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Nuclear Abl Drives miR-34c Transfer by Extracellular Vesicles to Induce Radiation Bystander Effects
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1 of the 39 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1038/nature12201 (notice 2019-04-11).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471143030.cb0322s30openalex-snapshot
Isolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids
inferredcites →https://doi.org/10.1002/jcb.24694openalex-snapshot
Radiation‐induced microRNA: Discovery, functional analysis, and cancer radiotherapy
inferredcites →https://doi.org/10.1002/path.4299openalex-snapshot
Responses to ionizing radiation mediated by inflammatory mechanisms
inferredcites →https://doi.org/10.1007/s10456-011-9241-1openalex-snapshot
Exosomes released by K562 chronic myeloid leukemia cells promote angiogenesis in a src-dependent fashion
inferredcites →https://doi.org/10.1016/j.canlet.2011.12.012openalex-snapshot
Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury
inferredcites →https://doi.org/10.1016/j.canlet.2013.12.017openalex-snapshot
Bystander effects as manifestation of intercellular communication of DNA damage and of the cellular oxidative status
inferredcites →https://doi.org/10.1016/j.canlet.2014.01.023openalex-snapshot
The role of oxidative DNA damage in radiation induced bystander effect
inferredcites →https://doi.org/10.1016/j.cell.2016.01.043openalex-snapshot
Communication by Extracellular Vesicles: Where We Are and Where We Need to Go
inferredcites →https://doi.org/10.1016/j.mrrev.2017.05.003openalex-snapshot
Significance and nature of bystander responses induced by various agents
inferredcites →https://doi.org/10.1016/j.tcb.2008.11.003openalex-snapshot
Shedding microvesicles: artefacts no more
inferredcites →https://doi.org/10.1016/s0092-8674(00)81847-4openalex-snapshot
Association of BRCA1 with Rad51 in Mitotic and Meiotic Cells
inferredcites →https://doi.org/10.1038/21690openalex-snapshot
The tyrosine kinase c-Abl regulates p73 in apoptotic response to cisplatin-induced DNA damage
inferredcites →https://doi.org/10.1038/387516a0openalex-snapshot
Ataxia telangiectasia mutant protein activates c-Abl tyrosine kinase in response to ionizing radiation
inferredcites →https://doi.org/10.1038/cdd.2013.42openalex-snapshot
Genetic disruption of Abl nuclear import reduces renal apoptosis in a mouse model of cisplatin-induced nephrotoxicity
inferredcites →https://doi.org/10.1038/nature05939openalex-snapshot
A microRNA component of the p53 tumour suppressor network
inferredcites →https://doi.org/10.1038/nature12201openalex-snapshot
KAT5 tyrosine phosphorylation couples chromatin sensing to ATM signalling
inferredcites →https://doi.org/10.1038/ncb1596openalex-snapshot
Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells
inferredcites →https://doi.org/10.1038/nrc2232openalex-snapshot
microRNAs join the p53 network — another piece in the tumour-suppression puzzle
inferredcites →https://doi.org/10.1038/nrc2603openalex-snapshot
Radiation-induced bystander signalling in cancer therapy
inferredcites →https://doi.org/10.1038/sj.cdd.4400626openalex-snapshot
c-Abl: activation and nuclear targets
inferredcites →https://doi.org/10.1038/sj.cdd.4402119openalex-snapshot
Delayed activation of Bax by DNA damage in embryonic stem cells with knock-in mutations of the Abl nuclear localization signals
inferredcites →https://doi.org/10.1038/sj.cr.7290261openalex-snapshot
Role of c-Abl in the DNA damage stress response
inferredcites →https://doi.org/10.1038/sj.onc.1202303openalex-snapshot
Stress-induced secretion of growth inhibitors: a novel tumor suppressor function of p53
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.1209467openalex-snapshot
Irradiation induces DNA damage and modulates epigenetic effectors in distant bystander tissue in vivo
inferredcites →https://doi.org/10.1073/pnas.0910015107openalex-snapshot
p38 MAPK/MK2-mediated induction of miR-34c following DNA damage prevents Myc-dependent DNA replication
inferredcites →https://doi.org/10.1088/0952-4746/36/1/r23openalex-snapshot
Non-targeted effects and radiation-induced carcinogenesis: a review
inferredcites →https://doi.org/10.1089/dna.2014.2401openalex-snapshot
microRNA Expression and Biogenesis in Cellular Response to Ionizing Radiation
inferredcites →https://doi.org/10.1126/scisignal.aaa4468openalex-snapshot
The kinase ABL phosphorylates the microprocessor subunit DGCR8 to stimulate primary microRNA processing in response to DNA damage
inferredcites →https://doi.org/10.1128/mcb.01454-13openalex-snapshot
The Capable ABL: What Is Its Biological Function?
inferredcites →https://doi.org/10.1158/0008-5472.can-08-0545openalex-snapshot
ATM Acts Downstream of ATR in the DNA Damage Response Signaling of Bystander Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-08-0698openalex-snapshot
Chromosomal Instability in Unirradiated Hemaopoietic Cells Induced by Macrophages Exposed In vivo to Ionizing Radiation
inferredcites →https://doi.org/10.1158/0008-5472.can-10-1181openalex-snapshot
Evidence of an Adaptive Response Targeting DNA Nonhomologous End Joining and Its Transmission to Bystander Cells
inferredcites →https://doi.org/10.1371/journal.pgen.1002797openalex-snapshot
Intact p53-Dependent Responses in miR-34–Deficient Mice
inferredcites →https://doi.org/10.1371/journal.pone.0067581openalex-snapshot
MiR-34a/c-Dependent PDGFR-α/β Downregulation Inhibits Tumorigenesis and Enhances TRAIL-Induced Apoptosis in Lung Cancer
inferredcites →https://doi.org/10.1371/journal.pone.0149866openalex-snapshot
Comparative Analysis of Technologies for Quantifying Extracellular Vesicles (EVs) in Clinical Cerebrospinal Fluids (CSF)
inferredcites →https://doi.org/10.2174/0929866523666160427105138openalex-snapshot
The Influence of Ionizing Radiation on Exosome Composition, Secretion and Intercellular Communication
inferredcites →https://doi.org/10.2174/1568009614666141020100337openalex-snapshot
MicroRNA-34 Family, Mechanisms of Action in Cancer: A Review
inferredcites →https://doi.org/10.7554/elife.19276openalex-snapshot
Y-box protein 1 is required to sort microRNAs into exosomes in cells and in a cell-free reaction
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