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Bettencourt, C., Santos, C., Coutinho, P., Rizzu, P., et al. (2011). Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): A two-case report. BMC Neurology, 11.
Bettencourt, C., Santos, C., Montiel, R., do Carmo Costa, M., et al. (2010). Increased transcript diversity: Novel splicing variants of Machado-Joseph Disease gene (ATXN3). Neurogenetics, 11(2), 193 - 202.
Bettencourt, C., Fialho, R. N., Santos, C., Montiel, R., et al. (2008). Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: A study in normal families from the Azores islands (Portugal). Journal of Human Genetics, 53(4), 333 - 339.
Bettencourt, B. F., Rocha, F. L., Alves, H., Amorim, R., et al. (2013). Protective effect of an ERAP1 haplotype in ankylosing spondylitis: Investigating non-MHC genes in HLA-B27-positive individuals. Rheumatology (United Kingdom), 52(12), 2168 - 2176.
Bettencourt, C., Santos, C., Montiel, R., Kay, T., et al. (2010). The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): A comparison between DNA and mRNA in patients and controls. European Journal of Human Genetics, 18(5), 621 - 623.
Bettencourt, B. F., Santos, M. R., Pereira, J., Amaro, B., et al. (2016). HLA-A, -B, -C, -DQA1, -DQB1, -DRB1, -E, -F and -G genotyping of 130 individuals from Terceira Island, Azores, Portugal. Human Immunology, 77(6), 445 - 446.
Bettencourt, C., & Lima, M. (2013). "Mimicking" capacity of spinocerebellar ataxia type 3: The details matter. Journal of the Neurological Sciences.
Bettencourt, C., Hensman-Moss, D., Flower, M., Wiethoff, S., et al. (2016). DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Annals of Neurology, 79(6), 983 - 990.
Bettencourt, C., & Lima, M. (2011). Machado-Joseph disease: From first descriptions to new perspectives. Orphanet Journal of Rare Diseases, 6(1).
Bettencourt, C., Raposo, M., Ros, R., Montiel, R., et al. (2012). Transcript Diversity of Machado-Joseph Disease Gene (ATXN3) Is Not Directly Determined by SNPs in Exonic or Flanking Intronic Regions. Journal of Molecular Neuroscience.
Bettencourt, B. F., Santos, M. R., Fialho, R. N., Couto, A. R., et al. (2008). Evaluation of two methods for computational HLA haplotypes inference using a real dataset. BMC Bioinformatics, 9.
Beubler, E., Eisenberg, E., Castro-Lopes, J., & Rhodin, A. (2007). Prescribing policies of opioids for chronic pain. Journal of Pain and Palliative Care Pharmacotherapy, 21(2), 53 - 55.
Birder, L. A., Kanai, A. J., Cruz, F., Moore, K., & Fry, C. H. (2010). Is the urothelium intelligent?. Neurourology and Urodynamics, 29(4), 598 - 602.
Blaya, D. S., Guimaräes, M. B., Pozza, D. H., Weber, J. B. B., & De Oliveira, M. G. (2008). Histologic study of the effect of laser therapy on bone repair. Journal of Contemporary Dental Practice, 9(6), 041 - 048.
Boaventura, P., Batista, R., Pestana, A., Reis, M., et al. (2017). TERT promoter mutations: A genetic signature of benign and malignant thyroid tumours occurring in the context of tinea capitis irradiation. European Journal of Endocrinology, 176(1), 49 - 55.
Boelaert, J. R., Vandecasteele, S. J., Appelberg, R., & Gordeuk, V. R. (2007). The effect of the host's iron status on tuberculosis. Journal of Infectious Diseases, 195(12), 1745 - 1753.
Boneca, I. G., Dussurget, O., Cabanes, D., Nahori, M. - A., et al. (2007). A critical role for peptidoglycan N-deacetylation in Listeria evasion from the host innate immune system. Proceedings of the National Academy of Sciences of the United States of America, 104(3), 997 - 1002.
Bonekamp, N. A., Sampaio, P., de Abreu, F. V., Lüers, G. H., & Schrader, M. (2012). Transient Complex Interactions of Mammalian Peroxisomes Without Exchange of Matrix or Membrane Marker Proteins. Traffic, 13(7), 960 - 978.
Borges, M., Barreira-Silva, P., Flórido, M., Jordan, M. B., et al. (2012). Molecular and cellular mechanisms of Mycobacterium avium-induced thymic atrophy. Journal of Immunology, 189(7), 3600 - 3608.
Borges, O., Borchard, G., de Sousa, A., Junginger, H. E., & Cordeiro-da-Silva, A. (2007). Induction of lymphocytes activated marker CD69 following exposure to chitosan and alginate biopolymers. International Journal of Pharmaceutics, 337(1-2), 254 - 264.
Borges, M., Rosa, G. T., & Appelberg, R. (2011). The death-promoting molecule tumour necrosis factor-related apoptosis inducing ligand (TRAIL) is not required for the development of peripheral lymphopenia or granuloma necrosis during infection with virulent Mycobacterium avium. Clinical and Experimental Immunology, 164(3), 407 - 416.
Borges, G. S., Berrocoso, E., Ortega-Alvaro, A., Mico, J. A., & Neto, F. L. (2013). Extracellular signal-regulated kinase activation in the chronic constriction injury model of neuropathic pain in anaesthetized rats. European Journal of Pain (United Kingdom), 17(1), 35 - 45.
Borges, O., Cordeiro-da-Silva, A., Tavares, J., Santarém, N., et al. (2008). Immune response by nasal delivery of hepatitis B surface antigen and codelivery of a CpG ODN in alginate coated chitosan nanoparticles. European Journal of Pharmaceutics and Biopharmaceutics, 69(2), 405 - 416.
Borges, O., Tavares, J., de Sousa, A., Borchard, G., et al. (2007). Evaluation of the immune response following a short oral vaccination schedule with hepatitis B antigen encapsulated into alginate-coated chitosan nanoparticles. European Journal of Pharmaceutical Sciences, 32(4-5), 278 - 290.
Borges, A., Borges, M., Fernandes, J., Nascimento, H., et al. (2011). Apoptosis of peripheral CD4 ++ T-lymphocytes in end-stage renal disease patients under hemodialysis and rhEPO therapies. Renal Failure, 33(2), 138 - 143.

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