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knockdown of GPx-4 by small interfering RNA technique in a human ovarian cancer cell line significantly enhances the cytotoxic effect of docosahexaenoic acid in a time- and concentration-dependent manner. This cytotoxic effect of docosahexaenoic acid is reversed by pretreatment with vitamin E, suggesting that the enhanced toxicity ofGPx-4 knockdown is due to changes in the ability of the cells to handle oxidative stress
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transgenic mouse
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smooth muscle cells
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subclone s6, SV40 large T antigen-transformed human airway epithelial cells
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in the blastomeres, Gpx4 granules are formed, and in the blastocysts, even clusters are present mainly around the cell nuclei
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in the blastomeres, Gpx4 granules are formed, and in the blastocysts, even clusters are present mainly around the cell nuclei
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resting blood platelet
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COH-BR1 cells
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PHGPx expression levels are downregulated in poorly differentiated (grade 3) breast invasive ductal carcinoma. PHGPx expression levels decrease gradually with tumor grade from grade 1 to grade 3. Downregulation of PHGPx in cases that showed p53 accumulation compared with cases without p53 immunostaining is observed. PHGPx is downregulated in cases without progesterone receptors immunostaining compared with cases with PR immunostaining
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treatment with docosahexaenoic acid results in 95% decrease in GPx-4 level
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ovular callus, salt-sensitive and adapted salt-tolerant cell lines
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extraction of genomic DNA
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keratinized surface epithelium
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treatment with docosahexaenoic acid results in 90% decrease in GPx-4 level
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basophil leucemia cell line S1 wild-type cell line and (RBL)2H3 cell line overexpressing mitochondrial phospholipid hydroperoxide glutathione peroxidase
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expression level may vary during mammary gland development
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treatment with docosahexaenoic acid results in 90% decrease in GPx-4 level
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treatment with docosahexaenoic acid results in 60% decrease in GPx-4 level
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treatment with docosahexaenoic acid results in 21% decrease in GPx-4 level
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pituicytes
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in the oocytes, Gpx4 is homogeneously diffused
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the enzyme is present in the epithelium, stroma, blood vessels, and smooth muscles of oviduct
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treatment with docosahexaenoic acid results in 95% decrease in GPx-4 level
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extracellular localisation
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treatment with docosahexaenoic acid results in 85% decrease in GPx-4 level
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PHGPx-overexpressed cell
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100 nM 8(S/R)-hydroxy-11(S),12S-trans-epoxyeicosa-5Z,9E,14Z-trienoic acid upregulates phospholipid hydroperoxide glutathione peroxidase (PHGPx) mRNA and protein expressions. Under persistent oxidative stress the formation of 8(S/R)-hydroxy-11(S),12S-trans-epoxyeicosa-5Z,9E,14Z-trienoic acid and the 8(S/R)-hydroxy-11(S),12S-trans-epoxyeicosa-5Z,9E,14Z-trienoic acid-induced upregulation of PHGPx constitute a compensatory defense response to protect the vitality and functionality of the cell
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of arteries
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enzyme is expressed as active peroxidase
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PHGPx expression is tightly regulated in pachytene spermatocytes, with any spatial-temporal increase in PHGPx expression resulting in damage to spermatogenesis and eventual loss of haploid cells
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cDNA library
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white matter
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mouse embryonic fibroblasts
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parenchym
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treatment with docosahexaenoic acid results in 60% decrease in GPx-4 level
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Paneth cells
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tubular epithelium
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parenchym
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parenchym
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endogenous GPX4 is mainly expressed in neurons, usage of primary cultured cortical neurons
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endogenous GPX4 is mainly expressed in neurons, usage of primary cultured cortical neurons
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Gpx4 is found inside the ovary in the corpus luteum, stroma, follicles, and blood vessels
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exocrine portion
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insulin-producing beta-cells and primary islets. Pancreatic beta-cells are endowed with a unique high expression level of GPx4, while GPx4 expression is significantly lower in insulin-producing RINm5F cells
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insulin-producing beta-cells and primary islets. Pancreatic beta-cells are endowed with a unique high expression level of GPx4, while GPx4 expression is significantly lower in insulin-producing RINm5F cells
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assessment of GPx4 expression in different pancreatic islet cell types reveals a predominant expression in beta-cells
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assessment of GPx4 expression in different pancreatic islet cell types reveals a predominant expression in beta-cells
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enzyme is transformed to an oxidatively inactivated protein in mature sperm, where it is a major constituent of the mitochondrial capsule in the midpiece
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mitochondrial capsule
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activity does not differ between normo- and hypomotile human sperm samples
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epididymal, hormone regulated appearance
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red pulp
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PHGPx mRNA is highly expressed in spermiogenic cells and Leydig cell
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hormone regulated appearance
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strongly linked to mitochondria of cells undergoing differentiation to spermatozoa, under gonadotropin control
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treatment with testosterone slightly decreases PHGPx mRNA levels in testes by the reverse transcription-polymerase chain reaction. Anti-androgenic compounds (flutamide, ketoconazole, and diethylhexyl phthalate) and estrogenic compounds (nonylphenol, octylphenol, and diethylstilbestrol) significantly upregulate PHGPx mRNA in the testes. Endocrine disrupting chemicals might have a detrimental effect on spermatogenesis via abnormal enhancement of PHGPx expression in testes
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parafollicular cells and follicular basement membrane
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Gpx4 is found in the endometrium, myometrium, blood vessels, and stroma of uterus
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additional information
In situ RT-PCR analyses of GPx4 in rat pancreas sections, immunohistochemic analysis
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additional information
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In situ RT-PCR analyses of GPx4 in rat pancreas sections, immunohistochemic analysis
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