1,765 research outputs found
A national health information strategy for Malta
In 1992 a national health information strategy was developed jointly by the Department of Health and the Information Systems Division. A detailed strategy study report was compiled, with recommendations for the development of a number of information systems. The main system proposed was an integrated and comprehensive health care information system encompassing all of Malta’s hospitals and health centres, based on a single Patient Master Index. This system would support the concepts of an integrated health record and of a person-based view for resource management.peer-reviewe
Thinking and communicating outside the box: a new perspective in chemical pathology instruction and communication
Controlling crystallization damage by the use of salt inhibitors on Malta's limestone
Parallel text in Spanish and EnglishThe main building stone in the Maltese Islands is the Globigerina Limestone, of which the Lower member is commonly used. This occurs in two types, the durable franka and the more easily weathered soll. Two types of fresh franka (bajda (white) and safra (yellow)), as well as fresh soll stone blocks, were obtained, based on the identification by quarry owners. Their designation was confirmed by geochemistry. Physical and mechanical properties of the three were investigated, including uniaxial compressive strength, water absorption by capillarity, permeability and porosimetry. Porosimetry results confirmed outcomes of previous research work. Soll was found to have a lower overall porosity, but a high percentage of small pores with practically no large pores. Some of the tested stones were then treated with a non-toxic phospho- organic compound containing carboxylic moieties as a salt inhibitor and the corresponding non-phosphorylated compound.peer-reviewe
Theoretical study of the mechanism of dry oxidation of 4H-SiC
Possible defect structures, arising from the interaction of O-2 molecules with an ideal portion of the SiC/SiO2 interface, have been investigated systematically using density functional theory. Based on the calculated total energies and assuming thermal quasiequilibrium during oxidation, the most likely routes leading to complete oxidation have been determined. The defect structures produced along these routes will remain at the interface in significant concentration when stopping the oxidation process. The results obtained for their properties are well supported by experimental findings about the SiC/SiO2 interface. It is found that carbon-carbon bonds can explain most of the observed interface states but not the high density near the conduction band of 4H-SiC
Defects in SiO2 as the possible origin of near interface traps in the SiC∕SiO2 system: A systematic theoretical study
A systematic study of the level positions of intrinsic and carbon defects in SiO2 is presented, based on density functional calculations with a hybrid functional in an alpha-quartz supercell. The results are analyzed from the point of view of the near interface traps (NIT), observed in both SiC/SiO2 and Si/SiO2 systems, and assumed to have their origins in the oxide. It is shown that the vacancies and the oxygen interstitial can be excluded as the origin of such NIT, while the silicon interstitial and carbon dimers give rise to gap levels in the energy range inferred from experiments. The properties of these defects are discussed in light of the knowledge about the SiC/SiO2 interface
Stability and Electronic Properties of TiO2 Nanostructures With and Without B and N Doping
We address one of the main challenges to TiO2-photocatalysis, namely band gap
narrowing, by combining nanostructural changes with doping. With this aim we
compare TiO2's electronic properties for small 0D clusters, 1D nanorods and
nanotubes, 2D layers, and 3D surface and bulk phases using different
approximations within density functional theory and GW calculations. In
particular, we propose very small (R < 0.5 nm) but surprisingly stable
nanotubes with promising properties. The nanotubes are initially formed from
TiO2 layers with the PtO2 structure, with the smallest (2,2) nanotube relaxing
to a rutile nanorod structure. We find that quantum confinement effects - as
expected - generally lead to a widening of the energy gap. However,
substitutional doping with boron or nitrogen is found to give rise to
(meta-)stable structures and the introduction of dopant and mid-gap states
which effectively reduce the band gap. Boron is seen to always give rise to
n-type doping while depending on the local bonding geometry, nitrogen may give
rise to n-type or p-type doping. For under coordinated TiO2 surface structures
found in clusters, nanorods, nanotubes, layers and surfaces nitrogen gives rise
to acceptor states while for larger clusters and bulk structures donor states
are introduced
Methods for the analysis of histone H3 and H4 acetylation in blood
LBH589 is one of the many histone deacetylase inhibitors (HDACi) that are currently in clinical trial. Despite their wide-spread use, there is little literature available describing the typical levels of histone acetylation in untreated peripheral blood, the treatment and storage of samples to retain optimal measurement of histone acetylation nor methods by which histone acetylation analysis may be monitored and measured during the course of a patient’s treatment. In this study, we have used cord or peripheral blood as a source of human leukocytes, performed a comparative analysis of sample processing methods and developed a flow cytometric method suitable for monitoring histone acetylation in isolated lymphocytes and liquid tumors. Western blotting and immunohistochemistry techniques have also been addressed. We have tested these methods on blood samples collected from four patients treated with LBH589 as part of an Australian Children’s Cancer Clinical Trial (CLBH589AAU03T) and show comparable results when comparing in vitro and in vivo data. This paper does not seek to correlate histone acetylation levels in peripheral blood with clinical outcome but describes methods of analysis that will be of interest to clinicians and scientists monitoring the effects of HDACi on histone acetylation in blood samples in clinical trials or in related research studies
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