human | Q5 |
P9985 | EMBO member ID | helder-maiato |
P496 | ORCID iD | 0000-0002-6200-9997 |
P3829 | Publons author ID | 2608497 |
P1053 | ResearcherID | J-9466-2013 |
P1153 | Scopus author ID | 6507722675 |
P734 | family name | Maiato | Q37447550 |
Maiato | Q37447550 | ||
Maiato | Q37447550 | ||
P735 | given name | Helder | Q20000413 |
Helder | Q20000413 | ||
P106 | occupation | researcher | Q1650915 |
Q46494033 | A Regulatory Switch Alters Chromosome Motions at the Metaphase-to-Anaphase Transition. |
Q38932588 | A chromosome separation checkpoint: A midzone Aurora B gradient mediates a chromosome separation checkpoint that regulates the anaphase-telophase transition. |
Q30524914 | A nuclear-derived proteinaceous matrix embeds the microtubule spindle apparatus during mitosis |
Q27309143 | An organelle-exclusion envelope assists mitosis and underlies distinct molecular crowding in the spindle region |
Q24307694 | Asymmetric CLASP-dependent nucleation of noncentrosomal microtubules at the trans-Golgi network |
Q30540082 | Aurora B spatially regulates EB3 phosphorylation to coordinate daughter cell adhesion with cytokinesis |
Q53219310 | Aurora Mitochondrialis drives fission during mitosis. |
Q24300214 | CLASP1, astrin and Kif2b form a molecular switch that regulates kinetochore-microtubule dynamics to promote mitotic progression and fidelity |
Q39401246 | CLASPs prevent irreversible multipolarity by ensuring spindle-pole resistance to traction forces during chromosome alignment. |
Q36317230 | Cdk1 and Plk1 mediate a CLASP2 phospho-switch that stabilizes kinetochore-microtubule attachments |
Q47978327 | Cell Division: NuMA Bears the Load in the Spindle. |
Q47072589 | Chromator is required for proper microtubule spindle formation and mitosis in Drosophila |
Q47292194 | Closing the tubulin detyrosination cycle. |
Q33922318 | Conformational mechanism for the stability of microtubule-kinetochore attachments. |
Q24803351 | Dissecting mitosis by RNAi inDrosophila tissue culture cells |
Q33454757 | Dissecting mitosis with laser microsurgery and RNAi in Drosophila cells |
Q33662953 | Drosophila S2 cells as a model system to investigate mitotic spindle dynamics, architecture, and function. |
Q39834291 | Dynein and mast/orbit/CLASP have antagonistic roles in regulating kinetochore-microtubule plus-end dynamics. |
Q39984175 | Dynein prevents erroneous kinetochore-microtubule attachments in mitosis |
Q30419902 | Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant |
Q28189031 | Essential roles of Drosophila inner centromere protein (INCENP) and aurora B in histone H3 phosphorylation, metaphase chromosome alignment, kinetochore disjunction, and chromosome segregation |
Q36702322 | Establishment and mitotic characterization of new Drosophila acentriolar cell lines from DSas-4 mutant |
Q38985265 | Feedback control of chromosome separation by a midzone Aurora B gradient |
Q37977547 | Fluorescent speckle microscopy in cultured cells. |
Q35047358 | Genes involved in centrosome-independent mitotic spindle assembly in Drosophila S2 cells |
Q39521875 | Heterochromatin boundaries are hotspots for de novo kinetochore formation |
Q28204481 | How do kinetochores CLASP dynamic microtubules? |
Q24306616 | Human CLASP1 is an outer kinetochore component that regulates spindle microtubule dynamics |
Q39455958 | Imidazole-grafted chitosan-mediated gene delivery: in vitro study on transfection, intracellular trafficking and degradation |
Q53347612 | Improved kymography tools and its applications to mitosis. |
Q27309106 | Inducible fluorescent speckle microscopy |
Q35406761 | Kinetochore motors drive congression of peripheral polar chromosomes by overcoming random arm-ejection forces. |
Q54686811 | Kinetochore regulation: Let there be light. |
Q24676290 | Kinetochore-driven formation of kinetochore fibers contributes to spindle assembly during animal mitosis |
Q30342478 | Kinetochore-microtubule interactions during cell division. |
Q30495542 | Kinetochores use a novel mechanism for coordinating the dynamics of individual microtubules. |
Q38815404 | Late mitotic functions of Aurora kinases |
Q30695098 | MAST/Orbit has a role in microtubule-kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity |
Q24299951 | Mammalian CLASP1 and CLASP2 cooperate to ensure mitotic fidelity by regulating spindle and kinetochore function |
Q38026773 | Maturation of the kinetochore-microtubule interface and the meaning of metaphase. |
Q37728193 | Mechanisms of Chromosome Congression during Mitosis. |
Q39328012 | Membrane-based mechanisms of mitotic spindle assembly. |
Q38188211 | Microtubule plus-end tracking proteins and their roles in cell division |
Q47767599 | Miguel Mota (1922-2016)-the kinetochore engine(er). |
Q47071247 | Mitch a rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila |
Q35864212 | Mitosis. Microtubule detyrosination guides chromosomes during mitosis |
Q57618837 | Mitotic progression, arrest, exit or death relies on centromere structural integrity, rather than de novo transcription |
Q38219034 | Mitotic spindle multipolarity without centrosome amplification. |
Q84433099 | Motor-dependent and -independent roles of CENP-E at kinetochores: the cautionary tale of UA62784 |
Q30491189 | Motor-independent targeting of CLASPs to kinetochores by CENP-E promotes microtubule turnover and poleward flux. |
Q50451045 | N-terminus-modified Hec1 suppresses tumour growth by interfering with kinetochore-microtubule dynamics. |
Q92282182 | No chromosome left behind: The importance of metaphase alignment for mitotic fidelity |
Q38798467 | Plk1 puts a (Has)pin on the mitotic histone code |
Q28268443 | Polar Ejection Forces Promote the Conversion from Lateral to End-on Kinetochore-Microtubule Attachments on Mono-oriented Chromosomes |
Q42262874 | Protein Phosphatase 1 inactivates Mps1 to ensure efficient Spindle Assembly Checkpoint silencing. |
Q27309002 | Reed-Sternberg cells form by abscission failure in the presence of functional Aurora B kinase |
Q37513982 | Robust gap repair in the contractile ring ensures timely completion of cytokinesis. |
Q43208276 | Spatial control of the anaphase-telophase transition |
Q83230151 | Spatiotemporal control of mitotic exit during anaphase by an aurora B-Cdk1 crosstalk |
Q37411011 | Spindle assembly checkpoint robustness requires Tpr-mediated regulation of Mad1/Mad2 proteostasis |
Q37267720 | Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores. |
Q101048427 | The Tubulin Code in Mitosis and Cancer |
Q38877127 | The Tubulin Code: A Navigation System for Chromosomes during Mitosis. |
Q34362671 | The dynamic kinetochore-microtubule interface |
Q38184761 | The dynamic spindle matrix. |
Q33403935 | The microtubule plus-end tracking protein CLASP2 is required for hematopoiesis and hematopoietic stem cell maintenance |
Q37715836 | The perpetual movements of anaphase. |
Q30613021 | The tumour suppressor DLC2 ensures mitotic fidelity by coordinating spindle positioning and cell-cell adhesion |
Q52756145 | Unbiased about chromosome segregation: give me a mechanism and I will make you "immortal". |