| Q28391506 | Basic principles and emerging concepts in the redox control of transcription factors |
| Q38822665 | Characterizations of Three Major Cysteine Sensors of Keap1 in Stress Response. |
| Q36813967 | Contrasting roles of dietary selenium and selenoproteins in chemically induced hepatocarcinogenesis |
| Q27346748 | Cytoprotective Nrf2 pathway is induced in chronically txnrd 1-deficient hepatocytes |
| Q36012410 | Dietary Selenium Levels Affect Selenoprotein Expression and Support the Interferon-γ and IL-6 Immune Response Pathways in Mice |
| Q58576444 | Emerging Regulatory Role of Nrf2 in Iron, Heme, and Hemoglobin Metabolism in Physiology and Disease |
| Q35652974 | Expression of Selenoproteins Is Maintained in Mice Carrying Mutations in SECp43, the tRNA Selenocysteine 1 Associated Protein (Trnau1ap). |
| Q36362863 | Genetic evidence of an evolutionarily conserved role for Nrf2 in the protection against oxidative stress |
| Q92704403 | Interaction of Genetic Variations in NFE2L2 and SELENOS Modulates the Risk of Hashimoto's Thyroiditis |
| Q28394732 | Mechanisms of activation of the transcription factor Nrf2 by redox stressors, nutrient cues, and energy status and the pathways through which it attenuates degenerative disease |
| Q36281925 | Mouse models targeting selenocysteine tRNA expression for elucidating the role of selenoproteins in health and development |
| Q37682067 | New Strategy of Functional Analysis of PHGPx Knockout Mice Model Using Transgenic Rescue Method and Cre-LoxP System |
| Q28295619 | Nrf1 and Nrf2 play distinct roles in activation of antioxidant response element-dependent genes |
| Q41687488 | Nrf2 target genes are induced under marginal selenium-deficiency |
| Q21563337 | Osteo-chondroprogenitor-specific deletion of the selenocysteine tRNA gene, Trsp, leads to chondronecrosis and abnormal skeletal development: a putative model for Kashin-Beck disease |
| Q28392715 | Paradoxical Roles of Antioxidant Enzymes: Basic Mechanisms and Health Implications |
| Q33427719 | Penultimate selenocysteine residue replaced by cysteine in thioredoxin reductase from selenium-deficient rat liver. |
| Q39776218 | Protective signalling effect of manganese superoxide dismutase in hypoxia-reoxygenation of hepatocytes |
| Q35202342 | Role of selenium-containing proteins in T-cell and macrophage function |
| Q88736653 | Roles for selenium and selenoprotein P in the development, progression, and prevention of intestinal disease |
| Q33652130 | Selective up-regulation of human selenoproteins in response to oxidative stress |
| Q58076433 | Selenium at the redox interface of the genome, metabolome and exposome |
| Q37281599 | Selenoprotein H is an essential regulator of redox homeostasis that cooperates with p53 in development and tumorigenesis |
| Q89455910 | Selenoprotein P as an in vivo redox regulator: disorders related to its deficiency and excess |
| Q38937720 | Selenoproteins and oxidative stress-induced inflammatory tumorigenesis in the gut. |
| Q47622822 | Selenoproteins in Tumorigenesis and Cancer Progression |
| Q33513325 | Selenoproteins regulate macrophage invasiveness and extracellular matrix-related gene expression |
| Q46371968 | Simvastatin activates Keap1/Nrf2 signaling in rat liver |
| Q24626002 | The human selenoproteome: recent insights into functions and regulation |
| Q39316517 | Thiophosphate and selenite conversely modulate cell death induced by glutathione depletion or cisplatin: effects related to activity and Sec contents of thioredoxin reductase. |
| Q28080723 | TrxR1 as a potent regulator of the Nrf2-Keap1 response system |
| Q95276643 | Understanding Metal Dynamics Between Cancer Cells and Macrophages: Competition or Synergism? |
| Q36129752 | Understanding selenoprotein function and regulation through the use of rodent models |
| Q41962064 | Validation of the multiple sensor mechanism of the Keap1-Nrf2 system |