review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Aaron H Rose | |
Peter R Hoffmann | |||
P2860 | cites work | The activity of aldose reductase is elevated in diabetic mouse heart | Q80034133 |
GPx-3 gene promoter variation and the risk of arterial ischemic stroke | Q80227009 | ||
Increased gene expression of glutathione peroxidase-3 in diabetic mouse heart | Q83229452 | ||
Determinants of selenium status in healthy adults | Q21245924 | ||
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy | Q21560937 | ||
Selenium supplementation for the primary prevention of cardiovascular disease | Q24201670 | ||
Association between the 15-kDa selenoprotein and UDP-glucose:glycoprotein glucosyltransferase in the endoplasmic reticulum of mammalian cells | Q24291018 | ||
Identification and characterization of selenoprotein K: an antioxidant in cardiomyocytes | Q24302087 | ||
Methionine sulfoxide reduction in mammals: characterization of methionine-R-sulfoxide reductases | Q24303517 | ||
Selenoprotein K knockout mice exhibit deficient calcium flux in immune cells and impaired immune responses | Q24336556 | ||
Essential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart function | Q24563493 | ||
Endothelial cell injury due to copper-catalyzed hydrogen peroxide generation from homocysteine | Q24563588 | ||
The human selenoproteome: recent insights into functions and regulation | Q24626002 | ||
Thioredoxin and ventricular remodeling | Q24683258 | ||
Selenium and cardiometabolic health: inconclusive yet intriguing evidence | Q26851701 | ||
Calmodulin-dependent protein kinase II: linking heart failure and arrhythmias | Q26999872 | ||
Synthesis and decoding of selenocysteine and human health | Q27022391 | ||
Aging: a theory based on free radical and radiation chemistry | Q27860549 | ||
Characterization of mammalian selenoproteomes. | Q27863319 | ||
Both selenium deficiency and modest selenium supplementation lead to myocardial fibrosis in mice via effects on redox-methylation balance | Q36537901 | ||
Thioredoxin in the cardiovascular system | Q36615058 | ||
Maintenance of proteins and aging: the role of oxidized protein repair. | Q36647411 | ||
Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study. | Q36685043 | ||
Thiol-based mechanisms of the thioredoxin and glutaredoxin systems: implications for diseases in the cardiovascular system | Q36685478 | ||
Selenistasis: epistatic effects of selenium on cardiovascular phenotype | Q36792384 | ||
Emerging potential of thioredoxin and thioredoxin interacting proteins in various disease conditions | Q37060626 | ||
Eukaryotic selenoprotein synthesis: mechanistic insight incorporating new factors and new functions for old factors | Q37111365 | ||
Oxidative stress is involved in the pathogenesis of Keshan disease (an endemic dilated cardiomyopathy) in China | Q37162946 | ||
Decreased platelet inhibition by nitric oxide in two brothers with a history of arterial thrombosis | Q37352044 | ||
Transgenic mouse models for the vital selenoenzymes cytosolic thioredoxin reductase, mitochondrial thioredoxin reductase and glutathione peroxidase 4. | Q37477495 | ||
Mammalian target of rapamycin signaling in cardiac physiology and disease. | Q37715817 | ||
Selenium in human health and disease | Q37784804 | ||
NMR structures of the selenoproteins Sep15 and SelM reveal redox activity of a new thioredoxin-like family | Q27863341 | ||
Selenoprotein H is a redox-sensing high mobility group family DNA-binding protein that up-regulates genes involved in glutathione synthesis and phase II detoxification | Q27863359 | ||
Selenoprotein T is a PACAP-regulated gene involved in intracellular Ca2+ mobilization and neuroendocrine secretion | Q27863376 | ||
Selenoprotein R is a zinc-containing stereo-specific methionine sulfoxide reductase | Q27936169 | ||
Cloning, sequencing and functional expression of a novel human thioredoxin reductase | Q28115611 | ||
Trends in oxidative aging theories | Q28237122 | ||
Selenium regulation of transcript abundance and translational efficiency of glutathione peroxidase-1 and -4 in rat liver | Q28344447 | ||
Glutathione peroxidase knockout mice are susceptible to myocardial ischemia reperfusion injury | Q28507903 | ||
Targeted disruption of the type 2 selenodeiodinase gene (DIO2) results in a phenotype of pituitary resistance to T4 | Q28509795 | ||
Cytoplasmic thioredoxin reductase is essential for embryogenesis but dispensable for cardiac development | Q28510029 | ||
The PACAP-regulated gene selenoprotein T is abundantly expressed in mouse and human β-cells and its targeted inactivation impairs glucose tolerance | Q28510300 | ||
Deletion of selenoprotein P alters distribution of selenium in the mouse | Q28512024 | ||
The mammalian cytosolic selenoenzyme thioredoxin reductase reduces ubiquinone. A novel mechanism for defense against oxidative stress | Q28570071 | ||
Effects of dietary selenium on post-ischemic expression of antioxidant mRNA | Q28578810 | ||
The selenoprotein GPX4 is essential for mouse development and protects from radiation and oxidative damage insults | Q28587364 | ||
Selenoprotein K is required for palmitoylation of CD36 in macrophages: implications in foam cell formation and atherogenesis | Q28588228 | ||
SelT, SelW, SelH, and Rdx12: genomics and molecular insights into the functions of selenoproteins of a novel thioredoxin-like family | Q28591945 | ||
Heterozygous cellular glutathione peroxidase deficiency in the mouse: abnormalities in vascular and cardiac function and structure | Q28592048 | ||
MsrB1 and MICALs regulate actin assembly and macrophage function via reversible stereoselective methionine oxidation | Q28592880 | ||
Mice with combined disruption of Gpx1 and Gpx2 genes have colitis | Q28593227 | ||
Selenoprotein oxidoreductase with specificity for thioredoxin and glutathione systems | Q28593944 | ||
Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1-/- mice | Q28594703 | ||
Deletion of selenoprotein M leads to obesity without cognitive deficits | Q28594967 | ||
Physiological functions of thioredoxin and thioredoxin reductase | Q29615600 | ||
Reactive oxygen species, antioxidants, and the mammalian thioredoxin system | Q29619367 | ||
Physiological roles of mitochondrial reactive oxygen species | Q29620297 | ||
A dynamic pathway for calcium-independent activation of CaMKII by methionine oxidation | Q29620430 | ||
Alterations in mitochondrial and cytosolic methionine sulfoxide reductase activity during cardiac ischemia and reperfusion. | Q30354240 | ||
Diabetes increases mortality after myocardial infarction by oxidizing CaMKII | Q30540314 | ||
MsrB1 (methionine-R-sulfoxide reductase 1) knock-out mice: roles of MsrB1 in redox regulation and identification of a novel selenoprotein form | Q30850851 | ||
Reactive oxygen species mediate alpha-adrenergic receptor-stimulated hypertrophy in adult rat ventricular myocytes | Q31763854 | ||
Thyroid hormone and the cardiovascular system | Q31921377 | ||
Redox regulation of MAPK pathways and cardiac hypertrophy in adult rat cardiac myocyte | Q32055216 | ||
Strain-stimulated hypertrophy in cardiac myocytes is mediated by reactive oxygen species-dependent Ras S-glutathiolation | Q33248213 | ||
The distal sequence element of the selenocysteine tRNA gene is a tissue-dependent enhancer essential for mouse embryogenesis | Q33758295 | ||
Selenium status and cardiometabolic health: State of the evidence | Q37811279 | ||
Hypoxia-inducible factor-1 alpha in the heart: a double agent? | Q38016690 | ||
Post-transcriptional control of selenoprotein biosynthesis | Q38019545 | ||
Impact of dietary selenium intake on cardiac health: experimental approaches and human studies | Q38023790 | ||
HIF expression and the role of hypoxic microenvironments within primary tumours as protective sites driving cancer stem cell renewal and metastatic progression | Q38112399 | ||
Potential impact of genetic variants in Nrf2 regulated antioxidant genes and risk prediction of diabetes and associated cardiac complications | Q38119999 | ||
The cardiac hypoxic niche: emerging role of hypoxic microenvironment in cardiac progenitors | Q38166731 | ||
Redox signaling in cardiac renewal | Q38226891 | ||
Selenoprotein H is a nucleolar thioredoxin-like protein with a unique expression pattern | Q40163311 | ||
Determinants of human plasma glutathione peroxidase (GPx-3) expression | Q40564755 | ||
Electrophilic prostaglandins and lipid aldehydes repress redox-sensitive transcription factors p53 and hypoxia-inducible factor by impairing the selenoprotein thioredoxin reductase | Q40691219 | ||
Further investigation on the role of selenium deficiency in the aetiology and pathogenesis of Keshan disease | Q41604403 | ||
Gene disruption discloses role of selenoprotein P in selenium delivery to target tissues | Q42127289 | ||
Glutathione peroxidase 1-deficient mice are more susceptible to doxorubicin-induced cardiotoxicity | Q42239399 | ||
Cellular glutathione peroxidase knockout mice express normal levels of selenium-dependent plasma and phospholipid hydroperoxide glutathione peroxidases in various tissues | Q42441950 | ||
Inhibition of basal and interleukin-1-induced VCAM-1 expression by phospholipid hydroperoxide glutathione peroxidase and 15-lipoxygenase in rabbit aortic smooth muscle cells | Q42456158 | ||
Thyroid hormone-targeting the heart | Q43516251 | ||
Ras/Erk signaling is essential for activation of protein synthesis by Gq protein-coupled receptor agonists in adult cardiomyocytes | Q44201590 | ||
Deficiency of glutathione peroxidase-1 sensitizes hyperhomocysteinemic mice to endothelial dysfunction | Q44249751 | ||
Beta-adrenergic receptor-stimulated apoptosis in cardiac myocytes is mediated by reactive oxygen species/c-Jun NH2-terminal kinase-dependent activation of the mitochondrial pathway | Q44306725 | ||
Overexpression of PHGPx and HSP60/10 protects against ischemia/reoxygenation injury | Q44635310 | ||
Effects of dietary selenium on glutathione peroxidase and thioredoxin reductase activity and recovery from cardiac ischemia-reperfusion | Q45109173 | ||
Alpha-adrenergic receptor-stimulated hypertrophy in adult rat ventricular myocytes is mediated via thioredoxin-1-sensitive oxidative modification of thiols on Ras. | Q45277153 | ||
Homocysteine down-regulates cellular glutathione peroxidase (GPx1) by decreasing translation | Q45285244 | ||
Nrf2-dependent upregulation of antioxidative enzymes: a novel pathway for proteasome inhibitor-mediated cardioprotection | Q46058228 | ||
Increased gene expression of antioxidant enzymes in KKAy diabetic mice but not in STZ diabetic mice | Q46591086 | ||
Selenium prevents diabetes-induced alterations in [Zn2+]i and metallothionein level of rat heart via restoration of cell redox cycle | Q46743940 | ||
Targeted disruption of the type 1 selenodeiodinase gene (Dio1) results in marked changes in thyroid hormone economy in mice | Q46751893 | ||
Role of promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene as a risk factor for cerebral venous thrombosis | Q46838350 | ||
Counteraction of adriamycin-induced oxidative damage in rat heart by selenium dietary supplementation | Q46944451 | ||
Glutathione peroxidase: a selenoenzyme | Q47965043 | ||
Selenium: Biochemical Role as a Component of Glutathione Peroxidase | Q48014453 | ||
Transgenic mice overexpressing glutathione peroxidase are resistant to myocardial ischemia reperfusion injury | Q48948258 | ||
Glutathione peroxidase protects mice from viral-induced myocarditis. | Q52531835 | ||
NK-lysin, a disulfide-containing effector peptide of T-lymphocytes, is reduced and inactivated by human thioredoxin reductase. Implication for a protective mechanism against NK-lysin cytotoxicity. | Q54590051 | ||
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts | Q57315334 | ||
Benign human enterovirus becomes virulent in selenium-deficient mice | Q58983545 | ||
Calmodulin kinase II inhibition protects against structural heart disease | Q59975125 | ||
Keshan disease: an endemic cardiomyopathy in China | Q70110313 | ||
Selenium in diet, blood, and toenails in relation to human health in a seleniferous area | Q70143028 | ||
[Detection of enteroviral RNA in paraffin-embedded myocardial tissue from patients with Keshan by nested PCR] | Q71727943 | ||
Preconditioning potentiates molecular signaling for myocardial adaptation to ischemia | Q71754539 | ||
Homocyst(e)ine decreases bioavailable nitric oxide by a mechanism involving glutathione peroxidase | Q73456320 | ||
Effects of homocysteine on endothelial nitric oxide production | Q74346361 | ||
Inhibitory effects of antioxidants on neonatal rat cardiac myocyte hypertrophy induced by tumor necrosis factor-alpha and angiotensin II | Q77198542 | ||
Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial stroke | Q78122067 | ||
Regulation of cardiomyocyte apoptosis in ischemic reperfused mouse heart by glutathione peroxidase | Q78130140 | ||
Attenuation of doxorubicin-induced contractile and mitochondrial dysfunction in mouse heart by cellular glutathione peroxidase | Q79743967 | ||
The role of Nrf2-mediated pathway in cardiac remodeling and heart failure | Q33914944 | ||
Overexpression of cellular glutathione peroxidase rescues homocyst(e)ine-induced endothelial dysfunction | Q33947823 | ||
Characterization of enterovirus isolates from patients with heart muscle disease in a selenium-deficient area of China. | Q33969834 | ||
Homocysteine and coronary risk | Q34027229 | ||
Inhibition of endogenous thioredoxin in the heart increases oxidative stress and cardiac hypertrophy | Q34274405 | ||
Cloning and sequencing of a human thioredoxin reductase | Q34297828 | ||
Glutathione peroxidases | Q34314833 | ||
Oxidized Ca(2+)/calmodulin-dependent protein kinase II triggers atrial fibrillation. | Q34370565 | ||
Molecular and cellular aspects of thiol-disulfide exchange. | Q34373608 | ||
Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD). | Q34396448 | ||
Cardiac-specific elevations in thyroid hormone enhance contractility and prevent pressure overload-induced cardiac dysfunction | Q34509413 | ||
Impacts of dietary selenium deficiency on metabolic phenotypes of diet-restricted GPX1-overexpressing mice | Q34519430 | ||
Selenium and human health. | Q34636304 | ||
Reduction in glutathione peroxidase 4 increases life span through increased sensitivity to apoptosis | Q34693231 | ||
Hypoxia. 2. Hypoxia regulates cellular metabolism | Q34718056 | ||
Development of insulin resistance and obesity in mice overexpressing cellular glutathione peroxidase | Q34827699 | ||
Antioxidant nutrients and adriamycin toxicity. | Q34904589 | ||
Reduced utilization of selenium by naked mole rats due to a specific defect in GPx1 expression | Q34947894 | ||
Specific antioxidant selenoproteins are induced in the heart during hypertrophy | Q35085592 | ||
Selenium-dependent enzymes in endothelial cell function | Q35115463 | ||
Translational regulation of GPx-1 and GPx-4 by the mTOR pathway. | Q35137710 | ||
Thyroid hormone deiodinases: physiology and clinical disorders | Q35188882 | ||
Roles of the 15-kDa selenoprotein (Sep15) in redox homeostasis and cataract development revealed by the analysis of Sep 15 knockout mice | Q35312958 | ||
Selenoprotein K binds multiprotein complexes and is involved in the regulation of endoplasmic reticulum homeostasis | Q35604604 | ||
Promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene: a novel risk factor for arterial ischemic stroke among young adults and children. | Q35608361 | ||
Assessment of requirements for selenium and adequacy of selenium status: a review | Q35676276 | ||
Glutathione peroxidase potentiates the inhibition of platelet function by S-nitrosothiols | Q35750794 | ||
Stimulation of unprimed macrophages with immune complexes triggers a low output of nitric oxide by calcium-dependent neuronal nitric-oxide synthase | Q35762897 | ||
The selenoproteome exhibits widely varying, tissue-specific dependence on selenoprotein P for selenium supply | Q35891602 | ||
Oxidation of CaMKII determines the cardiotoxic effects of aldosterone. | Q35903753 | ||
The Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production | Q36118624 | ||
Early embryonic lethality caused by targeted disruption of the mouse selenocysteine tRNA gene (Trsp). | Q36149734 | ||
Selenoprotein synthesis: a unique translational mechanism used by a diverse family of proteins | Q36244481 | ||
P433 | issue | 3 | |
P304 | page(s) | 494-504 | |
P577 | publication date | 2014-10-30 | |
P1433 | published in | Thrombosis and Haemostasis | Q15724413 |
P1476 | title | Selenoproteins and cardiovascular stress | |
P478 | volume | 113 |
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