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regulates thioredoxin to play an important role in the preservation of cellular viability [RGD, Feb 2006].. Additionally we are shipping TXNIP Antibodies (76) and TXNIP Proteins (7) and many more products for this protein.
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The crystal structure of the complex between a phosphorylated PPxY motif of TXNIP and the SH2 domain of Vav2 (show VAV2 ELISA Kits) reveals a conserved recognition mechanism.
Activation of the miR (show MLXIP ELISA Kits)-373-TXNIP-HIF1alpha (show HIF1A ELISA Kits)-TWIST signaling axis is correlated with a worse outcome in patients with breast cancer.
Metformin down-regulates high-glucose-induced TXNIP transcription by inactivating ChREBP (show MLXIPL ELISA Kits) and FOXO1 (show FOXO1 ELISA Kits) in endothelial cells, partially through AMP-activated protein kinase (show PRKAA2 ELISA Kits) activation
Foam cell-released 4-hydroxnonenal activates PPARdelta (show PPARD ELISA Kits) in Vascular endothelial cells, leading to increased TXNIP expression and consequently to senescence.
our data support the hypothesis that TXNIP is an effective target for the treatment of breast cancer.
Expression of TXNIP was up-regulated in all three NSCLC cell lines.
Data identify the metastasis suppressor TXNIP as new target of miR (show MLXIP ELISA Kits)-224/miR (show MLXIP ELISA Kits)-452 that induces feedback inhibition of E2F1 (show E2F1 ELISA Kits) and show that miR (show MLXIP ELISA Kits)-224/452-mediated downregulation of TXNIP is essential for E2F1 (show E2F1 ELISA Kits)-induced EMT (show ITK ELISA Kits) and invasion
HG-induced NADPH oxidase (show NOX1 ELISA Kits) activation is driven by TXNIP which subsequently triggers NALP3 (show NLRP3 ELISA Kits) inflammasome activation in podocytes and ultimately led to podocyte injury
Suggest that TXNIP plays a critical role in anti-Her-1 (show EGFR ELISA Kits)/Her-2 (show ERBB2 ELISA Kits) treatment and may be a potential prognostic marker in breast cancer.
The expression of TXNIP was significantly higher in normal-weight type- 2 diabetic patients than in obese ones.
The molecular characterization of porcine TXNIP gene, is described.
single-marker and haplotype analyses revealed significant effects of TXNIP on hot carcass weight, test daily gain, and lifetime daily gain
Txnip plays an important role in oxidative inflammatory response and atherosclerotic lesion development in ApoE (show APOE ELISA Kits) knockout mice.
The results indicate that a lack of TxNIP protects against diabetic nephropathy (DN) and support in vitro data that upregulation of TxNIP by glucose is a key mediator of early oxidative stress and a trigger for the development and progression of DN.
Reactive oxygen species regulation through REDD1 (show DDIT4 ELISA Kits)/TXNIP is physiological rheostat controlling stress-induced autophagy.
These findings suggest that TXNIP is required for endothelial cell survival and homeostasis especially under stress conditions including hyperoxia.
Data indicate that thioredoxin-interacting protein (TXNIP)levels are induced in erythroid differentiation.
In vivo, levels of lipogenic proteins, inflammatory molecules, PGC-1alpha (show PPARGC1A ELISA Kits), and PRMT1 (show PRMT1 ELISA Kits) were increased in the livers of HFD mice compared with those fed a chow diet, and were ameliorated in HFD Txnip(-/-) mice.
we demonstrated that TXNIP-mediated NLRP3 (show NLRP3 ELISA Kits) inflammasome activation in cardiac microvascular endothelial cells was a novel mechanism of myocardial ischemia/reperfusion injury
Genetic deletion of Txnip in cells and mice led to increased protein ubiquitination and splicing of the unfolded protein response regulated transcription factor X-box-binding protein 1 (show XBP1 ELISA Kits) at baseline as well as under endoplasmic reticulum stress.
results demonstrate that TXNIP binding to NLRP3 (show NLRP3 ELISA Kits) is a key signaling mechanism necessary for hHcys-induced NLRP3 (show NLRP3 ELISA Kits) inflammasome formation and activation and subsequent glomerular injury.
regulates thioredoxin to play an important role in the preservation of cellular viability
thioredoxin interacting protein
, Thioredoxin-interacting protein
, thioredoxin binding protein 2
, thioredoxin-binding protein 2
, thioredoxin-interacting protein
, upregulated by 1,25-dihydroxyvitamin D-3
, vitamin D3 up-regulated protein 1
, hyperlipidemia 1
, thioredoxin binding protein-2