ChREBP, a glucose-responsive transcriptional factor, enhances glucose metabolism to support biosynthesis in human cytomegalovirus-infected cells.
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Regulation of Wnt/β-catenin signaling by herpesvirusesInfection homeostasis: implications for therapeutic and immune programming of metabolism in controlling infectionStealing the Keys to the Kitchen: Viral Manipulation of the Host Cell Metabolic NetworkViral Infections and Obesity.Cytomegalovirus-mediated activation of pyrimidine biosynthesis drives UDP-sugar synthesis to support viral protein glycosylationViral activation of cellular metabolismPositive role of promyelocytic leukemia protein in type I interferon response and its regulation by human cytomegalovirus.Identification of HNF-4α as a key transcription factor to promote ChREBP expression in response to glucoseHuman Cytomegalovirus Can Procure Deoxyribonucleotides for Viral DNA Replication in the Absence of Retinoblastoma Protein Phosphorylation.Effects of low-carbohydrate diet therapy in overweight subjects with autoimmune thyroiditis: possible synergism with ChREBP.Metabolic reprogramming: a hallmark of viral oncogenesis.Lactate dehydrogenase inhibition: exploring possible applications beyond cancer treatment.Fatty acid elongase 7 catalyzes lipidome remodeling essential for human cytomegalovirus replication.The IGF2 mRNA binding protein p62/IGF2BP2-2 induces fatty acid elongation as a critical feature of steatosis.ACSS2-mediated acetyl-CoA synthesis from acetate is necessary for human cytomegalovirus infectionHPV31 utilizes the ATR-Chk1 pathway to maintain elevated RRM2 levels and a replication-competent environment in differentiating Keratinocytes.Essential role of HCMV deubiquitinase in promoting oncogenesis by targeting anti-viral innate immune signaling pathways.Targeting viperin improves diet-induced glucose intolerance but not adipose tissue inflammation.Mechanisms of AMPK in the maintenance of ATP balance during energy metabolism.Flightless-I Controls Fat Storage in Drosophila.
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ChREBP, a glucose-responsive transcriptional factor, enhances glucose metabolism to support biosynthesis in human cytomegalovirus-infected cells.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 21 January 2014
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@en
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@nl
type
label
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@en
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@nl
prefLabel
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@en
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@nl
P2093
P2860
P921
P356
P1476
ChREBP, a glucose-responsive t ...... ytomegalovirus-infected cells.
@en
P2093
James C Alwine
Tobi G Maguire
Yongjun Yu
P2860
P304
P356
10.1073/PNAS.1310779111
P407
P577
2014-01-21T00:00:00Z