16,894 research outputs found
The role of prolactin in autoimmune demyelination: suppression of experimental allergic encephalomyelitis by bromocriptine.
Comparison of the COBE FIRAS and DIRBE Calibrations
We compare the independent FIRAS and DIRBE observations from the COBE in the
wavelength range 100-300 microns. This cross calibration provides checks of
both data sets. The results show that the data sets are consistent within the
estimated gain and offset uncertainties of the two instruments. They show the
possibility of improving the gain and offset determination of DIRBE at 140 and
240 microns.Comment: Accepted for publication in the Astrophysical Journal 11 pages, plus
3 figures in separate postscript files. Figure 3 has three part
Proton induced reaction cross section measurements on Se isotopes for the astrophysical p process
As a continuation of a systematic study of reactions relevant to the
astrophysical p process, the cross sections of the 74,76Se(p,gamma)75,77Br and
82Se(p,n)82Br reactions have been measured at energies from 1.3 to 3.6 MeV
using an activation technique. The results are compared to the predictions of
Hauser-Feshbach statistical model calculations using the NON-SMOKER and MOST
codes. The sensitivity of the calculations to variations in the optical proton
potential and the nuclear level density was studied. Good agreement between
theoretical and experimental reaction rates was found for the reactions
74Se(p,gamma)75Br and 82Se(p,n)82Br.Comment: 9 pages, 6 figures (in 12 eps files), accepted for publication in
Phys. Rev C, RevTeX styl
Infrared study of spin crossover Fe-picolylamine complex
Infrared (IR) absorption spectroscopy has been used to probe the evolution of
microscopic vibrational states upon the temperature- and photo-induced spin
crossovers in [Fe(2-picolylamine)3]Cl2EtOH (Fe-pic). To overcome the small
sizes and the strong IR absorption of the crystal samples used, an IR
synchrotron radiation source and an IR microscope have been used. The obtained
IR spectra of Fe-pic show large changes between high-spin and low-spin states
for both the temperature- and the photo- induced spin crossovers. Although the
spectra in the temperature- and photo-induced high-spin states are relatively
similar to each other, they show distinct differences below 750 cm-1. This
demonstrates that the photo-induced high-spin state involves microscopically
different characters from those of the temperature-induced high-spin state. The
results are discussed in terms of local pressure and structural deformations
within the picolylamine ligands, and in terms of their possible relevance to
the development of macroscopic photo-induced phase in Fe-pic.Comment: 6 pages (text) and 6 figures,submitted to J. Phys. Soc. Jp
Frequency Domain Functional Near-Infrared Spectrometer (fNIRS) for Crew State Monitoring
A frequency domain functional near-infrared spectrometer (fNIRS) and accompanying software have been developed by the NASA Glenn Research Center as part of the Airspace Operations and Safety Program (AOSP) Technologies for Airplane State Awareness (TASA)SE211 Crew State Monitoring (CSM) Project. The goal of CSM was to develop a suite of instruments to measure the cognitive state of operators while performing operational activities. The fNIRS was one of the instruments intended for the CSM, developed to measure changes in oxygen levels in the brain noninvasively
POM2/CSI1 is essential for functional association of cellulose synthase and microtubules in Arabidopsis
In plants, regulation of cellulose synthesis is fundamental for morphogenesis and plant growth. Cellulose is synthesized at the plasma membrane, and the orientation of synthesis is guided by cortical microtubules; however, the guiding mechanism is currently unknown. We show that the conditional root elongation pom2 mutants are impaired in cell elongation, fertility, and microtubule-related functions. Map-based cloning of the POM-POM2 locus revealed that it is allelic to CELLULOSE SYNTHASE INTERACTING1 (CSI1). Fluorescently tagged POM2/CSI1s associated with both plasma membrane-located cellulose synthases (CESAs) and post-Golgi CESA-containing compartments. Interestingly, while CESA insertions coincided with cortical microtubules in the pom2/csi1 mutants, the microtubule-defined movement of the CESAs was significantly reduced in the mutant. We propose that POM2/CSI1 provides a scaffold between the CESAs and cortical microtubules that guide cellulose synthesis
Adolescents\u27 Behavior in the Presence of Interparental Hostility: Developmental and Emotion Regulatory Influences
Within-family covariation between interparental hostility and adolescent behavior across three interactions over a 2-year period was explored in a sample that included 37 typical adolescents and 35 adolescents recently hospitalized for psychiatric difficulties. More interparental hostility across the three interactions was associated with more adolescent hostility and more positive engagement (at a trend level) regardless of psychiatric background. Parent-to-child hostility in each interaction mediated the link for adolescent hostility but not for positive adolescent engagement. Emotion regulation capacities and age were linked to variability in adolescents\u27 behavior in the presence of interparental conflict. In interactions with more interparental hostility, adolescents with greater capacity to tolerate negative affect were more likely to show increased positive engagement, and adolescents who were better able to modulate their emotional expression were less likely to show increased hostility. Covariation between interparental and adolescent hostility across the three family interactions decreased as the adolescent aged. These findings are consistent with the theory that exposure to inter-parental hostility is emotionally disequilibrating, and that adolescent responses may reflect differences in emotion regulation and other developmentally based capacities. Gender and variations across families in overall levels of hostile parenting were also linked with adolescent behavior in the presence of interparental hostility
Adolescents\u27 Behavior in the Presence of Interparental Hostility: Developmental and Emotion Regulatory Influences
Within-family covariation between interparental hostility and adolescent behavior across three interactions over a 2-year period was explored in a sample that included 37 typical adolescents and 35 adolescents recently hospitalized for psychiatric difficulties. More interparental hostility across the three interactions was associated with more adolescent hostility and more positive engagement (at a trend level) regardless of psychiatric background. Parent-to-child hostility in each interaction mediated the link for adolescent hostility but not for positive adolescent engagement. Emotion regulation capacities and age were linked to variability in adolescents\u27 behavior in the presence of interparental conflict. In interactions with more interparental hostility, adolescents with greater capacity to tolerate negative affect were more likely to show increased positive engagement, and adolescents who were better able to modulate their emotional expression were less likely to show increased hostility. Covariation between interparental and adolescent hostility across the three family interactions decreased as the adolescent aged. These findings are consistent with the theory that exposure to inter-parental hostility is emotionally disequilibrating, and that adolescent responses may reflect differences in emotion regulation and other developmentally based capacities. Gender and variations across families in overall levels of hostile parenting were also linked with adolescent behavior in the presence of interparental hostility
Multigene interactions and the prediction of depression in the Wisconsin Longitudinal Study
Objectives: Single genetic loci offer little predictive power for the identification of depression. This study examined whether an analysis of gene-gene (G x G) interactions of 78 single nucleotide polymorphisms (SNPs) in genes associated with depression and agerelated diseases would identify significant interactions with increased predictive power for depression. Design: A retrospective cohort study. Setting: A survey of participants in the Wisconsin Longitudinal Study. Participants: A total of 4811 persons (2464 women and 2347 men) who provided saliva for genotyping; the group comes from a randomly selected sample of Wisconsin high school graduates from the class of 1957 as well as a randomly selected sibling, almost all of whom are non-Hispanic white. Primary outcome measure: Depression as determine by the Composite International Diagnostic Interview-Short-Form. Results: Using a classification tree approach (recursive partitioning (RP)), the authors identified a number of candidate G 3 G interactions associated with depression. The primary SNP splits revealed by RP (ANKK1 rs1800497 (also known as DRD2 Taq1A) in men and DRD2 rs224592 in women) were found to be significant as single factors by logistic regression (LR) after controlling for multiple testing (p=0.001 for both). Without considering interaction effects, only one of the five subsequent RP splits reached nominal significance in LR (FTO rs1421085 in women, p=0.008). However, after controlling for G x G interactions by running LR on RP-specific subsets, every split became significant and grew larger in magnitude (OR (before) → (after): men: GNRH1 novel SNP: (1.43 → 1.57); women: APOC3 rs2854116: (1.28 → 1.55), ACVR2B rs3749386: (1.11 → 2.17), FTO rs1421085: (1.32 → 1.65), IL6 rs1800795: (1.12 → 1.85)). Conclusions: The results suggest that examining G x G interactions improves the identification of genetic associations predictive of depression. 4 of the SNPs identified in these interactions were located in two pathways well known to impact depression: neurotransmitter (ANKK1 and DRD2) and neuroendocrine (GNRH1 and ACVR2B) signalling. This study demonstrates the utility of RP analysis as an efficient and powerful exploratory analysis technique for uncovering genetic and molecular pathway interactions associated with disease aetiology
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