4,017 research outputs found

    EXPLAINING INTERNATIONAL DIFFERENCES IN GENETICALLY MODIFIED FOOD LABELING REGULATIONS

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    Replaced with revised version of paper 07/13/04.Food Consumption/Nutrition/Food Safety,

    Large N Scaling Behavior of the Lipkin-Meshkov-Glick Model

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    We introduce a novel semiclassical approach to the Lipkin model. In this way the well-known phase transition arising at the critical value of the coupling is intuitively understood. New results -- showing for strong couplings the existence of a threshold energy which separates deformed from undeformed states as well as the divergence of the density of states at the threshold energy -- are explained straightforwardly and in quantitative terms by the appearance of a double well structure in a classical system corresponding to the Lipkin model. Previously unnoticed features of the eigenstates near the threshold energy are also predicted and found to hold.Comment: 4 pages, 2 figures, to appear in PR

    Functional and computational identification of a rescue mutation near the active site of an mRNA methyltransferase

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    RNA-based drugs are an emerging class of therapeutics combining the immense potential of DNA gene-therapy with the absence of genome integration-associated risks. While the synthesis of such molecules is feasible, large scale in vitro production of humanised mRNA remains a biochemical and economical challenge. Human mRNAs possess two post-transcriptional modifcations at their 5′ end: an inverted methylated guanosine and a unique 2′O-methylation on the ribose of the penultimate nucleotide. One strategy to precisely methylate the 2′ oxygen is to use viral mRNA methyltransferases that have evolved to escape the host’s cell immunity response following virus infection. However, these enzymes are ill-adapted to industrial processes and sufer from low turnovers. We have investigated the efects of homologous and orthologous active-site mutations on both stability and transferase activity, and identifed new functional motifs in the interaction network surrounding the catalytic lysine. Our fndings suggest that despite their low catalytic efciency, the active-sites of viral mRNA methyltransferases have low mutational plasticity, while mutations in a defned third shell around the active site have strong efects on folding, stability and activity in the variant enzymes, mostly via network-mediated efects

    Quantum breaking time near classical equilibrium points

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    By using numerical and semiclassical methods, we evaluate the quantum breaking, or Ehrenfest time for a wave packet localized around classical equilibrium points of autonomous one-dimensional systems with polynomial potentials. We find that the Ehrenfest time diverges logarithmically with the inverse of the Planck constant whenever the equilibrium point is exponentially unstable. For stable equilibrium points, we have a power law divergence with exponent determined by the degree of the potential near the equilibrium point.Comment: 4 pages, 5 figure

    Eigenfunction statistics for a point scatterer on a three-dimensional torus

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    In this paper we study eigenfunction statistics for a point scatterer (the Laplacian perturbed by a delta-potential) on a three-dimensional flat torus. The eigenfunctions of this operator are the eigenfunctions of the Laplacian which vanish at the scatterer, together with a set of new eigenfunctions (perturbed eigenfunctions). We first show that for a point scatterer on the standard torus all of the perturbed eigenfunctions are uniformly distributed in configuration space. Then we investigate the same problem for a point scatterer on a flat torus with some irrationality conditions, and show uniform distribution in configuration space for almost all of the perturbed eigenfunctions.Comment: Revised according to referee's comments. Accepted for publication in Annales Henri Poincar

    AMP-activated protein kinase (AMPK) as a potential therapeutic target independent of PI3K/Akt signaling in prostate cancer

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    Depletion of cellular energy activates the AMP-activated protein kinase (AMPK) to favor energy-producing catabolic processes during tumorigenesis. Using a panel of in vitro cell lines and resected tumors, we investigated the therapeutic value of manipulating AMPK in prostate cancer (PC). Phospho-AMPK expression was significantly elevated in human PC cells and clinical PC samples. In clinical PC, we observed a trend for increasing phospho-AMPK with increasing Gleason sum score; Phospho-AMPK expression was associated with phospho-ACC (p=0.0023). Using the paired PC3 and PC3M cells to model progressive androgen-independent PC, treatment with either 5-aminoimidazole-4-carboxamide riboside (AICAR) or A-769662 suppressed proliferation, migration and invasion in both cell lines, and down-regulated mTOR and P70S6Ki levels regardless of the Akt status. Involvement of AMPK was confirmed by Compound C (AMPK inhibitor) and siRNA-mediated AMPK silencing. Despite similar functional responses in PC3 and PC3M cells, AMPK activation resulted in sustained phospho-Akt activation in PC3M cells, but not in PC3 cells. This prompted the addition of the PI3K inhibitor LY-294002 to AICAR treatment of PC3M cells in a proliferation assay. Interestingly, we found no synergistic effects upon combined treatment. Collectively, these findings support AMPK as a potential therapeutic target independent of PI3K/Akt signalling

    Topological properties of quantum periodic Hamiltonians

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    We consider periodic quantum Hamiltonians on the torus phase space (Harper-like Hamiltonians). We calculate the topological Chern index which characterizes each spectral band in the generic case. This calculation is made by a semi-classical approach with use of quasi-modes. As a result, the Chern index is equal to the homotopy of the path of these quasi-modes on phase space as the Floquet parameter (\theta) of the band is varied. It is quite interesting that the Chern indices, defined as topological quantum numbers, can be expressed from simple properties of the classical trajectories.Comment: 27 pages, 14 figure

    CDM, Feedback and the Hubble Sequence

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    We have performed TreeSPH simulations of galaxy formation in a standard LCDM cosmology, including effects of star formation, energetic stellar feedback processes and a meta-galactic UV field, and obtain a mix of disk, lenticular and elliptical galaxies. The disk galaxies are deficient in angular momentum by only about a factor of two compared to observed disk galaxies. The stellar disks have approximately exponential surface density profiles, and those of the bulges range from exponential to r^{1/4}, as observed. The bulge-to-disk ratios of the disk galaxies are consistent with observations and likewise are their integrated B-V colours, which have been calculated using stellar population synthesis techniques. Furthermore, we can match the observed I-band Tully-Fisher (TF) relation, provided that the mass-to-light ratio of disk galaxies, (M/L_I), is about 0.8. The ellipticals and lenticulars have approximately r^{1/4} stellar surface density profiles, are dominated by non-disklike kinematics and flattened due to non-isotropic stellar velocity distributions, again consistent with observations.Comment: 6 pages, incl. 4 figs. To appear in the proceedings of the EuroConference "The Evolution of Galaxies: II - Basic Building Blocks", Ile de La Reunion (France), 16-21 October 2001 (Slightly updated version). A much more comprehensive paper about this work with links to pictures of some of the galaxies can be found at http://babbage.sissa.it/abs/astro-ph/020436

    Eigenvalues of Laplacian with constant magnetic field on non-compact hyperbolic surfaces with finite area

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    We consider a magnetic Laplacian ΔA=(id+A)(id+A)-\Delta_A=(id+A)^\star (id+A) on a noncompact hyperbolic surface \mM with finite area. AA is a real one-form and the magnetic field dAdA is constant in each cusp. When the harmonic component of AA satifies some quantified condition, the spectrum of ΔA-\Delta_A is discrete. In this case we prove that the counting function of the eigenvalues of ΔA-\Delta_{A} satisfies the classical Weyl formula, even when $dA=0.
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