375 research outputs found

    Policing and the Likelihood of Terrorism: A Community Structural Approach to an Uncertain Relationship

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    Prior research on terrorism has argued that local law enforcement play an important role in counterterrorism though the mechanisms by which the police should prevent terrorism are empirically unsettled and atheoretical in nature. Even less understood is how policing might differentially impact terrorism across specific ideological movements (e.g., far-right, environmental, Islamic extremism). Drawing from prominent sociological and criminological theories (i.e., Environmental perspectives, Social Disorganization, Conflict/Marxist) the current study addresses several key gaps in prior literature by utilizing data from the American Terrorism Study (ATS) paired with data from the FBI Uniform Crime Report and U.S. Census Bureau. Results suggest that counties with greater police presence and heavier officer workloads are associated with greater likelihood of terrorism, for terrorism overall and also equally across unique ideological movements, net of key controls. These findings have strong theoretical implications for the study of terrorism outcomes going forward. Additional implications for policy and future research are discussed

    Somatic Mitochondrial DNA Mutations in Diffuse Large B-Cell Ly

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    Diffuse Large B-Cell Lymphoma (DLBCL) is an aggressive hematological cancer for which mitochondrial metabolism may play an important role. Mitochondrial DNA (mtDNA) encodes crucial mitochondrial proteins, yet the relationship between mtDNA and DLBCL remains unclear. We analyzed the functional consequences and mutational spectra of mtDNA somatic mutations and private constitutional variants in 40 DLBCL tumour-normal pairs. While private constitutional variants occurred frequently in the D-Loop, somatic mutations were randomly distributed across the mitochondrial genome. Heteroplasmic constitutional variants showed a trend towards loss of heteroplasmy in the corresponding tumour regardless of whether the reference or variant allele was being lost, suggesting that these variants are selectively neutral. The mtDNA mutational spectrum showed minimal support for ROS damage and revealed strand asymmetry with increased C > T and A > G transitions on the heavy strand, consistent with a replication-associated mode of mutagenesis. These heavy strand transitions carried higher proportions of amino acid changes – which were also more pathogenic – than equivalent substitutions on the light strand. Taken together, endogenous replication-associated events underlie mtDNA mutagenesis in DLBCL and preferentially generate functionally consequential mutations. Yet mtDNA somatic mutations remain selectively neutral, suggesting that mtDNA-encoded mitochondrial functions may not play an important role in DLBCL

    Positive selection on loci associated with drug and alcohol dependence

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    Much of the evolution of human behavior remains a mystery, including how certain disadvantageous behaviors are so prevalent. Nicotine addiction is one such phenotype. Several loci have been implicated in nicotine related phenotypes including the nicotinic receptor gene clusters (CHRNs) on chromosomes 8 and 15. Here we use 1000 Genomes sequence data from 3 populations (Africans, Asians and Europeans) to examine whether natural selection has occurred at these loci. We used Tajima's D and the integrated haplotype score (iHS) to test for evidence of natural selection. Our results provide evidence for strong selection in the nicotinic receptor gene cluster on chromosome 8, previously found to be significantly associated with both nicotine and cocaine dependence, as well as evidence selection acting on the region containing the CHRNA5 nicotinic receptor gene on chromosome 15, that is genome wide significant for risk for nicotine dependence. To examine the possibility that this selection is related to memory and learning, we utilized genetic data from the Collaborative Studies on the Genetics of Alcoholism (COGA) to test variants within these regions with three tests of memory and learning, the Wechsler Adult Intelligence Scale (WAIS) Block Design, WAIS Digit Symbol and WAIS Information tests. Of the 17 SNPs genotyped in COGA in this region, we find one significantly associated with WAIS digit symbol test results. This test captures aspects of reaction time and memory, suggesting that a phenotype relating to memory and learning may have been the driving force behind selection at these loci. This study could begin to explain why these seemingly deleterious SNPs are present at their current frequencies

    Building SAWE Capability as an ANSI Accredited Standards Developer

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    This paper presents a 2014 status of the Society of Allied Weight Engineers' process towards becoming an Accredited Standards Developer (ASD) under certification by the United States American National Standards Institute (ANSI). Included is material from the committee's 2013 International presentation, current status, and additional general background material. The document strives to serve as a reference point to assist SAWE Recommended Practice and Standards developers in negotiating United States Standards Strategy, international standards strategy, and the association of SAWE standards and recommended practices to those efforts. Required procedures for SAWE to develop and maintain Recommended Practices and ANSI/SAWE Standards are reviewed

    Multiple AMPK activators inhibit L-Carnitine uptake in C2C12 skeletal muscle myotubes

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    Mutations in the gene that encodes the principal L-Carnitine transporter, OCTN2, can lead to a reduced intracellular L-Carnitine pool and the disease Primary Carnitine Deficiency. L-Carnitine supplementation is used therapeutically to increase intracellular L-Carnitine. As AMPK and insulin regulate fat metabolism and substrate uptake we hypothesised that AMPK activating compounds and insulin would increase L-Carnitine uptake in C2C12myotubes. The cells express all three OCTN transporters at the mRNA level and immunohistochemistry confirmed expression at the protein level. Contrary to our hypothesis, despite significant activation of PKB and 2DG uptake, insulin did not increase L-Carnitine uptake at 100nM. However, L-Carnitine uptake was modestly increased at a dose of 150nM insulin. A range of AMPK activators that increase intracellular calcium content [caffeine (10mM, 5mM, 1mM, 0.5mM), A23187 (10μM)], inhibit mitochondrial function [Sodium Azide (75μM), Rotenone (1μM), Berberine (100μM), DNP (500μM)] or directly activate AMPK [AICAR (250μM)] were assessed for their ability to regulate L-Carnitine uptake. All compounds tested significantly inhibited L-Carnitine uptake. Inhibition by caffeine was not dantrolene (10μM) sensitive. Saturation curve analysis suggested that caffeine did not competitively inhibit L-Carnitine transport. However, the AMPK inhibitor Compound C (10μM) partially rescued the effect of caffeine suggesting that AMPK may play a role in the inhibitory effects of caffeine. However, caffeine likely inhibits L-Carnitine uptake by alternative mechanisms independently of calcium release. PKA activation or direct interference with transporter function may play a role

    Understanding the Relationship between Solar Coronal Abundances and F10.7 cm Radio Emission

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    Sun-as-a-star coronal plasma composition, derived from full-Sun spectra, and the F10.7 radio flux (2.8 GHz) have been shown to be highly correlated (r = 0.88) during solar cycle 24. However, this correlation becomes nonlinear during increased solar magnetic activity. Here we use cotemporal, high spatial resolution, multiwavelength images of the Sun to investigate the underlying causes of the nonlinearity between coronal composition (FIP bias) and F10.7 solar index correlation. Using the Karl G. Jansky Very Large Array, Hinode/EIS (EUV Imaging Spectrometer), and the Solar Dynamics Observatory, we observed a small active region, AR 12759, throughout the solar atmosphere from the photosphere to the corona. The results of this study show that the magnetic field strength (flux density) in active regions plays an important role in the variability of coronal abundances, and it is likely the main contributing factor to this nonlinearity during increased solar activity. Coronal abundances above cool sunspots are lower than in dispersed magnetic plage regions. Strong magnetic concentrations are associated with stronger F10.7 cm gyroresonance emission. Considering that as the solar cycle moves from minimum to maximum, the sizes of sunspots and their field strength increase with the gyroresonance component, the distinctly different tendencies of radio emission and coronal abundances in the vicinity of sunspots is the likely cause of saturation of Sun-as-a-star coronal abundances during solar maximum, while the F10.7 index remains well correlated with the sunspot number and other magnetic field proxies

    Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: Evidence for pleiotropy

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    In the U.S.A., cocaine is the second most abused illicit drug. Variants within the CHRNB3-A6 gene cluster have been associated with cigarette consumption in several GWAS. These receptors represent intriguing candidates for the study of cocaine dependence because nicotinic receptors are thought to be involved in generalized addiction pathways. Using genotypic data from a GWAS of the Study of Addiction: Genetics and Environment (SAGE) dataset, we tested for association of CHRNB3-A6 SNPs with DSM-5 cocaine use disorder. Multiple SNPs in the region were significantly associated with increased risk of cocaine use disorder. Inclusion of the most significant SNP as a covariate in a linear regression model provided evidence for an additional independent signal within this locus for cocaine use disorder. These results suggest that the CHRNB3-A6 locus contains multiple variants affecting risk for vulnerability to cocaine and nicotine dependence as well as bipolar disorder, suggesting that they have pleiotropic effects
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