2,562 research outputs found

    Ariel - Volume 4 Number 1

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    Editors David A. Jacoby Eugenia Miller Tom Williams Associate Editors Paul Bialas Terry Burt Michael Leo Gail Tenikat Editor Emeritus and Business Manager Richard J. Bonnano Movie Editor Robert Breckenridg

    Global foot and mouth disease research update and gap analysis 2014

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    Scalar hairy black holes and solitons in asymptotically flat spacetimes

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    A numerical analysis shows that a class of scalar-tensor theories of gravity with a scalar field minimally and nonminimally coupled to the curvature allows static and spherically symmetric black hole solutions with scalar-field hair in asymptotically flat spacetimes. In the limit when the horizon radius of the black hole tends to zero, regular scalar solitons are found. The asymptotically flat solutions are obtained provided that the scalar potential V(ϕ)V(\phi) of the theory is not positive semidefinite and such that its local minimum is also a zero of the potential, the scalar field settling asymptotically at that minimum. The configurations for the minimal coupling case, although unstable under spherically symmetric linear perturbations, are regular and thus can serve as counterexamples to the no-scalar-hair conjecture. For the nonminimal coupling case, the stability will be analyzed in a forthcoming paper.Comment: 7 pages, 10 postscript figures, file tex, new postscript figs. and references added, stability analysis revisite

    An alternative approach to the construction of Schur-Weyl transform

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    We propose an alternative approach for the construction of the unitary matrix which performs generalized unitary rotations of the system consisting of independent identical subsystems (for example spin system). This matrix, when applied to the system, results in a change of degrees of freedom, uncovering the information hidden in non-local degrees of freedom. This information can be used, inter alia, to study the structure of entangled states, their classification and may be useful for construction of quantum algorithms.Comment: 6 page

    Liver fat in adults with GH deficiency: comparison to matched controls and the effect of GH replacement

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    CONTEXT: Existing data regarding the association between growth hormone deficiency (GHD) and liver fat content are conflicting. OBJECTIVE: We aimed i) to assess intrahepatocellular lipid (IHCL) content in hypopituitary adults with GHD compared to matched controls and ii) to evaluate the effect of growth hormone (GH) replacement on IHCL content. DESIGN: Cross-sectional comparison and controlled intervention study. PATIENTS, PARTICIPANTS: Cross-sectional comparison: 22 hypopituitary adults with GHD and 44 healthy controls matched for age, BMI, gender and ethnicity. Intervention study: 9 GHD patients starting GH replacement (GH Rx group), 9 GHD patients not starting replacement therapy (non-GH Rx group). INTERVENTION: Intervention study:GH replacement for 6 months in the GH Rx group, dosage was titrated to achieve normal IGF-1 levels. MAIN OUTCOME MEASURES: IHCL content determined by proton magnetic resonance spectroscopy (1 H MRS). RESULTS: Cross-sectional comparison: There was no difference in IHCL content between GHD patients and healthy controls (1.89% (0.30, 4.03) vs. 1.14% (0.22, 2.32); p=0.2), the prevalence of patients with hepatic steatosis (IHCL of ≥ 5.56%) was similar in the two groups (22.7% vs. 15.9%; chi square probability = 0.4). Intervention study: The change in IHCL content over 6 months did not differ between the GH Rx group and the non-GH Rx group (-0.63 ± 4.53% vs. +0.11 ± 1.46%; p=0.6). CONCLUSIONS: In our study liver fat content and the prevalence of hepatic steatosis did not differ between hypopituitary adults with GHD and matched controls. In GHD patients GH replacement had no effect on liver fat content

    Real-time PCR based on SYBR-Green I fluorescence: An alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions

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    BACKGROUND: Real-time PCR is increasingly being adopted for RNA quantification and genetic analysis. At present the most popular real-time PCR assay is based on the hybridisation of a dual-labelled probe to the PCR product, and the development of a signal by loss of fluorescence quenching as PCR degrades the probe. Though this so-called 'TaqMan' approach has proved easy to optimise in practice, the dual-labelled probes are relatively expensive. RESULTS: We have designed a new assay based on SYBR-Green I binding that is quick, reliable, easily optimised and compares well with the published assay. Here we demonstrate its general applicability by measuring copy number in three different genetic contexts; the quantification of a gene rearrangement (T-cell receptor excision circles (TREC) in peripheral blood mononuclear cells); the detection and quantification of GLI, MYC-C and MYC-N gene amplification in cell lines and cancer biopsies; and detection of deletions in the OPA1 gene in dominant optic atrophy. CONCLUSION: Our assay has important clinical applications, providing accurate diagnostic results in less time, from less biopsy material and at less cost than assays currently employed such as FISH or Southern blotting

    Cold Plasma Dispersion Relations in the Vicinity of a Schwarzschild Black Hole Horizon

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    We apply the ADM 3+1 formalism to derive the general relativistic magnetohydrodynamic equations for cold plasma in spatially flat Schwarzschild metric. Respective perturbed equations are linearized for non-magnetized and magnetized plasmas both in non-rotating and rotating backgrounds. These are then Fourier analyzed and the corresponding dispersion relations are obtained. These relations are discussed for the existence of waves with positive angular frequency in the region near the horizon. Our results support the fact that no information can be extracted from the Schwarzschild black hole. It is concluded that negative phase velocity propagates in the rotating background whether the black hole is rotating or non-rotating.Comment: 27 pages, 11 figures accepted for publication in Gen. Relat. & Gravi

    The Robinson-Trautman Type III Prolongation Structure Contains K2_2

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    The minimal prolongation structure for the Robinson-Trautman equations of Petrov type III is shown to always include the infinite-dimensional, contragredient algebra, K2_2, which is of infinite growth. Knowledge of faithful representations of this algebra would allow the determination of B\"acklund transformations to evolve new solutions.Comment: 20 pages, plain TeX, no figures, submitted to Commun. Math. Phy

    Degeneracies when T=0 Two Body Matrix Elements are Set Equal to Zero and Regge's 6j Symmetry Relations

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    The effects of setting all T=0 two body interaction matrix elements equal to a constant (or zero) in shell model calculations (designated as =0=0) are investigated. Despite the apparent severity of such a procedure, one gets fairly reasonable spectra. We find that using =0=0 in single j shell calculations degeneracies appear e.g. the I=1/2I={1/2} ^{-} and 13/2{13/2}^{-} states in 43^{43}Sc are at the same excitation energies; likewise the I=32+3_{2}^{+},72+7_{2}^{+},91+^{+}_{1} and 101+^{+}_{1} states in 44^{44}Ti. The above degeneracies involve the vanishing of certain 6j and 9j symbols. The symmetry relations of Regge are used to explain why these vanishings are not accidental. Thus for these states the actual deviation from degeneracy are good indicators of the effects of the T=0 matrix elements. A further indicator of the effects of the T=0 interaction in an even - even nucleus is to compare the energies of states with odd angular momentum with those that are even

    Association of FCGR3A and FCGR3B haplotypes with rheumatoid arthritis and primary Sjögren's syndrome [POSTER PRESENTATION]

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    Background Rheumatoid arthritis (RA) is an autoimmune disease that is thought to arise from a complex interaction between multiple genetic factors and environmental triggers. We have previously demonstrated an association between a Fc gamma receptor (FcγR) haplotype and RA in a cross-sectional cohort of RA patients. We have sought to confirm this association in an inception cohort of RA patients and matched controls. We also extended our study to investigate a second autoanti-body associated rheumatic disease, primary Sjögren's syndrome (PSS). Methods The FCGR3A-158F/V and FCGR3B-NA1/NA2 functional polymorphisms were examined for association in an inception cohort of RA patients (n = 448), and a well-characterised PSS cohort (n = 83) from the United Kingdom. Pairwise disequilibrium coefficients (D') were calculated in 267 Blood Service healthy controls. The EHPlus program was used to estimate haplotype frequencies for patients and controls and to determine whether significant linkage disequilibrium was present. A likelihood ratio test is performed to test for differences between the haplotype frequencies in cases and controls. A permutation procedure implemented in this program enabled 1000 permutations to be performed on all haplotype associations to assess significance. Results There was significant linkage disequilibrium between FCGR3A and FCGR3B (D' = -0.445, P = 0.001). There was no significant difference in the FCGR3A or FCGR3B allele or genotype frequencies in the RA or PSS patients compared with controls. However, there was a significant difference in the FCGR3A-FCGR3B haplotype distributions with increased homozygosity for the FCGR3A-FCGR3B 158V-NA2 haplotype in both our inception RA cohort (odds ratio = 2.15, 95% confidence interval = 1.1–4.2 P = 0.027) and PSS (odds ratio = 2.83, 95% confidence interval = 1.0–8.2, P = 0.047) compared with controls. The reference group for these analyses comprised individuals who did not possess a copy of the FCGR3A-FCGR3B 158V-NA2 haplotype. Conclusions We have confirmed our original findings of association between the FCGR3A-FCGR3B 158V-NA2 haplotype and RA in a new inception cohort of RA patients. This suggests that there may be an RA-susceptibility gene at this locus. The significant increased frequency of an identical haplotype in PSS suggests the FcγR genetic locus may contribute to the pathogenesis of diverse autoantibody-mediated rheumatic diseases
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