| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Emmanuelle Fabre | Q57260761 |
| Christophe Zimmer | Q67484290 | ||
| P2860 | cites work | Initial genomics of the human nucleolus | Q21090208 |
| Population genomics of domestic and wild yeasts | Q22122208 | ||
| Chromosome territories, nuclear architecture and gene regulation in mammalian cells | Q22122379 | ||
| The chromosome end in yeast: its mosaic nature and influence on recombinational dynamics | Q24532914 | ||
| Gene recruitment of the activated INO1 locus to the nuclear membrane | Q24794933 | ||
| Life with 6000 genes | Q27860877 | ||
| Clustering of yeast tRNA genes is mediated by specific association of condensin with tRNA gene transcription complexes. | Q27932659 | ||
| RLF2, a subunit of yeast chromatin assembly factor-I, is required for telomeric chromatin function in vivo | Q27932921 | ||
| Telomere anchoring at the nuclear periphery requires the budding yeast Sad1-UNC-84 domain protein Mps3. | Q27934898 | ||
| The nuclear envelope and spindle pole body-associated Mps3 protein bind telomere regulators and function in telomere clustering | Q27936387 | ||
| Role for perinuclear chromosome tethering in maintenance of genome stability. | Q27936989 | ||
| The inner nuclear membrane protein Src1 associates with subtelomeric genes and alters their regulated gene expression | Q27937035 | ||
| Genetic and epigenetic regulation of the FLO gene family generates cell-surface variation in yeast | Q27937126 | ||
| Gene loops function to maintain transcriptional memory through interaction with the nuclear pore complex | Q27937326 | ||
| Esc1, a nuclear periphery protein required for Sir4-based plasmid anchoring and partitioning | Q27937349 | ||
| SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope | Q27937982 | ||
| Interaction of a DNA Zip Code with the Nuclear Pore Complex Promotes H2A.Z Incorporation and INO1 Transcriptional Memory | Q27938380 | ||
| Nucleoporins prevent DNA damage accumulation by modulating Ulp1-dependent sumoylation processes | Q27938451 | ||
| Nuclear pore complexes in the organization of silent telomeric chromatin | Q27939276 | ||
| Cdk phosphorylation of a nucleoporin controls localization of active genes through the cell cycle | Q27939682 | ||
| Nuclear architecture and spatial positioning help establish transcriptional states of telomeres in yeast. | Q27939863 | ||
| Suppression of homologous recombination by the Saccharomyces cerevisiae linker histone | Q27940005 | ||
| Colocalization of multiple DNA double-strand breaks at a single Rad52 repair centre | Q27940019 | ||
| DNA zip codes control an ancient mechanism for gene targeting to the nuclear periphery | Q27940091 | ||
| Specific distribution of the Saccharomyces cerevisiae linker histone homolog HHO1p in the chromatin | Q27940216 | ||
| Telomere tethering at the nuclear periphery is essential for efficient DNA double strand break repair in subtelomeric region | Q27940251 | ||
| Position effect at S. cerevisiae telomeres: reversible repression of Pol II transcription | Q28131683 | ||
| Comprehensive mapping of long-range interactions reveals folding principles of the human genome | Q28131819 | ||
| Capturing chromosome conformation | Q28201750 | ||
| Genome-wide localization of the nuclear transport machinery couples transcriptional status and nuclear organization | Q28261156 | ||
| Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions | Q28279406 | ||
| Histone H3 and H4 N-termini interact with SIR3 and SIR4 proteins: a molecular model for the formation of heterochromatin in yeast | Q29614857 | ||
| Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres | Q47946111 | ||
| Lab-on-Chip for fast 3D particle tracking in living cells | Q48833299 | ||
| Dynamics of DNA double-strand breaks revealed by clustering of damaged chromosome domains. | Q51830570 | ||
| The Smc5-Smc6 complex and SUMO modification of Rad52 regulates recombinational repair at the ribosomal gene locus. | Q53539192 | ||
| Comparative Genomics in Hemiascomycete Yeasts: Evolution of Sex, Silencing, and Subtelomeres | Q57009027 | ||
| Nuclear pore association confers optimal expression levels for an inducible yeast gene | Q59054249 | ||
| Evidence for silencing compartments within the yeast nucleus: a role for telomere proximity and Sir protein concentration in silencer-mediated repression | Q61783589 | ||
| Global identification of yeast chromosome interactions using Genome conformation capture | Q61784902 | ||
| Live-cell super-resolution imaging with trimethoprim conjugates | Q64027672 | ||
| Silent domains are assembled continuously from the telomere and are defined by promoter distance and strength, and by SIR3 dosage | Q72802227 | ||
| Centromere clustering is a major determinant of yeast interphase nuclear organization | Q73777745 | ||
| Localization of yeast telomeres to the nuclear periphery is separable from transcriptional repression and telomere stability functions | Q74394179 | ||
| Spatial organisation and behaviour of the parental chromosome sets in the nuclei of Saccharomyces cerevisiae x S. paradoxus hybrids | Q74796400 | ||
| Functional compartmentalization of the nucleus in the budding yeast Saccharomyces cerevisiae | Q77922968 | ||
| Live imaging of telomeres: yKu and Sir proteins define redundant telomere-anchoring pathways in yeast | Q78708973 | ||
| Actively transcribed GAL genes can be physically linked to the nuclear pore by the SAGA chromatin modifying complex | Q79421818 | ||
| Behaviour of nucleolus organizing regions (NORs) and nucleoli during mitotic and meiotic divisions in budding yeast | Q80337742 | ||
| Sir-mediated repression can occur independently of chromosomal and subnuclear contexts | Q81201128 | ||
| Recombination proteins in yeast | Q29617872 | ||
| Yeast kinetochore microtubule dynamics analyzed by high-resolution three-dimensional microscopy | Q30476783 | ||
| Intermingling of chromosome territories in interphase suggests role in translocations and transcription-dependent associations | Q33240304 | ||
| H2A.Z-mediated localization of genes at the nuclear periphery confers epigenetic memory of previous transcriptional state | Q33279444 | ||
| Recruitment to the nuclear periphery can alter expression of genes in human cells | Q33325909 | ||
| Structure and dynamics of interphase chromosomes | Q33363082 | ||
| Chromosome-wide Rad51 spreading and SUMO-H2A.Z-dependent chromosome fixation in response to a persistent DNA double-strand break | Q33409251 | ||
| Chromatin-bound nuclear pore components regulate gene expression in higher eukaryotes | Q33652562 | ||
| Chromosome arm length and nuclear constraints determine the dynamic relationship of yeast subtelomeres | Q33719988 | ||
| Nucleolus: from structure to dynamics | Q33991847 | ||
| High-resolution whole-genome sequencing reveals that specific chromatin domains from most human chromosomes associate with nucleoli | Q34136894 | ||
| SIR3 and SIR4 proteins are required for the positioning and integrity of yeast telomeres | Q34343500 | ||
| The concept of self-organization in cellular architecture | Q34403925 | ||
| Long-range directional movement of an interphase chromosome site | Q34516449 | ||
| Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C). | Q34573154 | ||
| Domains of gene silencing near the left end of chromosome III in Saccharomyces cerevisiae | Q34614877 | ||
| High-density mapping of single-molecule trajectories with photoactivated localization microscopy | Q34735689 | ||
| Nucleosome repeat length and linker histone stoichiometry determine chromatin fiber structure | Q34789571 | ||
| Chromosome positioning in the interphase nucleus | Q34831329 | ||
| Cotranscriptional recruitment to the mRNA export receptor Mex67p contributes to nuclear pore anchoring of activated genes | Q35131387 | ||
| Chromatin assembly factor I contributes to the maintenance, but not the re-establishment, of silencing at the yeast silent mating loci | Q35188576 | ||
| Collisions between yeast chromosomal loci in vivo are governed by three layers of organization | Q35201786 | ||
| Yeast telomeres exert a position effect on recombination between internal tracts of yeast telomeric DNA | Q35210267 | ||
| Lack of chromosome territoriality in yeast: promiscuous rejoining of broken chromosome ends. | Q35938806 | ||
| Centromere identity is specified by a single centromeric nucleosome in budding yeast | Q35990276 | ||
| Yeast evolution and comparative genomics | Q36118448 | ||
| Chromosome condensation and sister chromatid pairing in budding yeast | Q36234068 | ||
| The clustering of telomeres and colocalization with Rap1, Sir3, and Sir4 proteins in wild-type Saccharomyces cerevisiae | Q36237437 | ||
| Interaction of the bacteriophage P1 recombinase Cre with the recombining site loxP | Q36248787 | ||
| In vivo localization of DNA sequences and visualization of large-scale chromatin organization using lac operator/repressor recognition | Q36257776 | ||
| Actin-dependent intranuclear repositioning of an active gene locus in vivo. | Q36274498 | ||
| Chromosome looping in yeast: telomere pairing and coordinated movement reflect anchoring efficiency and territorial organization | Q36321341 | ||
| Controlled exchange of chromosomal arms reveals principles driving telomere interactions in yeast | Q36388826 | ||
| A genetic locus targeted to the nuclear periphery in living cells maintains its transcriptional competence | Q36404918 | ||
| Differential nuclear localization does not determine the silencing status of Saccharomyces cerevisiae telomeres | Q36416213 | ||
| Functional targeting of DNA damage to a nuclear pore-associated SUMO-dependent ubiquitin ligase | Q36456463 | ||
| Positional stability of single double-strand breaks in mammalian cells | Q36742792 | ||
| Meiotic chromosomes move by linkage to dynamic actin cables with transduction of force through the nuclear envelope | Q37013008 | ||
| Yeast silent mating type loci form heterochromatic clusters through silencer protein-dependent long-range interactions | Q37168902 | ||
| Yeast telomerase and the SUN domain protein Mps3 anchor telomeres and repress subtelomeric recombination | Q37175957 | ||
| Mechanisms that regulate localization of a DNA double-strand break to the nuclear periphery | Q37175976 | ||
| Separation of silencing from perinuclear anchoring functions in yeast Ku80, Sir4 and Esc1 proteins. | Q37270623 | ||
| Molecular analysis of the replication program in unicellular model organisms | Q37685965 | ||
| Long-range compaction and flexibility of interphase chromatin in budding yeast analyzed by high-resolution imaging techniques. | Q37692307 | ||
| Chromatin structure: does the 30-nm fibre exist in vivo? | Q37719900 | ||
| In vivo protein architecture of the eukaryotic kinetochore with nanometer scale accuracy | Q39413546 | ||
| Centromere position in budding yeast: evidence for anaphase A. | Q40387545 | ||
| A three-dimensional model of the yeast genome | Q40674029 | ||
| Conservation of relative chromosome positioning in normal and cancer cells | Q40700082 | ||
| Mapping in vivo chromatin interactions in yeast suggests an extended chromatin fiber with regional variation in compaction | Q41175894 | ||
| A network of nuclear envelope membrane proteins linking centromeres to microtubules | Q42044145 | ||
| Subdiffusive motion of a polymer composed of subdiffusive monomers | Q42070408 | ||
| Yeast nuclei display prominent centromere clustering that is reduced in nondividing cells and in meiotic prophase | Q42083945 | ||
| Nucleolar clustering of dispersed tRNA genes. | Q42116159 | ||
| A physiological role for gene loops in yeast. | Q42116820 | ||
| In Saccharomyces cerevisiae, yKu and subtelomeric core X sequences repress homologous recombination near telomeres as part of the same pathway | Q42590640 | ||
| Limitations of silencing at native yeast telomeres | Q42673247 | ||
| Higher order structure is present in the yeast nucleus: autoantibody probes demonstrate that the nucleolus lies opposite the spindle pole body | Q43740711 | ||
| Chromosome dynamics in the yeast interphase nucleus | Q43820233 | ||
| High-resolution statistical mapping reveals gene territories in live yeast | Q44852389 | ||
| The polar arrangement of telomeres in interphase and meiosis. Rabl organization and the bouquet | Q46225059 | ||
| Interphase chromosomes undergo constrained diffusional motion in living cells | Q46252294 | ||
| Nup-PI: the nucleopore-promoter interaction of genes in yeast | Q46925405 | ||
| Perinuclear localization of chromatin facilitates transcriptional silencing | Q47675987 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | nucleoprotein | Q419245 |
| cell | Q7868 | ||
| eukaryote | Q19088 | ||
| yeast | Q45422 | ||
| P304 | page(s) | 723-733 | |
| P577 | publication date | 2011-03-01 | |
| 2011-03-07 | |||
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Principles of chromosomal organization: lessons from yeast | |
| P478 | volume | 192 |
| Q35674570 | A decade of 3C technologies: insights into nuclear organization |
| Q38948551 | A decade of understanding spatio-temporal regulation of DNA repair by the nuclear architecture |
| Q35770629 | Accurate identification of centromere locations in yeast genomes using Hi-C. |
| Q28484846 | Allele-specific behavior of molecular networks: understanding small-molecule drug response in yeast |
| Q37343895 | An array of nuclear microtubules reorganizes the budding yeast nucleus during quiescence |
| Q35758599 | Analysis of Single Locus Trajectories for Extracting In Vivo Chromatin Tethering Interactions |
| Q54292741 | Analysis of interactions between genomic loci through Chromosome Conformation Capture (3C). |
| Q57465056 | Brr6 plays a role in gene recruitment and transcriptional regulation at the nuclear envelope |
| Q37423477 | Centromere tethering confines chromosome domains |
| Q37612740 | Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts |
| Q38685445 | Chromatin stiffening underlies enhanced locus mobility after DNA damage in budding yeast |
| Q36137510 | Chromosome domain architecture and dynamic organization of the fission yeast genome. |
| Q46805879 | Chromosome positioning and the clustering of functionally related loci in yeast is driven by chromosomal interactions |
| Q37417779 | Chromosome-refolding model of mating-type switching in yeast |
| Q35584337 | Comparative 3D genome structure analysis of the fission and the budding yeast |
| Q24622426 | Complete DNA sequence of Kuraishia capsulata illustrates novel genomic features among budding yeasts (Saccharomycotina) |
| Q43078159 | Csi1 illuminates the mechanism and function of Rabl configuration. |
| Q64389659 | DNA Repair: The Search for Homology |
| Q93116236 | DNA double-strand breaks in telophase lead to coalescence between segregated sister chromatid loci |
| Q37338273 | Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III-transcribed genes in budding yeast. |
| Q64099428 | Destabilization of chromosome structure by histone H3 lysine 27 methylation |
| Q40483820 | Dynamical modeling of three-dimensional genome organization in interphase budding yeast. |
| Q35206444 | Effect of chromosome tethering on nuclear organization in yeast |
| Q27930266 | Effect of nuclear architecture on the efficiency of double-strand break repair |
| Q47353418 | Enrichment of dynamic chromosomal crosslinks drive phase separation of the nucleolus. |
| Q27323070 | Entropy gives rise to topologically associating domains |
| Q38804258 | Finding a place in the SUN: telomere maintenance in a diverse nuclear landscape. |
| Q48358485 | From dynamic chromatin architecture to DNA damage repair and back. |
| Q38086775 | Functional implications of genome topology. |
| Q37686820 | Genetic and epigenetic control of the spatial organization of the genome. |
| Q49909575 | Heterogeneous Spatial Distribution of Transcriptional Activity in Budding Yeast Nuclei |
| Q41777561 | High-throughput chromatin motion tracking in living yeast reveals the flexibility of the fiber throughout the genome |
| Q37987659 | Higher-order chromatin structure: bridging physics and biology |
| Q39883960 | History of chromosome rearrangements reflects the spatial organization of yeast chromosomes |
| Q42736680 | How to build a yeast nucleus. |
| Q92756287 | Hyperosmotic Stress Response Memory is Modulated by Gene Positioning in Yeast |
| Q92452330 | Impact of Chromosome Fusions on 3D Genome Organization and Gene Expression in Budding Yeast |
| Q63965533 | Increased chromosome mobility facilitates homology search during recombination |
| Q38806570 | Inferring the physical properties of yeast chromatin through Bayesian analysis of whole nucleus simulations. |
| Q40633884 | Involvement of the SATB1/F-actin complex in chromatin reorganization during active cell death. |
| Q64389080 | Keep moving and stay in a good shape to find your homologous recombination partner |
| Q36917558 | Long-range heterochromatin association is mediated by silencing and double-strand DNA break repair proteins |
| Q37028399 | Loss of the integral nuclear envelope protein SUN1 induces alteration of nucleoli |
| Q34040940 | Mechanisms and principles of homology search during recombination |
| Q35887923 | Mechanistic Modeling of Dose and Dose Rate Dependences of Radiation-Induced DNA Double Strand Break Rejoining Kinetics in Saccharomyces cerevisiae |
| Q41827167 | Microtubule dynamics drive enhanced chromatin motion and mobilize telomeres in response to DNA damage. |
| Q38196677 | Microtubules move the nucleus to quiescence |
| Q34263005 | Modeling meiotic chromosomes indicates a size dependent contribution of telomere clustering and chromosome rigidity to homologue juxtaposition. |
| Q42224115 | Nuclear GPS for interchromosomal clustering |
| Q38675814 | Physical properties of the chromosomes and implications for development |
| Q42236154 | Physical tethering and volume exclusion determine higher-order genome organization in budding yeast |
| Q38682331 | Position effects influencing intrachromosomal repair of a double-strand break in budding yeast |
| Q38821202 | Put your 3D glasses on: plant chromatin is on show. |
| Q27936606 | Quiescent Saccharomyces cerevisiae forms telomere hyperclusters at the nuclear membrane vicinity through a multifaceted mechanism involving Esc1, the Sir complex, and chromatin condensation. |
| Q38263582 | Ribosomal proteins' association with transcription sites peaks at tRNA genes in Schizosaccharomyces pombe |
| Q55651799 | Sad1 Spatiotemporally Regulates Kinetochore Clustering To Ensure High-Fidelity Chromosome Segregation in the Human Fungal Pathogen Cryptococcus neoformans. |
| Q37723762 | Something silent this way forms: the functional organization of the repressive nuclear compartment |
| Q42056140 | Spatial localization of co-regulated genes exceeds genomic gene clustering in the Saccharomyces cerevisiae genome |
| Q36887445 | Spatial telomere organization and clustering in yeast Saccharomyces cerevisiae nucleus is generated by a random dynamics of aggregation-dissociation |
| Q50964160 | Stalled RNAP-II molecules bound to non-coding rDNA spacers are required for normal nucleolus architecture. |
| Q36198201 | Structure and function in the budding yeast nucleus. |
| Q37297123 | Subnuclear positioning and interchromosomal clustering of the GAL1-10 locus are controlled by separable, interdependent mechanisms |
| Q34575600 | The 3D organization of the yeast genome correlates with co-expression and reflects functional relations between genes |
| Q36376474 | The Conformation of Yeast Chromosome III Is Mating Type Dependent and Controlled by the Recombination Enhancer |
| Q64077072 | The Rabl configuration limits topological entanglement of chromosomes in budding yeast |
| Q38201247 | The biogenesis of chromosome translocations. |
| Q41991701 | The eukaryotic genome is structurally and functionally more like a social insect colony than a book |
| Q40170607 | The genome in space and time: does form always follow function? How does the spatial and temporal organization of a eukaryotic genome reflect and influence its functions? |
| Q39108767 | The telomere profile distinguishes two classes of genetically distinct cutaneous squamous cell carcinomas. |
| Q89499360 | Understanding the 3D genome: Emerging impacts on human disease |
| Q37696369 | Unexpected function of the glucanosyltransferase Gas1 in the DNA damage response linked to histone H3 acetyltransferases in Saccharomyces cerevisiae |
| Q64086145 | tRNA Genes Affect Chromosome Structure and Function via Local Effects |
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