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Unexpected Sensitivity to the Induction of Mutations by Very Low Doses of Alpha-Particle Radiation: Evidence for a Bystander Effect
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/s0027-5107(96)00118-2openalex-snapshot
Hypersensitivity to very-low single radiation doses: Its relationship to the adaptive response and induced radioresistance
inferredcites →https://doi.org/10.1073/pnas.94.8.3765openalex-snapshot
Mutagenic effects of a single and an exact number of α particles in mammalian cells
inferredcites →https://doi.org/10.1073/pnas.96.9.4959openalex-snapshot
Targeted cytoplasmic irradiation with alpha particles induces mutations in mammalian cells
inferredcites →https://doi.org/10.1080/09553009014550321openalex-snapshot
Induction of Chromosomal Aberrations and Sister Chromatid Exchanges by Alpha Particles in Density-inhibited Cultures of Mouse 10T½ and 3T3 Cells
inferredcites →https://doi.org/10.1080/09553009414550021openalex-snapshot
Initial Events in the Cellular Effects of Ionizing Radiations: Clustered Damage in DNA
inferredcites →https://doi.org/10.1080/095530097144030openalex-snapshot
Medium from irradiated human epithelial cells but not human fibroblasts reduces the clonogenic survival of unirradiated cells
inferredcites →https://doi.org/10.1080/095530097144364openalex-snapshot
Review: Proximity effects in the production of chromosome aberrations by ionizing radiation
inferredcites →https://doi.org/10.1080/095530098141087openalex-snapshot
Studies of bystander effects in human fibroblasts using a charged particle microbeam
inferredcites →https://doi.org/10.1080/095530098142176openalex-snapshot
Track structure in radiation biology: theory and applications
inferredcites →https://doi.org/10.1093/jnci/87.11.817openalex-snapshot
Lung Cancer in Radon-Exposed Miners and Estimation of Risk From Indoor Exposure
inferredcites →https://doi.org/10.1093/jnci/89.1.49openalex-snapshot
Lung Cancer Risk From Residential Radon: Meta-analysis of Eight Epidemiologic Studies
inferredcites →https://doi.org/10.1097/00004032-199505000-00012openalex-snapshot
Design of a Benchtop Alpha Particle Irradiator
inferredcites →https://doi.org/10.2307/3574995openalex-snapshot
Mutagenicity and Cytotoxicity of 4.4-MeV α Particles Emitted by Plutonium-238
inferredcites →https://doi.org/10.2307/3576010openalex-snapshot
The Mutagenicity of α Particles from Plutonium-238
inferredcites →https://doi.org/10.2307/3576209openalex-snapshot
Oncogenic Transformation of Mouse BALB/3T3 Cells by Plutonium-238 Alpha Particles
inferredcites →https://doi.org/10.2307/3577523openalex-snapshot
Radiobiology of Ultrasoft X Rays: IV. Flat and Round-Shaped Hamster Cells (CHO-10B, HS-23)
inferredcites →https://doi.org/10.2307/3577917openalex-snapshot
Response of X-Ray-Sensitive CHO Mutant Cells (xrs-6c) to Radiation: II. Relationship between Cell Survival and the Induction of Chromosomal Damage with Low Doses of α Particles
inferredcites →https://doi.org/10.2307/3578090openalex-snapshot
The Dose-Dependent Fragmentation of Chromatin in Human Fibroblasts by 3.5-MeV a Particles from 238 Pu: Experimental and Theoretical Considerations Pertaining to Single-Track Effects
inferredcites →https://doi.org/10.2307/3578979openalex-snapshot
Cellular and Molecular Analysis of Mutagenesis Induced by Charged Particles of Defined Linear Energy Transfer
inferredcites →https://doi.org/10.2307/3578980openalex-snapshot
Alpha-Particle-Induced Sister Chromatid Exchange in Normal Human Lung Fibroblasts: Evidence for an Extranuclear Target
inferredcites →https://doi.org/10.2307/3579145openalex-snapshot
Radiation Mutagenesis: The Initial DNA Lesions Responsible
inferredcites →https://doi.org/10.2307/3579865openalex-snapshot
Intercellular Communication Is Involved in the Bystander Regulation of Gene Expression in Human Cells Exposed to Very Low Fluences of Alpha Particles
inferredcites →https://doi.org/10.2307/3579958openalex-snapshot
Cell-Cell Contact during Gamma Irradiation Is Not Required to Induce a Bystander Effect in Normal Human Keratinocytes: Evidence for Release during Irradiation of a Signal Controlling Survival into the Medium
inferredcites →https://doi.org/10.2307/3580049openalex-snapshot
Alpha Particles Induce the Production of Interleukin-8 by Human Cells
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Differential response of two cell lines sequentially irradiated with low X-ray doses
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What can we say about the dose-effect relationship at very low doses?
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A contribution to the linear no-threshold discussion
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Non-targeted effects and radiation-induced carcinogenesis: a review
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Non-targeted effects and radiation-induced cancer
inferred← citeshttps://doi.org/10.1088/1361-6560/aaf26aopenalex-snapshot
The linear quadratic model: usage, interpretation and challenges
inferred← citeshttps://doi.org/10.1088/1742-6596/101/1/012005openalex-snapshot
Bystander responses in low dose irradiated cells treated with plasma from gamma irradiated blood
inferred← citeshttps://doi.org/10.1089/ars.2013.5649openalex-snapshot
Health Risks of Space Exploration: Targeted and Nontargeted Oxidative Injury by High-Charge and High-Energy Particles
inferred← citeshttps://doi.org/10.1089/cbr.2010.0940openalex-snapshot
Mitochondrial Gene Expression in Directly Irradiated and Nonirradiated Bystander Cells
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1093/jnci/djj001openalex-snapshot
Cancer Survivorship—Genetic Susceptibility and Second Primary Cancers: Research Strategies and Recommendations
inferred← citeshttps://doi.org/10.1093/jrr/rrad059openalex-snapshot
Radiation-quality-dependent bystander cellular effects induced by heavy-ion microbeams through different pathways
inferred← citeshttps://doi.org/10.1093/jrr/rrt068openalex-snapshot
X-ray-induced bystander responses reduce spontaneous mutations in V79 cells
inferred← citeshttps://doi.org/10.1093/jrr/rrw110openalex-snapshot
Modeling cell survival and change in amount of DNA during protracted irradiation
inferred← citeshttps://doi.org/10.1093/milmed/167.suppl_1.44openalex-snapshot
Genomic Instability and Bystander Effects: A Paradigm Shift in Radiation Biology?
inferred← citeshttps://doi.org/10.1093/mutage/16.6.529openalex-snapshot
Chromosome instability induced in the cell progeny of human T lymphocytes irradiated in G0 with gamma-rays
inferred← citeshttps://doi.org/10.1093/occmed/kql010openalex-snapshot
New advances in radiation biology
inferred← citeshttps://doi.org/10.1093/oxfordjournals.rpd.a006769openalex-snapshot
Genotoxic Damage in Non-irradiated Cells: Contribution from the Bystander Effect
inferred← citeshttps://doi.org/10.1093/rpd/ncl430openalex-snapshot
Keeping up with the neighbours—measuring the bystander response
inferred← citeshttps://doi.org/10.1093/rpd/ncl433openalex-snapshot
A model for the induction of chromosome aberrations through direct and bystander mechanisms
inferred← citeshttps://doi.org/10.1093/rpd/ncl446openalex-snapshot
Modelling radiation-induced bystander effect and cellular communication
inferred← citeshttps://doi.org/10.1093/rpd/ncr169openalex-snapshot
Radiation-induced bystander effects induce radioadaptive response by low-dose radiation
inferred← citeshttps://doi.org/10.1097/00004032-200104000-00010openalex-snapshot
RESOLVING THE MOLECULAR MECHANISMS OF RADIATION TUMORIGENESIS
inferred← citeshttps://doi.org/10.1097/00004032-200307000-00005openalex-snapshot
THE STATE OF THE ART IN THE 1990’S: NCRP REPORT No. 136 ON THE SCIENTIFIC BASES FOR LINEARITY IN THE DOSE-RESPONSE RELATIONSHIP FOR IONIZING RADIATION
inferred← citeshttps://doi.org/10.1097/01.hp.0000232847.23192.3eopenalex-snapshot
LAURISTON S. TAYLOR LECTURE: NONTARGETED EFFECTS OF RADIATION: IMPLICATIONS FOR LOW-DOSE EXPOSURES
inferred← citeshttps://doi.org/10.1097/hp.0000000000000430openalex-snapshot
Health Benefits of Exposure to Low-dose Radiation
inferred← citeshttps://doi.org/10.1101/435487openalex-snapshot
Relative biological effect of alpha particle radiation on low dose phenomena: lethal mutation, hyper-radiosensitivity and increased radioresistance
inferred← citeshttps://doi.org/10.1134/s0026893312030041openalex-snapshot
Differential regulation of MicroRNA expression in irradiated and bystander cells
inferred← citeshttps://doi.org/10.1142/9789812779489_0005openalex-snapshot
CANCER MODELS, IONIZING RADIATION, AND GENOMIC INSTABILITY: A REVIEW
inferred← citeshttps://doi.org/10.1155/2012/389095openalex-snapshot
A Simulation Study of the Radiation-Induced Bystander Effect: Modeling with Stochastically Defined Signal Reemission
inferred← citeshttps://doi.org/10.1158/0008-5472.can-08-0545openalex-snapshot
ATM Acts Downstream of ATR in the DNA Damage Response Signaling of Bystander Cells
inferred← citeshttps://doi.org/10.1159/000485971openalex-snapshot
Thyroid Cancer Induction: Nitrates as Independent Risk Factors or Risk Modulators after Radiation Exposure, with a Focus on the Chernobyl Accident
inferred← citeshttps://doi.org/10.1177/153303460500400209openalex-snapshot
Precautions in the Use of Intensity-Modulated Radiation Therapy
inferred← citeshttps://doi.org/10.1186/s41181-025-00393-0openalex-snapshot
Assessing the radiation-induced bystander effect in radionuclide therapy using targeted radiopharmaceuticals
inferred← citeshttps://doi.org/10.1191/0960327104ht417edopenalex-snapshot
Bystander effects and the dose response
inferred← citeshttps://doi.org/10.1191/0960327104ht418oaopenalex-snapshot
The radiation-induced bystander effect: evidence and significance
inferred← citeshttps://doi.org/10.1191/0960327104ht420oaopenalex-snapshot
In vivo validation of the bystander effect
inferred← citeshttps://doi.org/10.1191/0960327104ht423oaopenalex-snapshot
Review of radiation-induced bystander effects
inferred← citeshttps://doi.org/10.1201/9780203913284-16openalex-snapshot
Track Structure Studies of Biological Systems
inferred← citeshttps://doi.org/10.1201/9780203913284.ch17openalex-snapshot
Track Structure Studies of Biological Systems
inferred← citeshttps://doi.org/10.1201/b11448-19openalex-snapshot
Late Effects from Scattered and Secondary Radiation
inferred← citeshttps://doi.org/10.1201/b11448-24openalex-snapshot
Late Effects from Scattered and Secondary Radiation
inferred← citeshttps://doi.org/10.1259/bjr.75.889.750050openalex-snapshot
Evidence for humoral effects on the radiation response of rat foot skin
inferred← citeshttps://doi.org/10.1269/jrr.42.157openalex-snapshot
Comet Assay to Assess the Non-target Effect of Neutron-radiation in Human Peripheral Blood
inferred← citeshttps://doi.org/10.1371/journal.pone.0041431openalex-snapshot
Lung Cancer Mortality (1950–1999) among Eldorado Uranium Workers: A Comparison of Models of Carcinogenesis and Empirical Excess Risk Models
inferred← citeshttps://doi.org/10.1371/journal.pone.0067174openalex-snapshot
Bioavailability and Efficacy of a Gap Junction Enhancer (PQ7) in a Mouse Mammary Tumor Model
inferred← citeshttps://doi.org/10.1504/ijlr.2004.003875openalex-snapshot
Radiation-induced genomic instability: manifestations and mechanisms
inferred← citeshttps://doi.org/10.1667/0033-7587(2000)154[0073:aotnos]2.0.co;2openalex-snapshot
Activation of the Nitric Oxide Synthase 2 Pathway in the Response of Bone Marrow Stromal Cells to High Doses of Ionizing Radiation
inferred← citeshttps://doi.org/10.1667/0033-7587(2000)154[0351:mibapr]2.0.co;2openalex-snapshot
Mutations Induced by Alpha-Particle Radiation—No Evidence for a Bystander Effect
inferred← citeshttps://doi.org/10.1667/0033-7587(2000)154[0352:rttcoc]2.0.co;2openalex-snapshot
Response to the Comments of Chadwick and Leenhouts
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)155[0335:friagj]2.0.co;2openalex-snapshot
Free Radical-Initiated and Gap Junction-Mediated Bystander Effect due to Nonuniform Distribution of Incorporated Radioactivity in a Three-Dimensional Tissue Culture Model
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)155[0402:tbeiro]2.0.co;2openalex-snapshot
The Bystander Effect in Radiation Oncogenesis: II. A Quantitative Model
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)155[0759:ribeph]2.0.co;2openalex-snapshot
Radiation-Induced Bystander Effects: Past History and Future Directions
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)155[0870:ricici]2.0.co;2openalex-snapshot
Radiation-Induced Cell Inactivation can Increase the Cancer Risk
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)156[0521:hmiibc]2.0.co;2openalex-snapshot
HPRTMutants Induced in Bystander Cells by Very Low Fluences of Alpha Particles Result Primarily from Point Mutations
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)156[0612:tpiobe]2.0.co;2openalex-snapshot
The Potential Impact of Bystander Effects on Radiation Risks in a Mars Mission
inferred← citeshttps://doi.org/10.1667/0033-7587(2001)156[0695:tbeicc]2.0.co;2openalex-snapshot
The Bystander Effect in C3H 10T Cells and Radon-Induced Lung Cancer
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1667/0033-7587(2003)159[0262:iotnej]2.0.co;2openalex-snapshot
Involvement of the Nonhomologous End Joining DNA Repair Pathway in the Bystander Effect for Chromosomal Aberrations
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1667/0033-7587(2003)160[0052:gdibiv]2.0.co;2openalex-snapshot
Genetic Damage Induced byIn VitroIrradiation of Human G0Lymphocytes with Low-Energy Protons (28 keV/μm):HPRTMutations and Chromosome Aberrations
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/rr0742.1openalex-snapshot
Detrimental and Protective Bystander Effects: A Model Approach
inferred← citeshttps://doi.org/10.1667/rr1014.1openalex-snapshot
Effective Target Size for the Induction of Bystander Effects in Medium Transfer Experiments
inferred← citeshttps://doi.org/10.1667/rr1293.1openalex-snapshot
Triggering-Response Model for Radiation-Induced Bystander Effects
inferred← citeshttps://doi.org/10.1667/rr14053.1openalex-snapshot
Early and Delayed Induction of DSBs by Nontargeted Effects in ICR Mouse Lymphocytes afterIn VivoX Irradiation
inferred← citeshttps://doi.org/10.1667/rr1508.1openalex-snapshot
A Bystander Effect is Induced in Human Cells Treated with UVA Radiation but Not UVB Radiation
inferred← citeshttps://doi.org/10.1667/rr1866.1openalex-snapshot
Investigation of Adaptive Responses in Bystander Cells in 3D Cultures Containing Tritium-Labeled and Unlabeled Normal Human Fibroblasts
inferred← citeshttps://doi.org/10.1667/rr1895.1openalex-snapshot
Induction of Bystander Response in Human Glioma Cells using High-Energy Electrons: A Role for TGF-β1
inferred← citeshttps://doi.org/10.1667/rr2023.1openalex-snapshot
Investigation of Bystander Effects in Hybrid Cells by Means of Cell Fusion and Premature Chromosome Condensation Induction
inferred← citeshttps://doi.org/10.1667/rr2223.1openalex-snapshot
Persistence of DNA Double-Strand Breaks in Normal Human Cells Induced by Radiation-Induced Bystander Effect
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