548 research outputs found
The nonlinear Bernstein-Schr\"odinger equation in Economics
In this paper we relate the Equilibrium Assignment Problem (EAP), which is
underlying in several economics models, to a system of nonlinear equations that
we call the "nonlinear Bernstein-Schr\"odinger system", which is well-known in
the linear case, but whose nonlinear extension does not seem to have been
studied. We apply this connection to derive an existence result for the EAP,
and an efficient computational method.Comment: 8 pages, submitted to Lecture Notes in Computer Scienc
Infiltration of the synovial membrane with macrophage subsets and polymorphonuclear cells reflects global disease activity in spondyloarthropathy
Considering the relation between synovial inflammation and global disease activity in rheumatoid arthritis (RA) and the distinct but heterogeneous histology of spondyloarthropathy (SpA) synovitis, the present study analyzed whether histopathological features of synovium reflect specific phenotypes and/or global disease activity in SpA. Synovial biopsies obtained from 99 SpA and 86 RA patients with active knee synovitis were analyzed for 15 histological and immunohistochemical markers. Correlations with swollen joint count, serum C-reactive protein concentrations, and erythrocyte sedimentation rate were analyzed using classical and multiparameter statistics. SpA synovitis was characterized by higher vascularity and infiltration with CD163(+) macrophages and polymorphonuclear leukocytes (PMNs) and by lower values for lining-layer hyperplasia, lymphoid aggregates, CD1a(+) cells, intracellular citrullinated proteins, and MHC-HC gp39 complexes than RA synovitis. Unsupervised clustering of the SpA samples based on synovial features identified two separate clusters that both contained different SpA subtypes but were significantly differentiated by concentration of C-reactive protein and erythrocyte sedimentation rate. Global disease activity in SpA correlated significantly with lining-layer hyperplasia as well as with inflammatory infiltration with macrophages, especially the CD163+ subset, and with PMNs. Accordingly, supervised clustering using these synovial parameters identified a cluster of 20 SpA patients with significantly higher disease activity, and this finding was confirmed in an independent SpA cohort. However, multiparameter models based on synovial histopathology were relatively poor predictors of disease activity in individual patients. In conclusion, these data indicate that inflammatory infiltration of the synovium with CD163+ macrophages and PMNs as well as lining-layer hyperplasia reflect global disease activity in SpA, independently of the SpA subtype. These data support a prominent role for innate immune cells in SpA synovitis and warrant further evaluation of synovial histopathology as a surrogate marker in early-phase therapeutic trials in SpA.</p
On-line Excited-State Laser Spectroscopy of Trapped Short-Lived Ra Ions
As an important step towards an atomic parity violation experiment in one
single trapped Ra ion, laser spectroscopy experiments were performed with
on-line produced short-lived Ra ions. The isotope shift of
the 6\,^2D\,-\,7\,^2P and
6\,^2D\,-\,7\,^2P transitions and the hyperfine structure
constant of the 7\,^2S and 6\,^2D states in Ra
were measured. These values provide a benchmark for the required atomic theory.
A lower limit of ms for the lifetime of the metastable
6\,^2D state was measured by optical shelving.Comment: 4.2 pages, 6 figures, 2 tables
Alpha, Betti and the Megaparsec Universe: on the Topology of the Cosmic Web
We study the topology of the Megaparsec Cosmic Web in terms of the
scale-dependent Betti numbers, which formalize the topological information
content of the cosmic mass distribution. While the Betti numbers do not fully
quantify topology, they extend the information beyond conventional cosmological
studies of topology in terms of genus and Euler characteristic. The richer
information content of Betti numbers goes along the availability of fast
algorithms to compute them.
For continuous density fields, we determine the scale-dependence of Betti
numbers by invoking the cosmologically familiar filtration of sublevel or
superlevel sets defined by density thresholds. For the discrete galaxy
distribution, however, the analysis is based on the alpha shapes of the
particles. These simplicial complexes constitute an ordered sequence of nested
subsets of the Delaunay tessellation, a filtration defined by the scale
parameter, . As they are homotopy equivalent to the sublevel sets of
the distance field, they are an excellent tool for assessing the topological
structure of a discrete point distribution. In order to develop an intuitive
understanding for the behavior of Betti numbers as a function of , and
their relation to the morphological patterns in the Cosmic Web, we first study
them within the context of simple heuristic Voronoi clustering models.
Subsequently, we address the topology of structures emerging in the standard
LCDM scenario and in cosmological scenarios with alternative dark energy
content. The evolution and scale-dependence of the Betti numbers is shown to
reflect the hierarchical evolution of the Cosmic Web and yields a promising
measure of cosmological parameters. We also discuss the expected Betti numbers
as a function of the density threshold for superlevel sets of a Gaussian random
field.Comment: 42 pages, 14 figure
Isotope Shifts of the 6d\,^2D - 7p\,^2P Transition in Trapped Short-Lived Ra
Laser spectroscopy of short-lived radium isotopes in a linear Paul trap has
been performed. The isotope shifts of the 6d\,^2D -
7p\,^2P transition in Ra were measured, which are
sensitive to the short range part of the atomic wavefunctions. The results are
essential experimental input for improving the precision of atomic structure
calculation. This is indispensable for parity violation in Ra aiming at the
determination of the weak mixing angle.Comment: Accepted for publication in Physical Review A as a Rapid
Communicatio
Changes in rheumatoid factor reflect the inflammatory response (CRP and ESR) to infliximab treatment
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