(Q34559902)

3 August 2017

Bile alcohols function as the ligands of membrane-type bile acid-activated G protein-coupled receptor (English)

1 reference

G protein-coupled receptor

3 August 2017

0 references

author name string

Yusuke Iguchi

1

1 reference

3 August 2017

Masafumi Yamaguchi

2

1 reference

3 August 2017

Hiroyuki Sato

3

1 reference

3 August 2017

Kenji Kihira

4

1 reference

3 August 2017

Tomoko Nishimaki-Mogami

5

1 reference

3 August 2017

Mizuho Une

6

1 reference

3 August 2017

18 December 2009

1 reference

Journal of Lipid Research

3 August 2017

1 reference

3 August 2017

51

1 reference

3 August 2017

6

1 reference

3 August 2017

1432-1441

1 reference

Structure-activity relationship of bile alcohols as human farnesoid X receptor agonist

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

TGR5-mediated bile acid sensing controls glucose homeostasis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

The G-protein coupled bile salt receptor TGR5 is expressed in liver sinusoidal endothelial cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

5Alpha-bile alcohols function as farnesoid X receptor antagonists

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Nuclear receptors as targets for drug development: regulation of cholesterol and bile acid metabolism by nuclear receptors

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Bile acids promote glucagon-like peptide-1 secretion through TGR5 in a murine enteroendocrine cell line STC-1.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Protein measurement with the Folin phenol reagent

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Structure-activity relationship of bile acids and bile acid analogs in regard to FXR activation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

A G protein-coupled receptor responsive to bile acids

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Bile acids: natural ligands for an orphan nuclear receptor

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Identification of a nuclear receptor for bile acids

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Inflammatory and immunologic effects of obstructive jaundice: pathogenesis and treatment

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Synthesis of biological precursors of cholic acid II.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Formation and metabolism of bile alcohols in man.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Chemistry and Metabolism of Bile Alcohols and Higher Bile Acids

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Identification of new bile alcohols, 5 beta-cholestane-3 alpha,7 alpha,24,26-tetrol, 5 beta-cholestane-3 alpha,7 alpha,25,26-tetrol, and 5 beta-cholestane-3 alpha,7 alpha,26,27-tetrol in human gallbladder bile

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Synthesis of biological precursors of cholic acid

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Preparation of 24(R)- and 24(S)-5beta-cholestane-3alpha,7alpha,24-triols and 25(R)- and 25(S)-5beta-cholestane-3alpha,7alpha,26-triols by a hydroboration procedure

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3035506

Novel potent and selective bile acid derivatives as TGR5 agonists: biological screening, structure-activity relationships, and molecular modeling studies

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1194%2FJLR.M004051

Identification of intermediates in the bile acid synthetic pathway as ligands for the farnesoid X receptor

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1194%2FJLR.M004051

Nongenomic actions of bile acids. Synthesis and preliminary characterization of 23- and 6,23-alkyl-substituted bile acid derivatives as selective modulators for the G-protein coupled receptor TGR5.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1194%2FJLR.M004051

Study of reticuloendothelial phagocytic capacity in patients with cholestasis

21 January 2018

1 reference

12 December 2020

Circadian distribution of bile acid in the enterohepatic circulatory system in hamsters

1 reference

12 December 2020

Bile salts of frogs: a new higher bile acid, 3 alpha, 7 alpha, 12 alpha, 26-tetrahydroxy-5 beta-cholestanoic acid from the bile Rana plancyi

1 reference

12 December 2020

Synthesis of (22R and 22S)-3 alpha, 7 alpha, 22-trihydroxy-5 beta-cholan-24-oic acids and structure of haemulcholic acid, a unique bile acid isolated from fish bile

1 reference

12 December 2020

The identification of urinary bile alcohols by gas chromatography-mass spectrometry in patients with liver disease and in healthy individuals

1 reference

12 December 2020

Impairment of human lymphocyte function by bile salts

1 reference

12 December 2020

Stero-bile acids and bile sterols. LXXIV. Biosynthesis of bile acids and bile alcohols in toad

1 reference

12 December 2020

The separation of the stereo-isomers of bile steroids, 5-beta-cholestane-3-alpha, 7-alpha, 12-alpha, 24-alpha-tetrol and 5-beta-cholestane-3-alpha, 7-alpha, 12-alpha, 24-beta-tetrol, by thin layer chromatography

1 reference

12 December 2020

Conversion of 7-alpha,12-alpha-dihydroxycholest-4-en-3-one to 5-alpha-cholestane-3-alpha, 7-alpha,12-alpha-triol by iguana liver microsomes

1 reference

12 December 2020

Synthesis of 5beta-cholestane-3alpha, 7alpha, 12alpha, 25-tetrol and 5beta-cholestane-3alpha, 7alpha, 245, 25-pentol

1 reference

12 December 2020

Identification of bile alcohols in human bile

1 reference

12 December 2020

Steady-state kinetics of serum bile acids in healthy human subjects: single and dual isotope techniques using stable isotopes and mass spectrometry

1 reference

12 December 2020

Synthesis of new bile salt analogues, sodium 3 alpha, 7 alpha-dihydroxy-5 beta-cholane-24-sulfonate and sodium 3 alpha, 7 beta-dihydroxy-5 beta-cholane-24-sulfonate

1 reference

12 December 2020

Synthesis of sulfonate analogs of bile acids

1 reference

12 December 2020

Synthesis and metabolism of sodium 3 alpha,7 alpha-dihydroxy-25,26-bishomo-5 beta-cholane-26-sulfonate in the hamster

1 reference

12 December 2020

Stero-bile acids and bile sterols. 36. Isolation of a new bile sterol, 3 alpha, 7 alpha, 12 alpha, 26-tetrahydroxy-delta23-bishomocholene, from bull frog bile

1 reference

12 December 2020

New bile alcohols--synthesis of 5beta-cholestane-3alpha, 7alpha, 25-triol and 5beta-cholestane-3alpha, 7alpha, 25-24 (14C)-triol

1 reference

12 December 2020

Identifiers

DOI

10.1194/JLR.M004051

1 reference

3 August 2017

1 reference

3 August 2017

1 reference