21 Analogs for Treating Metabolic Disorders.Fundamentals of FGF19 & FGF21 action in vitro and in vivoCharacterization of a FGF19 variant with altered receptor specificity revealed a central role for FGFR1c in the regulation of glucose metabolismFGF19 regulates cell proliferation, glucose and bile acid metabolism via FGFR4-dependent and independent pathwaysTherapeutic utilities of fibroblast growth factor 19.Separating mitogenic and metabolic activities of fibroblast growth factor 19 (FGF19).The Fibroblast Growth Factor signaling pathwayCurrent and upcoming pharmacotherapy for non-alcoholic fatty liver disease.FGF21 can be mimicked in vitro and in vivo by a novel anti-FGFR1c/β-Klotho bispecific protein.Identification of a therapeutic strategy targeting amplified FGF19 in liver cancer by Oncogenomic screeningTissue-specific actions of the metabolic hormones FGF15/19 and FGF21.Enterohepatic bacterial infections dysregulate the FGF15-FGFR4 endocrine axis.Fibroblast growth factor 21 induces glucose transporter-1 expression through activation of the serum response factor/Ets-like protein-1 in adipocytes.Klotho-beta overexpression as a novel target for suppressing proliferation and fibroblast growth factor receptor-4 signaling in hepatocellular carcinoma.Advances in pharmacotherapy for primary biliary cirrhosis.The structural biology of the FGF19 subfamilyFGF19 promotes epithelial-mesenchymal transition in hepatocellular carcinoma cells by modulating the GSK3β/β- catenin signaling cascade via FGFR4 activation.Modulation of fibroblast growth factor 19 expression by bile acids, meal replacement and energy drinks, milk, and coffee.Increased FGF19 copy number is frequently detected in hepatocellular carcinoma with a complete response after sorafenib treatment.Up-regulation of fibroblast growth factor 19 and its receptor associates with progression from fatty liver to hepatocellular carcinoma.Fibroblast growth factor receptor 4 (FGFR4): a targetable regulator of drug resistance in colorectal cancer.Molecular subclasses of hepatocellular carcinoma predict sensitivity to fibroblast growth factor receptor inhibitionAssociation between fibroblast growth factor receptor-4 gene polymorphism and risk of prostate cancer: a meta-analysis.Targeting fibroblast growth factor receptor signaling in hepatocellular carcinoma.The role of fibroblast growth factor 21 in the pathogenesis of liver disease: a novel predictor and therapeutic target.Targeting fibroblast growth factor 19 in liver disease: a potential biomarker and therapeutic target.Fibroblast growth factor 19-targeted therapies for the treatment of metabolic disease.Chronic Over-expression of Fibroblast Growth Factor 21 Increases Bile Acid Biosynthesis by Opposing FGF15/19 ActionIL-1β inhibits β-Klotho expression and FGF19 signaling in hepatocytes.Fibroblast growth factor family as a potential target in the treatment of hepatocellular carcinoma.Cardiac actions of fibroblast growth factor 23.Preclinical evaluation of combined TKI-258 and RAD001 in hepatocellular carcinoma.Sulfated glycosaminoglycan-assisted receptor specificity of human fibroblast growth factor (FGF) 19 signaling in a mouse system is different from that in a human system.Hepatocellular carcinoma treatment: a comparative review of emerging growth factor receptor antagonists.Deguelin-induced blockade of PI3K/protein kinase B/MAP kinase signaling in zebrafish and breast cancer cell lines is mediated by down-regulation of fibroblast growth factor receptor 4 activity.
P2860
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P2860
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@ast
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@en
type
label
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@ast
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@en
prefLabel
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@ast
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@en
P2093
P2860
P356
P1476
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation.
@en
P2093
Bryan Lemon
Hongfei Ge
Jamila Gupte
Jennifer Weiszmann
Randy Hecht
Richard Lindberg
Steven Vonderfecht
Todd Hager
P2860
P304
P356
10.1074/JBC.M109.068783
P407
P577
2009-12-15T00:00:00Z