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Journal Article
Wiese, S., Gronemeyer, T., Ofman, R., Kunze, M., et al. (2007). Proteomics characterization of mouse kidney peroxisomes by tandem mass spectrometry and protein correlation profiling. Molecular and Cellular Proteomics, 6(12), 2045 - 2057.
Wiese, S., Gronemeyer, T., Ofman, R., Kunze, M., et al. (2007). Proteomics characterization of mouse kidney peroxisomes by tandem mass spectrometry and protein correlation profiling. Molecular and Cellular Proteomics, 6(12), 2045 - 2057.
Tarafder, A. K., Wasmeier, C., Figueiredo, A. C., Booth, A. E. G., et al. (2011). Rab27a targeting to melanosomes requires nucleotide exchange but not effector binding. Traffic, 12(8), 1056 - 1066.
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.
Currie, S. P., Luz, L. L., Booker, S. A., Wyllie, D. J. A., et al. (2017). Reduced local input to fast-spiking interneurons in the somatosensory cortex in the GABAA γ2 R43Q mouse model of absence epilepsy. Epilepsia, 58(4), 597 - 607.
McGovern, M. M., Elles, R., Beretta, I., Somerville, M. J., et al. (2007). Report of an international survey of molecular genetic testing laboratories. Community Genetics, 10(3), 123 - 131.
Köhler, A., Collymore, C., Finger-Baier, K., Geisler, R., et al. (2017). Report of workshop on euthanasia for zebrafish - a matter of welfare and science. Zebrafish, 14(6), 547 - 551.
Moran, C., Azziz, R., Weintrob, N., Witchel, S. F., et al. (2006). Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 91(9), 3451 - 3456.
Moran, C., Azziz, R., Weintrob, N., Witchel, S. F., et al. (2006). Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 91(9), 3451 - 3456.
Sneddon, L. U., Lopez-Luna, J., Wolfenden, D. C. C., Leach, M. C., et al. (2017). Response to: Responses of larval zebrafish to low pH immersion assay. Comment on Lopez-Luna et al. Comment. Journal of Experimental Biology, 220(17), 3192 - 3194.
Martins, I., Cabral, L., Pinto, A., Wilson, S. P., et al. (2011). Reversal of inflammatory pain by HSV-1-mediated overexpression of enkephalin in the caudal ventrolateral medulla. European Journal of Pain, 15(10), 1008 - 1014.
Pinto, P. A. B., Henriques, T., Freitas, M. O., Martins, T., et al. (2011). RNA polymerase II kinetics in polo polyadenylation signal selection. EMBO Journal, 30(12), 2431 - 2444.
Rutledge, S. D., Douglas, T. A., Nicholson, J. M., Vila-Casadesús, M., et al. (2016). Selective advantage of trisomic human cells cultured in non-standard conditions. Scientific Reports, 6.
Moreira, M. - C., Klur, S., Watanabe, M., Németh, A. H., et al. (2004). Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nature Genetics, 36(3), 225 - 227.
Moreira, M. - C., Klur, S., Watanabe, M., Németh, A. H., et al. (2004). Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nature Genetics, 36(3), 225 - 227.
White, J. P. M., Ko, C. W., Fidalgo, A. R., Cibelli, M., et al. (2011). Severe burn injury induces a characteristic activation of extracellular signal-regulated kinase 1/2 in spinal dorsal horn neurons. European Journal of Pain, 15(7), 683 - 690.
Pereira, P., Pedrosa, S. S., Wymant, J. M., Sayers, E., et al. (2015). SiRNA inhibition of endocytic pathways to characterize the cellular uptake mechanisms of folate-functionalized glycol chitosan nanogels. Molecular Pharmaceutics, 12(6), 1970 - 1979.
Martindale, J. E., Seneca, S., Wieczorek, S., & Sequeiros, J. (2012). Spinocerebellar ataxias: An example of the challenges associated with genetic databases for dynamic mutations. Human Mutation, 33(9), 1359 - 1365.
Trott, A., Jardim, L. B., Ludwig, H. T., Saute, J. A. M., et al. (2006). Spinocerebellar ataxias in 114 Brazilian families: Clinical and molecular findings [3]. Clinical Genetics, 70(2), 173 - 176.
Fuchs, S., Herzog, D., Sumara, G., Büchmann-Møller, S., et al. (2009). Stage-Specific Control of Neural Crest Stem Cell Proliferation by the Small Rho GTPases Cdc42 and Rac1. Cell Stem Cell, 4(3), 236 - 247.
Niederhauser, J., Lobrinus, J. A., Ochsner, F., Wider, C., et al. (2011). Successful heart and liver transplantation in a swiss patient with glu89lys transthyretin amyloidosis. Transplantation, 91(6), e40 - e42.
Altland, K., Winter, P., Saraiva, M. J. M., & Suhr, O. (2004). Sulfite and base for the treatment of familial amyloidotic polyneuropathy: Two additive approaches to stabilize the conformation of human amyloidogenic transthyretin. Neurogenetics, 5(1), 61 - 67.
Soares, M. L., Coelho, T., Sousa, A., Batalov, S., et al. (2005). Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: Complexity in a single-gene disease. Human Molecular Genetics, 14(4), 543 - 553.
Roussaki, M., Hall, B., Lima, S. C., Da Silva, A. C., et al. (2013). Synthesis and anti-parasitic activity of a novel quinolinone-chalcone series. Bioorganic and Medicinal Chemistry Letters, 23(23), 6436 - 6441.

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