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Journal Article
Martins, S., Costa-Lima, S., Carneiro, T., Cordeiro-da-Silva, A., et al. (2012). Solid lipid nanoparticles as intracellular drug transporters: An investigation of the uptake mechanism and pathway. International Journal of Pharmaceutics, 430(1-2), 216 - 227.
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.
Ogun, S. A., Martins, S., Adebayo, P. B., Dawodu, C. O., et al. (2015). Machado-Joseph disease in a Nigerian family: Mutational origin and review of the literature. European Journal of Human Genetics, 23(2), 271 - 273.
Martins, S., Seixas, A. I., Magalhães, P., Coutinho, P., et al. (2005). Haplotype diversity and somatic instability in normal and expanded SCA8 alleles. American Journal of Medical Genetics - Neuropsychiatric Genetics, 139 B(1), 109 - 114.
Pessoa, J., Sárkány, Z., Ferreira-Da-Silva, F., Martins, S., et al. (2010). Functional characterization of Arabidopsis thaliana transthyretin-like protein. BMC Plant Biology, 10.
Maia, N., Loureiro, J. R., Oliveira, B., Marques, I., et al. (2017). Contraction of fully expanded FMR1 alleles to the normal range: Predisposing haplotype or rare events?. Journal of Human Genetics, 62(2), 269 - 275.
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.
Martins, S., Coutinho, P., Silveira, I., Giunti, P., et al. (2008). Cis-acting factors promoting the CAG intergenerational instability in Machado-Joseph disease. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 147(4), 439 - 446.
Martins, S., Calafell, F., Gaspar, C., Wong, V. C. N., et al. (2007). Asian origin for the worldwide-spread mutational event in Machado-Joseph disease. Archives of Neurology, 64(10), 1502 - 1508.
Almeida, T., Alonso, I., Martins, S., Ramos, E. M., et al. (2009). Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10). PLoS ONE, 4(2).

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