| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1028207524 |
| P356 | DOI | 10.1038/NCB1845 |
| P698 | PubMed publication ID | 19182789 |
| P50 | author | Hisao Masukata | Q89574387 |
| Takuro Nakagawa | Q41848343 | ||
| Tatsuro S Takahashi | Q41848347 | ||
| Jun-Ichi Nakayama | Q57338785 | ||
| Makoto Hayashi | Q58173535 | ||
| P2860 | cites work | Telomere binding protein Taz1 establishes Swi6 heterochromatin independently of RNAi at telomeres | Q81389440 |
| Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome | Q81886031 | ||
| Shugoshin enables tension-generating attachment of kinetochores by loading Aurora to centromeres | Q24669659 | ||
| Structure of HP1 chromodomain bound to a lysine 9-methylated histone H3 tail | Q27638012 | ||
| Ordered assembly of Sld3, GINS and Cdc45 is distinctly regulated by DDK and CDK for activation of replication origins | Q27935990 | ||
| Regulation of replication timing in fission yeast | Q28363094 | ||
| Heterochromatin revisited | Q29614716 | ||
| Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
| Epigenetic regulation of heterochromatic DNA stability | Q33622619 | ||
| swi6, a gene required for mating-type switching, prohibits meiotic recombination in the mat2-mat3 "cold spot" of fission yeast | Q33958793 | ||
| A role for DNA polymerase alpha in epigenetic control of transcriptional silencing in fission yeast | Q34079851 | ||
| Common themes in mechanisms of gene silencing | Q34388956 | ||
| Replication timing and transcriptional control: beyond cause and effect | Q34688494 | ||
| Early-replicating heterochromatin | Q35963910 | ||
| Replication of Centromere II of Schizosaccharomyces pombe | Q36554830 | ||
| Replication in context: dynamic regulation of DNA replication patterns in metazoans | Q36875519 | ||
| A novel intermediate in initiation complex assembly for fission yeast DNA replication. | Q39284579 | ||
| A chromodomain protein, Chp1, is required for the establishment of heterochromatin in fission yeast. | Q40197642 | ||
| The silent P mating type locus in fission yeast contains two autonomously replicating sequences | Q40405409 | ||
| Genome-wide localization of pre-RC sites and identification of replication origins in fission yeast | Q41893574 | ||
| Establishment and maintenance of a heterochromatin domain | Q44128134 | ||
| A chromodomain protein, Swi6, performs imprinting functions in fission yeast during mitosis and meiosis | Q73881224 | ||
| Chromodomain protein Swi6-mediated role of DNA polymerase alpha in establishment of silencing in fission Yeast | Q74582431 | ||
| Hsk1-Dfp1 is required for heterochromatin-mediated cohesion at centromeres | Q79305190 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 357-362 | |
| P577 | publication date | 2009-02-01 | |
| P1433 | published in | Nature Cell Biology | Q1574111 |
| P1476 | title | The heterochromatin protein Swi6/HP1 activates replication origins at the pericentromeric region and silent mating-type locus. | |
| P478 | volume | 11 |
| Q53077173 | A replication-time-controlling sequence element in Schizosaccharomyces pombe. |
| Q33881228 | A surrogate approach to study the evolution of noncoding DNA elements that organize eukaryotic genomes |
| Q37503456 | An acetyltransferase-independent function of Eso1 regulates centromere cohesion |
| Q33818720 | Auxin-inducible protein depletion system in fission yeast. |
| Q36189251 | Behavior of replication origins in Eukaryota - spatio-temporal dynamics of licensing and firing |
| Q91825484 | Cdc7 kinase stimulates Aurora B kinase in M-phase |
| Q39010240 | Centromere Stability: The Replication Connection |
| Q37790557 | Chromatin landscape: methylation beyond transcription. |
| Q41813815 | Clusters, factories and domains: The complex structure of S-phase comes into focus. |
| Q93064854 | Control of DNA replication timing in the 3D genome |
| Q64087221 | DNA Replication Timing Enters the Single-Cell Era |
| Q38496732 | DNA replication origin activation in space and time |
| Q34654036 | DNA replication timing |
| Q36736144 | DNA replication timing, genome stability and cancer: late and/or delayed DNA replication timing is associated with increased genomic instability. |
| Q36160604 | DNA sequence templates adjacent nucleosome and ORC sites at gene amplification origins in Drosophila |
| Q54967259 | Distinct 'safe zones' at the nuclear envelope ensure robust replication of heterochromatic chromosome regions. |
| Q37211356 | Diverse roles of HP1 proteins in heterochromatin assembly and functions in fission yeast. |
| Q33684292 | Domain-wide regulation of DNA replication timing during mammalian development |
| Q43765606 | Drosophila SUUR protein associates with PCNA and binds chromatin in a cell cycle-dependent manner. |
| Q64280786 | Dynamic relocalization of replication origins by Fkh1 requires execution of DDK function and Cdc45 loading at origins |
| Q64268272 | Dynamics of DNA replication in a eukaryotic cell |
| Q38171275 | Epigenetic landscape for initiation of DNA replication |
| Q42158675 | Establishment of expression-state boundaries by Rif1 and Taz1 in fission yeast |
| Q34139588 | Eukaryotic DNA replication origins: many choices for appropriate answers |
| Q34232735 | Evaluating genome-scale approaches to eukaryotic DNA replication |
| Q33853216 | Fission yeast Hsk1 (Cdc7) kinase is required after replication initiation for induced mutagenesis and proper response to DNA alkylation damage |
| Q35195952 | Genome-scale analysis of metazoan replication origins reveals their organization in specific but flexible sites defined by conserved features |
| Q36245258 | Genome-wide identification and characterization of replication origins by deep sequencing |
| Q46949847 | HP1 knockdown is associated with abnormal condensation of almost all chromatin types in a grasshopper (Eyprepocnemis plorans). |
| Q40784286 | Heterochromatin protein 1 (HP1) modulates replication timing of the Drosophila genome |
| Q60911595 | Heterochromatin suppresses gross chromosomal rearrangements at centromeres by repressing Tfs1/TFIIS-dependent transcription |
| Q41668818 | Histone demethylation and timely DNA replication |
| Q38359785 | How the cell cycle impacts chromatin architecture and influences cell fate |
| Q41874160 | Identification of two telomere-proximal fission yeast DNA replication origins constrained by nearby cis-acting sequences to replicate in late S phase |
| Q33495181 | Impact of chromatin structures on DNA processing for genomic analyses |
| Q38420057 | Inner nuclear membrane protein Lem2 facilitates Rad3-mediated checkpoint signaling under replication stress induced by nucleotide depletion in fission yeast |
| Q37500876 | Interplay between Epigenetics and Genetics in Cancer |
| Q27940145 | Kinetochores coordinate pericentromeric cohesion and early DNA replication by Cdc7-Dbf4 kinase recruitment |
| Q38076662 | Location, location, location: it's all in the timing for replication origins |
| Q36285411 | Maintaining replication origins in the face of genomic change |
| Q37685965 | Molecular analysis of the replication program in unicellular model organisms |
| Q38909131 | Multiple pathways can bypass the essential role of fission yeast Hsk1 kinase in DNA replication initiation |
| Q21559664 | Mutations disrupting histone methylation have different effects on replication timing in S. pombe centromere |
| Q34392191 | Neocentromeres: a place for everything and everything in its place |
| Q93103545 | Next-Generation Sequencing Enables Spatiotemporal Resolution of Human Centromere Replication Timing |
| Q39014876 | Order from clutter: selective interactions at mammalian replication origins |
| Q64056900 | Origin Firing Regulations to Control Genome Replication Timing |
| Q89996449 | Overlapping Roles in Chromosome Segregation for Heterochromatin Protein 1 (Swi6) and DDK in Schizosaccharomyces pombe |
| Q33450714 | Polycomb mediated epigenetic silencing and replication timing at the INK4a/ARF locus during senescence |
| Q27934621 | Quantitative BrdU immunoprecipitation method demonstrates that Fkh1 and Fkh2 are rate-limiting activators of replication origins that reprogram replication timing in G1 phase |
| Q37965791 | RNA and epigenetic silencing: insight from fission yeast |
| Q42228801 | RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol II. |
| Q34422701 | RNAi-dependent formation of heterochromatin and its diverse functions |
| Q34014307 | Rad3 decorates critical chromosomal domains with gammaH2A to protect genome integrity during S-Phase in fission yeast |
| Q35156797 | Rad51-Rad52 mediated maintenance of centromeric chromatin in Candida albicans |
| Q40311595 | Reconciling stochastic origin firing with defined replication timing |
| Q37777343 | Regulation of DNA replication by chromatin structures: accessibility and recruitment. |
| Q44542200 | Regulation of DNA replication timing |
| Q47404896 | Regulation of transcriptional silencing and chromodomain protein localization at centromeric heterochromatin by histone H3 tyrosine 41 phosphorylation in fission yeast |
| Q39168142 | Regulation of DNA Replication through Natural Impediments in the Eukaryotic Genome. |
| Q30539756 | Replication fork stability is essential for the maintenance of centromere integrity in the absence of heterochromatin |
| Q37432729 | Replication timing and transcriptional control: beyond cause and effect--part II. |
| Q37208139 | Replication timing as an epigenetic mark |
| Q34249766 | Rif1 is a global regulator of timing of replication origin firing in fission yeast |
| Q35176804 | Rif1 regulates initiation timing of late replication origins throughout the S. cerevisiae genome |
| Q42256342 | S. pombe replication protein Cdc18 (Cdc6) interacts with Swi6 (HP1) heterochromatin protein: region specific effects and replication timing in the centromere. |
| Q41417327 | SUMOylation of HP1α supports association with ncRNA to define responsiveness of breast cancer cells to chemotherapy |
| Q89574390 | Shelterin promotes tethering of late replication origins to telomeres for replication-timing control |
| Q64230645 | Short-Homology-Mediated CRISPR/Cas9-Based Method for Genome Editing in Fission Yeast |
| Q36240918 | Telomere-binding protein Taz1 controls global replication timing through its localization near late replication origins in fission yeast |
| Q43130012 | Telomere-binding proteins play roles in control of replication timing |
| Q30541456 | The C-terminus of S. pombe DDK subunit Dfp1 is required for meiosis-specific transcription and cohesin cleavage |
| Q37503847 | The CINs of the centromere |
| Q36958166 | The Histone Variant H3.3 Is Enriched at Drosophila Amplicon Origins but Does Not Mark Them for Activation. |
| Q37142528 | The Transcription Cofactor Swi6 of the Fusarium graminearum Is Involved in Fusarium Graminearum Virus 1 Infection-Induced Phenotypic Alterations |
| Q37985257 | The chromatin backdrop of DNA replication: lessons from genetics and genome-scale analyses |
| Q90408550 | The regulation of chromosome segregation via centromere loops |
| Q42039702 | The spatial and temporal organization of origin firing during the S-phase of fission yeast |
| Q27008596 | Three wise centromere functions: see no error, hear no break, speak no delay |
| Q24648278 | Transcriptional co-activator LEDGF interacts with Cdc7-activator of S-phase kinase (ASK) and stimulates its enzymatic activity |
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