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Journal Article
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.
Karageorgos, L., Brooks, D. A., Pollard, A., Melville, E. L., et al. (2007). Mutational analysis of 105 mucopolysaccharidosis type VI patients. Human Mutation, 28(9), 897 - 903.
Martins, S., Calafell, F., Wong, V. C. N., Sequeiros, J., & Amorim, A. (2006). A multistep mutation mechanism drives the evolution of the CAG repeat at MJD/SCA3 locus. European Journal of Human Genetics, 14(8), 932 - 940.
Olsson, I. A. S., & Westlund, K. (2007). More than numbers matter: The effect of social factors on behaviour and welfare of laboratory rodents and non-human primates. Applied Animal Behaviour Science, 103(3-4), 229 - 254.
Neves, J. V., Caldas, C., Wilson, J. M., & Rodrigues, P. N. S. (2011). Molecular mechanisms of hepcidin regulation in sea bass (Dicentrarchus labrax). Fish and Shellfish Immunology, 31(6), 1154 - 1161.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Kolb, A. F., Huber, R. C., Lillico, S. G., Carlisle, A., et al. (2011). Milk lacking α-casein leads to permanent reduction in body size in mice. PLoS ONE, 6(7).
Coelho-Santos, V., Socodato, R., Portugal, C., Leitão, R. A., et al. (2016). Methylphenidate-triggered ROS generation promotes caveolae-mediated transcytosis via Rac1 signaling and c-Src-dependent caveolin-1 phosphorylation in human brain endothelial cells. Cellular and Molecular Life Sciences, 73(24), 4701 - 4716.
Borsari, C., Santarém, N., Torrado, J., Olías, A. I., et al. (2017). Methoxylated 2'-hydroxychalcones as antiparasitic hit compounds. European Journal of Medicinal Chemistry, 126, 1129 - 1135.
Borsari, C., Santarém, N., Torrado, J., Olías, A. I., et al. (2017). Methoxylated 2'-hydroxychalcones as antiparasitic hit compounds. European Journal of Medicinal Chemistry, 126, 1129 - 1135.
Rodrigues, L. G., Tavares, M. A., Wood, J. P. M., Schmidt, K. - G., & Osborne, N. N. (2004). Methamphetamine exacerbates the toxic effect of kainic acid in the adult rat retina. Neurochemistry International, 45(8), 1133 - 1141.
Williams, G. S., Collinson, L. M., Brzostek, J., Eissmann, P., et al. (2007). Membranous ctructures transfer cell surface proteins across NK cell immune synapses. Traffic, 8(9), 1190 - 1204.
Mayr, C., Bund, D., Schlee, M., Bamberger, M., et al. (2006). MDM2 is recognized as a tumor-associated antigen in chronic lymphocytic leukemia by CD8+ autologous T lymphocytes. Experimental Hematology, 34(1), 44 - 53.
Weber, E. M., & Olsson, I. A. S. (2008). Maternal behaviour in Mus musculus sp.: An ethological review. Applied Animal Behaviour Science, 114(1-2), 1 - 22.
Hoischen, A., Gilissen, C., Arts, P., Wieskamp, N., et al. (2010). Massively parallel sequencing of ataxia genes after array-based enrichment. Human Mutation, 31(4), 492 - 499.
Ferraz, M. J., Marques, A. R. A., Gaspar, P., Mirzaian, M., et al. (2016). Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders. Molecular Genetics and Metabolism, 117(2), 186 - 193.
Martin, E., Schüle, R., Smets, K., Rastetter, A., et al. (2013). Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. American Journal of Human Genetics, 92(2), 238 - 244.
Harmatz, P., Giugliani, R., D. Schwartz, I. V., Guffon, N., et al. (2008). Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase. Molecular Genetics and Metabolism, 94(4), 469 - 475.
Harmatz, P., Giugliani, R., D. Schwartz, I. V., Guffon, N., et al. (2008). Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase. Molecular Genetics and Metabolism, 94(4), 469 - 475.
Afonso-Barroso, A., Clark, S. O., Williams, A., Rosa, G. T., et al. (2013). Lipoarabinomannan mannose caps do not affect mycobacterial virulence or the induction of protective immunity in experimental animal models of infection and have minimal impact on in vitro inflammatory responses. Cellular Microbiology, 15(4), 660 - 674.
van Meurs, J. B. J., Trikalinos, T. A., Ralston, S. H., Balcells, S., et al. (2008). Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis. JAMA - Journal of the American Medical Association, 299(11), 1277 - 1290.
Moosvi, S. A., Pacheco, C. C., McDonald, I. R., de Marco, P., et al. (2005). Isolation and properties of methanesulfonate-degrading Afipia felis from Antarctica and comparison with other strains of A. felis. Environmental Microbiology, 7(1), 22 - 33.

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