| Q24294298 | A cryptic TOG domain with a distinct architecture underlies CLASP-dependent bipolar spindle formation |
| Q34643436 | A kinetochore-independent mechanism drives anaphase chromosome separation during acentrosomal meiosis |
| Q36869073 | A new mechanism controlling kinetochore-microtubule interactions revealed by comparison of two dynein-targeting components: SPDL-1 and the Rod/Zwilch/Zw10 complex |
| Q35946782 | Acentrosomal spindle assembly and chromosome segregation during oocyte meiosis |
| Q60954706 | BUB-1 promotes amphitelic chromosome biorientation via multiple activities at the kinetochore |
| Q36692554 | CLASPs function redundantly to regulate astral microtubules in the C. elegans embryo |
| Q36432441 | Cenp-F (mitosin) is more than a mitotic marker |
| Q30654802 | Chromatids segregate without centrosomes during Caenorhabditis elegans mitosis in a Ran- and CLASP-dependent manner |
| Q30608755 | Dynamic SUMO modification regulates mitotic chromosome assembly and cell cycle progression in Caenorhabditis elegans |
| Q35795603 | Emergent Properties of the Metaphase Spindle |
| Q34450046 | Fluorescent proteins as proteomic probes. |
| Q30481416 | Genetic analysis of the spindle checkpoint genes san-1, mdf-2, bub-3 and the CENP-F homologues hcp-1 and hcp-2 in Caenorhabditis elegans |
| Q36579406 | How to build a centromere: from centromeric and pericentromeric chromatin to kinetochore assembly |
| Q88058993 | Human CLASP2 specifically regulates microtubule catastrophe and rescue |
| Q37349399 | Key players in chromosome segregation in Caenorhabditis elegans |
| Q36337950 | Kinetochore capture and bi-orientation on the mitotic spindle. |
| Q27313276 | Kinetochore components are required for central spindle assembly |
| Q35642690 | Kinetochore-localized BUB-1/BUB-3 complex promotes anaphase onset in C. elegans |
| Q37971172 | Kinetochores and disease: keeping microtubule dynamics in check! |
| Q34395178 | LAB-1 targets PP1 and restricts Aurora B kinase upon entrance into meiosis to promote sister chromatid cohesion. |
| Q24299951 | Mammalian CLASP1 and CLASP2 cooperate to ensure mitotic fidelity by regulating spindle and kinetochore function |
| Q24298000 | Mammalian CLASPs are required for mitotic spindle organization and kinetochore alignment |
| Q37671350 | Mechanisms of force generation by end-on kinetochore-microtubule attachments. |
| Q37085042 | Mechanisms of mitotic spindle assembly and function |
| Q41860233 | Meiotic double-strand breaks uncover and protect against mitotic errors in the C. elegans germline |
| Q54106319 | Microtubule Dynamics Scale with Cell Size to Set Spindle Length and Assembly Timing |
| Q35863030 | Mitotic spindle form and function |
| Q35124404 | Molecular Biology of Kaposi's Sarcoma-associated Herpesvirus and Related Oncogenesis |
| Q29620741 | Molecular architecture of the kinetochore-microtubule interface |
| Q30491189 | Motor-independent targeting of CLASPs to kinetochores by CENP-E promotes microtubule turnover and poleward flux. |
| Q30512268 | Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts |
| Q47344725 | NudE regulates dynein at kinetochores but is dispensable for other dynein functions in the C. elegans early embryo |
| Q36274493 | RMD-1, a novel microtubule-associated protein, functions in chromosome segregation in Caenorhabditis elegans |
| Q27007105 | Reconstituting the kinetochore–microtubule interface: what, why, and how |
| Q90123490 | Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development |
| Q37904130 | Regulation of microtubule dynamics by TOG-domain proteins XMAP215/Dis1 and CLASP. |
| Q33495558 | Spermatogenesis-specific features of the meiotic program in Caenorhabditis elegans |
| Q37781881 | Still entangled: Assembly of the central spindle by multiple microtubule modulators |
| Q92021724 | Structures of TOG1 and TOG2 from the human microtubule dynamics regulator CLASP1 |
| Q42123710 | Stu1 inversely regulates kinetochore capture and spindle stability |
| Q93051383 | Sumoylation regulates protein dynamics during meiotic chromosome segregation in C. elegans oocytes |
| Q42986632 | Synthetic lethal interactions identify phenotypic "interologs" of the spindle assembly checkpoint components |
| Q30485999 | Systematic analysis in Caenorhabditis elegans reveals that the spindle checkpoint is composed of two largely independent branches |
| Q50665190 | The Arabidopsis CLASP gene encodes a microtubule-associated protein involved in cell expansion and division. |
| Q40135294 | The Drosophila CLASP homologue, Mast/Orbit regulates the dynamic behaviour of interphase microtubules by promoting the pause state. |
| Q47559208 | Tumor suppressor APC is an attenuator of spindle-pulling forces during C. elegans asymmetric cell division. |
| Q24292895 | Unstable microtubule capture at kinetochores depleted of the centromere-associated protein CENP-F. |
| Q30480345 | Xorbit/CLASP links dynamic microtubules to chromosomes in the Xenopus meiotic spindle |