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M
Moutinho-Pereira, S., Debec, A., & Maiato, H. (2009). Microtubule cytoskeleton remodeling by acentriolar microtubule-organizing centers at the entry and exit from mitosis in Drosophila somatic cells. Molecular Biology of the Cell, 20(11), 2796 - 2808.
Maiato, H., Gomes, A. M., Sousa, F., & Barisic, M. (2017). Mechanisms of chromosome congression during mitosis. Biology, 6(1).
Pereira, A. J., & Maiato, H. (2012). Maturation of the kinetochore-microtubule interface and the meaning of metaphase. Chromosome Research, 20(5), 563 - 577.
Pereira, A. L., Pereira, A. J., Maia, A. R. R., Drabek, K., et al. (2006). Mammalian CLASP1 and CLASP2 cooperate to ensure mitotic fidelity by regulating spindle and kinetochore function. Molecular Biology of the Cell, 17(10), 4526 - 4542.
L
Afonso, O., Figueiredo, A. C., & Maiato, H. (2017). Late mitotic functions of Aurora kinases. Chromosoma, 126(1), 93 - 103.
K
Vandenbeldt, K. J., Barnard, R. M., Hergert, P. J., Meng, X., et al. (2006). Kinetochores Use a Novel Mechanism for Coordinating the Dynamics of Individual Microtubules. Current Biology, 16(12), 1217 - 1223.
Maiato, H., & Sunkel, C. E. (2004). Kinetochore-microtubule interactions during cell division. Chromosome Research, 12(6), 585 - 597.
Maiato, H., Rieder, C. L., & Khodjakov, A. (2004). Kinetochore-driven formation of kinetochore fibers contributes to spindle assembly during animal mitosis. Journal of Cell Biology, 167(5), 831 - 840.
Figueiredo, A. C., & Maiato, H. (2017). Kinetochore regulation: Let there be light. Nature Chemical Biology, 13(10), 1058 - 1059.
I
Pereira, A. J., Aguiar, P., Belsley, M., & Maiato, H. (2016). Inducible fluorescent speckle microscopy. Journal of Cell Biology, 212(2), 245 - 255.
Pereira, A. J., & Maiato, H. (2010). Improved kymography tools and its applications to mitosis. Methods, 51(2), 214 - 219.
Pires, L. R., Oliveira, H., Barrias, C. C., Sampaio, P., et al. (2011). Imidazole-grafted chitosan-mediated gene delivery: In vitro study on transfection, intracellular trafficking and degradation. Nanomedicine, 6(9), 1499 - 1512.
H
Wandke, C., Barisic, M., Sigl, R., Rauch, V., et al. (2012). Human chromokinesins promote chromosome congression and spindle microtubule dynamics during mitosis. Journal of Cell Biology, 198(5), 847 - 863.
Olszak, A. M., Van Essen, D., Pereira, A. J., Diehl, S., et al. (2011). Heterochromatin boundaries are hotspots for de novo kinetochore formation. Nature Cell Biology, 13(7), 799 - 808.
F
Barisic, M., Pereira, A. J., & Maiato, H. (2012). Fluorescent speckle microscopy in cultured cells. Methods in Enzymology (Vol. 504, pp. 147 - 161).
E
Earnshaw, W. C., Allshire, R. C., Black, B. E., Bloom, K., et al. (2013). Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant. Chromosome Research, 21(2), 101 - 106.
Tan, C. H., Gasic, I., Huber-Reggi, S. P., Dudka, D., et al. (2015). The equatorial position of the metaphase plate ensures symmetric cell divisions. eLife, 4(JULY2015).
D
Reis, R., Feijão, T., Gouveia, S., Pereira, A. J., et al. (2009). Dynein and Mast/Orbit/CLASP have antagonistic roles in regulating kinetochore-microtubule plus-end dynamics. Journal of Cell Science, 122(14), 2543 - 2553.
Maiato, H., DeLuca, J., Salmon, E. D., & Earnshaw, W. C. (2004). The dynamic kinetochore-microtubule interface. Journal of Cell Science, 117(23), 5461 - 5477.
Coelho, P. A., Queiroz-Machado, J., Carmo, A. M., Moutinho-Pereira, S., et al. (2008). Dual role of topoisomerase II in centromere resolution and aurora B activity. PLoS Biology, 6(8), 1758 - 1777.
Coelho, P. A., Queiroz-Machado, J., Carmo, A. M., Moutinho-Pereira, S., et al. (2008). Dual role of topoisomerase II in centromere resolution and aurora B activity. PLoS biology, 6(8).
Moutinho-Pereira, S., Matos, I., & Maiato, H. (2010). Drosophila S2 Cells as a Model System to Investigate Mitotic Spindle Dynamics, Architecture, and Function. Methods in Cell Biology (Vol. 97, pp. 243 - 257).
Conde, C., Osswald, M., Barbosa, J., Moutinho-Santos, T., et al. (2013). Drosophila Polo regulates the spindle assembly checkpoint through Mps1-dependent BubR1 phosphorylation. EMBO Journal, 32(12), 1761 - 1777.
Maiato, H., Khodjakov, A., & Rieder, C. L. (2005). Drosophila CLASP is required for the incorporation of microtubule subunits into fluxing kinetochore fibres. Nature Cell Biology, 7(1), 42 - 47.
C
Barisic, M., & Maiato, H. (2015). Cracking the (tubulin) code of mitosis. Oncotarget, 6(23), 19356 - 19357.

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