Oxidative stress activates metal-responsive transcription factor-1 binding activity. Occupancy in vivo of metal response elements in the metallothionein-I gene promoter.
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Induction of metallothionein l by phenolic antioxidants requires metal-activated transcription factor 1 (MTF-1) and zincInduction of human metallothionein 1G promoter by VEGF and heavy metals: differential involvement of E2F and metal transcription factorsVanin-1-/- mice exhibit a glutathione-mediated tissue resistance to oxidative stressRegulation of translocator protein 18 kDa (TSPO) expression in health and disease statesTwo major branches of anti-cadmium defense in the mouse: MTF-1/metallothioneins and glutathioneActivation of gene expression by metal-responsive signal transduction pathways.Copper-inducible transcription: regulation by metal- and oxidative stress-responsive pathwaysRegulation of metallothionein transcription by the metal-responsive transcription factor MTF-1: identification of signal transduction cascades that control metal-inducible transcriptionNucleo-cytoplasmic trafficking of metal-regulatory transcription factor 1 is regulated by diverse stress signalsNrf1 and Nrf2 play distinct roles in activation of antioxidant response element-dependent genesCadmium-mediated activation of the metal response element in human neuroblastoma cells lacking functional metal response element-binding transcription factor-1Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1Hypoxia acts through multiple signaling pathways to induce metallothionein transactivation by the metal-responsive transcription factor-1 (MTF-1)Nutrient-gene interactions: a single nutrient and hundreds of target genes.A novel chimeric promoter that is highly responsive to hypoxia and metals.Zinc is a potent and specific inhibitor of IFN-λ3 signalling.Identification of ATF-7 and the insulin signaling pathway in the regulation of metallothionein in C. elegans suggests roles in aging and reactive oxygen species.Induction, regulation, degradation, and biological significance of mammalian metallothioneins.A potential role for alterations of zinc and zinc transport proteins in the progression of Alzheimer's disease.The Drosophila homolog of mammalian zinc finger factor MTF-1 activates transcription in response to heavy metalsThe parkin mutant phenotype in the fly is largely rescued by metal-responsive transcription factor (MTF-1)Identification of two nickel ion-induced genes, NCI16 and PcGST1, in Paramecium caudatum.Putting its fingers on stressful situations: the heavy metal-regulatory transcription factor MTF-1.The transcription factors MTF-1 and USF1 cooperate to regulate mouse metallothionein-I expression in response to the essential metal zinc in visceral endoderm cells during early developmentDifferential regulation of the rainbow trout (Oncorhynchus mykiss) MT-A gene by nuclear factor interleukin-6 and activator protein-1.Target gene search for the metal-responsive transcription factor MTF-1.Mycobacterial p(1)-type ATPases mediate resistance to zinc poisoning in human macrophages.The role of small ubiquitin-like modifier-interacting motif in the assembly and regulation of metal-responsive transcription factor 1.Zinc inhibits the reproductive toxicity of Zearalenone in immortalized murine ovarian granular KK-1 cells.Zinc and cancer: implications for LIV-1 in breast cancer.Activation of metallothionein transcription by 4-hydroxynonenalMetallothionein induction in response to restraint stress. Transcriptional control, adaptation to stress, and role of glucocorticoidHypothermia enhances induction of protective protein metallothionein under ischemia.Activity of metal-responsive transcription factor 1 by toxic heavy metals and H2O2 in vitro is modulated by metallothionein.Serum zinc in the progression of Alzheimer's disease.Metal-responsive transcription factor 1 (MTF-1) activity is regulated by a nonconventional nuclear localization signal and a metal-responsive transactivation domain.Overexpression of the large subunit of the protein Ku suppresses metallothionein-I induction by heavy metals.Cellular stress response pathway system as a sentinel ensemble in toxicological screening.Nuclear proteins that bind to metal response element a (MREa) in the Wilson disease gene promoter are Ku autoantigens and the Ku-80 subunit is necessary for basal transcription of the WD gene.Nuclear factor-1 and metal transcription factor-1 synergistically activate the mouse metallothionein-1 gene in response to metal ions.
P2860
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P2860
Oxidative stress activates metal-responsive transcription factor-1 binding activity. Occupancy in vivo of metal response elements in the metallothionein-I gene promoter.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Oxidative stress activates met ...... tallothionein-I gene promoter.
@en
type
label
Oxidative stress activates met ...... tallothionein-I gene promoter.
@en
prefLabel
Oxidative stress activates met ...... tallothionein-I gene promoter.
@en
P2093
P356
P1476
Oxidative stress activates met ...... tallothionein-I gene promoter.
@en
P2093
P304
26233-26241
P356
10.1074/JBC.271.42.26233
P407
P577
1996-10-01T00:00:00Z