1,002 research outputs found

    Long tails, short telomeres: Dyskeratosis congenita

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    The effects of elevated temperature and dissolved �CO2 on a marine foundation species

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    Understanding how climate change and other environmental stressors will affect species is a fundamental concern of modern ecology. Indeed, numerous studies have documented how climate stressors affect species distributions and population persistence. However, relatively few studies have investigated how multiple climate stressors might affect species. In this study, we investigate the impacts of how two climate change factors affect an important foundation species. Specifically, we tested how ocean acidification from dissolution of CO2 and increased sea surface temperatures affect multiple characteristics of juvenile eastern oysters (Crassostrea virginica). We found strong impacts of each stressor, but no interaction between the two. Simulated warming to mimic heat stressed summers reduced oyster growth, survival, and filtration rates. Additionally, we found that CO2-induced acidification reduced strength of oyster shells, which could potentially facilitate crab predation. As past studies have detected few impacts of these stressors on adult oysters, these results indicate that early life stages of calcareous marine organisms may be more susceptible to effects of ocean acidification and global warming. Overall, these data show that predicted changes in temperature and CO2 can differentially influence direct effects on individual species, which could have important implications for the nature of their trophic interactions.ECU Open Access Publishing Fun

    Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

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    Financial support provided by The Medical Research Council-MR/K000292/1, Children with Cancer- 2013/144 and Blood Wise-14032 (AJW, LC, SC, AE, TV, HT and ID). KMG is supported by the National Institute for Health Research through the NIHR Southampton Biomedical Research Centre

    Is the LITE version of the usability metric for user experience (UMUX-LITE) a reliable tool to support rapid assessment of new healthcare technology?

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    Objective To ascertain the reliability of a standardised, short-scale measure of satisfaction in the use of new healthcare technology i.e., the LITE version of the usability metric for user experience (UMUX-LITE). Whilst previous studies have demonstrated the reliability of UMUX-LITE, and its relationship with measures of likelihood to recommend a product, such as the Net Promoter Score (NPS) in other sectors no such testing has been undertaken with healthcare technology. Materials and methods Six point-of-care products at different stages of development were assessed by 120 healthcare professionals. UMUX-LITE was used to gather their satisfaction in use, and NPS to declare their intention to promote the product. Inferential statistics were used to: i) ascertain the reliability of UMUX-LITE, and ii) assess the relationship between UMUX-LITE and NPS at different stages of products development. Results UMUX-LITE showed an acceptable reliability (α = 0.7) and a strong positive correlation with NPS (r = 0.455, p < .001). This is similar to findings in other fields of application. The level of product development did not affect the UMUX-LITE scores, while the stage of development was a significant predictor (R2 = 0.49) of the intention to promote. Discussion and conclusion Practitioners may apply UMUX-LITE alone, or in combination with the NPS, to complement interview and ‘homemade’ scales to investigate the quality of new products at different stages of development. This shortened scale is appropriate for use in the context of healthcare in which busy professionals have a minimal amount of time to support innovation

    The royal Great Seals Deputed of South Carolina

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    This paper gives a history of the royal seals used in South Carolina from 1719 to the Revolution. It also has pictures of the seals

    Ecotoxicological effects of chemical contaminants adsorbed to microplastics in the clam Scrobicularia plana

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    Although microplastics (MPs) are distributed globally in the marine environment, a great deal of unknowns relating to their ecotoxicological effects on the marine biota remains. Due to their lipophilic nature, microplastics have the potential to adsorb persistent organic pollutants present in contaminated regions, which may increase their detrimental impact once assimilated by organisms. This study investigates the ecotoxicological effects of exposure to low-density polyethylene (LDPE) microplastics (11-13 beta m), with and without adsorbed contaminants (benzo[a]pyrene- BaP and perfluorooctane sulfonic acid-PFOS), in the peppery furrow shell clam, Scrobicularia plana. Environmentally relevant concentrations of contaminants (BaP-16.87 +/- 0.22 mu g g(-1) and PFOS-70.22 +/- 12.41 mu g g(-1)) were adsorbed to microplastics to evaluate the potential role of plastic particles as a source of chemical contamination once ingested. S. plana were exposed to microplastics, at a concentration of 1 mg L-1, in a water-sediment exposure setup for 14 days. Clams were sampled at the beginning of the experiment (day 0) and after 3, 7, and 14 days. BaP accumulation, in whole clam tissues, was analyzed. A multi-biomarker assessment was conducted in the gills, digestive gland, and haemolymph of clams to clarify the effects of exposure. This included the quantification of antioxidant (superoxide dismutase, catalase, glutathione peroxidase) and biotransformation (glutathione-Stransferases) enzyme activities, oxidative damage (lipid peroxidation levels), genotoxicity (single and double strand DNA breaks), and neurotoxicity (acetylcholinesterase activity). Results suggest a potential mechanical injury of gills caused by ingestion of microplastics that may also affect the analyzed biomarkers. The digestive gland seems less affected by mechanical damage caused by virgin microplastic exposure, with the MPs-adsorbed BaP and PFOS exerting a negative influence over the assessed biomarkers in this tissue.JPI Oceans FCT JPIOCEANS/0005/2015 JPI Oceans (BELSPO) JPI Oceans (FWO) JPI Oceans (FORMAS) JPI Oceans (SwAM) FCT UID/MAR/00350/2013info:eu-repo/semantics/publishedVersio

    Novel functions of UPF1 in safeguarding DNA replication fidelity in S-phase and beyond

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    Maintaining DNA replication fidelity is required to allow for the successful duplication of genetic information that will be passed on to the next generation of daughter cells. Interfering with this process leads to replication stress that can promote mutagenesis, double-stranded DNA breaks and loss of genetic stability. The fundamental process of transcription is a well described promotor of DNA replication stress through changes in chromatin dynamics, DNA structure and direct transcription-replication collisions (TRCs). In this thesis, we have identified a novel function for the RNA/DNA helicase UPF1 in preventing harmful consequences between the DNA replicative and transcriptional machineries. Loss of UPF1 resulted in an increase in spontaneous transcription-dependent replication fork stalling, double stranded breaks and an accumulation of R-loops. UPF1-deficient cells following mild replicative stress show a reduced frequency of replication fork stalling, mitotic delay and the DNA replication salvage pathway of mitotic DNA synthesis (MiDAS). However, no increase in markers of under-replicated DNA such as 53BP1 nuclear bodies in the subsequent G1 is observed, suggesting that cells deficient for UPF1 are able to fully replicate their DNA prior to mitotic entry under such conditions. Together these data demonstrate UPF1 as vital for protecting the genome from spontaneous TRCs, most likely through its role in regulating the dissociation of nascent R-loop associated-mRNAs. Loss or down-regulation of UPF1 also represents a potential mechanism whereby cells could display resistance to DNA replication-targeting chemotherapeutics. Targeting UPF1- deficient cancers or UPF1 inhibition with drugs known to synergize with high levels of TRCs such as PARP inhibitors, could be a promising therapeutic approach
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