940 research outputs found

    Intentions to work with older adults: a critical exploration of psychology students’ motivations and ambition

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    Objectives: Previous studies offer insight into volunteering intentions and career aspirations but reveal little about work with older adults. Given the aging population, this research investigates attitudes towards older adults amongst Psychology undergraduates. Associated volunteer intentions and motivations, as well as career aspirations were also explored. Design: A questionnaire design was used in order to access motivations, intentions and attitudes. Method: Psychology undergraduates (N = 188) completed the Volunteer Function Inventory and the Attitudes to Older Adults Scale. Current volunteering status and career aspirations were measured, including likelihood of seeking future employment with older adults. Results: Negative statements about older people were rejected by these students, however, positive statements were not highly endorsed. Intentions to volunteer were high (although only 26.6% were currently volunteering), with career enhancement being the most important motivational factor (x2 (5) = 609.59, p < .001). The majority aspired to work in the applied psychologies or some sort of public service role. Despite this, only 5 students (2.7%) thought themselves very likely to work with older people. Conclusions: Despite an encouraging absence of negative attitudes to older adults amongst these students, there was an evident lack of positive attitudes and plans to work with this demographic group. Given their career aspirations and the ageing population, this may suggest a worrying naivety within the sample regarding their likelihood of working with older adults. Pedagogical input around the realities of the social world appears warranted. Longitudinal research should explore how the current measures map onto actual career trajectories

    Challenges and opportunities in the development of novel antimicrobial therapeutics for cystic fibrosis

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    Chronic respiratory infection is the primary driver of mortality in individuals with cystic fibrosis (CF). Existing drug screening models utilised in preclinical antimicrobial development are unable to mimic the complex CF respiratory environment. Consequently, antimicrobials showing promising activity in preclinical models often fail to translate through to clinical efficacy in people with CF. Model systems used in CF anti-infective drug discovery and development range from antimicrobial susceptibility testing in nutrient broth, through to 2D and 3D in vitro tissue culture systems and in vivo models. No single model fully recapitulates every key aspect of the CF lung. To improve the outcomes of people with CF (PwCF) it is necessary to develop a set of preclinical models that collectively recapitulate the CF respiratory environment to a high degree of accuracy. Models must be validated for their ability to mimic aspects of the CF lung and associated lung infection, through evaluation of biomarkers that can also be assessed following treatment in the clinic. This will give preclinical models greater predictive power for identification of antimicrobials with clinical efficacy. The landscape of CF is changing, with the advent of modulator therapies that correct the function of the CFTR protein, while antivirulence drugs and phage therapy are emerging alternative treatments to chronic infection. This review discusses the challenges faced in current antimicrobial development pipelines, including the advantages and disadvantages of current preclinical models and the impact of emerging treatments

    Some Abnormal Reactions of Organomagnesium Halides

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    Nitro and nitroso groups react with methylmagnesium halides (and other RMgX compounds) to give methane and some ethane. The gases so evolved make it necessary to correct for the ordinary determination of active hydrogen by means of the Zerewitinoff method. Accordingly, the new hydroxy structure proposed for o-nitrobenzaladehyde finds no support on the basis of gas evolved when treated with alkylmagnesium halides

    Comparative genomics of isolates of a pseudomonas aeruginosa epidemic strain associated with chronic lung infections of cystic fibrosis patients

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    Pseudomonas aeruginosa is the main cause of fatal chronic lung infections among individuals suffering from cystic fibrosis (CF). During the past 15 years, particularly aggressive strains transmitted among CF patients have been identified, initially in Europe and more recently in Canada. The aim of this study was to generate high-quality genome sequences for 7 isolates of the Liverpool epidemic strain (LES) from the United Kingdom and Canada representing different virulence characteristics in order to: (1) associate comparative genomics results with virulence factor variability and (2) identify genomic and/or phenotypic divergence between the two geographical locations. We performed phenotypic characterization of pyoverdine, pyocyanin, motility, biofilm formation, and proteolytic activity. We also assessed the degree of virulence using the Dictyostelium discoideum amoeba model. Comparative genomics analysis revealed at least one large deletion (40-50 kb) in 6 out of the 7 isolates compared to the reference genome of LESB58. These deletions correspond to prophages, which are known to increase the competitiveness of LESB58 in chronic lung infection. We also identified 308 non-synonymous polymorphisms, of which 28 were associated with virulence determinants and 52 with regulatory proteins. At the phenotypic level, isolates showed extensive variability in production of pyocyanin, pyoverdine, proteases and biofilm as well as in swimming motility, while being predominantly avirulent in the amoeba model. Isolates from the two continents were phylogenetically and phenotypically undistinguishable. Most regulatory mutations were isolate-specific and 29% of them were predicted to have high functional impact. Therefore, polymorphism in regulatory genes is likely to be an important basis for phenotypic diversity among LES isolates, which in turn might contribute to this strain's adaptability to varying conditions in the CF lung

    Coaxial multi-mode cavities for fundamental SRF research in an unprecedented parameter space

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    Recent developments in superconducting radio-frequency (SRF) research have focused primarily on high frequency elliptical cavities for electron accelerators. Advances have been made in both reducing RF surface resistance and pushing the readily achievable accelerating gradient by using novel SRF cavity treatments including surface processing, custom heat treatments, and flux expulsion. Despite the global demand for SRF based hadron accelerators, the advancement of TEM mode cavities has lagged behind. To address this, two purpose-built research cavities, one quarter-wave and one half-wave resonator, have been designed and built to allow characterization of TEM-mode cavities with standard and novel surface treatments. The cavities are intended as the TEM mode equivalent to the 1.3GHz single cell cavity, which is the essential tool for high frequency cavity research. Given their coaxial structure, the cavities allow testing at the fundamental mode and higher harmonics, giving unique insight into the role of RF frequency on fundamental loss mechanisms from intrinsic and extrinsic sources. In this paper, the cavities and testing infrastructure are described and the first performance measurements of both cavities are presented

    Inhibitors of Leishmania mexicana phosphoglycerate mutase identified by virtual screening and verified by inhibition studies

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    Cofactor-independent phosphoglycerate mutase has been proposed as a therapeutic target for the treatment of trypanosomatid diseases. In this paper, we report the identification of compounds that could potentially be developed as selective inhibitors of cofactor-independent phosphoglycerate mutase from Leishmania mexicana (LmiPGAM). Virtual screening was used in this search, as well as compounds identified by high-throughput screening. A ligand-based virtual screen programme, ultra fast shape recognition with atom types (UFSRAT), was used to screen for compounds resembling the substrate/product, before a structure-based approach was applied using AutoDock 4 and AutoDock Vina in a consensus docking scheme. In this way eight selected compounds were identified. In addition, three compounds from the Library of Pharmacologically Active Compounds (LOPAC) were selected from the published results of high-throughput screening of this library. The inhibitory effects of these compounds were tested at a fixed concentration of 1 mM. The results showed that seven compounds inhibited LmiPGAM activity and of these, two compounds (one each from high-throughput and virtual screening) showed substantial inhibition (i.e. 14% and 49% remaining activity, respectively). Taken together, the findings from this study indicate that these compounds have potential as novel inhibitors that specifically target LmiPGAM
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