469 research outputs found

    Normative climates of parenthood across Europe : judging voluntary childlessness and working parents

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    Erworben im Rahmen der Schweizer Nationallizenzen (http://www.nationallizenzen.ch)Past research on gender role attitudes has often focused on individual- rather than country-level explanations. Drawing on European Social Survey data from 21 countries, we examine the effect of societal normative climates (i.e., shared perceptions of others’ attitudes) on personal attitudes towards two non-traditional gender roles: Voluntary childlessness and working full-time while children are young. To detect potential gender differences, we analyse disapproval of men and women separately. Findings reveal that there are strong differences in normative climates across countries, and that people generally perceive more disapproval of women than of men for both behaviours. Most importantly, in countries where a higher share of respondents perceives disapproval of these behaviours, respondents themselves disapprove more strongly – even if they do not believe that others disapprove, and even after controlling for other relevant individual- and country-level characteristics. What is more, the independent effect of normative climate explains most of the differences between countries. This robust finding demonstrates the power of country-level normative climates in explaining individuals’ attitudes and between-country differences in attitudes toward gender roles

    The Proteomics of N-terminal Methionine Cleavage

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    Methionine aminopeptidase (MAP) is a ubiquitous, essential enzyme involved in protein N-terminal methionine excision. According to the generally accepted cleavage rules for MAP, this enzyme cleaves all proteins with small side chains on the residue in the second position (P1′), but many exceptions are known. The substrate specificity of Escherichia coli MAP1 was studied in vitro with a large (\u3e120) coherent array of peptides mimicking the natural substrates and kinetically analyzed in detail. Peptides with Val or Thr at P1′ were much less efficiently cleaved than those with Ala, Cys, Gly, Pro, or Ser in this position. Certain residues at P2′, P3′, and P4′ strongly slowed the reaction, and some proteins with Val and Thr at P1′ could not undergo Met cleavage. These in vitro data were fully consistent with data for 862 E. coli proteins with known N-terminal sequences in vivo. The specificity sites were found to be identical to those for the other type of MAPs, MAP2s, and a dedicated prediction tool for Met cleavage is now available. Taking into account the rules of MAP cleavage and leader peptide removal, the N termini of all proteins were predicted from the annotated genome and compared with data obtained in vivo. This analysis showed that proteins displaying N-Met cleavage are overrepresented in vivo. We conclude that protein secretion involving leader peptide cleavage is more frequent than generally thought

    Study of the dissolved organic matter (DOM) of the Auzon cut-off meander (Allier River, France) by spectral and photoreactivity approaches

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    International audienceWetlands are recognized for the importance of their hydrological function and biodiversity, and there is now a consensus to protect and restore them as well as to complete the knowledge on their functioning. Here, we studied the dissolved organic matter (DOM) of a wetland composed of the Auzon cutoff meander, the Allier River, the alluvial fluvial flow, and watershed aquifer. Water was sampled at different locations, in spring, summer, and autumn. For each sample, DOM was characterized for its chemical and optical properties and its photooxidant capacity through its ability to generate DOM triplet excited states (3 DOM*) and singlet oxygen upon simulated solar light exposure. UV-visible and fluorescence indices revealed that DOM was mainly microbial-derived whatever the sampling sites with spatial and temporal variations in terms of aromaticity (5.5-22%), specific UV absorbance at 254 nm (0.28-2.82 L m −1 mgC −1), ratio of the absorbance at 254 and 365 nm (4.6-10.8), fluorescence index (1.35-166), and biological index (0.812-2.25). All the samples generated 3 DOM* and singlet oxygen, rates of formation of which showed parallel variations. Using principal component analysis (PCA), we found positive correlations between the sensitizing properties of DOM samples and parameters associated to the abundance of low molecular weight and low absorbing chromophores. Moreover, the parameter variation across the wetland reinforced the hydrological movements observed in a previous study, suggesting that these parameters could be used as water connection tracers

    Place du dispositif intra-utérin dans l arsenal contraceptif de la jeune femme nullipare en soins primaires

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    Les dispositifs intra-utérins sont le premier moyen de contraception réversible dans le monde. En 2004, l HAS statue que "les DIU ne sont pas uniquement destinés aux multipares". Malgré les nouvelles recommandations, en France leur utilisation chez la nullipare reste marginale : environ 1% des femmes nullipares l'utilisent. L objectif de cette étude était de déterminer les freins à la diffusion du dispositif intra-utérin chez la jeune femme nullipare en soins primaires ambulatoires. Une étude qualitative a été menée auprès de médecins généralistes libéraux ou salariés de l Isère, dans leur cabinet d exercice. Les entretiens enregistrés ont été menés par deux enquêtrices. L étude a été conduite en recherche de variation maximale, suivant un guide d entretien et jusqu à saturation des données. Après retranscription exhaustive des entretiens, une analyse thématique a été réalisée par les deux investigatrices respectant ainsi la triangulation des données. Vingt médecins généralistes ont été interviewés entre janvier et avril 2013. Les freins mis en évidence sont de quatre ordres. Tout d abord ceux liés aux professionnels de santé, qu ils soient médecins généralistes ou gynécologues. Deuxièmement, ceux en rapport avec les patientes nullipares, principalement induits par un manque d information. Troisièmement viennent les freins en lien avec la société et enfin ceux dépendant des laboratoires pharmaceutiques. Chez les médecins généralistes, les réticences restent ancrées, en dépit des nombreuses études et recommandations qui en découlent depuis bientôt 10 ans. Par ailleurs, les médecins favorables à cette méthode se heurtent à un problème de compétence pratique.GRENOBLE1-BU Médecine pharm. (385162101) / SudocSudocFranceF

    Fluorescence analysis allows to predict the oxidative capacity of humic quinones in dissolved organic matter: implication for pollutant degradation

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    AbstractDissolved organic matter (DOM) controls the degradation and sequestration of aquatic pollutants and, in turn, water quality. In particular, pollutant degradation is performed by oxidant species that are generated by exposure of DOM to solar light, yet, since DOM is a very complex mixture of poorly known substances, the relationships between potential oxidant precursors in DOM and their oxydative capacity is poorly known. Here, we hypothesized that production of oxidant species could be predicted using fluorescence analysis. We analysed water samples from an alluvial plain by fluorescence spectroscopy; the three-dimensional spectra were then decomposed into seven individual components using a multi-way algorithm. Components include a protein-like fluorophore, e.g. tryptophan-like and tyrosine-like, three humic fluorophores, 2-naphthoxyacetic acid, and a by-product. We compared component levels with the ability of water samples to generate reactive species under solar light. The results show a strong correlation between reactive species production and the intensity of two humic-like fluorophores assigned to reduced quinones. Monitoring these fluorophores should thus allow to predict the ability of DOM degradation of pollutants in surface waters

    Continuous Casting of Multi-Alloy Metal Products and Related Methods

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    Described are multi-alloy metal products formed by a continuous casting system, as well as methods of continuously casting multi-alloy metal products. The disclosed multi-alloy metal product includes a plurality of layers of metallurgically bonded together metal alloys. The layers can be distributed along the thickness of the metal product or along the width of the metal product. The disclosed continuous casting system includes a plurality of injectors configured to simultaneously inject a plurality of metal alloys into a casting cavity to form the multi-alloy metal product

    Temporal regulation of embryonic M-phases.

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    Temporal regulation of M-phases of the cell cycle requires precise molecular mechanisms that differ among different cells. This variable regulation is particularly clear during embryonic divisions. The first embryonic mitosis in the mouse lasts twice as long as the second one. In other species studied so far (C. elegans, Sphaerechinus granularis, Xenopus laevis), the first mitosis is also longer than the second, yet the prolongation is less pronounced than in the mouse. We have found recently that the mechanisms prolonging the first embryonic M-phase differ in the mouse and in Xenopus embryos. In the mouse, the metaphase of the first mitosis is specifically prolonged by the unknown mechanism acting similarly to the CSF present in oocytes arrested in the second meiotic division. In Xenopus, higher levels of cyclins B participate in the M-phase prolongation, however, without any cell cycle arrest. In Xenopus embryo cell-free extracts, the inactivation of the major M-phase factor, MPF, depends directly on dissociation of cyclin B from CDK1 subunit and not on cyclin B degradation as was thought before. In search for other mitotic proteins behaving in a similar way as cyclins B we made two complementary proteomic screens dedicated to identifying proteins ubiquitinated and degraded by the proteasome upon the first embryonic mitosis in Xenopus laevis. The first screen yielded 175 proteins. To validate our strategy we are verifying now which of them are really ubiquitinated. In the second one, we identified 9 novel proteins potentially degraded via the proteasome. Among them, TCTP (Translationally Controlled Tumor Protein), a 23-kDa protein, was shown to be partially degraded during mitosis (as well as during meiotic exit). We characterized the expression and the role of this protein in Xenopus, mouse and human somatic cells, Xenopus and mouse oocytes and embryos. TCTP is a mitotic spindle protein positively regulating cellular proliferation. Analysis of other candidates is in progress

    A Shift from Cellular to Humoral Responses Contributes to Innate Immune Memory in the Vector Snail Biomphalaria glabrata

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    International audienceDiscoveries made over the past ten years have provided evidence that invertebrate anti-parasitic responses may be primed in a sustainable manner, leading to the failure of a secondary encounter with the same pathogen. This phenomenon called " immune priming " or "innate immune memory" was mainly phenomenological. The demonstration of this process remains to be obtained and the underlying mechanisms remain to be discovered and exhaustively tested with rigorous functional and molecular methods, to eliminate all alternative explanations. In order to achieve this ambitious aim, the present study focuses on the Lophotrochozoan snail, Biomphalaria glabrata, in which innate immune memory was recently reported. We provide herein the first evidence that a shift from a cellular immune response (encapsulation) to a humoral immune response (biomphalysin) occurs during the development of innate memory. The molecular characterisation of this process in Biompha-laria/Schistosoma system was undertaken to reconcile mechanisms with phenomena

    Developing a flexible automated continuous downstream processing system for research to clinical supply

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    Continuous manufacturing has gained a lot of attention over the last 10-15 years for numerous reasons such as the potential for higher efficiencies, reduced cost of goods, and improved product quality. However, the adoption of these technologies has been slow due to concerns over operating these processes in a GMP manufacturing environment. Some of these concerns relate to the operation of multiple continuous unit operations in an integrated process sequence. This presentation will highlight these concerns and show how these issues were addressed by developing an overarching automated and modular platform which can be easily reconfigured for processing most products. The developed automation platform is the result of a project funded by Innovate UK that brings together a number of biopharmaceutical companies including Allergan, AstraZeneca, Fujifilm Diosynth Biotechnologies and GSK to identify and address these issues. One objective of the project is to develop a flexible automated biologics downstream process consisting of multiple unit operations that can be rapidly reconfigured for manufacturing different products. To that end the process has been design with modularity in mind with each module having common inputs and outputs. The automation software has also been developed in a way that most typical downstream processes can be implemented in the system with little to no software updates. The ability to rapidly reconfigure the process has been demonstrated by using the system to produce three products with different process sequences. Another issue that inhibits the adoption of continuous technologies is the concern over simultaneously operating multiple unit operations. This presentation will detail how the automation software was developed to control both the key unit operations such as chromatography and filtration steps but also intermediate operations such as feed conditioning and viral inactivation steps. The automated system reduces the complexity of downstream processes, which can have in excess of eleven unit operations, to a single user-friendly interface. Implementing this control platform enables a single operator to control the entire process. This presentation will also detail how the automation strategy has been developed to enable a single operator to deal with start-up/shutdown, perturbations in the process and mid-process equipment turnover. It will highlight the challenges that have been faced when developing this system and how these have been overcome. The aim of this project was to improve efficiency by reducing processing time when compared to the current batch process and this was demonstrated by testing the system with three different products (a MAb and a MAb fusion protein). Furthermore, this presentation with show data from the production of three products that demonstrates comparability between the continuous process and the original batch processes. It will then detail how this was used to demonstrate the production of a large-scale clinical batch run
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