FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
about
Characterization of FGFR signaling pathway as therapeutic targets for sarcoma patientsN-3 polyunsaturated fatty acids increase hepatic fibroblast growth factor 21 sensitivity via a PPAR-γ-β-klotho pathway.Bile acid homeostasis controls CAR signaling pathways in mouse testis through FXRalpha.Commensal bacteria at the crossroad between cholesterol homeostasis and chronic inflammation in atherosclerosis.Hepatic farnesoid X receptor protein level and circulating fibroblast growth factor 19 concentration in children with NAFLD.INT-767 improves histopathological features in a diet-induced ob/ob mouse model of biopsy-confirmed non-alcoholic steatohepatitis.Postprandial FGF19-induced phosphorylation by Src is critical for FXR function in bile acid homeostasis.
P2860
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P2860
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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2015年學術文章
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2015年學術文章
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name
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@ast
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@en
type
label
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@ast
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@en
prefLabel
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@ast
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@en
P2093
P2860
P356
P1476
FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.
@en
P2093
Byron Kemper
Dong-Hyun Kim
Jongsook Kim Kemper
Kelly Suino-Powell
Sangwon Byun
Sunmi Seok
Young-Chae Kim
P2860
P304
P356
10.1210/ME.2015-1226
P577
2015-10-27T00:00:00Z