Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation (Q28290455)

11

0 references

Johan Auwerx

13

0 references

Nadia Messaddeq

7

0 references

Antonio Bianco

12

Antonio C Bianco

0 references

Marcelo A Christoffolete

Marcelo A Christoffolete

4

0 references

Sander M. Houten

Sander M Houten

2

0 references

Chikage Mataki

3

Chikage Mataki

0 references

Mitsuhiro Watanabe

1

Mitsuhiro Watanabe

0 references

John W. Harney

8

John W Harney

0 references

author name string

Brian W Kim

5

0 references

Hiroyuki Sato

6

0 references

Osamu Ezaki

9

0 references

Tatsuhiko Kodama

Down-regulation of cholesterol 7alpha-hydroxylase (CYP7A1) gene expression by bile acids in primary rat hepatocytes is mediated by the c-Jun N-terminal kinase pathway

10

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language of work or name

English

0 references

publication date

26 January 2006

0 references

published in

Nature

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volume

439

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issue

7075

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page(s)

484-9

0 references

cites work

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Bile Acid Regulation of C/EBPβ, CREB, and c-Jun Function, via the Extracellular Signal-Regulated Kinase and c-Jun NH2-Terminal Kinase Pathways, Modulates the Apoptotic Response of Hepatocytes

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A G protein-coupled receptor responsive to bile acids

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Identification of membrane-type receptor for bile acids (M-BAR)

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Identification of a nuclear receptor for bile acids

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Bile acids: natural ligands for an orphan nuclear receptor

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Endogenous bile acids are ligands for the nuclear receptor FXR/BAR

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A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis

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Molecular basis for feedback regulation of bile acid synthesis by nuclear receptors

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Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1c

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Measurement of mitochondrial calcium in single living cardiomyocytes by selective removal of cytosolic indo 1

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Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis

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Mice with targeted disruption of the Dio2 gene have cold-induced overexpression of the uncoupling protein 1 gene but fail to increase brown adipose tissue lipogenesis and adaptive thermogenesis.

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The type 2 iodothyronine deiodinase is essential for adaptive thermogenesis in brown adipose tissue

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The type 2 deiodinase A/G (Thr92Ala) polymorphism is associated with decreased enzyme velocity and increased insulin resistance in patients with type 2 diabetes mellitus

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Association between a novel variant of the human type 2 deiodinase gene Thr92Ala and insulin resistance: evidence of interaction with the Trp64Arg variant of the beta-3-adrenergic receptor

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SRC-1 and TIF2 control energy balance between white and brown adipose tissues

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The human type 2 iodothyronine deiodinase is a selenoprotein highly expressed in a mesothelioma cell line

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Simultaneous determination of bile acids in rat bile and serum by high-performance liquid chromatography

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