| P50 | author | Kozo Tanaka | Q54956791 |
| P2093 | author name string | Kozo Tanaka | |
| P2860 | cites work | Characterization of the kinetochore binding domain of CENP-E reveals interactions with the kinetochore proteins CENP-F and hBUBR1 | Q22003896 |
| | Induced ectopic kinetochore assembly bypasses the requirement for CENP-A nucleosomes | Q24300684 |
| | CENP-T-W-S-X forms a unique centromeric chromatin structure with a histone-like fold | Q24304369 |
| | CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment. | Q24306547 |
| | Tex14, a Plk1-regulated protein, is required for kinetochore-microtubule attachment and regulation of the spindle assembly checkpoint | Q24306949 |
| | Human NUF2 interacts with centromere-associated protein E and is essential for a stable spindle microtubule-kinetochore attachment | Q24307444 |
| | Timely anaphase onset requires a novel spindle and kinetochore complex comprising Ska1 and Ska2 | Q24313155 |
| | The conserved KMN network constitutes the core microtubule-binding site of the kinetochore | Q24320105 |
| | Genome stability is ensured by temporal control of kinetochore-microtubule dynamics | Q24322655 |
| | Analysis of mitotic microtubule-associated proteins using mass spectrometry identifies astrin, a spindle-associated protein | Q24555066 |
| | A new look at kinetochore structure in vertebrate somatic cells using high-pressure freezing and freeze substitution | Q24607318 |
| | The kinesin-8 motor Kif18A suppresses kinetochore movements to control mitotic chromosome alignment | Q24653914 |
| | Three-dimensional ultrastructural analysis of the Saccharomyces cerevisiae mitotic spindle | Q24657131 |
| | Kinetochore fiber maturation in PtK1 cells and its implications for the mechanisms of chromosome congression and anaphase onset | Q24680015 |
| | Implications for kinetochore-microtubule attachment from the structure of an engineered Ndc80 complex | Q27324199 |
| | Chromosomes can congress to the metaphase plate before biorientation | Q27332199 |
| | The Ndc80/HEC1 complex is a contact point for kinetochore-microtubule attachment | Q27643451 |
| | Structural and functional organization of the Ska complex, a key component of the kinetochore-microtubule interface | Q27678365 |
| | The spindle-assembly checkpoint in space and time | Q27860766 |
| | Phospho-regulation of kinetochore-microtubule attachments by the Aurora kinase Ipl1p | Q27931713 |
| | CENP-T proteins are conserved centromere receptors of the Ndc80 complex | Q27931916 |
| | Formation of a dynamic kinetochore- microtubule interface through assembly of the Dam1 ring complex | Q27933177 |
| | The yeast DASH complex forms closed rings on microtubules. | Q27935179 |
| | Molecular mechanisms of microtubule-dependent kinetochore transport toward spindle poles | Q27936713 |
| | Cnn1 inhibits the interactions between the KMN complexes of the yeast kinetochore | Q27937573 |
| | Molecular organization of the Ndc80 complex, an essential kinetochore component | Q27940063 |
| | NudC is required for Plk1 targeting to the kinetochore and chromosome congression | Q28253469 |
| | Cdc42 and mDia3 regulate microtubule attachment to kinetochores | Q28256623 |
| | Kinetochore-microtubule interactions "in check" by Bub1, Bub3 and BubR1: The dual task of attaching and signalling | Q28285820 |
| | Sds22 regulates aurora B activity and microtubule-kinetochore interactions at mitosis | Q28294849 |
| | Recruitment of the human Cdt1 replication licensing protein by the loop domain of Hec1 is required for stable kinetochore-microtubule attachment | Q28771763 |
| | Molecular architecture of the kinetochore-microtubule interface | Q29620741 |
| | Multiple mechanisms of chromosome movement in vertebrate cells mediated through the Ndc80 complex and dynein/dynactin | Q30439804 |
| | The DASH complex and Klp5/Klp6 kinesin coordinate bipolar chromosome attachment in fission yeast | Q30476087 |
| | Bod1, a novel kinetochore protein required for chromosome biorientation | Q30480574 |
| | Examining the link between chromosomal instability and aneuploidy in human cells | Q30481428 |
| | Different assemblies of the DAM1 complex follow shortening microtubules by distinct mechanisms. | Q30481907 |
| | Phosphoregulation and depolymerization-driven movement of the Dam1 complex do not require ring formation | Q30491892 |
| | Spindly/CCDC99 is required for efficient chromosome congression and mitotic checkpoint regulation | Q30494847 |
| | Chromosome congression in the absence of kinetochore fibres | Q30495251 |
| | Direct binding of Cenp-C to the Mis12 complex joins the inner and outer kinetochore | Q30499448 |
| | Tension directly stabilizes reconstituted kinetochore-microtubule attachments. | Q30500849 |
| | Zwint-1 is a novel Aurora B substrate required for the assembly of a dynein-binding platform on kinetochores. | Q30504218 |
| | Regulated targeting of protein phosphatase 1 to the outer kinetochore by KNL1 opposes Aurora B kinase | Q33751737 |
| | Abnormal kinetochore-generated pulling forces from expressing a N-terminally modified Hec1. | Q33813043 |
| | Aurora B phosphorylates spatially distinct targets to differentially regulate the kinetochore-microtubule interface | Q33863228 |
| | The outer plate in vertebrate kinetochores is a flexible network with multiple microtubule interactions | Q33956248 |
| | Aurora kinases and protein phosphatase 1 mediate chromosome congression through regulation of CENP-E. | Q34066062 |
| | The MIS12 complex is a protein interaction hub for outer kinetochore assembly | Q34111005 |
| | Complete kinetochore tracking reveals error-prone homologous chromosome biorientation in mammalian oocytes | Q34209347 |
| | Aurora B kinase controls the targeting of the Astrin-SKAP complex to bioriented kinetochores. | Q34218832 |
| | MCAK activity at microtubule tips regulates spindle microtubule length to promote robust kinetochore attachment | Q34267263 |
| | The dynamic kinetochore-microtubule interface | Q34362671 |
| | Aurora kinase promotes turnover of kinetochore microtubules to reduce chromosome segregation errors. | Q34562965 |
| | Spindle microtubules generate tension-dependent changes in the distribution of inner kinetochore proteins | Q34854555 |
| | The spatial arrangement of chromosomes during prometaphase facilitates spindle assembly | Q35793140 |
| | Aurora B controls kinetochore-microtubule attachments by inhibiting Ska complex-KMN network interaction | Q35839779 |
| | PRP4 is a spindle assembly checkpoint protein required for MPS1, MAD1, and MAD2 localization to the kinetochores | Q36149288 |
| | Kinetochores are transported poleward along a single astral microtubule during chromosome attachment to the spindle in newt lung cells | Q36222387 |
| | Kinetochore capture and bi-orientation on the mitotic spindle. | Q36337950 |
| | Augmin: a protein complex required for centrosome-independent microtubule generation within the spindle | Q36625777 |
| | A new mechanism controlling kinetochore-microtubule interactions revealed by comparison of two dynein-targeting components: SPDL-1 and the Rod/Zwilch/Zw10 complex | Q36869073 |
| | Kinetochore stretching inactivates the spindle assembly checkpoint | Q37106715 |
| | Intrakinetochore stretch is associated with changes in kinetochore phosphorylation and spindle assembly checkpoint activity | Q37106724 |
| | Chromosomes and cancer cells. | Q37165291 |
| | Spindly switch controls anaphase: spindly and RZZ functions in chromosome attachment and mitotic checkpoint control | Q37831015 |
| | Merotelic kinetochore attachment: causes and effects. | Q37838569 |
| | Formation of stable attachments between kinetochores and microtubules depends on the B56-PP2A phosphatase | Q38625831 |
| | Crm1 is a mitotic effector of Ran-GTP in somatic cells | Q40418909 |
| | Kinetochore-dependent microtubule rescue ensures their efficient and sustained interactions in early mitosis. | Q41050003 |
| | Ndc80 internal loop interacts with Dis1/TOG to ensure proper kinetochore-spindle attachment in fission yeast | Q41808587 |
| | Connecting with Ska, a key complex at the kinetochore-microtubule interface | Q41846300 |
| | The Ndc80 loop region facilitates formation of kinetochore attachment to the dynamic microtubule plus end. | Q42056835 |
| | The Ndc80 internal loop is required for recruitment of the Ska complex to establish end-on microtubule attachment to kinetochores | Q43596550 |
| | The Dam1 kinetochore ring complex moves processively on depolymerizing microtubule ends. | Q46038669 |
| | Architecture of the Dam1 kinetochore ring complex and implications for microtubule-driven assembly and force-coupling mechanisms | Q46088120 |
| | Molecular mechanisms of kinetochore capture by spindle microtubules | Q48951524 |
| | Chk1 is required for spindle checkpoint function. | Q52576772 |
| P433 | issue | 5 | |
| P921 | main subject | kinetochore | Q908912 |
| P304 | page(s) | 415-424 | |
| P577 | publication date | 2012-09-20 | |
| P1433 | published in | Journal of Biochemistry | Q6294839 |
| P1476 | title | Dynamic regulation of kinetochore-microtubule interaction during mitosis | |
| P478 | volume | 152 | |