| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.3389/FGENE.2014.00296 |
| P8608 | Fatcat ID | release_jaxzytqq45dudiqqct3bh3qypu |
| P932 | PMC publication ID | 4155812 |
| P698 | PubMed publication ID | 25250043 |
| P5875 | ResearchGate publication ID | 266086312 |
| P50 | author | Nealia C M House | Q86572927 |
| P2093 | author name string | Melissa R Koch | |
| Catherine H Freudenreich | |||
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| RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly | Q24300428 | ||
| A YY1-INO80 complex regulates genomic stability through homologous recombination-based repair | Q24300998 | ||
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| Roles of human INO80 chromatin remodeling enzyme in DNA replication and chromosome segregation suppress genome instability | Q24303693 | ||
| WSTF regulates the H2A.X DNA damage response via a novel tyrosine kinase activity | Q24309061 | ||
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| The mINO80 chromatin remodeling complex is required for efficient telomere replication and maintenance of genome stability | Q42853694 | ||
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| Ino80 chromatin remodeling complex promotes recovery of stalled replication forks | Q46649401 | ||
| UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways | Q46713104 | ||
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| The ACF1 complex is required for DNA double-strand break repair in human cells. | Q50530840 | ||
| Histone H2A phosphorylation and H3 methylation are required for a novel Rad9 DSB repair function following checkpoint activation. | Q50731881 | ||
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| Changes in nuclear protein acetylation in u.v.-damaged human cells. | Q53535802 | ||
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| Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene | Q72073093 | ||
| Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements | Q72333265 | ||
| Trinucleotide repeats affect DNA replication in vivo | Q73839003 | ||
| Expansion and length-dependent fragility of CTG repeats in yeast | Q74128701 | ||
| Expanded CAG repeats activate the DNA damage checkpoint pathway | Q80354669 | ||
| Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II | Q24314310 | ||
| Cockayne syndrome group B protein enhances elongation by RNA polymerase II | Q24317053 | ||
| ATM-dependent chromatin changes silence transcription in cis to DNA double-strand breaks | Q24321489 | ||
| The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα | Q24339204 | ||
| DNA damage triggers nucleotide excision repair-dependent monoubiquitylation of histone H2A | Q24546161 | ||
| Mdc1 couples DNA double-strand break recognition by Nbs1 with its H2AX-dependent chromatin retention | Q24563397 | ||
| SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging | Q24595900 | ||
| Histone H3 lysine 56 acetylation and the response to DNA replication fork damage | Q24612284 | ||
| A PP4-phosphatase complex dephosphorylates gamma-H2AX generated during DNA replication | Q24626425 | ||
| The Dot1 histone methyltransferase and the Rad9 checkpoint adaptor contribute to cohesin-dependent double-strand break repair by sister chromatid recombination in Saccharomyces cerevisiae | Q24650576 | ||
| Orchestration of the DNA-damage response by the RNF8 ubiquitin ligase | Q24653776 | ||
| DNA damage-dependent acetylation and ubiquitination of H2AX enhances chromatin dynamics | Q24681614 | ||
| The balancing act of DNA repeat expansions | Q27001959 | ||
| Impact of histone H4 lysine 20 methylation on 53BP1 responses to chromosomal double strand breaks | Q27337186 | ||
| Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development | Q27347595 | ||
| Dual recognition of phosphoserine and phosphotyrosine in histone variant H2A.X by DNA damage response protein MCPH1 | Q27671621 | ||
| Acetylation limits 53BP1 association with damaged chromatin to promote homologous recombination | Q27676128 | ||
| The ctf13-30/CTF13 genomic haploinsufficiency modifier screen identifies the yeast chromatin remodeling complex RSC, which is required for the establishment of sister chromatid cohesion | Q27930793 | ||
| COMPASS: a complex of proteins associated with a trithorax-related SET domain protein | Q27931344 | ||
| Regulation of NuA4 histone acetyltransferase activity in transcription and DNA repair by phosphorylation of histone H4. | Q27931428 | ||
| Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites | Q27931488 | ||
| Dephosphorylation of gamma H2A by Glc7/protein phosphatase 1 promotes recovery from inhibition of DNA replication. | Q27932022 | ||
| Acetylation of histone H3 lysine 56 regulates replication-coupled nucleosome assembly | Q27932260 | ||
| A chromatin remodelling complex involved in transcription and DNA processing. | Q27932458 | ||
| Rad4-Rad23 interaction with SWI/SNF links ATP-dependent chromatin remodeling with nucleotide excision repair | Q27932672 | ||
| A phosphatase complex that dephosphorylates gammaH2AX regulates DNA damage checkpoint recovery | Q27933727 | ||
| Chromatin remodelling complex RSC promotes base excision repair in chromatin of Saccharomyces cerevisiae | Q27933831 | ||
| INO80 and gamma-H2AX interaction links ATP-dependent chromatin remodeling to DNA damage repair. | Q27933934 | ||
| The DNA damage checkpoint response requires histone H2B ubiquitination by Rad6-Bre1 and H3 methylation by Dot1. | Q27934025 | ||
| Histone variant Htz1 promotes histone H3 acetylation to enhance nucleotide excision repair in Htz1 nucleosomes | Q27934483 | ||
| Distinct roles for SWR1 and INO80 chromatin remodeling complexes at chromosomal double-strand breaks. | Q27934708 | ||
| The p400 ATPase regulates nucleosome stability and chromatin ubiquitination during DNA repair | Q34191583 | ||
| NuA4 initiates dynamic histone H4 acetylation to promote high-fidelity sister chromatid recombination at postreplication gaps. | Q34216700 | ||
| Involvement of a chromatin remodeling complex in damage tolerance during DNA replication | Q34280451 | ||
| Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases | Q34280857 | ||
| PARP1 promotes nucleotide excision repair through DDB2 stabilization and recruitment of ALC1 | Q34304600 | ||
| H2AX post-translational modifications in the ionizing radiation response and homologous recombination | Q34306825 | ||
| Distribution and dynamics of chromatin modification induced by a defined DNA double-strand break | Q34354650 | ||
| Localized histone acetylation and deacetylation triggered by the homologous recombination pathway of double-strand DNA repair. | Q34422309 | ||
| The DDB1-CUL4ADDB2 ubiquitin ligase is deficient in xeroderma pigmentosum group E and targets histone H2A at UV-damaged DNA sites | Q34479820 | ||
| The WSTF-SNF2h chromatin remodeling complex interacts with several nuclear proteins in transcription | Q34512121 | ||
| X-ray survival characteristics and genetic analysis for nine Saccharomyces deletion mutants that show altered radiation sensitivity | Q34570137 | ||
| CAF-I-dependent control of degradation of the discontinuous strands during mismatch repair | Q34582950 | ||
| GCN5 and E2F1 stimulate nucleotide excision repair by promoting H3K9 acetylation at sites of damage. | Q34609350 | ||
| The structural determinants of checkpoint activation | Q34619662 | ||
| ATR-dependent phosphorylation and activation of ATM in response to UV treatment or replication fork stalling | Q34653133 | ||
| An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae | Q34659849 | ||
| 30 nm chromatin fibre decompaction requires both H4-K16 acetylation and linker histone eviction | Q34800325 | ||
| Systematic identification of fragile sites via genome-wide location analysis of gamma-H2AX. | Q34841266 | ||
| Replication stress induces 53BP1-containing OPT domains in G1 cells | Q34854577 | ||
| Nucleotide excision repair-induced H2A ubiquitination is dependent on MDC1 and RNF8 and reveals a universal DNA damage response | Q35006034 | ||
| Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast | Q35049665 | ||
| Analysis of protein dynamics at active, stalled, and collapsed replication forks. | Q35080080 | ||
| Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice | Q35134204 | ||
| Mechanisms of trinucleotide repeat instability during human development | Q35219284 | ||
| SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination | Q35680031 | ||
| Overcoming natural replication barriers: differential helicase requirements | Q35740570 | ||
| ATP-dependent chromatin remodeling in the DNA-damage response. | Q35744850 | ||
| Interplay between mismatch repair and chromatin assembly | Q35750965 | ||
| Different structural states in oligonucleosomes are required for early versus late steps of base excision repair. | Q35917003 | ||
| ATP-dependent chromatin remodeling is required for base excision repair in conventional but not in variant H2A.Bbd nucleosomes. | Q35950275 | ||
| Chromatin dynamics in DNA double-strand break repair | Q36012981 | ||
| Chromatin changes in the development and pathology of the Fragile X-associated disorders and Friedreich ataxia | Q36016607 | ||
| Requirement of ATM-dependent monoubiquitylation of histone H2B for timely repair of DNA double-strand breaks | Q36095690 | ||
| Acetylation of histone H4 by Esa1 is required for DNA double-strand break repair. | Q27935926 | ||
| The NEF4 complex regulates Rad4 levels and utilizes Snf2/Swi2-related ATPase activity for nucleotide excision repair | Q27936146 | ||
| NuA4-dependent acetylation of nucleosomal histones H4 and H2A directly stimulates incorporation of H2A.Z by the SWR1 complex. | Q27936275 | ||
| The RAD6/BRE1 histone modification pathway in Saccharomyces confers radiation resistance through a RAD51-dependent process that is independent of RAD18 | Q27936359 | ||
| RAD26, the yeast homolog of human Cockayne's syndrome group B gene, encodes a DNA-dependent ATPase | Q27936827 | ||
| Methylation of histone H3 lysine-79 by Dot1p plays multiple roles in the response to UV damage in Saccharomyces cerevisiae. | Q27937420 | ||
| Evidence that the histone methyltransferase Dot1 mediates global genomic repair by methylating histone H3 on lysine 79. | Q27938606 | ||
| A histone acetylation switch regulates H2A.Z deposition by the SWR-C remodeling enzyme | Q27940293 | ||
| PP4 is a gamma H2AX phosphatase required for recovery from the DNA damage checkpoint | Q28117742 | ||
| DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
| CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae | Q28139592 | ||
| A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage | Q28144576 | ||
| A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome | Q28183834 | ||
| Histone H2AX is phosphorylated in an ATR-dependent manner in response to replicational stress | Q28201846 | ||
| Association of CBP/p300 acetylase and thymine DNA glycosylase links DNA repair and transcription | Q28203698 | ||
| Histone H3 and H4 ubiquitylation by the CUL4-DDB-ROC1 ubiquitin ligase facilitates cellular response to DNA damage | Q28238604 | ||
| Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks | Q28286203 | ||
| MDC1 maintains genomic stability by participating in the amplification of ATM-dependent DNA damage signals | Q28292900 | ||
| Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae | Q28343956 | ||
| ATP-dependent chromatin remodeling facilitates nucleotide excision repair of UV-induced DNA lesions in synthetic dinucleosomes | Q28362241 | ||
| A reversible histone H3 acetylation cooperates with mismatch repair and replicative polymerases in maintaining genome stability | Q28534685 | ||
| Inhibition of histone deacetylase 3 causes replication stress in cutaneous T cell lymphoma | Q28534761 | ||
| Histone H3K56 acetylation, Rad52, and non-DNA repair factors control double-strand break repair choice with the sister chromatid | Q28563892 | ||
| The DNA-dependent protein kinase: requirement for DNA ends and association with Ku antigen | Q28608938 | ||
| Double strand break repair functions of histone H2AX | Q28661754 | ||
| DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae | Q28709604 | ||
| ATP-dependent chromatin remodeling shapes the DNA replication landscape | Q28754502 | ||
| Histone H4-K16 acetylation controls chromatin structure and protein interactions | Q29614521 | ||
| Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks | Q29617463 | ||
| Recruitment of the INO80 complex by H2A phosphorylation links ATP-dependent chromatin remodeling with DNA double-strand break repair | Q29620305 | ||
| Gene silencing: trans-histone regulatory pathway in chromatin | Q30309681 | ||
| Histone H3 Thr 45 phosphorylation is a replication-associated post-translational modification in S. cerevisiae | Q30436419 | ||
| The Rtt109 histone acetyltransferase facilitates error-free replication to prevent CAG/CTG repeat contractions | Q30493921 | ||
| Histone H2B ubiquitylation controls processive methylation but not monomethylation by Dot1 and Set1. | Q33220208 | ||
| Replisome instability, fork collapse, and gross chromosomal rearrangements arise synergistically from Mec1 kinase and RecQ helicase mutations | Q33229596 | ||
| Perturbed gap-filling synthesis in nucleotide excision repair causes histone H2AX phosphorylation in human quiescent cells | Q33275895 | ||
| The ATM repair pathway inhibits RNA polymerase I transcription in response to chromosome breaks | Q33286997 | ||
| Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II | Q33551567 | ||
| Double-strand break repair pathways protect against CAG/CTG repeat expansions, contractions and repeat-mediated chromosomal fragility in Saccharomyces cerevisiae | Q33628502 | ||
| Methylated H3K4, a Transcription-Associated Histone Modification, Is Involved in the DNA Damage Response Pathway | Q33701701 | ||
| Rad26p, a transcription-coupled repair factor, is recruited to the site of DNA lesion in an elongating RNA polymerase II-dependent manner in vivo | Q33719420 | ||
| DNA double-strand breaks promote methylation of histone H3 on lysine 9 and transient formation of repressive chromatin | Q33834990 | ||
| UV irradiation stimulates histone acetylation and chromatin remodeling at a repressed yeast locus | Q33853904 | ||
| Expanded CAG/CTG repeat DNA induces a checkpoint response that impacts cell proliferation in Saccharomyces cerevisiae | Q33855685 | ||
| Deletion of the CSB homolog, RAD26, yields Spt(-) strains with proficient transcription-coupled repair | Q33940642 | ||
| How chromatin is remodelled during DNA repair of UV-induced DNA damage in Saccharomyces cerevisiae | Q33940737 | ||
| Role for hACF1 in the G2/M damage checkpoint | Q33957455 | ||
| MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair | Q33963853 | ||
| ATP-dependent chromatin remodeling factors tune S phase checkpoint activity | Q34022692 | ||
| The mammalian INO80 chromatin remodeling complex is required for replication stress recovery | Q34044332 | ||
| Methylation of histone H3 by COMPASS requires ubiquitination of histone H2B by Rad6. | Q34133875 | ||
| Requirement of the MRN complex for ATM activation by DNA damage | Q36267304 | ||
| MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells | Q36368825 | ||
| ATR protects the genome against CGG.CCG-repeat expansion in Fragile X premutation mice | Q36457201 | ||
| H2AX haploinsufficiency modifies genomic stability and tumor susceptibility | Q36533572 | ||
| Five repair pathways in one context: chromatin modification during DNA repair | Q36579359 | ||
| CAG/CTG repeats alter the affinity for the histone core and the positioning of DNA in the nucleosome | Q36594935 | ||
| Chromatin structure of repeating CTG/CAG and CGG/CCG sequences in human disease | Q36814097 | ||
| Chromosome fragility: molecular mechanisms and cellular consequences | Q36849639 | ||
| Expandable DNA repeats and human disease. | Q36854284 | ||
| Regulation of DNA repair throughout the cell cycle | Q37088926 | ||
| Histone H3 Lys79 methylation is required for efficient nucleotide excision repair in a silenced locus of Saccharomyces cerevisiae | Q37128155 | ||
| Chromatin remodeling in the noncoding repeat expansion diseases | Q37134343 | ||
| The biological effects of simple tandem repeats: lessons from the repeat expansion diseases | Q37204533 | ||
| Regulation of H3K4 trimethylation via Cps40 (Spp1) of COMPASS is monoubiquitination independent: implication for a Phe/Tyr switch by the catalytic domain of Set1. | Q37233447 | ||
| Protein modifications in transcription elongation | Q37249177 | ||
| Histone H2BK123 monoubiquitination is the critical determinant for H3K4 and H3K79 trimethylation by COMPASS and Dot1. | Q37309152 | ||
| Formation of dynamic gamma-H2AX domains along broken DNA strands is distinctly regulated by ATM and MDC1 and dependent upon H2AX densities in chromatin. | Q37347174 | ||
| Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous end-joining | Q37365625 | ||
| The role of RAD6 in recombinational repair, checkpoints and meiosis via histone modification | Q37397286 | ||
| Marks to stop the clock: histone modifications and checkpoint regulation in the DNA damage response | Q37398637 | ||
| Checkpoint responses to unusual structures formed by DNA repeats. | Q37420602 | ||
| Modulation of nucleotide excision repair by mammalian SWI/SNF chromatin-remodeling complex | Q37431761 | ||
| Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells | Q37446019 | ||
| Human SNF5/INI1, a component of the human SWI/SNF chromatin remodeling complex, promotes nucleotide excision repair by influencing ATM recruitment and downstream H2AX phosphorylation | Q37451917 | ||
| Core and linker histone modifications involved in the DNA damage response | Q37655471 | ||
| Histone modifications: crucial elements for damage response and chromatin restoration | Q37683656 | ||
| Chromatin dynamics and the repair of DNA double strand breaks | Q37826623 | ||
| Nucleotide excision repair in chromatin: damage removal at the drop of a HAT. | Q37877924 | ||
| Histone tails: Directing the chromatin response to DNA damage | Q37881417 | ||
| Chromatin response to DNA double-strand break damage | Q37961878 | ||
| Histone marks: repairing DNA breaks within the context of chromatin | Q37995722 | ||
| The complex basis underlying common fragile site instability in cancer | Q37998801 | ||
| Nucleosome remodelers in double-strand break repair. | Q38076899 | ||
| Chromatin remodeling at DNA double-strand breaks | Q38090114 | ||
| Chromatin movement in the maintenance of genome stability. | Q38090115 | ||
| Chromatin modifications and chromatin remodeling during DNA repair in budding yeast | Q38100439 | ||
| Saccharomyces cerevisiae Rad16 mediates ultraviolet-dependent histone H3 acetylation required for efficient global genome nucleotide-excision repair | Q38296363 | ||
| The RAD7 and RAD16 genes, which are essential for pyrimidine dimer removal from the silent mating type loci, are also required for repair of the nontranscribed strand of an active gene in Saccharomyces cerevisiae | Q38304692 | ||
| The chromatin remodeling factor BRG1 stimulates nucleotide excision repair by facilitating recruitment of XPC to sites of DNA damage | Q38349017 | ||
| RSC facilitates Rad59-dependent homologous recombination between sister chromatids by promoting cohesin loading at DNA double-strand breaks. | Q38630544 | ||
| Human ISWI complexes are targeted by SMARCA5 ATPase and SLIDE domains to help resolve lesion-stalled transcription | Q38978584 | ||
| Histone H4 deacetylation facilitates 53BP1 DNA damage signaling and double-strand break repair | Q39208600 | ||
| GCN5 protects vertebrate cells against UV-irradiation via controlling gene expression of DNA polymerase η. | Q39266637 | ||
| A role for chromatin remodellers in replication of damaged DNA. | Q39341270 | ||
| Bat3 facilitates H3K79 dimethylation by DOT1L and promotes DNA damage-induced 53BP1 foci at G1/G2 cell-cycle phases | Q39388766 | ||
| ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. | Q39455992 | ||
| Replisome stalling and stabilization at CGG repeats, which are responsible for chromosomal fragility | Q39592950 | ||
| 53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress | Q39593027 | ||
| Human HDAC1 and HDAC2 function in the DNA-damage response to promote DNA nonhomologous end-joining | Q39662092 | ||
| Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctions | Q39687235 | ||
| p53 is a chromatin accessibility factor for nucleotide excision repair of DNA damage | Q39714641 | ||
| Physical interaction between the histone acetyl transferase Tip60 and the DNA double-strand breaks sensor MRN complex. | Q39752528 | ||
| Mutations in Yeast Replication Proteins That Increase CAG/CTG Expansions Also Increase Repeat Fragility | Q39940361 | ||
| gamma-H2AX dephosphorylation by protein phosphatase 2A facilitates DNA double-strand break repair | Q40347113 | ||
| ATM and DNA-PK function redundantly to phosphorylate H2AX after exposure to ionizing radiation | Q40570996 | ||
| The Ino80 chromatin-remodeling complex restores chromatin structure during UV DNA damage repair | Q41157072 | ||
| Nucleosome remodeling by hMSH2-hMSH6. | Q41479268 | ||
| Monitoring the spatiotemporal dynamics of proteins at replication forks and in assembled chromatin using isolation of proteins on nascent DNA. | Q41490747 | ||
| Histone deacetylases 1 and 2 maintain S-phase chromatin and DNA replication fork progression | Q41772663 | ||
| Rad26p, a transcription-coupled repair factor, promotes the eviction and prevents the reassociation of histone H2A-H2B dimer during transcriptional elongation in vivo | Q41786276 | ||
| Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis | Q42132322 | ||
| DNA repair choice defines a common pathway for recruitment of chromatin regulators | Q42144432 | ||
| Phosphorylation of histone H3(T118) alters nucleosome dynamics and remodeling | Q42230215 | ||
| Drosophila p53 Is Required to Increase the Levels of the dKDM4B Demethylase after UV-induced DNA Damage to Demethylate Histone H3 Lysine 9 | Q42274730 | ||
| MOF and H4 K16 acetylation play important roles in DNA damage repair by modulating recruitment of DNA damage repair protein Mdc1. | Q42375517 | ||
| Histone H2A.Z controls a critical chromatin remodeling step required for DNA double-strand break repair | Q42418108 | ||
| Dual chromatin remodeling roles for RSC during DNA double strand break induction and repair at the yeast MAT locus | Q42516363 | ||
| P304 | page(s) | 296 | |
| P577 | publication date | 2014-09-05 | |
| P1433 | published in | Frontiers in Genetics | Q2499875 |
| P1476 | title | Chromatin modifications and DNA repair: beyond double-strand breaks | |
| P478 | volume | 5 |
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