45 research outputs found
Uncertainty Analyses in the Finite-Difference Time-Domain Method
Providing estimates of the uncertainty in results obtained by Computational Electromagnetic (CEM) simulations is essential when determining the acceptability of the results. The Monte Carlo method (MCM) has been previously used to quantify the uncertainty in CEM simulations. Other computationally efficient methods have been investigated more recently, such as the polynomial chaos method (PCM) and the method of moments (MoM). This paper introduces a novel implementation of the PCM and the MoM into the finite-difference time -domain method. The PCM and the MoM are found to be computationally more efficient than the MCM, but can provide poorer estimates of the uncertainty in resonant electromagnetic compatibility data
Next-to-Leading Order QCD Analysis of Polarized Deep Inelastic Scattering Data
We present a Next-to-Leading order perturbative QCD analysis of world data on
the spin dependent structure functions , and , including
the new experimental information on the dependence of . Careful
attention is paid to the experimental and theoretical uncertainties. The data
constrain the first moments of the polarized valence quark distributions, but
only qualitatively constrain the polarized sea quark and gluon distributions.
The NLO results are used to determine the dependence of the ratio
and evolve the experimental data to a constant . We
determine the first moments of the polarized structure functions of the proton
and neutron and find agreement with the Bjorken sum rule.Comment: 21 pages, 4 figures; final version to be published in Phys. Lett. B.
References updated. Uses elsart.cls version 1996/04/22, 2e-1.4
Exploring attachment behavior versus non-attachment behavior: Issues in the clinical assessment of relationships with significant caregivers
15-deoxy-Delta(12,14)-prostaglandin J(2)-induced apoptosis in amnion-like WISH cells
Apoptosis at the site of rupture has been proposed to play a role in premature rupture of the fetal membranes, a condition associated with increased risk of neonatal sepsis and preterm birth. We investigated the ability of peroxisome proliferator-activated receptor (PPAR)-gamma ligands 15-deoxy-Delta(12,14)PGJ(2) (15d-PGJ(2)), Delta(12)PGJ2(,) ciglitizone and rosiglitazone to induce apoptosis in the amnion-like WISH cell line. 15d-PGJ(2) (10 muM) induced morphological characteristics of apoptosis within 2 h, with biochemical indices (caspase activation and substrate cleavage) following shortly after; maximum cell death (approximately 60%) was observed by 16 h, with an EC50 of approximately 7 muM 15d-PGJ(2). Delta(12)-PGJ(2) also induced apoptosis but was less potent and acted at a much slower rate. While ciglitizone also induced apoptosis, rosiglitazone had no effect on cell viability. The mechanism of induction of apoptosis by 15d-PGJ(2) and Delta(12)PGJ(2), which may be independent of PPAR-gamma activation, requires further elucidation. (C) 2001 Elsevier Science Inc. All rights reserved