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Tyrosine kinase c-Abl couples RNA polymerase II transcription to DNA double-strand breaks
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1 of the 84 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 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/10.1007/978-1-4939-3792-9_10openalex-snapshot
A Nonradioactive Assay to Measure Production and Processing of Ribosomal RNA by 4sU-Tagging
inferredcites →https://doi.org/10.1016/j.cell.2010.04.038openalex-snapshot
ATM-Dependent Chromatin Changes Silence Transcription In cis to DNA Double-Strand Breaks
inferredcites →https://doi.org/10.1016/j.cell.2012.03.002openalex-snapshot
A Role for Small RNAs in DNA Double-Strand Break Repair
inferredcites →https://doi.org/10.1016/j.cell.2013.02.011openalex-snapshot
Chromatin Remodeling at DNA Double-Strand Breaks
inferredcites →https://doi.org/10.1016/j.cell.2014.10.040openalex-snapshot
A Variety of Dicer Substrates in Human and C. elegans
inferredcites →https://doi.org/10.1016/j.cell.2016.09.053openalex-snapshot
Conflict Resolution in the Genome: How Transcription and Replication Make It Work
inferredcites →https://doi.org/10.1016/j.cell.2016.10.001openalex-snapshot
Transient RNA-DNA Hybrids Are Required for Efficient Double-Strand Break Repair
inferredcites →https://doi.org/10.1016/j.cell.2018.08.056openalex-snapshot
Human Rad52 Promotes XPG-Mediated R-loop Processing to Initiate Transcription-Associated Homologous Recombination Repair
inferredcites →https://doi.org/10.1016/j.celrep.2014.04.023openalex-snapshot
BRCA2 Coordinates the Activities of Cell-Cycle Kinases to Promote Genome Stability
inferredcites →https://doi.org/10.1016/j.devcel.2014.11.004openalex-snapshot
A Requirement for ERK-Dependent Dicer Phosphorylation in Coordinating Oocyte-to-Embryo Transition in C. elegans
inferredcites →https://doi.org/10.1016/j.febslet.2010.07.029openalex-snapshot
The MRN complex in double‐strand break repair and telomere maintenance
inferredcites →https://doi.org/10.1016/j.molcel.2007.10.008openalex-snapshot
Damage-Induced Ubiquitylation of Human RNA Polymerase II by the Ubiquitin Ligase Nedd4, but Not Cockayne Syndrome Proteins or BRCA1
inferredcites →https://doi.org/10.1016/j.molcel.2015.03.023openalex-snapshot
Transcriptional Elongation Factor ENL Phosphorylated by ATM Recruits Polycomb and Switches Off Transcription for DSB Repair
inferredcites →https://doi.org/10.1016/j.molcel.2016.11.029openalex-snapshot
Distinctive Patterns of Transcription and RNA Processing for Human lincRNAs
inferredcites →https://doi.org/10.1016/j.molcel.2017.05.015openalex-snapshot
ATM, ATR, and DNA-PK: The Trinity at the Heart of the DNA Damage Response
inferredcites →https://doi.org/10.1016/j.molcel.2017.10.008openalex-snapshot
R-ChIP Using Inactive RNase H Reveals Dynamic Coupling of R-loops with Transcriptional Pausing at Gene Promoters
inferredcites →https://doi.org/10.1016/j.molcel.2017.11.020openalex-snapshot
MPK1/SLT2 Links Multiple Stress Responses with Gene Expression in Budding Yeast by Phosphorylating Tyr1 of the RNAP II CTD
inferredcites →https://doi.org/10.1016/j.molcel.2017.12.009openalex-snapshot
Tyrosine-1 of RNA Polymerase II CTD Controls Global Termination of Gene Transcription in Mammals
inferredcites →https://doi.org/10.1016/s0021-9258(18)34669-6openalex-snapshot
Studies of in vitro transcription by calf thymus RNA polymerase II using a novel duplex DNA template.
inferredcites →https://doi.org/10.1016/s0304-419x(97)00020-6openalex-snapshot
Functional role for the c-Abl protein tyrosine kinase in the cellular response to genotoxic stress
inferredcites →https://doi.org/10.1017/s1355838200992318openalex-snapshot
Determination of preferential binding sites for anti-dsRNA antibodies on double-stranded RNA by scanning force microscopy
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The many substrates and functions of ATM
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Ataxia telangiectasia mutant protein activates c-Abl tyrosine kinase in response to ionizing radiation
inferredcites →https://doi.org/10.1038/387520a0openalex-snapshot
Interaction between ATM protein and c-Abl in response to DNA damage
inferredcites →https://doi.org/10.1038/emboj.2010.38openalex-snapshot
High‐resolution profiling of γH2AX around DNA double strand breaks in the mammalian genome
inferredcites →https://doi.org/10.1038/nature03097openalex-snapshot
Cell-cycle checkpoints and cancer
inferredcites →https://doi.org/10.1038/nature05842openalex-snapshot
The ATM repair pathway inhibits RNA polymerase I transcription in response to chromosome breaks
inferredcites →https://doi.org/10.1038/nature08041openalex-snapshot
qiRNA is a new type of small interfering RNA induced by DNA damage
inferredcites →https://doi.org/10.1038/nature08467openalex-snapshot
The DNA-damage response in human biology and disease
inferredcites →https://doi.org/10.1038/nature11179openalex-snapshot
Site-specific DICER and DROSHA RNA products control the DNA-damage response
inferredcites →https://doi.org/10.1038/nature11273openalex-snapshot
Chromatin organization is a major influence on regional mutation rates in human cancer cells
inferredcites →https://doi.org/10.1038/nature12201openalex-snapshot
KAT5 tyrosine phosphorylation couples chromatin sensing to ATM signalling
inferredcites →https://doi.org/10.1038/nature13682openalex-snapshot
Transcript-RNA-templated DNA recombination and repair
inferredcites →https://doi.org/10.1038/nature13787openalex-snapshot
R-loops induce repressive chromatin marks over mammalian gene terminators
inferredcites →https://doi.org/10.1038/ncb3643openalex-snapshot
Damage-induced lncRNAs control the DNA damage response through interaction with DDRNAs at individual double-strand breaks
inferredcites →https://doi.org/10.1038/nchembio.63openalex-snapshot
A forward chemical genetic screen reveals an inhibitor of the Mre11–Rad50–Nbs1 complex
inferredcites →https://doi.org/10.1038/ncomms13049openalex-snapshot
Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes
inferredcites →https://doi.org/10.1038/ncomms15656openalex-snapshot
A damaged genome’s transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks
inferredcites →https://doi.org/10.1038/nprot.2016.012openalex-snapshot
Mammalian NET-seq analysis defines nascent RNA profiles and associated RNA processing genome-wide
inferredcites →https://doi.org/10.1038/nrg3355openalex-snapshot
RNA interference in the nucleus: roles for small RNAs in transcription, epigenetics and beyond
inferredcites →https://doi.org/10.1038/nrg3961openalex-snapshot
R loops: new modulators of genome dynamics and function
inferredcites →https://doi.org/10.1038/nrm.2017.10openalex-snapshot
The code and beyond: transcription regulation by the RNA polymerase II carboxy-terminal domain
inferredcites →https://doi.org/10.1038/nrm3523openalex-snapshot
Charity begins at home: non-coding RNA functions in DNA repair
inferredcites →https://doi.org/10.1038/nrm3994openalex-snapshot
Swiss army knives: non-canonical functions of nuclear Drosha and Dicer
inferredcites →https://doi.org/10.1038/nsmb.1710openalex-snapshot
DNA resection in eukaryotes: deciding how to fix the break
inferredcites →https://doi.org/10.1038/nsmb.2399openalex-snapshot
Cyclin-dependent kinase control of the initiation-to-elongation switch of RNA polymerase II
inferredcites →https://doi.org/10.1038/nsmb.2796openalex-snapshot
Transcriptionally active chromatin recruits homologous recombination at DNA double-strand breaks
inferredcites →https://doi.org/10.1038/nsmb.2827openalex-snapshot
Human nuclear Dicer restricts the deleterious accumulation of endogenous double-stranded RNA
inferredcites →https://doi.org/10.1038/nsmb.3000openalex-snapshot
CDK9 inhibitors define elongation checkpoints at both ends of RNA polymerase II–transcribed genes
inferredcites →https://doi.org/10.1038/nsmb.3285openalex-snapshot
The pol II CTD: new twists in the tail
inferredcites →https://doi.org/10.1038/nsmb.3395openalex-snapshot
DNA–RNA hybrids: the risks of DNA breakage during transcription
inferredcites →https://doi.org/10.1038/s41467-018-02893-xopenalex-snapshot
Drosha drives the formation of DNA:RNA hybrids around DNA break sites to facilitate DNA repair
inferredcites →https://doi.org/10.1038/s41467-018-02894-wopenalex-snapshot
Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations
inferredcites →https://doi.org/10.1038/s41467-018-07799-2openalex-snapshot
BRCA2 controls DNA:RNA hybrid level at DSBs by mediating RNase H2 recruitment
inferredcites →https://doi.org/10.1038/sj.onc.1206087openalex-snapshot
BCR/ABL regulates response to DNA damage: the role in resistance to genotoxic treatment and in genomic instability
inferredcites →https://doi.org/10.1073/pnas.1810409116openalex-snapshot
DNA damage and genome instability by G-quadruplex ligands are mediated by R loops in human cancer cells
inferredcites →https://doi.org/10.1073/pnas.90.23.11167openalex-snapshot
Tyrosine phosphorylation of mammalian RNA polymerase II carboxyl-terminal domain.
inferredcites →https://doi.org/10.1074/jbc.272.30.18905openalex-snapshot
Tyrosine Phosphorylation of RNA Polymerase II Carboxyl-terminal Domain by the Abl-related Gene Product
inferredcites →https://doi.org/10.1074/jbc.m112.364661openalex-snapshot
Preferential Repair of DNA Double-strand Break at the Active Gene in Vivo
inferredcites →https://doi.org/10.1083/jcb.201612131openalex-snapshot
Nuclear phosphorylated Dicer processes double-stranded RNA in response to DNA damage
inferredcites →https://doi.org/10.1093/nar/gks711openalex-snapshot
A small RNA response at DNA ends in Drosophila
inferredcites →https://doi.org/10.1093/nar/gkt1309openalex-snapshot
Quantitation of DNA double-strand break resection intermediates in human cells
inferredcites →https://doi.org/10.1093/nar/gkv1166openalex-snapshot
Cross talk of tyrosine kinases with the DNA damage signaling pathways
inferredcites →https://doi.org/10.1093/nar/gkw121openalex-snapshot
The human DNA ends proteome uncovers an unexpected entanglement of functional pathways
inferredcites →https://doi.org/10.1093/nar/gkx403openalex-snapshot
Strong transcription blockage mediated by R-loop formation within a G-rich homopurine–homopyrimidine sequence localized in the vicinity of the promoter
inferredcites →https://doi.org/10.1093/nar/gky1107openalex-snapshot
Next-generation sequencing reveals two populations of damage-induced small RNAs at endogenous DNA double-strand breaks
inferredcites →https://doi.org/10.1101/cshperspect.a012716openalex-snapshot
DNA Damage Sensing by the ATM and ATR Kinases
inferredcites →https://doi.org/10.1101/gad.200303.112openalex-snapshot
The RNA polymerase II CTD coordinates transcription and RNA processing
inferredcites →https://doi.org/10.1126/science.1140321openalex-snapshot
ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage
inferredcites →https://doi.org/10.1126/science.1164096openalex-snapshot
RNA Exosome Depletion Reveals Transcription Upstream of Active Human Promoters
inferredcites →https://doi.org/10.1126/science.1219651openalex-snapshot
CTD Tyrosine Phosphorylation Impairs Termination Factor Recruitment to RNA Polymerase II
inferredcites →https://doi.org/10.1126/scisignal.3139re6openalex-snapshot
ABL Tyrosine Kinases: Evolution of Function, Regulation, and Specificity
inferredcites →https://doi.org/10.1128/jvi.80.10.5059-5064.2006openalex-snapshot
Double-Stranded RNA Is Produced by Positive-Strand RNA Viruses and DNA Viruses but Not in Detectable Amounts by Negative-Strand RNA Viruses
inferredcites →https://doi.org/10.1158/0008-5472.can-04-3451openalex-snapshot
Deficiency in the Catalytic Subunit of DNA-Dependent Protein Kinase Causes Down-Regulation of ATM
inferredcites →https://doi.org/10.1242/jcs.182188openalex-snapshot
DICER, DROSHA and DNA damage response RNAs are necessary for the secondary recruitment of DNA damage response factors
inferredcites →https://doi.org/10.1371/journal.pgen.1002460openalex-snapshot
Cohesin Protects Genes against γH2AX Induced by DNA Double-Strand Breaks
inferredcites →https://doi.org/10.1371/journal.pgen.1007151openalex-snapshot
Nuclear re-localization of Dicer in primary mouse embryonic fibroblast nuclei following DNA damage
inferredcites →https://doi.org/10.18632/oncotarget.7452openalex-snapshot
Overcoming resistance of targeted EGFR monotherapy by inhibition of STAT3 escape pathway in soft tissue sarcoma
inferredcites →https://doi.org/10.4161/23723548.2014.970072openalex-snapshot
The PBAF chromatin remodeling complex represses transcription and promotes rapid repair at DNA double-strand breaks
inferredcites →https://doi.org/10.7554/elife.02105openalex-snapshot
Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells
inferredcites →https://doi.org/10.7554/elife.02112openalex-snapshot
RNAP II CTD tyrosine 1 performs diverse functions in vertebrate cells
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.4781335openalex-extracted
The Abl1 Tyrosine Kinase and p53 are Key Players in Doxorubicin-Induced Cardiomyopathy and Their Cell Death Signaling Differs in Atrial and Ventricular Cardiomyocytes
inferred← citeshttps://doi.org/10.1002/bies.201900225openalex-snapshot
RNA at DNA Double‐Strand Breaks: The Challenge of Dealing with DNA:RNA Hybrids
inferred← citeshttps://doi.org/10.1007/s10735-025-10662-6openalex-snapshot
Detection of c-Abl and mTERT expression by DMBA-ınduced mouse model of premature ovarian ınsufficiency
inferred← citeshttps://doi.org/10.1016/j.ccell.2023.05.002openalex-snapshot
Circular RNAs drive oncogenic chromosomal translocations within the MLL recombinome in leukemia
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107603openalex-snapshot
Senataxin Ortholog Sen1 Limits DNA:RNA Hybrid Accumulation at DNA Double-Strand Breaks to Control End Resection and Repair Fidelity
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110097openalex-snapshot
RNA-DNA hybrids regulate meiotic recombination
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111526openalex-snapshot
DNA double-strand break-derived RNA drives TIRR/53BP1 complex dissociation
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113489openalex-snapshot
The phosphorylated trimeric SOSS1 complex and RNA polymerase II trigger liquid-liquid phase separation at double-strand breaks
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116386openalex-snapshot
Break-induced replication is activated to repair R-loop-associated double-strand breaks in SETX-deficient cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116605openalex-snapshot
DROSHA, DICER, and damage-induced long ncRNA control BMI1-dependent transcriptional repression at DNA double-strand break
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117699openalex-snapshot
ABL kinase inactivation induces transcription-replication conflicts and impairs replication fork progression in metastatic small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.102661openalex-snapshot
Non-canonical DNA/RNA structures during Transcription-Coupled Double-Strand Break Repair: Roadblocks or Bona fide repair intermediates?
inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103139openalex-snapshot
Repair of DNA double-strand breaks in RNAPI- and RNAPII-transcribed loci
inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103211openalex-snapshot
Transcription-coupled DNA double-strand break repair
inferred← citeshttps://doi.org/10.1016/j.gendis.2024.101401openalex-snapshot
Update on R-loops in genomic integrity: Formation, functions, and implications for human diseases
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.111010openalex-snapshot
Distinct mechanisms of recognition of phosphorylated RNAPII C-terminal domain by BRCT repeats of the BRCA1–BARD1 complex
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.10.002openalex-snapshot
R-Loops Promote Antisense Transcription across the Mammalian Genome
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.04.014openalex-snapshot
Walking a tightrope: The complex balancing act of R-loops in genome stability
inferred← citeshttps://doi.org/10.1016/j.mrrev.2020.108300openalex-snapshot
The dark side of RNA:DNA hybrids
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2020.12.005openalex-snapshot
Regulation of DNA break repair by RNA
inferred← citeshttps://doi.org/10.1016/j.tig.2021.08.016openalex-snapshot
Integration of DNA damage responses with dynamic spatial genome organization
inferred← citeshttps://doi.org/10.1016/j.tig.2026.06.004openalex-snapshot
Transcription in check at DNA double-strand breaks
inferred← citeshttps://doi.org/10.1016/j.tiv.2022.105323openalex-snapshot
Deficiency of TRDMT1 impairs exogenous RNA-based response and promotes retrotransposon activity during long-term culture of osteosarcoma cells
inferred← citeshttps://doi.org/10.1021/acschembio.9b00610openalex-snapshot
Mapping RNAPII CTD Phosphorylation Reveals That the Identity and Modification of Seventh Heptad Residues Direct Tyr1 Phosphorylation
inferred← citeshttps://doi.org/10.1038/s41416-019-0624-1openalex-snapshot
The roles of RNA in DNA double-strand break repair
inferred← citeshttps://doi.org/10.1038/s41418-026-01873-9openalex-snapshot
DDX3X regulates DNA repair pathway choice at double-strand breaks via RNA-DNA hybrid formation
inferred← citeshttps://doi.org/10.1038/s41419-020-2464-6openalex-snapshot
DNA:RNA hybrids form at DNA double-strand breaks in transcriptionally active loci
inferred← citeshttps://doi.org/10.1038/s41467-020-16903-4openalex-snapshot
Specificity of end resection pathways for double-strand break regions containing ribonucleotides and base lesions
inferred← citeshttps://doi.org/10.1038/s41467-021-24201-wopenalex-snapshot
UPF1 promotes the formation of R loops to stimulate DNA double-strand break repair
inferred← citeshttps://doi.org/10.1038/s41467-022-28646-5openalex-snapshot
Small Cajal body-associated RNA 2 (scaRNA2) regulates DNA repair pathway choice by inhibiting DNA-PK
inferred← citeshttps://doi.org/10.1038/s41467-025-63220-9openalex-snapshot
NSUN2 facilitates DICER cleavage of DNA damage-associated R-loops to promote repair
inferred← citeshttps://doi.org/10.1038/s41556-021-00663-4openalex-snapshot
R-loops as Janus-faced modulators of DNA repair
inferred← citeshttps://doi.org/10.1038/s41556-025-01669-yopenalex-snapshot
Transcriptional repression facilitates RNA:DNA hybrid accumulation at DNA double-strand breaks
inferred← citeshttps://doi.org/10.1038/s41576-019-0203-6openalex-snapshot
Conserved chromosomal functions of RNA interference
inferred← citeshttps://doi.org/10.1038/s41580-020-00308-8openalex-snapshot
Causes and consequences of RNA polymerase II stalling during transcript elongation
inferred← citeshttps://doi.org/10.1038/s41580-021-00447-6openalex-snapshot
Mechanisms of lncRNA biogenesis as revealed by nascent transcriptomics
inferred← citeshttps://doi.org/10.1038/s42003-026-10230-yopenalex-snapshot
Site-specific DNA double-strand break induces local transcription in cis and protein expression
inferred← citeshttps://doi.org/10.1038/s44318-024-00111-7openalex-snapshot
The GATAD2B-NuRD complex drives DNA:RNA hybrid-dependent chromatin boundary formation upon DNA damage
inferred← citeshttps://doi.org/10.1042/ebc20200008openalex-snapshot
Jack of all trades? The versatility of RNA in DNA double-strand break repair
inferred← citeshttps://doi.org/10.1080/10409238.2019.1670131openalex-snapshot
RNA–DNA hybrids and the convergence with DNA repair
inferred← citeshttps://doi.org/10.1080/15476286.2021.2014694openalex-snapshot
RNA polymerase II is recruited to DNA double-strand breaks for dilncRNA transcription in Drosophila
inferred← citeshttps://doi.org/10.1080/21541264.2020.1762468openalex-snapshot
A combinatorial view of old and new RNA polymerase II modifications
inferred← citeshttps://doi.org/10.1080/21541264.2024.2406717openalex-snapshot
From silence to symphony: transcriptional repression and recovery in response to DNA damage
inferred← citeshttps://doi.org/10.1093/nar/gkac843openalex-snapshot
DDX17 is required for efficient DSB repair at DNA:RNA hybrid deficient loci
inferred← citeshttps://doi.org/10.1093/nar/gkae937openalex-snapshot
Tetrameric INTS6-SOSS1 complex facilitates DNA:RNA hybrid autoregulation at double-strand breaks
inferred← citeshttps://doi.org/10.1093/nargab/lqad059openalex-snapshot
Regulation of mature mRNA levels by RNA processing efficiency
inferred← citeshttps://doi.org/10.1101/2022.10.24.513557openalex-snapshot
Cytoplasmic mRNA levels are regulated by a combination of chromatin retention and RNA stability
inferred← citeshttps://doi.org/10.1101/2023.02.17.528960openalex-snapshot
Human Integrator provides a quality checkpoint during elongation to facilitate RNA polymerase II processivity
inferred← citeshttps://doi.org/10.1101/2023.10.20.563274openalex-snapshot
RNA Polymerase II-mediated transcription is required for repair of ribosomal DNA breaks in nucleolar caps, guarding against genomic instability
inferred← citeshttps://doi.org/10.1101/2024.02.05.578920openalex-snapshot
NEAT1 promotes genome stability via m6A methylation-dependent regulation of CHD4
inferred← citeshttps://doi.org/10.1101/2024.02.19.581003openalex-snapshot
GATAD2B containing NuRD complex drives R-loop dependent chromatin boundary formation at double strand breaks
inferred← citeshttps://doi.org/10.1101/2025.01.22.634233openalex-snapshot
Distinct Mechanisms of Recognition of Phosphorylated RNAPII C-Terminal Domain by BRCT Repeats of the BRCA1–BARD1 Complex: Insights from Structural and Functional Analyses
inferred← citeshttps://doi.org/10.1101/gad.351913.124openalex-snapshot
NEAT1 promotes genome stability via m 6 A methylation-dependent regulation of CHD4
inferred← citeshttps://doi.org/10.1101/gr.278644.123openalex-snapshot
Tyrosine 1–phosphorylated RNA polymerase II transcribes PROMPTs to facilitate proximal promoter pausing and induce global transcriptional repression in response to DNA damage
inferred← citeshttps://doi.org/10.1111/febs.16561openalex-snapshot
RNAPII response to transcription‐blocking DNA lesions in mammalian cells
inferred← citeshttps://doi.org/10.1126/sciadv.abi6896openalex-snapshot
Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity
inferred← citeshttps://doi.org/10.1126/science.ads7152openalex-snapshot
Direct targeting and regulation of RNA polymerase II by cell signaling kinases
inferred← citeshttps://doi.org/10.1128/mcb.00181-19openalex-snapshot
Regional Gene Repression by DNA Double-Strand Breaks in G 1 Phase Cells
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-20-0396openalex-snapshot
Platinum-Induced Ubiquitination of Phosphorylated H2AX by RING1A Is Mediated by Replication Protein A in Ovarian Cancer
inferred← citeshttps://doi.org/10.1186/s12967-024-05623-8openalex-snapshot
The Abl1 tyrosine kinase is a key player in doxorubicin-induced cardiomyopathy and its p53/p73 cell death mediated signaling differs in atrial and ventricular cardiomyocytes
inferred← citeshttps://doi.org/10.1242/jcs.263423openalex-snapshot
DNA double-strand break response at a glance
inferred← citeshttps://doi.org/10.1515/hsz-2023-0136openalex-snapshot
Structure and phase separation of the C-terminal domain of RNA polymerase II
inferred← citeshttps://doi.org/10.15252/embr.202357801openalex-snapshot
Break‐induced RNA–DNA hybrids (BIRDHs) in homologous recombination: friend or foe?
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1214613/v1openalex-snapshot
DROSHA and DICER RNA products control BMI1-dependent transcriptional repression at DNA damage sites
inferred← citeshttps://doi.org/10.3389/fcell.2025.1537731openalex-snapshot
Mechanisms underlining R-loop biology and implications for human disease
inferred← citeshttps://doi.org/10.3389/fgene.2021.779554openalex-snapshot
A Mutation-Related Long Noncoding RNA Signature of Genome Instability Predicts Immune Infiltration and Hepatocellular Carcinoma Prognosis
inferred← citeshttps://doi.org/10.3389/fmolb.2019.00055openalex-snapshot
Regulation of DNA Double Strand Breaks Processing: Focus on Barriers
inferred← citeshttps://doi.org/10.3389/fmolb.2019.00061openalex-snapshot
Beyond the Trinity of ATM, ATR, and DNA-PK: Multiple Kinases Shape the DNA Damage Response in Concert With RNA Metabolism
inferred← citeshttps://doi.org/10.3389/fmolb.2020.00024openalex-snapshot
Studying DNA Double-Strand Break Repair: An Ever-Growing Toolbox
inferred← citeshttps://doi.org/10.3389/fmolb.2021.655786openalex-snapshot
Sweet Melody or Jazz? Transcription Around DNA Double-Strand Breaks
inferred← citeshttps://doi.org/10.3389/fmolb.2021.664872openalex-snapshot
The Emerging Role of RNA Modifications in DNA Double-Strand Break Repair
inferred← citeshttps://doi.org/10.3389/fmolb.2022.914873openalex-snapshot
In vivo Proximity Labeling of Nuclear and Nucleolar Proteins by a Stably Expressed, DNA Damage-Responsive NONO-APEX2 Fusion Protein
inferred← citeshttps://doi.org/10.3390/cells12162041openalex-snapshot
The Role of c-Abl Tyrosine Kinase in Brain and Its Pathologies
inferred← citeshttps://doi.org/10.3390/cimb45090478openalex-snapshot
Interactions between the DNA Damage Response and the Telomere Complex in Carcinogenesis: A Hypothesis
inferred← citeshttps://doi.org/10.3390/genes12101475openalex-snapshot
Home and Away: The Role of Non-Coding RNA in Intracellular and Intercellular DNA Damage Response
inferred← citeshttps://doi.org/10.3390/ijms21051706openalex-snapshot
One, No One, and One Hundred Thousand: The Many Forms of Ribonucleotides in DNA
inferred← citeshttps://doi.org/10.3390/ijms21186684openalex-snapshot
Inhibition of DNA Repair in Cancer Therapy: Toward a Multi-Target Approach
inferred← citeshttps://doi.org/10.3390/ijms21218039openalex-snapshot
The Role of Small Noncoding RNA in DNA Double-Strand Break Repair
inferred← citeshttps://doi.org/10.3390/ncrna7030042openalex-snapshot
Commuting to Work: Nucleolar Long Non-Coding RNA Control Ribosome Biogenesis from Near and Far
inferred← citeshttps://doi.org/10.3892/mmr.2025.13529openalex-snapshot
Application of non‑coding RNAs in tumors (Review)
inferred← citeshttps://doi.org/10.4103/1673-5374.346540openalex-snapshot
c-Abl kinase at the crossroads of healthy synaptic remodeling and synaptic dysfunction in neurodegenerative diseases
inferred← citeshttps://doi.org/10.5281/zenodo.33320openalex-snapshot
Становлення І Розвиток Опікунської Педагогіки У Польщі
inferred← citeshttps://doi.org/10.62347/aiid7730openalex-snapshot
Study on serum tRF-30-RRJ89O9NF5W8 as a potential biomarker for clinical diagnosis of gastric cancer
inferred← citeshttps://doi.org/10.64898/2026.01.30.702603openalex-snapshot
The glycine-arginine-rich motif of 53BP1 modulates RNA interactions necessary for its liquid-liquid phase separation during DNA Damage Response
inferred← citeshttps://doi.org/10.70675/4bab1779z812bz45d6zbcd4z9eea765b52e7openalex-snapshot
Contrôle de l'expression génique par la RNP 7SK
inferred← citeshttps://doi.org/10.70675/9ac3610bz2f0ez4ce2zac24zd9863979d34eopenalex-snapshot
Characterizing the interplay between DNA : RNA hybrids and genome stability
inferred← citeshttps://doi.org/10.70675/dce63b34z1573z4c87z9c02z6d5c0807db2aopenalex-snapshot
L'implication des hybrides ADN : ARN et de la modification m6A des ARN dans la réparation des cassures double-brins de l'ADN
inferred← citeshttps://doi.org/10.7150/ijbs.47203openalex-snapshot
miRNA-based biomarkers, therapies, and resistance in Cancer
inferred← citeshttps://doi.org/10.7554/elife.48725openalex-snapshot
Tyr1 phosphorylation promotes phosphorylation of Ser2 on the C-terminal domain of eukaryotic RNA polymerase II by P-TEFb
inferred← citeshttps://doi.org/10.7554/elife.69881openalex-snapshot
DNA-RNA hybrids at DSBs interfere with repair by homologous recombination
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