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GPX1 and SEPP1 (show SEPP1 Proteins) Single Nucleotide Polymorphism were not associated with any changes in the expression of related genes. GPX1 was shown to modulate the expression of unrelated target, SEP15 (show SEP15 Proteins), upon Se supplementation, both alone and in combination with SEPP1 (show SEPP1 Proteins).
Study demonstrates that SOD2 (show SOD2 Proteins) rs4880, GPX1 rs1050450 and CAT rs1001179 are not associated with an increased susceptibility to epilepsy after neonatal hypoxic-ischemic encephalopathyor its drug resistance
Data show that antioxidant enzymes SOD2 (show SOD2 Proteins) and GPX1 expression and GPX1 and SOD1 (show SOD1 Proteins) activity were significantly higher in patients at diagnosis of bladder cancer (BC) in comparison to controls.
Data show that the placement of rectus sheath block (RSB) analgesia did not significantly affect the level of oxidative stress biomarker plasma glutathione peroxidase (show GPX3 Proteins) (GPX1) level in patients with benign disease or cancer.
Adiponectin gene promoter -11377C/G (CG), -11377C/G (GG), GPx-1 gene C594T (CT), C594T (TT), and cigarette smoking are risk factors in nonalcoholic fatty liver disease (NAFLD).
Our results suggest that GSTP1 rs1695 and GPX1 rs1050450 single nucleotide polymorphisms have no effect on the risk of preeclampsia in the Chinese Han population.
Results show no significant association between glutathione peroxidase 1 (GPX1) Pro198Leu polymorphism and risk of bladder cancer.
It was concluded that the genotype for SNPs in GPX1 and gender affected biomarkers of Se status in this pilot study with healthy Brazilians.
The effects of oleuropein (OL) on hydrogen peroxide-induced oxidative stress in L02 cells showed that SOD1 (show SOD1 Proteins), GPx1, and catalase (show CAT Proteins) levels were all increased, and suggested that OL is a potent antioxidant and may be therapeutically useful in liver disease prevention.
This meta-analysis showed a significant association between low GPx level and vitiligo (show MITF Proteins).
Exposure to far infrared rays significantly protects acute restraint stress oxidative burdens via inhibition of JAK2 (show JAK2 Proteins)/STAT3 (show STAT3 Proteins) signaling by induction of GPx-1.
Genetic inhibition of Gpx1 potentiates cocaine-induced renal damage via activation of AT1R (show AGTRAP Proteins) by inhibition of PI3K-Akt (show AKT1 Proteins) signaling.
Glutathione peroxidase 1 deficiency attenuates concanavalin A-induced liver injury by induction of T-cell hyporesponsiveness through chronic reactive oxygen species exposure.
GPx1 was found to play a critical role in regulating pro-inflammatory pathways in vascular endothelium.
Plasmalogen enrichment via batyl alcohol supplementation attenuated atherosclerosis in ApoE (show APOE Proteins)- and ApoE (show APOE Proteins)/GPx1-deficient mice.
Gpx1 expression in the mouse skeletal muscle can be altered by both exercise and dyslipidemia through changes in DNA methylation (show HELLS Proteins), leading to a fine regulation of free radical metabolism.
our findings unveil a new metabolic role for Reg3beta in protein nitration and a new biosynthesis control of GPX1 by a completely "unrelated" regenerating protein, Reg3beta, via transcriptional activation of Scly (show SCLY Proteins)
Rora (show RORA Proteins) induces the mRNA level of antioxidant enzymes, superoxide dismutase 2 (show SOD2 Proteins) and glutathione peroxidase 1, through the Rora (show RORA Proteins) response elements located in the upstream promoters of Sod2 (show SOD2 Proteins) and Gpx1.
High-fat-fed Gpx1(-/-) mice also exhibited decreased hepatic steatosis and liver damage accompanied by decreased plasma insulin (show INS Proteins) and decreased glucose-induced insulin (show INS Proteins) secretion.
we propose that ileocolitis in the DKO mice is caused by Nox1 (show NOX1 Proteins), which is induced by TNF (show TNF Proteins). The milder disease in female het-TKO (show MRPS12 Proteins) intestine is probably due to random or imprinted X-chromosome inactivation, which produces mosaic Nox1 (show NOX1 Proteins) expression.
Studied the importance of selenium in bovine female reproductive function. Gene expression analysis revealed selenoprotein gene GPX1 was significantly up-regulated in large healthy follicles.
did not find any significant inhibition of bovine GPx-1 by (S)- or (R)-misonidazole.
Data indicate mRNA level and activity of GPx1 are regulated by level of selenium supplied to hepatocytes.
homocysteine decreases GPx1 activity by altering the translational mechanism
glutathione peroxidase-1 activity is decreased by aminoglycosides through interference with selenocysteine incorporation
GPx1 plays a key role in blocking the promotion of porcine circovirus type 2 replication
The developmental expression of GPX1 and thioredoxin reductase during fetal development and the effect of maternal selenium consumption on the expression of these proteins are reported.
This gene encodes a member of the glutathione peroxidase family. Glutathione peroxidase functions in the detoxification of hydrogen peroxide, and is one of the most important antioxidant enzymes in humans. This protein is one of only a few proteins known in higher vertebrates to contain selenocysteine, which occurs at the active site of glutathione peroxidase and is coded by UGA, that normally functions as a translation termination codon. In addition, this protein is characterized in a polyalanine sequence polymorphism in the N-terminal region, which includes three alleles with five, six or seven alanine (ALA) repeats in this sequence. The allele with five ALA repeats is significantly associated with breast cancer risk. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
glutathione peroxidase Gpx1
, glutathione peroxidase
, putative glutathione peroxidase
, glutathione peroxidase 1
, cellular glutathione peroxidase
, selenium-dependent glutathione peroxidase 1
, cytosolic glutathione peroxidase