9,545 research outputs found

    Nerve growth factor (NGF)

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    Physics Behind Precision

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    This document provides a writeup of contributions to the FCC-ee mini-workshop on "Physics behind precision" held at CERN, on 2-3 February 2016.Comment: https://indico.cern.ch/event/469561

    Top quark pair + jet production at next-to-leading order: NLO QCD corrections to gg -> t tbar g

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    The reaction pp/pbar p -> t tbar jet+X is an important background process for Higgs boson searches in the mass range below 200 GeV. Apart from that it is also an ideal laboratory for precision measurements in the top quark sector. Both applications require a solid theoretical prediction, which can be achieved only through a full next-to-leading order (NLO) calculation. In this work we describe the NLO computation of the subprocess gg -> t tbar g.Comment: To appear in the proceedings of 7th DESY Workshop on Elementary Particle Theory: Loops and Legs in Quantum Field Theory, Zinnowitz, Germany, 25-30 Apr 200

    Flavor changing scalar couplings and tγ(Z)t\gamma(Z) production at hadron colliders

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    We calculate the contributions of the flavor changing scalar (FCSFCS) couplings arised from topcolor-assisted technicolor (TC2TC2) models at tree-level to the tγt\gamma and tZtZ production at the Tevatron and LHCLHC experiments. We find that the production cross sections are very small at the Tevatron with s=1.96TeV\sqrt{s}=1.96TeV, which is smaller than 5 fb in most of the parameter space of TC2TC2 models. However, the virtual effects of the FCSFCS couplings on the tγ(Z)t\gamma(Z) production can be easily detected at the LHCLHC with s=14TeV\sqrt{s}=14TeV via the final state γlνˉb\gamma l\bar{\nu}b (l+llνˉbl^{+}l^{-}l\bar{\nu}b).Comment: 10 pages,5 figure

    TLR7-mediated skin inflammation remotely triggers chemokine expression and leukocyte accumulation in the brain

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    Background: The relationship between the brain and the immune system has become increasingly topical as, although it is immune-specialised, the CNS is not free from the influences of the immune system. Recent data indicate that peripheral immune stimulation can significantly affect the CNS. But the mechanisms underpinning this relationship remain unclear. The standard approach to understanding this relationship has relied on systemic immune activation using bacterial components, finding that immune mediators, such as cytokines, can have a significant effect on brain function and behaviour. More rarely have studies used disease models that are representative of human disorders. Methods: Here we use a well-characterised animal model of psoriasis-like skin inflammation—imiquimod—to investigate the effects of tissue-specific peripheral inflammation on the brain. We used full genome array, flow cytometry analysis of immune cell infiltration, doublecortin staining for neural precursor cells and a behavioural read-out exploiting natural burrowing behaviour. Results: We found that a number of genes are upregulated in the brain following treatment, amongst which is a subset of inflammatory chemokines (CCL3, CCL5, CCL9, CXCL10, CXCL13, CXCL16 and CCR5). Strikingly, this model induced the infiltration of a number of immune cell subsets into the brain parenchyma, including T cells, NK cells and myeloid cells, along with a reduction in neurogenesis and a suppression of burrowing activity. Conclusions: These findings demonstrate that cutaneous, peripheral immune stimulation is associated with significant leukocyte infiltration into the brain and suggest that chemokines may be amongst the key mediators driving this response

    Identifying Ligand Binding Conformations of the β2-Adrenergic Receptor by Using Its Agonists as Computational Probes

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    Recently available G-protein coupled receptor (GPCR) structures and biophysical studies suggest that the difference between the effects of various agonists and antagonists cannot be explained by single structures alone, but rather that the conformational ensembles of the proteins need to be considered. Here we use an elastic network model-guided molecular dynamics simulation protocol to generate an ensemble of conformers of a prototypical GPCR, β2-adrenergic receptor (β2AR). The resulting conformers are clustered into groups based on the conformations of the ligand binding site, and distinct conformers from each group are assessed for their binding to known agonists of β2AR. We show that the select ligands bind preferentially to different predicted conformers of β2AR, and identify a role of β2AR extracellular region as an allosteric binding site for larger drugs such as salmeterol. Thus, drugs and ligands can be used as "computational probes" to systematically identify protein conformers with likely biological significance. © 2012 Isin et al

    Oropharyngeal Group A Streptococcal Colonization Disrupts Latent Epstein-Barr Virus Infection

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    Epstein-Barr virus (EBV) infects >90% of the human population within the first 2 decades of life and establishes reversible latent infection in B cells. The stimuli that lead to switching from latent to lytic EBV infection in vivo are still elusive. Group A streptococci (GAS) are a common cause of bacterial pharyngotonsillitis in children and adolescents and colonize the tonsils and pharynx of up to 20% of healthy children. Thus, concomitant presence of EBV and GAS in the same individual is frequent. Here, we show that EBV carriers who are colonized with GAS shed EBV particles in higher numbers in their saliva, compared with EBV carriers not colonized with GAS. Messenger RNA levels of the master lytic regulatory EBV gene BZLF1 were more frequently detected in tonsils from EBV carriers colonized with GAS than from EBV carriers not colonized. Heat-killed GAS, potentially mimicking GAS colonization, elicited lytic EBV in latently infected lymphoblastoid cell lines (LCLs) partially via Toll-like receptor 2 triggering, as did purified GAS peptidoglycan. Thus, colonization by GAS might benefit EBV by increasing the EBV load in saliva and thereby enhancing the likelihood of EBV spread to other host

    Search for the Supersymmetric Partner of the Top-Quark in ppˉp \bar{p} Collisions at s=1.8TeV\sqrt{s} = 1.8 {\rm TeV}

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    We report on a search for the supersymmetric partner of the top quark (stop) produced in ttˉt \bar{t} events using 110pb1110 {\rm pb}^{-1} of ppˉp \bar{p} collisions at s=1.8TeV\sqrt{s} = 1.8 {\rm TeV} recorded with the Collider Detector at Fermilab. In the case of a light stop squark, the decay of the top quark into stop plus the lightest supersymmetric particle (LSP) could have a significant branching ratio. The observed events are consistent with Standard Model ttˉt \bar{t} production and decay. Hence, we set limits on the branching ratio of the top quark decaying into stop plus LSP, excluding branching ratios above 45% for a LSP mass up to 40 {\rm GeV/c}2^{2}.Comment: 11 pages, 4 figure

    Measurement of the ttbar Production Cross Section in ppbar Collisions at sqrt(s) = 1.96 TeV

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    We present a measurement of the top quark pair production cross section in ppbar collisions at sqrt(s)=1.96 TeV using 318 pb^{-1} of data collected with the Collider Detector at Fermilab. We select ttbar decays into the final states e nu + jets and mu nu + jets, in which at least one b quark from the t-quark decays is identified using a secondary vertex-finding algorithm. Assuming a top quark mass of 178 GeV/c^2, we measure a cross section of 8.7 +-0.9 (stat) +1.1-0.9 (syst) pb. We also report the first observation of ttbar with significance greater than 5 sigma in the subsample in which both b quarks are identified, corresponding to a cross section of 10.1 +1.6-1.4(stat)+2.0-1.3 (syst) pb.Comment: Accepted for publication in Physics Review Letters, 7 page
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