204 research outputs found
Interaction-assisted propagation of Coulomb-correlated electron-hole pairs in disordered semiconductors
A two-band model of a disordered semiconductor is used to analyze dynamical
interaction induced weakening of localization in a system that is accessible to
experimental verification. The results show a dependence on the sign of the
two-particle interaction and on the optical excitation energy of the
Coulomb-correlated electron-hole pair.Comment: 4 pages and 3 ps figure
Off-diagonal disorder in the Anderson model of localization
We examine the localization properties of the Anderson Hamiltonian with
additional off-diagonal disorder using the transfer-matrix method and
finite-size scaling. We compute the localization lengths and study the
metal-insulator transition (MIT) as a function of diagonal disorder, as well as
its energy dependence. Furthermore we investigate the different influence of
odd and even system sizes on the localization properties in quasi
one-dimensional systems. Applying the finite-size scaling approach in
conjunction with a nonlinear fitting procedure yields the critical parameters
of the MIT. In three dimensions, we find that the resulting critical exponent
of the localization length agrees with the exponent for the Anderson model with
pure diagonal disorder.Comment: 12 pages including 4 EPS figures, accepted for publication in phys.
stat. sol. (b
Magnetohydrodynamic equilibria of a cylindrical plasma with poloidal mass flow and arbitrary cross section shape
The equilibrium of a cylindrical plasma with purely poloidal mass flow and
cross section of arbitrary shape is investigated within the framework of the
ideal MHD theory. For the system under consideration it is shown that only
incompressible flows are possible and, conscequently, the general two
dimensional flow equilibrium equations reduce to a single second-order
quasilinear partial differential equation for the poloidal magnetic flux
function , in which four profile functionals of appear. Apart from
a singularity occuring when the modulus of Mach number associated with the
Alfv\'en velocity for the poloidal magnetic field is unity, this equation is
always elliptic and permits the construction of several classes of analytic
solutions. Specific exact equlibria for a plasma confined within a perfectly
conducting circular cylindrical boundary and having i) a flat current density
and ii) a peaked current density are obtained and studied.Comment: Accepted to Plasma Physics & Controlled Fusion, 14 pages, revte
Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processes
<p>Abstract</p> <p>Background</p> <p>Down syndrome (DS; trisomy 21) is the most common genetic cause of mental retardation in the human population and key molecular networks dysregulated in DS are still unknown. Many different experimental techniques have been applied to analyse the effects of dosage imbalance at the molecular and phenotypical level, however, currently no integrative approach exists that attempts to extract the common information.</p> <p>Results</p> <p>We have performed a statistical meta-analysis from 45 heterogeneous publicly available DS data sets in order to identify consistent dosage effects from these studies. We identified 324 genes with significant genome-wide dosage effects, including well investigated genes like <it>SOD1</it>, <it>APP</it>, <it>RUNX1 </it>and <it>DYRK1A </it>as well as a large proportion of novel genes (N = 62). Furthermore, we characterized these genes using gene ontology, molecular interactions and promoter sequence analysis. In order to judge relevance of the 324 genes for more general cerebral pathologies we used independent publicly available microarry data from brain studies not related with DS and identified a subset of 79 genes with potential impact for neurocognitive processes. All results have been made available through a web server under <url>http://ds-geneminer.molgen.mpg.de/</url>.</p> <p>Conclusions</p> <p>Our study represents a comprehensive integrative analysis of heterogeneous data including genome-wide transcript levels in the domain of trisomy 21. The detected dosage effects build a resource for further studies of DS pathology and the development of new therapies.</p
Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6.
Early detection of the behavioural deficits of neurodegenerative diseases may help to describe the pathogenesis of such diseases and establish important biomarkers of disease progression. The aim of this study was to identify how sensorimotor adaptation of the upper limb, a cerebellar-dependent process restoring movement accuracy after introduction of a perturbation, is affected at the pre-clinical and clinical stages of spinocerebellar ataxia type 6 (SCA6), an inherited neurodegenerative disease. We demonstrate that initial adaptation to the perturbation was significantly impaired in the eighteen individuals with clinical motor symptoms but mostly preserved in the five pre-clinical individuals. Moreover, the amount of error reduction correlated with the clinical symptoms, with the most symptomatic patients adapting the least. Finally both pre-clinical and clinical individuals showed significantly reduced de-adaptation performance after the perturbation was removed in comparison to the control participants. Thus, in this large study of motor features in SCA6, we provide novel evidence for the existence of subclinical motor dysfunction at a pre-clinical stage of SCA6. Our findings show that testing sensorimotor de-adaptation could provide a potential predictor of future motor deficits in SCA6
Exposure to aircraft and road traffic noise and associations with heart disease and stroke in six European countries: a cross-sectional study
This work was supported by the Economic and Social Research Council (grant ES/F038763/1) with additional funding from the European Network for Noise and Health (ENNAH, EU FP7 grant number 226442)
Soluble and Cell-Associated Insulin Receptor Dysfunction Correlates with Severity of HAND in HIV-Infected Women
Blood sugar metabolism abnormalities have been identified in HIV-infected individuals and associated with HIV-associated neurocognitive disorders (HAND). These abnormalities may occur as a result of chronic HIV infection, long-term use of combined antiretroviral treatment (CART), aging, genetic predisposition, or a combination of these factors, and may increase morbidity and mortality in this population.To determine if changes in soluble and cell-associated insulin receptor (IR) levels, IR substrate-1 (IRS-1) levels, and IRS-1 tyrosine phosphorylation are associated with the presence and severity of HAND in a cohort of HIV-seropositive women.This is a retrospective cross-sectional study using patient database information and stored samples from 34 HIV-seropositive women and 10 controls without history of diabetes from the Hispanic-Latino Longitudinal Cohort of Women. Soluble IR subunits [sIR, ectodomain (α) and full-length or intact (αβ)] were assayed in plasma and CSF samples by ELISA. Membrane IR levels, IRS-1 levels, and IRS-1 tyrosine phosphorylation were analyzed in CSF white cell pellets (WCP) using flow cytometry. HIV-seropositive women had significantly increased levels of intact or full-length sIR in plasma (p<0.001) and CSF (p<0.005) relative to controls. Stratified by HAND, increased levels of full-length sIR in plasma were associated with the presence (p<0.001) and severity (p<0.005) of HAND. A significant decrease in IRS-1 tyrosine-phosphorylation in the WCP was also associated with the presence (p<0.02) and severity (p<0.02) of HAND.This study provides evidence that IR secretion is increased in HIV-seropositive women, and increased IR secretion is associated with cognitive impairment in these women. Thus, IR dysfunction may have a role in the progression of HAND and could represent a biomarker for the presence and severity of HAND
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