54 research outputs found
Extended Hauser-Feshbach Method for Statistical Binary-Decay of Light-Mass Systems
An Extended Hauser-Feshbach Method (EHFM) is developed for light heavy-ion
fusion reactions in order to provide a detailed analysis of all the possible
decay channels by including explicitly the fusion-fission phase-space in the
description of the cascade chain. The mass-asymmetric fission component is
considered as a complex-fragment binary-decay which can be treated in the same
way as the light-particle evaporation from the compound nucleus in
statistical-model calculations. The method of the phase-space integrations for
the binary-decay is an extension of the usual Hauser-Feshbach formalism to be
applied to the mass-symmetric fission part. The EHFM calculations include
ground-state binding energies and discrete levels in the low excitation-energy
regions which are essential for an accurate evaluation of the phase-space
integrations of the complex-fragment emission (fission). In the present
calculations, EHFM is applied to the first-chance binary-decay by assuming that
the second-chance fission decay is negligible. In a similar manner to the
description of the fusion-evaporation process, the usual cascade calculation of
light-particle emission from the highly excited complex fragments is applied.
This complete calculation is then defined as EHFM+CASCADE. Calculated
quantities such as charge-, mass- and kinetic-energy distributions are compared
with inclusive and/or exclusive data for the S+Mg and
Cl+C reactions which have been selected as typical examples.
Finally, the missing charge distributions extracted from exclusive measurements
are also successfully compared with the EHFM+CASCADE predictions.Comment: 34 pages, 6 Figures available upon request, Phys. Rev. C (to be
published
Population Health Science: A Core Element of Health Science Education in Sub-Saharan Africa
Sub-Saharan Africa suffers an inordinate burden of disease and does not have the numbers of suitably trained health care workers to address this challenge. New concepts in health sciences education are needed to offer alternatives to current training approaches. A perspective of integrated training in population health for undergraduate medical and nursing education is advanced, rather than continuing to take separate approaches for clinical and public health education. Population health science educates students in the social and environmental origins of disease, thus complementing disease-specific training and providing opportunities for learners to take the perspective of the community as a critical part of their education.
Many of the recent initiatives in health science education in sub-Saharan Africa are reviewed, and two case studies of innovative change in undergraduate medical education are presented that begin to incorporate such population health thinking. The focus is on East Africa, one of the most rapidly growing economies in sub-Saharan Africa where opportunities for change in health science education are opening. The authors conclude that a focus on population health is a timely and effective way for enhancing training of health care professionals to reduce the burden of disease in sub-Saharan Africa
Highly deformed Ca configurations in Si + C
The possible occurrence of highly deformed configurations in the Ca
di-nuclear system formed in the Si + C reaction is investigated
by analyzing the spectra of emitted light charged particles. Both inclusive and
exclusive measurements of the heavy fragments (A 10) and their
associated light charged particles (protons and particles) have been
made at the IReS Strasbourg {\sc VIVITRON} Tandem facility at bombarding
energies of Si) = 112 MeV and 180 MeV by using the {\sc ICARE}
charged particle multidetector array. The energy spectra, velocity
distributions, and both in-plane and out-of-plane angular correlations of light
charged particles are compared to statistical-model calculations using a
consistent set of parameters with spin-dependent level densities. The analysis
suggests the onset of large nuclear deformation in Ca at high spin.Comment: 33 pages, 11 figure
ANSI/NISO Z39.99-2017 ResourceSync Framework Specification
This ResourceSync specification describes a synchronization framework for the web consisting of various capabilities that allow third-party systems to remain synchronized with a server’s evolving resources. The capabilities may be combined in a modular manner to meet local or community requirements. This specification also describes how a server should advertise the synchronization capabilities it supports and how third-party systems may discover this information. The specification repurposes the document formats defined by the Sitemap protocol and introduces extensions for them
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
OBJECTIVE: Proinsulin is a precursor of mature insulin and C-peptide. Higher circulating proinsulin levels are associated with impaired β-cell function, raised glucose levels, insulin resistance, and type 2 diabetes (T2D). Studies of the insulin processing pathway could provide new insights about T2D pathophysiology. RESEARCH DESIGN AND METHODS: We have conducted a meta-analysis of genome-wide association tests of ∼2.5 million genotyped or imputed single nucleotide polymorphisms (SNPs) and fasting proinsulin levels in 10,701 nondiabetic adults of European ancestry, with follow-up of 23 loci in up to 16,378 individuals, using additive genetic models adjusted for age, sex, fasting insulin, and study-specific covariates. RESULTS: Nine SNPs at eight loci were associated with proinsulin levels (P < 5 × 10(-8)). Two loci (LARP6 and SGSM2) have not been previously related to metabolic traits, one (MADD) has been associated with fasting glucose, one (PCSK1) has been implicated in obesity, and four (TCF7L2, SLC30A8, VPS13C/C2CD4A/B, and ARAP1, formerly CENTD2) increase T2D risk. The proinsulin-raising allele of ARAP1 was associated with a lower fasting glucose (P = 1.7 × 10(-4)), improved β-cell function (P = 1.1 × 10(-5)), and lower risk of T2D (odds ratio 0.88; P = 7.8 × 10(-6)). Notably, PCSK1 encodes the protein prohormone convertase 1/3, the first enzyme in the insulin processing pathway. A genotype score composed of the nine proinsulin-raising alleles was not associated with coronary disease in two large case-control datasets. CONCLUSIONS: We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis
Mining the human phenome using allelic scores that index biological intermediates
J. Kaprio ja M-L. Lokki työryhmien jäseniä.It is common practice in genome-wide association studies (GWAS) to focus on the relationship between disease risk and genetic variants one marker at a time. When relevant genes are identified it is often possible to implicate biological intermediates and pathways likely to be involved in disease aetiology. However, single genetic variants typically explain small amounts of disease risk. Our idea is to construct allelic scores that explain greater proportions of the variance in biological intermediates, and subsequently use these scores to data mine GWAS. To investigate the approach's properties, we indexed three biological intermediates where the results of large GWAS meta-analyses were available: body mass index, C-reactive protein and low density lipoprotein levels. We generated allelic scores in the Avon Longitudinal Study of Parents and Children, and in publicly available data from the first Wellcome Trust Case Control Consortium. We compared the explanatory ability of allelic scores in terms of their capacity to proxy for the intermediate of interest, and the extent to which they associated with disease. We found that allelic scores derived from known variants and allelic scores derived from hundreds of thousands of genetic markers explained significant portions of the variance in biological intermediates of interest, and many of these scores showed expected correlations with disease. Genome-wide allelic scores however tended to lack specificity suggesting that they should be used with caution and perhaps only to proxy biological intermediates for which there are no known individual variants. Power calculations confirm the feasibility of extending our strategy to the analysis of tens of thousands of molecular phenotypes in large genome-wide meta-analyses. We conclude that our method represents a simple way in which potentially tens of thousands of molecular phenotypes could be screened for causal relationships with disease without having to expensively measure these variables in individual disease collections.Peer reviewe
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