68 research outputs found

    Definition of valid proteomic biomarkers: a bayesian solution

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    Clinical proteomics is suffering from high hopes generated by reports on apparent biomarkers, most of which could not be later substantiated via validation. This has brought into focus the need for improved methods of finding a panel of clearly defined biomarkers. To examine this problem, urinary proteome data was collected from healthy adult males and females, and analysed to find biomarkers that differentiated between genders. We believe that models that incorporate sparsity in terms of variables are desirable for biomarker selection, as proteomics data typically contains a huge number of variables (peptides) and few samples making the selection process potentially unstable. This suggests the application of a two-level hierarchical Bayesian probit regression model for variable selection which assumes a prior that favours sparseness. The classification performance of this method is shown to improve that of the Probabilistic K-Nearest Neighbour model

    Isospin-Violating Meson-Nucleon Vertices as an Alternate Mechanism of Charge-Symmetry Breaking

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    We compute isospin-violating meson-nucleon coupling constants and their consequent charge-symmetry-breaking nucleon-nucleon potentials. The couplings result from evaluating matrix elements of quark currents between nucleon states in a nonrelativistic constituent quark model; the isospin violations arise from the difference in the up and down constituent quark masses. We find, in particular, that isospin violation in the omega-meson--nucleon vertex dominates the class IV CSB potential obtained from these considerations. We evaluate the resulting spin-singlet--triplet mixing angles, the quantities germane to the difference of neutron and proton analyzing powers measured in elastic np\vec{n}-\vec{p} scattering, and find them commensurate to those computed originally using the on-shell value of the ρ\rho-ω\omega mixing amplitude. The use of the on-shell ρ\rho-ω\omega mixing amplitude at q2=0q^2=0 has been called into question; rather, the amplitude is zero in a wide class of models. Our model possesses no contribution from ρ\rho-ω\omega mixing at q2=0q^2=0, and we find that omega-meson exchange suffices to explain the measured npn-p analyzing power difference~at~183 MeV.Comment: 20 pages, revtex, 3 uuencoded PostScript figure

    On the pion-nucleon coupling constant

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    In view of persisting misunderstanding about the determination of the pion-nucleon coupling constants in the Nijmegen multienergy partial-wave analyses of pp, np, and pbar-p scattering data, we present additional information which may clarify several points of discussion. We comment on several recent papers addressing the issue of the pion-nucleon coupling constant and criticizing the Nijmegen analyses.Comment: 19 pages, Nijmegen preprint THEF-NYM-92-0

    The alpha-particle based on modern nuclear forces

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    The Faddeev-Yakubovsky equations for the alpha-particle are solved. Accurate results are obtained for several modern NN interaction models, which include charge-symmetry breaking effects in the NN force, nucleon mass dependences as well as the Coulomb interaction. These models are augmented by three-nucleon forces of different types and adjusted to the 3N binding energy. Our results are close to the experimental binding energy with a slight overbinding. Thus there is only little room left for the contribution of possible 4N interactions to the alpha-particle binding energy. We also discuss model dependences of the binding energies and the wave functions.Comment: 22 pages REVTeX 4, 12 figures, table with TM parameters added, typos corrected, version as published in PR

    Tri-meson-mixing of π\pi-η\eta-η\eta' and ρ\rho-ω\omega-ϕ\phi in the light-cone quark model

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    The radiative transition form factors of the pseudoscalar mesons {π\pi, η\eta, η\eta'} and the vector mesons {ρ\rho, ω\omega, ϕ\phi} are restudied with π\pi-η\eta-η\eta' and ρ\rho-ω\omega-ϕ\phi in tri-meson-mixing pattern, which is described by tri-mixing matrices in the light-cone constituent quark model. The experimental transition decay widths are better reproduced with tri-meson-mixing than previous results in a two-mixing-angle scenario of only two-meson η\eta-η\eta' mixing and ω\omega-ϕ\phi mixing.Comment: 8 pages, 6 figures, final version to appear in EPJ

    Weak capture of protons by protons

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    The cross section for the proton weak capture reaction 1H(p,e+νe)2H^1H(p,e^+\nu_e)^2H is calculated with wave functions obtained from a number of modern, realistic high-precision interactions. To minimize the uncertainty in the axial two-body current operator, its matrix element has been adjusted to reproduce the measured Gamow-Teller matrix element of tritium β\beta decay in model calculations using trinucleon wave functions from these interactions. A thorough analysis of the ambiguities that this procedure introduces in evaluating the two-body current contribution to the pp capture is given. Its inherent model dependence is in fact found to be very weak. The overlap integral Λ2(E=0)\Lambda^2(E=0) for the pp capture is predicted to be in the range 7.05--7.06, including the axial two-body current contribution, for all interactions considered.Comment: 17 pages RevTeX (twocolumn), 5 postscript figure

    Search for Neutrinoless Double-Beta Decay with the Upgraded EXO-200 Detector

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    Results from a search for neutrinoless double-beta decay (0νββ) of Xe136 are presented using the first year of data taken with the upgraded EXO-200 detector. Relative to previous searches by EXO-200, the energy resolution of the

    Structure and functionality of a multimeric human COQ7:COQ9 complex.

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    Coenzyme Q (CoQ) is a redox-active lipid essential for core metabolic pathways and antioxidant defense. CoQ is synthesized upon the mitochondrial inner membrane by an ill-defined "complex Q" metabolon. Here, we present structure-function analyses of a lipid-, substrate-, and NADH-bound complex comprising two complex Q subunits: the hydroxylase COQ7 and the lipid-binding protein COQ9. We reveal that COQ7 adopts a ferritin-like fold with a hydrophobic channel whose substrate-binding capacity is enhanced by COQ9. Using molecular dynamics, we further show that two COQ7:COQ9 heterodimers form a curved tetramer that deforms the membrane, potentially opening a pathway for the CoQ intermediates to translocate from the bilayer to the proteins' lipid-binding sites. Two such tetramers assemble into a soluble octamer with a pseudo-bilayer of lipids captured within. Together, these observations indicate that COQ7 and COQ9 cooperate to access hydrophobic precursors within the membrane and coordinate subsequent synthesis steps toward producing CoQ
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