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Seabra, A., Katzmarzyk, P., Carvalho, M. J., Seabra, A., et al. (2016). Effects of 6-month soccer and traditional physical activity programmes on body composition, cardiometabolic risk factors, inflammatory, oxidative stress markers and cardiorespiratory fitness in obese boys. Journal of Sports Sciences, 34(19), 1822 - 1829.
Seabra, A. R., Carvalho, H., & Pereira, P. J. B. (2009). Crystallization and preliminary crystallographic characterization of glutamine synthetase from Medicago truncatula. Acta Crystallographica Section F: Structural Biology and Crystallization Communications, 65(12), 1309 - 1312.
Seabra, A. R., Pereira, P. A., Becker, J. D., & Carvalho, H. G. (2012). Inhibition of glutamine synthetase by phosphinothricin leads to transcriptome reprograming in root nodules of Medicago truncatula. Molecular Plant-Microbe Interactions, 25(7), 976 - 992.
Seabra, R., Santos, A., Pereira, S., Moradas-Ferreira, P., & Tamagnini, P. (2009). Immunolocalization of the uptake hydrogenase in the marine cyanobacterium Lyngbya majuscula CCAP 1446/4 and two Nostoc strains. FEMS Microbiology Letters, 292(1), 57 - 62.
Segundo, M. A., Abreu, V. L. R. G., Osório, M. V., Nogueira, S., et al. (2016). Development and validation of HPLC method with fluorometric detection for quantification of bisnaphthalimidopropyldiaminooctane in animal tissues following administration in polymeric nanoparticles. Journal of Pharmaceutical and Biomedical Analysis, 120, 290 - 296.
Seixas, A. I., Vale, J., Jorge, P., Marques, I., et al. (2011). FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes. Behavioral and Brain Functions, 7.
Seixas, A. I., Holmes, S. E., Takeshima, H., Pavlovich, A., et al. (2012). Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis. Annals of Neurology, 71(2), 245 - 257.
Seixas, A. I., Maurer, M. H., Lin, M., Callahan, C., et al. (2005). FXTAS, SCA10, and SCA17 in American patients with movement disorders [1]. American Journal of Medical Genetics, 136 A(1), 87 - 89.
Seixas, D., Palace, J., & Tracey, I. (2016). Chronic pain disrupts the reward circuitry in multiple sclerosis. European Journal of Neuroscience, 44(3), 1928 - 1934.
Seixas, D., & Lima, D. (2011). Accuracy, reliability, validity and limitations of functional and structural magnetic resonance imaging data. Cortex, 47(10), 1266 - 1269.
Seixas, D., & Ayres Basto, M. (2008). Ethics in fMRI studies: A review of the EMBASE and MEDLINE literature. Clinical Neuroradiology, 18(2), 79 - 87.
Seixas, D., Galhardo, V., Sá, M. J., Guimarães, J., & Lima, D. (2009). Pain in multiple sclerosis: Characterization of a Portuguese population of 85 patients. Dor na esclerose múltipla: Caracterização de uma população Portuguesa de 85 doentesActa Medica Portuguesa, 22(3), 233 - 240.
Seixas, A. I., Loureiro, J. R., Costa, C., Ordóñez-Ugalde, A., et al. (2017). A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia. American Journal of Human Genetics, 101(1), 87 - 103.
Seneca, S., Morris, M. A., Patton, S., Elles, R., & Sequeiros, J. (2008). Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias. European Journal of Human Genetics, 16(8), 913 - 920.
Sequeiros, J., Santos, C., & Jardim, L. B. (2009). Response to Tumas et al. Clinical Genetics, 75(2), 208.
Sequeiros, J. (2006). Corino Andrade (1906-2005): a clinical geneticist before its own time. Clinical genetics, 69(2), 194 - 196.
Sequeiros, J., Gibbon, S., & Clarke, A. (2015). Genetics and ethics in Latin America. Journal of Community Genetics, 6(3), 185 - 187.
Sequeiros, J., Ramos, E. M., Cerqueira, J., Costa, M. C., et al. (2010). Large normal and reduced penetrance alleles in Huntington disease: Instability in families and frequency at the laboratory, at the clinic and in the population. Clinical Genetics, 78(4), 381 - 387.
Sequeiros, J., Seneca, S., & Martindale, J. (2010). Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias. European Journal of Human Genetics, 18(11), 1188 - 1195.
Sequeiros, J., Martindale, J., & Seneca, S. (2010). EMQN Best Practice Guidelines for molecular genetic testing of SCAs. European Journal of Human Genetics, 18(11), 1173 - 1176.
Sequeiros, J., Paneque, M., Guimarães, B., Rantanen, E., et al. (2012). The wide variation of definitions of genetic testing in international recommendations, guidelines and reports. Journal of Community Genetics, 3(2), 113 - 124.
Sequeiros, J., Martins, S., & Silveira, I. (2011). Epidemiology and population genetics of degenerative ataxias. Handbook of Clinical Neurology (Vol. 103, pp. 227 - 251).
Sereno, D., Monte Alegre, A., Silvestre, R., Vergnes, B., & Ouaissi, A. (2005). In vitro antileishmanial activity of nicotinamide. Antimicrobial Agents and Chemotherapy, 49(2), 808 - 812.
Sereno, D., Cordeiro Da Silva, A., Mathieu-Daude, F., & Ouaissi, A. (2007). Advances and perspectives in Leishmania cell based drug-screening procedures. Parasitology International, 56(1), 3 - 7.
Sereno, D., Vergnes, B., Mathieu-Daude, F., Cordeiro Da Silva, A., & Ouaissi, A. (2006). Looking for putative functions of the Leishmania cytosolic SIR2 deacetylase. Parasitology Research, 100(1), 1 - 9.

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