2,980 research outputs found

    Scalar leptoquarks and the rare B meson decays

    Full text link
    We study some rare decays of BB meson involving the quark level transition bql+l(q=d,s)b \to q l^+l^- (q=d,s) in the scalar leptoquark model. We constrain the leptoquark parameter space using the recently measured branching ratios of Bs,dμ+μB_{s,d} \to \mu^+ \mu^- processes. Using such parameters, we obtain the branching ratios, direct CP violation parameters and isospin asymmetries in BKμ+μB \to K \mu^+ \mu^- and Bπμ+μB \to \pi \mu^+ \mu^- processes. We also obtain the branching ratios for some lepton flavour violating decays Bli+ljB \to l_i^+ l_j^-. We find that the various anomalies associated with the isospin asymmetries of BKμ+μB \to K \mu^+ \mu^- process can be explained in the scalar leptoquark model.Comment: 28 pages, 7 figures. typos corrected, to appear in Phys. Rev.

    Dynamic self- and other-focused emotional intelligence: A theoretical framework and research agenda

    Get PDF
    This paper introduces a theoretical framework for research on the dynamics of self- and otherfocused \nemotional intelligence (EI). The EI-framework focuses specifically on the interplay \nbetween different EI dimensions when individuals are processing their own emotions and the \nemotions of others. The framework captures different phases of processing self- and otheremotions. \nThe first phase consists of situational cues (e.g., an argument) that elicit \ninterdependent emotions in the self and others. The next phase specifies differential and \ninteracting effects of EI dimensions when processing these emotions, and the third phase \ndescribes what proximal and distal consequences this processing may have. In addition, the \nframework includes candidate dispositional and contextual factors (e.g., emotion-type, \nmotivation) that may qualify the process

    Moderation of antipsychotic-induced weight gain by energy balance gene variants in the RUPP autism network risperidone studies.

    Get PDF
    Second-generation antipsychotic exposure, in both children and adults, carries significant risk for excessive weight gain that varies widely across individuals. We queried common variation in key energy balance genes (FTO, MC4R, LEP, CNR1, FAAH) for their association with weight gain during the initial 8 weeks in the two NIMH Research Units on Pediatric Psychopharmacology Autism Network trials (N=225) of risperidone for treatment of irritability in children/adolescents aged 4-17 years with autism spectrum disorders. Variants in the cannabinoid receptor (CNR)-1 promoter (P=1.0 × 10(-6)), CNR1 (P=9.6 × 10(-5)) and the leptin (LEP) promoter (P=1.4 × 10(-4)) conferred robust-independent risks for weight gain. A model combining these three variants was highly significant (P=1.3 × 10(-9)) with a 0.85 effect size between lowest and highest risk groups. All results survived correction for multiple testing and were not dependent on dose, plasma level or ethnicity. We found no evidence for association with a reported functional variant in the endocannabinoid metabolic enzyme, fatty acid amide hydrolase, whereas body mass index-associated single-nucleotide polymorphisms in FTO and MC4R showed only trend associations. These data suggest a substantial genetic contribution of common variants in energy balance regulatory genes to individual antipsychotic-associated weight gain in children and adolescents, which supersedes findings from prior adult studies. The effects are robust enough to be detected after only 8 weeks and are more prominent in this largely treatment naive population. This study highlights compelling directions for further exploration of the pharmacogenetic basis of this concerning multifactorial adverse event

    The Process " Pbar P -> E- E+ " with Polarized Initial Particles and Proton Form Factors in Time-Like Region

    Full text link
    The discussion on the asymptotical behaviour of the form factors in the space-like and time-like regions have been corrected and clarified. Fig.3 has been replaced by an improved analysis of the data.Comment: DFTT 13/93. LaTeX file, 11 pages + 3 figures (included

    Drug resistance in non-B subtype HIV-1: Impact of HIV-1 reverse transcriptase inhibitors

    Get PDF
    Human immunodeficiency virus (HIV) causes approximately 2.5 million new infections every year, and nearly 1.6 million patients succumb to HIV each year. Several factors, including cross-species transmission and error-prone replication have resulted in extraordinary genetic diversity of HIV groups. One of these groups, known as group M (main) contains nine subtypes (A-D, F-H and J-K) and causes ∼95% of all HIV infections. Most reported data on susceptibility and resistance to anti-HIV therapies are from subtype B HIV infections, which are prevalent in developed countries but account for only ∼12% of all global HIV infections, whereas non-B subtype HIV infections that account for ∼88% of all HIV infections are prevalent primarily in low and middle-income countries. Although the treatments for subtype B infections are generally effective against non-B subtype infections, there are differences in response to therapies. Here, we review how polymorphisms, transmission efficiency of drug-resistant strains, and differences in genetic barrier for drug resistance can differentially alter the response to reverse transcriptase-targeting therapies in various subtypes

    Numerical Computations with H(div)-Finite Elements for the Brinkman Problem

    Full text link
    The H(div)-conforming approach for the Brinkman equation is studied numerically, verifying the theoretical a priori and a posteriori analysis in previous work of the authors. Furthermore, the results are extended to cover a non-constant permeability. A hybridization technique for the problem is presented, complete with a convergence analysis and numerical verification. Finally, the numerical convergence studies are complemented with numerical examples of applications to domain decomposition and adaptive mesh refinement.Comment: Minor clarifications, added references. Reordering of some figures. To appear in Computational Geosciences, final article available at http://www.springerlink.co

    Self-Organization, Layered Structure, and Aggregation Enhance Persistence of a Synthetic Biofilm Consortium

    Get PDF
    Microbial consortia constitute a majority of the earth’s biomass, but little is known about how these cooperating communities persist despite competition among community members. Theory suggests that non-random spatial structures contribute to the persistence of mixed communities; when particular structures form, they may provide associated community members with a growth advantage over unassociated members. If true, this has implications for the rise and persistence of multi-cellular organisms. However, this theory is difficult to study because we rarely observe initial instances of non-random physical structure in natural populations. Using two engineered strains of Escherichia coli that constitute a synthetic symbiotic microbial consortium, we fortuitously observed such spatial self-organization. This consortium forms a biofilm and, after several days, adopts a defined layered structure that is associated with two unexpected, measurable growth advantages. First, the consortium cannot successfully colonize a new, downstream environment until it selforganizes in the initial environment; in other words, the structure enhances the ability of the consortium to survive environmental disruptions. Second, when the layered structure forms in downstream environments the consortium accumulates significantly more biomass than it did in the initial environment; in other words, the structure enhances the global productivity of the consortium. We also observed that the layered structure only assembles in downstream environments that are colonized by aggregates from a previous, structured community. These results demonstrate roles for self-organization and aggregation in persistence of multi-cellular communities, and also illustrate a role for the techniques of synthetic biology in elucidating fundamental biological principles
    corecore