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Prestes, P. R., Saraiva-Pereira, M. L., Silveira, I., Sequeiros, J., & Jardim, L. B. (2008). Machado-Joseph disease enhances genetic fitness: A comparison between affected and unaffected women and between MJD and the general population. Annals of Human Genetics, 72(1), 57 - 64.
Corti, A., Duarte, T. L., Giommarelli, C., De Tata, V., et al. (2009). Membrane gamma-glutamyl transferase activity promotes iron-dependent oxidative DNA damage in melanoma cells. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 669(1-2), 112 - 121.
Barisic, M., Silva E Sousa, R., Tripathy, S. K., Magiera, M. M., et al. (2015). Microtubule detyrosination guides chromosomes during mitosis. Science, 348(6236), 799 - 803.
Silvia, F., Joana, B., Pedro, M., Céu, F., et al. (2015). Mismatch discrimination in fluorescent in situ hybridization using different types of nucleic acids. Applied Microbiology and Biotechnology, 99(9), 3961 - 3969.
Silvia, F., Joana, B., Pedro, M., Céu, F., et al. (2015). Mismatch discrimination in fluorescent in situ hybridization using different types of nucleic acids. Applied Microbiology and Biotechnology, 99(9), 3961 - 3969.
Teixeira, F., Castro, H., Cruz, T., Tse, E., et al. (2015). Mitochondrial peroxiredoxin functions as crucial chaperone reservoir in Leishmania infantum. Proceedings of the National Academy of Sciences of the United States of America, 112(7), E616 - E624.
Borges, M., Barreira-Silva, P., Flórido, M., Jordan, M. B., et al. (2012). Molecular and cellular mechanisms of Mycobacterium avium-induced thymic atrophy. Journal of Immunology, 189(7), 3600 - 3608.
Maffini, S., Maia, A. R. R., Manning, A. L., Maliga, Z., et al. (2009). Motor-Independent Targeting of CLASPs to Kinetochores by CENP-E Promotes Microtubule Turnover and Poleward Flux. Current Biology, 19(18), 1566 - 1572.
Guimarães, C. P., Domingues, P., Aubourg, P., Fouquet, F., et al. (2004). Mouse liver PMP70 and ALDP: Homomeric interactions prevail in vivo. Biochimica et Biophysica Acta - Molecular Basis of Disease, 1689(3), 235 - 243.
Martin, C. - A., Murray, J. E., Carroll, P., Leitch, A., et al. (2016). Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. Genes and Development, 30(19), 2158 - 2172.
Martin, C. - A., Murray, J. E., Carroll, P., Leitch, A., et al. (2016). Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. Genes and Development, 30(19), 2158 - 2172.

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