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Ferreira-Gomes, J., Neto, F. L., & Castro-Lopes, J. M. (2006). GABAB2 receptor subunit mRNA decreases in the thalamus of monoarthritic animals. Brain Research Bulletin, 71(1-3), 252 - 258.
Flórido, M., Pearl, J. E., Solache, A., Borges, M., et al. (2005). Gamma interferon-induced T-cell loss in virulent Mycobacterium avium infection. Infection and Immunity, 73(6), 3577 - 3586.
Pereira, D. M., Vinholes, J., De Pinho, P. G., Valentão, P., et al. (2012). A gas chromatography-mass spectrometry multi-target method for the simultaneous analysis of three classes of metabolites in marine organisms. Talanta, 100, 391 - 400.
Rodríguez-Seguí, S. A., & Bessa, J. (2015). Gatekeepers of pancreas: TEAD and YAP. Oncotarget, 6(18), 15736 - 15737.
Cherif, W., Ben Turkia, H., Ben Rhouma, F., Riahi, I., et al. (2009). Gaucher disease in Tunisia: High frequency of the most common mutations. Blood Cells, Molecules, and Diseases, 43(2), 161 - 162.
Barsch, A., Carvalho, H. G., Cullimore, J. V., & Niehaus, K. (2006). GC-MS based metabolite profiling implies three interdependent ways of ammonium assimilation in Medicago truncatula root nodules. Journal of Biotechnology, 127(1), 79 - 83.
Plissonneau, M., Pansieri, J., Heinrich-Balard, L., Morfin, J. - F., et al. (2016). Gd-nanoparticles functionalization with specific peptides for ß-amyloid plaques targeting. Journal of Nanobiotechnology, 14(1).
Gonçalves, A. F., Dias, N. G., Moransard, M., Correia, R., et al. (2010). Gelsolin is required for macrophage recruitment during remyelination of the peripheral nervous system. GLIA, 58(6), 706 - 715.
Oliveira, S. M., Ribeiro, C. A., Cardoso, I., & Saraiva, M. J. (2011). Gender-dependent transthyretin modulation of brain amyloid-β Levels: Evidence from a mouse model of alzheimer's disease. Journal of Alzheimer's Disease, 27(2), 429 - 439.
Fonseca, N. A., Vieira, C. P., & Vieira, J. (2009). Gene classification based on amino acid motifs and residues: The DLX (distal-less) test case. PLoS ONE, 4(6).
Pavani, K. C., Baron, E., Correia, P., Lourenço, J., et al. (2016). Gene expression, oocyte nuclear maturation and developmental competence of bovine oocytes and embryos produced after in vivo and in vitro heat shock. Zygote, 24(5), 748 - 759.
Teixeira, C. A. F., Lin, S., Mangas, M., Quinta, R., et al. (2006). Gene expression profiling in vLINCL CLN6-deficient fibroblasts: Insights into pathobiology. Biochimica et Biophysica Acta - Molecular Basis of Disease, 1762(7), 637 - 646.
Duarte, T. L., Cooke, M. S., & Jones, G. D. D. (2009). Gene expression profiling reveals new protective roles for vitamin C in human skin cells. Free Radical Biology and Medicine, 46(1), 78 - 87.
Crespo, R., Rocha, F. A., Damas, A. M., & Martins, P. M. (2012). A generic crystallization-like model that describes the kinetics of amyloid fibril formation. Journal of Biological Chemistry, 287(36), 30585 - 30594.
Leitão, E., Pereira, S., Bondoso, J., Ferreira, D., et al. (2006). Genes involved in the maturation of hydrogenase(s) in the nonheterocystous cyanobacterium Lyngbya majuscula CCAP 1446/4. International Journal of Hydrogen Energy, 31(11), 1469 - 1477.
Crespo, T. C., Silva, B., Marques, L., Marcelino, E., et al. (2014). Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation. Neurobiology of Aging, 35(4), 777 - 785.
Tsukamoto, T., Potter, D., Tao, R., Vieira, C. P., et al. (2008). Genetic and molecular characterization of three novel S-haplotypes in sour cherry (Prunus cerasus L.). Journal of Experimental Botany, 59(11), 3169 - 3185.
Neto, J. L., Lee, J. - M., Afridi, A., Gillis, T., et al. (2017). Genetic contributors to intergenerational CAG repeat instability in Huntington’s disease knock-in mice. Genetics, 205(2), 503 - 516.
Flórido, M., & Appelberg, R. (2006). Genetic control of immune-mediated necrosis of Mycobacterium avium granulomas. Immunology, 118(1), 122 - 130.
Paneque, M., Mendes, Á., Saraiva, J., & Sequeiros, J. (2015). Genetic Counseling in Portugal: Education, Practice and a Developing Profession. Journal of Genetic Counseling, 24(4), 548 - 552.
Duarte, T. L., Caldas, C., Santos, A. G., Silva-Gomes, S., et al. (2017). Genetic disruption of NRF2 promotes the development of necroinflammation and liver fibrosis in a mouse model of HFE-hereditary hemochromatosis. Redox Biology, 11, 157 - 169.
Skirton, H., Lewis, C., Kent, A., & Coviello, D. A. (2010). Genetic education and the challenge of genomic medicine: Development of core competences to support preparation of health professionals in Europe. European Journal of Human Genetics, 18(9), 972 - 977.
Munar-Qués, M., Saraiva, M. J. M., Viader-Farré, C., Zabay-Becerril, J. M., & Mulet-Ferrer, J. (2005). Genetic epidemiology of familial amyloid polyneuropathy in the Balearic Islands (Spain). Amyloid, 12(1), 54 - 61.
Couto, A. R., & Brown, M. A. (2007). Genetic factors in the pathogenesis of CPPD crystal deposition disease. Current Rheumatology Reports, 9(3), 231 - 236.
Altland, K., Benson, M. D., Costello, C. E., Ferlini, A., et al. (2007). Genetic microheterogeneity of human transthyretin detected by IEF. Electrophoresis, 28(12), 2053 - 2064.

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