587 research outputs found

    On the Construction of Trigonometric Solutions of the Yang-Baxter Equation

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    We describe the construction of trigonometric R-matrices corresponding to the (multiplicity-free) tensor product of any two irreducible representations of a quantum algebra U_q(\G). Our method is a generalization of the tensor product graph method to the case of two different representations. It yields the decomposition of the R-matrix into projection operators. Many new examples of trigonometric R-matrices (solutions to the spectral parameter dependent Yang-Baxter equation) are constructed using this approach.Comment: latex file, 29 pages, Universitaet Bielefeld and University of Queensland preprint, BI-TP-94/13, UQMATH-94-02 (minor correction: in eq. (4.63) the number 32 should be replaced by 36 and in eq. (4.64) -16 becomes -18 and -10 becomes -8.

    Bethe Equations for a g_2 Model

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    We prove, using the coordinate Bethe ansatz, the exact solvability of a model of three particles whose point-like interactions are determined by the root system of g_2. The statistics of the wavefunction are left unspecified. Using the properties of the Weyl group, we are also able to find Bethe equations. It is notable that the method relies on a certain generalized version of the well-known Yang-Baxter equation. A particular class of non-trivial solutions to this equation emerges naturally.Comment: 10 pages, 3 figure

    Many Body Problems with "Spin"-Related Contact Interactions

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    We study quantum mechanical systems with "spin"-related contact interactions in one dimension. The boundary conditions describing the contact interactions are dependent on the spin states of the particles. In particular we investigate the integrability of NN-body systems with δ\delta-interactions and point spin couplings. Bethe ansatz solutions, bound states and scattering matrices are explicitly given. The cases of generalized separated boundary condition and some Hamiltonian operators corresponding to special spin related boundary conditions are also discussed.Comment: 13 pages, Late

    Current Algebraic Structures over Manifolds: Poisson Algebras, q-Deformations and Quantization

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    Poisson algebraic structures on current manifolds (of maps from a finite dimensional Riemannian manifold into a 2-dimensional manifold) are investigated in terms of symplectic geometry. It is shown that there is a one to one correspondence between such current manifolds and Poisson current algebras with three generators. A geometric meaning is given to q-deformations of current algebras. The geometric quantization of current algebras and quantum current algebraic maps is also studied.Comment: 25 pages, Late

    Hospitalized poisonings after renal transplantation in the United States

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    BACKGROUND: The national incidence of and risk factors for hospitalized poisonings in renal transplant recipients has not been reported. METHODS: Historical cohort study of 39,628 renal transplant recipients in the United States Renal Data System between 1 July 1994 and 30 June 1998. Associations with time to hospitalizations for a primary diagnosis of poisonings (ICD-9 codes 960.x-989.x) within three years after renal transplant were assessed by Cox Regression. RESULTS: The incidence of hospitalized poisonings was 2.3 patients per 1000 person years. The most frequent causes of poisonings were immunosuppressive agents (25.3%), analgesics/antipyretics (14.1%), psychotropic agents (10.0%), and insulin/antidiabetic agents (7.1%). In Cox Regression analysis, low body mass index (BMI, <21.6 vs. >28.3 kg/m(2), adjusted hazard ratio (AHR), 3.02, 95% CI, 1.45–6.28, and allograft rejection, AHR 1.83, 95% CI, 1.15–2.89, were the only factors independently associated with hospitalized poisonings. Hospitalized poisonings were independently associated with increased mortality (AHR, 1.54, 95% CI 1.22–1.92, p = 0.002). CONCLUSIONS: Hospitalized poisonings were associated with increased mortality after renal transplantation. However, almost all reported poisonings in renal transplant recipients were due to the use of prescribed medications. Allograft rejection and low BMI were the only independent risk factors for poisonings identified in this population

    Galilean quantum gravity with cosmological constant and the extended q-Heisenberg algebra

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    We define a theory of Galilean gravity in 2+1 dimensions with cosmological constant as a Chern-Simons gauge theory of the doubly-extended Newton-Hooke group, extending our previous study of classical and quantum gravity in 2+1 dimensions in the Galilean limit. We exhibit an r-matrix which is compatible with our Chern-Simons action (in a sense to be defined) and show that the associated bi-algebra structure of the Newton-Hooke Lie algebra is that of the classical double of the extended Heisenberg algebra. We deduce that, in the quantisation of the theory according to the combinatorial quantisation programme, much of the quantum theory is determined by the quantum double of the extended q-deformed Heisenberg algebra.Comment: 22 page

    Residual enhancing disease after surgery for glioblastoma: Evaluation of practice in the United Kingdom

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    Background: A growing body of clinical data highlights the prognostic importance of achieving gross total resection (GTR) in patients with glioblastoma. The aim of this study was to determine nationwide practice and attitudes towards achieving GTR and dealing with residual enhancing disease. // Methods: The study was in 2 parts: an electronic questionnaire sent to United Kingdom neuro-oncology surgeons to assess surgical practice followed by a 3-month prospective, multicenter observational study of current neurosurgical oncology practice. // Results: Twenty-seven surgeons representing 22 neurosurgical units completed the questionnaire. Prospective data were collected for 113 patients from 15 neurosurgical units. GTR was deemed to be achieved at time of surgery in 82% (91/111) of cases, but in only 45% (36/80) on postoperative MRI. Residual enhancing disease was deemed operable in 16.3% (13/80) of cases, however, no patient underwent early repeat surgery for residual enhancing disease. The most commonly cited reason (38.5%, 5/13) was perceived lack of clinical benefit. // Conclusion: There is a subset of patients for whom GTR is thought possible, but not achieved at surgery. For these patients, early repeat resection may improve overall survival. Further prospective surgical research is required to better define the prognostic implications of GTR for residual enhancing disease and examine the potential benefit of this early re-intervention

    Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma

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    Genome-wide association studies (GWAS) have identified ~20 melanoma susceptibility loci, most of which are not functionally characterized. Here we report an approach integrating massively-parallel reporter assays (MPRA) with cell-type-specific epigenome and expression quantitative trait loci (eQTL) to identify susceptibility genes/variants from multiple GWAS loci. From 832 high-LD variants, we identify 39 candidate functional variants from 14 loci displaying allelic transcriptional activity, a subset of which corroborates four colocalizing melanocyte cis-eQTL genes. Among these, we further characterize the locus encompassing the HIV-1 restriction gene, MX2 (Chr21q22.3), and validate a functional intronic variant, rs398206. rs398206 mediates the binding of the transcription factor, YY1, to increase MX2 levels, consistent with the cis-eQTL of MX2 in primary human melanocytes. Melanocyte-specific expression of human MX2 in a zebrafish model demonstrates accelerated melanoma formation in a BRAFV600E background. Our integrative approach streamlines GWAS follow-up studies and highlights a pleiotropic function of MX2 in melanoma susceptibility

    Beer and its Non-Alcoholic Compounds: Role in Pancreatic Exocrine Secretion, Alcoholic Pancreatitis and Pancreatic Carcinoma

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    In this article we provide an overview of the newest data concerning the effect of non-alcoholic constituents of alcoholic beverages, especially of beer, on pancreatic secretion, and their possible role in alcoholic pancreatitis and pancreatic carcinoma. The data indicate that non-alcoholic constituents of beer stimulate pancreatic enzyme secretion in humans and rats, at least in part, by direct action on pancreatic acinar cells. Some non-alcoholic compounds of beer, such as quercetin, resveratrol, ellagic acid or catechins, have been shown to be protective against experimentally induced pancreatitis by inhibiting pancreatic secretion, stellate cell activation or by reducing oxidative stress. Quercetin, ellagic acid and resveratrol also show anti-carcinogenic potential in vitro and in vivo. However, beer contains many more non-alcoholic ingredients. Their relevance in beer-induced functional alterations of pancreatic cells leading to pancreatitis and pancreatic cancer in humans needs to be further evaluated

    Immunotoxins and Anticancer Drug Conjugate Assemblies: The Role of the Linkage between Components

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    Immunotoxins and antibody-drug conjugates are protein-based drugs combining a target-specific binding domain with a cytotoxic domain. Such compounds are potentially therapeutic against diseases including cancer, and several clinical trials have shown encouraging results. Although the targeted elimination of malignant cells is an elegant concept, there are numerous practical challenges that limit conjugates’ therapeutic use, including inefficient cellular uptake, low cytotoxicity, and off-target effects. During the preparation of immunoconjugates by chemical synthesis, the choice of the hinge component joining the two building blocks is of paramount importance: the conjugate must remain stable in vivo but must afford efficient release of the toxic moiety when the target is reached. Vast efforts have been made, and the present article reviews strategies employed in developing immunoconjugates, focusing on the evolution of chemical linkers
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