173 research outputs found

    q-Analog of Gelfand-Graev Basis for the Noncompact Quantum Algebra U_q(u(n,1))

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    For the quantum algebra U_q(gl(n+1)) in its reduction on the subalgebra U_q(gl(n)) an explicit description of a Mickelsson-Zhelobenko reduction Z-algebra Z_q(gl(n+1),gl(n)) is given in terms of the generators and their defining relations. Using this Z-algebra we describe Hermitian irreducible representations of a discrete series for the noncompact quantum algebra U_q(u(n,1)) which is a real form of U_q(gl(n+1)), namely, an orthonormal Gelfand-Graev basis is constructed in an explicit form.Comment: Invited talk given by V.N.T. at XVIII International Colloquium "Integrable Systems and Quantum Symmetries", June 18--20, 2009, Prague, Czech Republi

    The Diamond Lemma and the PBW Property in Quantum Algebras

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    (so3) is demonstrated. The approach presented here is successful in other cases of quantum algebras and superalgebras

    On Representations of sl(n, C) Compatible with a Z2-grading

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    This paper extends existing Lie algebra representation theory related to Lie algebra gradings. The notion of a representation compatible with a given grading is applied to finite-dimensional representations of sl(n,C) in relation to its Z2-gradings. For representation theory of sl(n,C) the Gel’fand-Tseitlin method turned out very efficient. We show that it is not generally true that every irreducible representation can be compatibly graded

    Trisubstituted pyrazolopyrimidines as novel angiogenesis inhibitors.

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    Current inhibitors of angiogenesis comprise either therapeutic antibodies (e.g. bevacicumab binding to VEGF-A) or small molecular inhibitors of receptor tyrosin kinases like e.g. sunitinib, which inhibits PDGFR and VEGFR. We have recently identified cyclin-dependent kinase 5 (Cdk5) as novel alternative and pharmacologically accessible target in the context of angiogenesis. In the present work we demonstrate that trisubstituted pyrazolo[4,3-d]pyrimidines constitute a novel class of compounds which potently inhibit angiogenesis. All seven tested compounds inhibited endothelial cell proliferation with IC(50) values between 1 and 18 µM. Interestingly, this seems not to be due to cytotoxicity, since none of them showed acute cytotoxic effects on endothelial cells at a concentration of 10 µM,. The three most potent compounds (LGR1404, LGR1406 and LGR1407) also inhibited cell migration (by 27, 51 and 31%, resp.), chemotaxis (by 50, 70 and 60% in accumulative distance, resp.), and tube formation (by 25, 60 and 30% of total tube length, resp.) at the non-toxic concentration of 10 µM. Furthermore, angiogenesis was reduced in vivo in the CAM assay by these three compounds. A kinase selectivity profiling revealed that the compounds prevalently inhibit Cdk2, Cdk5 and Cdk9. The phenotype of the migrating cells (reduced formation of lamellipodia, loss of Rac-1 translocation to the membrane) resembles the previously described effects of silencing of Cdk5 in endothelial cells. We conclude that especially LGR1406 and LGR1407 are highly attractive anti-angiogenic compounds, whose effects seem to largely depend on their Cdk5 inhibiting properties

    q-Analog of Gelfand-Graev Basis for the Noncompact Quantum Algebra Uq(u(n,1))

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    For the quantum algebra Uq(gl(n+1)) in its reduction on the subalgebra Uq(gl(n)) an explicit description of a Mickelsson-Zhelobenko reduction Z-algebra Zq(gl(n+1),gl(n)) is given in terms of the generators and their defining relations. Using this Z-algebra we describe Hermitian irreducible representations of a discrete series for the noncompact quantum algebra Uq(u(n,1)) which is a real form of Uq(gl(n+1)), namely, an orthonormal Gelfand-Graev basis is constructed in an explicit form

    The qq-boson-fermion realizations of quantum suprealgebra Uq(gl(2/1))U_q(gl(2/1))

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    We show that our construction of realizations for Lie algebras and quantum algebras can be generalized to quantum superalgebras, too. We study an example of quantum superalgebra Uq(gl(2/1))U_q(gl(2/1)) and give the boson-fermion realization with respect to one pair od q-deformed boson operator and 2 pairs of fermions.Comment: 8 page

    Multi-device study of temporal characteristics of magnetohydrodynamic modes initiating disruptions

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    Disruptions in tokamaks are often preceded by magnetohydrodynamic (MHD) instabilities that can rotate or become locked to the wall. Measurements from magnetic diagnostics in the presence of MHD mode precursors to disruptions can yield potentially valuable input to the plasma control system, with a view to disruption avoidance, prediction and mitigation. This paper presents an exploratory analysis of the growth of MHD modes and corresponding time scales on the basis of magnetic measurements in multiple tokamaks. To this end, a database was compiled using disruptive discharges from COMPASS, ASDEX Upgrade, DIII-D and JET, manually classified according to disruption root cause, and characterized by a great diversity of operational conditions and mode dynamics. The typical time during which a mode can be detected using saddle coils and the duration of the locked mode phase in the database both extend over several orders of magnitude, but generally the time scales increase with plasma size. Several additional factors are discussed that can influence these durations, including the disruption root cause. A scaling law for the locked phase duration was estimated, yielding predictions toward ITER of the order of hundreds of milliseconds or even seconds. In addition, a scaling law for the mode amplitude at the disruption onset, proposed earlier by de Vries et al. (2016), is applied to the database, and its predictive capabilities are assessed. Despite significant uncertainty on the predictions from both scaling laws, encouraging trends are observed of the fraction of disruptions that may be detected with sufficient warning time to allow mitigation or even avoidance, based solely on observations of MHD mode dynamics. When combined with similar analysis of measurements from diagnostics that are sensitive to other disruption precursors, our analysis methods and results may contribute to the reliability, robustness and generalization of disruption warning schemes for ITER

    Increased incidence of traffic accidents in Toxoplasma-infected military drivers and protective effect RhD molecule revealed by a large-scale prospective cohort study

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    <p>Abstract</p> <p>Background</p> <p>Latent toxoplasmosis, protozoan parasitosis with prevalence rates from 20 to 60% in most populations, is known to impair reaction times in infected subjects, which results, for example, in a higher risk of traffic accidents in subjects with this life-long infection. Two recent studies have reported that RhD-positive subjects, especially RhD heterozygotes, are protected against latent toxoplasmosis-induced impairment of reaction times. In the present study we searched for increased incidence of traffic accidents and for protective effect of RhD positivity in 3890 military drivers.</p> <p>Methods</p> <p>Male draftees who attended the Central Military Hospital in Prague for regular entrance psychological examinations between 2000 and 2003 were tested for <it>Toxoplasma </it>infection and RhD phenotype at the beginning of their 1 to1.5-year compulsory military service. Subsequently, the data on <it>Toxoplasma </it>infection and RhD phenotype were matched with those on traffic accidents from military police records and the effects of RhD phenotype and <it>Toxoplasma </it>infection on probability of traffic accident was estimated with logistic regression.</p> <p>Results</p> <p>We confirmed, using for the first time a prospective cohort study design, increased risk of traffic accidents in <it>Toxoplasma</it>-infected subjects and demonstrated a strong protective effect of RhD positivity against the risk of traffic accidents posed by latent toxoplasmosis. Our results show that RhD-negative subjects with high titers of anti-<it>Toxoplasma </it>antibodies had a probability of a traffic accident of about 16.7%, i.e. a more than six times higher rate than <it>Toxoplasma</it>-free or RhD-positive subjects.</p> <p>Conclusion</p> <p>Our results showed that a common infection by <it>Toxoplasma gondii </it>could have strong impact on the probability of traffic accident in RhD negative subjects. The observed effects could provide not only a clue to the long-standing evolutionary enigma of the origin of RhD polymorphism in humans (the effect of balancing selection), but might also be the missing piece in the puzzle of the physiological function of the RhD molecule.</p
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