899 research outputs found

    PAR22 FIBROMYALGIA SYNDROM: A FRENCH EPIDEMIOLOGICAL SURVEY

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    Finite element analysis of a fluid-structure interaction in flexible pipe line

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    This paper describes the basic theory and computing method for transient flow of liquid in flexible pipe such as rubber tubing and arterial system. A mathematical model taking into account tube wall axial and radial motion (in which the dynamic fluid pressure causes circumferential and axial motion of the tube wall) is presented. The tube wall is assumed to be elastic material and the compressibility of the liquid is neglected. Circumferential and axial strain-stress relationships for the tube are considered. The obtained mathematical system is constituted of four non-linear hyperbolic partial differential equations describing the wave  propagation in both pipe wall and liquid flow. The fluid-structure interaction is found to be governed by Poisson’s ratio. In this steady finite element method based on Galerkin formulation is applied. Numerical results show a good similarity with those of the literature obtained by the characteristics method.Key words : Fluid-structure interaction, flexible pipe, rubber, finite element method

    PCV58 CHRONIC VENOUS DISEASE: CARE IMPACT

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    PSN22 SENSITIVE SKIN: IMPACT ON QUALITY OF LIFE

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    PFM6 CROSS-SURVEY OF FRENCH AND PORTUGUESE GENERAL PRACTITIONERS AWARENESS AND KNOWLEDGE OF FIBROMYALGIA

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    Evaporation residues produced in spallation of 208Pb by protons at 500A MeV

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    The production cross sections of fragmentation-evaporation residues in the reaction Pb+p at 500A MeV have been measured using the inverse-kinematics method and the FRS spectrometer (GSI). Fragments were identified in nuclear charge using ionisation chambers. The mass identification was performed event-by-event using the B-rho - TOF - Delta-E technique. Although partially-unresolved ionic charge states induced an ambiguity on the mass of some heavy fragments, production rates could be obtained with a high accuracy by systematically accounting for the polluting ionic charge states. The contribution of multiple reactions in the target was subtracted using a new, partly self-consistent code. The isobaric distributions are found to have a shape very close to the one observed in experiments at higher energy. Kinematic properties of the fragments were also measured. The total and the isotopic cross sections, including charge-pickup cross sections, are in good agreement with previous measurements. The data are discussed in the light of previous spallation measurements, especially on lead at 1 GeV

    Bub1 is activated by the protein kinase p90Rsk during Xenopus oocyte maturation

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    AbstractBackground: The kinetochore attachment (spindle assembly) checkpoint arrests cells in metaphase to prevent exit from mitosis until all the chromosomes are aligned properly at the metaphase plate. The checkpoint operates by preventing activation of the anaphase-promoting complex (APC), which triggers anaphase by degrading mitotic cyclins and other proteins. This checkpoint is active during normal mitosis and upon experimental disruption of the mitotic spindle. In yeast, the serine/threonine protein kinase Bub1 and the WD-repeat protein Bub3 are elements of a signal transduction cascade that regulates the kinetochore attachment checkpoint. In mammalian cells, activated MAPK is present on kinetochores during mitosis and activity is upregulated by the spindle assembly checkpoint. In vertebrate unfertilized eggs, a special form of meiotic metaphase arrest by cytostatic factor (CSF) is mediated by MAPK activation of the protein kinase p90Rsk, which leads to inhibition of the APC. However, it is not known whether CSF-dependent metaphase arrest caused by p90Rsk involves components of the spindle assembly checkpoint.Results: xBub1 is present in resting oocytes and its protein level increases slightly during oocyte maturation and early embryogenesis. In Xenopus oocytes, Bub1 is localized to kinetochores during both meiosis I and meiosis II, and the electrophoretic mobility of Bub1 upon SDS-PAGE decreases during meiosis I, reflecting phosphorylation and activation of the enzyme. The activation of Bub1 can be induced in interphase egg extracts by selective stimulation of the MAPK pathway by c-Mos, a MAPKKK. In oocytes treated with the MEK1 inhibitor U0126, the MAPK pathway does not become activated, and Bub1 remains in its low-activity, unshifted form. Injection of a constitutively active target of MAPK, the protein kinase p90Rsk, restores the activation of Bub1 in the presence of U0126. Moreover, purified p90Rsk phosphorylates Bub1 in vitro and increases its protein kinase activity.Conclusions: Bub1, an upstream component of the kinetochore attachment checkpoint, is activated during meiosis in Xenopus in a MAPK-dependent manner. Moreover, a single substrate of MAPK, p90Rsk, is sufficient to activate Bub1 in vitro and in vivo. These results indicate that in vertebrate eggs, kinetochore attachment/spindle assembly checkpoint proteins, including Bub1, are downstream of p90Rsk and may be effectors of APC inhibition and CSF-dependent metaphase arrest by p90Rsk
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