scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | José Pedro Castro | Q92616183 |
Tilman Grune | Q42577412 | ||
Annika Höhn | Q47503915 | ||
Tobias Jung | Q48013635 | ||
Martín Hugo | Q54023035 | ||
Daniela Weber | Q56383616 | ||
P2093 | author name string | Ioanna Korovila | |
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The Immunoproteasome Cleans up after Inflammation | Q84772673 | ||
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Purification of an 11 S regulator of the multicatalytic protease | Q28202111 | ||
Proteasome-mediated processing of Nrf1 is essential for coordinate induction of all proteasome subunits and p97 | Q28243388 | ||
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Antioxidants Enhance Mammalian Proteasome Expression through the Keap1-Nrf2 Signaling Pathway | Q37062266 | ||
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Mixed proteasomes function to increase viral peptide diversity and broaden antiviral CD8+ T cell responses | Q37146941 | ||
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Activation of Nrf2-antioxidant signaling attenuates NFkappaB-inflammatory response and elicits apoptosis | Q37241323 | ||
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S-glutathionylation of the Rpn2 regulatory subunit inhibits 26 S proteasomal function | Q37372263 | ||
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The proteasomal system. | Q37446143 | ||
Methionine sulfoxides in serum proteins as potential clinical biomarkers of oxidative stress | Q37483905 | ||
The molecular chaperone Hsp70 promotes the proteolytic removal of oxidatively damaged proteins by the proteasome. | Q37545942 | ||
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The Ubiquitin System and Kaposi's Sarcoma-Associated Herpesvirus | Q37989143 | ||
Changes of the proteasomal system during the aging process. | Q38021168 | ||
The Nrf2 cell defence pathway: Keap1-dependent and -independent mechanisms of regulation | Q38065567 | ||
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Relationship between the proteasomal system and autophagy | Q38103557 | ||
The MHC I loading complex: a multitasking machinery in adaptive immunity | Q38121190 | ||
The proteasome and the degradation of oxidized proteins: Part I-structure of proteasomes. | Q38136226 | ||
Early signalling events of autophagy | Q38144264 | ||
Selective autophagy | Q38144281 | ||
The nrf1 and nrf2 balance in oxidative stress regulation and androgen signaling in prostate cancer cells | Q38166575 | ||
The machinery of macroautophagy | Q38173673 | ||
Redox regulation of the proteasome via S-glutathionylation. | Q38176369 | ||
Mechanisms for regulating deubiquitinating enzymes | Q38176851 | ||
The proteasome and the degradation of oxidized proteins: part III-Redox regulation of the proteasomal system | Q38190556 | ||
Melatonin feedback on clock genes: a theory involving the proteasome | Q38264948 | ||
Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules | Q28248180 | ||
Transcription factor Nrf1 mediates the proteasome recovery pathway after proteasome inhibition in mammalian cells | Q28279454 | ||
Proteasomal Degradation Is Transcriptionally Controlled by TCF11 via an ERAD-Dependent Feedback Loop | Q28295179 | ||
p97-dependent retrotranslocation and proteolytic processing govern formation of active Nrf1 upon proteasome inhibition | Q28306282 | ||
Evolution of proteasome regulators in eukaryotes | Q28334391 | ||
Regulation of cell function by methionine oxidation and reduction | Q28349109 | ||
Redox regulation of mitochondrial function | Q28383361 | ||
The Keap1-Nrf2 pathway: Mechanisms of activation and dysregulation in cancer | Q28387975 | ||
The complexity of the Nrf2 pathway: beyond the antioxidant response | Q28389296 | ||
Regulation of proteasome activity in health and disease | Q28392708 | ||
Nrf2, a regulator of the proteasome, controls self-renewal and pluripotency in human embryonic stem cells | Q28394410 | ||
Microautophagy of cytosolic proteins by late endosomes | Q28509224 | ||
Altered proteasome function and subunit composition in aged muscle | Q28565158 | ||
Systematic survey of deubiquitinase localization identifies USP21 as a regulator of centrosome- and microtubule-associated functions | Q28575853 | ||
Selective autophagy: xenophagy | Q28652564 | ||
Induction of autophagy by spermidine promotes longevity | Q29614498 | ||
Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple | Q29615232 | ||
The unfolded protein response: controlling cell fate decisions under ER stress and beyond | Q29615499 | ||
Inducibility of kappa immunoglobulin enhancer-binding protein Nf-kappa B by a posttranslational mechanism | Q29619866 | ||
Inflammation meets cancer, with NF-κB as the matchmaker | Q29620242 | ||
Methionine residues may protect proteins from critical oxidative damage. | Q30322097 | ||
HSPA8/HSC70 chaperone protein: structure, function, and chemical targeting. | Q30354473 | ||
Catalytic site-specific inhibition of the 20S proteasome by 4-hydroxynonenal | Q31135318 | ||
The IKK complex, a central regulator of NF-kappaB activation | Q33693802 | ||
Nuclear erythroid factor 2-mediated proteasome activation delays senescence in human fibroblasts | Q33707090 | ||
Mining the TRAF6/p62 interactome for a selective ubiquitination motif | Q33893441 | ||
Uric acid: the oxidant-antioxidant paradox | Q33956678 | ||
Methionine oxidation and aging | Q33984659 | ||
Assembly, structure, and function of the 26S proteasome. | Q33988314 | ||
Conformational constraints in protein degradation by the 20S proteasome | Q34058982 | ||
An optimal ubiquitin-proteasome pathway in the nervous system: the role of deubiquitinating enzymes | Q34063163 | ||
Properties of the hybrid form of the 26S proteasome containing both 19S and PA28 complexes. | Q34088438 | ||
Catalytic activities of the 20 S proteasome, a multicatalytic proteinase complex | Q34092896 | ||
Microautophagy: lesser-known self-eating | Q34232209 | ||
Chaperones, but not oxidized proteins, are ubiquitinated after oxidative stress | Q34298650 | ||
Signals from the lysosome: a control centre for cellular clearance and energy metabolism | Q34340780 | ||
Autophagy and ageing: implications for age-related neurodegenerative diseases. | Q34373575 | ||
PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome | Q34381697 | ||
Chaperone-mediated autophagy: roles in disease and aging | Q34388237 | ||
Muscle wasting in aged, sarcopenic rats is associated with enhanced activity of the ubiquitin proteasome pathway | Q34400761 | ||
Selective mitochondrial autophagy, or mitophagy, as a targeted defense against oxidative stress, mitochondrial dysfunction, and aging | Q34556311 | ||
NF-kappaB/p65 antagonizes Nrf2-ARE pathway by depriving CBP from Nrf2 and facilitating recruitment of HDAC3 to MafK. | Q34744211 | ||
Dependence of proteasome processing rate on substrate unfolding | Q34978877 | ||
Ubiquitin-proteasome pathway and cellular responses to oxidative stress | Q35027877 | ||
20S proteasome activation promotes life span extension and resistance to proteotoxicity in Caenorhabditis elegans | Q35039312 | ||
Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome. | Q35202606 | ||
Peroxiredoxin 3 is a key molecule regulating adipocyte oxidative stress, mitochondrial biogenesis, and adipokine expression. | Q35604034 | ||
Lifespan of mice and primates correlates with immunoproteasome expression | Q35720093 | ||
Induction and adaptation of chaperone-assisted selective autophagy CASA in response to resistance exercise in human skeletal muscle | Q35852833 | ||
Age-dependent inhibition of proteasome chymotrypsin-like activity in the retina | Q35858136 | ||
Nrf2-dependent induction of proteasome and Pa28αβ regulator are required for adaptation to oxidative stress | Q35880062 | ||
Quantitative time-resolved analysis reveals intricate, differential regulation of standard- and immuno-proteasomes | Q36177598 | ||
Dissecting molecular cross-talk between Nrf2 and NF-κB response pathways | Q36184638 | ||
Proteasome function is not impaired in healthy aging of the lung | Q36260235 | ||
NF-κB controls energy homeostasis and metabolic adaptation by upregulating mitochondrial respiration | Q36291524 | ||
mTORC1 maintains metabolic balance | Q36293517 | ||
Coordinate regulation of the human TAP1 and LMP2 genes from a shared bidirectional promoter | Q36364703 | ||
Chaperones in autophagy | Q36413186 | ||
Multiple nuclear localization signals function in the nuclear import of the transcription factor Nrf2. | Q36512148 | ||
Constitutive activation of chaperone-mediated autophagy in cells with impaired macroautophagy | Q36631143 | ||
Proteasomal adaptation to environmental stress links resistance to proteotoxicity with longevity in Caenorhabditis elegans | Q36657540 | ||
Thymoproteasome subunit-β5T generates peptide-MHC complexes specialized for positive selection | Q36799097 | ||
Standard and immunoproteasomes show similar peptide degradation specificities. | Q38268527 | ||
S-glutathionylation reactions in mitochondrial function and disease | Q38276703 | ||
The proteasome and the degradation of oxidized proteins: Part II - protein oxidation and proteasomal degradation | Q38280561 | ||
Regulation of NADPH oxidase subunit p22(phox) by NF-kB in human aortic smooth muscle cells | Q38294991 | ||
Role of glutathione, glutathione transferase, and glutaredoxin in regulation of redox-dependent processes. | Q38369963 | ||
The demographics of the ubiquitin system | Q38439051 | ||
Redox- and non-redox-metal-induced formation of free radicals and their role in human disease | Q38581859 | ||
Targeting the lysosome in cancer | Q38645365 | ||
The role of E3 ubiquitin-ligases MuRF-1 and MAFbx in loss of skeletal muscle mass | Q38688717 | ||
Structural and Biological Interaction of hsc-70 Protein with Phosphatidylserine in Endosomal Microautophagy | Q38758528 | ||
Metabolic Syndrome, Redox State, and the Proteasomal System | Q38842149 | ||
Chaperone mediated autophagy in aging: Starve to prosper | Q38916473 | ||
Proteasome isoforms exhibit only quantitative differences in cleavage and epitope generation | Q38955527 | ||
Differential roles of proteasome and immunoproteasome regulators Pa28αβ, Pa28γ and Pa200 in the degradation of oxidized proteins. | Q39352530 | ||
Proteins bearing oxidation-induced carbonyl groups are not preferentially ubiquitinated. | Q39576384 | ||
SCF/{beta}-TrCP promotes glycogen synthase kinase 3-dependent degradation of the Nrf2 transcription factor in a Keap1-independent manner. | Q39606140 | ||
Ubiquitin-independent degradation of antiapoptotic MCL-1. | Q39715640 | ||
Chromatin repair after oxidative stress: role of PARP-mediated proteasome activation | Q39760680 | ||
Quantification of age-related changes of α-tocopherol in lysosomal membranes in murine tissues and human fibroblasts. | Q39837797 | ||
NADH binds and stabilizes the 26S proteasomes independent of ATP. | Q39997925 | ||
The olive constituent oleuropein exhibits proteasome stimulatory properties in vitro and confers life span extension of human embryonic fibroblasts | Q40129325 | ||
A new infant case of Nakajo-Nishimura syndrome with a genetic mutation in the immunoproteasome subunit: an overlapping entity with JMP and CANDLE syndrome related to PSMB8 mutations. | Q40238045 | ||
Intracellular distribution of oxidized proteins and proteasome in HT22 cells during oxidative stress. | Q40288929 | ||
Glycogen synthase kinase-3beta inhibits the xenobiotic and antioxidant cell response by direct phosphorylation and nuclear exclusion of the transcription factor Nrf2. | Q40301567 | ||
A mathematical model of protein degradation by the proteasome | Q40324090 | ||
Circadian modulation of proteasome activities and removal of carbonylated proteins | Q40438284 | ||
Central role of the proteasome in senescence and survival of human fibroblasts: induction of a senescence-like phenotype upon its inhibition and resistance to stress upon its activation. | Q40649321 | ||
Protein oxidation and degradation during cellular senescence of human BJ fibroblasts: part I--effects of proliferative senescence | Q40839462 | ||
Hydrogen peroxide-mediated protein oxidation in young and old human MRC-5 fibroblasts. | Q40899090 | ||
Biochemical basis of lipofuscin, ceroid, and age pigment-like fluorophores | Q41197191 | ||
Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination | Q41589996 | ||
Mitochondrial contribution to lipofuscin formation. | Q42042230 | ||
Macroautophagy is impaired in old murine brain tissue as well as in senescent human fibroblasts. | Q42372625 | ||
Mitochondrial autophagy promotes healthy aging. | Q42389288 | ||
Autophagosomes, phagosomes, autolysosomes, phagolysosomes, autophagolysosomes... wait, I'm confused | Q42729278 | ||
Genetic evidence linking age-dependent attenuation of the 26S proteasome with the aging process | Q43179672 | ||
Glutathiolation of the proteasome is enhanced by proteolytic inhibitors | Q43599231 | ||
Age-dependent declines in proteasome activity in the heart | Q43857550 | ||
Age-related increase in the immunoproteasome content in rat hippocampus: molecular and functional aspects. | Q43903490 | ||
Stability of the nuclear protein turnover during cellular senescence of human fibroblasts | Q44535787 | ||
Nrf1 can be processed and activated in a proteasome-independent manner | Q45043665 | ||
Macroxyproteinase (M.O.P.): a 670 kDa proteinase complex that degrades oxidatively denatured proteins in red blood cells. | Q45054752 | ||
Role of glutaredoxin 2 and cytosolic thioredoxins in cysteinyl-based redox modification of the 20S proteasome | Q46627706 | ||
Identifying, by first-principles simulations, Cu[amyloid-β] species making Fenton-type reactions in Alzheimer's disease | Q46650994 | ||
RPN-6 determines C. elegans longevity under proteotoxic stress conditions | Q46942610 | ||
Age-related changes in the 20S and 26S proteasome activities in the liver of male F344 rats | Q47847864 | ||
Activation of the proteasome during Xenopus egg activation implies a link between proteasome activation and intracellular calcium release | Q49022344 | ||
Cardioprotection of exercise preconditioning involving heat shock protein 70 and concurrent autophagy: a potential chaperone-assisted selective macroautophagy effect. | Q51280141 | ||
Reduced autophagy leads to an impaired ferritin turnover in senescent fibroblasts. | Q51358844 | ||
Thymoproteasome shapes immunocompetent repertoire of CD8+ T cells. | Q53350619 | ||
PARP-1: a new player in the asthma field? | Q53830448 | ||
Altered dynamics of the lysosomal receptor for chaperone-mediated autophagy with age. | Q54557545 | ||
The Lysosome | Q55037468 | ||
Lipofuscin inhibits the proteasome by binding to surface motifs | Q59240639 | ||
Protein oxidation and degradation during cellular senescence of human BJ fibroblasts: part II—aging of nondividing cells | Q60284685 | ||
Proteasome β-type subunits: unequal roles of propeptides in core particle maturation and a hierarchy of active site function | Q60656421 | ||
Age-related differences in oxidative protein-damage in young and senescent fibroblasts | Q60705157 | ||
Human erythrocyte contains a factor that stimulates the peptidase activities of multicatalytic proteinase complex | Q67925446 | ||
Proteasome activator PA28 and its interaction with 20 S proteasomes | Q71053872 | ||
Fibroblast cultures from healthy centenarians have an active proteasome | Q73128693 | ||
Hydrogen peroxide-induced structural alterations of RNAse A | Q73294198 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International | Q24082749 |
P921 | main subject | proteostasis | Q2892805 |
human ageing | Q332154 | ||
oxidative stress | Q898814 | ||
P304 | page(s) | 550-567 | |
P577 | publication date | 2017-07-12 | |
2017-10-01 | |||
P1433 | published in | Redox Biology | Q27724751 |
P1476 | title | Proteostasis, oxidative stress and aging | |
P478 | volume | 13 |
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