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2017
Paneque, M., Moldovan, R., Cordier, C., Serra-Juhé, C., et al. (2017). The perceived impact of the European registration system for genetic counsellors and nurses. European Journal of Human Genetics, 25(9), 1075 - 1077.
Ghaeli, I., De Moraes, M. A., Beppu, M. M., Lewandowska, K., et al. (2017). Phase behaviour and miscibility studies of collagen/silk fibroin macromolecular system in dilute solutions and solid state. Molecules, 22(8).
Moreira, A. C., Silva, A. M., Branco, A. F., Baldeiras, I., et al. (2017). Phytoestrogen coumestrol improves mitochondrial activity and decreases oxidative stress in the brain of ovariectomized Wistar-Han rats. Journal of Functional Foods, 34, 329 - 339.
Silva, A., de Almeida, A. V., & Macedo-Ribeiro, S. (2017). Polyglutamine expansion diseases: More than simple repeats. Journal of Structural Biology.
Sousa, A. L., Alonso, I., & Magalhães, M. (2017). A Portuguese rapid-onset dystonia-parkinsonism case with atypical features. Neurological Sciences, 38(9), 1713 - 1714.
Cecílio, P., Pérez-Cabezas, B., Fernandez, L., Moreno, J., et al. (2017). Pre-clinical antigenicity studies of an innovative multivalent vaccine for human visceral leishmaniasis. PLoS Neglected Tropical Diseases, 11(11).
Melo, S., Figueiredo, J., Fernandes, M. S., Gonçalves, M., et al. (2017). Predicting the functional impact of CDH1 missense mutations in hereditary diffuse gastric cancer. International Journal of Molecular Sciences, 18(12).
Melo, S., Figueiredo, J., Fernandes, M. S., Gonçalves, M., et al. (2017). Predicting the functional impact of CDH1 missense mutations in hereditary diffuse gastric cancer. International Journal of Molecular Sciences, 18(12).
Kazachkova, N., Raposo, M., Ramos, A., Montiel, R., & Lima, M. (2017). Promoter Variant Alters Expression of the Autophagic BECN1 Gene: Implications for Clinical Manifestations of Machado-Joseph Disease. Cerebellum, 16(5-6), 957 - 963.
Moura, M., Osswald, M., Leça, N., Barbosa, J., et al. (2017). Protein phosphatase 1 inactivates Mps1 to ensure efficient spindle assembly checkpoint silencing. eLife, 6.
Moura, M., Osswald, M., Leça, N., Barbosa, J., et al. (2017). Protein phosphatase 1 inactivates Mps1 to ensure efficient spindle assembly checkpoint silencing. eLife, 6.
Anjo, S. I., Figueiredo, F., Fernandes, R., Manadas, B., & Oliveira, M. (2017). A proteomic and ultrastructural characterization of Aspergillus fumigatus' conidia adaptation at different culture ages. Journal of Proteomics, 161, 47 - 56.
Deng, S., Kain, L., Pereira, C. S., Mata, S., et al. (2017). Psychosine variants as antigens for natural killer T cells. Chemical Science, 8(3), 2204 - 2208.
Deng, S., Kain, L., Pereira, C. S., Mata, S., et al. (2017). Psychosine variants as antigens for natural killer T cells. Chemical Science, 8(3), 2204 - 2208.
Gaskell, G., Bard, I., Allansdottir, A., Da Cunha, R. V., et al. (2017). Public views on gene editing and its uses. Nature Biotechnology, 35(11), 1022 - 1023.
Matilla-Duenas, A., Corral-Juan, M., A. Seuma, R. - P., Vilas, D., et al. (2017). Rare neurodegenerative diseases: Clinical and genetic update. Advances in Experimental Medicine and Biology (Vol. 1031, pp. 443 - 496).
Matilla-Duenas, A., Corral-Juan, M., A. Seuma, R. - P., Vilas, D., et al. (2017). Rare neurodegenerative diseases: Clinical and genetic update. Advances in Experimental Medicine and Biology (Vol. 1031, pp. 443 - 496).
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.

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