Zin, W. W. May, Buttachon, S., Dethoup, T., Pereira, J. A., et al. (2017). Antibacterial and antibiofilm activities of the metabolites isolated from the culture of the mangrove-derived endophytic fungus Eurotium chevalieri KUFA 0006. Phytochemistry, 141, 86 - 97.

Kennelly, M., Dmochowski, R., Schulte-Baukloh, H., Ethans, K., et al. (2017). Efficacy and safety of onabotulinumtoxinA therapy are sustained over 4 years of treatment in patients with neurogenic detrusor overactivity: Final results of a long-term extension study. Neurourology and Urodynamics, 36(2), 368 - 375.

Afshin, A., Forouzanfar, M. H., Reitsma, M. B., Sur, P., et al. (2017). Health effects of overweight and obesity in 195 countries over 25 years. New England Journal of Medicine, 377(1), 13 - 27.

Barber, R. M., Fullman, N., Sorensen, R. J. D., Bollyky, T., et al. (2017). Healthcare Access and Quality Index based on mortality from causes amenable to personal health care in 195 countries and territories, 1990?2015: a novel analysis from the Global Burden of Disease Study 2015. The Lancet, 390(10091), 231 - 266.

Zhao, Y., Goldschen-Ohm, M. P., Morais-Cabral, J. H., Chanda, B., & Robertson, G. A. (2017). The intrinsically liganded cyclic nucleotide-binding homology domain promotes KCNH channel activation. Journal of General Physiology, 149(2), 249 - 260.

Ziermann, J. M., Freitas, R., & Diogo, R. (2017). Muscle development in the shark Scyliorhinus canicula: Implications for the evolution of the gnathostome head and paired appendage musculature. Frontiers in Zoology, 14(1).

Burisch, J., Vegh, Z., Katsanos, K. H., Christodoulou, D. K., et al. (2017). Occurrence of anaemia in the first year of inflammatory bowel disease in a European population-based inception cohort-An ECCO-EpiCom study. Journal of Crohn's and Colitis, 11(10), 1213 - 1222.

Gaskell, G., Bard, I., Allansdottir, A., Da Cunha, R. V., et al. (2017). Public views on gene editing and its uses. Nature Biotechnology, 35(11), 1022 - 1023.

Kilinc, E., Guerrero-Toro, C., Zakharov, A., Vitale, C., et al. (2017). Serotonergic mechanisms of trigeminal meningeal nociception: Implications for migraine pain. Neuropharmacology, 116, 160 - 173.

Aday, S., Zoldan, J., Besnier, M., Carreto, L., et al. (2017). Synthetic microparticles conjugated with VEGF165improve the survival of endothelial progenitor cells via microRNA-17 inhibition. Nature Communications, 8(1).

Liu, X., Freitas, J., Zheng, D., Oliveira, M. S., et al. (2017). Transcription elongation rate has a tissue-specific impact on alternative cleavage and polyadenylation in Drosophila melanogaster. RNA, 23(12), 1807 - 1816.

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.

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.

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.

Martínez-Salamanca, J. I., Zurita, M., Costa, C., Martínez-Salamanca, E., et al. (2016). Dual Strategy With Oral Phosphodiesterase Type 5 Inhibition and Intracavernosal Implantation of Mesenchymal Stem Cells Is Superior to Individual Approaches in the Recovery of Erectile and Cavernosal Functions After Cavernous Nerve Injury in Rats. Journal of Sexual Medicine, 13(1), 1 - 11.

Porto, G., Brissot, P., Swinkels, D. W., Zoller, H., et al. (2016). EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). European Journal of Human Genetics, 24(4), 479 - 495.

Fais, S., O'Driscoll, L., Borras, F. E., Buzas, E., et al. (2016). Evidence-Based Clinical Use of Nanoscale Extracellular Vesicles in Nanomedicine. ACS Nano, 10(4), 3886 - 3899.

Zin, W. W. M., Buttachon, S., Dethoup, T., Fernandes, C., et al. (2016). New cyclotetrapeptides and a new diketopiperzine derivative from the marine sponge-associated fungus Neosartorya glabra KUFA 0702. Marine Drugs, 14(7).

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.

Buttachon, S., Zin, W. W. May, Dethoup, T., Gales, L., et al. (2016). Secondary Metabolites from the Culture of the Marine Sponge-Associated Fungi Talaromyces tratensis and Sporidesmium circinophorum. Planta Medica, 82(9-10), 888 - 896.

Porto, G., Brissot, P., Swinkels, D. W., Zoller, H., et al. (2015). EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). European Journal of Human Genetics.

Zipor, G., Duarte, P., Carqueijeiro, I., Shahar, L., et al. (2015). In planta anthocyanin degradation by a vacuolar class III peroxidase in Brunfelsia calycina flowers. New Phytologist, 205(2), 653 - 665.

Barisic, M., Silva E Sousa, R., Tripathy, S. K., Magiera, M. M., et al. (2015). Microtubule detyrosination guides chromosomes during mitosis. Science, 348(6236), 799 - 803.

Zin, W. W. M., Buttachon, S., Buaruang, J., Gales, L., et al. (2015). A new meroditerpene and a new tryptoquivaline analog from the algicolous fungus Neosartorya takakii KUFC 7898. Marine Drugs, 13(6), 3776 - 3790.

Rothaug, M., Zunke, F., Mazzulli, J. R., Schweizer, M., et al. (2014). LIMP-2 expression is critical for Î²-glucocerebrosidase activity and Î±-synuclein clearance. Proceedings of the National Academy of Sciences of the United States of America, 111(43), 15573 - 15578.

Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.

Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.

Silva, D. S., Pereira, L. M. G., Moreira, A. R., Ferreira-Da-Silva, F., et al. (2013). The Apoptogenic Toxin AIP56 Is a Metalloprotease A-B Toxin that Cleaves NF-?b P65. PLoS Pathogens, 9(2).

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.

Laforge, M., Limou, S., Harper, F., Casartelli, N., et al. (2013). DRAM Triggers Lysosomal Membrane Permeabilization and Cell Death in CD4+ T Cells Infected with HIV. PLoS Pathogens, 9(5).

Petrakis, I., Mavroeidi, V., Stylianou, K., Andronikidi, E., et al. (2013). Hsf-1 affects podocyte markers NPHS1, NPHS2 and WT1 in a transgenic mouse model of TTRVal30Met-related amyloidosis. Amyloid, 20(3), 164 - 172.

Martin, E., Schüle, R., Smets, K., Rastetter, A., et al. (2013). Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. American Journal of Human Genetics, 92(2), 238 - 244.

Maia, A. R. R., Zhu, X., Miller, P., Gu, G., et al. (2013). Modulation of Golgi-associated microtubule nucleation throughout the cell cycle. Cytoskeleton, 70(1), 32 - 43.

Mota, R., Guimarães, R., Büttel, Z., Rossi, F., et al. (2013). Production and characterization of extracellular carbohydrate polymer from Cyanothece sp. CCY 0110. Carbohydrate Polymers, 92(2), 1408 - 1415.

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.

Lee, J. - M., Gillis, T., Mysore, J. S., Ramos, E. M., et al. (2012). Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics, 90(3), 434 - 444.

Lopo, M., Montagud, A., Navarro, E., Cunha, I., et al. (2012). Experimental and modeling analysisof synechocystis sp. PCC 6803 growth. Journal of Molecular Microbiology and Biotechnology, 22(2), 71 - 82.

Couto, A. R., Zhang, Y., Timms, A., Bruges-Armas, J., et al. (2012). Investigating ANKH and ENPP1 in Slovakian families with chondrocalcinosis. Rheumatology International, 32(9), 2745 - 2751.

Gómez-Ros, L. V., Gabaldón, C., López Núñez-Flores, M. J., GutiéRrez, J., et al. (2012). The promoter region of the Zinnia elegans basic peroxidase isoenzyme gene contains cis-elements responsive to nitric oxide and hydrogen peroxide. Planta, 236(2), 327 - 342.

Figueiredo, A. C., Clement, C. C., Zakia, S., Gingold, J., et al. (2012). Rational design and characterization of D-Phe-Pro-D-Arg-derived direct thrombin inhibitors. PLoS ONE, 7(3).

Lee, J. - H., Lee, J. - M., Ramos, E. M., Gillis, T., et al. (2012). TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and Biophysical Research Communications, 424(3), 404 - 408.

Marks, D. J. B., Fisk, M. D., Koo, C. Y., Pavlou, M., et al. (2012). Thoracic empyema: A 12-year study from a UK tertiary cardiothoracic referral centre. PLoS ONE, 7(1).

Pellegrino, R. M., Coutinho, M., D'Ascola, D., Lopes, A. M., et al. (2012). Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form. British Journal of Haematology, 158(5), 668 - 672.

Becker, F., Van El, C. G., Ibarreta, D., Zika, E., et al. (2011). Genetic testing and common disorders in a public health framework: How to assess relevance and possibilities. European Journal of Human Genetics, 19(SUPPL. 1), S6 - S44.

Noborna, F., O'Callaghan, P., Hermansson, E., Zhang, X., et al. (2011). Heparan sulfate/heparin promotes transthyretin fibrillization through selective binding to a basic motif in the protein. Proceedings of the National Academy of Sciences of the United States of America, 108(14), 5584 - 5589.

Evans, D. M., Spencer, C. C. A., Pointon, J. J., Su, Z., et al. (2011). Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nature Genetics, 43(8), 761 - 767.

Pereira, S., Micheletti, E., Zille, A., Santos, A., et al. (2011). Using extracellular polymeric substances (EPS)-producing cyanobacteria for the bioremediation of heavy metals: Do cations compete for the EPS functional groups and also accumulate inside the cell?. Microbiology, 157(2), 451 - 458.

Hollak, C. E. M., vom Dahl, S., Aerts, J. M. F. G., Belmatoug, N., et al. (2010). Force Majeure: Therapeutic measures in response to restricted supply of imiglucerase (Cerezyme) for patients with Gaucher disease. Blood Cells, Molecules, and Diseases, 44(1), 41 - 47.

Pinto, J. P., Dias, V., Zoller, H., Porto, G., et al. (2010). Hepcidin messenger RNA expression in human lymphocytes. Immunology, 130(2), 217 - 230.

Perdu, B., De Freitas, F., Frints, S. G. M., Schouten, M., et al. (2010). Osteopathia striata with cranial sclerosis owing to WTX gene defect. Journal of Bone and Mineral Research, 25(1), 82 - 90.

Melo, P., Zanon-Moreno, V., Alves, C. J., Magalhães, A., et al. (2010). Oxidative stress response in the adult rat retina and plasma after repeated administration of methamphetamine. Neurochemistry International, 56(3), 431 - 436.

Kim, S., Silva, C., Zille, A., Lopez, C., et al. (2009). Characterisation of enzymatically oxidised lignosulfonates and their application on lignocellulosic fabrics. Polymer International, 58(8), 863 - 868.

Pereira, S., Zille, A., Micheletti, E., Moradas-Ferreira, P., et al. (2009). Complexity of cyanobacterial exopolysaccharides: Composition, structures, inducing factors and putative genes involved in their biosynthesis and assembly. FEMS Microbiology Reviews, 33(5), 917 - 941.

Song, R., Duarte, T. L., Almeida, G. M., Farmer, P. B., et al. (2009). Cytotoxicity and gene expression profiling of two hydroxylated polybrominated diphenyl ethers in human H295R adrenocortical carcinoma cells. Toxicology Letters, 185(1), 23 - 31.

Franciscon, E., Zille, A., Fantinatti-Garboggini, F., Silva, I. S., et al. (2009). Microaerophilic-aerobic sequential decolourization/biodegradation of textile azo dyes by a facultative Klebsiella sp. strain VN-31. Process Biochemistry, 44(4), 446 - 452.

Beetz, N., Harrison, M. D., Brede, M., Zong, X., et al. (2009). Phosducin influences sympathetic activity and prevents stress-induced hypertension in humans and mice. Journal of Clinical Investigation, 119(12), 3597 - 3612.

Nunes, A. F., Montero, M., Franquinho, F., Santos, S. D., et al. (2009). Transthyretin knockout mice display decreased susceptibility to AMPA-induced neurodegeneration. Neurochemistry International, 55(7), 454 - 457.

Javaher, P., Kääriäinen, H., Kristoffersson, U., Nippert, I., et al. (2008). EuroGentest: DNA-based testing for heritable disorders in Europe. Community Genetics, 11(2), 75 - 120.

Zanon-Moreno, V., Melo, P., Mendes-Pinto, M. M., Alves, C. J., et al. (2008). Serotonin levels in aqueous humor of patients with primary open-angle glaucoma. Molecular Vision, 14, 2143 - 2147.

Pons-Vázquez, S., Vila-Bou, V., Zanon-Moreno, V., Iborra, F. J., et al. (2008). Study of apoptosis and mitosis mechanisms in the eye. Experimental model of gestational toxic syndrome. Estudio de los mecanismos de apoptosis y mitosis en el globo ocular. Modelo experimental del síndrome tóxico gestacionalArchivos de la Sociedad Espanola de Oftalmologia, 83(1), 37 - 44.

Freitas, R., Zhang, G., & Cohn, M. J. (2007). Biphasic Hoxd gene expression in shark paired fins reveals an ancient origin of the distal limb domain. PLoS ONE, 2(8).

Nascimento, D. S., Vale, A. D., Tomás, A. M., Zou, J., et al. (2007). Cloning, promoter analysis and expression in response to bacterial exposure of sea bass (Dicentrarchus labrax L.) interleukin-12 p40 and p35 subunits. Molecular Immunology, 44(9), 2277 - 2291.

Nascimento, D. S., Pereira, P. J. B., Reis, M. I. R., do Vale, A., et al. (2007). Molecular cloning and expression analysis of sea bass (Dicentrarchus labrax L.) tumor necrosis factor-? (TNF-?). Fish and Shellfish Immunology, 23(3), 701 - 710.

Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.

Pons, S., Zanón-Moreno, V., Melo, P., Vila, V., et al. (2007). Optic neuropathy induced by prenatal drug or alcohol exposure. Neuropatía óptica inducida por exposición prenatal a drogas o alcoholArchivos de la Sociedad Espanola de Oftalmologia, 82(1), 21 - 26.

Stendel, C., Roos, A., Deconinck, T., Pereira, J., et al. (2007). Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics, 81(1), 158 - 164.

Rolim, L., Zagalo-Cardoso, J. A., Paúl, C., Sequeiros, J., & Fleming, M. (2006). The perceived advantages and disadvantages of presymptomatic testing for Machado-Joseph disease: Development of a new self-response inventory. Journal of Genetic Counseling, 15(5), 375 - 391.

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.