review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1024521373 |
P356 | DOI | 10.1023/B:CHRO.0000036588.42225.2F |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1023/b:chro.0000036588.42225.2f |
P698 | PubMed publication ID | 15289669 |
P50 | author | Karen Oegema | Q42317492 |
Iain M Cheeseman | Q55298744 | ||
P2093 | author name string | Arshad Desai | |
Paul S Maddox | |||
P2860 | cites work | Mitotic phosphorylation of histone H3 is governed by Ipl1/aurora kinase and Glc7/PP1 phosphatase in budding yeast and nematodes | Q24290197 |
Specification of kinetochore-forming chromatin by the histone H3 variant CENP-A | Q24291840 | ||
Differential contributions of condensin I and condensin II to mitotic chromosome architecture in vertebrate cells | Q24297107 | ||
Conservation of the centromere/kinetochore protein ZW10 | Q24312091 | ||
Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway | Q24338369 | ||
A new look at kinetochore structure in vertebrate somatic cells using high-pressure freezing and freeze substitution | Q24607318 | ||
Functional analysis of kinetochore assembly in Caenorhabditis elegans. | Q24679016 | ||
HIM-10 is required for kinetochore structure and function on Caenorhabditis elegans holocentric chromosomes | Q24679230 | ||
Here, there, and everywhere: kinetochore function on holocentric chromosomes | Q24679340 | ||
HCP-1, a protein involved in chromosome segregation, is localized to the centromere of mitotic chromosomes in Caenorhabditis elegans | Q28611296 | ||
The survivin-like C. elegans BIR-1 protein acts with the Aurora-like kinase AIR-2 to affect chromosomes and the spindle midzone | Q28611298 | ||
Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling | Q29547850 | ||
Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III | Q29618444 | ||
Localization of Mad2 to kinetochores depends on microtubule attachment, not tension | Q29620330 | ||
Distinct developmental function of two Caenorhabditis elegans homologs of the cohesin subunit Scc1/Rad21. | Q30479877 | ||
Polarity controls forces governing asymmetric spindle positioning in the Caenorhabditis elegans embryo | Q30654911 | ||
Components of the spindle-assembly checkpoint are essential in Caenorhabditis elegans | Q33882831 | ||
The ZW10 and Rough Deal checkpoint proteins function together in a large, evolutionarily conserved complex targeted to the kinetochore | Q34094048 | ||
A solid foundation: functional specialization of centromeric chromatin | Q34183863 | ||
The Formation, Structure, and Composition of the Mammalian Kinetochore and Kinetochore Fiber | Q34249698 | ||
Kinetochore motility after severing between sister centromeres using laser microsurgery: Evidence that kinetochore directional instability and position is regulated by tension | Q34298395 | ||
Determining centromere identity: cyclical stories and forking paths. | Q34325316 | ||
Segregation of holocentric chromosomes at meiosis in the nematode, Caenorhabditis elegans | Q34338341 | ||
The making of the mitotic chromosome: modern insights into classical questions | Q34532415 | ||
Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice | Q35008528 | ||
Structure, Function, and Regulation of Budding Yeast Kinetochores | Q35564845 | ||
Caenorhabditis elegans EVL-14/PDS-5 and SCC-3 Are Essential for Sister Chromatid Cohesion in Meiosis and Mitosis | Q36139047 | ||
Direct observation of microtubule dynamics at kinetochores in Xenopus extract spindles: implications for spindle mechanics | Q36322983 | ||
Morphologically distinct microtubule ends in the mitotic centrosome of Caenorhabditis elegans | Q36324773 | ||
KNL-1 directs assembly of the microtubule-binding interface of the kinetochore in C. elegans | Q36335836 | ||
HCP-4, a CENP-C-like protein in Caenorhabditis elegans, is required for resolution of sister centromeres | Q36364884 | ||
Conserved organization of centromeric chromatin in flies and humans | Q38692366 | ||
The vertebrate cell kinetochore and its roles during mitosis | Q38717231 | ||
Unusual kinetochores and chromatin diminution in Parascaris | Q38727787 | ||
C. elegans condensin promotes mitotic chromosome architecture, centromere organization, and sister chromatid segregation during mitosis and meiosis | Q39753833 | ||
Characterization of HCP-6, a C. elegans protein required to prevent chromosome twisting and merotelic attachment | Q39859891 | ||
A Caenorhabditis elegans cohesion protein with functions in meiotic chromosome pairing and disjunction | Q40424054 | ||
CSC-1: a subunit of the Aurora B kinase complex that binds to the survivin-like protein BIR-1 and the incenp-like protein ICP-1 | Q42120394 | ||
Suspended Animation in C. elegans Requires the Spindle Checkpoint | Q42612760 | ||
Holocentric chromosomes in Oncopeltus: kinetochore plates are present in mitosis but absent in meiosis | Q44221271 | ||
Interphase chromosomes undergo constrained diffusional motion in living cells | Q46252294 | ||
Chromosome cohesion is regulated by a clock gene paralogue TIM-1. | Q46560873 | ||
A histone-H3-like protein in C. elegans | Q47068912 | ||
Cell division: feeling tense enough? | Q48002364 | ||
Chromosome-wide control of meiotic crossing over in C. elegans. | Q52100230 | ||
The Caenorhabditis elegans SCC-3 homologue is required for meiotic synapsis and for proper chromosome disjunction in mitosis and meiosis | Q61455359 | ||
Incenp and an Aurora-like kinase form a complex essential for chromosome segregation and efficient completion of cytokinesis | Q61455361 | ||
Fine structure of kinetochore in Indian muntjac | Q64958663 | ||
The kinetochores of Caenorhabditis elegans | Q70598101 | ||
P433 | issue | 6 | |
P921 | main subject | Caenorhabditis elegans | Q91703 |
kinetochore | Q908912 | ||
P304 | page(s) | 641-653 | |
P577 | publication date | 2004-01-01 | |
P1433 | published in | Chromosome Research | Q15765850 |
P1476 | title | "Holo"er than thou: chromosome segregation and kinetochore function in C. elegans | |
P478 | volume | 12 |
Q90720382 | "Lessons from the extremes: Epigenetic and genetic regulation in point monocentromere and holocentromere establishment on artificial chromosomes" |
Q24304199 | A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension |
Q34643436 | A kinetochore-independent mechanism drives anaphase chromosome separation during acentrosomal meiosis |
Q38157699 | A multitasking Argonaute: exploring the many facets of C. elegans CSR-1. |
Q34701093 | A satellite explosion in the genome of holocentric nematodes |
Q30856481 | A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo |
Q30596591 | Alternative meiotic chromatid segregation in the holocentric plant Luzula elegans |
Q28078705 | Anaphase B |
Q34548272 | Broad chromosomal domains of histone modification patterns in C. elegans |
Q38170221 | C. elegans epigenetic regulation in development and aging |
Q43266934 | CDE-1 affects chromosome segregation through uridylation of CSR-1-bound siRNAs |
Q38055344 | CENP-A: the key player behind centromere identity, propagation, and kinetochore assembly |
Q34613778 | Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 |
Q21558513 | Caenorhabditis elegans cyclin B3 is required for multiple mitotic processes including alleviation of a spindle checkpoint-dependent block in anaphase chromosome segregation |
Q39042190 | Cell Biology of the Caenorhabditis elegans Nucleus |
Q60938313 | Centromere and Pericentromere Transcription: Roles and Regulation … in Sickness and in Health |
Q34123197 | Centromere identity: a challenge to be faced. |
Q34603834 | Centromere sequence and dynamics in Dictyostelium discoideum |
Q34132489 | Centromere-associated repeat arrays on Trypanosoma brucei chromosomes are much more extensive than predicted |
Q35765130 | Centromeres Off the Hook: Massive Changes in Centromere Size and Structure Following Duplication of CenH3 Gene in Fabeae Species |
Q35973370 | Centromeres were derived from telomeres during the evolution of the eukaryotic chromosome |
Q37147265 | Centromeres: old tales and new tools |
Q35785958 | Centromeric chromatin and the pathway that drives its propagation |
Q25256473 | Characterization of sub-nuclear changes in Caenorhabditis elegans embryos exposed to brief, intermediate and long-term anoxia to analyze anoxia-induced cell cycle arrest |
Q52715877 | Chromosome Segregation Is Biased by Kinetochore Size. |
Q89686824 | Conserved chromosomal functions of RNA interference |
Q37284900 | Control of oocyte growth and meiotic maturation in Caenorhabditis elegans |
Q34897855 | Developmental modulation of nonhomologous end joining in Caenorhabditis elegans |
Q35548405 | Different roles for Aurora B in condensin targeting during mitosis and meiosis |
Q39469348 | Differential Chromosomal Localization of Centromeric Histone CENP-A Contributes to Nematode Programmed DNA Elimination |
Q47069400 | Differential role of CENP-A in the segregation of holocentric C. elegans chromosomes during meiosis and mitosis |
Q33543520 | Down the rabbit hole of centromere assembly and dynamics |
Q30608755 | Dynamic SUMO modification regulates mitotic chromosome assembly and cell cycle progression in Caenorhabditis elegans |
Q37256638 | Emerging roles for centromeres in meiosis I chromosome segregation |
Q42506171 | Evolution of the karyotype and sex chromosome systems in basal clades of araneomorph spiders (Araneae: Araneomorphae). |
Q28750638 | Extensive conserved synteny of genes between the karyotypes of Manduca sexta and Bombyx mori revealed by BAC-FISH mapping |
Q33903518 | Finding the middle ground: how kinetochores power chromosome congression. |
Q24683353 | Functional genomics identifies a Myb domain-containing protein family required for assembly of CENP-A chromatin |
Q38868512 | Gene silencing and sex determination by programmed DNA elimination in parasitic nematodes |
Q28743833 | Genome-wide characterization of centromeric satellites from multiple mammalian genomes |
Q35940986 | Histone H3 Variants in Trichomonas vaginalis |
Q97932961 | Holocentric chromosomes |
Q53250470 | Holocentric chromosomes of Luzula elegans are characterized by a longitudinal centromere groove, chromosome bending, and a terminal nucleolus organizer region. |
Q38024240 | Holocentric chromosomes: convergent evolution, meiotic adaptations, and genomic analysis. |
Q38928957 | Holocentromere identity: from the typical mitotic linear structure to the great plasticity of meiotic holocentromeres. |
Q36579406 | How to build a centromere: from centromeric and pericentromeric chromatin to kinetochore assembly |
Q42022155 | Identification and molecular characterization of a sex chromosome rearrangement causing a soft and pliable (spli) larval body phenotype in the silkworm, Bombyx mori |
Q37349399 | Key players in chromosome segregation in Caenorhabditis elegans |
Q36942436 | LAB-1 antagonizes the Aurora B kinase in C. elegans |
Q34395178 | LAB-1 targets PP1 and restricts Aurora B kinase upon entrance into meiosis to promote sister chromatid cohesion. |
Q37728193 | Mechanisms of Chromosome Congression during Mitosis. |
Q37936478 | Mitotic motors and chromosome segregation: the mechanism of anaphase B. |
Q30478181 | Molecular analysis of mitotic chromosome condensation using a quantitative time-resolved fluorescence microscopy assay |
Q29620741 | Molecular architecture of the kinetochore-microtubule interface |
Q39432997 | Molecular characterization of heterochromatin proteins 1a and 1b from the silkworm, Bombyx mori |
Q36734912 | Molecular underpinnings of centromere identity and maintenance |
Q34730895 | N-glycosylation is required for secretion and mitosis in C. elegans |
Q41946221 | Natural Loss of Mps1 Kinase in Nematodes Uncovers a Role for Polo-like Kinase 1 in Spindle Checkpoint Initiation. |
Q34392191 | Neocentromeres: a place for everything and everything in its place |
Q30412014 | Putting CENP-A in its place |
Q79142672 | Rapid adaptive divergence of life-history traits in response to abiotic stress within a natural population of a parthenogenetic nematode |
Q38355891 | Recent advances in plant centromere biology |
Q35176510 | Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects |
Q38023216 | Regulatory mechanisms of kinetochore-microtubule interaction in mitosis. |
Q39315224 | Repetitive DNA is associated with centromeric domains in Trypanosoma brucei but not Trypanosoma cruzi. |
Q48148054 | Repressive Chromatin in Caenorhabditis elegans: Establishment, Composition, and Function |
Q41642442 | Restructuring of Holocentric Centromeres During Meiosis in the Plant Rhynchospora pubera. |
Q27308707 | Separase Cleaves the N-Tail of the CENP-A Related Protein CPAR-1 at the Meiosis I Metaphase-Anaphase Transition in C. elegans |
Q34465647 | Sequence features and transcriptional stalling within centromere DNA promote establishment of CENP-A chromatin. |
Q33495558 | Spermatogenesis-specific features of the meiotic program in Caenorhabditis elegans |
Q37398640 | Structural and temporal regulation of centromeric chromatin |
Q27681275 | Structural basis for microtubule recognition by the human kinetochore Ska complex |
Q27304802 | Structural comparison of the Caenorhabditis elegans and human Ndc80 complexes bound to microtubules reveals distinct binding behavior |
Q37969468 | Structure, assembly and reading of centromeric chromatin |
Q52729138 | Subcellular scaling: does size matter for cell division? |
Q93051383 | Sumoylation regulates protein dynamics during meiotic chromosome segregation in C. elegans oocytes |
Q53170886 | T time for point centromeres. |
Q42590501 | The Argonaute CSR-1 and its 22G-RNA cofactors are required for holocentric chromosome segregation |
Q34184923 | The Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in Lepidoptera |
Q36723456 | The MAP kinase pathway coordinates crossover designation with disassembly of synaptonemal complex proteins during meiosis |
Q47823343 | The cenH3 histone variant defines centromeres in Giardia intestinalis. |
Q38193190 | The cytogenetic architecture of the aphid genome |
Q53514992 | The first karyotype study in palpigrades, a primitive order of arachnids (Arachnida: Palpigradi). |
Q53108045 | The holocentric species Luzula elegans shows interplay between centromere and large-scale genome organization. |
Q33796368 | The kinetochore |
Q22065973 | The most frequent short sequences in non-coding DNA |
Q42244934 | Unlocking holocentric chromosomes: new perspectives from comparative and functional genomics? |
Q53672298 | Visualization of diffuse centromeres with centromere-specific histone H3 in the holocentric plant Luzula nivea. |
Q46261914 | X exceptionalism in Caenorhabditis speciation. |
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