160 research outputs found

    Trading Places: Somerset Maugham’s Tales From Abroad

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    Dans cet article, Glenn Hooper Ă©tudie les nouvelles d’un Ă©crivain qui, bien que nĂ© en France, reprĂ©sente pour beaucoup l’anglais type par excellence. Figure cosmopolite Ă  l’aise dans de nombreuses cultures, Maugham dĂ©peint ce qu’il connaĂźt le mieux. Cependant, en narrateur passionnĂ©, il ne cessa d’ĂȘtre motivĂ© par ce qu’il vendait Ă  ses lecteurs : des dĂ©cors exotiques, des rĂ©cits d’aventure avec des pertes frĂ©quentes en “haute mer” et des vies remplies de dĂ©sirs et d’animositĂ©s intenses. Les nouvelles de Maugham reprĂ©sentent l’une des Ă©tudes les plus dĂ©taillĂ©es et Ă©vocatrices de la fin de l’ùre impĂ©rialiste et s’intĂ©ressent de prĂšs Ă  l’identitĂ© coloniale soumise Ă  la mouvance, Ă  l’angoisse du voyage, aux difficultĂ©s de l’adaptation. (Traduction Martine Rimbourg

    Sward Structure Effects on Light Interception in Rotationally-Grazed Orchardgrass (\u3cem\u3eDactylis glomerata\u3c/em\u3e L.)

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    Grazing managers need to know the relationship of sward height and mass to photosynthetic capacity. The aim of this study was to measure the interception of photosynthetically active radiation (PAR) and relate it to sward structure throughout the grazing season on rotationally-grazed orchardgrass/cocksfoot (Dactylis glomerata L.) pastures

    Trading Places: Somerset Maugham’s Tales From Abroad

    Get PDF
    Dans cet article, Glenn Hooper Ă©tudie les nouvelles d’un Ă©crivain qui, bien que nĂ© en France, reprĂ©sente pour beaucoup l’anglais type par excellence. Figure cosmopolite Ă  l’aise dans de nombreuses cultures, Maugham dĂ©peint ce qu’il connaĂźt le mieux. Cependant, en narrateur passionnĂ©, il ne cessa d’ĂȘtre motivĂ© par ce qu’il vendait Ă  ses lecteurs : des dĂ©cors exotiques, des rĂ©cits d’aventure avec des pertes frĂ©quentes en “haute mer” et des vies remplies de dĂ©sirs et d’animositĂ©s intenses. Les nouvelles de Maugham reprĂ©sentent l’une des Ă©tudes les plus dĂ©taillĂ©es et Ă©vocatrices de la fin de l’ùre impĂ©rialiste et s’intĂ©ressent de prĂšs Ă  l’identitĂ© coloniale soumise Ă  la mouvance, Ă  l’angoisse du voyage, aux difficultĂ©s de l’adaptation. (Traduction Martine Rimbourg

    Genome Sequence Conservation of Hendra Virus Isolates during Spillover to Horses, Australia

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    Bat-to-horse transmission of Hendra virus has occurred at least 14 times. Although clinical signs in horses have differed, genome sequencing has demonstrated little variation among the isolates. Our sequencing of 5 isolates from recent Hendra virus outbreaks in horses found no correlation between sequences and time or geographic location of outbreaks

    Factors associated with reporting multiple causes of death

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    BACKGROUND: There is analytical potential for multiple cause of death data collected from death certificates. This study examines relationships of multiple causes of death as a function of factors available on the death certificate (demographics of decedent, place of death, type of certifier, disposal method, whether an autopsy was performed, and year of death). METHODS: Data from 326,332 Minnesota death certificates from 1990–1998 are examined. Underlying and non-underlying causes of death are examined (based on record axis codes) as well as demographic and death-related covariates. Associations between covariates and prevalence of multiple causes of death and conditional probability of underlying compared to non-underlying causes of death are examined. The occurrence of ischemic heart disease or diabetes as underlying causes are specifically examined. RESULTS: Both the probability of multiple causes of death and the proportion of underlying cause compared to non-underlying cause of death are associated with demographic characteristics of the deceased and other non-medical conditions related to filing death certificate such as place of death. CONCLUSIONS: Multiple cause of death data provide a potentially useful way of looking for inaccuracies in reporting of causes of death. Differences across demographics in the proportion of time a cause is selected as underlying compared to non-underlying exist and can potentially provide useful information about the overall impact of causes of death in different populations

    Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle

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    Polyclonal antibodies, derived from humans or hyperimmunized animals, have been used prophylactically or therapeutically as countermeasures for a variety of infectious diseases. SAB Biotherapeutics has successfully developed a transchromosomic (Tc) bovine platform technology that can produce fully human immunoglobulins rapidly, and in substantial quantities, against a variety of disease targets. In this study, two Tc bovines expressing high levels of fully human IgG were hyperimmunized with a recombinant glycoprotein (GP) vaccine consisting of the 2014 Ebola virus (EBOV) Makona isolate. Serum collected from these hyperimmunized Tc bovines contained high titers of human IgG against EBOV GP as determined by GP specific ELISA, surface plasmon resonance (SPR), and virus neutralization assays. Fully human polyclonal antibodies against EBOV were purified and evaluated in a mouse challenge model using mouse adapted Ebola virus (maEBOV). Intraperitoneal administration of the purified anti-EBOV IgG (100 mg/kg) to BALB/c mice one day after lethal challenge with maEBOV resulted in 90% protection; whereas 100% of the control animals succumbed. The results show that hyperimmunization of Tc bovines with EBOV GP can elicit protective and potent neutralizing fully human IgG antibodies rapidly and in commercially viable quantities

    Immune Modulation by Adjuvants Combined with Diphtheria Toxoid Administered Topically in BALB/c Mice After Microneedle Array Pretreatment

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    Purpose. In this study, modulation of the immune response against diphtheria toxoid (DT) by various adjuvants in transcutaneous immunization (TCI) with microneedle array pretreatment was investigated. Methods. TCI was performed on BALB/c mice with or without microneedle array pretreatment using DT as a model antigen co-administrated with lipopolysaccharide (LPS), Quil A, CpG oligo deoxynucleotide (CpG) or cholera toxin (CT) as adjuvant. The immunogenicity was evaluated by measuring serum IgG subtype titers and neutralizing antibody titers. Results. TCI with microneedle array pretreatment resulted in a 1,000-fold increase of DT-specific serum IgG levels as compared to TCI. The immune response was further improved by co-administration of adjuvants, showing a progressive increase in serum IgG titers when adjuvanted with LPS, Quil A, CpG and CT. IgG titers of the CT-adjuvanted group reached levels comparable to those obtained after DTalum subcutaneous injection. The IgG1/IgG2a ratio of DT-specific antibodies decreased in the following sequence: plain DT, Quil A, CT and CpG, suggesting that the immune response was skewed towards the Th1 direction. Conclusions. The potency and the quality of the immune response against DT administered by microneedle array mediated TCI can be modulated by co-administration of adjuvants. KEY WORDS: cholera toxin; CpG; diphtheria toxoid; microneedle array; transcutaneous immunization

    A small-molecule PI3Kα activator for cardioprotection and neuroregeneration

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    Harnessing the potential beneficial effects of kinase signalling through the generation of direct kinase activators remains an underexplored area of drug development1,2,3,4,5. This also applies to the PI3K signalling pathway, which has been extensively targeted by inhibitors for conditions with PI3K overactivation, such as cancer and immune dysregulation. Here we report the discovery of UCL-TRO-1938 (referred to as 1938 hereon), a small-molecule activator of the PI3Kα isoform, a crucial effector of growth factor signalling. 1938 allosterically activates PI3Kα through a distinct mechanism by enhancing multiple steps of the PI3Kα catalytic cycle and causes both local and global conformational changes in the PI3Kα structure. This compound is selective for PI3Kα over other PI3K isoforms and multiple protein and lipid kinases. It transiently activates PI3K signalling in all rodent and human cells tested, resulting in cellular responses such as proliferation and neurite outgrowth. In rodent models, acute treatment with 1938 provides cardioprotection from ischaemia–reperfusion injury and, after local administration, enhances nerve regeneration following nerve crush. This study identifies a chemical tool to directly probe the PI3Kα signalling pathway and a new approach to modulate PI3K activity, widening the therapeutic potential of targeting these enzymes through short-term activation for tissue protection and regeneration. Our findings illustrate the potential of activating kinases for therapeutic benefit, a currently largely untapped area of drug development
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