نتایج جستجو برای: t dual rickartmodules
تعداد نتایج: 849204 فیلتر نتایج به سال:
: \ We obtain a very good description of all available large angle pp elastic scattering data using a dual model with logarithmic trajectories. Our fit strongly suggests that the dual amplitude is responsible for filling in ,a pronounced dip produced by the Pomeranchuk singularity. This new explanation of the shoulder in pp data survives the test of an enormous extrapolation from s N, 26-(GeV/~...
Myasthenia gravis (MG) and experimental autoimmune MG are T cell-dependent antibody-mediated autoimmune diseases. A dual altered peptide ligand (APL), composed of the tandemly arranged two single amino acid analogs of two myasthenogenic peptides, p195-212 and p259-271, down-regulated in vitro and in vivo MG-associated T cell responses. In the present study, we investigated the role of CD8(+)CD2...
Starting from the classification of 6–dimensional real Drinfeld doubles and their decomposition into Manin triples we construct 3–dimensional Poisson–Lie T–dual or more precisely T–plural sigma models. Of special interest are those that are conformally invariant. Examples of models that satisfy vanishing β–function equations with zero dilaton are presented and their duals are calculated. It tur...
The nonlinear second order differential equation d dt h(t, x′(t)) + g(t, x(t)) = 0, t ∈ [0, T ] a.e. x′(0) = x′(T ) = 0 with superlinear function g is investigated. Based on dual variational method the existence of solution is proved. Dependence on parameters and approximation method are also presented.
Abstract. Certain facts about frames and generalized frames (g- frames) are extended for the g-frames for Hilbert C*-modules. It is shown that g-frames for Hilbert C*-modules share several useful properties with those for Hilbert spaces. The paper also character- izes the operators which preserve the class of g-frames for Hilbert C*-modules. Moreover, a necessary and suffcient condition is ob- ...
CD134- and CD137-primed CD8 T cells mount powerful effector responses upon recall, but even without recall these dual-costimulated T cells respond to signal 3 cytokines such as IL-12. We searched for alternative signal 3 receptor pathways and found the IL-1 family member IL-36R. Although IL-36 alone did not stimulate effector CD8 T cells, in combination with IL-12, or more surprisingly IL-2, it...
In this talk the dual of an abelian variety will be defined. It will be shown that this dual is an abelian variety again. Using dual morphisms, we will finally show that the dual of the dual is canonically isomorphic to the orginal abelian variety. The author would like to thank Bas Edixhoven, Julian Lyczak and the other participants to the seminar for their valuable contributions. 0 Convention...
We prove that a homogeneous Banach space B on the unit circle T can be embedded as a closed subspace of a dual space ΞB contained in the space of bounded Borel measures on T in such a way that the map B → ΞB defines a bijective correspondence between the class of homogeneous Banach spaces on T and the class of prehomogeneous Banach spaces on T. We apply our results to show that the algebra of a...
Let Y denote a D-class symmetric association scheme with D ≥ 3, and suppose Y is almostbipartite Pand Q-polynomial. Let x denote a vertex of Y and let T = T (x) denote the corresponding Terwilliger algebra. We prove that any irreducible T -module W is both thin and dual thin in the sense of Terwilliger. We produce two bases for W and describe the action of T on these bases. We prove that the is...
The methods currently available for genotype-specific diagnosis of T. cruzi infection still present relevant limitations, especially to identify mixed infection. In the present investigation, we have evaluated the performance of Chagas-Flow ATE-IgG2a test for early and late differential diagnosis of single and dual genotype-specific T. cruzi infections. Serum samples from Swiss mice at early an...
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