scholarly article | Q13442814 |
P2093 | author name string | L L Moore | |
M B Roth | |||
P2860 | cites work | CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 |
Human Zw10 and ROD are mitotic checkpoint proteins that bind to kinetochores | Q24290711 | ||
ZW10 helps recruit dynactin and dynein to the kinetochore | Q24322833 | ||
Human CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromere | Q24337253 | ||
CENP-C, an autoantigen in scleroderma, is a component of the human inner kinetochore plate | Q24337772 | ||
Purification of the centromere-specific protein CENP-A and demonstration that it is a distinctive histone | Q24562780 | ||
Automated assembly of protein blocks for database searching | Q24627190 | ||
Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients | Q24681500 | ||
Assembly of CENP-A into centromeric chromatin requires a cooperative array of nucleosomal DNA contact sites | Q24681628 | ||
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans | Q27860867 | ||
Combining evidence using p-values: application to sequence homology searches | Q28265811 | ||
HCP-1, a protein involved in chromosome segregation, is localized to the centromere of mitotic chromosomes in Caenorhabditis elegans | Q28611296 | ||
Identification and characterization of a nuclear pore complex protein | Q29616069 | ||
Cse4p is a component of the core centromere of Saccharomyces cerevisiae | Q29616168 | ||
Evidence that the MIF2 gene of Saccharomyces cerevisiae encodes a centromere protein with homology to the mammalian centromere protein CENP-C | Q29616337 | ||
Three-dimensional multiple-wavelength fluorescence microscopy for the structural analysis of biological phenomena | Q33268169 | ||
The kinetochore of higher eucaryotes: a molecular view | Q33737157 | ||
The ultrastructure and spatial organization of the metaphase kinetochore in mitotic rat cells | Q34231879 | ||
C. elegans nuclear envelope proteins emerin, MAN1, lamin, and nucleoporins reveal unique timing of nuclear envelope breakdown during mitosis | Q34757049 | ||
Heterochromatic deposition of centromeric histone H3-like proteins | Q34975731 | ||
Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice | Q35008528 | ||
Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo death | Q35795981 | ||
A 17-kD centromere protein (CENP-A) copurifies with nucleosome core particles and with histones | Q36215978 | ||
CENP-C is required for maintaining proper kinetochore size and for a timely transition to anaphase. | Q36233891 | ||
ncl-1 is required for the regulation of cell size and ribosomal RNA synthesis in Caenorhabditis elegans | Q36255131 | ||
The centromere-kinetochore complex: a repeat subunit model | Q36529852 | ||
Identification of overlapping DNA-binding and centromere-targeting domains in the human kinetochore protein CENP-C. | Q36560751 | ||
Superresolution three-dimensional images of fluorescence in cells with minimal light exposure. | Q36706369 | ||
Structure and dynamic organization of centromeres/prekinetochores in the nucleus of mammalian cells. | Q36834703 | ||
CENP-C is necessary but not sufficient to induce formation of a functional centromere | Q38322242 | ||
Mitosis. | Q40016377 | ||
Efficient conditional mutation of the vertebrate CENP-C gene | Q41059410 | ||
A histone-H3-like protein in C. elegans | Q47068912 | ||
Mis6, a fission yeast inner centromere protein, acts during G1/S and forms specialized chromatin required for equal segregation | Q48047339 | ||
Light and electron microscopy of rat kangaroo cells in mitosis. II. Kinetochore structure and function. | Q54762829 | ||
Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres | Q59483611 | ||
Light and electron microscopy of rat kangaroo cells in mitosis. III. Patterns of chromosome behavior during prometaphase | Q67438582 | ||
Human centromere protein C (CENP-C) is a DNA-binding protein which possesses a novel DNA-binding motif | Q72614562 | ||
Requirement of Mis6 centromere connector for localizing a CENP-A-like protein in fission yeast | Q73919521 | ||
RNAi in C. elegans: soaking in the genome sequence | Q77642002 | ||
Ultrastructure of the prophase kinetochore in cultured cells of rat-kangaroo (Potorous tridactylis) | Q93499719 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
HoloCentric chromosome binding Protein CELE_T03F1.9 | Q29798511 | ||
HoloCentric chromosome binding Protein CELE_ZK1055.1 | Q29806589 | ||
P1104 | number of pages | 10 | |
P304 | page(s) | 1199-1208 | |
P577 | publication date | 2001-06-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | HCP-4, a CENP-C-like protein in Caenorhabditis elegans, is required for resolution of sister centromeres | |
P478 | volume | 153 |
Q35853959 | "Holo"er than thou: chromosome segregation and kinetochore function in C. elegans |
Q38765635 | A Molecular View of Kinetochore Assembly and Function |
Q24304199 | A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension |
Q28473655 | A monoclonal antibody toolkit for C. elegans |
Q48216188 | A pathway for mitotic chromosome formation. |
Q30856481 | A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo |
Q24794896 | Adaptive evolution of centromere proteins in plants and animals |
Q34621622 | Beyond the ABCs of CKC and SCC. Do centromeres orchestrate sister chromatid cohesion or vice versa? |
Q39753833 | C. elegans condensin promotes mitotic chromosome architecture, centromere organization, and sister chromatid segregation during mitosis and meiosis |
Q28183451 | CENP-B Interacts with CENP-C Domains Containing Mif2 Regions Responsible for Centromere Localization |
Q35810683 | CENP-C is involved in chromosome segregation, mitotic checkpoint function, and kinetochore assembly |
Q40736425 | CENP-I is essential for centromere function in vertebrate cells |
Q21558513 | Caenorhabditis elegans cyclin B3 is required for multiple mitotic processes including alleviation of a spindle checkpoint-dependent block in anaphase chromosome segregation |
Q35142905 | Captivating capture: how microtubules attach to kinetochores. |
Q27310847 | Centromere protein F includes two sites that couple efficiently to depolymerizing microtubules |
Q59483490 | Centromere round-up at the heterochromatin corral |
Q30309525 | Centromeres and variant histones: what, where, when and why? |
Q34179745 | Centromeres: unique chromatin structures that drive chromosome segregation |
Q37388735 | Centromeric DNA sequences in the pathogenic yeast Candida albicans are all different and unique |
Q39859891 | Characterization of HCP-6, a C. elegans protein required to prevent chromosome twisting and merotelic attachment |
Q38692366 | Conserved organization of centromeric chromatin in flies and humans |
Q47907787 | Critical Foundation of the Kinetochore: The Constitutive Centromere-Associated Network (CCAN). |
Q36021367 | Cyc17, a meiosis-specific cyclin, is essential for anaphase initiation and chromosome segregation in Tetrahymena thermophila. |
Q33787810 | Dephosphorylation of cell cycle-regulated proteins correlates with anoxia-induced suspended animation in Caenorhabditis elegans |
Q34325316 | Determining centromere identity: cyclical stories and forking paths. |
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 |
Q30437632 | Dissection of CENP-C-directed centromere and kinetochore assembly |
Q28469022 | Drosophila CENP-A mutations cause a BubR1-dependent early mitotic delay without normal localization of kinetochore components |
Q39652517 | Drosophila CENP-C is essential for centromere identity |
Q38992391 | Duplication and Adaptive Evolution of a Key Centromeric Protein in Mimulus, a Genus with Female Meiotic Drive |
Q37369861 | Function and assembly of DNA looping, clustering, and microtubule attachment complexes within a eukaryotic kinetochore |
Q42953788 | Genetic interactions of separase regulatory subunits reveal the diverged Drosophila Cenp-C homolog. |
Q46301631 | Genome Architecture and Evolution of a Unichromosomal Asexual Nematode |
Q33707741 | HCP-4/CENP-C promotes the prophase timing of centromere resolution by enabling the centromere association of HCP-6 in Caenorhabditis elegans |
Q24679340 | Here, there, and everywhere: kinetochore function on holocentric chromosomes |
Q33581966 | Histone variant H2A.Z regulates centromere silencing and chromosome segregation in fission yeast |
Q34414322 | Holocentromeres are dispersed point centromeres localized at transcription factor hotspots |
Q36579406 | How to build a centromere: from centromeric and pericentromeric chromatin to kinetochore assembly |
Q38697149 | Insights from the reconstitution of the divergent outer kinetochore of Drosophila melanogaster |
Q36335836 | KNL-1 directs assembly of the microtubule-binding interface of the kinetochore in C. elegans |
Q37349399 | Key players in chromosome segregation in Caenorhabditis elegans |
Q34947399 | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
Q30478181 | Molecular analysis of mitotic chromosome condensation using a quantitative time-resolved fluorescence microscopy assay |
Q29620741 | Molecular architecture of the kinetochore-microtubule interface |
Q93017200 | Multiple phosphorylations control recruitment of the KMN network onto kinetochores |
Q35855722 | Reconstruction of the kinetochore: a prelude to meiosis |
Q41762544 | Spatial organization of a ubiquitous eukaryotic kinetochore protein network in Drosophila chromosomes |
Q37317531 | Sperm chromatin proteomics identifies evolutionarily conserved fertility factors |
Q35097684 | Stretching it: putting the CEN(P-A) in centromere |
Q30485999 | Systematic analysis in Caenorhabditis elegans reveals that the spindle checkpoint is composed of two largely independent branches |
Q42590501 | The Argonaute CSR-1 and its 22G-RNA cofactors are required for holocentric chromosome segregation |
Q33463367 | The C-terminal domain of CENP-C displays multiple and critical functions for mammalian centromere formation |
Q34298429 | The CNA1 histone of the ciliate Tetrahymena thermophila is essential for chromosome segregation in the germline micronucleus |
Q37595514 | The Caenorhabditis elegans kinetochore reorganizes at prometaphase and in response to checkpoint stimuli |
Q47070469 | The Drosophila melanogaster condensin subunit Cap-G interacts with the centromere-specific histone H3 variant CID. |
Q28217817 | The aurora B kinase AIR-2 regulates kinetochores during mitosis and is required for separation of homologous Chromosomes during meiosis |
Q41825513 | The dimerization domain of PfCENP-C is required for its functions as a centromere protein in human malaria parasite Plasmodium falciparum |
Q53672298 | Visualization of diffuse centromeres with centromere-specific histone H3 in the holocentric plant Luzula nivea. |
Q41825913 | cin-4, a gene with homology to topoisomerase II, is required for centromere resolution by cohesin removal from sister kinetochores during mitosis |
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