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A
Se, H. C., Leight, S. N., Lee, V. M. - Y., Li, T., et al. (2007). Accelerated Aβ deposition in APPswe/PS1ΔE9 mice with hemizygous deletions of TTR (transthyretin). Journal of Neuroscience, 27(26), 7006 - 7010.
Castro, J. P., Jung, T., Grune, T., & Almeida, H. (2013). Actin carbonylation: From cell dysfunction to organism disorder. Journal of Proteomics, 92, 171 - 180.
Borges, O., Silva, M., de Sousa, A., Borchard, G., et al. (2008). Alginate coated chitosan nanoparticles are an effective subcutaneous adjuvant for hepatitis B surface antigen. International Immunopharmacology, 8(13-14), 1773 - 1780.
Gryseels, S., Amissah, D., Durnez, L., Vandelannoote, K., et al. (2012). Amoebae as Potential Environmental Hosts for Mycobacterium ulcerans and Other Mycobacteria, but Doubtful Actors in Buruli Ulcer Epidemiology. PLoS Neglected Tropical Diseases, 6(8).
Cho, K., Jang, J. H., Kim, S. - P., Lee, S. H., et al. (2016). Analysis of nociceptive information encoded in the temporal discharge patterns of cutaneous C-fibers. Frontiers in Computational Neuroscience, 10(NOV).
Cho, K., Jang, J. H., Kim, S. - P., Lee, S. H., et al. (2016). Analysis of nociceptive information encoded in the temporal discharge patterns of cutaneous C-fibers. Frontiers in Computational Neuroscience, 10(NOV).
Cho, K., Jang, J. H., Kim, S. - P., Lee, S. H., et al. (2016). Analysis of nociceptive information encoded in the temporal discharge patterns of cutaneous C-fibers. Frontiers in Computational Neuroscience, 10(NOV).
Almeida, T., Alonso, I., Martins, S., Ramos, E. M., et al. (2009). Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10). PLoS ONE, 4(2).
Bettencourt, C., Raposo, M., Kazachkova, N., Cymbron, T., et al. (2011). The APOE ε 2 allele increases the risk of earlier age at onset in Machado-Joseph disease. Archives of Neurology, 68(12), 1580 - 1583.
Tejera, E., Jose Areias, M., Rodrigues, A., Rama, A., et al. (2011). Artificial neural network for normal, hypertensive, and preeclamptic pregnancy classification using maternal heart rate variability indexes. Journal of Maternal-Fetal and Neonatal Medicine, 24(9), 1147 - 1151.
Martins, S., Calafell, F., Gaspar, C., Wong, V. C. N., et al. (2007). Asian origin for the worldwide-spread mutational event in Machado-Joseph disease. Archives of Neurology, 64(10), 1502 - 1508.
Saute, J. A. M., Donis, K. C., Serrano-Munuera, C., Genis, D., et al. (2012). Ataxia rating scales-psychometric profiles, natural history and their application in clinical trials. Cerebellum, 11(2), 488 - 504.
Huntington, N. D., Alves, N. L., Legrand, N., Lim, A., et al. (2011). Autonomous and extrinsic regulation of thymopoiesis inhuman immune system (HIS) mice. European Journal of Immunology, 41(10), 2883 - 2893.
C
Lee, J. - M., Ramos, E. M., Lee, J. - H., Gillis, T., et al. (2012). CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology, 78(10), 690 - 695.
Chen, Z., Zheng, C., Long, Z., Cao, L., et al. (2016). (CAG)nloci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China. Brain, 139(8), e41.
Ramos, E. M., Latourelle, J. C., Gillis, T., Mysore, J. S., et al. (2013). Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics, 14(3-4), 173 - 179.
Castro, J. P., Ott, C., Jung, T., Grune, T., & Almeida, H. (2012). Carbonylation of the cytoskeletal protein actin leads to aggregate formation. Free Radical Biology and Medicine, 53(4), 916 - 925.
Sonawane, A., Santos, J. C., Mishra, B. B., Jena, P., et al. (2011). Cathelicidin is involved in the intracellular killing of mycobacteria in macrophages. Cellular Microbiology, 13(10), 1601 - 1617.
Borry, P., Bentzen, H. B., Budin-Ljøsne, I., Cornel, M. C., et al. (2017). The challenges of the expanded availability of genomic information: an agenda-setting paper. Journal of Community Genetics.
Harley, C. A., Jesus, C. S. H., Carvalho, R., Brito, R. M. M., & Morais-Cabral, J. H. (2012). Changes in channel trafficking and protein stability caused by lqt2 mutations in the pas domain of the herg channel. PLoS ONE, 7(3).

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