scholarly article | Q13442814 |
P356 | DOI | 10.1038/NG1602 |
P698 | PubMed publication ID | 15976807 |
P50 | author | Tomoyasu Sugiyama | Q42790301 |
P2093 | author name string | Ee Sin Chen | |
Xi Chen | |||
Shiv I S Grewal | |||
Hugh P Cam | |||
Peter C FitzGerald | |||
P2860 | cites work | The genome sequence of Schizosaccharomyces pombe | Q21972841 |
Regulation of chromatin structure by site-specific histone H3 methyltransferases | Q24290115 | ||
Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin | Q24537593 | ||
RNA-dependent RNA polymerase is an essential component of a self-enforcing loop coupling heterochromatin assembly to siRNA production | Q24557548 | ||
RNAi-mediated targeting of heterochromatin by the RITS complex | Q24623437 | ||
Genetic and functional diversification of small RNA pathways in plants | Q24797901 | ||
Global expression changes resulting from loss of telomeric DNA in fission yeast | Q24805476 | ||
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain | Q27860477 | ||
Asymmetry in the assembly of the RNAi enzyme complex | Q27860763 | ||
RNA interference is mediated by 21- and 22-nucleotide RNAs | Q27860764 | ||
The small RNA profile during Drosophila melanogaster development | Q28201894 | ||
Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi | Q28218870 | ||
Regulation of heterochromatin by histone methylation and small RNAs | Q28261891 | ||
RNA silencing in plants | Q28282572 | ||
RITS acts in cis to promote RNA interference-mediated transcriptional and post-transcriptional silencing | Q28287265 | ||
RNAi-mediated pathways in the nucleus | Q28300961 | ||
Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
Role of transposable elements in heterochromatin and epigenetic control | Q29616253 | ||
Endogenous and silencing-associated small RNAs in plants | Q29618383 | ||
Rb targets histone H3 methylation and HP1 to promoters | Q29620452 | ||
Transitions in distinct histone H3 methylation patterns at the heterochromatin domain boundaries | Q29622865 | ||
Retrotransposons and their recognition of pol II promoters: a comprehensive survey of the transposable elements from the complete genome sequence of Schizosaccharomyces pombe | Q33678105 | ||
Global effects on gene expression in fission yeast by silencing and RNA interference machineries. | Q33694831 | ||
The profile of repeat-associated histone lysine methylation states in the mouse epigenome | Q33868292 | ||
RNA polymerase IV directs silencing of endogenous DNA. | Q33984841 | ||
Small RNAs correspond to centromere heterochromatic repeats | Q34145801 | ||
RNA interference machinery regulates chromosome dynamics during mitosis and meiosis in fission yeast | Q34168055 | ||
A protein sensor for siRNA asymmetry | Q34369235 | ||
Gardening the genome: DNA methylation in Arabidopsis thaliana | Q34414767 | ||
Heterochromatic deposition of centromeric histone H3-like proteins | Q34975731 | ||
An epigenetic road map for histone lysine methylation | Q35120983 | ||
Small RNAs in genome rearrangement in Tetrahymena. | Q35804621 | ||
A chromodomain protein, Chp1, is required for the establishment of heterochromatin in fission yeast. | Q40197642 | ||
RNA interference (RNAi)-dependent and RNAi-independent association of the Chp1 chromodomain protein with distinct heterochromatic loci in fission yeast. | Q41864606 | ||
Correlation between histone lysine methylation and developmental changes at the chicken beta-globin locus | Q43703042 | ||
Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component | Q43890842 | ||
Establishment and maintenance of a heterochromatin domain | Q44128134 | ||
Sir2 regulates histone H3 lysine 9 methylation and heterochromatin assembly in fission yeast | Q44515864 | ||
RNAi-independent heterochromatin nucleation by the stress-activated ATF/CREB family proteins | Q44952131 | ||
Atypical RNA polymerase subunits required for RNA-directed DNA methylation | Q48136173 | ||
Plant nuclear RNA polymerase IV mediates siRNA and DNA methylation-dependent heterochromatin formation | Q48146967 | ||
spRap1 and spRif1, recruited to telomeres by Taz1, are essential for telomere function in fission yeast | Q48336594 | ||
Two RNAi complexes, RITS and RDRC, physically interact and localize to noncoding centromeric RNAs. | Q55039785 | ||
Hairpin RNAs and retrotransposon LTRs effect RNAi and chromatin-based gene silencing | Q56765302 | ||
Transposon silencing in the Caenorhabditis elegans germ line by natural RNAi | Q59093938 | ||
Requirement of Mis6 centromere connector for localizing a CENP-A-like protein in fission yeast | Q73919521 | ||
Heterochromatin regulates cell type-specific long-range chromatin interactions essential for directed recombination | Q80987684 | ||
P433 | issue | 8 | |
P304 | page(s) | 809-819 | |
P577 | publication date | 2005-06-24 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome | |
P478 | volume | 37 |
Q38655732 | A Matter of Scale and Dimensions: Chromatin of Chromosome Landmarks in the Fungi |
Q35927018 | A Novel Epigenetic Silencing Pathway Involving the Highly Conserved 5'-3' Exoribonuclease Dhp1/Rat1/Xrn2 in Schizosaccharomyces pombe |
Q34998845 | A computational model for histone mark propagation reproduces the distribution of heterochromatin in different human cell types |
Q60907776 | A conserved dimer interface connects ERH and YTH family proteins to promote gene silencing |
Q34507364 | A diffusion model for the coordination of DNA replication in Schizosaccharomyces pombe |
Q33295222 | A discrete class of intergenic DNA dictates meiotic DNA break hotspots in fission yeast |
Q40469556 | A global non-coding RNA system modulates fission yeast protein levels in response to stress. |
Q28829593 | A histone H3K9M mutation traps histone methyltransferase Clr4 to prevent heterochromatin spreading |
Q35558859 | A homolog of male sex-determining factor SRY cooperates with a transposon-derived CENP-B protein to control sex-specific directed recombination. |
Q42321072 | A novel RNAi protein, Dsh1, assembles RNAi machinery on chromatin to amplify heterochromatic siRNA. |
Q33751932 | A paucity of heterochromatin at functional human neocentromeres |
Q39253895 | A requirement for DICER to maintain full promoter CpG island hypermethylation in human cancer cells |
Q54942389 | A somatic role for the histone methyltransferase Setdb1 in endogenous retrovirus silencing. |
Q91739281 | Abo1 is required for the H3K9me2 to H3K9me3 transition in heterochromatin |
Q36478645 | Abo1, a conserved bromodomain AAA-ATPase, maintains global nucleosome occupancy and organisation. |
Q49576014 | Accumulation of RNA on chromatin disrupts heterochromatic silencing |
Q34500908 | Advancing our understanding of functional genome organisation through studies in the fission yeast |
Q27655247 | An Alpha Motif at Tas3 C Terminus Mediates RITS cis Spreading and Promotes Heterochromatic Gene Silencing |
Q26786228 | An Ancient Yeast for Young Geneticists: A Primer on the Schizosaccharomyces pombe Model System |
Q33304439 | An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1. |
Q27671800 | An extended dsRBD with a novel zinc-binding motif mediates nuclear retention of fission yeast Dicer |
Q36287893 | Analysis of Drosophila species genome size and satellite DNA content reveals significant differences among strains as well as between species |
Q24655215 | Analysis of small RNA in fission yeast; centromeric siRNAs are potentially generated through a structured RNA |
Q34562251 | Asf1/HIRA Facilitate Global Histone Deacetylation and Associate with HP1 to Promote Nucleosome Occupancy at Heterochromatic Loci |
Q53253347 | Assembly and Functions of Heterochromatin in the Fission Yeast Genome |
Q41356353 | Balance between distinct HP1 family proteins controls heterochromatin assembly in fission yeast |
Q38105192 | Brc1 links replication stress response and centromere function |
Q64103229 | Bub1 kinase- and H2A phosphorylation-independent regulation of Shugoshin proteins under glucose-restricted conditions |
Q28727510 | CENP-B Cooperates with Set1 in Bidirectional Transcriptional Silencing and Genome Organization of Retrotransposons |
Q46793624 | Cell cycle control of centromeric repeat transcription and heterochromatin assembly |
Q42989297 | Cell cycle-dependent accumulation of histone H3.3 and euchromatic histone modifications in pericentromeric heterochromatin in response to a decrease in DNA methylation levels |
Q92295550 | Cellular Dynamics and Genomic Identity of Centromeres in Cereal Blast Fungus |
Q60938313 | Centromere and Pericentromere Transcription: Roles and Regulation … in Sickness and in Health |
Q38023244 | Centromeres of filamentous fungi |
Q40758954 | Centromeric barrier disruption leads to mitotic defects in Schizosaccharomyces pombe |
Q33597872 | Centromeric localization of dispersed Pol III genes in fission yeast. |
Q35172232 | Characterization of the short RNAs bound by the P19 suppressor of RNA silencing in mouse embryonic stem cells |
Q33760091 | Characterization of the small RNA content of Trypanosoma cruzi extracellular vesicles. |
Q33312107 | Checkpoint effects and telomere amplification during DNA re-replication in fission yeast |
Q33311412 | Checkpoint independence of most DNA replication origins in fission yeast |
Q42090694 | Chp1-Tas3 interaction is required to recruit RITS to fission yeast centromeres and for maintenance of centromeric heterochromatin. |
Q37591539 | Chromatin remodeling by the small RNA machinery in mammalian cells |
Q26827448 | Chromosome boundary elements and regulation of heterochromatin spreading |
Q36137510 | Chromosome domain architecture and dynamic organization of the fission yeast genome. |
Q35497934 | Chromosome segregation and organization are targets of 5'-Fluorouracil in eukaryotic cells |
Q35047551 | Clustered regulatory elements at nucleosome-depleted regions punctuate a constant nucleosomal landscape in Schizosaccharomyces pombe |
Q35737747 | Cohesin-dependent globules and heterochromatin shape 3D genome architecture in S. pombe |
Q36932903 | Comparative transcriptome analysis of small noncoding RNAs in different stages of Trypanosoma brucei |
Q82212529 | Competing to destroy: a fight between two RNA-degradation systems |
Q37773106 | Confining euchromatin/heterochromatin territory: jumonji crosses the line |
Q89686824 | Conserved chromosomal functions of RNA interference |
Q36419788 | Conserved factor Dhp1/Rat1/Xrn2 triggers premature transcription termination and nucleates heterochromatin to promote gene silencing |
Q94948190 | Conserved protein Pir2ARS2 mediates gene repression through cryptic introns in lncRNAs |
Q35301089 | Defects in RNA quality control factors reveal RNAi-independent nucleation of heterochromatin. |
Q41735227 | Defining heterochromatin in C. elegans through genome-wide analysis of the heterochromatin protein 1 homolog HPL-2. |
Q35171295 | Determinants of heterochromatic siRNA biogenesis and function |
Q53283775 | Dicer associates with chromatin to repress genome activity in Schizosaccharomyces pombe |
Q33668649 | Dicer is associated with ribosomal DNA chromatin in mammalian cells |
Q34487325 | Dicer-independent primal RNAs trigger RNAi and heterochromatin formation |
Q35903171 | Different means, same end—heterochromatin formation by RNAi and RNAi-independent RNA processing factors in fission yeast |
Q35978300 | Dimethylated H3K27 Is a Repressive Epigenetic Histone Mark in the Protist Entamoeba histolytica and Is Significantly Enriched in Genes Silenced via the RNAi Pathway |
Q46185049 | Dissecting Arabidopsis thaliana DICER function in small RNA processing, gene silencing and DNA methylation patterning |
Q54967259 | Distinct 'safe zones' at the nuclear envelope ensure robust replication of heterochromatic chromosome regions. |
Q35020139 | Distinct DNA methylation patterns associated with active and inactive centromeres of the maize B chromosome |
Q34338241 | Distinct roles for Sir2 and RNAi in centromeric heterochromatin nucleation, spreading and maintenance. |
Q80195998 | Distinct roles of HDAC complexes in promoter silencing, antisense suppression and DNA damage protection |
Q37211356 | Diverse roles of HP1 proteins in heterochromatin assembly and functions in fission yeast. |
Q26851994 | Diversity in requirement of genetic and epigenetic factors for centromere function in fungi |
Q37098598 | Domesticated DNA transposon proteins mediate retrotransposon control |
Q36881872 | Dynamic transcriptome of Schizosaccharomyces pombe shown by RNA-DNA hybrid mapping |
Q35239502 | Element 1360 and RNAi components contribute to HP1-dependent silencing of a pericentric reporter |
Q37345835 | Elimination of shelterin components bypasses RNAi for pericentric heterochromatin assembly |
Q36687330 | Enhancer of Rudimentary Cooperates with Conserved RNA-Processing Factors to Promote Meiotic mRNA Decay and Facultative Heterochromatin Assembly |
Q37185627 | Epe1 recruits BET family bromodomain protein Bdf2 to establish heterochromatin boundaries |
Q38541784 | Epigenetic Regulation of Chromatin States in Schizosaccharomyces pombe |
Q48075232 | Epigenetic modification of centromeric chromatin: hypomethylation of DNA sequences in the CENH3-associated chromatin in Arabidopsis thaliana and maize |
Q36981211 | Epigenetic regulation of centromeric chromatin: old dogs, new tricks? |
Q33622619 | Epigenetic regulation of heterochromatic DNA stability |
Q37384283 | Epigenetics: heterochromatin meets RNAi. |
Q51544587 | Euchromatic Subdomains in Rice Centromeres Are Associated with Genes and Transcription |
Q34789444 | Evidence for Two Different Regulatory Mechanisms Linking Replication and Segregation of Vibrio cholerae Chromosome II |
Q25257059 | Evolutionary-conserved telomere-linked helicase genes of fission yeast are repressed by silencing factors, RNAi components and the telomere-binding protein Taz1 |
Q34924069 | Fission yeast Cactin restricts telomere transcription and elongation by controlling Rap1 levels |
Q35914168 | Fission yeast Lem2 and Man1 perform fundamental functions of the animal cell nuclear lamina |
Q89542319 | Fission yeast telosomes: non-canonical histone-containing chromatin structures dependent on shelterin and RNA |
Q36440376 | Gene Expression and Chromatin Modifications Associated with Maize Centromeres |
Q37077306 | Genome-wide approaches to studying chromatin modifications |
Q41893574 | Genome-wide localization of pre-RC sites and identification of replication origins in fission yeast |
Q82679247 | Genome-wide patterns of histone modifications in fission yeast |
Q36567360 | Genome-wide patterns of histone modifications in yeast. |
Q36306107 | Genome-wide redistribution of H3K27me3 is linked to genotoxic stress and defective growth |
Q50720987 | Genomic and genetic characterization of rice Cen3 reveals extensive transcription and evolutionary implications of a complex centromere |
Q41461673 | Global regulation of heterochromatin spreading by Leo1. |
Q36421393 | Global role for polyadenylation-assisted nuclear RNA degradation in posttranscriptional gene silencing |
Q31098054 | Graph rigidity reveals well-constrained regions of chromosome conformation embeddings |
Q35079154 | H3.3 is deposited at centromeres in S phase as a placeholder for newly assembled CENP-A in G1phase |
Q33641829 | H3K9 methylation and RNA interference regulate nucleolar organization and repeated DNA stability |
Q36380674 | H3K9 methylation extends across natural boundaries of heterochromatin in the absence of an HP1 protein |
Q33799141 | H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases. |
Q33688942 | HAATI survivors replace canonical telomeres with blocks of generic heterochromatin. |
Q36866340 | HDAC-mediated suppression of histone turnover promotes epigenetic stability of heterochromatin. |
Q34091900 | Hairpin RNA induces secondary small interfering RNA synthesis and silencing in trans in fission yeast |
Q42074056 | Heterochromatin assembly and transcriptome repression by Set1 in coordination with a class II histone deacetylase |
Q36408600 | Heterochromatin assembly: a new twist on an old model |
Q34057278 | Heterochromatin controls γH2A localization in Neurospora crassa |
Q41763284 | Heterochromatin is required for normal distribution of Neurospora crassa CenH3. |
Q29614716 | Heterochromatin revisited |
Q60911595 | Heterochromatin suppresses gross chromosomal rearrangements at centromeres by repressing Tfs1/TFIIS-dependent transcription |
Q27654666 | High-Affinity Binding of Chp1 Chromodomain to K9 Methylated Histone H3 Is Required to Establish Centromeric Heterochromatin |
Q33276641 | High-resolution mapping reveals links of HP1 with active and inactive chromatin components |
Q35917373 | Highly condensed chromatins are formed adjacent to subtelomeric and decondensed silent chromatin in fission yeast |
Q37352034 | Histone H2A.Z cooperates with RNAi and heterochromatin factors to suppress antisense RNAs |
Q42410347 | Histone H2B mutations in inner region affect ubiquitination, centromere function, silencing and chromosome segregation |
Q36914566 | Histone H3K36 trimethylation is essential for multiple silencing mechanisms in fission yeast |
Q50278958 | Histone H3K9 methylation is dispensable for Caenorhabditis elegans development but suppresses RNA:DNA hybrid-associated repeat instability |
Q54508771 | Histone modifications associated with both A and B chromosomes of maize. |
Q36110128 | Histone modifications rather than the novel regional centromeres of Zymoseptoria tritici distinguish core and accessory chromosomes |
Q33492759 | Histone modifications within the human X centromere region |
Q33581966 | Histone variant H2A.Z regulates centromere silencing and chromosome segregation in fission yeast |
Q47728065 | Host genome surveillance for retrotransposons by transposon-derived proteins |
Q36440470 | Hrp3 controls nucleosome positioning to suppress non-coding transcription in eu- and heterochromatin |
Q38308578 | Human heterochromatin proteins form large domains containing KRAB-ZNF genes |
Q34181375 | Identification of noncoding transcripts from within CENP-A chromatin at fission yeast centromeres. |
Q26787215 | Identification of the Drosophila X chromosome: The long and short of it |
Q33954447 | Independent Chromatin Binding of ARGONAUTE4 and SPT5L/KTF1 Mediates Transcriptional Gene Silencing |
Q36132266 | Inner Kinetochore Protein Interactions with Regional Centromeres of Fission Yeast |
Q28257767 | Insulators: exploiting transcriptional and epigenetic mechanisms |
Q36186352 | Intercepting noncoding messages between germline and soma |
Q37797693 | Interplay Between Different Epigenetic Modifications and Mechanisms |
Q35851886 | Intrinsic Toxicity of Unchecked Heterochromatin Spread Is Suppressed by Redundant Chromatin Boundary Functions in Schizosacchromyces pombe |
Q88447305 | Iron homeostasis regulates facultative heterochromatin assembly in adaptive genome control |
Q34987501 | Kinetochore function and chromosome segregation rely on critical residues in histones H3 and H4 in budding yeast |
Q91964937 | Leo1 is essential for the dynamic regulation of heterochromatin and gene expression during cellular quiescence |
Q35629825 | Linking DNA replication to heterochromatin silencing and epigenetic inheritance |
Q41807702 | Localization of Smc5/6 to centromeres and telomeres requires heterochromatin and SUMO, respectively |
Q37379964 | Long noncoding RNA-based chromatin control of germ cell differentiation: a yeast perspective. |
Q41904552 | Lsd1 and lsd2 control programmed replication fork pauses and imprinting in fission yeast |
Q34401568 | Mapping of long-range associations throughout the fission yeast genome reveals global genome organization linked to transcriptional regulation |
Q34998301 | Maternal depletion of Piwi, a component of the RNAi system, impacts heterochromatin formation in Drosophila |
Q34961833 | Mediator directs co-transcriptional heterochromatin assembly by RNA interference-dependent and -independent pathways |
Q42602804 | Mediator regulates non-coding RNA transcription at fission yeast centromeres. |
Q37772649 | Meiotic silencing in Caenorhabditis elegans |
Q36000122 | Mmi1 RNA surveillance machinery directs RNAi complex RITS to specific meiotic genes in fission yeast |
Q33315573 | Molecular landscape of modified histones in Drosophila heterochromatic genes and euchromatin-heterochromatin transition zones |
Q37682692 | Mtr4-like protein coordinates nuclear RNA processing for heterochromatin assembly and for telomere maintenance. |
Q34427885 | Multifaceted genome control by Set1 Dependent and Independent of H3K4 methylation and the Set1C/COMPASS complex |
Q39070444 | Multiple Transcriptional and Post-transcriptional Pathways Collaborate to Control Sense and Antisense RNAs of Tf2 Retroelements in Fission Yeast |
Q21559664 | Mutations disrupting histone methylation have different effects on replication timing in S. pombe centromere |
Q22066043 | Non-coding RNA |
Q34389118 | Noncoding RNAs and the borders of heterochromatin |
Q47968225 | Noncoding RNAs prevent spreading of a repressive histone mark |
Q54652558 | Noncoding RNAs prevent spreading of a repressive histone mark. |
Q89659307 | Nuclear Argonaute Piwi Gene Mutation Affects rRNA by Inducing rRNA Fragment Accumulation, Antisense Expression, and Defective Processing in Drosophila Ovaries |
Q41879000 | Nucleosome positioning and transcription: fission yeast CHD remodellers make their move |
Q36346077 | Organization of interphase chromatin |
Q21203755 | Origin of the cell nucleus, mitosis and sex: roles of intracellular coevolution |
Q64389118 | Pericentromere-Specific Cohesin Complex Prevents Meiotic Pericentric DNA Double-Strand Breaks and Lethal Crossovers |
Q35313303 | Phylogenetic Comparison of Small RNA-triggered Transcriptional Gene Silencing |
Q34168342 | Plant centromeric retrotransposons: a structural and cytogenetic perspective |
Q27316324 | Plasmodium falciparum heterochromatin protein 1 marks genomic loci linked to phenotypic variation of exported virulence factors |
Q36967399 | Plasticity and epigenetic inheritance of centromere-specific histone H3 (CENP-A)-containing nucleosome positioning in the fission yeast |
Q33293168 | Plasticity of fission yeast CENP-A chromatin driven by relative levels of histone H3 and H4. |
Q33626243 | Post-transcriptional regulation of meiotic genes by a nuclear RNA silencing complex |
Q83009550 | Primal RNAs: The end of the beginning? |
Q37083495 | Programmed fluctuations in sense/antisense transcript ratios drive sexual differentiation in S. pombe |
Q33867438 | Proteomic and functional analysis of the noncanonical poly(A) polymerase Cid14 |
Q45939916 | Quantitative Genome-Wide Measurements of Meiotic DNA Double-Strand Breaks and Protein Binding in S. pombe. |
Q33412565 | Quelling targets the rDNA locus and functions in rDNA copy number control |
Q37791749 | RAGs’ eye view of the immunoglobulin heavy chain gene locus |
Q59323656 | RETRACTED ARTICLE: DDB1 and Cul4 are necessary for gene silencing and heterochromatin formation at pericentromeric regions in Neurospora |
Q37467376 | RIP140 in thyroid hormone-repression and chromatin remodeling of Crabp1 gene during adipocyte differentiation |
Q34028020 | RITS—connecting transcription, RNA interference, and heterochromatin assembly in fission yeast |
Q82821093 | RNA Elimination Machinery Targeting Meiotic mRNAs Promotes Facultative Heterochromatin Formation |
Q28307996 | RNA Interference and Heterochromatin Assembly |
Q36692156 | RNA interference guides histone modification during the S phase of chromosomal replication. |
Q28301544 | RNA turnover and chromatin-dependent gene silencing |
Q52589225 | RNAi drives nonreciprocal translocations at eroding chromosome ends to establish telomere-free linear chromosomes |
Q35882142 | RNAi keeps Atf1-bound stress response genes in check at nuclear pores |
Q42228801 | RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol II. |
Q36561712 | RNAi triggered by specialized machinery silences developmental genes and retrotransposons |
Q30444096 | RNAi-dependent H3K27 methylation is required for heterochromatin formation and DNA elimination in Tetrahymena |
Q34422701 | RNAi-dependent formation of heterochromatin and its diverse functions |
Q50705038 | RNAs regulate biology |
Q34014307 | Rad3 decorates critical chromosomal domains with gammaH2A to protect genome integrity during S-Phase in fission yeast |
Q41848290 | Rad51 suppresses gross chromosomal rearrangement at centromere in Schizosaccharomyces pombe |
Q35400929 | Rapid epigenetic adaptation to uncontrolled heterochromatin spreading |
Q30583633 | Reconsideration of in silico siRNA design from a perspective of heterogeneous data integration: problems and solutions |
Q36120395 | Regional centromeres in the yeast Candida lusitaniae lack pericentromeric heterochromatin. |
Q64972475 | Regulation of ectopic heterochromatin-mediated epigenetic diversification by the JmjC family protein Epe1. |
Q47404896 | Regulation of transcriptional silencing and chromodomain protein localization at centromeric heterochromatin by histone H3 tyrosine 41 phosphorylation in fission yeast |
Q24651946 | Relics of repeat-induced point mutation direct heterochromatin formation in Neurospora crassa |
Q43638477 | Reorganization of chromatin is an early response to nitrogen starvation in Schizosaccharomyces pombe |
Q41324231 | Replication stress affects the fidelity of nucleosome-mediated epigenetic inheritance. |
Q34125334 | Repression of Meiotic Genes by Antisense Transcription and by Fkh2 Transcription Factor in Schizosaccharomyces pombe |
Q37454582 | Requirement for the ERI/DICER complex in endogenous RNA interference and sperm development in Caenorhabditis elegans |
Q42363593 | Restriction of Retrotransposon Mobilization in Schizosaccharomyces pombe by Transcriptional Silencing and Higher-Order Chromatin Organization |
Q36733927 | Rice as a model for centromere and heterochromatin research |
Q34742174 | Role for Cohesin in the Formation of a Heterochromatic Domain at Fission Yeast Subtelomeres |
Q35954431 | Role of Ccr4-Not complex in heterochromatin formation at meiotic genes and subtelomeres in fission yeast |
Q37961784 | Roles of RNAi in Chromatin Regulation and Epigenetic Inheritance |
Q46698178 | Roles of the Clr4 methyltransferase complex in nucleation, spreading and maintenance of heterochromatin. |
Q50789005 | SNF2 Family Protein Fft3 Suppresses Nucleosome Turnover to Promote Epigenetic Inheritance and Proper Replication |
Q33294061 | SREBP controls oxygen-dependent mobilization of retrotransposons in fission yeast |
Q36244337 | Schizosaccharomyces pombe Hat1 (Kat1) is associated with Mis16 and is required for telomeric silencing. |
Q82718379 | Schizosaccharomyces pombe genome-wide nucleosome mapping reveals positioning mechanisms distinct from those of Saccharomyces cerevisiae |
Q34545114 | Selective elimination of messenger RNA prevents an incidence of untimely meiosis |
Q45141810 | Shelterin components mediate genome reorganization in response to replication stress. |
Q36534220 | Shugoshin forms a specialized chromatin domain at subtelomeres that regulates transcription and replication timing. |
Q27327527 | Silencing motifs in the Clr2 protein from fission yeast, Schizosaccharomyces pombe |
Q37560585 | Silent chromatin at the middle and ends: lessons from yeasts |
Q42601136 | Sir2 is required for Clr4 to initiate centromeric heterochromatin assembly in fission yeast. |
Q37079516 | Small RNA-directed heterochromatin formation in the context of development: what flies might learn from fission yeast |
Q38071437 | Small RNAs in Germline Development |
Q28307317 | Small RNAs in transcriptional gene silencing and genome defence |
Q36974244 | Specialization and evolution of endogenous small RNA pathways |
Q38629913 | Spt6 is required for heterochromatic silencing in the fission yeast Schizosaccharomyces pombe. |
Q34102684 | Stc1: a critical link between RNAi and chromatin modification required for heterochromatin integrity. |
Q35780099 | Strong epigenetic similarity between maize centromeric and pericentromeric regions at the level of small RNAs, DNA methylation and H3 chromatin modifications. |
Q37340740 | Subnuclear relocalization and silencing of a chromosomal region by an ectopic ribosomal DNA repeat. |
Q46293830 | Subtelomeres constitute a safeguard for gene expression and chromosome homeostasis. |
Q89610403 | Subtelomeric Transcription and its Regulation |
Q39094256 | Survival in Quiescence Requires the Euchromatic Deployment of Clr4/SUV39H by Argonaute-Associated Small RNAs |
Q52327611 | TOR complex 2 in fission yeast is required for chromatin-mediated gene silencing and assembly of heterochromatic domains at subtelomeres. |
Q35618796 | TRAMP-mediated RNA surveillance prevents spurious entry of RNAs into the Schizosaccharomyces pombe siRNA pathway |
Q51719045 | Taz1-Shelterin Promotes Facultative Heterochromatin Assembly at Chromosome-Internal Sites Containing Late Replication Origins. |
Q46162198 | Ten principles of heterochromatin formation and function. |
Q42378042 | The 19S proteasome is directly involved in the regulation of heterochromatin spreading in fission yeast |
Q48163258 | The 19S proteasome regulates subtelomere silencing and facultative heterochromatin formation in fission yeast |
Q34586818 | The Clr7 and Clr8 directionality factors and the Pcu4 cullin mediate heterochromatin formation in the fission yeast Schizosaccharomyces pombe |
Q36819834 | The Cul4-Ddb1Cdt2 Ubiquitin Ligase Inhibits Invasion of a Boundary-Associated Antisilencing Factor into Heterochromatin |
Q33855659 | The FUN30 chromatin remodeler, Fft3, protects centromeric and subtelomeric domains from euchromatin formation |
Q34703724 | The JmjC domain protein Epe1 prevents unregulated assembly and disassembly of heterochromatin |
Q38583047 | The Long Terminal Repeat Retrotransposons Tf1 and Tf2 of Schizosaccharomyces pombe |
Q35827849 | The Paf1 complex factors Leo1 and Paf1 promote local histone turnover to modulate chromatin states in fission yeast |
Q30884260 | The Schizosaccharomyces pombe JmjC-protein, Msc1, prevents H2A.Z localization in centromeric and subtelomeric chromatin domains |
Q34016589 | The Set1/COMPASS histone H3 methyltransferase helps regulate mitosis with the CDK1 and NIMA mitotic kinases in Aspergillus nidulans |
Q42112994 | The centromeric retrotransposons of rice are transcribed and differentially processed by RNA interference |
Q36408543 | The contradictory definitions of heterochromatin: transcription and silencing. |
Q37122968 | The double-stranded RNA binding domain of human Dicer functions as a nuclear localization signal |
Q98178019 | The epigenetic regulation of centromeres and telomeres in plants and animals |
Q90249962 | The euchromatic histone mark H3K36me3 preserves heterochromatin through sequestration of an acetyltransferase complex in fission yeast |
Q64883396 | The heterochromatin protein Swi6/HP1 activates replication origins at the pericentromeric region and silent mating-type locus. |
Q33429021 | The impact of local genome sequence on defining heterochromatin domains |
Q27937035 | The inner nuclear membrane protein Src1 associates with subtelomeric genes and alters their regulated gene expression |
Q41977257 | The kinetochore proteins Pcs1 and Mde4 and heterochromatin are required to prevent merotelic orientation |
Q35786141 | The many faces of Dicer: the complexity of the mechanisms regulating Dicer gene expression and enzyme activities |
Q35016886 | The potential regulation of L1 mobility by RNA interference. |
Q36452595 | The principles of guiding by RNA: chimeric RNA-protein enzymes |
Q35888810 | The telomeric transcriptome of Schizosaccharomyces pombe. |
Q34179511 | Transcription and RNA interference in the formation of heterochromatin. |
Q53650265 | Transcription and histone modifications in the recombination-free region spanning a rice centromere |
Q38159962 | Transcription and ncRNAs: at the cent(rome)re of kinetochore assembly and maintenance |
Q39846304 | Transcription facilitates sister chromatid cohesion on chromosomal arms |
Q26863161 | Transcriptional regulation at the yeast nuclear envelope |
Q57973165 | Two different Argonaute complexes are required for siRNA generation and heterochromatin assembly in fission yeast |
Q34793131 | UCSC genome browser: deep support for molecular biomedical research |
Q53659537 | Ubiquitin ligase component Cul4 associates with Clr4 histone methyltransferase to assemble heterochromatin |
Q35748195 | Uncoupling of Genomic and Epigenetic Signals in the Maintenance and Inheritance of Heterochromatin Domains in Fission Yeast |
Q90622274 | Unprogrammed epigenetic variation mediated by stochastic formation of ectopic heterochromatin |
Q41495422 | Untimely expression of gametogenic genes in vegetative cells causes uniparental disomy. |
Q90286803 | Vigilin protein Vgl1 is required for heterochromatin-mediated gene silencing in Schizosaccharomyces pombe |
Q28585218 | WDHD1 modulates the post-transcriptional step of the centromeric silencing pathway |
Q34338855 | Yeast X-chromosome-associated protein 5 (Xap5) functions with H2A.Z to suppress aberrant transcripts |
Q36954795 | siRNA-mediated heterochromatin establishment requires HP1 and is associated with antisense transcription |
Q82735335 | tRNA genes as chromatin barriers |
Q39790559 | γH2A-Binding Protein Brc1 Affects Centromere Function in Fission Yeast |
Search more.