| scholarly article | Q13442814 |
| P50 | author | Julie Ahringer | Q15709495 |
| Jason D Lieb | Q109084133 | ||
| Tao Liu | Q30347456 | ||
| Isabel Latorre | Q35703615 | ||
| Paulina Kolasinska-Zwierz | Q42458264 | ||
| Abby Dernburg | Q43167372 | ||
| Andreas Rechtsteiner | Q56515002 | ||
| Susan Strome | Q65088229 | ||
| P2093 | author name string | X Shirley Liu | |
| Arshad Desai | |||
| Hiroshi Kimura | |||
| Heidi Rosenbaum | |||
| A Leonardo Iniguez | |||
| Sevinc Ercan | |||
| Ming-Sin Cheung | |||
| Morten Jensen | |||
| Anne Vielle | |||
| Teruaki Takasaki | |||
| Hyunjin Shin | |||
| Thea A Egelhofer | |||
| Paulina Kolasinska-Zwierz | |||
| Kohta Ikegami | |||
| Scott Taing | |||
| P2860 | cites work | Combinatorial patterns of histone acetylations and methylations in the human genome | Q24647290 |
| The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets | Q24655245 | ||
| DOT1L/KMT4 recruitment and H3K79 methylation are ubiquitously coupled with gene transcription in mammalian cells | Q24655388 | ||
| A chromosomal memory triggered by Xist regulates histone methylation in X inactivation | Q24802695 | ||
| An integrated strategy to study muscle development and myofilament structure in Caenorhabditis elegans | Q27312196 | ||
| Genome sequence of the nematode C. elegans: a platform for investigating biology | Q27860527 | ||
| A comparison of normalization methods for high density oligonucleotide array data based on variance and bias | Q27860710 | ||
| Systematic functional analysis of the Caenorhabditis elegans genome using RNAi | Q27860839 | ||
| High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
| Chromatin modifications and their function | Q27861067 | ||
| Exploration, normalization, and summaries of high density oligonucleotide array probe level data | Q27861098 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| PR-Set7 is a nucleosome-specific methyltransferase that modifies lysine 20 of histone H4 and is associated with silent chromatin | Q28647369 | ||
| Meiotic recombination, noncoding DNA and genomic organization in Caenorhabditis elegans | Q28769447 | ||
| Partitioning and plasticity of repressive histone methylation states in mammalian chromatin | Q29614513 | ||
| CEAS: cis-regulatory element annotation system | Q30872386 | ||
| Model-based analysis of two-color arrays (MA2C). | Q33295457 | ||
| Molecular landscape of modified histones in Drosophila heterochromatic genes and euchromatin-heterochromatin transition zones | Q33315573 | ||
| The genomic distribution and function of histone variant HTZ-1 during C. elegans embryogenesis | Q33369072 | ||
| Recombinational landscape and population genomics of Caenorhabditis elegans | Q33417666 | ||
| Identification of genes expressed in the hermaphrodite germ line of C. elegans using SAGE. | Q33441953 | ||
| Partitioning the C. elegans genome by nucleosome modification, occupancy, and positioning | Q33587754 | ||
| Epigenetic regulation of heterochromatic DNA stability | Q33622619 | ||
| Cytoskeletal forces span the nuclear envelope to coordinate meiotic chromosome pairing and synapsis. | Q33674350 | ||
| The histone H3K36 methyltransferase MES-4 acts epigenetically to transmit the memory of germline gene expression to progeny. | Q33686906 | ||
| A native chromatin purification system for epigenomic profiling in Caenorhabditis elegans | Q33700093 | ||
| The profile of repeat-associated histone lysine methylation states in the mouse epigenome | Q33868292 | ||
| Targeting X chromosomes for repression | Q34003258 | ||
| A cellular memory of developmental history generates phenotypic diversity in C. elegans | Q34343843 | ||
| Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH. | Q34439696 | ||
| Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 | Q34613778 | ||
| Trans-generational epigenetic regulation of C. elegans primordial germ cells | Q34622455 | ||
| Intron size correlates positively with recombination rate in Caenorhabditis elegans | Q34644075 | ||
| C. elegans nuclear envelope proteins emerin, MAN1, lamin, and nucleoporins reveal unique timing of nuclear envelope breakdown during mitosis | Q34757049 | ||
| Members of the H3K4 trimethylation complex regulate lifespan in a germline-dependent manner in C. elegans | Q34784199 | ||
| HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis | Q35619440 | ||
| Chromosome sites play dual roles to establish homologous synapsis during meiosis in C. elegans | Q35619465 | ||
| "Holo"er than thou: chromosome segregation and kinetochore function in C. elegans | Q35853959 | ||
| Mouse centric and pericentric satellite repeats form distinct functional heterochromatin | Q36322196 | ||
| MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in the C. elegans germ line. | Q36731942 | ||
| X-Chromosome dosage compensation | Q37020494 | ||
| Germline chromatin | Q37020713 | ||
| Differential chromatin marking of introns and expressed exons by H3K36me3. | Q37111430 | ||
| A condensin-like dosage compensation complex acts at a distance to control expression throughout the genome | Q37135166 | ||
| X chromosome repression by localization of the C. elegans dosage compensation machinery to sites of transcription initiation | Q37367035 | ||
| Biochemical mechanisms of gene regulation by polycomb group protein complexes | Q37432734 | ||
| The C. elegans dosage compensation complex propagates dynamically and independently of X chromosome sequence | Q37437773 | ||
| Identification of chromosome sequence motifs that mediate meiotic pairing and synapsis in C. elegans | Q37727084 | ||
| PR-Set7-mediated monomethylation of histone H4 lysine 20 at specific genomic regions induces transcriptional repression | Q39698399 | ||
| The organization of histone H3 modifications as revealed by a panel of specific monoclonal antibodies | Q40129996 | ||
| A family of zinc-finger proteins is required for chromosome-specific pairing and synapsis during meiosis in C. elegans. | Q45933828 | ||
| Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans | Q47327774 | ||
| Composition and dynamics of the Caenorhabditis elegans early embryonic transcriptome. | Q52110050 | ||
| The kinetochores of Caenorhabditis elegans | Q70598101 | ||
| P433 | issue | 2 | |
| P921 | main subject | Caenorhabditis elegans | Q91703 |
| P304 | page(s) | 227-236 | |
| P577 | publication date | 2010-12-22 | |
| P1433 | published in | Genome Research | Q5533485 |
| P1476 | title | Broad chromosomal domains of histone modification patterns in C. elegans | |
| P478 | volume | 21 |
| Q90720382 | "Lessons from the extremes: Epigenetic and genetic regulation in point monocentromere and holocentromere establishment on artificial chromosomes" |
| Q64114668 | A DNA repair protein and histone methyltransferase interact to promote genome stability in the Caenorhabditis elegans germ line |
| Q49837559 | A Role for Mono-methylation of Histone H3-K27 in Gene Activity in Drosophila. |
| Q28730938 | A differential sequencing-based analysis of the C. elegans noncoding transcriptome |
| Q33576338 | A histone methylation network regulates transgenerational epigenetic memory in C. elegans |
| Q35976800 | A streamlined tethered chromosome conformation capture protocol. |
| Q33574854 | A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress |
| Q37099127 | An Abundant Class of Non-coding DNA Can Prevent Stochastic Gene Silencing in the C. elegans Germline. |
| Q57146396 | An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues |
| Q36511978 | An inverse relationship to germline transcription defines centromeric chromatin in C. elegans |
| Q36150010 | Anchoring of Heterochromatin to the Nuclear Lamina Reinforces Dosage Compensation-Mediated Gene Repression. |
| Q41960310 | Antagonism between MES-4 and Polycomb repressive complex 2 promotes appropriate gene expression in C. elegans germ cells |
| Q27022640 | Antigenic variation and the generation of diversity in malaria parasites |
| Q89610617 | Artificial generation of centromeres and kinetochores to understand their structure and function |
| Q42107385 | BLIMP-1/BLMP-1 and Metastasis-Associated Protein Regulate Stress Resistant Development in Caenorhabditis elegans. |
| Q38170221 | C. elegans epigenetic regulation in development and aging |
| Q90082889 | C. elegans synMuv B proteins regulate spatial and temporal chromatin compaction during development |
| Q28742637 | Caenorhabditis briggsae recombinant inbred line genotypes reveal inter-strain incompatibility and the evolution of recombination |
| Q90848690 | Caenorhabditis elegans as an emerging model system in environmental epigenetics |
| Q34613778 | Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 |
| Q35943305 | Caenorhabditis elegans dosage compensation regulates histone H4 chromatin state on X chromosomes |
| Q57425003 | Caenorhabditis elegans sperm carry a histone-based epigenetic memory of both spermatogenesis and oogenesis |
| Q45943868 | Chromatin accessibility dynamics reveal novel functional enhancers in C. elegans. |
| Q37983891 | Chromatin insulator elements: establishing barriers to set heterochromatin boundaries |
| Q42352275 | Chromatin signature discovery via histone modification profile alignments. |
| Q42376666 | Chromatin states responsible for the regulation of differentially expressed genes under 60Co~γ ray radiation in rice. |
| Q89946693 | Chromosome-Level Assembly of the Caenorhabditis remanei Genome Reveals Conserved Patterns of Nematode Genome Organization |
| Q21184018 | Cistrome: an integrative platform for transcriptional regulation studies |
| Q34486035 | Comparative analysis of metazoan chromatin organization |
| Q38367824 | Computational methodology for ChIP-seq analysis |
| Q34670135 | Condensin-driven remodelling of X chromosome topology during dosage compensation. |
| Q90110548 | Crossover Position Drives Chromosome Remodeling for Accurate Meiotic Chromosome Segregation |
| Q37412741 | Crossover heterogeneity in the absence of hotspots in Caenorhabditis elegans |
| Q33879043 | Crossover recombination mediated by HIM-18/SLX4-associated nucleases. |
| Q36637692 | Current trends in the development and application of molecular technologies for cancer epigenetics |
| Q37644161 | Decoupling the downstream effects of germline nuclear RNAi reveals that H3K9me3 is dispensable for heritable RNAi and the maintenance of endogenous siRNA-mediated transcriptional silencing in Caenorhabditis elegans |
| Q41735227 | Defining heterochromatin in C. elegans through genome-wide analysis of the heterochromatin protein 1 homolog HPL-2. |
| Q90196326 | Distinct functions and temporal regulation of methylated histone H3 during early embryogenesis |
| Q34036755 | Duplication and retention biases of essential and non-essential genes revealed by systematic knockdown analyses |
| Q52374550 | Dynamic Control of Chromosome Topology and Gene Expression by a Chromatin Modification. |
| Q46315066 | Dynamic Control of X Chromosome Conformation and Repression by a Histone H4K20 Demethylase. |
| Q34611127 | Dynamic epigenetic regulation of gene expression during the life cycle of malaria parasite Plasmodium falciparum |
| Q36263760 | Effect of mutation mechanisms on variant composition and distribution in Caenorhabditis elegans |
| Q36130861 | Effects of ADARs on small RNA processing pathways in C. elegans |
| Q35556683 | Embryonic stem cell specific "master" replication origins at the heart of the loss of pluripotency |
| Q33716759 | Emerging roles of chromatin in the maintenance of genome organization and function in plants |
| Q41139907 | Engineering new balancer chromosomes in C. elegans via CRISPR/Cas9 |
| Q36012704 | Enrichment of H3K9me2 on Unsynapsed Chromatin in Caenorhabditis elegans Does Not Target de Novo Sites |
| Q47105601 | Epigenetic Transitions and Knotted Solitons in Stretched Chromatin. |
| Q38042887 | Epigenetic landscape and miRNA involvement during neural crest development |
| Q37871545 | Epigenetics in C. elegans: facts and challenges |
| Q27320001 | Evolutionary change within a bipotential switch shaped the sperm/oocyte decision in hermaphroditic nematodes |
| Q38245426 | Expanded genetic code technologies for incorporating modified lysine at multiple sites |
| Q35910252 | Finding a balance: how diverse dosage compensation strategies modify histone h4 to regulate transcription |
| Q40812076 | Frequency and mitotic heritability of epimutations in Schistosoma mansoni |
| Q38086775 | Functional implications of genome topology. |
| Q30358248 | Generation and purification of highly specific antibodies for detecting post-translationally modified proteins in vivo. |
| Q38828884 | Genetic sources of population epigenomic variation |
| Q38578607 | Genome architecture: from linear organisation of chromatin to the 3D assembly in the nucleus |
| Q38709880 | Genome-wide analysis of condensin binding in Caenorhabditis elegans |
| Q55520981 | Genome-wide expert annotation of the epigenetic machinery of the plant-parasitic nematodes Meloidogyne spp., with a focus on the asexually reproducing species. |
| Q40395325 | Genome-wide prediction and analysis of human chromatin boundary elements |
| Q35534936 | Genome-wide profiling of the C. elegans dsRNAome |
| Q38930532 | Germ Granules Prevent Accumulation of Somatic Transcripts in the Adult Caenorhabditis elegans Germline |
| Q38208754 | Getting down to the core of histone modifications |
| Q33797064 | Global effects of the CSR-1 RNA interference pathway on the transcriptional landscape |
| Q34690818 | Global remodeling of nucleosome positions in C. elegans |
| Q64923274 | H3.3K27M-induced chromatin changes drive ectopic replication through misregulation of the JNK pathway in C. elegans. |
| Q36676559 | H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans |
| Q100526363 | H3K4me2 regulates the recovery of protein biosynthesis and homeostasis following DNA damage |
| Q27331824 | H4K20me1 contributes to downregulation of X-linked genes for C. elegans dosage compensation |
| Q27021442 | HP1a: a structural chromosomal protein regulating transcription |
| Q42588662 | High nucleosome occupancy is encoded at X-linked gene promoters in C. elegans |
| Q34350965 | Histone H2B monoubiquitination facilitates the rapid modulation of gene expression during Arabidopsis photomorphogenesis |
| Q52589500 | Histone H3K9 and H4 Acetylations and Transcription Facilitate the Initial CENP-AHCP-3 Deposition and De Novo Centromere Establishment in Caenorhabditis elegans Artificial Chromosomes. |
| Q50278958 | Histone H3K9 methylation is dispensable for Caenorhabditis elegans development but suppresses RNA:DNA hybrid-associated repeat instability. |
| Q38064095 | Histone lysine methylation dynamics: establishment, regulation, and biological impact |
| Q36110128 | Histone modifications rather than the novel regional centromeres of Zymoseptoria tritici distinguish core and accessory chromosomes |
| Q26770526 | Histones and histone modifications in perinuclear chromatin anchoring: from yeast to man |
| Q34414322 | Holocentromeres are dispersed point centromeres localized at transcription factor hotspots |
| Q37591542 | Homeland security in the C. elegans germ line: insights into the biogenesis and function of piRNAs |
| Q35018004 | Human genome replication proceeds through four chromatin states. |
| Q36218592 | Hyperhomocysteinemia in ApoE-/- Mice Leads to Overexpression of Enhancer of Zeste Homolog 2 via miR-92a Regulation |
| Q28301622 | Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project |
| Q24632836 | Integrative epigenomic mapping defines four main chromatin states in Arabidopsis |
| Q92875181 | Interplay between small RNA pathways shapes chromatin landscapes in C. elegans |
| Q28513559 | Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis |
| Q64993308 | Isolated C. elegans germ nuclei exhibit distinct genomic profiles of histone modification and gene expression. |
| Q38910234 | Joint annotation of chromatin state and chromatin conformation reveals relationships among domain types and identifies domains of cell-type-specific expression |
| Q37105600 | KdmA, a histone H3 demethylase with bipartite function, differentially regulates primary and secondary metabolism in Aspergillus nidulans |
| Q36075422 | LHP1 Regulates H3K27me3 Spreading and Shapes the Three-Dimensional Conformation of the Arabidopsis Genome. |
| Q91595909 | LSM2-8 and XRN-2 contribute to the silencing of H3K27me3-marked genes through targeted RNA decay |
| Q89916726 | Lamina-Dependent Stretching and Unconventional Chromosome Compartments in Early C. elegans Embryos |
| Q33698066 | Locking the genome: nuclear organization and cell fate |
| Q90089208 | Loss of an H3K9me anchor rescues laminopathy-linked changes in nuclear organization and muscle function in an Emery-Dreifuss muscular dystrophy model |
| Q33352054 | Making sense of chromatin states |
| Q92060510 | Mapping the dsRNA World |
| Q35002469 | Mechanisms of x chromosome dosage compensation |
| Q26991732 | Meiotic development in Caenorhabditis elegans |
| Q37371435 | Meiotic recombination and the crossover assurance checkpoint in Caenorhabditis elegans |
| Q38624791 | Molecular mechanism of the priming by jasmonic acid of specific dehydration stress response genes in Arabidopsis |
| Q34479071 | Mos1-mediated transgenesis to probe consequences of single gene mutations in variation-rich isolates of Caenorhabditis elegans |
| Q35748969 | Nonconsensus Protein Binding to Repetitive DNA Sequence Elements Significantly Affects Eukaryotic Genomes |
| Q92889647 | Normal transcription of cellulolytic enzyme genes relies on the balance between the methylation of H3K36 and H3K4 in Penicillium oxalicum |
| Q37548517 | Nucleosome fragility is associated with future transcriptional response to developmental cues and stress in C. elegans |
| Q46282702 | PCSD: a plant chromatin state database |
| Q35604396 | Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expression |
| Q36915003 | RNAi pathways contribute to developmental history-dependent phenotypic plasticity in C. elegans |
| Q34018995 | Random and targeted transgene insertion in Caenorhabditis elegans using a modified Mos1 transposon |
| Q46334220 | Recruitment of histone modifications to assist mRNA dosage maintenance after degeneration of cytosine DNA methylation during animal evolution |
| Q46244949 | Regulation of Crossover Frequency and Distribution during Meiotic Recombination. |
| Q27316903 | Regulation of DCC localization by HTZ-1/H2A.Z and DPY-30 does not correlate with H3K4 methylation levels |
| Q37618160 | Regulation of the X chromosomes in Caenorhabditis elegans |
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| Q48148054 | Repressive Chromatin in Caenorhabditis elegans: Establishment, Composition, and Function |
| Q91798076 | Repressive H3K9me2 protects lifespan against the transgenerational burden of COMPASS activity in C. elegans |
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| Q27001247 | Seeing elegance in gene regulatory networks of the worm |
| Q58083591 | Sex and death: from cell fate specification to dynamic control of X-chromosome structure and gene expression |
| Q37589376 | Sex-specific chromatin landscapes in an ultra-compact chordate genome. |
| Q27026725 | Single molecule and single cell epigenomics. |
| Q37417986 | Stable Caenorhabditis elegans chromatin domains separate broadly expressed and developmentally regulated genes |
| Q38442406 | Structural organization of human replication timing domains. |
| Q35071703 | Summarizing specific profiles in Illumina sequencing from whole-genome amplified DNA. |
| Q42373230 | Taxonomically Restricted Genes with Essential Functions Frequently Play Roles in Chromosome Segregation in Caenorhabditis elegans and Saccharomyces cerevisiae |
| Q35754687 | The Epigenome of Schistosoma mansoni Provides Insight about How Cercariae Poise Transcription until Infection |
| Q55395376 | The Memory of Environmental Chemical Exposure in C. elegans Is Dependent on the Jumonji Demethylases jmjd-2 and jmjd-3/utx-1. |
| Q51033425 | The gastrula transition reorganizes replication-origin selection in Caenorhabditis elegans. |
| Q53108045 | The holocentric species Luzula elegans shows interplay between centromere and large-scale genome organization. |
| Q37061192 | The landscape of RNA polymerase II transcription initiation in C. elegans reveals promoter and enhancer architectures |
| Q37379029 | The shelterin protein POT-1 anchors Caenorhabditis elegans telomeres through SUN-1 at the nuclear periphery |
| Q27313726 | The specification and global reprogramming of histone epigenetic marks during gamete formation and early embryo development in C. elegans |
| Q37313695 | The time-resolved transcriptome of C. elegans |
| Q46572295 | Three-dimensional genome organization: a lesson from the Polycomb-Group proteins |
| Q53649784 | Time for the zebrafish ENCODE. |
| Q36113113 | Tissue- and Time-Specific Expression of Otherwise Identical tRNA Genes |
| Q51827112 | Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development. |
| Q92523616 | Transcription-independent TFIIIC-bound sites cluster near heterochromatin boundaries within lamina-associated domains in C. elegans |
| Q35125239 | Transcriptional control of a whole chromosome: emerging models for dosage compensation |
| Q38117116 | Transcriptional regulation of gene expression in C. elegans |
| Q36010849 | Transgenerational epigenetic inheritance of longevity in Caenorhabditis elegans |
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| Q28635111 | pENCODE: a plant encyclopedia of DNA elements |
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