Romeríes del 1320

"Aquestes romeries faeren En P. Riber he En R. Torner en lany de nostre Senyor. M. CCCXX. que anaren a la perdonança de monsenyer sen Ffrancesch de Sis". Transcripció d'aquest manuscrit que es conserva en l'Arxiu de la Comunitat de Santa Maria de Ma

Education and older adults at the University of the Third Age

This article reports a critical analysis of older adult education in Malta. In educational gerontology, a critical perspective demands the exposure of how relations of power and inequality, in their myriad forms, combinations, and complexities, are manifest in late-life learning initiatives. Fieldwork conducted at the University of the Third Age (UTA) in Malta uncovered the political nature of elder-learning, especially with respect to three intersecting lines of inequality - namely, positive aging, elitism, and gender. A cautionary note is, therefore, warranted at the dominant positive interpretations of UTAs since late-life learning, as any other education activity, is not politically neutral.peer-reviewe

Interplay of Mre11 Nuclease with Dna2 plus Sgs1 in Rad51-Dependent Recombinational Repair

The Mre11/Rad50/Xrs2 complex initiates IR repair by binding to the end of a double-strand break, resulting in 5′ to 3′ exonuclease degradation creating a single-stranded 3′ overhang competent for strand invasion into the unbroken chromosome. The nuclease(s) involved are not well understood. Mre11 encodes a nuclease, but it has 3′ to 5′, rather than 5′ to 3′ activity. Furthermore, mutations that inactivate only the nuclease activity of Mre11 but not its other repair functions, mre11-D56N and mre11-H125N, are resistant to IR. This suggests that another nuclease can catalyze 5′ to 3′ degradation. One candidate nuclease that has not been tested to date because it is encoded by an essential gene is the Dna2 helicase/nuclease. We recently reported the ability to suppress the lethality of a dna2Δ with a pif1Δ. The dna2Δ pif1Δ mutant is IR-resistant. We have determined that dna2Δ pif1Δ mre11-D56N and dna2Δ pif1Δ mre11-H125N strains are equally as sensitive to IR as mre11Δ strains, suggesting that in the absence of Dna2, Mre11 nuclease carries out repair. The dna2Δ pif1Δ mre11-D56N triple mutant is complemented by plasmids expressing Mre11, Dna2 or dna2K1080E, a mutant with defective helicase and functional nuclease, demonstrating that the nuclease of Dna2 compensates for the absence of Mre11 nuclease in IR repair, presumably in 5′ to 3′ degradation at DSB ends. We further show that sgs1Δ mre11-H125N, but not sgs1Δ, is very sensitive to IR, implicating the Sgs1 helicase in the Dna2-mediated pathway

A COMPARISON BETWEEN THE VALUES OBTAINED FROM ACTIVE DRAG ANALYSIS COMPARED TO FORCES PRODUCED IN TETHERED SWIMMING

The purpose of this study was to identify in a maximum swim effort by elite freestyle swimmers, if the mean force produced in tethered swimming over a set number of whole strokes could reliably be utilised as an alternative measure for mean propulsive force over the same number of whole strokes. Tethered force can be measured relatively easily. Although mean propulsive force at a maximum swim velocity may be derived, the process of doing so is not direct, is time consuming and requires an extensive setup. Stepwise regression analysis indicated that mean tethered force was not an acceptable alternative for mean propulsive force. Therefore the use of mean propulsive power to monitor training would require the measurement of mean propulsive force rather than simply measuring the mean tethered force in a maximum swim effort

MEASURING PROPULSIVE FORCE WITHIN THE DIFFERENT PHASES OF BACKSTROKE SWIMMING

The purpose of this study was to identify the propulsive force profile associated within the different phases of backstroke to provide individual feedback to elite swimmers and coaches. Elite backstrokers (n=4) performed three maximal velocity time trials to determine the swimmers maximum velocity. This was followed by three passive drag trials and three active drag trials using a flux vector drive dynamometer mounted on a force platform to tow them at set velocities (derived from the swimmer’s maximum swim pace) while measuring the force to do so. The computed active drag and the propulsive propelling force profile were represented as a dynamic parameter, allowing identification of intra cyclic force fluctuations with respect to time. The force profiles were synchronised to video footage which provided unique quantitative and individual stroke kinematic feedback to the elite swimmers and coaches

Clumping factor B promotes adherence of <i>Staphylococcus aureus </i>to corneocytes in atopic dermatitis

Staphylococcus aureus skin infection is a frequent and recurrent problem in children with the common inflammatory skin disease atopic dermatitis (AD). S. aureus colonizes the skin of the majority of children with AD and exacerbates the disease. The first step during colonization and infection is bacterial adhesion to the cornified envelope of corneocytes in the outer layer, the stratum corneum. Corneocytes from AD skin are structurally different from corneocytes from normal healthy skin. The objective of this study was to identify bacterial proteins that promote the adherence of S. aureus to AD corneocytes. S. aureus strains from clonal complexes 1 and 8 were more frequently isolated from infected AD skin than from the nasal cavity of healthy children. AD strains had increased ClfB ligand binding activity compared to normal nasal carriage strains. Adherence of single S. aureus bacteria to corneocytes from AD patients ex vivo was studied using atomic force microscopy. Bacteria expressing ClfB recognized ligands distributed over the entire corneocyte surface. The ability of an isogenic ClfB-deficient mutant to adhere to AD corneocytes compared to that of its parent clonal complex 1 clinical strain was greatly reduced. ClfB from clonal complex 1 strains had a slightly higher binding affinity for its ligand than ClfB from strains from other clonal complexes. Our results provide new insights into the first step in the establishment of S. aureus colonization in AD patients. ClfB is a key adhesion molecule for the interaction of S. aureus with AD corneocytes and represents a target for interventio

THE USE OF PASSIVE DRAG TO INTERPRET VARIATION IN ACTIVE DRAG MEASUREMENTS

This study investigated if a measure of mean passive drag could explain the huge differences in propulsive force required by different swimmers to swim at a similar high velocity. Nineteen elite male and female national freestyle swimmers were subjects. The subject’s mean active and passive drag was measured at each swimmer’s top swimming pace. Stepwise regression analysis was used in the analysis. Passive drag was accepted into the equation to calculate mean propulsive force, prior to velocity being rejected. The correlation coefficient for the relationship between mean propelling force and mean passive drag was 0.77. This was statistically significant at the

What do older people learn from young people? : Intergenerational learning in ‘day centre’ community settings in Malta

This study analyses what motivates older people to attend ‘day centres’ in Malta and what they believe that they derive from young people who carry out their placements at these day ‘centres’ These young people, who are aged 16–17, attend a vocational college in Malta and are studying health and social care. The study is based on a qualitative approach and employs the usage of focus groups. The main findings are that the elderly see the students as helping them on an emotional level by giving them encouragement, and on a practical level, by offering them insights that help them in modern-day life

Tumor surveillance by circulating microRNAs: a hypothesis

A growing body of experimental evidence supports the diagnostic relevance of circulating microRNAs in various diseases including cancer. The biological relevance of circulating microRNAs is, however, largely unknown, particularly in healthy individuals. Here, we propose a hypothesis based on the relative abundance of microRNAs with predominant tumor suppressor activity in the blood of healthy individuals. According to our hypothesis, certain sets of circulating microRNAs might function as a tumor surveillance mechanism exerting continuous inhibition on tumor formation. The microRNA-mediated tumor surveillance might complement cancer immune surveillance