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A novel ChREBP isoform in adipose tissue regulates systemic glucose metabolism
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scholarly article
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stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
title
A novel ChREBP isoform in adipose tissue regulates systemic glucose metabolism
(English)
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
main subject
glucose
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author
Matthias Blüher
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6
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Mark A. Herman
object named as
Mark A. Herman
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1
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Barbara Kahn
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8
object named as
Barbara B. Kahn
1 reference
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PubMed
PubMed ID
22466288
retrieved
25 January 2017
Odile D Peroni
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2
object named as
Odile D. Peroni
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
author name string
Jorge Villoria
series ordinal
3
1 reference
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PubMed
PubMed ID
22466288
retrieved
25 January 2017
Michael R. Schön
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4
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
Nada A. Abumrad
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
Samuel Klein
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7
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
language of work or name
English
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publication date
19 April 2012
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stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
published in
Nature
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stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
volume
484
1 reference
stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
issue
7394
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stated in
PubMed
PubMed ID
22466288
retrieved
25 January 2017
page(s)
333–338
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PubMed
PubMed ID
22466288
retrieved
25 January 2017
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Europe PubMed Central
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11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3341994/fullTextXML
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Regulator of G protein signaling (RGS16) inhibits hepatic fatty acid oxidation in a carbohydrate response element-binding protein (ChREBP)-dependent manner
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PubMed Central
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PubMed Central
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PubMed Central
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Leptin
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PubMed Central
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29 September 2017
Glucose transporters and insulin action--implications for insulin resistance and diabetes mellitus
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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29 September 2017
Role of fatty acids in the pathogenesis of insulin resistance and NIDDM.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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29 September 2017
Adipose cell hyperplasia and enhanced glucose disposal in transgenic mice overexpressing GLUT4 selectively in adipose tissue
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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29 September 2017
Impaired subcutaneous adipocyte lipogenesis is associated with systemic insulin resistance and increased apolipoprotein B/AI ratio in men and women
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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2 June 2018
High level overexpression of glucose transporter-4 driven by an adipose-specific promoter is maintained in transgenic mice on a high fat diet, but does not prevent impaired glucose tolerance
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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2 June 2018
Fatty acid synthesis in liver and adipose tissue of normal and genetically obese (ob/ob) mice during the 24-hour cycle
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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2 June 2018
Response to carbohydrate and fat refeeding in the expression of genes involved in nutrient partitioning and metabolism: striking effects on fibroblast growth factor-21 induction.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
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27 November 2018
Markers of de novo lipogenesis in adipose tissue: associations with small adipocytes and insulin sensitivity in humans.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
retrieved
27 November 2018
Hepatic overexpression of dominant negative Mlx improves metabolic profile in diabetes-prone C57BL/6J mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
retrieved
27 November 2018
ChREBP*Mlx is the principal mediator of glucose-induced gene expression in the liver.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
retrieved
27 November 2018
Adipose-specific overexpression of GLUT4 reverses insulin resistance and diabetes in mice lacking GLUT4 selectively in muscle
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341994
retrieved
27 November 2018
Two CACGTG motifs with proper spacing dictate the carbohydrate regulation of hepatic gene transcription
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22466288
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Serum retinol-binding protein is more highly expressed in visceral than in subcutaneous adipose tissue and is a marker of intra-abdominal fat mass
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22466288
retrieved
12 December 2020
based on heuristic
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Identifiers
DOI
10.1038/NATURE10986
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1540288
Dimensions Publication ID
1036130232
0 references
OpenCitations bibliographic resource ID
1540288
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1540288
PMCID
3341994
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1540288
PubMed ID
22466288
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1540288
ResearchGate publication ID
223979224
0 references
Springer Nature article ID
10.1038/nature10986
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