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Genome instability: a mechanistic view of its causes and consequences
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.1999.2847openalex-snapshot
Analysis of DNA replication forks encountering a pyrimidine dimer in the template to the leading strand 1 1Edited by M. Yaniv
inferredcites →https://doi.org/10.1007/bf00268528openalex-snapshot
Hyper-recombination in dam mutants of Escherichia coli K-12
inferredcites →https://doi.org/10.1007/bf00272988openalex-snapshot
DNA polymerase ? inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
inferredcites →https://doi.org/10.1007/bf00329839openalex-snapshot
Asymmetric cytosine deamination revealed by spontaneous mutational specificity in an Ung− strain of Escherichia coli
inferredcites →https://doi.org/10.1016/0022-2836(76)90156-xopenalex-snapshot
A model for replication repair in mammalian cells
inferredcites →https://doi.org/10.1016/0042-6822(88)90489-8openalex-snapshot
Transcription stimulates recombination II. Generalized transduction of Escherichia coli by phages T1 and T4
inferredcites →https://doi.org/10.1016/0092-8674(87)90714-8openalex-snapshot
Recombination-stimulating sequences in yeast ribosomal DNA correspond to sequences regulating transcription by RNA polymerase I
inferredcites →https://doi.org/10.1016/0092-8674(88)90222-xopenalex-snapshot
A replication fork barrier at the 3′ end of yeast ribosomal RNA genes
inferredcites →https://doi.org/10.1016/0092-8674(89)90584-9openalex-snapshot
Elevated recombination rates in transcriptionally active DNA
inferredcites →https://doi.org/10.1016/0092-8674(94)90179-1openalex-snapshot
The saccharomyces PIF1 DNA helicase inhibits telomere elongation and de novo telomere formation
inferredcites →https://doi.org/10.1016/0092-8674(95)90074-8openalex-snapshot
Trinucleotide repeats that expand in human disease form hairpin structures in vitro
inferredcites →https://doi.org/10.1016/0921-8777(94)90057-4openalex-snapshot
Strand bias in mutation involving 5-methylcytosine deamination in the human hprt gene
inferredcites →https://doi.org/10.1016/j.ceb.2005.03.001openalex-snapshot
Cotranscriptional mRNP assembly: from the DNA to the nuclear pore
inferredcites →https://doi.org/10.1016/j.cell.2004.08.006openalex-snapshot
AID Is Required for c-myc/IgH Chromosome Translocations In Vivo
inferredcites →https://doi.org/10.1016/j.cell.2004.12.039openalex-snapshot
Chromosomal Translocations in Yeast Induced by Low Levels of DNA Polymerase
inferredcites →https://doi.org/10.1016/j.cell.2005.03.022openalex-snapshot
Gross Chromosomal Rearrangements and Elevated Recombination at an Inducible Site-Specific Replication Fork Barrier
inferredcites →https://doi.org/10.1016/j.cell.2005.06.008openalex-snapshot
Inactivation of the SR Protein Splicing Factor ASF/SF2 Results in Genomic Instability
inferredcites →https://doi.org/10.1016/j.dnarep.2007.02.023openalex-snapshot
Transcription-associated mutagenesis in yeast is directly proportional to the level of gene expression and influenced by the direction of DNA replication
inferredcites →https://doi.org/10.1016/j.gde.2004.02.007openalex-snapshot
Chromosome segregation and genomic stability
inferredcites →https://doi.org/10.1016/j.molcel.2003.08.010openalex-snapshot
Cotranscriptionally Formed DNA:RNA Hybrids Mediate Transcription Elongation Impairment and Transcription-Associated Recombination
inferredcites →https://doi.org/10.1016/j.molcel.2004.06.034openalex-snapshot
Expanded CAG Repeats Activate the DNA Damage Checkpoint Pathway
inferredcites →https://doi.org/10.1016/j.molcel.2004.11.026openalex-snapshot
Postreplicative Recruitment of Cohesin to Double-Strand Breaks Is Required for DNA Repair
inferredcites →https://doi.org/10.1016/j.molcel.2004.11.027openalex-snapshot
DNA Damage Response Pathway Uses Histone Modification to Assemble a Double-Strand Break-Specific Cohesin Domain
inferredcites →https://doi.org/10.1016/j.molcel.2005.05.001openalex-snapshot
Interdependence between Transcription and mRNP Processing and Export, and Its Impact on Genetic Stability
inferredcites →https://doi.org/10.1016/j.molcel.2005.06.004openalex-snapshot
RNA Polymerase Modulators and DNA Repair Activities Resolve Conflicts between DNA Replication and Transcription
inferredcites →https://doi.org/10.1016/j.molcel.2005.11.015openalex-snapshot
Multiple Mechanisms Control Chromosome Integrity after Replication Fork Uncoupling and Restart at Irreparable UV Lesions
inferredcites →https://doi.org/10.1016/j.molcel.2007.06.012openalex-snapshot
An AT-Rich Sequence in Human Common Fragile Site FRA16D Causes Fork Stalling and Chromosome Breakage in S. cerevisiae
inferredcites →https://doi.org/10.1016/j.tig.2005.02.013openalex-snapshot
The contested role of uracil DNA glycosylase in immunoglobulin gene diversification
inferredcites →https://doi.org/10.1016/s0021-9258(17)31881-1openalex-snapshot
Transcription induces the formation of a stable RNA.DNA hybrid in the immunoglobulin alpha switch region.
inferredcites →https://doi.org/10.1016/s0065-2776(06)94003-6openalex-snapshot
The Role of Activation‐Induced Deaminase in Antibody Diversification and Chromosome Translocations
inferredcites →https://doi.org/10.1016/s0092-8674(00)80621-2openalex-snapshot
Modulation of RNA Polymerase by (p)ppGpp Reveals a RecG-Dependent Mechanism for Replication Fork Progression
inferredcites →https://doi.org/10.1016/s0092-8674(00)80683-2openalex-snapshot
The Saccharomyces Pif1p DNA Helicase and the Highly Related Rrm3p Have Opposite Effects on Replication Fork Progression in Ribosomal DNA
inferredcites →https://doi.org/10.1016/s0092-8674(00)81772-9openalex-snapshot
RuvAB Acts at Arrested Replication Forks
inferredcites →https://doi.org/10.1016/s0092-8674(00)81846-2openalex-snapshot
A Novel Mutation Avoidance Mechanism Dependent on S. cerevisiae RAD27 Is Distinct from DNA Mismatch Repair
inferredcites →https://doi.org/10.1016/s0092-8674(01)00227-6openalex-snapshot
Suppression of Spontaneous Chromosomal Rearrangements by S Phase Checkpoint Functions in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/s0092-8674(02)00614-1openalex-snapshot
The Mre11 Complex Is Required for Repair of Hairpin-Capped Double-Strand Breaks and Prevention of Chromosome Rearrangements
inferredcites →https://doi.org/10.1016/s0092-8674(02)01113-3openalex-snapshot
ATR Regulates Fragile Site Stability
inferredcites →https://doi.org/10.1016/s1097-2765(00)80109-4openalex-snapshot
Chromosomal Rearrangements Occur in S. cerevisiae rfa1 Mutator Mutants Due to Mutagenic Lesions Processed by Double-Strand-Break Repair
inferredcites →https://doi.org/10.1016/s1097-2765(00)80236-1openalex-snapshot
Inhibition of FEN-1 Processing by DNA Secondary Structure at Trinucleotide Repeats
inferredcites →https://doi.org/10.1016/s1097-2765(02)00513-0openalex-snapshot
The Yeast CDK Inhibitor Sic1 Prevents Genomic Instability by Promoting Replication Origin Licensing in Late G1
inferredcites →https://doi.org/10.1016/s1097-2765(02)00679-2openalex-snapshot
Error-free Recombinational Repair Predominates over Mutagenic Translesion Replication in E. coli
inferredcites →https://doi.org/10.1016/s1097-2765(03)00456-8openalex-snapshot
The Saccharomyces cerevisiae Helicase Rrm3p Facilitates Replication Past Nonhistone Protein-DNA Complexes
inferredcites →https://doi.org/10.1021/bi00039a041openalex-snapshot
The Trinucleotide Repeat Sequence d(CGG)15 Forms a Heat-Stable Hairpin Containing Gsyn.cntdot.Ganti Base Pairs
inferredcites →https://doi.org/10.1021/bi00462a015openalex-snapshot
A sensitive genetic assay for the detection of cytosine deamination: determination of rate constants and the activation energy
inferredcites →https://doi.org/10.1038/12687openalex-snapshot
Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants
inferredcites →https://doi.org/10.1038/14281openalex-snapshot
Microarray ratio analysis under noisy background
inferredcites →https://doi.org/10.1038/289144a0openalex-snapshot
Intrachromosomal gene conversion in yeast
inferredcites →https://doi.org/10.1038/292306a0openalex-snapshot
Gene conversion between duplicated genetic elements in yeast
inferredcites →https://doi.org/10.1038/35082608openalex-snapshot
Multiple pathways cooperate in the suppression of genome instability in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/35087607openalex-snapshot
Regulation of DNA replication fork progression through damaged DNA by the Mec1/Rad53 checkpoint
inferredcites →https://doi.org/10.1038/35087613openalex-snapshot
The DNA replication checkpoint response stabilizes stalled replication forks
inferredcites →https://doi.org/10.1038/362709a0openalex-snapshot
Instability and decay of the primary structure of DNA
inferredcites →https://doi.org/10.1038/414660aopenalex-snapshot
AID is required to initiate Nbs1/γ-H2AX focus formation and mutations at sites of class switching
inferredcites →https://doi.org/10.1038/70598openalex-snapshot
Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice
inferredcites →https://doi.org/10.1038/nature01574openalex-snapshot
Transcription-targeted DNA deamination by the AID antibody diversification enzyme
inferredcites →https://doi.org/10.1038/nature01900openalex-snapshot
S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex
inferredcites →https://doi.org/10.1038/nature02821openalex-snapshot
Replication protein A interacts with AID to promote deamination of somatic hypermutation targets
inferredcites →https://doi.org/10.1038/nature03485openalex-snapshot
Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions
inferredcites →https://doi.org/10.1038/nature04329openalex-snapshot
Replication fork reactivation downstream of a blocked nascent leading strand
inferredcites →https://doi.org/10.1038/nature04495openalex-snapshot
Role of genomic instability and p53 in AID-induced c-myc–Igh translocations
inferredcites →https://doi.org/10.1038/nature05977openalex-snapshot
Expandable DNA repeats and human disease
inferredcites →https://doi.org/10.1038/nature06020openalex-snapshot
IgH class switching and translocations use a robust non-classical end-joining pathway
inferredcites →https://doi.org/10.1038/ncb1466openalex-snapshot
Smc5–Smc6 mediate DNA double-strand-break repair by promoting sister-chromatid recombination
inferredcites →https://doi.org/10.1038/ng0695-213openalex-snapshot
Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli
inferredcites →https://doi.org/10.1038/ng1103openalex-snapshot
Transcription-associated mutational asymmetry in mammalian evolution
inferredcites →https://doi.org/10.1038/ng1197-298openalex-snapshot
Trinucleotide repeats affect DNA replication in vivo
inferredcites →https://doi.org/10.1038/ng1587openalex-snapshot
Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice
inferredcites →https://doi.org/10.1038/ng1936openalex-snapshot
A viable allele of Mcm4 causes chromosome instability and mammary adenocarcinomas in mice
inferredcites →https://doi.org/10.1038/ni1498openalex-snapshot
Antigen receptor diversification and chromosome translocations
inferredcites →https://doi.org/10.1038/ni919openalex-snapshot
R-loops at immunoglobulin class switch regions in the chromosomes of stimulated B cells
inferredcites →https://doi.org/10.1038/nrg2111openalex-snapshot
RNA regulons: coordination of post-transcriptional events
inferredcites →https://doi.org/10.1038/nrm2058openalex-snapshot
Replisome assembly and the direct restart of stalled replication forks
inferredcites →https://doi.org/10.1038/sj.emboj.7600602openalex-snapshot
Impairment of replication fork progression mediates RNA polII transcription‐associated recombination
inferredcites →https://doi.org/10.1038/sj.emboj.7601045openalex-snapshot
ATM and ATR promote Mre11 dependent restart of collapsed replication forks and prevent accumulation of DNA breaks
inferredcites →https://doi.org/10.1038/sj.emboj.7601251openalex-snapshot
Genome‐wide replication profiles of S‐phase checkpoint mutants reveal fragile sites in yeast
inferredcites →https://doi.org/10.1038/sj.emboj.7601766openalex-snapshot
Replication blocking lesions present a unique substrate for homologous recombination
inferredcites →https://doi.org/10.1038/sj.embor.7400128openalex-snapshot
The absence of the yeast chromatin assembly factor Asf1 increases genomic instability and sister chromatid exchange
inferredcites →https://doi.org/10.1038/sj.embor.7400774openalex-snapshot
Double‐strand breaks arising by replication through a nick are repaired by cohesin‐dependent sister‐chromatid exchange
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.6071957.xopenalex-snapshot
Repair by recombination of DNA containing a palindromic sequence
inferredcites →https://doi.org/10.1073/pnas.0608566103openalex-snapshot
Suppression of spontaneous genome rearrangements in yeast DNA helicase mutants
inferredcites →https://doi.org/10.1073/pnas.062702199openalex-snapshot
Suppression of genome instability by redundant S-phase checkpoint pathways in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.0702836104openalex-snapshot
Activation-induced cytidine deaminase action is strongly stimulated by mutations of the THO complex
inferredcites →https://doi.org/10.1073/pnas.0730835100openalex-snapshot
Activation-induced cytidine deaminase deaminates deoxycytidine on single-stranded DNA but requires the action of RNase
inferredcites →https://doi.org/10.1073/pnas.091095898openalex-snapshot
Sequence conservation at human and mouse orthologous common fragile regions, FRA3B / FHIT and Fra14A2 / Fhit
inferredcites →https://doi.org/10.1073/pnas.1232239100openalex-snapshot
Saccharomyces cerevisiae chromatin-assembly factors that act during DNA replication function in the maintenance of genome stability
inferredcites →https://doi.org/10.1073/pnas.1934561100openalex-snapshot
Genetic regulation of telomere-telomere fusions in the yeast Saccharomyces cerevisae
inferredcites →https://doi.org/10.1073/pnas.252652399openalex-snapshot
Alternate pathways involving Sgs1/Top3, Mus81/ Mms4, and Srs2 prevent formation of toxic recombination intermediates from single-stranded gaps created by DNA replication
inferredcites →https://doi.org/10.1073/pnas.76.9.4571openalex-snapshot
Transcription promotes recA-independent recombination mediated by DNA-dependent RNA polymerase in Escherichia coli.
inferredcites →https://doi.org/10.1073/pnas.92.8.3526openalex-snapshot
Overexpression of RNase H partially complements the growth defect of an Escherichia coli delta topA mutant: R-loop formation is a major problem in the absence of DNA topoisomerase I.
inferredcites →https://doi.org/10.1073/pnas.93.24.13919openalex-snapshot
Transcription-induced mutations: Increase in C to T mutations in the nontranscribed strand during transcription in Escherichia coli
inferredcites →https://doi.org/10.1073/pnas.96.4.1504openalex-snapshot
Triplet repeats form secondary structures that escape DNA repair in yeast
inferredcites →https://doi.org/10.1074/jbc.271.6.2875openalex-snapshot
Molecular Basis of Genetic Instability of Triplet Repeats
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/10.1074/jbc.274.23.16659openalex-snapshot
Escherichia coli DNA Topoisomerase I Inhibits R-loop Formation by Relaxing Transcription-induced Negative Supercoiling
inferredcites →https://doi.org/10.1074/jbc.c100466200openalex-snapshot
ATM Phosphorylates Histone H2AX in Response to DNA Double-strand Breaks
inferredcites →https://doi.org/10.1074/jbc.m302900200openalex-snapshot
Nab2p and the Thp1p-Sac3p Complex Functionally Interact at the Interface between Transcription and mRNA Metabolism
inferredcites →https://doi.org/10.1084/jem.187.12.2081openalex-snapshot
Ku70 Is Required for Late B Cell Development and Immunoglobulin Heavy Chain Class Switching
inferredcites →https://doi.org/10.1084/jem.20061067openalex-snapshot
The in vivo pattern of AID targeting to immunoglobulin switch regions deduced from mutation spectra in msh2 −/− ung −/− mice
inferredcites →https://doi.org/10.1093/emboj/16.10.2826openalex-snapshot
Recombination between DNA repeats in yeast hpr1Δ cells is linked to transcription elongation
inferredcites →https://doi.org/10.1093/emboj/17.17.5095openalex-snapshot
Transcription through a simple DNA repeat blocks replication elongation
inferredcites →https://doi.org/10.1093/emboj/17.8.2404openalex-snapshot
Ku80 is required for immunoglobulin isotype switching
inferredcites →https://doi.org/10.1093/emboj/19.10.2381openalex-snapshot
Recombination‐induced CAG trinucleotide repeat expansions in yeast involve the MRE11–RAD50–XRS2 complex
inferredcites →https://doi.org/10.1093/emboj/21.3.195openalex-snapshot
The connection between transcription and genomic instability
inferredcites →https://doi.org/10.1093/genetics/110.3.381openalex-snapshot
ALTERED FIDELITY OF MITOTIC CHROMOSOME TRANSMISSION IN CELL CYCLE MUTANTS OF S. CEREVISIAE
inferredcites →https://doi.org/10.1093/genetics/119.4.779openalex-snapshot
Genetic control of intrachromosomal recombination in Saccharomyces cerevisiae. I. Isolation and genetic characterization of hyper-recombination mutations.
inferredcites →https://doi.org/10.1093/genetics/143.2.713openalex-snapshot
Destabilization of Simple Repetitive DNA Sequences by Transcription in Yeast
inferredcites →https://doi.org/10.1093/genetics/152.3.953openalex-snapshot
The Effect of DNA Replication Mutations on CAG Tract Stability in Yeast
inferredcites →https://doi.org/10.1093/genetics/165.2.457openalex-snapshot
Recombinogenic Effects of DNA-Damaging Agents Are Synergistically Increased by Transcription in Saccharomyces cerevisiae: New Insights Into Transcription-Associated Recombination
inferredcites →https://doi.org/10.1093/nar/23.24.5006openalex-snapshot
RNA: DNA complex formation upon transcription of immunoglobulin switch regions: implications for the mechanism and regualtion of class switch recombination
inferredcites →https://doi.org/10.1093/nar/gkm589openalex-snapshot
A persistent RNA{middle dot}DNA hybrid formed by transcription of the Friedreich ataxia triplet repeat in live bacteria, and by T7 RNAP in vitro
inferredcites →https://doi.org/10.1101/gad.1085403openalex-snapshot
Transcription-dependent recombination and the role of fork collision in yeast rDNA
inferredcites →https://doi.org/10.1101/gad.1200804openalex-snapshot
Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA
inferredcites →https://doi.org/10.1101/gad.1305005openalex-snapshot
Histone deposition protein Asf1 maintains DNA replisome integrity and interacts with replication factor C
inferredcites →https://doi.org/10.1101/gad.1392506openalex-snapshot
Cycles of chromosome instability are associated with a fragile site and are increased by defects in DNA replication and checkpoint controls in yeast
inferredcites →https://doi.org/10.1101/gad.1478906openalex-snapshot
The S. cerevisiae Rrm3p DNA helicase moves with the replication fork and affects replication of all yeast chromosomes
inferredcites →https://doi.org/10.1101/gad.322605openalex-snapshot
Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase
inferredcites →https://doi.org/10.1101/gad.337205openalex-snapshot
Molecular anatomy and regulation of a stable replisome at a paused eukaryotic DNA replication fork
inferredcites →https://doi.org/10.1101/gad.340905openalex-snapshot
Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability
inferredcites →https://doi.org/10.1101/gad.361805openalex-snapshot
Replisome instability, fork collapse, and gross chromosomal rearrangements arise synergistically from Mec1 kinase and RecQ helicase mutations
inferredcites →https://doi.org/10.1101/gad.417607openalex-snapshot
Replication fork stalling and cell cycle arrest in UV-irradiated Escherichia coli
inferredcites →https://doi.org/10.1126/science.1071398openalex-snapshot
ATR Homolog Mec1 Promotes Fork Progression, Thus Averting Breaks in Replication Slow Zones
inferredcites →https://doi.org/10.1126/science.1074023openalex-snapshot
Fork Reversal and ssDNA Accumulation at Stalled Replication Forks Owing to Checkpoint Defects
inferredcites →https://doi.org/10.1126/science.1083964openalex-snapshot
Uncoupling of Leading- and Lagging-Strand DNA Replication During Lesion Bypass in Vivo
inferredcites →https://doi.org/10.1126/science.1087706openalex-snapshot
An Age-Induced Switch to a Hyper-Recombinational State
inferredcites →https://doi.org/10.1126/science.1092481openalex-snapshot
Transcription-Coupled Events Associating with Immunoglobulin Switch Region Chromatin
inferredcites →https://doi.org/10.1126/science.1116102openalex-snapshot
Recombination Regulation by Transcription-Induced Cohesin Dissociation in rDNA Repeats
inferredcites →https://doi.org/10.1126/science.1455232openalex-snapshot
Consequences of Replication Fork Movement Through Transcription Units in Vivo
inferredcites →https://doi.org/10.1126/science.272.5264.1030openalex-snapshot
DNA Replication Fork Pause Sites Dependent on Transcription
inferredcites →https://doi.org/10.1126/science.279.5352.853openalex-snapshot
Expansion and Length-Dependent Fragility of CTG Repeats in Yeast
inferredcites →https://doi.org/10.1126/science.6239375openalex-snapshot
Constitutive Fragile Sites and Cancer
inferredcites →https://doi.org/10.1126/science.7777859openalex-snapshot
Association of Increased Spontaneous Mutation Rates with High Levels of Transcription in Yeast
inferredcites →https://doi.org/10.1126/science.877551openalex-snapshot
Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture Medium
inferredcites →https://doi.org/10.1128/jb.106.2.543-550.1971openalex-snapshot
Effect of Gene Induction on the Rate of Mutagenesis by ICR-191 in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.134.3.958-966.1978openalex-snapshot
Recombinant levels of Escherichia coli K-12 mutants deficient in various replication, recombination, or repair genes
inferredcites →https://doi.org/10.1128/mcb.02375-05openalex-snapshot
The Transcription Elongation Complex Directs Activation-Induced Cytidine Deaminase-Mediated DNA Deamination
inferredcites →https://doi.org/10.1128/mcb.10.9.4837openalex-snapshot
Transcription Stimulates Homologous Recombination in Mammalian Cells
inferredcites →https://doi.org/10.1128/mcb.11.1.289openalex-snapshot
The strong ADH1 promoter stimulates mitotic and meiotic recombination at the ADE6 gene of Schizosaccharomyces pombe.
inferredcites →https://doi.org/10.1128/mcb.14.12.8391openalex-snapshot
The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase.
inferredcites →https://doi.org/10.1128/mcb.16.12.6617openalex-snapshot
Orientation Dependence of Trinucleotide CAG Repeat Instability in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1128/mcb.17.4.2090openalex-snapshot
Stability of a CTG/CAG Trinucleotide Repeat in Yeast Is Dependent on Its Orientation in the Genome
inferredcites →https://doi.org/10.1128/mcb.21.16.5459-5470.2001openalex-snapshot
High-Copy-Number Expression of Sub2p, a Member of the RNA Helicase Superfamily, Suppresses hpr1-Mediated Genomic Instability
inferredcites →https://doi.org/10.1128/mcb.23.21.7849-7860.2003openalex-snapshot
Mutations in Yeast Replication Proteins That Increase CAG/CTG Expansions Also Increase Repeat Fragility
inferredcites →https://doi.org/10.1128/mcb.23.4.1349-1357.2003openalex-snapshot
Replication and Expansion of Trinucleotide Repeats in Yeast
inferredcites →https://doi.org/10.1128/mcb.24.6.2286-2295.2004openalex-snapshot
Replication Stalling at Friedreich's Ataxia (GAA)n Repeats In Vivo
inferredcites →https://doi.org/10.1128/mcb.25.3.888-895.2005openalex-snapshot
Mechanisms of Transcription-Replication Collisions in Bacteria
inferredcites →https://doi.org/10.1128/mcb.26.8.3327-3334.2006openalex-snapshot
Replication Fork Progression Is Impaired by Transcription in Hyperrecombinant Yeast Cells Lacking a Functional THO Complex
inferredcites →https://doi.org/10.1146/annurev.biochem.76.061705.090740openalex-snapshot
Molecular Mechanisms of Antibody Somatic Hypermutation
inferredcites →https://doi.org/10.1146/annurev.genet.39.073003.110544openalex-snapshot
Immunoglobulin Gene Diversification
inferredcites →https://doi.org/10.1146/annurev.genet.40.110405.090428openalex-snapshot
Cellular Responses to DNA Damage: One Signal, Multiple Choices
inferredcites →https://doi.org/10.1146/annurev.genet.41.042007.165900openalex-snapshot
Chromosome Fragile Sites
inferredcites →https://doi.org/10.1158/0008-5472.can-06-2419openalex-snapshot
G-Rich Proto-Oncogenes Are Targeted for Genomic Instability in B-Cell Lymphomas
inferredcites →https://doi.org/10.4049/jimmunol.179.9.6064openalex-snapshot
Activation-Induced Cytidine Deaminase-Dependent DNA Breaks in Class Switch Recombination Occur during G1 Phase of the Cell Cycle and Depend upon Mismatch Repair
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.4164236openalex-extracted
Super-Resolution Imaging Reveals T Lymphocyte Activation-Induced Chromatin Decondensation and Disruption of Nuclear Envelope Facilitate the Release of Nuclear DNA
inferred← citeshttps://doi.org/10.1002/1873-3468.70444openalex-snapshot
Synergistic perspectives—How single‐molecule biophysics complement biochemical understanding
inferred← citeshttps://doi.org/10.1002/1878-0261.12467openalex-snapshot
Exploiting DNA repair defects in colorectal cancer
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200300097.pub2openalex-snapshot
The Cell Nucleus: Biogenesis, Structure, and Function
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001041.pub2openalex-snapshot
DNA Replication: Mammalian
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001041.pub3openalex-snapshot
DNA Replication: Mammalian
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021478openalex-snapshot
DNA Strand Break Repair and Human Genetic Disease
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021478.pub2openalex-snapshot
DNA Strand Break Repair and Human Genetic Disease
inferred← citeshttps://doi.org/10.1002/9780470015902.a0023889openalex-snapshot
Somatic Genome Variations
inferred← citeshttps://doi.org/10.1002/9781118399668.ch13openalex-snapshot
Epithelial Tumours of the Stomach
inferred← citeshttps://doi.org/10.1002/ajmg.a.33346openalex-snapshot
Introductory comments on special section—Genomic microduplications: When adding may equal subtracting
inferred← citeshttps://doi.org/10.1002/ajmg.c.31492openalex-snapshot
Genome stability: What we have learned from cohesinopathies
inferred← citeshttps://doi.org/10.1002/em.21691openalex-snapshot
Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors
inferred← citeshttps://doi.org/10.1002/em.21740openalex-snapshot
High levels of transcription stimulate transversions at GC base pairs in yeast
inferred← citeshttps://doi.org/10.1002/etc.3741openalex-snapshot
Returning to normal? Assessing transcriptome recovery over time in male rainbow darter (Etheostoma caeruleum) liver in response to wastewater-treatment plant upgrades
inferred← citeshttps://doi.org/10.1002/gcc.20847openalex-snapshot
Chromosome‐specific segmentation revealed by structural analysis of individually isolated chromosomes
inferred← citeshttps://doi.org/10.1002/gcc.21956openalex-snapshot
Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data
inferred← citeshttps://doi.org/10.1002/ijc.27846openalex-snapshot
Chromosome stability in tonsillar squamous cell carcinoma is associated with HPV16 integration and indicates a favorable prognosis
inferred← citeshttps://doi.org/10.1002/ijc.32900openalex-snapshot
Cdc6 as a novel target in cancer: Oncogenic potential, senescence and subcellular localisation
inferred← citeshttps://doi.org/10.1002/iub.1276openalex-snapshot
DNA polymerase ε and its roles in genome stability
inferred← citeshttps://doi.org/10.1002/jbt.70332openalex-snapshot
Investigating the Genotoxic Potential of Pioglitazone in Hyperglycemic Conditions Using Chromosome Aberration and GADD45α Markers in TK6 Cells
inferred← citeshttps://doi.org/10.1002/jcb.21937openalex-snapshot
Chromosome instability and tumor lethality suppression in carcinogenesis
inferred← citeshttps://doi.org/10.1002/jcb.30074openalex-snapshot
R‐loops mediate transcription‐associated formation of human rDNA secondary constrictions
inferred← citeshttps://doi.org/10.1002/jcp.25792openalex-snapshot
Knockdown of REV3 synergizes with ATR inhibition to promote apoptosis induced by cisplatin in lung cancer cells
inferred← citeshttps://doi.org/10.1002/mc.20513openalex-snapshot
Transcriptional processing of G4 DNA
inferred← citeshttps://doi.org/10.1002/mco2.70369openalex-snapshot
Epigenetic Regulation of Aging and its Rejuvenation
inferred← citeshttps://doi.org/10.1002/pd.2215openalex-snapshot
De novo balanced chromosome rearrangements in prenatal diagnosis
inferred← citeshttps://doi.org/10.1002/pmic.201900184openalex-snapshot
Proteomic Analysis of DNA Synthesis on a Structured DNA Template in Human Cellular Extracts: Interplay Between NHEJ and Replication‐Associated Proteins
inferred← citeshttps://doi.org/10.1002/tpg2.20367openalex-snapshot
A review of plant epigenetics through the lens of almond
inferred← citeshttps://doi.org/10.1007/978-1-4614-4741-2_8openalex-snapshot
Poly(ADP) Ribose Polymerase at the Interface of DNA Damage Signaling and DNA Repair
inferred← citeshttps://doi.org/10.1007/978-1-4614-5037-5_5openalex-snapshot
Helicases at the Replication Fork
inferred← citeshttps://doi.org/10.1007/978-1-4939-0620-8_3openalex-snapshot
Hypoxia in Tumors: Pathogenesis-Related Classification, Characterization of Hypoxia Subtypes, and Associated Biological and Clinical Implications
inferred← citeshttps://doi.org/10.1007/978-1-4939-6545-8_10openalex-snapshot
Methods to Study the Atypical Roles of DNA Repair and SMC Proteins in Gene Silencing
inferred← citeshttps://doi.org/10.1007/978-1-61779-585-5_7openalex-snapshot
The Origin and Evolution of New Genes
inferred← citeshttps://doi.org/10.1007/978-3-030-00683-9_3openalex-snapshot
How Do Yeast and Other Fungi Recognize and Respond to Genome Perturbations?
inferred← citeshttps://doi.org/10.1007/978-3-030-04861-7_4openalex-snapshot
Pathological Diagnosis and Classification of Gastric Epithelial Tumours
inferred← citeshttps://doi.org/10.1007/978-3-030-21855-3_32openalex-snapshot
Photosensitivity, Pigmentary Changes, and Short Stature
inferred← citeshttps://doi.org/10.1007/978-3-030-30302-0_5openalex-snapshot
Epigenetic Regulation in Almond
inferred← citeshttps://doi.org/10.1007/978-3-319-14151-0_14openalex-snapshot
Targeting Tumour Hypoxia with PARP Inhibitors: Contextual Synthetic Lethality
inferred← citeshttps://doi.org/10.1007/978-3-319-70142-4_7openalex-snapshot
Future Paradigm of Breast Cancer Resistance and Treatment
inferred← citeshttps://doi.org/10.1007/978-3-662-49118-8_13openalex-snapshot
Applications of Single Cell Sequencing in Cancer
inferred← citeshttps://doi.org/10.1007/978-981-15-1067-0_6openalex-snapshot
Genomic Instability and Cancer Metastasis
inferred← citeshttps://doi.org/10.1007/978-981-15-4494-1_15openalex-snapshot
Single Cell Sequencing in Cancer Diagnostics
inferred← citeshttps://doi.org/10.1007/978-981-95-0457-2_2openalex-snapshot
Understanding Cancer Biology and Microenvironment
inferred← citeshttps://doi.org/10.1007/978-981-97-1658-6_21openalex-snapshot
Application of Micronucleus Test in African Toad as Biomarker of Genotoxic and Cytotoxic Assessment of Contaminants in the African Environment
inferred← citeshttps://doi.org/10.1007/s00011-025-02077-6openalex-snapshot
Prominent fibroblast growth factor 21 with less abundant tumor-associated macrophages in hepatic mass of the conditional mgmt-deleted mice using LysM-Cre system
inferred← citeshttps://doi.org/10.1007/s00018-009-0013-7openalex-snapshot
The multifaceted role of periostin in tumorigenesis
inferred← citeshttps://doi.org/10.1007/s00018-010-0337-3openalex-snapshot
Roles of human INO80 chromatin remodeling enzyme in DNA replication and chromosome segregation suppress genome instability
inferred← citeshttps://doi.org/10.1007/s00018-011-0910-4openalex-snapshot
Chromosome instability and deregulated proliferation: an unavoidable duo
inferred← citeshttps://doi.org/10.1007/s00018-014-1722-0openalex-snapshot
The FHIT gene product: tumor suppressor and genome “caretaker”
inferred← citeshttps://doi.org/10.1007/s00018-018-2900-2openalex-snapshot
Impact of DNA repair and stability defects on cortical development
inferred← citeshttps://doi.org/10.1007/s00066-012-0085-4openalex-snapshot
Acute versus chronic hypoxia in tumors
inferred← citeshttps://doi.org/10.1007/s00239-022-10088-8openalex-snapshot
Loss of Heterozygosity and Its Importance in Evolution
inferred← citeshttps://doi.org/10.1007/s00253-023-12865-xopenalex-snapshot
CRISPR/Cas9 system is a suitable gene targeting editing tool to filamentous fungus Monascus pilosus
inferred← citeshttps://doi.org/10.1007/s00280-009-0986-9openalex-snapshot
Thymidylate synthetase allelic imbalance in clear cell renal carcinoma
inferred← citeshttps://doi.org/10.1007/s00299-010-0946-1openalex-snapshot
Analysis of target sequences of DDM1s in Brassica rapa by MSAP
inferred← citeshttps://doi.org/10.1007/s00335-024-10082-zopenalex-snapshot
Investigating DNA damage caused by COVID-19 and influenza in post COVID-19
inferred← citeshttps://doi.org/10.1007/s00412-013-0398-9openalex-snapshot
Impediments to replication fork movement: stabilisation, reactivation and genome instability
inferred← citeshttps://doi.org/10.1007/s00412-013-0431-zopenalex-snapshot
Resolving branched DNA intermediates with structure-specific nucleases during replication in eukaryotes
inferred← citeshttps://doi.org/10.1007/s00412-018-00687-0openalex-snapshot
A new role for Drosophila Aurora-A in maintaining chromosome integrity
inferred← citeshttps://doi.org/10.1007/s10142-008-0099-2openalex-snapshot
Structure–function analysis of the barley genome: the gene-rich region of chromosome 2HL
inferred← citeshttps://doi.org/10.1007/s10142-016-0490-3openalex-snapshot
Genetic and physical mapping of the earliness per se locus Eps-A m 1 in Triticum monococcum identifies EARLY FLOWERING 3 (ELF3) as a candidate gene
inferred← citeshttps://doi.org/10.1007/s10327-010-0271-0openalex-snapshot
EGFP-Rhm51 foci enable the visualization and enumeration of DNA double-strand breaks in Magnaporthe oryzae
inferred← citeshttps://doi.org/10.1007/s10495-012-0711-8openalex-snapshot
Selective cell death of p53-insufficient cancer cells is induced by knockdown of the mRNA export molecule GANP
inferred← citeshttps://doi.org/10.1007/s10555-013-9427-7openalex-snapshot
Chromosomal instability (CIN): what it is and why it is crucial to cancer evolution
inferred← citeshttps://doi.org/10.1007/s10577-018-9594-zopenalex-snapshot
Keeping ribosomal DNA intact: a repeating challenge
inferred← citeshttps://doi.org/10.1007/s10682-022-10195-4openalex-snapshot
Multivariate selection and the making and breaking of mutational pleiotropy
inferred← citeshttps://doi.org/10.1007/s10689-011-9489-zopenalex-snapshot
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
inferred← citeshttps://doi.org/10.1007/s11154-022-09777-yopenalex-snapshot
The hallmarks of cancer… in pituitary tumors?
inferred← citeshttps://doi.org/10.1007/s11390-010-9300-xopenalex-snapshot
New Generations: Sequencing Machines and Their Computational Challenges
inferred← citeshttps://doi.org/10.1007/s11515-011-1122-xopenalex-snapshot
The spindle assembly checkpoint: perspectives in tumorigenesis and cancer therapy
inferred← citeshttps://doi.org/10.1007/s12539-013-0153-1openalex-snapshot
Structural, functional and molecular docking study to characterize GMI1 from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s13353-025-01001-2openalex-snapshot
Ataxia and oculomotor apraxia caused by a large-scale deletion in the senataxin gene
inferred← citeshttps://doi.org/10.1007/s42764-020-00027-6openalex-snapshot
Locked in a vicious cycle: the connection between genomic instability and a loss of protein homeostasis
inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.22715-7openalex-snapshot
Long Noncoding RNAs and Human Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-394279-1.00009-0openalex-snapshot
Recombination in the Stability, Repair and Evolution of the Mitochondrial Genome
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/b978-0-12-823579-9.00009-6openalex-snapshot
Chromoanagenesis phenomena and their formation mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-323-85679-9.00020-9openalex-snapshot
Homologous recombination in mammalian cells: From molecular mechanisms to pathology
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/j.arr.2014.10.004openalex-snapshot
DAMPs, ageing, and cancer: The ‘DAMP Hypothesis’
inferred← citeshttps://doi.org/10.1016/j.bbadis.2019.165561openalex-snapshot
RAD6B is a major mediator of triple negative breast cancer cisplatin resistance: Regulation of translesion synthesis/Fanconi anemia crosstalk and BRCA1 independence
inferred← citeshttps://doi.org/10.1016/j.bbadis.2024.167438openalex-snapshot
Current status and prospect of the DNA double-strand break repair pathway in colorectal cancer development and treatment
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.11.012openalex-snapshot
New clues to understand the role of THO and other functionally related factors in mRNP biogenesis
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.12.001openalex-snapshot
mRNA export and the TREX complex
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2013.02.012openalex-snapshot
RNA quality control in the nucleus: The Angels' share of RNA
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2017.02.009openalex-snapshot
Iwr1 facilitates RNA polymerase II dynamics during transcription elongation
inferred← citeshttps://doi.org/10.1016/j.bbalip.2015.06.001openalex-snapshot
Disruption of the mevalonate pathway induces dNTP depletion and DNA damage
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2026.120190openalex-snapshot
Inhibition of PrimPol by mevalonate pyrophosphate: A metabolic link between genome integrity and cytokinesis?
inferred← citeshttps://doi.org/10.1016/j.bbcan.2009.04.005openalex-snapshot
Translocations in epithelial cancers
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.10.021openalex-snapshot
Global chromatin fibre compaction in response to DNA damage
inferred← citeshttps://doi.org/10.1016/j.canlet.2021.01.021openalex-snapshot
Long noncoding RNA: A resident staff of genomic instability regulation in tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.cbi.2010.09.020openalex-snapshot
N-methyl-N′-nitro-N-nitrosoguanidine induces and cooperates with 12-O-tetradecanoylphorbol-1,3-acetate/sodium butyrate to enhance Epstein-Barr virus reactivation and genome instability in nasopharyngeal carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.cbi.2019.02.010openalex-snapshot
Downregulation of c-Myc and p21 expression and induction of S phase arrest by naphthalene diimide derivative in gastric adenocarcinoma cells
inferred← citeshttps://doi.org/10.1016/j.ccr.2010.10.035openalex-snapshot
EZH2 Promotes Expansion of Breast Tumor Initiating Cells through Activation of RAF1-β-Catenin Signaling
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.10.004openalex-snapshot
The replication fork's five degrees of freedom, their failure and genome rearrangements
inferred← citeshttps://doi.org/10.1016/j.ceb.2010.06.003openalex-snapshot
Dr Jekyll and Mr Hyde: role of aneuploidy in cellular adaptation and cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2008.06.035openalex-snapshot
Acetylated Lysine 56 on Histone H3 Drives Chromatin Assembly after Repair and Signals for the Completion of Repair
inferred← citeshttps://doi.org/10.1016/j.cell.2009.06.022openalex-snapshot
Genome-Organizing Factors Top2 and Hmo1 Prevent Chromosome Fragility at Sites of S phase Transcription
inferred← citeshttps://doi.org/10.1016/j.cell.2009.11.030openalex-snapshot
Nuclear Receptor-Induced Chromosomal Proximity and DNA Breaks Underlie Specific Translocations in Cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2010.03.036openalex-snapshot
The Transcription Factor DksA Prevents Conflicts between DNA Replication and Transcription Machinery
inferred← citeshttps://doi.org/10.1016/j.cell.2014.03.048openalex-snapshot
RECQL5 Controls Transcript Elongation and Suppresses Genome Instability Associated with Transcription Stress
inferred← citeshttps://doi.org/10.1016/j.cell.2017.06.006openalex-snapshot
Telomere Length Determines TERRA and R-Loop Regulation through the Cell Cycle
inferred← citeshttps://doi.org/10.1016/j.cell.2024.09.020openalex-snapshot
Genome integrity sensing by the broad-spectrum Hachiman antiphage defense complex
inferred← citeshttps://doi.org/10.1016/j.cell.2026.04.020openalex-snapshot
Mesenchymal drift: A convergent framework for the hallmarks of aging
inferred← citeshttps://doi.org/10.1016/j.cellin.2023.100112openalex-snapshot
The CHCHD2/Sirt1 corepressors involve in G9a-mediated regulation of RNase H1 expression to control R-loop
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.10.013openalex-snapshot
High-Frequency Promoter Firing Links THO Complex Function to Heavy Chromatin Formation
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.02.020openalex-snapshot
Structural Basis of SOSS1 Complex Assembly and Recognition of ssDNA
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.03.030openalex-snapshot
The RBBP6/ZBTB38/MCM10 Axis Regulates DNA Replication and Common Fragile Site Stability
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.08.076openalex-snapshot
BRCA1 Accelerates CtIP-Mediated DNA-End Resection
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.08.056openalex-snapshot
The Deubiquitylating Enzyme USP4 Cooperates with CtIP in DNA Double-Strand Break End Resection
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.10.016openalex-snapshot
PTEN Controls the DNA Replication Process through MCM2 in Response to Replicative Stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.12.093openalex-snapshot
Signaling from Mus81-Eme2-Dependent DNA Damage Elicited by Chk1 Deficiency Modulates Replication Fork Speed and Origin Usage
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.06.030openalex-snapshot
PCNA Retention on DNA into G2/M Phase Causes Genome Instability in Cells Lacking Elg1
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.08.058openalex-snapshot
Set2 Methyltransferase Facilitates DNA Replication and Promotes Genotoxic Stress Responses through MBF-Dependent Transcription
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.11.012openalex-snapshot
The Replisome Mediates A-NHEJ Repair of Telomeres Lacking POT1-TPP1 Independently of MRN Function
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107542openalex-snapshot
Systematic Analysis of Targets of Pumilio-Mediated mRNA Decay Reveals that PUM1 Repression by DNA Damage Activates Translesion Synthesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117051openalex-snapshot
Ski2-like helicase ASCC3 unwinds DNA upon fork stalling to control replication stress responses
inferred← citeshttps://doi.org/10.1016/j.comtox.2017.07.002openalex-snapshot
Classification of carcinogenic and mutagenic properties using machine learning method
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2008.12.002openalex-snapshot
Road to the crossroads of life and death: Linking sister chromatid cohesion and separation to aneuploidy, apoptosis and cancer
inferred← citeshttps://doi.org/10.1016/j.ctrv.2016.05.004openalex-snapshot
Can the response to a platinum-based therapy be predicted by the DNA repair status in non-small cell lung cancer?
inferred← citeshttps://doi.org/10.1016/j.dci.2010.12.009openalex-snapshot
Invertebrate immune diversity
inferred← citeshttps://doi.org/10.1016/j.diff.2018.02.002openalex-snapshot
Increased TERRA levels and RNase H sensitivity are conserved hallmarks of post-senescent survivors in budding yeast
inferred← citeshttps://doi.org/10.1016/j.dnarep.2008.06.014openalex-snapshot
Multiple pathways cooperate to facilitate DNA replication fork progression through alkylated DNA
inferred← citeshttps://doi.org/10.1016/j.dnarep.2008.12.010openalex-snapshot
Stimulation of direct-repeat recombination by RNA polymerase III transcription
inferred← citeshttps://doi.org/10.1016/j.dnarep.2009.04.023openalex-snapshot
DNA replication as a target of the DNA damage checkpoint
inferred← citeshttps://doi.org/10.1016/j.dnarep.2010.07.003openalex-snapshot
Regulation of tolerance to DNA alkylating damage by Dot1 and Rad53 in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.dnarep.2010.08.003openalex-snapshot
RecA protein assures fidelity of DNA repair and genome stability in Deinococcus radiodurans
inferred← citeshttps://doi.org/10.1016/j.dnarep.2010.12.004openalex-snapshot
DNA end resection—Unraveling the tail
inferred← citeshttps://doi.org/10.1016/j.dnarep.2011.04.013openalex-snapshot
Human DHX9 helicase preferentially unwinds RNA-containing displacement loops (R-loops) and G-quadruplexes
inferred← citeshttps://doi.org/10.1016/j.dnarep.2012.12.005openalex-snapshot
Early steps of double-strand break repair in Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.dnarep.2014.03.023openalex-snapshot
The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.11.005openalex-snapshot
RECQL5 has unique strand annealing properties relative to the other human RecQ helicase proteins
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.11.021openalex-snapshot
Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2016.05.032openalex-snapshot
Pathways controlling dNTP pools to maintain genome stability
inferred← citeshttps://doi.org/10.1016/j.dnarep.2018.04.006openalex-snapshot
Chromosome instability: From molecular mechanisms to disease
inferred← citeshttps://doi.org/10.1016/j.dnarep.2020.102902openalex-snapshot
Methylation of the central transcriptional regulator KLF4 by PRMT5 is required for DNA end resection and recombination
inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103070openalex-snapshot
GTPases, genome, actin: A hidden story in DNA damage response and repair mechanisms
inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103195openalex-snapshot
Genome maintenance during embryogenesis
inferred← citeshttps://doi.org/10.1016/j.dnarep.2024.103699openalex-snapshot
Broken strands, broken minds: Exploring the nexus of DNA damage and neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.dnarep.2024.103715openalex-snapshot
Human translesion DNA polymerases ι and κ mediate tolerance to temozolomide in MGMT-deficient glioblastoma cells.
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120525openalex-snapshot
Olaparib induces craniofacial cartilage malformations in zebrafish embryos through DNA damage, oxidative stress, and Wnt dysregulation
inferred← citeshttps://doi.org/10.1016/j.envint.2012.12.004openalex-snapshot
Role of genomic instability in arsenic-induced carcinogenicity. A review
inferred← citeshttps://doi.org/10.1016/j.exphem.2012.06.001openalex-snapshot
Epigenetic modifiers enhance the synergistic cytotoxicity of combined nucleoside analog-DNA alkylating agents in lymphoma cell lines
inferred← citeshttps://doi.org/10.1016/j.febslet.2010.07.029openalex-snapshot
The MRN complex in double‐strand break repair and telomere maintenance
inferred← citeshttps://doi.org/10.1016/j.foodchem.2014.01.047openalex-snapshot
Diversification of 13S globulins, allergenic seed storage proteins, of common buckwheat
inferred← citeshttps://doi.org/10.1016/j.gde.2013.10.010openalex-snapshot
Genetic screens in mice for genome integrity maintenance and cancer predisposition
inferred← citeshttps://doi.org/10.1016/j.gde.2017.07.014openalex-snapshot
Beyond speciation genes: an overview of genome stability in evolution and speciation
inferred← citeshttps://doi.org/10.1016/j.gde.2020.02.016openalex-snapshot
Shelterin and the replisome: at the intersection of telomere repair and replication
inferred← citeshttps://doi.org/10.1016/j.gendis.2023.101191openalex-snapshot
Guarding against digestive-system cancers: Unveiling the role of Chk2 as a potential therapeutic target
inferred← citeshttps://doi.org/10.1016/j.gene.2020.144400openalex-snapshot
Genetic variations and haplotypic diversity in the Myostatin gene of New Zealand cattle breeds
inferred← citeshttps://doi.org/10.1016/j.hoc.2019.10.003openalex-snapshot
Targeting Aberrant Splicing in Myelodysplastic Syndromes
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100968openalex-snapshot
The SUMOylated METTL8 Induces R-loop and Tumorigenesis via m3C
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115953openalex-snapshot
Universal principles of cell population growth follow from local contact inhibition
inferred← citeshttps://doi.org/10.1016/j.jare.2025.01.039openalex-snapshot
The urinary eccDNA landscape in prostate cancer reveals associations with genome instability and vital roles in cancer progression
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101036openalex-snapshot
Epithelial cell transforming factor ECT2 is an important regulator of DNA double-strand break repair and genome stability
inferred← citeshttps://doi.org/10.1016/j.jep.2018.05.016openalex-snapshot
Interrogation of ethnomedicinal plants for synthetic lethality effects in combination with deficiency in the DNA repair endonuclease RAD1 using a yeast cell-based assay
inferred← citeshttps://doi.org/10.1016/j.jip.2025.108520openalex-snapshot
Phenotypic and pathogenicity changes in Beauveria and Metarhizium isolates induced by serial subculturing and passage through different host species
inferred← citeshttps://doi.org/10.1016/j.jksus.2019.12.025openalex-snapshot
Biochemical characterization of human exonuclease1 (hExo1)
inferred← citeshttps://doi.org/10.1016/j.jmb.2013.04.023openalex-snapshot
Replication Stress-Induced Genome Instability: The Dark Side of Replication Maintenance by Homologous Recombination
inferred← citeshttps://doi.org/10.1016/j.jmb.2013.08.019openalex-snapshot
Dealing with Transcriptional Outbursts during S Phase to Protect Genomic Integrity
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169061openalex-snapshot
DDX37 and DDX50 Maintain Genome Stability by Preventing Transcription-dependent R-loop Formation
inferred← citeshttps://doi.org/10.1016/j.lungcan.2012.12.018openalex-snapshot
Aurora-B overexpression is correlated with aneuploidy and poor prognosis in non-small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.lungcan.2013.07.005openalex-snapshot
Response of CAIX and CAXII to in vitro re-oxygenation and clinical significance of the combined expression in NSCLC patients
inferred← citeshttps://doi.org/10.1016/j.mbs.2024.109343openalex-snapshot
Mechanical causes and implications of repetitive DNA motifs
inferred← citeshttps://doi.org/10.1016/j.mednuc.2009.11.003openalex-snapshot
De la cellule mammaire normale à la cellule cancéreuse
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.06.016openalex-snapshot
SR Proteins in Vertical Integration of Gene Expression from Transcription to RNA Processing to Translation
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.06.021openalex-snapshot
A Genome-wide siRNA Screen Reveals Diverse Cellular Processes and Pathways that Mediate Genome Stability
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.11.009openalex-snapshot
Rep Provides a Second Motor at the Replisome to Promote Duplication of Protein-Bound DNA
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.02.008openalex-snapshot
A Postincision-Deficient TFIIH Causes Replication Fork Breakage and Uncovers Alternative Rad51- or Pol32-Mediated Restart Mechanisms
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.07.015openalex-snapshot
Homologous Recombination Restarts Blocked Replication Forks at the Expense of Genome Rearrangements by Template Exchange
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.12.007openalex-snapshot
Yeast Sen1 Helicase Protects the Genome from Transcription-Associated Instability
inferred← citeshttps://doi.org/10.1016/j.molcel.2011.10.013openalex-snapshot
Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes
inferred← citeshttps://doi.org/10.1016/j.molcel.2011.10.017openalex-snapshot
RNase H and Multiple RNA Biogenesis Factors Cooperate to Prevent RNA:DNA Hybrids from Generating Genome Instability
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.01.017openalex-snapshot
R-Loop Formation Is a Distinctive Characteristic of Unmethylated Human CpG Island Promoters
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.04.009openalex-snapshot
R Loops: From Transcription Byproducts to Threats to Genome Stability
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.08.002openalex-snapshot
Genome-wide Screen Identifies Pathways that Govern GAA/TTC Repeat Fragility and Expansions in Dividing and Nondividing Yeast Cells
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.11.018openalex-snapshot
RETRACTED: RecA-Promoted, RecFOR-Independent Progressive Disassembly of Replisomes Stalled by Helicase Inactivation
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.08.019openalex-snapshot
TORC2 Signaling Pathway Guarantees Genome Stability in the Face of DNA Strand Breaks
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.10.034openalex-snapshot
PPL2 Translesion Polymerase Is Essential for the Completion of Chromosomal DNA Replication in the African Trypanosome
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.10.035openalex-snapshot
PrimPol Bypasses UV Photoproducts during Eukaryotic Chromosomal DNA Replication
inferred← citeshttps://doi.org/10.1016/j.molcel.2015.09.012openalex-snapshot
The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.12.030openalex-snapshot
Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.04.023openalex-snapshot
Heterochromatin-Encoded Satellite RNAs Induce Breast Cancer
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.mrfmmm.2011.07.014openalex-snapshot
Interactions between DNA damage, repair, and transcription
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.05.006openalex-snapshot
Homologous recombination in Arabidopsis seeds along the track of energetic carbon ions
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.07.003openalex-snapshot
Aberrant DNA replication in cancer
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.07.005openalex-snapshot
The DNA topoisomerase II catalytic inhibitor merbarone is genotoxic and induces endoreduplication
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2015.07.010openalex-snapshot
Micronucleus frequency in peripheral blood lymphocytes and frailty status in elderly. A lack of association with clinical features
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2010.04.009openalex-snapshot
Genotoxicity/mutagenicity of formaldehyde revealed by the Arabidopsis thaliana plants transgenic for homologous recombination substrates
inferred← citeshttps://doi.org/10.1016/j.mrrev.2014.11.005openalex-snapshot
Crosstalk between translesion synthesis, Fanconi anemia network, and homologous recombination repair pathways in interstrand DNA crosslink repair and development of chemoresistance
inferred← citeshttps://doi.org/10.1016/j.mrrev.2016.04.008openalex-snapshot
Molecular mechanisms by which in vivo exposure to exogenous chemical genotoxic agents can lead to micronucleus formation in lymphocytes in vivo and ex vivo in humans
inferred← citeshttps://doi.org/10.1016/j.mrrev.2022.108411openalex-snapshot
The potential role of COVID-19 in the induction of DNA damage
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