| P2093 | author name string | Jennifer Ortiz | |
| | Johannes Lechner | |
| | Astrid Schäfer | |
| | Caroline Funk | |
| P2860 | cites work | Mammalian CLASPs are required for mitotic spindle organization and kinetochore alignment | Q24298000 |
| | Human CLASP1 is an outer kinetochore component that regulates spindle microtubule dynamics | Q24306616 |
| | Drosophila CLASP is required for the incorporation of microtubule subunits into fluxing kinetochore fibres | Q24649746 |
| | Implication of a novel multiprotein Dam1p complex in outer kinetochore function | Q24652456 |
| | Evidence for a role of CLIP-170 in the establishment of metaphase chromosome alignment | Q24683148 |
| | The spindle-assembly checkpoint in space and time | Q27860766 |
| | A non-proteolytic function of separase links the onset of anaphase to mitotic exit | Q27930381 |
| | Cdc14-regulated midzone assembly controls anaphase B | Q27930729 |
| | Plus end-specific depolymerase activity of Kip3, a kinesin-8 protein, explains its role in positioning the yeast mitotic spindle | Q27931585 |
| | The Saccharomyces cerevisiae homolog of p24 is essential for maintaining the association of p150Glued with the dynactin complex | Q27933984 |
| | Slk19p is a centromere protein that functions to stabilize mitotic spindles | Q27934057 |
| | An in vivo map of the yeast protein interactome | Q27936680 |
| | Molecular mechanisms of microtubule-dependent kinetochore transport toward spindle poles | Q27936713 |
| | Analysis of the Saccharomyces spindle pole by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry | Q27936980 |
| | Polyploids require Bik1 for kinetochore-microtubule attachment | Q27937672 |
| | Mimicking Ndc80 phosphorylation triggers spindle assembly checkpoint signalling | Q27938932 |
| | Hierarchical assembly of the budding yeast kinetochore from multiple subcomplexes | Q27939140 |
| | The budding yeast protein kinase Ipl1/Aurora allows the absence of tension to activate the spindle checkpoint | Q28365645 |
| | Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections | Q29619579 |
| | Kinesin-related proteins required for structural integrity of the mitotic spindle | Q29636252 |
| | Xorbit/CLASP links dynamic microtubules to chromosomes in the Xenopus meiotic spindle | Q30480345 |
| | Stabilization of microtubule dynamics at anaphase onset promotes chromosome segregation | Q30484703 |
| | MAST/Orbit has a role in microtubule-kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity | Q30695098 |
| | The kinetochore protein Ndc10p is required for spindle stability and cytokinesis in yeast. | Q30856850 |
| | The spindle cycle in budding yeast | Q31846200 |
| | The coordination of centromere replication, spindle formation, and kinetochore-microtubule interaction in budding yeast | Q33385993 |
| | Molecular architecture of a kinetochore-microtubule attachment site | Q33839309 |
| | Stu1p is physically associated with beta-tubulin and is required for structural integrity of the mitotic spindle. | Q33898838 |
| | Closing mitosis: the functions of the Cdc14 phosphatase and its regulation | Q34371846 |
| | Microtubule plus-end-tracking proteins: mechanisms and functions. | Q34386396 |
| | The mitotic spindle is required for loading of the DASH complex onto the kinetochore | Q35004928 |
| | At the interface between signaling and executing anaphase--Cdc14 and the FEAR network | Q35936135 |
| | Spindle checkpoint proteins and chromosome-microtubule attachment in budding yeast | Q36321836 |
| | Asymmetric spindle positioning | Q36345298 |
| | Structures and functions of yeast kinetochore complexes | Q36760332 |
| | Assembling the spindle midzone in the right place at the right time. | Q37072270 |
| | Four new subunits of the Dam1-Duo1 complex reveal novel functions in sister kinetochore biorientation | Q39646433 |
| | Kinetochore microtubule interaction during S phase in Saccharomyces cerevisiae | Q41448908 |
| | Stabilization of overlapping microtubules by fission yeast CLASP. | Q41828687 |
| | S. pombe CLASP needs dynein, not EB1 or CLIP170, to induce microtubule instability and slows polymerization rates at cell tips in a dynein-dependent manner | Q41907752 |
| | Spc24 and Stu2 promote spindle integrity when DNA replication is stalled | Q42414556 |
| | Separase Regulates INCENP-Aurora B Anaphase Spindle Function Through Cdc14 | Q44647087 |
| | The CENP-F-like proteins HCP-1 and HCP-2 target CLASP to kinetochores to mediate chromosome segregation. | Q46810631 |
| | Distinct mechanisms govern the localisation of Drosophila CLIP-190 to unattached kinetochores and microtubule plus-ends. | Q47070135 |
| | Molecular mechanisms of kinetochore capture by spindle microtubules | Q48951524 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 23 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | kinetochore | Q908912 |
| | Kinetochore-associated Ndc80 complex subunit NDC80 YIL144W | Q27548593 |
| | Stu1p YBL034C | Q27549912 |
| P304 | page(s) | 2778-2791 | |
| P577 | publication date | 2009-12-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Stu1 inversely regulates kinetochore capture and spindle stability | |
| P478 | volume | 23 | |