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Intestinal xdh overexpression promotes organismal aging with early redox dysregulation
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/arch.21094openalex-snapshot
ACUTE EXPOSURE OF Drosophila melanogaster TO PARAQUAT CAUSES OXIDATIVE STRESS AND MITOCHONDRIAL DYSFUNCTION
inferredcites →https://doi.org/10.1016/0016-5085(81)90648-xopenalex-snapshot
Superoxide radicals in feline intestinal ischemia
inferredcites →https://doi.org/10.1016/j.cell.2013.09.021openalex-snapshot
Muscle Mitohormesis Promotes Longevity via Systemic Repression of Insulin Signaling
inferredcites →https://doi.org/10.1016/j.cell.2022.11.001openalex-snapshot
Hallmarks of aging: An expanding universe
inferredcites →https://doi.org/10.1016/j.celrep.2015.08.004openalex-snapshot
Distinct Shifts in Microbiota Composition during Drosophila Aging Impair Intestinal Function and Drive Mortality
inferredcites →https://doi.org/10.1016/j.cmet.2011.09.013openalex-snapshot
Modulation of Longevity and Tissue Homeostasis by the Drosophila PGC-1 Homolog
inferredcites →https://doi.org/10.1016/j.cmet.2016.03.009openalex-snapshot
Mitochondrial ROS Produced via Reverse Electron Transport Extend Animal Lifespan
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2009.11.012openalex-snapshot
Hydrogen peroxide is the major oxidant product of xanthine oxidase
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2011.04.002openalex-snapshot
Inhibition of xanthine oxidase reduces oxidative stress and improves skeletal muscle function in response to electrically stimulated isometric contractions in aged mice
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2011.10.445openalex-snapshot
The redox stress hypothesis of aging
inferredcites →https://doi.org/10.1016/j.stem.2008.07.024openalex-snapshot
JNK Activity in Somatic Stem Cells Causes Loss of Tissue Homeostasis in the Aging Drosophila Gut
inferredcites →https://doi.org/10.1016/j.stem.2010.12.006openalex-snapshot
Redox Regulation by Keap1 and Nrf2 Controls Intestinal Stem Cell Proliferation in Drosophila
inferredcites →https://doi.org/10.1038/ncb2466openalex-snapshot
Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation
inferredcites →https://doi.org/10.1038/ni.1765openalex-snapshot
Coordination of multiple dual oxidase–regulatory pathways in responses to commensal and infectious microbes in drosophila gut
inferredcites →https://doi.org/10.1038/s41573-021-00233-1openalex-snapshot
Targeting oxidative stress in disease: promise and limitations of antioxidant therapy
inferredcites →https://doi.org/10.1038/s41580-020-0230-3openalex-snapshot
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
inferredcites →https://doi.org/10.1038/s41580-022-00456-zopenalex-snapshot
Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology
inferredcites →https://doi.org/10.1038/s41598-022-11094-yopenalex-snapshot
Possible role of insulin resistance in activation of plasma xanthine oxidoreductase in health check-up examinees
inferredcites →https://doi.org/10.1038/s41598-022-16688-0openalex-snapshot
Xanthine oxidoreductase activity is correlated with hepatic steatosis
inferredcites →https://doi.org/10.1038/s42255-022-00591-zopenalex-snapshot
Guidelines for measuring reactive oxygen species and oxidative damage in cells and in vivo
inferredcites →https://doi.org/10.1056/nejmoa050373openalex-snapshot
Febuxostat Compared with Allopurinol in Patients with Hyperuricemia and Gout
inferredcites →https://doi.org/10.1073/pnas.1215849110openalex-snapshot
Intestinal barrier dysfunction links metabolic and inflammatory markers of aging to death in Drosophila
inferredcites →https://doi.org/10.1073/pnas.97.20.10723openalex-snapshot
Crystal structures of bovine milk xanthine dehydrogenase and xanthine oxidase: Structure-based mechanism of conversion
inferredcites →https://doi.org/10.1111/j.1474-9726.2006.00251.xopenalex-snapshot
Trade‐offs between longevity and pathogen resistance in Drosophila melanogaster are mediated by NFκB signaling
inferredcites →https://doi.org/10.1146/annurev-biochem-061516-045037openalex-snapshot
Oxidative Stress
inferredcites →https://doi.org/10.1161/01.cir.0000041431.57222.afopenalex-snapshot
Vascular Oxidative Stress and Endothelial Dysfunction in Patients With Chronic Heart Failure
inferredcites →https://doi.org/10.1253/circj.cj-18-0082openalex-snapshot
Plasma Xanthine Oxidoreductase Activity as a Novel Biomarker of Metabolic Disorders in a General Population
inferredcites →https://doi.org/10.1371/journal.pgen.1004568openalex-snapshot
Integration of UPRER and Oxidative Stress Signaling in the Control of Intestinal Stem Cell Proliferation
inferredcites →https://doi.org/10.1371/journal.pone.0110963openalex-snapshot
Oxidative Stress Induces Persistent Telomeric DNA Damage Responsible for Nuclear Morphology Change in Mammalian Cells
inferredcites →https://doi.org/10.2147/cia.s158513openalex-snapshot
Oxidative stress, aging, and diseases
inferredcites →https://doi.org/10.3164/jcbn.21-118openalex-snapshot
Associations of circulating xanthine oxidoreductase activity with cardiometabolic risk markers in overweight and obese Japanese men: a cross-sectional pilot study
inferredcites →https://doi.org/10.3390/biomedicines11051445openalex-snapshot
A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
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