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Journal Article
do Carmo Costa, M., Costa, C., Silva, A. P., Evangelista, P., et al. (2005). Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics, 6(4), 209 - 215.
Bettencourt, C., Santos, C., Montiel, R., do Carmo Costa, M., et al. (2010). Increased transcript diversity: Novel splicing variants of Machado-Joseph Disease gene (ATXN3). Neurogenetics, 11(2), 193 - 202.
Santos, M., do Carmo Costa, M., Edite Rio, M., José Sá, M., et al. (2004). Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin. Multiple Sclerosis, 10(2), 153 - 157.
do Carmo Costa, M., Gomes-da-Silva, J., Miranda, C. J., Sequeiros, J., et al. (2004). Genomic structure, promoter activity, and developmental expression of the mouse homologue of the Machado-Joseph disease (MJD) gene. Genomics, 84(2), 361 - 373.
Neves-Carvalho, A., Logarinho, E., Freitas, A., Duarte-Silva, S., et al. (2015). Dominant negative effect of polyglutamine expansion perturbs normal function of ataxin-3 in neuronal cells. Human Molecular Genetics, 24(1), 100 - 117.
do Carmo Costa, M., Bajanca, F., Rodrigues, A. J., Tomé, R. J., et al. (2010). Ataxin-3 plays a role in mouse myogenic differentiation through regulation of integrin subunit levels. PloS one, 5(7).
Rodrigues, A. - J., do Carmo Costa, M., Silva, T. - L., Ferreira, D., et al. (2010). Absence of ataxin-3 leads to cytoskeletal disorganization and increased cell death. Biochimica et Biophysica Acta - Molecular Cell Research, 1803(10), 1154 - 1163.

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