| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/ABBS/GMW033 |
| P698 | PubMed publication ID | 27151295 |
| P2093 | author name string | Na Kong | |
| Xiu-Jun Cai | |||
| Ji-Feng Xiang | |||
| An-Yong Xie | |||
| Yi-Li Feng | |||
| P2860 | cites work | The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway | Q22065419 |
| The role of heterochromatin in centromere function | Q22065919 | ||
| DNA Damage, Aging, and Cancer | Q22121931 | ||
| Finishing the euchromatic sequence of the human genome | Q22122488 | ||
| Involvement of the TIP60 histone acetylase complex in DNA repair and apoptosis | Q24290159 | ||
| RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins | Q24300411 | ||
| The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain | Q24301692 | ||
| ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage | Q24306743 | ||
| The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage | Q24309181 | ||
| RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins | Q24309287 | ||
| KAP1, a novel substrate for PIKK family members, colocalizes with numerous damage response factors at DNA lesions | Q24337449 | ||
| PARP1-dependent recruitment of KDM4D histone demethylase to DNA damage sites promotes double-strand break repair | Q24337719 | ||
| Genetic toxicology of oxygen | Q38683020 | ||
| Transcriptionally active chromatin recruits homologous recombination at DNA double-strand breaks. | Q39012832 | ||
| 53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair | Q39750906 | ||
| Physical interaction between the histone acetyl transferase Tip60 and the DNA double-strand breaks sensor MRN complex. | Q39752528 | ||
| gamma-radiation-induced gammaH2AX formation occurs preferentially in actively transcribing euchromatic loci | Q39783117 | ||
| Recruitment of heterochromatin protein 1 to DNA repair sites. | Q39845515 | ||
| The impact of heterochromatin on DSB repair | Q39851599 | ||
| Role for KAP1 serine 824 phosphorylation and sumoylation/desumoylation switch in regulating KAP1-mediated transcriptional repression | Q40066661 | ||
| Chromatin dynamics during DSB repair | Q40081910 | ||
| Chromatin relaxation in response to DNA double-strand breaks is modulated by a novel ATM- and KAP-1 dependent pathway | Q40252252 | ||
| Acetylation by Tip60 is required for selective histone variant exchange at DNA lesions | Q40495236 | ||
| Radiation-induced chromosome aberrations in human euchromatic (17cen-p53) and heterochromatic (1cen-1q12) regions | Q40797094 | ||
| Misrejoining of DNA double-strand breaks in primary and transformed human and rodent cells: a comparison between the HPRT region and other genomic locations | Q40952042 | ||
| The histone variant macroH2A1.1 is recruited to DSBs through a mechanism involving PARP1. | Q41425376 | ||
| Control of sister chromatid recombination by histone H2AX. | Q41549984 | ||
| The H4 tail domain participates in intra- and internucleosome interactions with protein and DNA during folding and oligomerization of nucleosome arrays | Q41888720 | ||
| DNA damage responses in progeroid syndromes arise from defective maturation of prelamin A. | Q42101728 | ||
| KAP-1 phosphorylation regulates CHD3 nucleosome remodeling during the DNA double-strand break response. | Q42152404 | ||
| Histone H2A.Z controls a critical chromatin remodeling step required for DNA double-strand break repair | Q42418108 | ||
| Histone H3 methylation links DNA damage detection to activation of the tumour suppressor Tip60. | Q42672338 | ||
| Distribution of breakpoints induced by etoposide and X-rays along the CHO X chromosome | Q44909817 | ||
| Non-random distribution of DNA double-strand breaks induced by particle irradiation | Q46120762 | ||
| Chromatin structure influences the sensitivity of DNA to gamma-radiation | Q46427208 | ||
| HP1-beta mobilization promotes chromatin changes that initiate the DNA damage response. | Q46625510 | ||
| End-joining of blunt DNA double-strand breaks in mammalian fibroblasts is precise and requires DNA-PK and XRCC4. | Q49172985 | ||
| The transcriptional histone acetyltransferase cofactor TRRAP associates with the MRN repair complex and plays a role in DNA double-strand break repair | Q24537586 | ||
| A comprehensive catalog of human KRAB-associated zinc finger genes: insights into the evolutionary history of a large family of transcriptional repressors | Q24546068 | ||
| Molecular determinants for targeting heterochromatin protein 1-mediated gene silencing: direct chromoshadow domain-KAP-1 corepressor interaction is essential | Q24551928 | ||
| The DNA-damage response in human biology and disease | Q24606586 | ||
| Megabase chromatin domains involved in DNA double-strand breaks in vivo | Q24680284 | ||
| Linking replication stress with heterochromatin formation | Q26778138 | ||
| Not All DDRs Are Created Equal: Non-Canonical DNA Damage Responses | Q26796371 | ||
| DNA-PK: a dynamic enzyme in a versatile DSB repair pathway | Q26866928 | ||
| Sources of DNA double-strand breaks and models of recombinational DNA repair | Q27005814 | ||
| Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA | Q27012760 | ||
| The DNA Damage Response: Making It Safe to Play with Knives | Q27861055 | ||
| Chromatin modifications and their function | Q27861067 | ||
| Constitutive heterochromatin formation and transcription in mammals | Q28080683 | ||
| The DNA-dependent protein kinase: A multifunctional protein kinase with roles in DNA double strand break repair and mitosis | Q28081821 | ||
| Envisioning the dynamics and flexibility of Mre11-Rad50-Nbs1 complex to decipher its roles in DNA replication and repair | Q28085622 | ||
| DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
| Histone H2AX is phosphorylated in an ATR-dependent manner in response to replicational stress | Q28201846 | ||
| Spatial organization of the mammalian genome surveillance machinery in response to DNA strand breaks | Q28235091 | ||
| Development and applications of CRISPR-Cas9 for genome engineering | Q28241526 | ||
| Mechanism of homologous recombination: mediators and helicases take on regulatory functions | Q28259452 | ||
| The DNA damage response: ten years after | Q28261230 | ||
| A role for the Tip60 histone acetyltransferase in the acetylation and activation of ATM | Q28270543 | ||
| Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks | Q28286203 | ||
| Nuclear organization of the genome and the potential for gene regulation | Q28303751 | ||
| Chromatin compaction protects genomic DNA from radiation damage | Q28534299 | ||
| Genomic instability in mice lacking histone H2AX | Q28589826 | ||
| Double strand break repair functions of histone H2AX | Q28661754 | ||
| Role of mammalian Mre11 in classical and alternative nonhomologous end joining | Q28751872 | ||
| Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage | Q29614218 | ||
| Histone H4-K16 acetylation controls chromatin structure and protein interactions | Q29614521 | ||
| Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks | Q29617463 | ||
| Histones: annotating chromatin | Q29619913 | ||
| Changes in chromatin structure and mobility in living cells at sites of DNA double-strand breaks | Q30480374 | ||
| Double-strand breaks in heterochromatin move outside of a dynamic HP1a domain to complete recombinational repair. | Q30524137 | ||
| gammaH2AX foci form preferentially in euchromatin after ionising-radiation. | Q33303665 | ||
| Higher-order chromatin structure in DSB induction, repair and misrepair | Q37689982 | ||
| ATR: a master conductor of cellular responses to DNA replication stress | Q37800265 | ||
| Heterochromatin and the DNA damage response: the need to relax | Q37843473 | ||
| KAP1 protein: an enigmatic master regulator of the genome | Q37886421 | ||
| Histone marks: repairing DNA breaks within the context of chromatin | Q37995722 | ||
| Classical and alternative end-joining pathways for repair of lymphocyte-specific and general DNA double-strand breaks | Q38051860 | ||
| The heterochromatic barrier to DNA double strand break repair: how to get the entry visa | Q38056496 | ||
| The role of the nucleosome acidic patch in modulating higher order chromatin structure | Q38085143 | ||
| The ATM protein kinase: regulating the cellular response to genotoxic stress, and more | Q38088935 | ||
| Chromatin remodeling at DNA double-strand breaks | Q38090114 | ||
| DNA damage sensing by the ATM and ATR kinases. | Q38134064 | ||
| INO80-C and SWR-C: guardians of the genome | Q38275882 | ||
| Mechanisms of ATM Activation | Q38314959 | ||
| The Ku heterodimer: function in DNA repair and beyond | Q38385852 | ||
| Patching Broken DNA: Nucleosome Dynamics and the Repair of DNA Breaks | Q38655184 | ||
| The redundancy of the mammalian heterochromatic compartment | Q38680093 | ||
| MRE11-RAD50-NBS1 complex dictates DNA repair independent of H2AX. | Q33569624 | ||
| Histone demethylase KDM5B is a key regulator of genome stability | Q33627079 | ||
| Chromatin as dynamic 10-nm fibers | Q33651467 | ||
| The NuRD chromatin-remodeling complex regulates signaling and repair of DNA damage | Q33678587 | ||
| A chromatin localization screen reveals poly (ADP ribose)-regulated recruitment of the repressive polycomb and NuRD complexes to sites of DNA damage | Q33715275 | ||
| DNA double-strand breaks promote methylation of histone H3 on lysine 9 and transient formation of repressive chromatin | Q33834990 | ||
| HP1alpha recruitment to DNA damage by p150CAF-1 promotes homologous recombination repair | Q33862272 | ||
| Increased ionizing radiation sensitivity and genomic instability in the absence of histone H2AX | Q34031720 | ||
| A macrohistone variant links dynamic chromatin compaction to BRCA1-dependent genome maintenance. | Q34132182 | ||
| Controlling the double helix | Q34172152 | ||
| Chromosome territories--a functional nuclear landscape. | Q34523990 | ||
| Activation of DNA damage response signaling by condensed chromatin | Q34713712 | ||
| Opposing ISWI- and CHD-class chromatin remodeling activities orchestrate heterochromatic DNA repair | Q34759375 | ||
| 30 nm chromatin fibre decompaction requires both H4-K16 acetylation and linker histone eviction | Q34800325 | ||
| ATM signaling facilitates repair of DNA double-strand breaks associated with heterochromatin | Q34801409 | ||
| Repair of endogenous DNA damage | Q35132488 | ||
| A Systematic Analysis of Factors Localized to Damaged Chromatin Reveals PARP-Dependent Recruitment of Transcription Factors | Q35640249 | ||
| A decade of 3C technologies: insights into nuclear organization | Q35674570 | ||
| HP1 and the dynamics of heterochromatin maintenance | Q35741016 | ||
| Mechanism and control of V(D)J recombination versus class switch recombination: similarities and differences | Q36037736 | ||
| Heterochromatin is refractory to gamma-H2AX modification in yeast and mammals | Q36118803 | ||
| A brief review of nucleosome structure | Q36137489 | ||
| The mechanism of telomere protection: a comparison between Drosophila and humans. | Q36192029 | ||
| Heterochromatic breaks move to the nuclear periphery to continue recombinational repair. | Q36235927 | ||
| Repeat instability: mechanisms of dynamic mutations | Q36277189 | ||
| DNA damage-induced acetylation of lysine 3016 of ATM activates ATM kinase activity | Q36316482 | ||
| Regulation of the H4 tail binding and folding landscapes via Lys-16 acetylation. | Q36397739 | ||
| Chromatin structure outside and inside the nucleus | Q36570241 | ||
| Facultative heterochromatin: is there a distinctive molecular signature? | Q36971377 | ||
| Live cell microscopy analysis of radiation-induced DNA double-strand break motion. | Q37096613 | ||
| Heterochromatin protein 1 is recruited to various types of DNA damage. | Q37263966 | ||
| Nuclear dynamics of radiation-induced foci in euchromatin and heterochromatin | Q37338520 | ||
| 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 | ||
| The emerging role of HP1 in the DNA damage response | Q37452573 | ||
| P433 | issue | 7 | |
| P304 | page(s) | 594-602 | |
| P577 | publication date | 2016-05-04 | |
| P1433 | published in | Acta Biochimica et Biophysica Sinica | Q2183997 |
| P1476 | title | Buried territories: heterochromatic response to DNA double-strand breaks | |
| P478 | volume | 48 |
| Q47614748 | A special issue on the DNA damage response and genomic instability |
| Q33574854 | A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress |
| Q37666874 | E3 ligase UHRF2 stabilizes the acetyltransferase TIP60 and regulates H3K9ac and H3K14ac via RING finger domain |
| Q47135566 | H2AX facilitates classical non-homologous end joining at the expense of limited nucleotide loss at repair junctions |
| Q64389148 | Is Required for Both Mitotic and Meiotic Recombination in Maize |
| Q28067125 | Repair of DNA Double-Strand Breaks in Heterochromatin |
| Q92864350 | SIRT6 coordinates with CHD4 to promote chromatin relaxation and DNA repair |
| Q58802841 | Using Persistent Homology as a New Approach for Super-Resolution Localization Microscopy Data Analysis and Classification of γH2AX Foci/Clusters |
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