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Journal Article
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.
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.
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.
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.
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.
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.
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.
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).
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).
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.
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.
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).
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.
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.
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.
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.
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.
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.
Sipe, J. D., Benson, M. D., Buxbaum, J. N., Ikeda, S. - I., et al. (2016). Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines. Amyloid, 23(4), 209 - 213.

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