639 research outputs found

    Critical Exponents near a Random Fractal Boundary

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    The critical behaviour of correlation functions near a boundary is modified from that in the bulk. When the boundary is smooth this is known to be characterised by the surface scaling dimension \xt. We consider the case when the boundary is a random fractal, specifically a self-avoiding walk or the frontier of a Brownian walk, in two dimensions, and show that the boundary scaling behaviour of the correlation function is characterised by a set of multifractal boundary exponents, given exactly by conformal invariance arguments to be \lambda_n = 1/48 (\sqrt{1+24n\xt}+11)(\sqrt{1+24n\xt}-1). This result may be interpreted in terms of a scale-dependent distribution of opening angles α\alpha of the fractal boundary: on short distance scales these are sharply peaked around α=π/3\alpha=\pi/3. Similar arguments give the multifractal exponents for the case of coupling to a quenched random bulk geometry.Comment: 13 pages. Comments on relation to results in quenched random bulk added, and on relation to other recent work. Typos correcte

    Femto-Photography of Protons to Nuclei with Deeply Virtual Compton Scattering

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    Developments in deeply virtual Compton scattering allow the direct measurements of scattering amplitudes for exchange of a highly virtual photon with fine spatial resolution. Real-space images of the target can be obtained from this information. Spatial resolution is determined by the momentum transfer rather than the wavelength of the detected photon. Quantum photographs of the proton, nuclei, and other elementary particles with resolution on the scale of a fraction of a femtometer is feasible with existing experimental technology.Comment: To be published in Physical Review D. Replaces previous version with minor changes in presentatio

    Renormalization Group Study of the A+B->0 Diffusion-Limited Reaction

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    The A+B0A + B\to 0 diffusion-limited reaction, with equal initial densities a(0)=b(0)=n0a(0) = b(0) = n_0, is studied by means of a field-theoretic renormalization group formulation of the problem. For dimension d>2d > 2 an effective theory is derived, from which the density and correlation functions can be calculated. We find the density decays in time as a,b \sim C\sqrt{\D}(Dt)^{-d/4} for d<4d < 4, with \D = n_0-C^\prime n_0^{d/2} + \dots, where CC is a universal constant, and CC^\prime is non-universal. The calculation is extended to the case of unequal diffusion constants DADBD_A \neq D_B, resulting in a new amplitude but the same exponent. For d2d \le 2 a controlled calculation is not possible, but a heuristic argument is presented that the results above give at least the leading term in an ϵ=2d\epsilon = 2-d expansion. Finally, we address reaction zones formed in the steady-state by opposing currents of AA and BB particles, and derive scaling properties.Comment: 17 pages, REVTeX, 13 compressed figures, included with epsf. Eq. (6.12) corrected, and a moderate rewriting of the introduction. Accepted for publication in J. Stat. Phy

    Application of Pauli-Villars regularization and discretized light-cone quantization to a single-fermion truncation of Yukawa theory

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    We apply Pauli-Villars regularization and discretized light-cone quantization to the nonperturbative solution of (3+1)-dimensional Yukawa theory in a single-fermion truncation. Three heavy scalars, including two with negative norm, are used to regulate the theory. The matrix eigenvalue problem is solved for the lowest-mass state with use of a new, indefinite-metric Lanczos algorithm. Various observables are extracted from the wave functions, including average multiplicities and average momenta of constituents, structure functions, and a form factor slope.Comment: 21 pages, 7 figures, RevTeX; published version: more extensive data in the tables of v

    Entanglement and correlation functions following a local quench: a conformal field theory approach

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    We show that the dynamics resulting from preparing a one-dimensional quantum system in the ground state of two decoupled parts, then joined together and left to evolve unitarily with a translational invariant Hamiltonian (a local quench), can be described by means of quantum field theory. In the case when the corresponding theory is conformal, we study the evolution of the entanglement entropy for different bi-partitions of the line. We also consider the behavior of one- and two-point correlation functions. All our findings may be explained in terms of a picture, that we believe to be valid more generally, whereby quasiparticles emitted from the joining point at the initial time propagate semiclassically through the system.Comment: 19 pages, 4 figures, v2 typos corrected and refs adde

    Search algorithms as a framework for the optimization of drug combinations

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    Combination therapies are often needed for effective clinical outcomes in the management of complex diseases, but presently they are generally based on empirical clinical experience. Here we suggest a novel application of search algorithms, originally developed for digital communication, modified to optimize combinations of therapeutic interventions. In biological experiments measuring the restoration of the decline with age in heart function and exercise capacity in Drosophila melanogaster, we found that search algorithms correctly identified optimal combinations of four drugs with only one third of the tests performed in a fully factorial search. In experiments identifying combinations of three doses of up to six drugs for selective killing of human cancer cells, search algorithms resulted in a highly significant enrichment of selective combinations compared with random searches. In simulations using a network model of cell death, we found that the search algorithms identified the optimal combinations of 6-9 interventions in 80-90% of tests, compared with 15-30% for an equivalent random search. These findings suggest that modified search algorithms from information theory have the potential to enhance the discovery of novel therapeutic drug combinations. This report also helps to frame a biomedical problem that will benefit from an interdisciplinary effort and suggests a general strategy for its solution.Comment: 36 pages, 10 figures, revised versio

    Consequence of the tumor-associated conversion to cyclin D1b.

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    Clinical evidence suggests that cyclin D1b, a variant of cyclin D1, is associated with tumor progression and poor outcome. However, the underlying molecular basis was unknown. Here, novel models were created to generate a genetic switch from cyclin D1 to cyclin D1b. Extensive analyses uncovered overlapping but non-redundant functions of cyclin D1b compared to cyclin D1 on developmental phenotypes, and illustrated the importance of the transcriptional regulatory functions of cyclin D1b in vivo. Data obtained identify cyclin D1b as an oncogene, wherein cyclin D1b expression under the endogenous promoter induced cellular transformation and further cooperated with known oncogenes to promote tumor growth in vivo. Further molecular interrogation uncovered unexpected links between cyclin D1b and the DNA damage/PARP1 regulatory networks, which could be exploited to suppress cyclin D1b-driven tumors. Collectively, these data are the first to define the consequence of cyclin D1b expression on normal cellular function, present evidence for cyclin D1b as an oncogene, and provide pre-clinical evidence of effective methods to thwart growth of cells dependent upon this oncogenic variant

    Kinome rewiring reveals AURKA limits PI3K-pathway inhibitor efficacy in breast cancer.

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    Dysregulation of the PI3K-AKT-mTOR signaling network is a prominent feature of breast cancers. However, clinical responses to drugs targeting this pathway have been modest, possibly because of dynamic changes in cellular signaling that drive resistance and limit drug efficacy. Using a quantitative chemoproteomics approach, we mapped kinome dynamics in response to inhibitors of this pathway and identified signaling changes that correlate with drug sensitivity. Maintenance of AURKA after drug treatment was associated with resistance in breast cancer models. Incomplete inhibition of AURKA was a common source of therapy failure, and combinations of PI3K, AKT or mTOR inhibitors with the AURKA inhibitor MLN8237 were highly synergistic and durably suppressed mTOR signaling, resulting in apoptosis and tumor regression in vivo. This signaling map identifies survival factors whose presence limits the efficacy of targeted therapies and reveals new drug combinations that may unlock the full potential of PI3K-AKT-mTOR pathway inhibitors in breast cancer

    The Star-Forming Galaxy Contribution to the Cosmic MeV and GeV Gamma-Ray Background

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    While star-forming galaxies could be major contributors to the cosmic GeV γ\gamma-ray background, they are expected to be MeV-dim because of the "pion bump" falling off below ~100 MeV. However, there are very few observations of galaxies in the MeV range, and other emission processes could be present. We investigate the MeV background from star-forming galaxies by running one-zone models of cosmic ray populations, including Inverse Compton and bremsstrahlung, as well as nuclear lines (including 26^{26}Al), emission from core-collapse supernovae, and positron annihilation emission, in addition to the pionic emission. We use the Milky Way and M82 as templates of normal and starburst galaxies, and compare our models to radio and GeV--TeV γ\gamma-ray data. We find that (1) higher gas densities in high-z normal galaxies lead to a strong pion bump, (2) starbursts may have significant MeV emission if their magnetic field strengths are low, and (3) cascades can contribute to the MeV emission of starbursts if they emit mainly hadronic γ\gamma-rays. Our fiducial model predicts that most of the unresolved GeV background is from star-forming galaxies, but this prediction is uncertain by an order of magnitude. About ~2% of the claimed 1 MeV background is diffuse emission from star-forming galaxies; we place a firm upper limit of <~10% based on the spectral shape of the background. The star-formation contribution is constrained to be small, because its spectrum is peaked, while the observed background is steeply falling with energy through the MeV-GeV range.Comment: Published in ApJ, 27 pages, emulateapj format. Readers may be interested in the concurrent paper by Chakraborty and Fields (arXiv:1206.0770), a calculation of the Inverse Compton background from star-forming galaxie
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