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2004
Vieira, L. M. M., Kijjoa, A., Wilairat, R., Nascimento, M. S. J., et al. (2004). Bioactive friedolanostanes and 11(10→8)-abeolanostanes from the bark of Garcinia speciosa. Journal of Natural Products, 67(12), 2043 - 2047.
Castelo-Branco, P., Furger, A., Wollerton, M., Smith, C., et al. (2004). Erratum: Polypyrimidine tract binding protein modulates efficiency of polyadenylation (Molecular and Cellular Biology (2004) 24, 10 (4174-4183)). Molecular and Cellular Biology, 24(15), 6889.
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.
Castelo-Branco, P., Furger, A., Wollerton, M., Smith, C., et al. (2004). Polypyrimidine tract binding protein modulates efficiency of polyadenylation. Molecular and Cellular Biology, 24(10), 4174 - 4183.
Moreira, M. - C., Klur, S., Watanabe, M., Németh, A. H., et al. (2004). Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nature Genetics, 36(3), 225 - 227.
Moreira, M. - C., Klur, S., Watanabe, M., Németh, A. H., et al. (2004). Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nature Genetics, 36(3), 225 - 227.
Altland, K., Winter, P., Saraiva, M. J. M., & Suhr, O. (2004). Sulfite and base for the treatment of familial amyloidotic polyneuropathy: Two additive approaches to stabilize the conformation of human amyloidogenic transthyretin. Neurogenetics, 5(1), 61 - 67.
2005
Marcao, A. M., Wiest, R., Schinaler, K., Wiesmann, U., et al. (2005). Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: A new mutation in the ARSA gene. Archives of Neurology, 62(2), 309 - 313.
Marcao, A. M., Wiest, R., Schinaler, K., Wiesmann, U., et al. (2005). Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: A new mutation in the ARSA gene. Archives of Neurology, 62(2), 309 - 313.
Marcao, A. M., Wiest, R., Schinaler, K., Wiesmann, U., et al. (2005). Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: A new mutation in the ARSA gene. Archives of Neurology, 62(2), 309 - 313.
Westermark, P., Benson, M. D., Buxbaum, J. N., Cohen, A. S., et al. (2005). Amyloid: Toward terminology clarification: Report from the Nomenclature Committee of the International Society Of Amyloidosis. Amyloid, 12(1), 1 - 4.
Lopes, C. S., Sampaio, P., Williams, B., Goldberg, M., & Sunkel, C. E. (2005). The Drosophila Bub3 protein is required for the mitotic checkpoint and for normal accumulation of cyclins during G2 and early stages of mitosis. Journal of Cell Science, 118(1), 187 - 198.
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.
De Matos Granja, N., Vinhas Ricardo, S. A., Longatto Filho, A., Ferreira Alves, V. A., et al. (2005). Potential use of loss of heterozygosity in pleural effusions of breast cancer metastases using the microsatellite marker of the 16q22.1 region of the CDH1 gene. Analytical and Quantitative Cytology and Histology, 27(2), 61 - 66.
Soares, M. L., Coelho, T., Sousa, A., Batalov, S., et al. (2005). Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: Complexity in a single-gene disease. Human Molecular Genetics, 14(4), 543 - 553.
Swiedler, S. J., Beck, M., Bajbouj, M., Giugliani, R., et al. (2005). Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). American Journal of Medical Genetics, 134 A(2), 144 - 150.
2006
Evans, E. J., Castro, M. A. A., O'Brien, R., Kearney, A., et al. (2006). Crystal structure and binding properties of the CD2 and CD244 (2B4)-binding protein, CD48. Journal of Biological Chemistry, 281(39), 29309 - 29320.
Cavadas, C., Céfai, D., Rosmaninho-Salgado, J., Vieira-Coelho, M. A., et al. (2006). Deletion of the neuropeptide Y (NPY) Y1 receptor gene reveals a regulatory role of NPY on catecholamine synthesis and secretion. Proceedings of the National Academy of Sciences of the United States of America, 103(27), 10497 - 10502.
Colombié, N., Vérollet, C., Sampaio, P., Moisand, A., et al. (2006). The Drosophila γ-tubulin small complex subunit Dgrip84 is required for structural and functional integrity of the spindle apparatus. Molecular Biology of the Cell, 17(1), 272 - 282.
Rodrigues, P. N. S., Vázquez-Dorado, S., Neves, J. V., & Wilson, J. M. (2006). Dual function of fish hepcidin: Response to experimental iron overload and bacterial infection in sea bass (Dicentrarchus labrax). Developmental and Comparative Immunology, 30(12), 1156 - 1167.
Harmatz, P., Giugliani, R., Schwartz, I., Guffon, N., et al. (2006). Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-l. Journal of Pediatrics, 148(4), 533 - 533.e.
Harmatz, P., Giugliani, R., Schwartz, I., Guffon, N., et al. (2006). Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-l. Journal of Pediatrics, 148(4), 533 - 533.e.
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.
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.
Holmes, S. E., Wentzell, J. S., Seixas, A. I., Callahan, C., et al. (2006). A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array. Human Genetics, 120(2), 193 - 200.

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