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Journal Article
Dias, C. C., Rodrigues, P. P., da Costa-Pereira, A., & Magro, F. (2013). Clinical prognostic factors for disabling Crohn's disease: A systematic review and meta-analysis. World Journal of Gastroenterology, 19(24), 3866 - 3871.
Garriga, D., Vives-Adrián, L., Buxaderas, M., Ferreira-Da-Silva, F., et al. (2011). Cloning, purification and preliminary crystallographic studies of the 2AB protein from hepatitis A virus. Acta Crystallographica Section F: Structural Biology and Crystallization Communications, 67(10), 1224 - 1227.
Akhmanova, A., & Maiato, H. (2017). Closing the tubulin detyrosination cycle. Science, 358(6369), 1381 - 1382.
Magalhães, J., & Saraiva, M. J. (2011). Clusterin overexpression and its possible protective role in transthyretin deposition in familial amyloidotic polyneuropathy. Journal of Neuropathology and Experimental Neurology, 70(12), 1097 - 1106.
Pais-Vieira, M., Mendes-Pinto, M. M., Lima, D., & Galhardo, V. (2009). Cognitive impairment of prefrontal-dependent decision-making in rats after the onset of chronic pain. Neuroscience, 161(3), 671 - 679.
Pittman, A. M., Naranjo, S., Webb, E., Broderick, P., et al. (2009). The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression. Genome Research, 19(6), 987 - 993.
Clayton, G. M., Aller, S. G., Wang, J., Unger, V., & Morais-Cabral, J. H. (2009). Combining electron crystallography and X-ray crystallography to study the MlotiK1 cyclic nucleotide-regulated potassium channel. Journal of Structural Biology, 167(3), 220 - 226.
Ramos, E. M., Martins, S., Alonso, I., Emmel, V. E., et al. (2010). Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2). American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 153(2), 524 - 531.
Ohmori, H., Ando, Y., Makita, Y., Onouchi, Y., et al. (2004). Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. Journal of medical genetics, 41(4).
Ohmori, H., Ando, Y., Makita, Y., Onouchi, Y., et al. (2004). Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. Journal of medical genetics, 41(4).
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.
Morales-Hojas, R., Vieira, C. P., Reis, M., & Vieira, J. (2009). Comparative analysis of five immunity-related genes reveals different levels of adaptive evolution in the virilis and melanogaster groups of Drosophila. Heredity, 102(6), 573 - 578.
Sanchez-Burgos, G., Mezquita-Vega, R. G., Escobedo-Ortegon, J., Ramirez-Sierra, M. J., et al. (2007). Comparative evaluation of therapeutic DNA vaccines against Trypanosoma cruzi in mice. FEMS Immunology and Medical Microbiology, 50(3), 333 - 341.
Morales-Hojas, R., Päällysaho, S., Vieira, C. P., Hoikkala, A., & Vieira, J. (2007). Comparative polytene chromosome maps of D. montana and D. virilis. Chromosoma, 116(1), 21 - 27.
Rodrigues, P., Lopes, C., Mascarenhas, C., Arosio, P., et al. (2006). Comparative study between Hfe-/- and β2m-/- mice: Progression with age of iron status and liver pathology. International Journal of Experimental Pathology, 87(4), 317 - 324.
Reis, M., Vieira, C. P., Morales-Hojas, R., Aguiar, B., et al. (2011). A comparative study of the short term cold resistance response in distantly related Drosophila species: The role of regucalcin and Frost. PLoS ONE, 6(10).
Paneque, M., Serra-Juhé, C., Pestoff, R., Cordier, C., et al. (2017). Complementarity between medical geneticists and genetic counsellors: Its added value in genetic services in Europe. European Journal of Human Genetics, 25(8), 918 - 923.
Pereira, S., Zille, A., Micheletti, E., Moradas-Ferreira, P., et al. (2009). Complexity of cyanobacterial exopolysaccharides: Composition, structures, inducing factors and putative genes involved in their biosynthesis and assembly. FEMS Microbiology Reviews, 33(5), 917 - 941.
Pereira, S., Zille, A., Micheletti, E., Moradas-Ferreira, P., et al. (2009). Complexity of cyanobacterial exopolysaccharides: Composition, structures, inducing factors and putative genes involved in their biosynthesis and assembly. FEMS Microbiology Reviews, 33(5), 917 - 941.

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