186 research outputs found

    Finite sum of gluon ladders and high energy cross sections

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    A model for the Pomeron at t=0t=0 is suggested. It is based on the idea of a finite sum of ladder diagrams in QCD. Accordingly, the number of ss-channel gluon rungs and correspondingly the powers of logarithms in the forward scattering amplitude depends on the phase space (energy) available, i.e. as energy increases, progressively new prongs with additional gluon rungs in the ss-channel open. Explicit expressions for the total cross section involving two and three rungs or, alternatively, three and four prongs (with ln⁥2(s)\ln^2(s) and ln⁥3(s)\ln^3(s) as highest terms, respectively) are fitted to the proton-proton and proton-antiproton total cross section data in the accelerator region. Both QCD calculation and fits to the data indicate fast convergence of the series. In the fit, two terms (a constant and a logarithmically rising one) almost saturate the whole series, the ln⁥2(s)\ln^2(s) term being small and the next one, ln⁥3(s)\ln^3(s), negligible. Theoretical predictions for the photon-photon total cross section are also given.Comment: 18 pages, LaTeX, 2 EPS figures, uses axodraw.st

    Autologous stem cell transplantation in multiple sclerosis: Results from a single centre

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    Background: In the last 2 decades, intensive immunosuppression followed by autologous stem cell transplantation (ASCT) has been proposed as a possible strategy for treatment of severe immune-mediated disorders, including multiple sclerosis (MS). Objective: To review the outcome of ASCT for MS in Western Australia. Methods: Eligibility criteria for ASCT were (1) progression of sustained disability with expanded disability status scale (EDSS) score increase of more than 1/10 over a 12 month period, (2) advanced MS with threatened loss of ambulation and (3) rapidly progressive disease not adequately assessed by EDSS. Stem cell mobilization was with cyclophosphamide (CY) 2g/m 2 and granu - locyte-colony stimulating factor 5ug/kg bd. conditioning chemo - therapy was with CY 50mg/kg and rabbit antithymocyte globulin 1mg/kg days -5 to -2. Patients were assessed at 3, 6, 12 and 24 months post-transplant. Results: Fourteen patients underwent ASCT. Median age was 47 years; median time from diagnosis to transplant was 12 years. Diagnosis at transplant was secondary progressive MS (12), pri - mary progressive MS (1) and neuromyelitis optica (1). About half the cohorts were neurologically stable at 24 months while the remainder had clinically relevant neurological deterioration. Two patients had meaningful improvement in bladder function. Follow-up MRI showed no Gd-enhancing lesions, but two patients developed new cerebral lesions on T2 weighted imaging. Conclusion: In this group of patients with advanced MS, neuro - logical function 24 months post-ASCT was essentially stable in half the cohort while the remainder experienced clinical progres - sion. It is not possible to conclude whether ASCT altered the natu - ral history of the disease

    Adiabatic following criterion, estimation of the nonadiabatic excitation fraction and quantum jumps

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    An accurate theory describing adiabatic following of the dark, nonabsorbing state in the three-level system is developed. An analytical solution for the wave function of the particle experiencing Raman excitation is found as an expansion in terms of the time varying nonadiabatic perturbation parameter. The solution can be presented as a sum of adiabatic and nonadiabatic parts. Both are estimated quantitatively. It is shown that the limiting value to which the amplitude of the nonadiabatic part tends is equal to the Fourier component of the nonadiabatic perturbation parameter taken at the Rabi frequency of the Raman excitation. The time scale of the variation of both parts is found. While the adiabatic part of the solution varies slowly and follows the change of the nonadiabatic perturbation parameter, the nonadiabatic part appears almost instantly, revealing a jumpwise transition between the dark and bright states. This jump happens when the nonadiabatic perturbation parameter takes its maximum value.Comment: 33 pages, 8 figures, submitted to PRA on 28 Oct. 200

    Domain Wall Junction in N=2 Supersymmetric QED in four dimensions

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    An exact solution of domain wall junction is obtained in N=2 supersymmetric (SUSY) QED with three massive hypermultiplets. The junction preserves two out of eight SUSY. Both a (magnetic) Fayet-Iliopoulos (FI) term and complex masses for hypermultiplets are needed to obtain the junction solution. There are zero modes corresponding to spontaneously broken translation, SUSY, and U(1). All broken and unbroken SUSY charges are explicitly worked out in the Wess-Zumino gauge in N=1 superfields as well as in components. The relation to models in five dimensions is also clarified.Comment: 27 pages, 6 figures, comments on zero modes added, a few references adde

    Energy Conditions in f(G)f(G) Modified Gravity with Non-minimal Coupling to Matter

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    In this paper we study a model of modified gravity with non-minimal coupling between a general function of the Gauss-Bonnet invariant, f(G)f(G), and matter Lagrangian from the point of view of the energy conditions. Such model has been introduced in Ref. [21] for description of early inflation and late-time cosmic acceleration. We present the suitable energy conditions for the above mentioned model and then, we use the estimated values of the Hubble, deceleration and jerk parameters to apply the obtained energy conditions to the specific class of modified Gauss-Bonnet models.Comment: 12 pages, no figur, Accepted for publication in Astrophysics and Space Scienc

    Trends in autoionization of Rydberg states converging to the 4s threshold in the Kr-Rbâș-SrÂČâș isoelectonic sequence: theory and experiment

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    We have measured the photoabsorption spectra of the Kr-like ions Rb+ and Sr2+ at photon energies corresponding to the excitation of 4s-np resonances using, the dual laser plasma photoabsorption technique. Dramatic changes in the line profiles, with increasing ionization and also proceeding along the Rydberg series of each ion, are observed and explained by the trends in 4s-transition amplitudes computed within a framework of configuration-interaction Pauli-Fock calculations. Total photoionization cross sections show very good agreement with relative absorption data extracted from the measured spectra

    Phantom Divide Crossing with General Non-minimal Kinetic Coupling

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    We propose a model of dark energy consists of a single scalar field with a general non-minimal kinetic couplings to itself and to the curvature. We study the cosmological dynamics of the equation of state in this setup. The coupling terms have the form Ο1Rf(ϕ)∂Όϕ∂Όϕ\xi_{1} R f(\phi)\partial_{\mu}\phi\partial^{\mu}\phi and Ο2RΌΜf(ϕ)∂Όϕ∂Μϕ\xi_{2} R_{\mu\nu}f(\phi)\partial^{\mu}\phi\partial^{\nu}\phi where Ο1\xi_{1} and Ο2\xi_{2} are coupling parameters and their dimensions depend on the type of function f(ϕ)f(\phi). We obtain the conditions required for phantom divide crossing and show numerically that a cosmological model with general non-minimal derivative coupling to the scalar and Ricci curvatures can realize such a crossing.Comment: 12 pages, 4 figures. Accepted for publication in Gen. Rel. Grav. arXiv admin note: substantial text overlap with arXiv:1105.4967, arXiv:1201.1627, and with arXiv:astro-ph/0610092 by other author

    An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

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    For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types
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