1,276 research outputs found
Addressing Facilitators and Barriers Related to Early Childhood Obesity Prevention in Rural Appalachian Communities
Through a community-focused needs assessment conducted in rural Appalachia, we gauged perceptions of facilitators and barriers related to healthful eating and physical activity for young children and identified suggestions for improvement. Thirty-seven key informant interviews and three caregiver focus group sessions were coded and analyzed for key themes. Limited community resources emerged as a barrier to both healthful eating and physical activity. Suboptimal communication about existing opportunities was also identified. Community members reviewed the needs assessment data and implemented initiatives to address identified needs. The importance of Extension-facilitated needs assessments in rural settings to shape health initiatives to local contexts is highlighted
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Agonist-induced endocytosis of rat somatostatin receptor 1
Somatostatin-receptor 1 (sst1) is an autoreceptor in the central nervous system that regulates the release of somatostatin. Sst1 is present intracellularly and at the cell surface. To investigate sst1 trafficking, rat sst1 tagged with epitope was expressed in rat insulinoma cells 1046-38 (RIN-1046-38) and tracked by antibody labeling. Confocal microscopic analysis revealed colocalization of intracellularly localized rat sst1-human simplex virus (HSV) with Rab5a-green fluorescent protein and Rab11a-green fluorescent protein, indicating the distribution of the receptor in endocytotic and recycling organelles. Somatostatin-14 induced internalization of cell surface receptors and reduction of binding sites on the cell surface. It also stimulated recruitment of intracellular sst1-HSV to the plasma membrane. Confocal analysis of sst1-HSV revealed that the receptor was initially transported within superficial vesicles. Prolonged stimulation of the cells with the peptide agonist induced intracellular accumulation of somatostatin-14. Because the number of cell surface binding sites did not change during prolonged stimulation, somatostatin-14 was internalized through a dynamic process of continuous endocytosis, recycling, and recruitment of intracellularly present sst1-HSV. Accumulated somatostatin-14 bypassed degradation via the endosomal-lysosomal route and was instead rapidly released as intact and biologically active somatostatin-14. Our results show for the first time that sst1 mediates a dynamic process of endocytosis, recycling, and re-endocytosis of its cognate ligand
Variational Multiscale Stabilization and the Exponential Decay of Fine-scale Correctors
This paper addresses the variational multiscale stabilization of standard
finite element methods for linear partial differential equations that exhibit
multiscale features. The stabilization is of Petrov-Galerkin type with a
standard finite element trial space and a problem-dependent test space based on
pre-computed fine-scale correctors. The exponential decay of these correctors
and their localisation to local cell problems is rigorously justified. The
stabilization eliminates scale-dependent pre-asymptotic effects as they appear
for standard finite element discretizations of highly oscillatory problems,
e.g., the poor approximation in homogenization problems or the pollution
effect in high-frequency acoustic scattering
Survey for Transiting Extrasolar Planets in Stellar Systems. II. Spectrophotometry and Metallicities of Open Clusters
We present metallicity estimates for seven open clusters based on
spectrophotometric indices from moderate-resolution spectroscopy. Observations
of field giants of known metallicity provide a correlation between the
spectroscopic indices and the metallicity of open cluster giants. We use \chi^2
analysis to fit the relation of spectrophotometric indices to metallicity in
field giants. The resulting function allows an estimate of the target-cluster
giants' metallicities with an error in the method of \pm0.08 dex. We derive the
following metallicities for the seven open clusters: NGC 1245,
[m/H]=-0.14\pm0.04; NGC 2099, [m/H]=+0.05\pm0.05; NGC 2324, [m/H]=-0.06\pm0.04;
NGC 2539, [m/H]=-0.04\pm0.03; NGC 2682 (M67), [m/H]=-0.05\pm0.02; NGC 6705,
[m/H]=+0.14\pm0.08; NGC 6819, [m/H]=-0.07\pm0.12. These metallicity estimates
will be useful in planning future extra-solar planet transit searches since
planets may form more readily in metal-rich environments.Comment: 38 pages, including 12 figures. Accepted for publication in A
Identification of medically actionable secondary findings in the 1000 genomes
The American College of Medical Genetics and Genomics (ACMG) recommends that clinical sequencing laboratories return secondary findings in 56 genes associated with medically actionable conditions. Our goal was to apply a systematic, stringent approach consistent with clinical standards to estimate the prevalence of pathogenic variants associated with such conditions using a diverse sequencing reference sample. Candidate variants in the 56 ACMG genes were selected from Phase 1 of the 1000 Genomes dataset, which contains sequencing information on 1,092 unrelated individuals from across the world. These variants were filtered using the Human Gene Mutation Database (HGMD) Professional version and defined parameters, appraised through literature review, and examined by a clinical laboratory specialist and expert physician. Over 70,000 genetic variants were extracted from the 56 genes, and filtering identified 237 variants annotated as disease causing by HGMD Professional. Literature review and expert evaluation determined that 7 of these variants were pathogenic or likely pathogenic. Furthermore, 5 additional truncating variants not listed as disease causing in HGMD Professional were identified as likely pathogenic. These 12 secondary findings are associated with diseases that could inform medical follow-up, including cancer predisposition syndromes, cardiac conditions, and familial hypercholesterolemia. The majority of the identified medically actionable findings were in individuals from the European (5/379) and Americas (4/181) ancestry groups, with fewer findings in Asian (2/286) and African (1/246) ancestry groups. Our results suggest that medically relevant secondary findings can be identified in approximately 1% (12/1092) of individuals in a diverse reference sample. As clinical sequencing laboratories continue to implement the ACMG recommendations, our results highlight that at least a small number of potentially important secondary findings can be selected for return. Our results also confirm that understudied populations will not reap proportionate benefits of genomic medicine, highlighting the need for continued research efforts on genetic diseases in these populations
A tight-binding potential for atomistic simulations of carbon interacting with transition metals: Application to the Ni-C system
We present a tight-binding potential for transition metals, carbon, and
transition metal carbides, which has been optimized through a systematic
fitting procedure. A minimal basis, including the s, p electrons of carbon and
the d electrons of the transition metal, is used to obtain a transferable
tight-binding model of the carbon-carbon, metal-metal and metal-carbon
interactions applicable to binary systems. The Ni-C system is more specifically
discussed. The successful validation of the potential for different atomic
configurations indicates a good transferability of the model and makes it a
good choice for atomistic simulations sampling a large configuration space.
This approach appears to be very efficient to describe interactions in systems
containing carbon and transition metal elements
Big Entropy Fluctuations in Statistical Equilibrium: The Macroscopic Kinetics
Large entropy fluctuations in an equilibrium steady state of classical
mechanics were studied in extensive numerical experiments on a simple
2--freedom strongly chaotic Hamiltonian model described by the modified Arnold
cat map. The rise and fall of a large separated fluctuation was shown to be
described by the (regular and stable) "macroscopic" kinetics both fast
(ballistic) and slow (diffusive). We abandoned a vague problem of "appropriate"
initial conditions by observing (in a long run)spontaneous birth and death of
arbitrarily big fluctuations for any initial state of our dynamical model.
Statistics of the infinite chain of fluctuations, reminiscent to the Poincar\'e
recurrences, was shown to be Poissonian. A simple empirical relation for the
mean period between the fluctuations (Poincar\'e "cycle") has been found and
confirmed in numerical experiments. A new representation of the entropy via the
variance of only a few trajectories ("particles") is proposed which greatly
facilitates the computation, being at the same time fairly accurate for big
fluctuations. The relation of our results to a long standing debates over
statistical "irreversibility" and the "time arrow" is briefly discussed too.Comment: Latex 2.09, 26 pages, 6 figure
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