3,253 research outputs found
EEG reinvestigations of visual statistical learning for faces, scenes, and objects
The objective of this ongoing, replication study is to understand temporal and spatial patterns in our environment by using the technique of electroencephalography (EEG). Visual statistical learning (VSL) helps us to understand conditional probabilities from our environments. This concept is why we know that chairs are located under tables, not above. The goal of this study is to understand whether participants can unconsciously associate pairs of items (faces, scenes, and objects) from their short-term memory. Strong pairs become more similar to each other, as compared to weak pairs, which become less similar. In the main task, participants saw items appear on the screen, on at a time, for 100ms each. Items directly followed each other without transitions. In the post-task, participants were asked to rate how familiar pairs of items were, using a sliding scale. There were three types of pairs presented: strong pairs where item B followed item A 100% of the time; weak pairs where item B followed item A 11% of the time; and foil pairs where item B followed item A 0% of the time. In conclusion, results are similar to the current study (n = 10) in that there are behavioral differences between strong vs. foil and strong vs. weak pairs
The Star Formation and Extinction Co-Evolution of UV-Selected Galaxies over 0.05<z<1.2
We use a new stacking technique to obtain mean mid IR and far IR to far UV
flux ratios over the rest near-UV/near-IR color-magnitude diagram. We employ
COMBO-17 redshifts and COMBO-17 optical, GALEX far and near UV, Spitzer IRAC
and MIPS Mid IR photometry. This technique permits us to probe infrared excess
(IRX), the ratio of far IR to far UV luminosity, and specific star formation
rate (SSFR) and their co-evolution over two orders of magnitude of stellar mass
and redshift 0.1<z<1.2. We find that the SSFR and the characteristic mass (M_0)
above which the SSFR drops increase with redshift (downsizing). At any given
epoch, IRX is an increasing function of mass up to M_0. Above this mass IRX
falls, suggesting gas exhaustion. In a given mass bin below M_0 IRX increases
with time in a fashion consistent with enrichment. We interpret these trends
using a simple model with a Schmidt-Kennicutt law and extinction that tracks
gas density and enrichment. We find that the average IRX and SSFR follows a
galaxy age parameter which is determined mainly by the galaxy mass and time
since formation. We conclude that blue sequence galaxies have properties which
show simple, systematic trends with mass and time such as the steady build-up
of heavy elements in the interstellar media of evolving galaxies and the
exhaustion of gas in galaxies that are evolving off the blue sequence. The IRX
represents a tool for selecting galaxies at various stages of evolution.Comment: Accepted for publication in GALEX Special Ap.J.Suppl., December, 200
Association of Simulated COVID-19 Vaccination and Nonpharmaceutical Interventions With Infections, Hospitalizations, and Mortality
IMPORTANCE Vaccination against SARS-CoV-2 has the potential to significantly reduce transmission and COVID-19 morbidity and mortality. The relative importance of vaccination strategies and nonpharmaceutical interventions (NPIs) is not well understood. OBJECTIVE To assess the association of simulated COVID-19 vaccine efficacy and coverage scenarios with and without NPIs with infections, hospitalizations, and deaths. DESIGN, SETTING, AND PARTICIPANTS An established agent-based decision analytical model was used to simulate COVID-19 transmission and progression from March 24, 2020, to September 23, 2021. The model simulated COVID-19 spread in North Carolina, a US state of 10.5 million people. A network of 1 017 720 agents was constructed from US Census data to represent the statewide population. EXPOSURES Scenarios of vaccine efficacy (50% and 90%), vaccine coverage (25%, 50%, and 75% at the end of a 6-month distribution period), and NPIs (reduced mobility, school closings, and use of face masks) maintained and removed during vaccine distribution. MAIN OUTCOMES AND MEASURES Risks of infection from the start of vaccine distribution and risk differences comparing scenarios. Outcome means and SDs were calculated across replications. RESULTS In the worst-case vaccination scenario (50% efficacy, 25%coverage), a mean (SD) of 2 231 134 (117 867) new infections occurred after vaccination began with NPIs removed, and a mean (SD) of 799 949 (60 279) new infections occurred with NPIs maintained during 11 months. In contrast, in the best-case scenario (90% efficacy, 75%coverage), a mean (SD) of 527 409 (40 637) new infections occurred with NPIs removed and a mean (SD) of 450 575 (32 716) new infections occurred with NPIs maintained. With NPIs removed, lower efficacy (50%) and higher coverage (75%) reduced infection risk by a greater magnitude than higher efficacy (90%) and lower coverage (25%) compared with theworst-case scenario (mean [SD] absolute risk reduction, 13%[1%] and 8%[1%], respectively). CONCLUSIONS AND RELEVANCE Simulation outcomes suggest that removing NPIs while vaccines are distributed may result in substantial increases in infections, hospitalizations, and deaths. Furthermore, as NPIs are removed, higher vaccination coverage with less efficacious vaccines can contribute to a larger reduction in risk of SARS-CoV-2 infection compared with more efficacious vaccines at lower coverage. These findings highlight the need for well-resourced and coordinated efforts to achieve high vaccine coverage and continued adherence to NPIs before many prepandemic activities can be resumed
UV Star Formation Rates in the Local Universe
We measure star formation rates of ~50,000 optically-selected galaxies in the
local universe (z~0.1), spanning a range from gas-rich dwarfs to massive
ellipticals. We obtain dust-corrected SFRs by fitting the GALEX (UV) and SDSS
(optical) photometry to a library of population synthesis models that include
dust attenuation. For star-forming galaxies, our UV-based SFRs compare
remarkably well with those derived from SDSS H alpha. Deviations from perfect
agreement between these two methods are due to differences in the dust
attenuation estimates. In contrast to H alpha, UV provides reliable SFRs for
galaxies with weak or no H alpha emission, and where H alpha is contaminated
with an emission from an AGN. We use full-SED SFRs to calibrate a simple
prescription that uses GALEX UV magnitudes to produce good SFRs for normal
star-forming galaxies. The specific SFR is considered as a function of stellar
mass for (1) star-forming galaxies with no AGN, (2) those hosting an AGN, and
for (3) galaxies without H alpha emission. We find that the three have distinct
star formation histories, with AGN lying intermediate between the star-forming
and the quiescent galaxies. Normal star forming galaxies (without an AGN) lie
on a relatively narrow linear sequence. Remarkably, galaxies hosting a strong
AGN appear to represent the massive continuation of this sequence. Weak AGN,
while also massive, have lower SFR, sometimes extending to the realm of
quiescent galaxies. We propose an evolutionary sequence for massive galaxies
that smoothly connects normal star-forming galaxies to quiescent (red sequence)
galaxies via strong and weak AGN. We confirm that some galaxies with no H alpha
emission show signs of SF in the UV. We derive a UV-based cosmic SFR density at
z=0.1 with smaller total error than previous measurements (abridged).Comment: Accepted for publication in ApJ (Special GALEX Supplement issue - Dec
2007). v2: Typo in Eq. 2 correcte
Cortical thickness, surface area and volume measures in Parkinson's disease, multiple system atrophy and progressive supranuclear palsy
OBJECTIVE
Parkinson's disease (PD), Multiple System Atrophy (MSA) and Progressive Supranuclear Palsy (PSP) are neurodegenerative diseases that can be difficult to distinguish clinically. The objective of the current study was to use surface-based analysis techniques to assess cortical thickness, surface area and grey matter volume to identify unique morphological patterns of cortical atrophy in PD, MSA and PSP and to relate these patterns of change to disease duration and clinical features.
METHODS
High resolution 3D T1-weighted MRI volumes were acquired from 14 PD patients, 18 MSA, 14 PSP and 19 healthy control participants. Cortical thickness, surface area and volume analyses were carried out using the automated surface-based analysis package FreeSurfer (version 5.1.0). Measures of disease severity and duration were assessed for correlation with cortical morphometric changes in each clinical group.
RESULTS
Results show that in PSP, widespread cortical thinning and volume loss occurs within the frontal lobe, particularly the superior frontal gyrus. In addition, PSP patients also displayed increased surface area in the pericalcarine. In comparison, PD and MSA did not display significant changes in cortical morphology.
CONCLUSION
These results demonstrate that patients with clinically established PSP exhibit distinct patterns of cortical atrophy, particularly affecting the frontal lobe. These results could be used in the future to develop a useful clinical application of MRI to distinguish PSP patients from PD and MSA patients
The Dkk3 gene encodes a vital intracellular regulator of cell proliferation
Members of the Dickkopf (Dkk) family of Wnt antagonists interrupt Wnt-induced receptor assembly and participate in axial patterning and cell fate determination. One family member, DKK3, does not block Wnt receptor activation. Loss of Dkk3 expression in cancer is associated with hyperproliferation and dysregulated ss-catenin signaling, and ectopic expression of Dkk3 halts cancer growth. The molecular events mediating the DKK3-dependent arrest of ss-catenin-driven cell proliferation in cancer cells are unknown. Here we report the identification of a new intracellular gene product originating from the Dkk3 locus. This Dkk3b transcript originates from a second transcriptional start site located in intron 2 of the Dkk3 gene. It is essential for early mouse development and is a newly recognized regulator of ss-catenin signaling and cell proliferation. Dkk3b interrupts nuclear translocation ss-catenin by capturing cytoplasmic, unphosphorylated ss-catenin in an extra-nuclear complex with ss-TrCP. These data reveal a new regulator of one of the most studied signal transduction pathways in metazoans and provides a novel, completely untapped therapeutic target for silencing the aberrant ss-catenin signaling that drives hyperproliferation in many cancers
Proposal for a revised taxonomy of the family Filoviridae: classification, names of taxa and viruses, and virus abbreviations
The taxonomy of the family Filoviridae (marburgviruses and ebolaviruses) has changed several times since the discovery of its members, resulting in a plethora of species and virus names and abbreviations. The current taxonomy has only been partially accepted by most laboratory virologists. Confusion likely arose for several reasons: species names that consist of several words or which (should) contain diacritical marks, the current orthographic identity of species and virus names, and the similar pronunciation of several virus abbreviations in the absence of guidance for the correct use of vernacular names. To rectify this problem, we suggest (1) to retain the current species names Reston ebolavirus, Sudan ebolavirus, and Zaire ebolavirus, but to replace the name Cote d'Ivoire ebolavirus [sic] with TaĂŻ Forest ebolavirus and Lake Victoria marburgvirus with Marburg marburgvirus; (2) to revert the virus names of the type marburgviruses and ebolaviruses to those used for decades in the field (Marburg virus instead of Lake Victoria marburgvirus and Ebola virus instead of Zaire ebolavirus); (3) to introduce names for the remaining viruses reminiscent of jargon used by laboratory virologists but nevertheless different from species names (Reston virus, Sudan virus, TaĂŻ Forest virus), and (4) to introduce distinct abbreviations for the individual viruses (RESTV for Reston virus, SUDV for Sudan virus, and TAFV for TaĂŻ Forest virus), while retaining that for Marburg virus (MARV) and reintroducing that used over decades for Ebola virus (EBOV). Paying tribute to developments in the field, we propose (a) to create a new ebolavirus species (Bundibugyo ebolavirus) for one member virus (Bundibugyo virus, BDBV); (b) to assign a second virus to the species Marburg marburgvirus (Ravn virus, RAVV) for better reflection of now available high-resolution phylogeny; and (c) to create a new tentative genus (Cuevavirus) with one tentative species (Lloviu cuevavirus) for the recently discovered Lloviu virus (LLOV). Furthermore, we explain the etymological derivation of individual names, their pronunciation, and their correct use, and we elaborate on demarcation criteria for each taxon and virus.S
Anti-schistosomal activities of quinoxaline-containing compounds:From hit identification to lead optimisation
Schistosomiasis is a neglected disease of poverty that is caused by infection with blood fluke species contained within the genus Schistosoma. For the last 40 years, control of schistosomiasis in endemic regions has predominantly been facilitated by administration of a single drug, praziquantel. Due to limitations in this mono-chemotherapeutic approach for sustaining schistosomiasis control into the future, alternative anti-schistosomal compounds are increasingly being sought by the drug discovery community. Herein, we describe a multi-pronged, integrated strategy that led to the identification and further exploration of the quinoxaline core as a promising anti-schistosomal scaffold
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