| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.YEXCR.2020.111898 |
| P698 | PubMed publication ID | 32035949 |
| P2093 | author name string | Tatsuo Fukagawa | |
| Tetsuya Hori | |||
| P2860 | cites work | Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini | Q40134828 |
| Telomere directed fragmentation of mammalian chromosomes | Q40404539 | ||
| The 10q25 neocentromere and its inactive progenitor have identical primary nucleotide sequence: further evidence for epigenetic modification | Q40414103 | ||
| Genome sequence, comparative analysis, and population genetics of the domestic horse | Q22065900 | ||
| Comparative and demographic analysis of orang-utan genomes | Q22122185 | ||
| Induced ectopic kinetochore assembly bypasses the requirement for CENP-A nucleosomes | Q24300684 | ||
| Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURP. | Q24321321 | ||
| HJURP is a cell-cycle-dependent maintenance and deposition factor of CENP-A at centromeres | Q24321377 | ||
| CCAN makes multiple contacts with centromeric DNA to provide distinct pathways to the outer kinetochore | Q24324027 | ||
| PHF8 mediates histone H4 lysine 20 demethylation events involved in cell cycle progression | Q24338563 | ||
| Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin | Q24537593 | ||
| Massive genomic rearrangement acquired in a single catastrophic event during cancer development | Q24631164 | ||
| Heterochromatin and RNAi are required to establish CENP-A chromatin at centromeres | Q24654940 | ||
| A chromosomal memory triggered by Xist regulates histone methylation in X inactivation | Q24802695 | ||
| Permissive transcriptional activity at the centromere through pockets of DNA hypomethylation | Q25257502 | ||
| PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription | Q26823191 | ||
| Comprehensive mapping of long-range interactions reveals folding principles of the human genome | Q28131819 | ||
| The CENP-H-I complex is required for the efficient incorporation of newly synthesized CENP-A into centromeres | Q28235274 | ||
| Variable and hierarchical size distribution of L1-retroelement-enriched CENP-A clusters within a functional human neocentromere | Q28292622 | ||
| Formation of de novo centromeres and construction of first-generation human artificial microchromosomes | Q28306987 | ||
| Molecular architecture of the kinetochore-microtubule interface | Q29620741 | ||
| HJURP interaction with the condensin II complex during G1 promotes CENP-A deposition | Q30275512 | ||
| Identification of the Post-translational Modifications Present in Centromeric Chromatin | Q30277890 | ||
| Histone variants and epigenetics | Q30301007 | ||
| A two-step mechanism for epigenetic specification of centromere identity and function | Q30405362 | ||
| The quantitative architecture of centromeric chromatin | Q30411797 | ||
| Putting CENP-A in its place | Q30412014 | ||
| Posttranslational modification of CENP-A influences the conformation of centromeric chromatin | Q30415280 | ||
| HJURP is a CENP-A chromatin assembly factor sufficient to form a functional de novo kinetochore | Q30428662 | ||
| Epigenetic centromere specification directs aurora B accumulation but is insufficient to efficiently correct mitotic errors | Q30433425 | ||
| Drosophila CAP-D2 is required for condensin complex stability and resolution of sister chromatids | Q40415592 | ||
| Chromosome size and origin as determinants of the level of CENP-A incorporation into human centromeres. | Q40460199 | ||
| CENP-B box is required for de novo centromere chromatin assembly on human alphoid DNA. | Q40686084 | ||
| Sequence analysis of an 80 kb human neocentromere | Q40825786 | ||
| Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25. | Q40829962 | ||
| Centromeric protein B null mice are viable with no apparent abnormalities | Q41008406 | ||
| Construction of YAC-based mammalian artificial chromosomes | Q41042021 | ||
| Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres | Q41887609 | ||
| The Chromatin of Candida albicans Pericentromeres Bears Features of Both Euchromatin and Heterochromatin. | Q42082600 | ||
| The requirement for the Dam1 complex is dependent upon the number of kinetochore proteins and microtubules | Q42738105 | ||
| Epigenetically induced paucity of histone H2A.Z stabilizes fission-yeast ectopic centromeres | Q43583151 | ||
| Repeatless and repeat-based centromeres in potato: implications for centromere evolution. | Q44446100 | ||
| Dynamic Control of X Chromosome Conformation and Repression by a Histone H4K20 Demethylase. | Q46315066 | ||
| Recurrent establishment of de novo centromeres in the pericentromeric region of maize chromosome 3. | Q46317620 | ||
| Decoding the centromeric nucleosome through CENP-N. | Q47252230 | ||
| Structural mechanisms of centromeric nucleosome recognition by the kinetochore protein CENP-N. | Q47263134 | ||
| RNA interference demonstrates a novel role for H2A.Z in chromosome segregation | Q47349040 | ||
| Spindle asymmetry drives non-Mendelian chromosome segregation. | Q47591701 | ||
| Expanded Satellite Repeats Amplify a Discrete CENP-A Nucleosome Assembly Site on Chromosomes that Drive in Female Meiosis. | Q47682737 | ||
| Association of M18BP1/KNL2 with CENP-A Nucleosome Is Essential for Centromere Formation in Non-mammalian Vertebrates | Q47881808 | ||
| Epigenetic modification of centromeric chromatin: hypomethylation of DNA sequences in the CENH3-associated chromatin in Arabidopsis thaliana and maize | Q48075232 | ||
| Micro-C XL: assaying chromosome conformation from the nucleosome to the entire genome | Q48265253 | ||
| Non-B-form DNA is enriched at centromeres. | Q49819293 | ||
| Molecular basis for CENP-N recognition of CENP-A nucleosome on the human kinetochore. | Q49925401 | ||
| Mis16 and Mis18 are required for CENP-A loading and histone deacetylation at centromeres. | Q50335532 | ||
| Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas. | Q51504406 | ||
| A Kinesin-14 Motor Activates Neocentromeres to Promote Meiotic Drive in Maize. | Q52328772 | ||
| Heterochromatin integrity affects chromosome reorganization after centromere dysfunction. | Q53458929 | ||
| Dissecting the centromere of the human Y chromosome with cloned telomeric DNA. | Q54692762 | ||
| A Dam1-based artificial kinetochore is sufficient to promote chromosome segregation in budding yeast | Q57887249 | ||
| HJURP Involvement in De Novo CenH3CENP-A and CENP-C Recruitment | Q57898678 | ||
| Sex and death: from cell fate specification to dynamic control of X-chromosome structure and gene expression | Q58083591 | ||
| 3D genomic architecture reveals that neocentromeres associate with heterochromatin regions | Q58610748 | ||
| The CENP-A centromere targeting domain facilitates H4K20 monomethylation in the nucleosome by structural polymorphism | Q61800373 | ||
| Centromere Repeats: Hidden Gems of the Genome | Q64084268 | ||
| CENP-A Ubiquitylation Contributes to Maintaining the Chromosomal Location of the Centromere | Q64268218 | ||
| A functional neo-centromere formed through activation of a latent human centromere and consisting of non-alpha-satellite DNA | Q73388111 | ||
| Epigenetic inactivation and subsequent heterochromatinization of a centromere stabilize dicentric chromosomes | Q83780163 | ||
| Centromere repositioning causes inversion of meiosis and generates a reproductive barrier | Q90616477 | ||
| Sub-nucleosomal Genome Structure Reveals Distinct Nucleosome Folding Motifs | Q91129373 | ||
| Centromeric Satellite DNAs: Hidden Sequence Variation in the Human Population | Q91891617 | ||
| Human Artificial Chromosomes that Bypass Centromeric DNA | Q92204339 | ||
| Cis- and Trans-chromosomal Interactions Define Pericentric Boundaries in the Absence of Conventional Heterochromatin | Q92381129 | ||
| Multiple phosphorylations control recruitment of the KMN network onto kinetochores | Q93017200 | ||
| H2A.Z contributes to the unique 3D structure of the centromere | Q30478722 | ||
| The cenpB gene is not essential in mice | Q31915856 | ||
| Intergenic locations of rice centromeric chromatin | Q33391509 | ||
| Neocentromeres form efficiently at multiple possible loci in Candida albicans. | Q33415450 | ||
| Human centromere repositioning "in progress" | Q33695623 | ||
| On the Anaphase Movement of Chromosomes | Q33747011 | ||
| A paucity of heterochromatin at functional human neocentromeres | Q33751932 | ||
| Histone H4 Lys 20 monomethylation of the CENP-A nucleosome is essential for kinetochore assembly | Q33844929 | ||
| Transmission of a fully functional human neocentromere through three generations | Q33858852 | ||
| A super-resolution map of the vertebrate kinetochore | Q33935029 | ||
| Epigenetics in Saccharomyces cerevisiae | Q34037400 | ||
| The case for epigenetic effects on centromere identity and function. | Q34065789 | ||
| Chickens possess centromeres with both extended tandem repeats and short non-tandem-repetitive sequences | Q34085140 | ||
| Neocentromeres: role in human disease, evolution, and centromere study | Q34146174 | ||
| The centromere: chromatin foundation for the kinetochore machinery | Q34160736 | ||
| Cdk activity couples epigenetic centromere inheritance to cell cycle progression. | Q34240608 | ||
| Sequencing of a rice centromere uncovers active genes | Q34289102 | ||
| Histone chaperones, a supporting role in the limelight | Q34305755 | ||
| Spatial and temporal regulation of Condensins I and II in mitotic chromosome assembly in human cells. | Q34321072 | ||
| Chromosome engineering allows the efficient isolation of vertebrate neocentromeres. | Q34333350 | ||
| Purification and characterization of CAF-I, a human cell factor required for chromatin assembly during DNA replication in vitro | Q34451628 | ||
| The architecture and evolution of cancer neochromosomes | Q34454339 | ||
| Epigenetic engineering shows H3K4me2 is required for HJURP targeting and CENP-A assembly on a synthetic human kinetochore | Q34513328 | ||
| Broad chromosomal domains of histone modification patterns in C. elegans | Q34548272 | ||
| Condensin-driven remodelling of X chromosome topology during dosage compensation. | Q34670135 | ||
| Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution | Q34746589 | ||
| H3.3 is deposited at centromeres in S phase as a placeholder for newly assembled CENP-A in G₁ phase | Q35079154 | ||
| Mislocalization of the Drosophila centromere-specific histone CID promotes formation of functional ectopic kinetochores | Q35335808 | ||
| Highly repeated DNA sequence limited to knob heterochromatin in maize | Q35406523 | ||
| CENP-C recruits M18BP1 to centromeres to promote CENP-A chromatin assembly | Q35514331 | ||
| DNA Sequence-Specific Binding of CENP-B Enhances the Fidelity of Human Centromere Function | Q35573549 | ||
| Centromere repositioning in mammals. | Q35614265 | ||
| Centromere sliding on a mammalian chromosome | Q35657166 | ||
| Mapping Nucleosome Resolution Chromosome Folding in Yeast by Micro-C | Q35871975 | ||
| Methylation of CenH3 arginine 37 regulates kinetochore integrity and chromosome segregation | Q36061323 | ||
| HJURP is involved in the expansion of centromeric chromatin | Q36063750 | ||
| Total centromere size and genome size are strongly correlated in ten grass species | Q36080983 | ||
| Propagation of centromeric chromatin requires exit from mitosis. | Q36117994 | ||
| Centromere protein B null mice are mitotically and meiotically normal but have lower body and testis weights | Q36289172 | ||
| The CCAN recruits CENP-A to the centromere and forms the structural core for kinetochore assembly | Q36525667 | ||
| Inbreeding drives maize centromere evolution | Q36646304 | ||
| Molecular architecture of the kinetochore-microtubule attachment site is conserved between point and regional centromeres | Q36660656 | ||
| Molecular underpinnings of centromere identity and maintenance | Q36734912 | ||
| Genetic manipulation of centromere function | Q36843287 | ||
| Epigenetic regulation of centromeric chromatin: old dogs, new tricks? | Q36981211 | ||
| Centromere assembly requires the direct recognition of CENP-A nucleosomes by CENP-N. | Q37248320 | ||
| Recruiting a microtubule-binding complex to DNA directs chromosome segregation in budding yeast | Q37363489 | ||
| Acetylation of histone H4 lysine 5 and 12 is required for CENP-A deposition into centromeres | Q37396227 | ||
| Induction of centromeric activity in maize by suppressor of meiotic drive 1. | Q37408565 | ||
| Maize centromeres expand and adopt a uniform size in the genetic background of oat. | Q37420321 | ||
| Mini-chromosomes derived from the human Y chromosome by telomere directed chromosome breakage | Q37489797 | ||
| Recurrent sites for new centromere seeding | Q37496061 | ||
| Constitutive centromere-associated network controls centromere drift in vertebrate cells. | Q37576596 | ||
| The ABCs of CENPs | Q37900520 | ||
| Establishment of the vertebrate kinetochores | Q38021698 | ||
| The molecular basis for centromere identity and function. | Q38645971 | ||
| Conserved organization of centromeric chromatin in flies and humans | Q38692366 | ||
| Genetic complementation analysis showed distinct contributions of the N-terminal tail of H2A.Z to epigenetic regulations | Q38797473 | ||
| Kinetochore assembly and function through the cell cycle | Q38885455 | ||
| Chromatin dynamics during the cell cycle at centromeres | Q39110341 | ||
| Critical histone post-translational modifications for centromere function and propagation | Q39361927 | ||
| Drosophila CENH3 is sufficient for centromere formation. | Q39448107 | ||
| Heterochromatin boundaries are hotspots for de novo kinetochore formation | Q39521875 | ||
| Genomic size of CENP-A domain is proportional to total alpha satellite array size at human centromeres and expands in cancer cells | Q39560198 | ||
| Characterization of HCP-6, a C. elegans protein required to prevent chromosome twisting and merotelic attachment | Q39859891 | ||
| Heterochromatin, satellite DNA, and cell function. Structural DNA of eucaryotes may support and protect genes and aid in speciation | Q40004460 | ||
| CENP-B controls centromere formation depending on the chromatin context | Q40030884 | ||
| Activation of Holliday junction recognizing protein involved in the chromosomal stability and immortality of cancer cells | Q40083781 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 111898 | |
| P577 | publication date | 2020-02-06 | |
| P1433 | published in | Experimental Cell Research | Q1524289 |
| P1476 | title | Artificial generation of centromeres and kinetochores to understand their structure and function | |
| P478 | volume | 389 |
| Q100295023 | Artificial chromosomes | cites work | P2860 |
Search more.