Salvar o país: o repertório nacional no FATAL de 2006 a 2010

Reflexão sobre o teatro universitário em Portugal.

Entre o público e o privado: a escolha da escola pelos país

Dissertação apresentada à Escola Superior de Educação de Lisboa para obtenção do grau de mestre em Ciências de Educação – Especialização em Administração Escolar

Diagnóstico da malária em Angola: um país em estreita ligação com Portugal

As migrações e a globalização dos viajantes têm apresentado grandes desafios no controlo da transmissão de doenças. Em 2012, o número estimado de pessoas em risco de contraíram malária foi de 3,4 biliões. Na Europa, esta é uma doença rara que, em 2012, apenas teve reportados 255 casos autóctones. Para turistas e emigrantes de áreas não endémicas, a malária representa um sério risco de morte e deve ser uma forte suspeita em casos de febre. Um diagnóstico correcto é de extrema importância para o controlo da malária. Este deve ser feito imediatamente após o aparecimento dos primeiros sintomas, daí que os serviços de saúde dos países visitados devem estar aptos a prontamente identificar e tratar esta doença. O objectivo deste trabalho doi determinar o impacto de uma formação na melhoria do diagnóstico da malária.

Study of thermochemical treatments of cork in the 150-400ºC range using colour analysis and Ftir spectroscopy

A study of chemical transformations of cork during heat treatments was made using colour variation and FTIR analysis. The cork enriched fractions from Quercus cerris bark were subjected to isothermal heating in the temperature range 150–400 ◦C and treatment time from 5 to 90 min. Mass loss ranged from 3% (90 min at 150 ◦C) to 71% (60 min at 350 ◦C). FTIR showed that hemicelluloses were thermally degraded first while suberin remained as the most heat resistant component. The change of CIE-Lab parameters was rapid for low intensity treatments where no significant mass loss occurred (at 150 ◦C L* decreased from the initial 51.5 to 37.3 after 20 min). The decrease in all colour parameters continued with temperature until they remained substantially constant with over 40% mass loss. Modelling of the thermally induced mass loss could be made using colour analysis. This is applicable to monitoring the production of heat expanded insulation agglomerates.

A comprehensive high-throughput FTIR spectroscopy-based method for evaluating the transfection event: estimating the transfection efficiency and extracting associated metabolic responses

Reporter genes are routinely used in every laboratory for molecular and cellular biology for studying heterologous gene expression and general cellular biological mechanisms, such as transfection processes. Although well characterized and broadly implemented, reporter genes present serious limitations, either by involving time-consuming procedures or by presenting possible side effects on the expression of the heterologous gene or even in the general cellular metabolism. Fourier transform mid-infrared (FT-MIR) spectroscopy was evaluated to simultaneously analyze in a rapid (minutes) and high-throughput mode (using 96-wells microplates), the transfection efficiency, and the effect of the transfection process on the host cell biochemical composition and metabolism. Semi-adherent HEK and adherent AGS cell lines, transfected with the plasmid pVAX-GFP using Lipofectamine, were used as model systems. Good partial least squares (PLS) models were built to estimate the transfection efficiency, either considering each cell line independently (R 2 ≥ 0.92; RMSECV ≤ 2 %) or simultaneously considering both cell lines (R 2 = 0.90; RMSECV = 2 %). Additionally, the effect of the transfection process on the HEK cell biochemical and metabolic features could be evaluated directly from the FT-IR spectra. Due to the high sensitivity of the technique, it was also possible to discriminate the effect of the transfection process from the transfection reagent on KEK cells, e.g., by the analysis of spectral biomarkers and biochemical and metabolic features. The present results are far beyond what any reporter gene assay or other specific probe can offer for these purposes.