| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Sophie E Polo | Q50199081 |
| P2093 | author name string | Anna Fortuny | |
| P2860 | cites work | The Smc5-Smc6 complex and SUMO modification of Rad52 regulates recombinational repair at the ribosomal gene locus. | Q53539192 |
| Chromatin fibers are formed by heterogeneous groups of nucleosomes in vivo. | Q53584742 | ||
| DNA methyltransferases control telomere length and telomere recombination in mammalian cells | Q57239953 | ||
| Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 | ||
| The deSUMOylase SENP7 promotes chromatin relaxation for homologous recombination DNA repair | Q24323354 | ||
| ATM and Artemis promote homologous recombination of radiation-induced DNA double-strand breaks in G2 | Q24647310 | ||
| Linking replication stress with heterochromatin formation | Q26778138 | ||
| Postreplicative mismatch repair | Q27690911 | ||
| Recombinational repair within heterochromatin requires ATP-dependent chromatin remodeling | Q27935713 | ||
| Constitutive heterochromatin formation and transcription in mammals | Q28080683 | ||
| DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
| DNA double-strand breaks in heterochromatin elicit fast repair protein recruitment, histone H2AX phosphorylation and relocation to euchromatin | Q28236172 | ||
| A role for the Tip60 histone acetyltransferase in the acetylation and activation of ATM | Q28270543 | ||
| Chromatin compaction protects genomic DNA from radiation damage | Q28534299 | ||
| Rif1 maintains telomere length homeostasis of ESCs by mediating heterochromatin silencing | Q28591651 | ||
| Double-strand breaks in heterochromatin move outside of a dynamic HP1a domain to complete recombinational repair. | Q30524137 | ||
| 53BP1 and the LINC Complex Promote Microtubule-Dependent DSB Mobility and DNA Repair | Q30673640 | ||
| Grabbing the genome by the NADs | Q30698865 | ||
| The telomeric DNA damage response occurs in the absence of chromatin decompaction | Q30845462 | ||
| gammaH2AX foci form preferentially in euchromatin after ionising-radiation. | Q33303665 | ||
| Epigenetic regulation of heterochromatic DNA stability | Q33622619 | ||
| Identification of the elementary structural units of the DNA damage response. | Q33804819 | ||
| Epigenome Maintenance in Response to DNA Damage | Q33811644 | ||
| 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 | ||
| Dynamic maps of UV damage formation and repair for the human genome | Q33865674 | ||
| RNAi and heterochromatin repress centromeric meiotic recombination | Q33928327 | ||
| Reduced local mutation density in regulatory DNA of cancer genomes is linked to DNA repair | Q33976821 | ||
| Understanding nucleotide excision repair and its roles in cancer and ageing. | Q34426055 | ||
| Nuclear position dictates DNA repair pathway choice | Q34518930 | ||
| Differential contribution of HP1 proteins to DNA end resection and homology-directed repair | Q34536140 | ||
| Transcription restores DNA repair to heterochromatin, determining regional mutation rates in cancer genomes. | Q34625791 | ||
| Activation of DNA damage response signaling by condensed chromatin | Q34713712 | ||
| Opposing ISWI- and CHD-class chromatin remodeling activities orchestrate heterochromatic DNA repair | Q34759375 | ||
| ATM signaling facilitates repair of DNA double-strand breaks associated with heterochromatin | Q34801409 | ||
| SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells. | Q35709996 | ||
| A localized nucleolar DNA damage response facilitates recruitment of the homology-directed repair machinery independent of cell cycle stage. | Q35750783 | ||
| DNA damage induces nuclear actin filament assembly by Formin -2 and Spire-½ that promotes efficient DNA repair. [corrected]. | Q36080669 | ||
| Heterochromatin is refractory to gamma-H2AX modification in yeast and mammals | Q36118803 | ||
| SCAI promotes DNA double-strand break repair in distinct chromosomal contexts | Q36184268 | ||
| Heterochromatic breaks move to the nuclear periphery to continue recombinational repair. | Q36235927 | ||
| The DDR at telomeres lacking intact shelterin does not require substantial chromatin decompaction | Q36337296 | ||
| Centromere mitotic recombination in mammalian cells | Q36718343 | ||
| Structure of Chromatin | Q39687258 | ||
| 53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair | Q39750906 | ||
| Chromatin relaxation in response to DNA double-strand breaks is modulated by a novel ATM- and KAP-1 dependent pathway | Q40252252 | ||
| Chromosome territory relocation during DNA repair requires nuclear myosin 1 recruitment to chromatin mediated by ϒ-H2AX signaling | Q41220276 | ||
| Linker histone H1 prevents R-loop accumulation and genome instability in heterochromatin | Q41448600 | ||
| Cervantes and Quijote protect heterochromatin from aberrant recombination and lead the way to the nuclear periphery | Q41887532 | ||
| KAP-1 phosphorylation regulates CHD3 nucleosome remodeling during the DNA double-strand break response. | Q42152404 | ||
| Histone H3 methylation links DNA damage detection to activation of the tumour suppressor Tip60. | Q42672338 | ||
| Temporal and Spatial Uncoupling of DNA Double Strand Break Repair Pathways within Mammalian Heterochromatin. | Q42809110 | ||
| Species conserved DNA damage response at the inactive human X chromosome | Q42820318 | ||
| Drosophila Histone Demethylase KDM4A Has Enzymatic and Non-enzymatic Roles in Controlling Heterochromatin Integrity | Q44889465 | ||
| ChromEMT: Visualizing 3D chromatin structure and compaction in interphase and mitotic cells | Q45235642 | ||
| Ten principles of heterochromatin formation and function. | Q46162198 | ||
| Regulation of mitotic recombination between DNA repeats in centromeres. | Q47107044 | ||
| Dynamic Organization of Chromatin Domains Revealed by Super-Resolution Live-Cell Imaging. | Q47918883 | ||
| Recombination at subtelomeres is regulated by physical distance, double-strand break resection and chromatin status. | Q48015207 | ||
| Carcinogen susceptibility is regulated by genome architecture and predicts cancer mutagenesis | Q48229411 | ||
| Nuclear topology modulates the mutational landscapes of cancer genomes. | Q48260617 | ||
| DNA Breaks and End Resection Measured Genome-wide by End Sequencing. | Q51603184 | ||
| Chromatin organization is a major influence on regional mutation rates in human cancer cells. | Q52837652 | ||
| Genome-wide kinetics of DNA excision repair in relation to chromatin state and mutagenesis | Q36821453 | ||
| Nucleotide-resolution DNA double-strand break mapping by next-generation sequencing | Q36834533 | ||
| HP1 promotes tumor suppressor BRCA1 functions during the DNA damage response | Q36909739 | ||
| Facultative heterochromatin: is there a distinctive molecular signature? | Q36971377 | ||
| A single double-strand break system reveals repair dynamics and mechanisms in heterochromatin and euchromatin | Q37151375 | ||
| Differential DNA lesion formation and repair in heterochromatin and euchromatin | Q37220505 | ||
| Heterochromatin protein 1 is recruited to various types of DNA damage. | Q37263966 | ||
| A 'higher order' of telomere regulation: telomere heterochromatin and telomeric RNAs | Q37293050 | ||
| Telomere-Internal Double-Strand Breaks Are Repaired by Homologous Recombination and PARP1/Lig3-Dependent End-Joining | Q37445974 | ||
| The emerging role of HP1 in the DNA damage response | Q37452573 | ||
| Hypermutation of the inactive X chromosome is a frequent event in cancer | Q37503144 | ||
| The chromatin response to DNA breaks: leaving a mark on genome integrity | Q38081947 | ||
| Chromatin movement in the maintenance of genome stability. | Q38090115 | ||
| Double strand break (DSB) repair in heterochromatin and heterochromatin proteins in DSB repair | Q38206320 | ||
| Noncoding RNAs and epigenetic mechanisms during X-chromosome inactivation. | Q38226983 | ||
| Repeat DNA in genome organization and stability. | Q38445548 | ||
| Analysis of human syndromes with disordered chromatin reveals the impact of heterochromatin on the efficacy of ATM-dependent G2/M checkpoint arrest. | Q38630610 | ||
| The molecular basis for centromere identity and function. | Q38645971 | ||
| Genome Organization Drives Chromosome Fragility | Q38696563 | ||
| Genome-wide mapping of long-range contacts unveils clustering of DNA double-strand breaks at damaged active genes. | Q38713512 | ||
| DNA double-strand-break repair in higher eukaryotes and its role in genomic instability and cancer: Cell cycle and proliferation-dependent regulation | Q38789304 | ||
| Transcription as a Threat to Genome Integrity | Q38792613 | ||
| ATM Dependent Silencing Links Nucleolar Chromatin Reorganization to DNA Damage Recognition | Q38829976 | ||
| Compartmentalization of DNA Damage Response between Heterochromatin and Euchromatin Is Mediated by Distinct H2A Histone Variants. | Q38845597 | ||
| Nuclear compartmentalization of DNA repair | Q38856344 | ||
| The molecular hallmarks of epigenetic control | Q38877902 | ||
| Differential DNA mismatch repair underlies mutation rate variation across the human genome | Q38906828 | ||
| The Chromatin Landscape of Cellular Senescence | Q38969345 | ||
| Organization and function of the 3D genome | Q38980344 | ||
| Nuclear Dynamics of Heterochromatin Repair. | Q39095474 | ||
| Opposing roles for 53BP1 during homologous recombination. | Q39106487 | ||
| Express or repress? The transcriptional dilemma of damaged chromatin | Q39148141 | ||
| Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression | Q39318399 | ||
| DSBCapture: in situ capture and sequencing of DNA breaks. | Q39489184 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International | Q24082749 |
| P433 | issue | 3 | |
| P921 | main subject | DNA damage | Q5205747 |
| P304 | page(s) | 291-300 | |
| P577 | publication date | 2018-03-29 | |
| 2018-09-01 | |||
| P1433 | published in | Chromosoma | Q15765851 |
| P1476 | title | The response to DNA damage in heterochromatin domains | |
| P478 | volume | 127 |
| Q92508214 | A cohesin/HUSH- and LINC-dependent pathway controls ribosomal DNA double-strand break repair |
| Q90307609 | Correlative Light and Electron Microscopy (CLEM) Analysis of Nuclear Reorganization Induced by Clustered DNA Damage Upon Charged Particle Irradiation |
| Q96022929 | H3K36 dimethylation by MMSET promotes classical non-homologous end-joining at unprotected telomeres |
| Q91678536 | Heterochromatin protein 1α interacts with parallel RNA and DNA G-quadruplexes |
| Q89977905 | Job Opening for Nucleosome Mechanic: Flexibility Required |
| Q64283787 | Kinesin-14 motor protein KIFC1 participates in DNA synthesis and chromatin maintenance |
| Q89719196 | Mathematical Model of ATM Activation and Chromatin Relaxation by Ionizing Radiation |
| Q103836664 | Radiation-induced DNA damage and repair effects on 3D genome organization |
| Q90182031 | Studying DNA Double-Strand Break Repair: An Ever-Growing Toolbox |
| Q92544102 | The Secret Life of Chromosome Loops upon DNA Double-Strand Break |
Search more.