27 research outputs found

    Structure and Message in Trobriand cricket

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    Ce texte est une version révisée des « Notes » afférentes à Trobriand cricket, film très connu parmi les anthropologues, qui fut réalisé à l’époque où leur attention se centrait (et c’est encore souvent le cas) sur le « message » décelable dans les comportements sociaux. Le thème principal de l’article se résume ainsi : comment les messages ont-ils été construits et insérés dans l’ensemble du documentaire, par le biais des relations entre ses bases constitutives, les images, le discours ? En formalisant quelque peu, l’auteur rend manifestes certains de ces messages du film. Bien sûr, ceux que perçoivent de facto un spectateur ou un public donnés relèvent d’un autre registre et restent ouverts à des recherches ultérieures.Structure and Message in Trobriand cricketThis paper is a modified version of the « Notes » to accompany the much talked-about film Trobriand cricket, that was made during a period in anthropology when attention was, and still is, focused on the message-bearing aspects of social behaviour. This dominant concern expressed in the article is about how messages were built into the whole film through the interrelations of its basic parts, images, and words. The author makes explicit, in a moderately formalized way, what some of the intended messages of Trobriand cricket are. The actual message to any given viewer or audience are, of course, another matter, and open to further investigation.El cricket de las Islas Trobriand : estructura y mensajeEste texto lo constituye una versión modificada de las « Notas » que respectan a Trobriand cricket, una película de mucha fama entre los antropólogos, que fue realizada cuando los trabajos de estos últimos enfocaban el « mensaje » traído por las conductas sociales (enfoque que sigue siendo vigente, a menudo). Una cuestión sintetiza el tema del artículo : ¿ De qué manera los mensajes han sido construídos e incorporados en el conjunto del filme, mediante las interrelaciones de sus partes básicas, de las imágenes y de las palabras ? El autor elucida algunos mensajes del documental, formalizándolos en cierta medida. Por supuesto, los que perciben tal espectador o tal público son datos distintos que quedan abiertos para investigaciones ulteriores

    Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

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    Dimethyl fumarate (DMF) inhibits inflammasome-mediated inflammation and has been proposed as a treatment for patients hospitalised with COVID-19. This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple treatments in patients hospitalised for COVID-19 (NCT04381936, ISRCTN50189673). In this assessment of DMF performed at 27 UK hospitals, adults were randomly allocated (1:1) to either usual standard of care alone or usual standard of care plus DMF. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. Between 2 March 2021 and 18 November 2021, 713 patients were enroled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients received corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.86-1.47; p = 0.40). There was no significant effect of DMF on any secondary outcome

    Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

    Get PDF
    Dimethyl fumarate (DMF) inhibits inflammasome-mediated inflammation and has been proposed as a treatment for patients hospitalised with COVID-19. This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple treatments in patients hospitalised for COVID-19 (NCT04381936, ISRCTN50189673). In this assessment of DMF performed at 27 UK hospitals, adults were randomly allocated (1:1) to either usual standard of care alone or usual standard of care plus DMF. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. Between 2 March 2021 and 18 November 2021, 713 patients were enroled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients received corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.86-1.47; p = 0.40). There was no significant effect of DMF on any secondary outcome

    Targeting eIF4A-Dependent Translation of KRAS Signaling Molecules.

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    Pancreatic adenocarcinoma (PDAC) epitomizes a deadly cancer driven by abnormal KRAS signaling. Here, we show that the eIF4A RNA helicase is required for translation of key KRAS signaling molecules and that pharmacological inhibition of eIF4A has single-agent activity against murine and human PDAC models at safe dose levels. EIF4A was uniquely required for the translation of mRNAs with long and highly structured 5\u27 untranslated regions, including those with multiple G-quadruplex elements. Computational analyses identified these features in mRNAs encoding KRAS and key downstream molecules. Transcriptome-scale ribosome footprinting accurately identified eIF4A-dependent mRNAs in PDAC, including critical KRAS signaling molecules such as PI3K, RALA, RAC2, MET, MYC, and YAP1. These findings contrast with a recent study that relied on an older method, polysome fractionation, and implicated redox-related genes as eIF4A clients. Together, our findings highlight the power of ribosome footprinting in conjunction with deep RNA sequencing in accurately decoding translational control mechanisms and define the therapeutic mechanism of eIF4A inhibitors in PDAC. SIGNIFICANCE: These findings document the coordinate, eIF4A-dependent translation of RAS-related oncogenic signaling molecules and demonstrate therapeutic efficacy of eIF4A blockade in pancreatic adenocarcinoma
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