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2017
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.
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.
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.
Chen, Z., Wang, C., Zheng, C., Long, Z., et al. (2017). Ubiquitin-related network underlain by (CAG)nloci modulate age at onset in Machado-Joseph disease. Brain, 140(4), e25.
2016
Sipe, J. D., Benson, M. D., Buxbaum, J. N., Ikeda, S. - I., et al. (2016). Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines. Amyloid, 23(4), 209 - 213.
Fontenete, S., Carvalho, D., Guimarães, N., Madureira, P., et al. (2016). Application of locked nucleic acid-based probes in fluorescence in situ hybridization. Applied Microbiology and Biotechnology, 100(13), 5897 - 5906.
Dias, D. M., Furtado, J., Wasielewski, E., Cruz, R., et al. (2016). Biophysical characterization of laforin-carbohydrate interaction. Biochemical Journal, 473(3), 335 - 345.
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.
Meyer, P. A., Socias, S., Key, J., Ransey, E., et al. (2016). Data publication with the structural biology data grid supports live analysis. Nature Communications, 7.
Meyer, P. A., Socias, S., Key, J., Ransey, E., et al. (2016). Data publication with the structural biology data grid supports live analysis. Nature Communications, 7.
Meyer, P. A., Socias, S., Key, J., Ransey, E., et al. (2016). Data publication with the structural biology data grid supports live analysis. Nature Communications, 7.
Howes, A., Taubert, C., Blankley, S., Spink, N., et al. (2016). Differential production of Type I IFN Determines the Reciprocal Levels of IL-10 and proinflammatory cytokines produced by C57BL/6 and BALB/c macrophages. Journal of Immunology, 197(7), 2838 - 2853.
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., 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.
Weber, E. M., Hultgren, J., Algers, B., & Olsson, I. A. S. (2016). Do laboratory mouse females that lose their litters behave differently around parturition?. PLoS ONE, 11(8).
Kramer, G., Wegdam, W., Donker-Koopman, W., Ottenhoff, R., et al. (2016). Elevation of glycoprotein nonmetastatic melanoma protein B in type 1 Gaucher disease patients and mouse models. FEBS Open Bio, 6(9), 902 - 913.
Ferraz, M. J., Marques, A. R. A., Gaspar, P., Mirzaian, M., et al. (2016). Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders. Molecular Genetics and Metabolism, 117(2), 186 - 193.
Coelho-Santos, V., Socodato, R., Portugal, C., Leitão, R. A., et al. (2016). Methylphenidate-triggered ROS generation promotes caveolae-mediated transcytosis via Rac1 signaling and c-Src-dependent caveolin-1 phosphorylation in human brain endothelial cells. Cellular and Molecular Life Sciences, 73(24), 4701 - 4716.
Martin, C. - A., Murray, J. E., Carroll, P., Leitch, A., et al. (2016). Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. Genes and Development, 30(19), 2158 - 2172.
Martin, C. - A., Murray, J. E., Carroll, P., Leitch, A., et al. (2016). Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. Genes and Development, 30(19), 2158 - 2172.
Laforge, M., Rodrigues, V., Silvestre, R., Gautier, C., et al. (2016). NF-κB pathway controls mitochondrial dynamics. Cell Death and Differentiation, 23(1), 89 - 98.
Butler, J. S., Chan, A., Costelha, S., Fishman, S., et al. (2016). Preclinical evaluation of RNAi as a treatment for transthyretin-mediated amyloidosis. Amyloid, 23(2), 109 - 118.
Borsari, C., Lucian, R., Pozzi, C., Poehner, I., et al. (2016). Profiling of flavonol derivatives for the development of antitrypanosomatidic drugs. Journal of Medicinal Chemistry, 59(16), 7598 - 7616.
Borsari, C., Lucian, R., Pozzi, C., Poehner, I., et al. (2016). Profiling of flavonol derivatives for the development of antitrypanosomatidic drugs. Journal of Medicinal Chemistry, 59(16), 7598 - 7616.

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