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2005
Sousa, S., Lecuit, M., & Cossart, P. (2005). Microbial strategies to target, cross or disrupt epithelia. Current Opinion in Cell Biology, 17(5 SPEC. ISS.), 489 - 498.
Silles, E., Osorio, H., Maia, R., Günther Sillero, M. A., & Sillero, A. (2005). Micromolar HgCl2 concentrations transitorily duplicate the ATP level in Saccharomyces cerevisiae cells. FEBS Letters, 579(19), 4044 - 4048.
Silles, E., Osorio, H., Maia, R., Günther Sillero, M. A., & Sillero, A. (2005). Micromolar HgCl2 concentrations transitorily duplicate the ATP level in Saccharomyces cerevisiae cells. FEBS Letters, 579(19), 4044 - 4048.
Ascensão, A., Magalhães, J., Soares, J. M. C., Ferreira, R., et al. (2005). Moderate endurance training prevents doxorubicin-induced in vivo mitochondriopathy and reduces the development of cardiac apoptosis. American Journal of Physiology - Heart and Circulatory Physiology, 289(2 58-2), H722 - H731.
MacIel, P., Cruz, V. T., Constante, M., Iniesta, I., et al. (2005). Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology, 65(4), 603 - 605.
MacIel, P., Cruz, V. T., Constante, M., Iniesta, I., et al. (2005). Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology, 65(4), 603 - 605.
MacIel, P., Cruz, V. T., Constante, M., Iniesta, I., et al. (2005). Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology, 65(4), 603 - 605.
Duarte, M., Schulte, U., Ushakova, A. V., & Videira, A. (2005). Neurospora strains harboring mitochondrial disease-associated mutations in iron-sulfur subunits of complex I. Genetics, 171(1), 91 - 99.
do Carmo Costa, M., Costa, C., Silva, A. P., Evangelista, P., et al. (2005). Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics, 6(4), 209 - 215.
do Carmo Costa, M., Costa, C., Silva, A. P., Evangelista, P., et al. (2005). Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics, 6(4), 209 - 215.
do Carmo Costa, M., Costa, C., Silva, A. P., Evangelista, P., et al. (2005). Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics, 6(4), 209 - 215.
Alonso, I., Costa, C., Gomes, A., Ferro, A., et al. (2005). A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14. Journal of Human Genetics, 50(10), 523 - 529.
Alonso, I., Costa, C., Gomes, A., Ferro, A., et al. (2005). A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14. Journal of Human Genetics, 50(10), 523 - 529.
Alonso, I., Costa, C., Gomes, A., Ferro, A., et al. (2005). A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14. Journal of Human Genetics, 50(10), 523 - 529.
Alonso, I., Costa, C., Gomes, A., Ferro, A., et al. (2005). A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14. Journal of Human Genetics, 50(10), 523 - 529.
Pereira, C. S., Soares Da Costa, D., Teixeira, J., & Pereira, S. (2005). Organ-specific distribution and subcellular localisation of ascorbate peroxidase isoenzymes in potato (Solanum tuberosum L.) plants. Protoplasma, 226(3-4), 223 - 230.
Belo, L., Santos-Silva, A., Caslake, M., Pereira-Leite, L., et al. (2005). Oxidized-LDL levels in normal and pre-eclamptic pregnancies: Contribution of LDL particle size [2]. Atherosclerosis, 183(1), 185 - 186.
Costa-Rodrigues, J., Carvalho, A. F., Fransen, M., Hambruch, E., et al. (2005). Pex5p, the peroxisomal cycling receptor, is a monomeric non-globular protein. Journal of Biological Chemistry, 280(26), 24404 - 24411.
Costa-Rodrigues, J., Carvalho, A. F., Fransen, M., Hambruch, E., et al. (2005). Pex5p, the peroxisomal cycling receptor, is a monomeric non-globular protein. Journal of Biological Chemistry, 280(26), 24404 - 24411.
Souto, L., Alves, C., Gusmão, L., Ferreira, E., et al. (2005). Population data on 15 autosomal STRs in a sample from East Timor. Forensic Science International, 155(1), 77 - 80.
Lima, M., Costa, M. C., Montiel, R., Ferro, A., et al. (2005). Population genetics of wild-type CAG repeats in the Machado-Joseph Disease gene in Portugal. Human Heredity, 60(3), 156 - 163.
Lima, M., Costa, M. C., Montiel, R., Ferro, A., et al. (2005). Population genetics of wild-type CAG repeats in the Machado-Joseph Disease gene in Portugal. Human Heredity, 60(3), 156 - 163.
Lima, M., Costa, M. C., Montiel, R., Ferro, A., et al. (2005). Population genetics of wild-type CAG repeats in the Machado-Joseph Disease gene in Portugal. Human Heredity, 60(3), 156 - 163.
Lima, M., Costa, M. C., Montiel, R., Ferro, A., et al. (2005). Population genetics of wild-type CAG repeats in the Machado-Joseph Disease gene in Portugal. Human Heredity, 60(3), 156 - 163.
De Matos Granja, N., Vinhas Ricardo, S. A., Longatto Filho, A., Ferreira Alves, V. A., et al. (2005). Potential use of loss of heterozygosity in pleural effusions of breast cancer metastases using the microsatellite marker of the 16q22.1 region of the CDH1 gene. Analytical and Quantitative Cytology and Histology, 27(2), 61 - 66.

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