922 research outputs found

    Search for the rare decays B0 (s) - ÎŒ+Ό− and K0 S - ÎŒ+Ό− with 1 fb−1 at LHCb

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    This thesis is devoted to the explanation of the searches for the very rare decays B0 (s) ! + and K0 S ! + , performed using the 1 fb1 of data taken by LHCb during 2011 from the LHC proton{ proton collisions at an energy of p s=7 TeV. The most relevant theory aspects concerning these searches will be presented. Furthermore, the LHCb experiment will be described, and some of its most interesting results in the rare decays area reported. The B0 (s) ! + search has not resulted in any signal excess above background, but has produced world best upper limits in the branching ratios of both channels: B(B0 ! + ) < 1:0 109 and B(B0 s ! + ) < 4:5 109, both at 95% con dence level. Finally, no signi cant signal excess has been found in the search for K0 S ! + neither, and again an upper limit on its branching ratio has been set: B(K0 S ! + ) < 11:2 109 at 95% con dence level. This upper limit is a factor of 35 better than the previous world best

    Discovering True Muonium at LHCb

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    We study the potential of the LHCb experiment to discover, for the first time, the ÎŒ+Ό−\mu^+\mu^- true muonium bound state. We propose a search for the vector 13S11^3S_1 state, T ⁣M\mathcal{T\!M}, which kinetically mixes with the photon and dominantly decays to e+e−e^+e^-. We demonstrate that a search for η→γT ⁣M\eta \to \gamma \mathcal{T\!M}, T ⁣M→e+e−\mathcal{T\!M}\to e^+e^- in a displaced vertex can exceed a significance of 5 standard deviations assuming statistical uncertainties. We present two possible searches: an inclusive search for the e+e−e^+e^- vertex, and an exclusive search which requires an additional photon and a reconstruction of the η\eta mass.Comment: 12 pages, 5 figures; v2: edits from comments and review, matched to PRD versio

    Exclusive displaced hadronic signatures in the LHC forward region

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    The LHCb detector provides accurate vertex reconstruction and hadronic particle identification, which make the experiment an ideal place to look for light long-lived particles (LLP) decaying into Standard Model (SM) hadrons. In contrast with the typical search strategy relying on energetic jets and a high multiplicity of tracks from the LLP decay, LHCb can identify LLPs in exclusive, specific hadronic final states. To illustrate the idea, we study the sensitivity of LHCb to an exotic Higgs decay h → SS, followed by the displaced decay of GeV-scale scalars into charged kaons S → K+K−. We show that the reconstruction of kaon vertices in narrow invariant mass windows can efficiently eliminate the combinatorial backgrounds from B-meson decays. While the same signal is extremely difficult to probe in the existing displaced jet searches at ATLAS/CMS, the LHCb search we propose can probe the branching ratio BR(h → SS) down to 0.1% (0.02%) level with 15 (300) fb−1 of data. We also apply this projected bound to two scenarios with Higgs portal couplings, where the scalar mediator S either couples to a) the SM quarks only, or b) to both quarks and leptons in the minimal flavor violation paradigm. In both scenarios we compare the reach of our proposed search with the expected constraints from ATLAS and CMS on the invisible Higgs width and with the constraints from rare B-decays studies at LHCb. We find that for 1 GeV < mS < 2 GeV and 0.5 mm . cτ . 10 mm our proposed search will be competitive with the ATLAS and CMS projections, while at the same time providing crucial information of the hadronic interactions of S, which can not be obtained from the indirect measurement of the Higgs invisible width.The work of XCV is supported by MINECO (Spain) through the RamÂŽon y Cajal program RYC-2016-20073 and by XuntaGal under the ED431F 2018/01 project. YT is supported in part by the National Science Foundation under Grant Number PHY-1620074. YT would like to thank Aspen Center for Physics for hospitality during the completion of this work, which is supported by National Science Foundation grant PHY-1607611.S

    Chloride channels in astrocytes: structure, roles in brain homeostasis and implications in disease

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    Astrocytes are the most abundant cell type in the CNS (central nervous system). They exert multiple functions during development and in the adult CNS that are essential for brain homeostasis. Both cation and anion channel activities have been identified in astrocytes and it is believed that they play key roles in astrocyte function. Whereas the proteins and the physiological roles assigned to cation channels are becoming very clear, the study of astrocytic chloride channels is in its early stages. In recent years, we have moved from the identification of chloride channel activities present in astrocyte primary culture to the identification of the proteins involved in these activities, the determination of their 3D structure and attempts to gain insights about their physiological role. Here, we review the recent findings related to the main chloride channels identified in astrocytes: the voltage-dependent ClC-2, the calcium-activated bestrophin, the volume-activated VRAC (volume-regulated anion channel) and the stress-activated Maxi-Cl−. We discuss key aspects of channel biophysics and structure with a focus on their role in glial physiology and human disease

    Real-time discrimination of photon pairs using machine learning at the LHC

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    ALP-mediated decays and other as-yet unobserved B decays to di-photon final states are a challenge to select in hadron collider environments due to the large backgrounds that come directly from the p p collision. We present the strategy implemented by the LHCb experiment in 2018 to efficiently select such photon pairs. A fast neural network topology, implemented in the LHCb real-time selection framework achieves high efficiency across a mass range of 4−20 GeV/c2. We discuss implications and future prospects for the LHCb experimentS
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