6,642 research outputs found
Conjunction search is relational: Behavioral and electrophysiological evidence
Attention selects behaviorally relevant stimuli for further capacity-limited processing and gates their access to awareness. Given the importance of attention for conscious perception, it is important to determine the factors and mechanisms that drive attention. A widespread view is that attention is biased to the specific feature values of a conjunction target (e.g., vertical, red, medium). By contrast, the results of the present study show that attention is tuned to the 2 relative features that distinguish a conjunction target from the irrelevant nontargets (e.g., larger and bluer). Moreover, an irrelevant conjunction cue that is briefly presented prior to the target can automatically attract attention, even in the absence of any feature contrasts. Importantly, automatic orienting to the conjunction cue was completely independent of the physical similarity between cue and target, and depended only on whether the conjunction cue matched the relative features of the target. These results demonstrate that attentional orienting is determined by a mechanism that can rapidly extract information about feature relationships and guide attention to the stimulus that best matches the relative attributes of the target. These results are difficult to reconcile with extant feature-specific accounts or object-based accounts of attention and argue for a relational account of conjunction search. (PsycINFO Database Recor
A Poissonian explanation for heavy-tails in e-mail communication
Patterns of deliberate human activity and behavior are of utmost importance
in areas as diverse as disease spread, resource allocation, and emergency
response. Because of its widespread availability and use, e-mail correspondence
provides an attractive proxy for studying human activity. Recently, it was
reported that the probability density for the inter-event time between
consecutively sent e-mails decays asymptotically as , with
. The slower than exponential decay of the inter-event time
distribution suggests that deliberate human activity is inherently
non-Poissonian. Here, we demonstrate that the approximate power-law scaling of
the inter-event time distribution is a consequence of circadian and weekly
cycles of human activity. We propose a cascading non-homogeneous Poisson
process which explicitly integrates these periodic patterns in activity with an
individual's tendency to continue participating in an activity. Using standard
statistical techniques, we show that our model is consistent with the empirical
data. Our findings may also provide insight into the origins of heavy-tailed
distributions in other complex systems.Comment: 9 pages, 5 figure
Crossover and scaling in a nearly antiferromagnetic Fermi liquid in two dimensions
We consider two-dimensional Fermi liquids in the vicinity of a quantum
transition to a phase with commensurate, antiferromagnetic long-range order.
Depending upon the Fermi surface topology, mean-field spin-density-wave theory
predicts two different types of such transitions, with mean-field dynamic
critical exponents (when the Fermi surface does not cross the magnetic
zone boundary, type ) and (when the Fermi surface crosses the magnetic
zone boundary, type ). The type system only displays behavior at
all energies and its scaling properties are similar (though not identical) to
those of an insulating Heisenberg antiferromagnet. Under suitable conditions
precisely stated in this paper, the type system displays a crossover from
relaxational behavior at low energies to type behavior at high energies. A
scaling hypothesis is proposed to describe this crossover: we postulate a
universal scaling function which determines the entire, temperature-,
wavevector-, and frequency-dependent, dynamic, staggered spin susceptibility in
terms of 4 measurable, , parameters (determining the distance, energy, and
order parameter scales, plus one crossover parameter). The scaling function
contains the full scaling behavior in all regimes for both type and
systems. The crossover behavior of the uniform susceptibility and the specific
heat is somewhat more complicated and is also discussed. Explicit computation
of the crossover functions is carried out in a large expansion on a
mean-field model. Some new results for the critical properties on the ordered
side of the transition are also obtained in a spin-density wave formalism. The
possible relevance of our results to the doped cuprate compounds is briefly
discussed.Comment: 20 pages, REVTeX, 6 figures (uuencoded compressed PostScript file for
figures is appended
Impact of Vitamin D Supplementation on Arterial Vasomotion, Stiffness and Endothelial Biomarkers in Chronic Kidney Disease Patients
Background: Cardiovascular events are frequent and vascular endothelial function is abnormal in patients with chronic
kidney disease (CKD). We demonstrated endothelial dysfunction with vitamin D deficiency in CKD patients; however the impact of cholecalciferol supplementation on vascular stiffness and vasomotor function, endothelial and bone biomarkers in CKD patients with low 25-hydroxy vitamin D [25(OH)D] is unknown, which this study investigated.
Methods: We assessed non-diabetic patients with CKD stage 3/4, age 17–80 years and serum 25(OH)D ,75 nmol/L. Brachial
artery Flow Mediated Dilation (FMD), Pulse Wave Velocity (PWV), Augmentation Index (AI) and circulating blood biomarkers were evaluated at baseline and at 16 weeks. Oral 300,000 units cholecalciferol was administered at baseline and 8-weeks.
Results: Clinical characteristics of 26 patients were: age 50614 (mean61SD) years, eGFR 41611 ml/min/1.73 m2, males
73%, dyslipidaemia 36%, smokers 23% and hypertensives 87%. At 16-week serum 25(OH)D and calcium increased (43616
to 84629 nmol/L, p,0.001 and 2.3760.09 to 2.4260.09 mmol/L; p = 0.004, respectively) and parathyroid hormone
decreased (10.868.6 to 7.464.4; p = 0.001). FMD improved from 3.163.3% to 6.163.7%, p = 0.001. Endothelial biomarker
concentrations decreased: E-Selectin from 566662123 to 525662058 pg/mL; p = 0.032, ICAM-1, 3.4560.01 to
3.1061.04 ng/mL; p = 0.038 and VCAM-1, 54633 to 42633 ng/mL; p = 0.006. eGFR, BP, PWV, AI, hsCRP, von Willebrand
factor and Fibroblast Growth Factor-23, remained unchanged.
Conclusion: This study demonstrates for the first time improvement of endothelial vasomotor and secretory functions with vitamin D in CKD patients without significant adverse effects on arterial stiffness, serum calcium or FGF-23.
Trial Registration: ClinicalTrials.gov NCT0200571
Characterization of Nonjunctional Hemichannels in Caterpillar Cells
Recent studies have demonstrated that hemichannels, which form gap junctions when paired from apposing cells, may serve additional roles when unpaired including cell adhesion and paracrine communication. Hemichannels in mammals are formed by connexins or pannexins, while in insects they are formed by pannexin homologues termed innexins. The formation of functional gap junctions by insect innexins has been established, although their ability to form functional nonjunctional hemichannels has not been reported. Here the characteristics of nonjunctional hemichannels were examined in three lepidopteran cell types, two cell lines (High Five and Sf9) and explanted hemocytes from Heliothis virescens (Fabricius) (Lepidoptera: Noctuidae). Selective fluorescent dye uptake by hemichannels was observed in a significant minority of cells, using fluorescence microscopy and flow cytometry. Carbenoxelone, an inhibitor of mammalian junctions, disrupted dye uptake, while flufenamic acid and mefloquine did not. The presence of Ca2+ and Mg2+ in the media increased hemichannel activity. Additionally, lipopolysaccharide, a stimulator of immune activity in lepidopterans, decreased dye uptake. These results demonstrate for the first time the activity of nonjunctional hemichannels in insect cells, as well as pharmacological tools to manipulate them. These results will facilitate the further examination of the role of innexins and nonjunctional hemichannels in insect cell biology, including paracrine signaling, and comparative studies of mammalian pannexins and insect innexins
Singular Fermi Liquids
An introductory survey of the theoretical ideas and calculations and the
experimental results which depart from Landau Fermi-liquids is presented.
Common themes and possible routes to the singularities leading to the breakdown
of Landau Fermi liquids are categorized following an elementary discussion of
the theory. Soluble examples of Singular Fermi liquids (often called Non-Fermi
liquids) include models of impurities in metals with special symmetries and
one-dimensional interacting fermions. A review of these is followed by a
discussion of Singular Fermi liquids in a wide variety of experimental
situations and theoretical models. These include the effects of low-energy
collective fluctuations, gauge fields due either to symmetries in the
hamiltonian or possible dynamically generated symmetries, fluctuations around
quantum critical points, the normal state of high temperature superconductors
and the two-dimensional metallic state. For the last three systems, the
principal experimental results are summarized and the outstanding theoretical
issues highlighted.Comment: 170 pages; submitted to Physics Reports; a single pdf file with high
quality figures is available from http://www.lorentz.leidenuniv.nl/~saarloo
Implications of MMP9 for Blood Brain Barrier Disruption and Hemorrhagic Transformation Following Ischemic Stroke.
Numerous studies have documented increases in matrix metalloproteinases (MMPs), specifically MMP-9 levels following stroke, with such perturbations associated with disruption of the blood brain barrier (BBB), increased risk of hemorrhagic complications, and worsened outcome. Despite this, controversy remains as to which cells release MMP-9 at the normal and pathological BBB, with even less clarity in the context of stroke. This may be further complicated by the influence of tissue plasminogen activator (tPA) treatment. The aim of the present review is to examine the relationship between neutrophils, MMP-9 and tPA following ischemic stroke to elucidate which cells are responsible for the increases in MMP-9 and resultant barrier changes and hemorrhage observed following stroke
A Triple Protostar System Formed via Fragmentation of a Gravitationally Unstable Disk
Binary and multiple star systems are a frequent outcome of the star formation
process, and as a result, almost half of all sun-like stars have at least one
companion star. Theoretical studies indicate that there are two main pathways
that can operate concurrently to form binary/multiple star systems: large scale
fragmentation of turbulent gas cores and filaments or smaller scale
fragmentation of a massive protostellar disk due to gravitational instability.
Observational evidence for turbulent fragmentation on scales of 1000~AU has
recently emerged. Previous evidence for disk fragmentation was limited to
inferences based on the separations of more-evolved pre-main sequence and
protostellar multiple systems. The triple protostar system L1448 IRS3B is an
ideal candidate to search for evidence of disk fragmentation. L1448 IRS3B is in
an early phase of the star formation process, likely less than 150,000 years in
age, and all protostars in the system are separated by 200~AU. Here we
report observations of dust and molecular gas emission that reveal a disk with
spiral structure surrounding the three protostars. Two protostars near the
center of the disk are separated by 61 AU, and a tertiary protostar is
coincident with a spiral arm in the outer disk at a 183 AU separation. The
inferred mass of the central pair of protostellar objects is 1 M,
while the disk surrounding the three protostars has a total mass of 0.30
M_{\sun}. The tertiary protostar itself has a minimum mass of 0.085
M. We demonstrate that the disk around L1448 IRS3B appears susceptible
to disk fragmentation at radii between 150~AU and 320~AU, overlapping with the
location of the tertiary protostar. This is consistent with models for a
protostellar disk that has recently undergone gravitational instability,
spawning one or two companion stars.Comment: Published in Nature on Oct. 27th. 24 pages, 8 figure
A genome-wide association study identifies protein quantitative trait loci (pQTLs)
There is considerable evidence that human genetic variation influences gene expression. Genome-wide studies have revealed that mRNA levels are associated with genetic variation in or close to the gene coding for those mRNA transcripts - cis effects, and elsewhere in the genome - trans effects. The role of genetic variation in determining protein levels has not been systematically assessed. Using a genome-wide association approach we show that common genetic variation influences levels of clinically relevant proteins in human serum and plasma. We evaluated the role of 496,032 polymorphisms on levels of 42 proteins measured in 1200 fasting individuals from the population based InCHIANTI study. Proteins included insulin, several interleukins, adipokines, chemokines, and liver function markers that are implicated in many common diseases including metabolic, inflammatory, and infectious conditions. We identified eight Cis effects, including variants in or near the IL6R (p = 1.8×10 -57), CCL4L1 (p = 3.9×10-21), IL18 (p = 6.8×10-13), LPA (p = 4.4×10-10), GGT1 (p = 1.5×10-7), SHBG (p = 3.1×10-7), CRP (p = 6.4×10-6) and IL1RN (p = 7.3×10-6) genes, all associated with their respective protein products with effect sizes ranging from 0.19 to 0.69 standard deviations per allele. Mechanisms implicated include altered rates of cleavage of bound to unbound soluble receptor (IL6R), altered secretion rates of different sized proteins (LPA), variation in gene copy number (CCL4L1) and altered transcription (GGT1). We identified one novel trans effect that was an association between ABO blood group and tumour necrosis factor alpha (TNF-alpha) levels (p = 6.8×10-40), but this finding was not present when TNF-alpha was measured using a different assay , or in a second study, suggesting an assay-specific association. Our results show that protein levels share some of the features of the genetics of gene expression. These include the presence of strong genetic effects in cis locations. The identification of protein quantitative trait loci (pQTLs) may be a powerful complementary method of improving our understanding of disease pathways. © 2008 Melzer et al
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