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A Hypothesis to Explain How the DNA of Elderly People Is Prone to Damage: Genome-Wide Hypomethylation Drives Genomic Instability in the Elderly by Reducing Youth-Associated Gnome-Stabilizing DNA Gaps
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The Discovery of 5‐Formylcytosine in Embryonic Stem Cell DNA
inferredcites →https://doi.org/10.1007/s13148-010-0017-zopenalex-snapshot
Epigenetic mechanisms and genome stability
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Regulating the HO endonuclease in yeast
inferredcites →https://doi.org/10.1016/j.bbadis.2015.08.017openalex-snapshot
Sirtuin regulation in aging and injury
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HMGB proteins: Interactions with DNA and chromatin
inferredcites →https://doi.org/10.1016/j.cell.2011.02.013openalex-snapshot
Hallmarks of Cancer: The Next Generation
inferredcites →https://doi.org/10.1016/j.cell.2011.03.022openalex-snapshot
Hydroxylation of 5-Methylcytosine by TET1 Promotes Active DNA Demethylation in the Adult Brain
inferredcites →https://doi.org/10.1016/j.cell.2015.10.055openalex-snapshot
Molecular Mechanism of V(D)J Recombination from Synaptic RAG1-RAG2 Complex Structures
inferredcites →https://doi.org/10.1016/j.cub.2004.12.065openalex-snapshot
Yeast Nhp6A/B and Mammalian Hmgb1 Facilitate the Maintenance of Genome Stability
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.06.027openalex-snapshot
An epigenetic perspective on the free radical theory of development
inferredcites →https://doi.org/10.1016/j.molcel.2007.06.029openalex-snapshot
HMGB1 Is a Cofactor in Mammalian Base Excision Repair
inferredcites →https://doi.org/10.1016/j.molcel.2007.11.015openalex-snapshot
The DNA Damage Response: Ten Years After
inferredcites →https://doi.org/10.1016/j.molcel.2010.09.019openalex-snapshot
The DNA Damage Response: Making It Safe to Play with Knives
inferredcites →https://doi.org/10.1016/j.mrfmmm.2014.11.009openalex-snapshot
DNA damage in non-communicable diseases: A clinical and epidemiological perspective
inferredcites →https://doi.org/10.1016/j.mrfmmm.2016.02.009openalex-snapshot
Radiation-induced changes in DNA methylation of repetitive elements in the mouse heart
inferredcites →https://doi.org/10.1016/j.mrrev.2015.07.001openalex-snapshot
Persistent γH2AX: A promising molecular marker of DNA damage and aging
inferredcites →https://doi.org/10.1016/j.tig.2007.11.004openalex-snapshot
Age to survive: DNA damage and aging
inferredcites →https://doi.org/10.1016/s0165-4608(98)00143-5openalex-snapshot
Frequent Hypomethylation in Wilms Tumors of Pericentromeric DNA in Chromosomes 1 and 16
inferredcites →https://doi.org/10.1016/s1476-5586(03)80039-8openalex-snapshot
Exceptionally High Protection of Photocarcinogenesis by Topical Application of (-)-Epi gal locatechin-3-Gal late in Hydrophilic Cream in SKH-1 Hairless Mouse Model: Relationship to Inhibition of UVB-Induced Global DNA Hypomethylation
inferredcites →https://doi.org/10.1038/25779openalex-snapshot
DNA hypomethylation leads to elevated mutation rates
inferredcites →https://doi.org/10.1038/46052openalex-snapshot
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
inferredcites →https://doi.org/10.1038/nature03001openalex-snapshot
Finishing the euchromatic sequence of the human genome
inferredcites →https://doi.org/10.1038/nature05456openalex-snapshot
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis
inferredcites →https://doi.org/10.1038/sj.onc.1208137openalex-snapshot
Distinctive pattern of LINE-1 methylation level in normal tissues and the association with carcinogenesis
inferredcites →https://doi.org/10.1038/srep15971openalex-snapshot
Deacetylation-mediated interaction of SIRT1-HMGB1 improves survival in a mouse model of endotoxemia
inferredcites →https://doi.org/10.1042/bj2980415openalex-snapshot
Folate-deficiency-induced homocysteinaemia in rats: disruption of S-adenosylmethionine's co-ordinate regulation of homocysteine metabolism
inferredcites →https://doi.org/10.1073/pnas.011506198openalex-snapshot
The Sir2 protein family: A novel deacetylase for gene silencing and more
inferredcites →https://doi.org/10.1073/pnas.94.6.2545openalex-snapshot
DNA methylation and genetic instability in colorectal cancer cells
inferredcites →https://doi.org/10.1080/10715760600953859openalex-snapshot
Clinical oxidation parameters of aging
inferredcites →https://doi.org/10.1093/emboj/16.10.2656openalex-snapshot
Initiation of V(D)J recombination in vivo: role of recombination signal sequences in formation of single and paired double‐strand breaks
inferredcites →https://doi.org/10.1093/mutage/geh025openalex-snapshot
Endogenous DNA damage in humans: a review of quantitative data
inferredcites →https://doi.org/10.1093/nar/gkm756openalex-snapshot
Changes in DNA repair during aging
inferredcites →https://doi.org/10.1093/nar/gkn261openalex-snapshot
LINE-1 methylation status of endogenous DNA double-strand breaks
inferredcites →https://doi.org/10.1093/nar/gkn571openalex-snapshot
LINE-1 methylation patterns of different loci in normal and cancerous cells
inferredcites →https://doi.org/10.1093/nar/gkw059openalex-snapshot
An interplay of the base excision repair and mismatch repair pathways in active DNA demethylation
inferredcites →https://doi.org/10.1093/nar/gkw925openalex-snapshot
L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomes
inferredcites →https://doi.org/10.1093/nar/gkx587openalex-snapshot
Prediction of genome-wide DNA methylation in repetitive elements
inferredcites →https://doi.org/10.1096/fj.201800218rropenalex-snapshot
Reduction in replication‐independent endogenous DNA double‐strand breaks promotes genomic instability during chronological aging in yeast
inferredcites →https://doi.org/10.1101/cshperspect.a012716openalex-snapshot
DNA Damage Sensing by the ATM and ATR Kinases
inferredcites →https://doi.org/10.1111/1567-1364.12115openalex-snapshot
Yeast sirtuins and the regulation of aging
inferredcites →https://doi.org/10.1111/bpa.12216openalex-snapshot
Oxidative Glial Cell Damage Associated with White Matter Lesions in the Aging Human Brain
inferredcites →https://doi.org/10.1111/j.1753-4887.2008.00070.xopenalex-snapshot
Folate, DNA methylation, and mouse models of breast tumorigenesis
inferredcites →https://doi.org/10.1111/nyas.13533openalex-snapshot
Revisiting the genomic hypomethylation hypothesis of aging
inferredcites →https://doi.org/10.1126/science.1083557openalex-snapshot
Chromosomal Instability and Tumors Promoted by DNA Hypomethylation
inferredcites →https://doi.org/10.1126/science.1210597openalex-snapshot
Tet Proteins Can Convert 5-Methylcytosine to 5-Formylcytosine and 5-Carboxylcytosine
inferredcites →https://doi.org/10.1126/science.1210944openalex-snapshot
Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA
inferredcites →https://doi.org/10.1128/mcb.06147-11openalex-snapshot
SIRT1 Deacetylates the DNA Methyltransferase 1 (DNMT1) Protein and Alters Its Activities
inferredcites →https://doi.org/10.1128/mcb.18.4.2029openalex-snapshot
Structure of Nonhairpin Coding-End DNA Breaks in Cells Undergoing V(D)J Recombination
inferredcites →https://doi.org/10.1152/physiolgenomics.00146.2009openalex-snapshot
Distinctive patterns of age-dependent hypomethylation in interspersed repetitive sequences
inferredcites →https://doi.org/10.1155/2012/135206openalex-snapshot
Free Radicals and Extrinsic Skin Aging
inferredcites →https://doi.org/10.1158/0008-5472.can-06-2995openalex-snapshot
Changes in DNA Methylation Patterns in Subjects Exposed to Low-Dose Benzene
inferredcites →https://doi.org/10.1159/000334368openalex-snapshot
Measuring Genome Instability in Aging – A Mini-Review
inferredcites →https://doi.org/10.1186/1471-2164-15-750openalex-snapshot
Characteristics of replication-independent endogenous double-strand breaks in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1186/1476-4598-9-70openalex-snapshot
Replication independent DNA double-strand break retention may prevent genomic instability
inferredcites →https://doi.org/10.1186/s12881-016-0335-xopenalex-snapshot
Association between global leukocyte DNA methylation and cardiovascular risk in postmenopausal women
inferredcites →https://doi.org/10.1186/s12977-018-0442-1openalex-snapshot
Nomenclature for endogenous retrovirus (ERV) loci
inferredcites →https://doi.org/10.1186/s13148-017-0395-6openalex-snapshot
The association between Alu hypomethylation and severity of type 2 diabetes mellitus
inferredcites →https://doi.org/10.1200/jco.2013.51.1055openalex-snapshot
Aging and Risk of Severe, Disabling, Life-Threatening, and Fatal Events in the Childhood Cancer Survivor Study
inferredcites →https://doi.org/10.1371/journal.pone.0015367openalex-snapshot
Tissue Distribution of 5-Hydroxymethylcytosine and Search for Active Demethylation Intermediates
inferredcites →https://doi.org/10.1371/journal.pone.0017934openalex-snapshot
Hypomethylation of Intragenic LINE-1 Represses Transcription in Cancer Cells through AGO2
inferredcites →https://doi.org/10.1371/journal.pone.0037009openalex-snapshot
Long Interspersed Nuclear Element-1 Hypomethylation and Oxidative Stress: Correlation and Bladder Cancer Diagnostic Potential
inferredcites →https://doi.org/10.1371/journal.pone.0045292openalex-snapshot
Patterns and Possible Roles of LINE-1 Methylation Changes in Smoke-Exposed Epithelia
inferredcites →https://doi.org/10.1371/journal.pone.0070386openalex-snapshot
Hypomethylation of Alu Elements in Post-Menopausal Women with Osteoporosis
inferredcites →https://doi.org/10.1371/journal.pone.0072706openalex-snapshot
Replication-Independent Endogenous DNA Double-Strand Breaks in Saccharomyces cerevisiae Model
inferredcites →https://doi.org/10.1371/journal.pone.0120032openalex-snapshot
Higher Alu Methylation Levels in Catch-Up Growth in Twenty-Year-Old Offsprings
inferredcites →https://doi.org/10.1371/journal.pone.0177119openalex-snapshot
EnHERV: Enrichment analysis of specific human endogenous retrovirus patterns and their neighboring genes
inferredcites →https://doi.org/10.18632/oncotarget.13562openalex-snapshot
Whole genome DNA methylation: beyond genes silencing
inferredcites →https://doi.org/10.18632/oncotarget.5899openalex-snapshot
DNA damage response (DDR) and senescence: shuttled inflamma-miRNAs on the stage of inflamm-aging
inferredcites →https://doi.org/10.2217/epi-2017-0096openalex-snapshot
Alu siRNA to Increase Alu Element Methylation and Prevent DNA Damage
inferredcites →https://doi.org/10.2217/epi.13.72openalex-snapshot
Epigenetics: The Language of the Cell?
inferredcites →https://doi.org/10.3389/fgene.2018.00501openalex-snapshot
Pathologic Replication-Independent Endogenous DNA Double-Strand Breaks Repair Defect in Chronological Aging Yeast
inferredcites →https://doi.org/10.3389/fonc.2018.00015openalex-snapshot
DNA Damage, Repair, and Cancer Metabolism
inferredcites →https://doi.org/10.3945/an.111.000992openalex-snapshot
Folate and DNA Methylation: A Review of Molecular Mechanisms and the Evidence for Folate's Role
inferredcites →https://doi.org/10.7150/ijbs.11218openalex-snapshot
DNA Methylation, Its Mediators and Genome Integrity
inferredcites →https://doi.org/10.7314/apjcp.2013.14.9.5495openalex-snapshot
Alu Hypomethylation in Smoke-Exposed Epithelia and Oral Squamous Carcinoma
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4628537openalex-extracted
Changes in Immune Cell Subtypes During Ageingchanges in Immune Cell Subtypes During Ageing
inferred← citeshttps://doi.org/10.1016/j.archger.2024.105376openalex-snapshot
Changes in immune cell subtypes during ageing
inferred← citeshttps://doi.org/10.1016/j.burns.2021.10.002openalex-snapshot
Alu repetitive sequence CpG methylation changes in burn scars
inferred← citeshttps://doi.org/10.1016/j.imbio.2026.153220openalex-snapshot
Changes of systemic immune cells subtypes in colorectal carcinoma patients
inferred← citeshttps://doi.org/10.1101/2024.08.26.609793openalex-snapshot
Immunophenotypic changes in peripheral blood of colorectal cancer patients: a potential diagnostic marker for CD4+ monocytes
inferred← citeshttps://doi.org/10.1186/s13148-020-00972-9openalex-snapshot
Altered immune phenotype and DNA methylation in panic disorder
inferred← citeshttps://doi.org/10.2217/epi-2019-0064openalex-snapshot
Is Global Hypomethylation a Nidus for Molecular Pathogenesis of Age-Related Noncommunicable Diseases?
inferred← citeshttps://doi.org/10.31557/apjcp.2022.23.11.3753openalex-snapshot
Upregulation of p16INK4A in Peripheral White Blood Cells as a Novel Screening Marker for Colorectal Carcinoma
inferred← citeshttps://doi.org/10.3389/fcell.2021.802024openalex-snapshot
B1 siRNA Increases de novo DNA Methylation of B1 Elements and Promotes Wound Healing in Diabetic Rats
inferred← citeshttps://doi.org/10.3389/fgene.2019.00580openalex-snapshot
Transposable Elements and Their Epigenetic Regulation in Mental Disorders: Current Evidence in the Field
inferred← citeshttps://doi.org/10.3389/fgene.2019.00645openalex-snapshot
Argonaute 4 as an Effector Protein in RNA-Directed DNA Methylation in Human Cells
inferred← citeshttps://doi.org/10.58837/chula.the.2019.29openalex-snapshot
Argonaute 4 promotes genomic methylation
inferred← citeshttps://doi.org/10.58837/chula.the.2021.21openalex-snapshot
Deprogramming senescence by genomic stabilizing molecules in vivo
inferred← citeshttps://doi.org/10.58837/chula.the.2022.24openalex-snapshot
The role of b1 methylation, physiologic replication independent endogenous dna double strand breaks (phy-rind-edsb) and laminin 511 e8 proteins in rat second degree burn wound healing
inferred← citeshttps://doi.org/10.58837/chula.the.2022.25openalex-snapshot
Senescent white blood cells in colorectal carcinoma patients
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