704 research outputs found

    An optimal sensor placement method for SHM based on Bayesian experimental design and polynomial chaos expansion

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    We present an optimal sensor placement methodology for structural health monitoring (SHM) purposes, relying on a Bayesian experimental design approach. The unknown structural properties, e.g. the residual strength and stiffness, are inferred from data collected through a network of sensors, whose architecture, i.e., type and position may largely affect the accuracy of the monitoring system. In tackling this issue, an optimal network configuration is herein sought by maximizing the expected information gain between prior and posterior probability distributions of the parameters to be estimated. Since the objective function linked to the network topology cannot be analytically computed, a numerical approximation is provided by means of a Monte Carlo analysis, wherein each realization is obtained via finite element modeling. Since the computational burden linked to this procedure often grows infeasible, a Polynomial Chaos Expansion (PCE) approach is adopted for accelerating the computation of the forward problem. The analysis expands over joint samples covering both structural state and design variables, i.e., sensor locations. Via increase of the number of deployed sensors in the network, the optimization procedure soon turns computationally costly due to the curse of dimensionality. To this end, a stochastic optimization method is adopted for accelerating the convergence of the optimization process and thereby the damage detection capability of the SHM system. The proposed method is applied to thin flexible structures, and the resulting optimal sensor configuration is shown. The effects of the number of training samples, the polynomial degree of the approximation expansion and the optimization settings are also discussed

    Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother-child cohort in Crete, Greece.

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    OBJECTIVE: This study aims to investigate relations of serum leptin at age 4 with development of adiposity and linear growth during 3 years of follow-up among 75 Greek children and to identify serum metabolites associated with leptin at age 4 and to characterize their associations with adiposity gain and linear growth. METHODS: Linear regression models that accounted for maternal age, education and gestational weight gain and child's age and sex were used to examine associations of leptin and leptin-associated metabolites measured at age 4 with indicators of adiposity and linear growth at age 7. RESULTS: Each 1-unit increment in natural log-(ln)-transformed leptin corresponded with 0.33 (95% CI: 0.10, 0.55) units greater body mass index-for-age z-score gain during follow-up. Likewise, higher levels of the leptin-associated metabolites methylmalonyl-carnitine and glutaconyl-carnitine corresponded with 0.14 (95% CI: 0.01, 0.27) and 0.07 (95% CI: -0.01, 0.16) units higher body mass index-for-age z-score gain, respectively. These relationships did not differ by sex or baseline weight status and were independent of linear growth. CONCLUSIONS: These findings suggest that leptin, methylmalonyl-carnitine and possibly glutaconyl-carnitine are associated with weight gain during early childhood. Future studies are warranted to confirm these findings in other populations

    Reactivity to AQP4 epitopes in relapsing–remitting multiple sclerosis

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    Autoantibodies against the water channel AQP4, expressed predominately in central nervous system astrocytes, are markers and pathogenic factors in Devic's disease. In this study we examined whether Multiple Sclerosis (MS) patients recognize antigenic epitopes on AQP4 that may define distinct disease subsets. We screened sera from 45 patients with relapsing–remitting MS (RRMS) and 13 patients with primary progressive MS (PMS). 23 Neuromyelitis Optica (NMO) patients previously characterized were used as assay positive/negative controls. Sera from 23 patients with Systemic Lupus Erythematosus, 23 with primary Sjogren syndrome without neurological involvement and from 28 healthy individuals were also used as controls. NMO-positive sera exhibited reactivity against the intracellular epitope AQPaa252-275, confirming previous observations. All RRMS sera tested negative for anti-AQP4 antibodies using a cell-based assay, but surprisingly, 13% of them reacted with the epitope AQPaa252-275. PMS, healthy and disease controls showed no specific reactivity. Whether these antibodies define distinct MS subsets and have a pathogenic potential pointing to convergent pathogenetic mechanism with NMO, or are simply markers of astrocytic damage, remains to be determined

    A hysteretic multiscale formulation for validating computational models of heterogeneous structures

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    A framework for the development of accurate yet computationally efficient numerical models is proposed in this work, within the context of computational model validation. The accelerated computation achieved herein relies on the implementation of a recently derived multiscale finite element formulation, able to alternate between scales of different complexity. In such a scheme, the micro-scale is modelled using a hysteretic finite elements formulation. In the micro-level, nonlinearity is captured via a set of additional hysteretic degrees of freedom compactly described by an appropriate hysteric law, which gravely simplifies the dynamic analysis task. The computational efficiency of the scheme is rooted in the interaction between the micro- and a macro-mesh level, defined through suitable interpolation fields that map the finer mesh displacement field to the coarser mesh displacement field. Furthermore, damage related phenomena that are manifested at the micro-level are accounted for, using a set of additional evolution equations corresponding to the stiffness degradation and strength deterioration of the underlying material. The developed modelling approach is utilized for the purpose of model validation; firstly, in the context of reliability analysis; and secondly, within an inverse problem formulation where the identification of constitutive parameters via availability of acceleration response data is sought

    Urinary metabolic profiles in early pregnancy are associated with preterm birth and fetal growth restriction in the Rhea mother-child cohort study

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    Syftet med studien var att undersöka vilka möjligheter matematikundervisning utomhus kan ge för elevernas utveckling och lärande. Syftet var även att undersöka hur utomhusmatematik kan användas som ett komplement till den traditionella inomhusundervisningen i ämnet matematik. Studien baserades på en kvalitativ forskningsansats där kvalitativa semistrukturerade intervjuer och ostrukturerade observationer användes som metoder för att besvara studiens forskningsfrågor. Sex lärare i F-3 intervjuades och två observationer på två olika skolor genomfördes. Resultatet visar att utomhusmatematiken kompletterar matematikundervisningen inomhus genom ett samspel mellan arbetssätt och miljöer. Resultatet visar även på flera positiva effekter med utomhusmatematik så som verklighetsanknytning, motivation, fysisk aktivitet, hälsa, sinnligt lärande, tillåtande miljö och sociala effekter.  De positiva effekter utomhusmatematiken medföljer för elevernas utveckling och lärande bör uppmärksamma fler lärare om dess möjligheter.

    Preprotein mature domains contain translocase targeting signals that are essential for secretion

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    Secretory proteins are only temporary cytoplasmic residents. They are typically synthesized as preproteins, carrying signal peptides N-terminally fused to their mature domains. In bacteria secretion largely occurs posttranslationally through the membrane-embedded SecA-SecYEG translocase. Upon crossing the plasma membrane, signal peptides are cleaved off and mature domains reach their destinations and fold. Targeting to the translocase is mediated by signal peptides. The role of mature domains in targeting and secretion is unclear. We now reveal that mature domains harbor their own independent targeting signals (mature domain targeting signals [MTSs]). These are multiple, degenerate, interchangeable, linear or 3D hydrophobic stretches that become available because of the unstructured states of targeting-competent preproteins. Their receptor site on the cytoplasmic face of the SecYEG-bound SecA is also of hydrophobic nature and is located adjacent to the signal peptide cleft. Both the preprotein MTSs and their receptor site on SecA are essential for protein secretion. Evidently, mature domains have their own previously unsuspected distinct roles in preprotein targeting and secretion
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