Absence of RIP140 reveals a pathway regulating glut4-dependent glucose uptake in oxidative skeletal muscle through UCP1-mediated activation of AMPK. (Q34184597)

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English	Absence of RIP140 reveals a pathway regulating glut4-dependent glucose uptake in oxidative skeletal muscle through UCP1-mediated activation of AMPK.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

31 July 2017

Absence of RIP140 reveals a pathway regulating glut4-dependent glucose uptake in oxidative skeletal muscle through UCP1-mediated activation of AMPK. (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Jennifer H Steel

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Jennifer H Steel

2

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Mark Christian

5

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David Carling

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author name string

Asmaà Fritah

1

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Europe PubMed Central

PubMed publication ID

31 July 2017

Nadeene Parker

3

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Europe PubMed Central

PubMed publication ID

31 July 2017

Evanthia Nikolopoulou

4

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Europe PubMed Central

PubMed publication ID

31 July 2017

Malcolm G Parker

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Europe PubMed Central

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31 July 2017

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publication date

28 February 2012

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

PubMed publication ID

31 July 2017

7

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Europe PubMed Central

PubMed publication ID

31 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

e32520

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Creative Commons Attribution 4.0 International

28 February 2012

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April 2022 Public Data File from Crossref

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Metformin inhibits hepatic gluconeogenesis in mice independently of the LKB1/AMPK pathway via a decrease in hepatic energy state

1 reference

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The metabolic coregulator RIP140: an update

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A muscle-specific knockout implicates nuclear receptor coactivator MED1 in the regulation of glucose and energy metabolism

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The nuclear receptor cofactor receptor-interacting protein 140 is a positive regulator of amphiregulin expression and cumulus cell-oocyte complex expansion in the mouse ovary

1 reference

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Elevated expression of the metabolic regulator receptor-interacting protein 140 results in cardiac hypertrophy and impaired cardiac function

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A negative regulatory pathway of GLUT4 trafficking in adipocyte: new function of RIP140 in the cytoplasm via AS160.

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MicroRNA mir-346 targets the 5'-untranslated region of receptor-interacting protein 140 (RIP140) mRNA and up-regulates its protein expression

1 reference

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Control of skeletal muscle metabolic properties by the nuclear receptor corepressor RIP140.

1 reference

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A functional interaction between RIP140 and PGC-1alpha regulates the expression of the lipid droplet protein CIDEA

1 reference

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The regulation of AMP-activated protein kinase by upstream kinases.

1 reference

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Coactivator function of RIP140 for NFkappaB/RelA-dependent cytokine gene expression

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1 reference

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SUMOylation modulates the transcription repressor function of RIP140.

1 reference

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RIP140 directs histone and DNA methylation to silence Ucp1 expression in white adipocytes

1 reference

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Histone deacetylase degradation and MEF2 activation promote the formation of slow-twitch myofibers

1 reference

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The transcriptional corepressor RIP140 regulates oxidative metabolism in skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3289711

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The nuclear receptor cofactor, receptor-interacting protein 140, is required for the regulation of hepatic lipid and glucose metabolism by liver X receptor

1 reference

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AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1alpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3289711

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Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages.

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The transcriptional coactivator PGC-1beta drives the formation of oxidative type IIX fibers in skeletal muscle

1 reference

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Investigating the mechanism for AMP activation of the AMP-activated protein kinase cascade

1 reference

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Suppression of receptor interacting protein 140 repressive activity by protein arginine methylation

1 reference

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Signaling pathways in skeletal muscle remodeling

1 reference

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Suppression of oxidative metabolism and mitochondrial biogenesis by the transcriptional corepressor RIP140 in mouse adipocytes.

1 reference

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RIP140-targeted repression of gene expression in adipocytes

1 reference

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Calmodulin-dependent protein kinase kinase-beta is an alternative upstream kinase for AMP-activated protein kinase

1 reference

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AMP-activated protein kinase: ancient energy gauge provides clues to modern understanding of metabolism

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Estrogen-related receptor alpha directs peroxisome proliferator-activated receptor alpha signaling in the transcriptional control of energy metabolism in cardiac and skeletal muscle

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Nuclear receptor corepressor RIP140 regulates fat accumulation

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Brown adipose tissue: function and physiological significance

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Complexes between the LKB1 tumor suppressor, STRAD alpha/beta and MO25 alpha/beta are upstream kinases in the AMP-activated protein kinase cascade

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The nuclear receptor co-repressor nrip1 (RIP140) is essential for female fertility

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Translocation of myocardial GLUT-4 and increased glucose uptake through activation of AMPK by AICAR.

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Evidence for 5' AMP-activated protein kinase mediation of the effect of muscle contraction on glucose transport

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AMP-activated protein kinase: greater AMP dependence, and preferential nuclear localization, of complexes containing the alpha2 isoform.

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A regulatory role for RIP140 in nuclear receptor activation

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RIP-140 interacts with multiple nuclear receptors by means of two distinct sites

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Inactivation of acetyl-CoA carboxylase and activation of AMP-activated protein kinase in muscle during exercise

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5'AMP activated protein kinase expression in human skeletal muscle: effects of strength training and type 2 diabetes.

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Transcriptional analysis of mouse skeletal myofiber diversity and adaptation to endurance exercise

1 reference

https://pubmed.ncbi.nlm.nih.gov/22389706

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunodetection of UCP1 in rat thymocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22389706

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based on heuristic

inferred from PubMed ID database lookup

Receptor-interacting protein 140 differentially regulates estrogen receptor-related receptor transactivation depending on target genes

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1371/JOURNAL.PONE.0032520

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

2012PLoSO...732520F

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https://api.fatcat.wiki/v0/release/lvjo2ivuf5ah5cjbtprzqsoyta

24 November 2022

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mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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