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Epigenetic changes and nontargeted radiation effects—Is there a link?
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1520-6823(1997)5:3<124::aid-roi8>3.0.co;2-#openalex-snapshot
Perpetuating radiation‐induced chromosomal instability
inferredcites →https://doi.org/10.1002/jcb.21485openalex-snapshot
Chromatin organization and nuclear microenvironments in cancer cells
inferredcites →https://doi.org/10.1007/3-7643-7378-4_12openalex-snapshot
Effects of ionizing radiation on cellular structures, induced instability and carcinogenesis
inferredcites →https://doi.org/10.1007/bf01221035openalex-snapshot
Transferable clastogenic activity in plasma from persons exposed as salvage personnel of the Chernobyl reactor
inferredcites →https://doi.org/10.1007/s00018-004-4177-xopenalex-snapshot
DNA damage repair and transcription
inferredcites →https://doi.org/10.1007/s00335-005-0066-3openalex-snapshot
Mammalian microRNAs: a small world for fine-tuning gene expression
inferredcites →https://doi.org/10.1016/0165-1110(80)90010-xopenalex-snapshot
Heritable translocation test in mice
inferredcites →https://doi.org/10.1016/0165-1218(87)90022-xopenalex-snapshot
A guide for mutagenicity testing using the dominant lethal assay
inferredcites →https://doi.org/10.1016/j.bbrc.2004.06.081openalex-snapshot
Dose-dependence, sex- and tissue-specificity, and persistence of radiation-induced genomic DNA methylation changes
inferredcites →https://doi.org/10.1016/j.bbrc.2004.10.002openalex-snapshot
Sex- and tissue-specific expression of maintenance and de novo DNA methyltransferases upon low dose X-irradiation in mice
inferredcites →https://doi.org/10.1016/j.bbrc.2005.09.084openalex-snapshot
Stable loss of global DNA methylation in the radiation-target tissue—A possible mechanism contributing to radiation carcinogenesis?
inferredcites →https://doi.org/10.1016/j.ceb.2007.04.011openalex-snapshot
Genomic patterns of DNA methylation: targets and function of an epigenetic mark
inferredcites →https://doi.org/10.1016/j.ejca.2007.04.002openalex-snapshot
The role of microRNAs in cancer: No small matter
inferredcites →https://doi.org/10.1016/j.etp.2004.12.001openalex-snapshot
Maternal effects and cancer risk in the progeny of mice exposed to X-rays before conception
inferredcites →https://doi.org/10.1016/j.exphem.2007.01.029openalex-snapshot
Bystander effects induced by serum from survivors of the Chernobyl accident
inferredcites →https://doi.org/10.1016/j.mrfmmm.2003.12.016openalex-snapshot
Methylation changes in muscle and liver tissues of male and female mice exposed to acute and chronic low-dose X-ray-irradiation
inferredcites →https://doi.org/10.1016/j.mrfmmm.2004.06.049openalex-snapshot
IR-inducible clusterin gene expression: a protein with potential roles in ionizing radiation-induced adaptive responses, genomic instability, and bystander effects
inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.03.035openalex-snapshot
Untargeted effects of ionizing radiation: Implications for radiation pathology
inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.06.032openalex-snapshot
Radiation-induced genomic instability is associated with DNA methylation changes in cultured human keratinocytes
inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.08.012openalex-snapshot
Bystander-induced differentiation: A major response to targeted irradiation of a urothelial explant model
inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.10.011openalex-snapshot
Radiation-induced bystander effects and the DNA paradigm: An “out of field” perspective
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.01.009openalex-snapshot
The offspring of irradiated parents, are they stable?
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.01.017openalex-snapshot
Detection of induced male germline mutation: Correlations and comparisons between traditional germline mutation assays, transgenic rodent assays and expanded simple tandem repeat instability assays
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.11.009openalex-snapshot
Non-targeted bystander effects induced by ionizing radiation
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.11.020openalex-snapshot
Effect of ATM heterozygosity on heritable DNA damage in mice following paternal F0 germline irradiation
inferredcites →https://doi.org/10.1016/j.mrgentox.2003.12.005openalex-snapshot
Transmission of genome damage from irradiated male rats to their progeny
inferredcites →https://doi.org/10.1016/j.mrrev.2003.05.003openalex-snapshot
Long-term genetic effects of radiation exposure
inferredcites →https://doi.org/10.1016/j.mrrev.2003.06.006openalex-snapshot
Transgenerational carcinogenesis: induction and transmission of genetic alterations and mechanisms of carcinogenesis
inferredcites →https://doi.org/10.1016/j.semcancer.2004.08.010openalex-snapshot
Integrative radiation carcinogenesis: interactions between cell and tissue responses to DNA damage
inferredcites →https://doi.org/10.1016/j.semradonc.2006.11.005openalex-snapshot
Responses of Normal Cells to Ionizing Radiation
inferredcites →https://doi.org/10.1016/j.tibs.2005.12.008openalex-snapshot
Genomic DNA methylation: the mark and its mediators
inferredcites →https://doi.org/10.1016/s0027-5107(01)00285-8openalex-snapshot
Effects of irradiated medium with or without cells on bystander cell responses
inferredcites →https://doi.org/10.1016/s0027-5107(02)00005-2openalex-snapshot
A novel single molecule analysis of spontaneous and radiation-induced mutation at a mouse tandem repeat locus
inferredcites →https://doi.org/10.1016/s0027-5107(99)00101-3openalex-snapshot
Lethal and teratogenic effects in two successive generations of the HLG mouse strain after radiation exposure of zygotes — association with genomic instability?
inferredcites →https://doi.org/10.1016/s0167-8140(02)00325-0openalex-snapshot
Partial volume rat lung irradiation; assessment of early DNA damage in different lung regions and effect of radical scavengers
inferredcites →https://doi.org/10.1016/s0168-9525(03)00080-5openalex-snapshot
The methyl-CpG binding domain and the evolving role of DNA methylation in animals
inferredcites →https://doi.org/10.1016/s0360-3016(97)00736-0openalex-snapshot
Partial volume rat lung irradiation: An evaluation of early DNA damage
inferredcites →https://doi.org/10.1016/s1472-6483(10)60676-1openalex-snapshot
Origins and consequences of DNA damage in male germ cells
inferredcites →https://doi.org/10.1021/es062978nopenalex-snapshot
Characterization of a Radiation-Induced Stress Response Communicated in Vivo between Zebrafish
inferredcites →https://doi.org/10.1038/380683a0openalex-snapshot
Human minisatellite mutation rate after the Chernobyl accident
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/ncponc0354openalex-snapshot
DNA methylation and gene silencing in cancer
inferredcites →https://doi.org/10.1038/ng0993-92openalex-snapshot
Mouse minisatellite mutations induced by ionizing radiation
inferredcites →https://doi.org/10.1038/ng1089openalex-snapshot
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
inferredcites →https://doi.org/10.1038/nrc1277openalex-snapshot
Radiation-induced bystander effects — implications for cancer
inferredcites →https://doi.org/10.1038/nrc1799openalex-snapshot
Epigenetic gene silencing in cancer – a mechanism for early oncogenic pathway addiction?
inferredcites →https://doi.org/10.1038/nrg2045openalex-snapshot
Environmental epigenomics and disease susceptibility
inferredcites →https://doi.org/10.1038/nrm1945openalex-snapshot
Chromatin remodelling: the industrial revolution of DNA around histones
inferredcites →https://doi.org/10.1038/sj.bjc.6600804openalex-snapshot
A proliferation-dependent bystander effect in primary porcine and human urothelial explants in response to targeted irradiation
inferredcites →https://doi.org/10.1038/sj.bjc.6603023openalex-snapshot
MicroRNAs in cell proliferation, cell death, and tumorigenesis
inferredcites →https://doi.org/10.1038/sj.onc.1204903openalex-snapshot
Inflammatory-type responses after exposure to ionizing radiation in vivo: a mechanism for radiation-induced bystander effects?
inferredcites →https://doi.org/10.1038/sj.onc.1205609openalex-snapshot
DNA methylation and chromatin – unraveling the tangled web
inferredcites →https://doi.org/10.1038/sj.onc.1206678openalex-snapshot
Roles of BRCA1 and BRCA2 in homologous recombination, DNA replication fidelity and the cellular response to ionizing radiation
inferredcites →https://doi.org/10.1038/sj.onc.1206680openalex-snapshot
Transcription factors activated in mammalian cells after clinically relevant doses of ionizing radiation
inferredcites →https://doi.org/10.1038/sj.onc.1206682openalex-snapshot
DNA damage checkpoint control in cells exposed to ionizing radiation
inferredcites →https://doi.org/10.1038/sj.onc.1206882openalex-snapshot
Radiation-induced bystander effects, carcinogenesis and models
inferredcites →https://doi.org/10.1038/sj.onc.1206990openalex-snapshot
Clinical implications of radiation-induced genomic instability
inferredcites →https://doi.org/10.1038/sj.onc.1206992openalex-snapshot
Is there a common mechanism underlying genomic instability, bystander effects and other nontargeted effects of exposure to ionizing radiation?
inferredcites →https://doi.org/10.1038/sj.onc.1206993openalex-snapshot
Radiation-induced transgenerational instability
inferredcites →https://doi.org/10.1038/sj.onc.1207037openalex-snapshot
Induced genomic instability in irradiated germ cells and in the offspring; reconciling discrepancies among the human and animal studies
inferredcites →https://doi.org/10.1038/sj.onc.1207044openalex-snapshot
Radiation-induced genomic instability and bystander effects: inter-related nontargeted effects of exposure to ionizing radiation
inferredcites →https://doi.org/10.1038/sj.onc.1208439openalex-snapshot
Medium-mediated intercellular communication is involved in bystander responses of X-ray-irradiated normal human fibroblasts
inferredcites →https://doi.org/10.1038/sj.onc.1208886openalex-snapshot
Ionizing radiation induces DNA double-strand breaks in bystander primary human fibroblasts
inferredcites →https://doi.org/10.1038/sj.onc.1209467openalex-snapshot
Irradiation induces DNA damage and modulates epigenetic effectors in distant bystander tissue in vivo
inferredcites →https://doi.org/10.1038/sj.onc.1209723openalex-snapshot
Radiation-induced transgenerational alterations in genome stability and DNA damage
inferredcites →https://doi.org/10.1038/sj.onc.1209863openalex-snapshot
ATR-dependent radiation-induced γH2AX foci in bystander primary human astrocytes and glioma cells
inferredcites →https://doi.org/10.1038/sj.onc.1210024openalex-snapshot
Constitutive nitric oxide acting as a possible intercellular signaling molecule in the initiation of radiation-induced DNA double strand breaks in non-irradiated bystander cells
inferredcites →https://doi.org/10.1038/sj.onc.1210253openalex-snapshot
Maternal effects of the scid mutation on radiation-induced transgenerational instability in mice
inferredcites →https://doi.org/10.1039/9781847557643-00149openalex-snapshot
Heritable Effects on DNA Damage Following Paternal F0 Germline Irradiation
inferredcites →https://doi.org/10.1073/pnas.0505020102openalex-snapshot
Biological effects in unirradiated human tissue induced by radiation damage up to 1 mm away
inferredcites →https://doi.org/10.1073/pnas.0505473102openalex-snapshot
Mechanism of radiation-induced bystander effect: Role of the cyclooxygenase-2 signaling pathway
inferredcites →https://doi.org/10.1073/pnas.0507119102openalex-snapshot
Effects of ionizing radiation in nonirradiated cells
inferredcites →https://doi.org/10.1073/pnas.0510565103openalex-snapshot
A microRNA expression signature of human solid tumors defines cancer gene targets
inferredcites →https://doi.org/10.1073/pnas.102015399openalex-snapshot
Elevated mutation rates in the germ line of first- and second-generation offspring of irradiated male mice
inferredcites →https://doi.org/10.1073/pnas.79.2.542openalex-snapshot
Mutation frequencies in male mice and the estimation of genetic hazards of radiation in men.
inferredcites →https://doi.org/10.1074/jbc.273.10.5858openalex-snapshot
DNA Double-stranded Breaks Induce Histone H2AX Phosphorylation on Serine 139
inferredcites →https://doi.org/10.1080/095530002317577330openalex-snapshot
Cellular reprogramming in the F 3 mouse with paternal F 0 radiation history
inferredcites →https://doi.org/10.1080/09553000600803904openalex-snapshot
Apoptosis is initiated in human keratinocytes exposed to signalling factors from microbeam irradiated cells
inferredcites →https://doi.org/10.1080/09553000600960027openalex-snapshot
Radiation-induced molecular changes in rat mammary tissue: Possible implications for radiation-induced carcinogenesis
inferredcites →https://doi.org/10.1080/095530097143824openalex-snapshot
Genetic factors influencing alpha-particle-induced chromosomal instability
inferredcites →https://doi.org/10.1088/0952-4746/23/2/304openalex-snapshot
Genomic instability and radiation
inferredcites →https://doi.org/10.1088/0952-4746/25/1/005openalex-snapshot
Chromosome intra- and inter-changes determined by G-banding in radiation workers within vivoexposure to plutonium
inferredcites →https://doi.org/10.1093/carcin/20.12.2351openalex-snapshot
Effect of ionizing radiation on transgenerational appearance of p un reversions in mice
inferredcites →https://doi.org/10.1093/carcin/20.2.325openalex-snapshot
Possible carcinogenic effects of X-rays in a transgenerational study with CBA mice
inferredcites →https://doi.org/10.1093/carcin/20.4.519openalex-snapshot
Environmental factors as regulators and effectors of multistep carcinogenesis
inferredcites →https://doi.org/10.1093/carcin/22.9.1465openalex-snapshot
Individual variation in the production of a `bystander signal' following irradiation of primary cultures of normal human urothelium
inferredcites →https://doi.org/10.1093/carcin/bgi224openalex-snapshot
The time and spatial effects of bystander response in mammalian cells induced by low dose radiation
inferredcites →https://doi.org/10.1093/carcin/bgm053openalex-snapshot
Role of epigenetic effectors in maintenance of the long-term persistent bystander effect in spleen in vivo
inferredcites →https://doi.org/10.1093/embo-reports/kve022openalex-snapshot
The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substrate recognition
inferredcites →https://doi.org/10.1093/genetics/148.4.1567openalex-snapshot
Differential Response of Mouse Male Germ-Cell Stages to Radiation-Induced Specific-Locus and Dominant Mutations
inferredcites →https://doi.org/10.1093/mutage/16.1.17openalex-snapshot
Heritable effects of paternal irradiation in mice on signaling protein kinase activities in F3 offspring
inferredcites →https://doi.org/10.1093/mutage/17.1.9openalex-snapshot
Germline drift in chimeric male mice possessing an F2 component with a paternal F0 radiation history
inferredcites →https://doi.org/10.1093/mutage/gei047openalex-snapshot
Gamma irradiation of Type B spermatogonia leads to heritable genomic instability in four generations of mice
inferredcites →https://doi.org/10.1093/nar/29.21.4493openalex-snapshot
Methyl-CpG-binding protein 2 represses LINE-1 expression and retrotransposition but not Alu transcription
inferredcites →https://doi.org/10.1093/oxfordjournals.rpd.a006775openalex-snapshot
Bystander-induced Apoptosis and Premature Differentiation in Primary Urothelial Explants after Charged Particle Microbeam Irradiation
inferredcites →https://doi.org/10.1093/rpd/ncl461openalex-snapshot
A microbeam study of DNA double-strand breaks in bystander primary human fibroblasts
inferredcites →https://doi.org/10.1093/rpd/ncl463openalex-snapshot
Mechanistic modelling of genetic and epigenetic events in radiation carcinogenesis
inferredcites →https://doi.org/10.1093/rpd/ncl495openalex-snapshot
Radiation-induced DNA damage responses
inferredcites →https://doi.org/10.1097/00004032-200307000-00008openalex-snapshot
THE BYSTANDER EFFECT
inferredcites →https://doi.org/10.1097/00004032-200307000-00009openalex-snapshot
MONITORING HUMAN RADIATION EXPOSURE BY GENE EXPRESSION PROFILING: POSSIBILITIES AND PITFALLS
inferredcites →https://doi.org/10.1097/ppo.0b013e31803c71f2openalex-snapshot
Cancer Susceptibility: Epigenetic Manifestation of Environmental Exposures
inferredcites →https://doi.org/10.1126/science.1068102openalex-snapshot
Nuclear Weapons Tests and Human Germline Mutation Rate
inferredcites →https://doi.org/10.1126/science.1073827openalex-snapshot
A microRNA in a Multiple-Turnover RNAi Enzyme Complex
inferredcites →https://doi.org/10.1126/science.1086887openalex-snapshot
Heterochromatin and Epigenetic Control of Gene Expression
inferredcites →https://doi.org/10.1139/o03-042openalex-snapshot
Characteristics of γ-H2AX foci at DNA double-strand breaks sites
inferredcites →https://doi.org/10.1146/annurev.genom.8.080706.092351openalex-snapshot
microRNAs in Vertebrate Physiology and Human Disease
inferredcites →https://doi.org/10.1158/0008-5472.can-04-2875openalex-snapshot
Assessment of Low Linear Energy Transfer Radiation–Induced Bystander Mutagenesis in a Three-Dimensional Culture Model
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0834openalex-snapshot
Chromosomal Instability in Unirradiated Hemopoietic Cells Resulting from a Delayed In vivo Bystander Effect of γ Radiation
inferredcites →https://doi.org/10.1158/0008-5472.can-06-1894openalex-snapshot
MicroRNA Responses to Cellular Stress
inferredcites →https://doi.org/10.1158/0008-5472.can-06-4442openalex-snapshot
DNA Double-Strand Breaks Form in Bystander Cells after Microbeam Irradiation of Three-dimensional Human Tissue Models
inferredcites →https://doi.org/10.1158/1535-7163.mct-06-0596openalex-snapshot
Radiation-induced cell signaling: inside-out and outside-in
inferredcites →https://doi.org/10.1158/1541-7786.mcr-05-0074openalex-snapshot
Fractionated Low-Dose Radiation Exposure Leads to Accumulation of DNA Damage and Profound Alterations in DNA and Histone Methylation in the Murine Thymus
inferredcites →https://doi.org/10.1159/000077499openalex-snapshot
Transgenerational transmission of radiation- and chemically induced tumors and congenital anomalies in mice: studies of their possible relationship to induced chromosomal and molecular changes
inferredcites →https://doi.org/10.1191/0960327104ht418oaopenalex-snapshot
The radiation-induced bystander effect: evidence and significance
inferredcites →https://doi.org/10.1191/0960327104ht419oaopenalex-snapshot
Evidence for ‘bystander effects’ in vivo
inferredcites →https://doi.org/10.1210/me.2004-0496openalex-snapshot
Epigenetic Regulation by Histone Methylation and Histone Variants
inferredcites →https://doi.org/10.1269/jrr.06084openalex-snapshot
Intercellular and Intracellular Signaling Pathways Mediating Ionizing Radiation-Induced Bystander Effects
inferredcites →https://doi.org/10.1269/jrr.39.271openalex-snapshot
Effects of X-ray Irradiation on Genomic DNA Methylation Levels in Mouse Tissues.
inferredcites →https://doi.org/10.1517/14712598.7.7.1009openalex-snapshot
Regulatory mechanisms of microRNAs involvement in cancer
inferredcites →https://doi.org/10.1667/0033-7587(2001)155[0397:tbeiro]2.0.co;2openalex-snapshot
The Bystander Effect in Radiation Oncogenesis: I. Transformation in C3H 10T½ CellsIn Vitrocan be Initiated in the Unirradiated Neighbors of Irradiated Cells
inferredcites →https://doi.org/10.1667/0033-7587(2001)156[0210:tcusim]2.0.co;2openalex-snapshot
The Columbia University Single-Ion Microbeam
inferredcites →https://doi.org/10.1667/0033-7587(2002)157[0661:piosro]2.0.co;2openalex-snapshot
Persistent Induction of Somatic Reversions of the Pink-Eyed Unstable Mutation in F1Mice Born to Fathers Irradiated at the Spermatozoa Stage
inferredcites →https://doi.org/10.1667/0033-7587(2003)159[0567:nadeoe]2.0.co;2openalex-snapshot
Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: I. Radiation-Induced Genomic Instability and Bystander EffectsIn Vitro
inferredcites →https://doi.org/10.1667/0033-7587(2003)159[0581:nadeoe]2.0.co;2openalex-snapshot
Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: II. Radiation-Induced Genomic Instability and Bystander EffectsIn Vivo,Clastogenic Factors and Transgenerational Effects
inferredcites →https://doi.org/10.1667/rr0159.1openalex-snapshot
Modulation of Radiation Responses by Pre-exposure to Irradiated Cell Conditioned Medium
inferredcites →https://doi.org/10.1667/rr0702.1openalex-snapshot
Intestinal Epithelial Cell Dysfunction is Mediated by an Endothelial-Specific Radiation-Induced Bystander Effect
inferredcites →https://doi.org/10.1667/rr0864.1openalex-snapshot
The Time Dependence of Bystander Responses Induced by Iron-Ion Radiation in Normal Human Skin Fibroblasts
inferredcites →https://doi.org/10.1667/rr3226openalex-snapshot
Effect of Medium on Chromatin Damage in Bystander Mammalian Cells
inferredcites →https://doi.org/10.1667/rr3325openalex-snapshot
Medium from Irradiated Cells Induces Dose-Dependent Mitochondrial Changes and BCL2 Responses in Unirradiated Human Keratinocytes
inferredcites →https://doi.org/10.1667/rr3580.1openalex-snapshot
A Dose Threshold for a Medium Transfer Bystander Effect for a Human Skin Cell Line
inferredcites →https://doi.org/10.2174/1568009043481641openalex-snapshot
Stress Signaling from Irradiated to Non-Irradiated Cells
inferredcites →https://doi.org/10.2174/1573406410602060555openalex-snapshot
Radiation-Induced Response of Micro RNA Expression in Murine Embryonic Stem Cells
inferredcites →https://doi.org/10.2187/bss.17.302openalex-snapshot
Qualitative and quantitative difference in mutation induction between carbon- and neon-ion beams in normal human cells.
inferredcites →https://doi.org/10.2187/bss.18.241openalex-snapshot
Heavy Charged Particles Produce a Bystander Effect via Cell-Cell Junctions
inferredcites →https://doi.org/10.2307/3572443openalex-snapshot
Breaks in Normal Human Chromosomes: Are They Induced by a Transferable Substance in the Plasma of Persons Exposed to Total-Body Irradiation?
inferredcites →https://doi.org/10.2307/3574086openalex-snapshot
Effect of 239 PuO 2 Particle Number and Size on the Frequency and Distribution of Chromosome Aberrations in the Liver of the Chinese Hamster
inferredcites →https://doi.org/10.2307/3577319openalex-snapshot
The Effect of γ Radiation on DNA Methylation
inferredcites →https://doi.org/10.2307/3579259openalex-snapshot
Clastogenic Factors in the Plasma of Chernobyl Accident Recovery Workers: Anticlastogenic Effect of Ginkgo biloba Extract
inferredcites →https://doi.org/10.2307/3579571openalex-snapshot
Impaired Cell Proliferation in Mice That Persists across at Least Two Generations after Paternal Irradiation
inferredcites →https://doi.org/10.2307/3580152openalex-snapshot
Gap Junction Intercellular Communication Mediates the Competitive Cell Proliferation Disadvantage of Irradiated Mouse Preimplantation Embryos in Aggregation Chimeras
inferredcites →https://doi.org/10.3760/cma.j.issn.1673-4114.2007.03.016openalex-snapshot
Non-targeted and delayed effects of exposure to ionizing radiation
inferredcites →https://doi.org/10.3892/ijo.21.2.337openalex-snapshot
Radiation-induced effects in unirradiated cells: A review and implications in cancer
inferredcites →https://doi.org/10.4161/cbt.2.3.373openalex-snapshot
Involvement of H2AX in the DNA Damage and Repair Response
inferredcites →https://doi.org/10.4161/cc.5.24.3569openalex-snapshot
γ-H2AX in Cancer Cells: A Potential Biomarker for Cancer Diagnostics, Prediction and Recurrence
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470613214.ch14openalex-snapshot
The Bystander Effect in Targeted Radiotherapy
inferred← citeshttps://doi.org/10.1002/9781394332175.ch8openalex-snapshot
The Biological Effects of Ionizing Radiation at the Molecular and Cellular Level
inferred← citeshttps://doi.org/10.1002/em.21701openalex-snapshot
Molecular and organismal changes in offspring of male mice treated with chemical stressors
inferred← citeshttps://doi.org/10.1002/em.21703openalex-snapshot
Direct and delayed X‐ray‐induced DNA damage in male mouse germ cells
inferred← citeshttps://doi.org/10.1002/em.21832openalex-snapshot
High LET 56Fe ion irradiation induces tissue‐specific changes in DNA methylation in the mouse
inferred← citeshttps://doi.org/10.1007/978-1-4939-1510-1_33openalex-snapshot
Radiation Therapy for Orbital Tumors
inferred← citeshttps://doi.org/10.1007/978-3-030-05526-4_51openalex-snapshot
Plant Behavior and Metabolic Response to the Space Environment as an Alternative Food and Therapeutic Source
inferred← citeshttps://doi.org/10.1007/978-3-319-31563-8_4openalex-snapshot
Radiation Therapy Towards Laser-Driven Particle Beams: An “OMICS” Approach in Radiobiology
inferred← citeshttps://doi.org/10.1007/978-3-319-48838-7_13openalex-snapshot
Strategies of Adaptation Under Prolonged Irradiation vs Chronic Exposure
inferred← citeshttps://doi.org/10.1007/978-3-319-50909-9_51-1openalex-snapshot
Plant Behavior and Metabolic Response to the Space Environment as an Alternative Food and Therapeutic Source
inferred← citeshttps://doi.org/10.1007/978-3-540-85516-3_11openalex-snapshot
Radiation-Induced Genomic Instability and Radiation Sensitivity
inferred← citeshttps://doi.org/10.1007/978-3-642-23380-7_5openalex-snapshot
Epigenetic Effects of Ionizing Radiation
inferred← citeshttps://doi.org/10.1007/978-4-431-88659-4_28openalex-snapshot
Adult Stem Cells, the Barker Hypothesis, Epigenetic Events, and Low-Level Radiation Effects
inferred← citeshttps://doi.org/10.1007/978-94-007-6630-3_2openalex-snapshot
Disturbance of Hereditary Material Reserves Is the Main Instrument of Stress
inferred← citeshttps://doi.org/10.1007/s00018-012-1148-5openalex-snapshot
What mechanisms/processes underlie radiation-induced genomic instability?
inferred← citeshttps://doi.org/10.1007/s00411-014-0532-yopenalex-snapshot
Intraclonal recovery of ‘slow clones’—a manifestation of genomic instability: Are mitochondria the key to an explanation?
inferred← citeshttps://doi.org/10.1007/s10577-011-9244-1openalex-snapshot
Double-strand break-induced transcriptional silencing is associated with loss of tri-methylation at H3K4
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.09122-3openalex-snapshot
Genome Effects and Mutational Risk of Radiation
inferred← citeshttps://doi.org/10.1016/b978-0-12-803309-8.00034-3openalex-snapshot
Sins of Fathers Through a Scientific Lens
inferred← citeshttps://doi.org/10.1016/b978-0-12-823761-8.00009-4openalex-snapshot
Interventions that target fundamental aging mechanisms: myths and realities
inferred← citeshttps://doi.org/10.1016/b978-0-323-85679-9.00033-7openalex-snapshot
Sins of fathers through a scientific lens: Transgenerational effects
inferred← citeshttps://doi.org/10.1016/b978-0-444-52272-6.00203-8openalex-snapshot
Genome Effects and Mutational Risk of Radiation
inferred← citeshttps://doi.org/10.1016/b978-0-444-63979-0.00035-5openalex-snapshot
Effect of Radiation on Biological Structures. Radiation Mutagenesis
inferred← citeshttps://doi.org/10.1016/j.arr.2011.01.004openalex-snapshot
Hormesis and epigenetics: Is there a link?
inferred← citeshttps://doi.org/10.1016/j.bcab.2022.102442openalex-snapshot
Photosynthetic performance of Terminalia arjuna Roxb towards different doses of 60Co γ-irradiation
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.06.012openalex-snapshot
Protein kinase C epsilon is involved in ionizing radiation induced bystander response in human cells
inferred← citeshttps://doi.org/10.1016/j.biochi.2009.03.010openalex-snapshot
DNA methylation during depleted uranium-induced leukemia
inferred← citeshttps://doi.org/10.1016/j.canlet.2013.09.018openalex-snapshot
Abscopal effects of radiation therapy: A clinical review for the radiobiologist
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2025.104843openalex-snapshot
Gender differences in radiotherapy: A critical review
inferred← citeshttps://doi.org/10.1016/j.dnarep.2009.02.001openalex-snapshot
X-irradiation and bystander effects induce similar changes of transcript profiles in most functional pathways in human melanoma cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2016.12.002openalex-snapshot
DNA damage, repair monitoring and epigenetic DNA methylation changes in seedlings of Chernobyl soybeans
inferred← citeshttps://doi.org/10.1016/j.ejphar.2009.07.028openalex-snapshot
Ionizing radiation-induced bystander effects, potential targets for modulation of radiotherapy
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2009.07.001openalex-snapshot
Characterization of metabolic disturbances closely linked to the delayed senescence of Arabidopsis leaves after γ irradiation
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.127002openalex-snapshot
Epigenetic and genotoxic effects of tritium in marine mussels: Comparing waterborne and metal-associated forms
inferred← citeshttps://doi.org/10.1016/j.envres.2015.11.019openalex-snapshot
Irradiation of rainbow trout at early life stages results in trans-generational effects including the induction of a bystander effect in non-irradiated fish
inferred← citeshttps://doi.org/10.1016/j.etap.2025.104832openalex-snapshot
Can bystander effects of metals in Daphnia magna be mediated by DNA methylation?
inferred← citeshttps://doi.org/10.1016/j.fct.2011.11.047openalex-snapshot
Interaction between γ-radiation and dietary folate starvation metabolically reprograms global hepatic histone H3 methylation at lysine 4 and lysine 27 residues
inferred← citeshttps://doi.org/10.1016/j.gene.2013.01.027openalex-snapshot
Integrated analysis of diverse transcriptomic data from Arabidopsis reveals genetic markers that reliably and reproducibly respond to ionizing radiation
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34460openalex-snapshot
Mediation of radiation-induced bystander effect and epigenetic modification: The role of exosomes in cancer radioresistance
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2009.11.033openalex-snapshot
Bystander Effects Induced by Medium From Irradiated Cells: Similar Transcriptome Responses in Irradiated and Bystander K562 Cells
inferred← citeshttps://doi.org/10.1016/j.jmb.2015.07.011openalex-snapshot
Epigenetic Modulation of Human Podocyte Vitamin D Receptor in HIV Milieu
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2010.01.002openalex-snapshot
Some important questions connected with non-targeted effects
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2010.01.014openalex-snapshot
Manifestations and mechanisms of non-targeted effects of ionizing radiation
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2014.04.010openalex-snapshot
Dose- and time-dependent changes of micronucleus frequency and gene expression in the progeny of irradiated cells: Two components in radiation-induced genomic instability?
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2015.08.003openalex-snapshot
The key role of miR-21-regulated SOD2 in the medium-mediated bystander responses in human fibroblasts induced by α-irradiated keratinocytes
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2010.11.001openalex-snapshot
Differential genetic responses to ionizing irradiation in individual families of Japanese medaka, Oryzias latipes
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2014.08.004openalex-snapshot
Role of DNA methylation in the adaptive responses induced in a human B lymphoblast cell line by long-term low-dose exposures to γ-rays and cadmium
inferred← citeshttps://doi.org/10.1016/j.mrrev.2012.12.001openalex-snapshot
Non-targeted effects of ionising radiation—Implications for low dose risk
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.10.013openalex-snapshot
Ionizing radiation manifesting DNA damage response in plants: An overview of DNA damage signaling and repair mechanisms in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.01.049openalex-snapshot
Flowering under enhanced ionising radiation conditions and its regulation through epigenetic mechanisms
inferred← citeshttps://doi.org/10.1016/j.radmp.2020.04.001openalex-snapshot
Research progress of radiation induced bystander and abscopal effects in normal tissue
inferred← citeshttps://doi.org/10.1016/j.survophthal.2009.06.004openalex-snapshot
Radiation Therapy for Orbital Tumors: Concepts, Current Use, and Ophthalmic Radiation Side Effects
inferred← citeshttps://doi.org/10.1021/es8035219openalex-snapshot
Communication of Radiation-Induced Signals in Vivo between DNA Repair Deficient and Proficient Medaka (Oryzias latipes)
inferred← citeshttps://doi.org/10.1038/bjc.2014.368openalex-snapshot
The role of TGF-β1–miR-21–ROS pathway in bystander responses induced by irradiated non-small-cell lung cancer cells
inferred← citeshttps://doi.org/10.1038/onc.2010.480openalex-snapshot
Methyltransferases mediate cell memory of a genotoxic insult
inferred← citeshttps://doi.org/10.1038/s41420-018-0132-8openalex-snapshot
Molecular and epigenetic regulatory mechanisms of normal stem cell radiosensitivity
inferred← citeshttps://doi.org/10.1038/srep11373openalex-snapshot
Radiation quality-dependence of bystander effect in unirradiated fibroblasts is associated with TGF-β1-Smad2 pathway and miR-21 in irradiated keratinocytes
inferred← citeshttps://doi.org/10.1073/pnas.0804186105openalex-snapshot
Oncogenic bystander radiation effects in Patched heterozygous mouse cerebellum
inferred← citeshttps://doi.org/10.1080/09553002.2017.1231943openalex-snapshot
Fractionated exposure to low doses of ionizing radiation results in accumulation of DNA damage in mouse spleen tissue and activation of apoptosis in a p53/Atm-independent manner
inferred← citeshttps://doi.org/10.1080/09553002.2018.1440092openalex-snapshot
Mechanisms of inflammatory responses to radiation and normal tissues toxicity: clinical implications
inferred← citeshttps://doi.org/10.1080/09553002.2018.1454617openalex-snapshot
The future impacts of non-targeted effects
inferred← citeshttps://doi.org/10.1080/09553002.2018.1484194openalex-snapshot
Low dose radiation, inflammation, cancer and chemoprevention
inferred← citeshttps://doi.org/10.1080/09553002.2018.1490042openalex-snapshot
Influence of diet and metabolism on hematopoietic stem cells and leukemia development following ionizing radiation exposure
inferred← citeshttps://doi.org/10.1080/09553002.2021.1941383openalex-snapshot
All for one, though not one for all: team players in normal tissue radiobiology
inferred← citeshttps://doi.org/10.1080/09553002.2021.1980630openalex-snapshot
Non-targeted effects of radiation: a personal perspective on the role of exosomes in an evolving paradigm
inferred← citeshttps://doi.org/10.1080/09553002.2023.2172623openalex-snapshot
Main radiation pathways in the landscape of Armenia
inferred← citeshttps://doi.org/10.1080/09553002.2026.2654430openalex-snapshot
Methodological approaches for estimating radiosensitivity in Quillaja saponaria : comparison of LD 50 models and a PCA-based integrative index
inferred← citeshttps://doi.org/10.1080/10934529.2020.1760016openalex-snapshot
Inter-retrotransposon amplified polymorphism markers revealed long terminal repeat retrotransposon insertion polymorphism in flax cultivated on the experimental fields around Chernobyl
inferred← citeshttps://doi.org/10.1080/15384101.2017.1320003openalex-snapshot
Low dose radiation effects on the brain – from mechanisms and behavioral outcomes to mitigation strategies
inferred← citeshttps://doi.org/10.1086/696005openalex-snapshot
Faster Development Covaries with Higher DNA Damage in Grasshoppers (Chorthippus albomarginatus) from Chernobyl
inferred← citeshttps://doi.org/10.1088/0952-4746/32/4/r13openalex-snapshot
Developmental defects and genomic instability after x-irradiation of wild-type and genetically modified mouse pre-implantation and early post-implantation embryos
inferred← citeshttps://doi.org/10.1088/0952-4746/36/1/r23openalex-snapshot
Non-targeted effects and radiation-induced carcinogenesis: a review
inferred← citeshttps://doi.org/10.1093/eep/dvx011openalex-snapshot
Transgenerational epigenetics and environmental justice
inferred← citeshttps://doi.org/10.1093/humupd/dmr047openalex-snapshot
Assisted reproduction treatment and epigenetic inheritance
inferred← citeshttps://doi.org/10.1093/jrr/rru078openalex-snapshot
Identification of low-dose responsive metabolites in X-irradiated human B lymphoblastoid cells and fibroblasts
inferred← citeshttps://doi.org/10.1093/molehr/gap098openalex-snapshot
Memoirs of an insult: sperm as a possible source of transgenerational epimutations and genetic instability
inferred← citeshttps://doi.org/10.1093/mp/ssr022openalex-snapshot
Genetic and Epigenetic Effects of Plant–Pathogen Interactions: An Evolutionary Perspective
inferred← citeshttps://doi.org/10.1097/hp.0000000000001074openalex-snapshot
Towards a New Concept of Low Dose
inferred← citeshttps://doi.org/10.1111/cga.12051openalex-snapshot
Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2012.02502.xopenalex-snapshot
Effects of parental radiation exposure on developmental instability in grasshoppers
inferred← citeshttps://doi.org/10.1134/s1062359012050068openalex-snapshot
Transgenerational effects of prenatal stress of different etiology
inferred← citeshttps://doi.org/10.1152/japplphysiol.00513.2014openalex-snapshot
Lungs at high-altitude: genomic insights into hypoxic responses
inferred← citeshttps://doi.org/10.11606/t.17.2015.tde-01072015-092135openalex-snapshot
Análise da Metilação do DNA de Seleções de Figueira (Ficus carica L.) por MSAP e Sequenciamento
inferred← citeshttps://doi.org/10.1177/1091581809337918openalex-snapshot
Effects of Mixtures of Polychlorinated Biphenyls, Methylmercury, and Organochlorine Pesticides on Hepatic DNA Methylation in Prepubertal Female Sprague-Dawley Rats
inferred← citeshttps://doi.org/10.1186/1471-2148-13-168openalex-snapshot
The Fukushima nuclear accident and the pale grass blue butterfly: evaluating biological effects of long-term low-dose exposures
inferred← citeshttps://doi.org/10.1186/1471-2164-12-2openalex-snapshot
Time-series clustering of gene expression in irradiated and bystander fibroblasts: an application of FBPA clustering
inferred← citeshttps://doi.org/10.1186/1471-2407-13-368openalex-snapshot
Axin gene methylation status correlates with radiosensitivity of lung cancer cells
inferred← citeshttps://doi.org/10.1269/jrr.08070openalex-snapshot
Recent Insights into the Biological Action of Heavy-Ion Radiation
inferred← citeshttps://doi.org/10.1269/jrr.10157openalex-snapshot
Photosynthetic Capacity of Arabidopsis Plants at the Reproductive Stage Tolerates γ Irradiation
inferred← citeshttps://doi.org/10.1371/journal.pone.0107722openalex-snapshot
Genetic and Epigenetic Changes in Chromosomally Stable and Unstable Progeny of Irradiated Cells
inferred← citeshttps://doi.org/10.1667/rade-24-00018.1openalex-snapshot
“Lethal Mutations” a Misnomer or the Start of a Scientific Revolution?
inferred← citeshttps://doi.org/10.1667/rade-24-00093.1openalex-snapshot
Transgenerational Effects on Lifespan and Pathology of Paternal Pre-conceptional Exposure to Continuous Low-dose-rate Gamma Rays in C57BL/6J Mice
inferred← citeshttps://doi.org/10.1667/rr13394.1openalex-snapshot
Characterization of Non-CG Genomic Hypomethylation Associated with Gamma-Ray-Induced Suppression of CMT3 Transcription in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1667/rr1374.1openalex-snapshot
The Range of the Bystander Effect Signal in Three-Dimensional Tissue and Estimation of the Range in Human Lung Tissue at Low Radon Levels
inferred← citeshttps://doi.org/10.1667/rr14532.1openalex-snapshot
Intrinsic LINE-1 Hypomethylation and Decreased Brca1 Expression are Associated with DNA Repair Delay in Irradiated Thyroid Cells
inferred← citeshttps://doi.org/10.1667/rr14587.1openalex-snapshot
Low-Dose Ionizing Radiation Exposure, Oxidative Stress and Epigenetic Programing of Health and Disease
inferred← citeshttps://doi.org/10.1667/rr15027.1openalex-snapshot
2017 Michael Fry Award Lecture When DNA is Actually Not a Target: Radiation Epigenetics as a Tool to Understand and Control Cellular Response to Ionizing Radiation
inferred← citeshttps://doi.org/10.1667/rr2674.1openalex-snapshot
Effects of Very Low Fluences of High-Energy Protons or Iron Ions on Irradiated and Bystander Cells
inferred← citeshttps://doi.org/10.1667/rr2803.1openalex-snapshot
In VitroEvaluation of Combined Temozolomide and Radiotherapy Using X Rays and High-Linear Energy Transfer Radiation for Glioblastoma
inferred← citeshttps://doi.org/10.17554/j.issn.2313-3406.2015.02.13openalex-snapshot
The Role of Epigenetic Modulation in the Cellular Response to Ionizing Radiation
inferred← citeshttps://doi.org/10.18632/aging.100447openalex-snapshot
Epigenetic bystander-like effects of stroke in somatic organs
inferred← citeshttps://doi.org/10.18632/oncotarget.12647openalex-snapshot
Methylation of promoter of RBL1 enhances the radioresistance of three dimensional cultured carcinoma cells
inferred← citeshttps://doi.org/10.18632/oncotarget.24311openalex-snapshot
Adverse effects of paternal chemotherapy exposure on the progeny brain: intergenerational chemobrain
inferred← citeshttps://doi.org/10.21037/2092openalex-snapshot
Cell and molecular response to IORT treatment
inferred← citeshttps://doi.org/10.21514/1998-426x-2026-19-2-27-33openalex-snapshot
Association of methylation and transcriptional activity of redox system genes with apoptosis and necrosis of lymphocytes in chronically irradiated individuals
inferred← citeshttps://doi.org/10.2187/bss.22.46openalex-snapshot
Heavy-Ion Microbeam Irradiation Induces Bystander Killing of Human Cells
inferred← citeshttps://doi.org/10.2187/bss.23.195openalex-snapshot
The Bystander Response to Heavy-Ion Radiation: Intercellular Signaling Between Irradiated and Non-Irradiated Cells
inferred← citeshttps://doi.org/10.22268/ajpp-001212openalex-snapshot
Genetic Profile of Gamma Irradiated Locusta migratoria migratorioides: A Futuristic Eco-friendly Control Approach
inferred← citeshttps://doi.org/10.2478/10004-1254-62-2011-2089openalex-snapshot
Long-Term Follow-Up Study of Genome Damage Elimination in Patients with Testicular Seminoma Exposed to Ionising Radiation during Radiotherapy
inferred← citeshttps://doi.org/10.3109/09553000903105452openalex-snapshot
Communication of ionising radiation signals – a tale of two fish
inferred← citeshttps://doi.org/10.3109/09553002.2010.522686openalex-snapshot
Radiation-induced genomic instability: Are epigenetic mechanisms the missing link?
inferred← citeshttps://doi.org/10.3109/09553002.2010.537431openalex-snapshot
Targeted and non-targeted effects from combinations of low doses of energetic protons and iron ions in human fibroblasts
inferred← citeshttps://doi.org/10.3109/09553002.2012.699698openalex-snapshot
Radiation hormesis: Autophagy and other cellular mechanisms
inferred← citeshttps://doi.org/10.3109/09553002.2012.704657openalex-snapshot
Transcriptional responses in irradiated and bystander fibroblasts after low dose α-particle radiation
inferred← citeshttps://doi.org/10.3109/09553002.2013.806832openalex-snapshot
Role of DNA methylation in long-term low-dose γ-rays induced adaptive response in human B lymphoblast cells
inferred← citeshttps://doi.org/10.3109/09553002.2014.925605openalex-snapshot
Radiation-induced conformational changes in chromatin structure in resting human peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.3109/09553002.2014.934929openalex-snapshot
Ionizing radiation-induced oxidative stress, epigenetic changes and genomic instability: The pivotal role of mitochondria
inferred← citeshttps://doi.org/10.3233/nib-190160openalex-snapshot
Innate Immunity, Stress and Evolution
inferred← citeshttps://doi.org/10.3389/fgene.2013.00040openalex-snapshot
Epigenetics in radiation biology: a new research frontier
inferred← citeshttps://doi.org/10.3389/fnbeh.2016.00084openalex-snapshot
Profound and Sexually Dimorphic Effects of Clinically-Relevant Low Dose Scatter Irradiation on the Brain and Behavior
inferred← citeshttps://doi.org/10.3389/fonc.2012.00117openalex-snapshot
Radiation-induced alterations in histone modification patterns and their potential impact on short-term radiation effects
inferred← citeshttps://doi.org/10.3389/fpubh.2014.00139openalex-snapshot
Role of microRNAs and DNA Methyltransferases in Transmitting Induced Genomic Instability between Cell Generations
inferred← citeshttps://doi.org/10.3390/agriculture15242541openalex-snapshot
Space Agriculture: A Comprehensive Systems-Level Review of Challenges and Opportunities
inferred← citeshttps://doi.org/10.3390/cells13060550openalex-snapshot
The Molecular Mechanisms in Senescent Cells Induced by Natural Aging and Ionizing Radiation
inferred← citeshttps://doi.org/10.3390/ijms20174093openalex-snapshot
Chromatin Remodeling and Epigenetic Regulation in Plant DNA Damage Repair
inferred← citeshttps://doi.org/10.3390/ijms21175993openalex-snapshot
Ionizing Radiation-Induced Epigenetic Modifications and Their Relevance to Radiation Protection
inferred← citeshttps://doi.org/10.3390/medicina55090591openalex-snapshot
Genomic Instability and Carcinogenesis of Heavy Charged Particles Radiation: Clinical and Environmental Implications
inferred← citeshttps://doi.org/10.4161/cc.25135openalex-snapshot
p53 Ser15 phosphorylation and histone modifications contribute to IR-induced miR-34a transcription in mammary epithelial cells
inferred← citeshttps://doi.org/10.46912/jbrcp.60openalex-snapshot
Epigenetics in Medical Practice in the Twenty First Century
inferred← citeshttps://doi.org/10.5513/jcea01/21.3.2709openalex-snapshot
Radioactive contamination in Chernobyl and (epi)genetic stability of plants – A review
inferred← citeshttps://doi.org/10.70675/70a73ff4z5e24z4244z8e55z410230ebf53copenalex-snapshot
Chromatin Disorganization as a Regulator of Irradiation-Induced L1Md Expression and Hematopoietic Stem Cell Function
inferred← citeshttps://doi.org/10.70675/ed42220dz616ez42e5z9603zef71b1522b94openalex-snapshot
A novel H2A.Z deposition pathway involving the Ku70/Ku80 heterodimer
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.