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Sipe, J. D., Benson, M. D., Buxbaum, J. N., Ikeda, S. - I., et al. (2012). Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis. Amyloid, 19(4), 167 - 170.
Mesquita, I., Moreira, D., Sampaio-Marques, B., Laforge, M., et al. (2016). AMPK in Pathogens. EXS, 107, 287 - 323.
Mesquita, I., Moreira, D., Sampaio-Marques, B., Laforge, M., et al. (2016). AMPK in Pathogens. EXS, 107, 287 - 323.
Moreira, D., Silvestre, R., Cordeiro-da-Silva, A., Estaquier, J., et al. (2016). AMP-activated protein kinase as a target for pathogens: Friends or foes?. Current Drug Targets, 17(8), 942 - 953.
Fonseca, N. A., Camacho, R., & Magalhães, A. L. (2008). Amino acid pairing at the N- and C-termini of helical segments in proteins. Proteins: Structure, Function and Genetics, 70(1), 188 - 196.
Conceiço Pereira, M., Loureiro, J. L., Pinto-Basto, J., Brando, E., et al. (2012). Alu elements mediate large SPG11 gene rearrangements: Further spatacsin mutations. Genetics in Medicine, 14(1), 143 - 151.
Conceiço Pereira, M., Loureiro, J. L., Pinto-Basto, J., Brando, E., et al. (2012). Alu elements mediate large SPG11 gene rearrangements: Further spatacsin mutations. Genetics in Medicine, 14(1), 143 - 151.
Maia, G. H., Soares, J. I., Andrade, P. A., Leite, J. F., et al. (2016). Altered taste preference and loss of limbic-projecting serotonergic neurons in the dorsal raphe nucleus of chronically epileptic rats. Behavioural Brain Research, 297, 28 - 36.
Beca, F., Pereira, M., Cameselle-Teijeiro, J. F., Martins, D., & Schmitt, F. (2015). Altered PPP2R2A and Cyclin D1 expression defines a subgroup of aggressive luminal-like breast cancer. BMC Cancer, 15(1).
Costa, E., Rocha, S., Rocha-Pereira, P., Castro, E., et al. (2008). Altered erythrocyte membrane protein composition in chronic kidney disease stage 5 patients under haemodialysis and recombinant human erythropoietin therapy. Blood Purification, 26(3), 267 - 273.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Brites, P., Ferreira, A. S., Da Silva, T. F., Sousa, V. F., et al. (2011). Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient mice. PLoS ONE, 6(12).
Moreira, S., Bishopp, A., Carvalho, H., & Campilho, A. (2013). AHP6 Inhibits Cytokinin Signaling to Regulate the Orientation of Pericycle Cell Division during Lateral Root Initiation. PLoS ONE, 8(2).
Guedes-Martins, L., Matos, L., Soares, A., Silva, E., & Almeida, H. (2013). AGEs, contributors to placental bed vascular changes leading to preeclampsia. Free Radical Research, 47(S1), 70 - 80.
Ribeiro, A., Freitas, C., Matos, L., Gouveia, A., et al. (2017). Age-related expression of TGF beta family receptors in human cumulus oophorus cells. Journal of Assisted Reproduction and Genetics, 34(9), 1121 - 1129.
Almeida, H., Matos, L., Ferreira, J., & Neves, D. (2006). Age-related effects of dexamethasone administration in adrenal zona reticularis. Annals of the New York Academy of Sciences (Vol. 1067, pp. 354 - 360).
Ribeiro, H., Abreu, I., Cunha, M., Mota, T., & Castro, R. (2005). Aeropalynological study of Vitis vinifera in the Braga region (1999-2003). Aerobiologia, 21(2), 131 - 138.
Miranda, C. O., Brites, P., Sousa, M. M., & Teixeira, C. A. (2013). Advances and pitfalls of cell therapy in metabolic leukodystrophies. Cell Transplantation, 22(2), 189 - 204.
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.
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.
Barrias, C. C., Martins, M. C. L., Miranda, M. C. S., & Barbosa, M. A. (2005). Adsorption of a therapeutic enzyme to self-assembled monolayers: Effect of surface chemistry and solution pH on the amount and activity of adsorbed enzyme. Biomaterials, 26(15), 2695 - 2704.

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