On the public citation graph

High-LET-Radiation-Induced Persistent DNA Damage Response Signaling and Gastrointestinal Cancer Development

https://doi.org/10.3390/curroncol30060416

0 signed · 192 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.10320openalex-snapshot

Cancer genetics

inferredcites →https://doi.org/10.1002/em.22087openalex-snapshot

Mechanisms of DNA damage, repair, and mutagenesis

inferredcites →https://doi.org/10.1002/ijc.34186openalex-snapshot

DNA methylation biomarkers in colorectal cancer: Clinical applications for precision medicine

inferredcites →https://doi.org/10.1002/path.4087openalex-snapshot

MLH1‐silenced and non‐silenced subgroups of hypermutated colorectal carcinomas have distinct mutational landscapes

inferredcites →https://doi.org/10.1002/wdev.56openalex-snapshot

Stress and stem cells

inferredcites →https://doi.org/10.1007/978-3-319-09216-4openalex-snapshot

Applications of EPR in Radiation Research

inferredcites →https://doi.org/10.1007/s002590100484openalex-snapshot

General aspects of the cellular response to low- and high-LET radiation

inferredcites →https://doi.org/10.1007/s00411-007-0105-4openalex-snapshot

Countermeasures against space radiation induced oxidative stress in mice

inferredcites →https://doi.org/10.1007/s00411-022-00997-zopenalex-snapshot

Predominant contribution of the dose received from constituent heavy-ions in the induction of gastrointestinal tumorigenesis after simulated space radiation exposure

inferredcites →https://doi.org/10.1007/s11670-012-0083-1openalex-snapshot

Typical cell signaling response to ionizing radiation: DNA damage and extranuclear damage

inferredcites →https://doi.org/10.1016/0046-8177(92)90345-4openalex-snapshot

Stromal neoplasms of the rectum and anal canal

inferredcites →https://doi.org/10.1016/b978-0-12-378630-2.00491-6openalex-snapshot

Nucleotide Excision Repair in Eukaryotes

inferredcites →https://doi.org/10.1016/b978-0-12-420117-0.00001-3openalex-snapshot

Reactive Oxygen Species in Normal and Tumor Stem Cells

inferredcites →https://doi.org/10.1016/j.bcp.2012.07.022openalex-snapshot

Redox modulation of the DNA damage response

inferredcites →https://doi.org/10.1016/j.biochi.2018.11.003openalex-snapshot

Role of adenomatous polyposis coli (APC) gene mutations in the pathogenesis of colorectal cancer; current status and perspectives

inferredcites →https://doi.org/10.1016/j.cell.2014.04.051openalex-snapshot

Gut Microbial Metabolism Drives Transformation of Msh2-Deficient Colon Epithelial Cells

inferredcites →https://doi.org/10.1016/j.celrep.2018.03.076openalex-snapshot

Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

inferredcites →https://doi.org/10.1016/j.celrep.2020.108434openalex-snapshot

DNA Damage Baseline Predicts Resilience to Space Radiation and Radiotherapy

inferredcites →https://doi.org/10.1016/j.celrep.2021.108840openalex-snapshot

DSB repair pathway choice is regulated by recruitment of 53BP1 through cell cycle-dependent regulation of Sp1

inferredcites →https://doi.org/10.1016/j.cels.2017.09.015openalex-snapshot

Orchestration of DNA Damage Checkpoint Dynamics across the Human Cell Cycle

inferredcites →https://doi.org/10.1016/j.csbj.2019.12.013openalex-snapshot

The genomics of oxidative DNA damage, repair, and resulting mutagenesis

inferredcites →https://doi.org/10.1016/j.dnarep.2008.01.010openalex-snapshot

The Ku-dependent non-homologous end-joining but not other repair pathway is inhibited by high linear energy transfer ionizing radiation

inferredcites →https://doi.org/10.1016/j.dnarep.2015.11.015openalex-snapshot

Mouse models of DNA mismatch repair in cancer research

inferredcites →https://doi.org/10.1016/j.dnarep.2019.01.004openalex-snapshot

Distinct response of adult neural stem cells to low versus high dose ionising radiation

inferredcites →https://doi.org/10.1016/j.dnarep.2022.103289openalex-snapshot

DNA damage-induced sumoylation of Sp1 induces its interaction with RNF4 and degradation in S phase to remove 53BP1 from DSBs and permit HR

inferredcites →https://doi.org/10.1016/j.eururo.2011.05.052openalex-snapshot

Late Gastrointestinal Toxicities Following Radiation Therapy for Prostate Cancer

inferredcites →https://doi.org/10.1016/j.ijrobp.2011.12.033openalex-snapshot

Exposure to Ionizing Radiation Causes Long-Term Increase in Serum Estradiol and Activation of PI3K-Akt Signaling Pathway in Mouse Mammary Gland

inferredcites →https://doi.org/10.1016/j.ijrobp.2015.10.057openalex-snapshot

Relative Biological Effectiveness of Energetic Heavy Ions for Intestinal Tumorigenesis Shows Male Preponderance and Radiation Type and Energy Dependence in APC1638N/+ Mice

inferredcites →https://doi.org/10.1016/j.lssr.2015.04.002openalex-snapshot

Safe days in space with acceptable uncertainty from space radiation exposure

inferredcites →https://doi.org/10.1016/j.lssr.2016.02.001openalex-snapshot

Galactic cosmic ray simulation at the NASA Space Radiation Laboratory

inferredcites →https://doi.org/10.1016/j.lssr.2017.01.005openalex-snapshot

Predictions of space radiation fatality risk for exploration missions

inferredcites →https://doi.org/10.1016/j.lssr.2017.04.003openalex-snapshot

Low and high dose rate heavy ion radiation-induced intestinal and colonic tumorigenesis in APC1638N/+ mice

inferredcites →https://doi.org/10.1016/j.lssr.2020.07.001openalex-snapshot

Heavy ion space radiation triggers ongoing DNA base damage by downregulating DNA repair pathways

inferredcites →https://doi.org/10.1016/j.lssr.2021.09.001openalex-snapshot

Effects of dietary aspirin on high-LET radiation-induced prostaglandin E2 levels and gastrointestinal tumorigenesis in Apc mice

inferredcites →https://doi.org/10.1016/j.lssr.2022.09.005openalex-snapshot

Countermeasure development against space radiation-induced gastrointestinal carcinogenesis: Current and future perspectives

inferredcites →https://doi.org/10.1016/j.molcel.2006.08.014openalex-snapshot

A Mechanism of Nucleotide Misincorporation during Transcription due to Template-Strand Misalignment

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.2019.08.023openalex-snapshot

Life or Death after a Break: What Determines the Choice?

inferredcites →https://doi.org/10.1016/j.mrfmmm.2010.11.002openalex-snapshot

Mechanism of cluster DNA damage repair in response to high-atomic number and energy particles radiation

inferredcites →https://doi.org/10.1016/j.mrfmmm.2011.02.012openalex-snapshot

Heavy charged particle radiobiology: Using enhanced biological effectiveness and improved beam focusing to advance cancer therapy

inferredcites →https://doi.org/10.1016/j.radonc.2018.12.028openalex-snapshot

DNA damage response of clinical carbon ion versus photon radiation in human glioblastoma cells

inferredcites →https://doi.org/10.1016/j.tranon.2020.100822openalex-snapshot

Quantifying DNA damage induced by ionizing radiation and hyperthermia using single DNA molecule imaging

inferredcites →https://doi.org/10.1016/j.trecan.2018.04.007openalex-snapshot

Epigenetic Priming in Cancer Initiation

inferredcites →https://doi.org/10.1016/s0016-5085(98)70478-0openalex-snapshot

Apc1638N: A mouse model for familial adenomatous polyposis–associated desmoid tumors and cutaneous cysts

inferredcites →https://doi.org/10.1016/s0140-6736(15)61167-9openalex-snapshot

Long-term effects of radiation exposure on health

inferredcites →https://doi.org/10.1038/cr.2007.115openalex-snapshot

Mechanisms and functions of DNA mismatch repair

inferredcites →https://doi.org/10.1038/cr.2008.1openalex-snapshot

Homologous recombination in DNA repair and DNA damage tolerance

inferredcites →https://doi.org/10.1038/ncb1909openalex-snapshot

Persistent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion

inferredcites →https://doi.org/10.1038/onc.2015.395openalex-snapshot

Radiation promotes colorectal cancer initiation and progression by inducing senescence-associated inflammatory responses

inferredcites →https://doi.org/10.1038/onc.2017.60openalex-snapshot

New factors in mammalian DNA repair—the chromatin connection

inferredcites →https://doi.org/10.1038/s41467-018-06308-9openalex-snapshot

Persistent repair intermediates induce senescence

inferredcites →https://doi.org/10.1038/s41588-020-0623-4openalex-snapshot

Cas9 activates the p53 pathway and selects for p53-inactivating mutations

inferredcites →https://doi.org/10.1038/s41596-022-00724-4openalex-snapshot

Designing and executing prime editing experiments in mammalian cells

inferredcites →https://doi.org/10.1038/s41598-017-02087-3openalex-snapshot

Non-Targeted Effects Models Predict Significantly Higher Mars Mission Cancer Risk than Targeted Effects Models

inferredcites →https://doi.org/10.1038/s41598-018-23202-yopenalex-snapshot

Integrated Modelling of Cell Responses after Irradiation for DNA-Targeted Effects and Non-Targeted Effects

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/srep14568openalex-snapshot

A generalized target theory and its applications

inferredcites →https://doi.org/10.1038/srep31853openalex-snapshot

Space radiation exposure persistently increased leptin and IGF1 in serum and activated leptin-IGF1 signaling axis in mouse intestine

inferredcites →https://doi.org/10.1039/9781839162541-00426openalex-snapshot

Chapter 31. Gamma- and Ion-beam DNA Radiation Damage: Theory and Experiment

inferredcites →https://doi.org/10.1073/pnas.0403131101openalex-snapshot

Gene interactions in the DNA damage-response pathway identified by genome-wide RNA-interference analysis of synthetic lethality

inferredcites →https://doi.org/10.1073/pnas.0800966105openalex-snapshot

Extreme resistance of bdelloid rotifers to ionizing radiation

inferredcites →https://doi.org/10.1073/pnas.1807522115openalex-snapshot

Space radiation triggers persistent stress response, increases senescent signaling, and decreases cell migration in mouse intestine

inferredcites →https://doi.org/10.1073/pnas.2119132119openalex-snapshot

Formation of clustered DNA damage in vivo upon irradiation with ionizing radiation: Visualization and analysis with atomic force microscopy

inferredcites →https://doi.org/10.1080/09553000902748591openalex-snapshot

Stress response of a p53 homologue in the radioresistant Sf9 insect cells

inferredcites →https://doi.org/10.1080/09553000902883836openalex-snapshot

Ionising radiation and cancer risks: What have we learned from epidemiology?

inferredcites →https://doi.org/10.1080/09553002.2019.1589020openalex-snapshot

The Million Person Study relevance to space exploration and Mars

inferredcites →https://doi.org/10.1080/09553002.2019.1665208openalex-snapshot

Primary and secondary bystander effect and genomic instability in cells exposed to high and low linear energy transfer radiations

inferredcites →https://doi.org/10.1080/10715762.2018.1452204openalex-snapshot

The effect of carbon irradiation is associated with greater oxidative stress in mouse intestine and colon relative to γ-rays

inferredcites →https://doi.org/10.1080/15384101.2018.1482136openalex-snapshot

Measuring cell cycle-dependent DNA damage responses and p53 regulation on a cell-by-cell basis from image analysis

inferredcites →https://doi.org/10.1080/19491034.2017.1384893openalex-snapshot

Heterochromatin and DNA damage repair: Use different histone variants and relax

inferredcites →https://doi.org/10.1089/ars.2012.5036openalex-snapshot

Oxidative DNA Damage and Nucleotide Excision Repair

inferredcites →https://doi.org/10.1091/mbc.e18-10-0668openalex-snapshot

Preserving genome integrity in human cells via DNA double-strand break repair

inferredcites →https://doi.org/10.1093/carcin/bgr236openalex-snapshot

Resveratrol protects mouse embryonic stem cells from ionizing radiation by accelerating recovery from DNA strand breakage

inferredcites →https://doi.org/10.1093/emboj/cdg203openalex-snapshot

Non‐homologous end joining as an important mutagenic process in cell cycle‐arrested cells

inferredcites →https://doi.org/10.1093/femsyr/fow071openalex-snapshot

Understanding how mismatch repair proteins participate in the repair/anti-recombination decision

inferredcites →https://doi.org/10.1093/jrr/rrv005openalex-snapshot

Low-dose energetic protons induce adaptive and bystander effects that protect human cells against DNA damage caused by a subsequent exposure to energetic iron ions

inferredcites →https://doi.org/10.1093/jrr/rry096openalex-snapshot

Clustered DNA double-strand break formation and the repair pathway following heavy-ion irradiation

inferredcites →https://doi.org/10.1093/mutage/geq022openalex-snapshot

RE: Multiple factors conferring high radioresistance in insect Sf9 cells. (Mutagenesis, 24, 259-269, 2009)

inferredcites →https://doi.org/10.1093/rpd/nci141openalex-snapshot

Implications of the space radiation environment for human exploration in deep space

inferredcites →https://doi.org/10.1097/cej.0b013e328341017aopenalex-snapshot

Curcumin prevents DNA damage and enhances the repair potential in a chronically arsenic-exposed human population in West Bengal, India

inferredcites →https://doi.org/10.1097/hp.0000000000001572openalex-snapshot

Medical Countermeasure Requirements to Meet NASA’s Space Radiation Permissible Exposure Limits for a Mars Mission Scenario

inferredcites →https://doi.org/10.1098/rsob.200253openalex-snapshot

The role of antioxidants in restoring MAPK 14 and a DNA damage marker level following autophagy suppression

inferredcites →https://doi.org/10.1101/cshperspect.a012609openalex-snapshot

Nucleotide Excision Repair in Eukaryotes

inferredcites →https://doi.org/10.1101/cshperspect.a016600openalex-snapshot

Homologous Recombination and Human Health: The Roles of BRCA1, BRCA2, and Associated Proteins

inferredcites →https://doi.org/10.1101/gad.13.10.1309openalex-snapshot

Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development

inferredcites →https://doi.org/10.1101/gad.2021311openalex-snapshot

Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications

inferredcites →https://doi.org/10.1109/tns.2020.3032946openalex-snapshot

Radiation Shielding Evaluation of Spacecraft Walls Against Heavy Ions Using Microdosimetry

inferredcites →https://doi.org/10.1111/acel.13013openalex-snapshot

Senescence‐associated tissue microenvironment promotes colon cancer formation through the secretory factor GDF15

inferredcites →https://doi.org/10.1111/tpj.15567openalex-snapshot

Cell cycle checkpoint control in response to DNA damage by environmental stresses

inferredcites →https://doi.org/10.1146/annurev-biochem-062917-012415openalex-snapshot

The MRE11–RAD50–NBS1 Complex Conducts the Orchestration of Damage Signaling and Outcomes to Stress in DNA Replication and Repair

inferredcites →https://doi.org/10.1155/2018/2389523openalex-snapshot

Targeting Oxidatively Induced DNA Damage Response in Cancer: Opportunities for Novel Cancer Therapies

inferredcites →https://doi.org/10.1155/2020/4834965openalex-snapshot

The Determinant of DNA Repair Pathway Choices in Ionising Radiation‐Induced DNA Double‐Strand Breaks

inferredcites →https://doi.org/10.1158/1535-7163.mct-08-0929openalex-snapshot

Base excision repair of reactive oxygen species–initiated 7,8-dihydro-8-oxo-2′-deoxyguanosine inhibits the cytotoxicity of platinum anticancer drugs

inferredcites →https://doi.org/10.1158/1538-7445.am2019-3728openalex-snapshot

Abstract 3728: Inverse effect of 28Si and 56Fe radiation on intestinal tumorigenesis vs. carcinogenesis in APC1638N/+ mice

inferredcites →https://doi.org/10.1158/1538-7445.am2019-3736openalex-snapshot

Abstract 3736: Space radiation-induced decline in gut autophagy and expansion of both mitotic and senescent population denotes an aging phenotype with enhanced cancer risk

inferredcites →https://doi.org/10.1172/jci43169openalex-snapshot

Genes methylated by DNA methyltransferase 3b are similar in mouse intestine and human colon cancer

inferredcites →https://doi.org/10.1177/0300985814559404openalex-snapshot

Epithelial Cell Shedding and Barrier Function

inferredcites →https://doi.org/10.1186/s12885-018-4609-xopenalex-snapshot

Gene promoter and exon DNA methylation changes in colon cancer development – mRNA expression and tumor mutation alterations

inferredcites →https://doi.org/10.1186/s12943-019-0962-xopenalex-snapshot

Stem cells in homeostasis and cancer of the gut

inferredcites →https://doi.org/10.1200/jco.2020.38.15_suppl.4064openalex-snapshot

The landscape of DNA damage response (DDR) pathway in colorectal cancer (CRC).

inferredcites →https://doi.org/10.1201/9780429490606openalex-snapshot

Basic Clinical Radiobiology

inferredcites →https://doi.org/10.1269/jrr.07123openalex-snapshot

Formation of Clustered DNA Damage after High-LET Irradiation: A Review

inferredcites →https://doi.org/10.1289/ehp.8563195openalex-snapshot

Multistage Models of Carcinogenesis

inferredcites →https://doi.org/10.1371/journal.pgen.1000110openalex-snapshot

Alternative-NHEJ Is a Mechanistically Distinct Pathway of Mammalian Chromosome Break Repair

inferredcites →https://doi.org/10.1371/journal.pgen.1003250openalex-snapshot

DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer

inferredcites →https://doi.org/10.1371/journal.pone.0021540openalex-snapshot

Increased Frequency of Spontaneous Neoplastic Transformation in Progeny of Bystander Cells from Cultures Exposed to Densely Ionizing Radiation

inferredcites →https://doi.org/10.1371/journal.pone.0042224openalex-snapshot

Exposure to Heavy Ion Radiation Induces Persistent Oxidative Stress in Mouse Intestine

inferredcites →https://doi.org/10.1371/journal.pone.0059295openalex-snapshot

Heavy Ion Radiation Exposure Triggered Higher Intestinal Tumor Frequency and Greater β-Catenin Activation than γ Radiation in APCMin/+ Mice

inferredcites →https://doi.org/10.1371/journal.pone.0085158openalex-snapshot

Dramatic Increase in Oxidative Stress in Carbon-Irradiated Normal Human Skin Fibroblasts

inferredcites →https://doi.org/10.1371/journal.pone.0155725openalex-snapshot

Both Complexity and Location of DNA Damage Contribute to Cellular Senescence Induced by Ionizing Radiation

inferredcites →https://doi.org/10.1371/journal.pone.0180412openalex-snapshot

Simulated space radiation-induced mutants in the mouse kidney display widespread genomic change

inferredcites →https://doi.org/10.14338/ijpt-18-00018.1openalex-snapshot

Comparing Photon and Charged Particle Therapy Using DNA Damage Biomarkers

inferredcites →https://doi.org/10.1667/rade-21-00059.1openalex-snapshot

Comparison of All Solid Cancer Mortality and Incidence Dose-Response in the Life Span Study of Atomic Bomb Survivors, 1958–2009

inferredcites →https://doi.org/10.1667/rr009cc.1openalex-snapshot

Scaling Human Cancer Risks from Low LET to High LET when Dose-Effect Relationships are Complex

inferredcites →https://doi.org/10.1667/rr1117.1openalex-snapshot

Biophysical Models of Radiation Bystander Effects: 1. Spatial Effects in Three-Dimensional Tissues

inferredcites →https://doi.org/10.1667/rr13572.1openalex-snapshot

Role of 53BP1 in the Regulation of DNA Double-Strand Break Repair Pathway Choice

inferredcites →https://doi.org/10.1667/rr13747.1openalex-snapshot

Biological Characterization of Low-Energy Ions with High-Energy Deposition on Human Cells

inferredcites →https://doi.org/10.1667/rr13770.1openalex-snapshot

Wip1 Abrogation Decreases Intestinal Tumor Frequency in APCMin/+Mice Irrespective of Radiation Quality

inferredcites →https://doi.org/10.1667/rr13804.1openalex-snapshot

Understanding Cancer Development Processes after HZE-Particle Exposure: Roles of ROS, DNA Damage Repair and Inflammation

inferredcites →https://doi.org/10.1667/rr13904.1openalex-snapshot

The Major DNA Repair Pathway after Both Proton and Carbon-Ion Radiation is NHEJ, but the HR Pathway is More Relevant in Carbon Ions

inferredcites →https://doi.org/10.1667/rr14092.1openalex-snapshot

Co-culturing with High-Charge and Energy Particle Irradiated Cells Increases Mutagenic Joining of Enzymatically Induced DNA Double-Strand Breaks in Nonirradiated Cells

inferredcites →https://doi.org/10.1667/rr1415.1openalex-snapshot

Two- and Three-Dimensional Models for Risk Assessment of Radiation-Enhanced Colorectal Tumorigenesis

inferredcites →https://doi.org/10.1667/rr1804.1openalex-snapshot

Comparative Analysis of Cell Killing and Autosomal Mutation in Mouse Kidney Epithelium Exposed to 1 GeV/nucleon Iron IonsIn VitroorIn Situ

inferredcites →https://doi.org/10.1667/rr2155.1openalex-snapshot

CDDO-Me Protects against Space Radiation-Induced Transformation of Human Colon Epithelial Cells

inferredcites →https://doi.org/10.1667/rr3489.1openalex-snapshot

Repair of DNA Damage Induced by Accelerated Heavy Ions in Mammalian Cells Proficient and Deficient in the Non-homologous End-Joining Pathway

inferredcites →https://doi.org/10.18632/aging.100587openalex-snapshot

Therapeutic and space radiation exposure of mouse brain causes impaired DNA repair response and premature senescence by chronic oxidant production

inferredcites →https://doi.org/10.18632/aging.102043openalex-snapshot

Intestinal stem cells acquire premature senescence and senescence associated secretory phenotype concurrent with persistent DNA damage after heavy ion radiation in mice

inferredcites →https://doi.org/10.18632/oncotarget.22679openalex-snapshot

3D-structured illumination microscopy reveals clustered DNA double-strand break formation in widespread γH2AX foci after high LET heavy-ion particle radiation

inferredcites →https://doi.org/10.21037/atm-20-2920openalex-snapshot

Alterations of DNA damage repair in cancer: from mechanisms to applications

inferredcites →https://doi.org/10.2147/ott.s175112openalex-snapshot

Elevated urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine and serum uric acid are associated with progression and are prognostic factors of colorectal cancer

inferredcites →https://doi.org/10.3109/10715762.2011.645207openalex-snapshot

Mitochondrial dysfunction, a probable cause of persistent oxidative stress after exposure to ionizing radiation

inferredcites →https://doi.org/10.3109/10715762.2011.653969openalex-snapshot

Mechanisms of free radical-induced damage to DNA

inferredcites →https://doi.org/10.31661/jbpe.v0i0.713openalex-snapshot

Radiation-induced Non-targeted Effect and Carcinogenesis; Implications in Clinical Radiotherapy

inferredcites →https://doi.org/10.3389/fcell.2021.661931openalex-snapshot

The Intestinal Epithelium – Fluid Fate and Rigid Structure From Crypt Bottom to Villus Tip

inferredcites →https://doi.org/10.3389/fgene.2015.00063openalex-snapshot

Bystander communication and cell cycle decisions after DNA damage

inferredcites →https://doi.org/10.3389/fonc.2015.00218openalex-snapshot

Decreased RXRα is Associated with Increased β-Catenin/TCF4 in 56Fe-Induced Intestinal Tumors

inferredcites →https://doi.org/10.3389/fonc.2020.549777openalex-snapshot

DNA Damage Repair Gene Mutations Are Indicative of a Favorable Prognosis in Colorectal Cancer Treated With Immune Checkpoint Inhibitors

inferredcites →https://doi.org/10.3390/biom6040047openalex-snapshot

Repair of DNA Double-Strand Breaks in Heterochromatin

inferredcites →https://doi.org/10.3390/cancers11111789openalex-snapshot

Ionizing Radiation and Complex DNA Damage: From Prediction to Detection Challenges and Biological Significance

inferredcites →https://doi.org/10.3390/cancers12103022openalex-snapshot

Carbon Ion Radiobiology

inferredcites →https://doi.org/10.3390/cancers12123560openalex-snapshot

Pathogenic Germline Mutations of DNA Repair Pathway Components in Early-Onset Sporadic Colorectal Polyp and Cancer Patients

inferredcites →https://doi.org/10.3390/cancers13092125openalex-snapshot

The Role of p53 Signaling in Colorectal Cancer

inferredcites →https://doi.org/10.3390/cancers14061388openalex-snapshot

Targeting the DNA Damage Response Pathway as a Novel Therapeutic Strategy in Colorectal Cancer

inferredcites →https://doi.org/10.3390/ijms161024094openalex-snapshot

Cancer Microenvironment: What Can We Learn from the Stem Cell Niche

inferredcites →https://doi.org/10.3390/life10120341openalex-snapshot

Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation

inferredcites →https://doi.org/10.3390/molecules27113567openalex-snapshot

Targeting Mechanisms of the DNA Damage Response (DDR) and DNA Repair by Natural Compounds to Improve cAT-Triggered Tumor Cell Death

inferredcites →https://doi.org/10.3978/j.issn.2218-676x.2013.04.02openalex-snapshot

DNA double strand break repair via non-homologous end-joining.

inferredcites →https://doi.org/10.4161/cc.7.18.6679openalex-snapshot

DNA repair by nonhomologous end joining and homologous recombination during cell cycle in human cells

inferredcites →https://doi.org/10.7150/jca.13387openalex-snapshot

Colorectal Carcinogenesis, Radiation Quality, and the Ubiquitin-Proteasome Pathway

inferredcites →https://doi.org/10.7554/elife.62852openalex-snapshot

DNA damage—how and why we age?

inferredcites →https://doi.org/10.7554/elife.79208openalex-snapshot

Highly efficient generation of isogenic pluripotent stem cell models using prime editing

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.4600643openalex-extracted

Assessment of Radioprotective Potential of Zingerone, Ibuprofen, and Sulfasalazine Compounds Against Gamma Radiation

inferred← citeshttps://doi.org/10.1002/cnma.70326openalex-snapshot

Integrating Biological and Physical Principles of Next‐Generation Radiotherapy to Fabricate Engineered Nanoplatforms for Improving Radiotherapy Efficacy

inferred← citeshttps://doi.org/10.1007/s00249-025-01765-9openalex-snapshot

From survival of irradiated mice to modern molecular insights: a seventy-year journey in radiobiology at the institute of biophysics, Czech academy of sciences

inferred← citeshttps://doi.org/10.1007/s00411-025-01174-8openalex-snapshot

Radiation shielding efficiency of rice husk ash-based low-density glasses: a comparative study

inferred← citeshttps://doi.org/10.1007/s00432-024-05757-8openalex-snapshot

A perspective on tumor radiation resistance following high-LET radiation treatment

inferred← citeshttps://doi.org/10.1007/s40778-026-00255-8openalex-snapshot

Genomic Instability and Clonal Hematopoiesis in the Deep-Space Environment: The Role of Sex-Chromosome Asymmetry and High-LET Radiation

inferred← citeshttps://doi.org/10.1016/j.apradiso.2025.111762openalex-snapshot

Resilient STR loci under gamma radiation: A preliminary study on DNA stability in buccal swabs

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119224openalex-snapshot

Biomolecular signatures of γ-irradiation exposure: Differential cell death pathways and Raman spectral profiles in human epidermal keratinocytes and melanocytes

inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39533openalex-snapshot

Transcriptomic analysis of embryonic mouse hypothalamic N38 cells exposed to high-energy protons and/or simulated microgravity

inferred← citeshttps://doi.org/10.1016/j.hoc.2024.11.007openalex-snapshot

Heavy Ion Particle Therapy in Modern Day Radiation Oncology

inferred← citeshttps://doi.org/10.1016/j.jenvrad.2025.107850openalex-snapshot

The unnatural selection: Plant evolution and adaptation in the Chernobyl and Fukushima Exclusion Zones

inferred← citeshttps://doi.org/10.1016/j.lssr.2026.01.006openalex-snapshot

Dose and LET-dependence of gastric cancer risk in Apc1638N/+ mice exposed to space-relevant radiation types

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.08.007openalex-snapshot

Low-dose ionizing radiation and cognitive function: evidence, mechanisms, and controversies

inferred← citeshttps://doi.org/10.1016/j.prenap.2025.100441openalex-snapshot

Natural guardians as radioprotective complements in oncological therapy: A review

inferred← citeshttps://doi.org/10.1016/j.prp.2025.156115openalex-snapshot

Mechanisms of aging-related secretory phenotype regulation in osteoporosis: Network regulation, trade-offs and homeostasis

inferred← citeshttps://doi.org/10.1016/j.radmp.2025.07.002openalex-snapshot

Understanding of FLASH radiotherapy through physical to biological interpretation

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.5c00678openalex-snapshot

Anthraquinone Rhein Mitigates Heavy Ion Radiation-Induced Lung Injury by Maintaining Thioredoxin Reductase/Thioredoxin (TrxR/Trx) Redox Homeostasis

inferred← citeshttps://doi.org/10.1038/s41526-025-00544-2openalex-snapshot

The role and mechanism of ARRB1 in simulated space radiation and microgravity-induced lung carcinogenesis

inferred← citeshttps://doi.org/10.1080/09553002.2024.2430250openalex-snapshot

Trichostatin A mitigates acute and late effects of radiation in intestine by regulation of DNA damage repair and Wnt/TGFβ/Smad signaling

inferred← citeshttps://doi.org/10.1186/s40360-024-00744-8openalex-snapshot

Iron overload induced submandibular glands toxicity in gamma irradiated rats with possible mitigation by hesperidin and rutin

inferred← citeshttps://doi.org/10.1227/neuprac.0000000000000220openalex-snapshot

Neoplastic Cauda Equina Syndrome: When Do We Not Operate?

inferred← citeshttps://doi.org/10.1515/ract-2025-0042openalex-snapshot

Assessing the protective properties of Anti-inflammatory and antioxidant compounds against gamma radiation

inferred← citeshttps://doi.org/10.1667/rade-23-00205.1openalex-snapshot

How We Got Here: One Laboratory's Odyssey in the Field of Radiation-Inducible Genes

inferred← citeshttps://doi.org/10.18632/aging.206183openalex-snapshot

Senolytic agent ABT-263 mitigates low- and high-LET radiation-induced gastrointestinal cancer development in Apc1638N/+ mice

inferred← citeshttps://doi.org/10.20944/preprints202406.0689.v1openalex-snapshot

FLASH Radiotherapy versus Conventional Therapy in Cancer Treatment; Promises, Paradoxes and Problems

inferred← citeshttps://doi.org/10.3389/fcimb.2025.1715061openalex-snapshot

Opposing fates: a bipolar cellular model for FMDV replication shaped by 12C6+heavy-ion mutagenesis

inferred← citeshttps://doi.org/10.3389/fcimb.2026.1852596openalex-snapshot

The gut microbiota-enteric nervous system axis: from bidirectional programming to precision therapeutics in digestive diseases

inferred← citeshttps://doi.org/10.3389/fonc.2026.1869974openalex-snapshot

Transcriptomic differences in chromatin and cell cycle regulation in A549 cells after irradiation with carbon ions and X-rays

inferred← citeshttps://doi.org/10.3390/app16041860openalex-snapshot

Medicinal Plants in the Space Exploration Era: Opportunities and Challenges for Mitigating Spaceflight-Induced Health Hazards

inferred← citeshttps://doi.org/10.3390/cancers16193392openalex-snapshot

Effects of High-Linear-Energy-Transfer Heavy Ion Radiation on Intestinal Stem Cells: Implications for Gut Health and Tumorigenesis

inferred← citeshttps://doi.org/10.3390/cells14221767openalex-snapshot

cGAS/STING Pathway Mediates Accelerated Intestinal Cell Senescence and SASP After GCR Exposure in Mice

inferred← citeshttps://doi.org/10.3390/dna4030015openalex-snapshot

8-OxodG: A Potential Biomarker for Chronic Oxidative Stress Induced by High-LET Radiation

inferred← citeshttps://doi.org/10.3390/genes16010085openalex-snapshot

Integrative Analysis of Radiation-Induced Senescence-Associated Secretory Phenotype Factors in Kidney Cancer Progression

inferred← citeshttps://doi.org/10.3390/gidisord6020025openalex-snapshot

Enteric Nervous System Alterations in Inflammatory Bowel Disease: Perspectives and Implications

inferred← citeshttps://doi.org/10.3390/horticulturae12050614openalex-snapshot

Carbon-Ion Irradiation Modulates Early Development of Lettuce Seedlings: A Morphotype-Specific Response

inferred← citeshttps://doi.org/10.3390/ijms27010211openalex-snapshot

Elevated SASP Factors, Reduced Antioxidant Enzymes, and Increased Tumor Susceptibility in Space Radiation-Exposed ApcMin/+ Mice

inferred← citeshttps://doi.org/10.3390/ijtm4030038openalex-snapshot

FLASH Radiotherapy Versus Conventional Cancer Therapy: Promises, Paradoxes and Problems

inferred← citeshttps://doi.org/10.3390/medicina60040653openalex-snapshot

Health Effects of Ionizing Radiation on the Human Body

inferred← citeshttps://doi.org/10.4038/kjms.v7i1.175openalex-snapshot

Health Physics Implications of Space Radiation for Astronauts

inferred← citeshttps://doi.org/10.5772/intechopen.1009748openalex-snapshot

In-Depth Exploration of Radiation-Induced Cell Death Mechanisms in Tumor

inferred← citeshttps://doi.org/10.70675/c231f089z5eaaz4a1azbaa6z5efcb63c119dopenalex-snapshot

The Role of α-Tubulin Acetyltransferase (αTAT1) in Glioblastoma Cellular Responses to Radiotherapy

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.