1,082 research outputs found

    Optimizing semiconductor devices by self-organizing particle swarm

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    A self-organizing particle swarm is presented. It works in dissipative state by employing the small inertia weight, according to experimental analysis on a simplified model, which with fast convergence. Then by recognizing and replacing inactive particles according to the process deviation information of device parameters, the fluctuation is introduced so as to driving the irreversible evolution process with better fitness. The testing on benchmark functions and an application example for device optimization with designed fitness function indicates it improves the performance effectively.Comment: Congress on Evolutionary Computation, 2004. CEC2004. Volume: 2, On page(s): 2017- 2022 Vol.

    Handling boundary constraints for numerical optimization by particle swarm flying in periodic search space

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    The periodic mode is analyzed together with two conventional boundary handling modes for particle swarm. By providing an infinite space that comprises periodic copies of original search space, it avoids possible disorganizing of particle swarm that is induced by the undesired mutations at the boundary. The results on benchmark functions show that particle swarm with periodic mode is capable of improving the search performance significantly, by compared with that of conventional modes and other algorithms.Comment: Congress on Evolutionary Computation, 2004. CEC2004. Volume: 2, On page(s): 2307- 2311 Vol.

    Anomalous U(1) symmetry and lepton flavor violation

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    We show that in a large class of models based on anomalous U(1) symmetry which addresses the fermion mass hierarchy problem, leptonic flavor changing processes are induced that are in the experimentally interesting range. The flavor violation occurs through the renormalization group evolution of the soft SUSY breaking parameters between the string scale and the U(1)_A breaking scale. We derive general expressions for the evolution of these parameters in the presence of higher dimensional operators. Several sources for the flavor violation are identified: flavor-dependent contributions to the soft masses from the U(1)_A gaugino, scalar mass corrections proportional to the trace of U(1)_A charge, non-proportional A-terms from vertex corrections, and the U(1)_A D-term. Quantitative estimates for the decays \mu -> e \gamma and \tau -> \mu \gamma are presented in supergravity models which accommodate the relic abundance of neutralino dark matter.Comment: References added, typos corrected, 28 pages LaTeX, includes 14 eps figure

    PAMELA/ATIC anomaly from the meta-stable extra dark matter component and the leptophilic Yukawa interaction

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    We present a supersymmetric model with two dark matter (DM) components explaining the galactic positron excess observed by PAMELA/HEAT and ATIC/PPB-BETS: One is the conventional (bino-like) lightest supersymmetric particle (LSP) \chi, and the other is a TeV scale meta-stable neutral singlet N_D, which is a Dirac fermion (N,N^c). In this model, N_D decays dominantly into \chi e^+e^- through an R parity preserving dimension 6 operator with the life time \tau_N\sim 10^{26} sec. We introduce a pair of vector-like superheavy SU(2) lepton doublets (L,L^c) and lepton singlets (E,E^c). The dimension 6 operator leading to the N_D decay is generated from the leptophilic Yukawa interactions by W\supset Ne^cE+Lh_dE^c+m_{3/2}l_1L^c with the dimensionless couplings of order unity, and the gauge interaction by {\cal L}\supset \sqrt{2} g'\tilde{e}^{c*}e^c\chi + h.c. The superheavy masses of the vector-like leptons (M_L, M_E\sim 10^{16} GeV) are responsible for the longevity of N_D. The low energy field spectrum in this model is just the MSSM fields and N_D. Even for the case that the portion of N_D is much smaller than that of \chi in the total DM density [{\cal O}(10^{-10}) \lesssim n_{N_D}/n_\chi], the observed positron excess can be explained by adopting relatively lighter masses of the vector-like leptons (10^{13} GeV \lesssim M_{L,E} \lesssim 10^{16} GeV). The smallness of the electron mass is also explained. This model is easily embedded in the flipped SU(5) grand unification, which is a leptophilic unified theory.Comment: 12 pages, published versio

    Spatiotemporal dynamics of hemorrhagic fever with renal syndrome, Beijing, People's Republic of Chin

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    We used geographic information systems to characterize the dynamic change in spatial distribution of hemorrhagic fever with renal syndrome (HFRS) in Beijing, People's Republic of China. The seasonal variation in its incidence was observed by creating an epidemic curve. HFRS was associated with developed land, orchards, and rice paddies

    Double-action dark matter, PAMELA and ATIC

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    Motivated by a two-bump (or 1-peak plus 1-hump) structure in the ATIC data, we perform a statistical analysis fitting the PAMELA and ATIC data to a dark matter model, in which the dark matter particle can undergo both annihilation and decay. Using a chi-square analysis we show that both data can be simultaneously fitted better with such a double-action dark matter particle. We use an existing neutrino mass model in literature to illustrate the idea.Comment: RevTex 18 pages, 4 figures; version 2: references corrected, an estimate modified; version 3, a new figure on annihilation, more discussion and reference

    Nitrated α-Synuclein Induces the Loss of Dopaminergic Neurons in the Substantia Nigra of Rats

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    BACKGROUND: The pathology of Parkinson's disease (PD) is characterized by the degeneration of the nigrostriatal dopaminergic pathway, as well as the formation of intraneuronal inclusions known as Lewy bodies and Lewy neurites in the substantia nigra. Accumulations of nitrated alpha-synuclein are demonstrated in the signature inclusions of Parkinson's disease. However, whether the nitration of alpha-synuclein is relevant to the pathogenesis of PD is unknown. METHODOLOGY/PRINCIPAL FINDINGS: In this study, effect of nitrated alpha-synuclein to dopaminergic (DA) neurons was determined by delivering nitrated recombinant TAT-alpha-synuclein intracellular. We provide evidence to show that the nitrated alpha-synuclein was toxic to cultured dopaminergic SHSY-5Y neurons and primary mesencephalic DA neurons to a much greater degree than unnitrated alpha-synuclein. Moreover, we show that administration of nitrated alpha-synuclein to the substantia nigra pars compacta of rats caused severe reductions in the number of DA neurons therein, and led to the down-regulation of D(2)R in the striatum in vivo. Furthermore, when administered to the substantia nigra of rats, nitrated alpha-synuclein caused PD-like motor dysfunctions, such as reduced locomotion and motor asymmetry, however unmodified alpha-synuclein had significantly less severe behavioral effects. CONCLUSIONS/SIGNIFICANCE: Our results provide evidence that alpha-synuclein, principally in its nitrated form, induce DA neuron death and may be a major factor in the etiology of PD

    Anti-angiogenic therapy for cancer: Current progress, unresolved questions and future directions

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    Tumours require a vascular supply to grow and can achieve this via the expression of pro-angiogenic growth factors, including members of the vascular endothelial growth factor (VEGF) family of ligands. Since one or more of the VEGF ligand family is overexpressed in most solid cancers, there was great optimism that inhibition of the VEGF pathway would represent an effective anti-angiogenic therapy for most tumour types. Encouragingly, VEGF pathway targeted drugs such as bevacizumab, sunitinib and aflibercept have shown activity in certain settings. However, inhibition of VEGF signalling is not effective in all cancers, prompting the need to further understand how the vasculature can be effectively targeted in tumours. Here we present a succinct review of the progress with VEGF-targeted therapy and the unresolved questions that exist in the field: including its use in different disease stages (metastatic, adjuvant, neoadjuvant), interactions with chemotherapy, duration and scheduling of therapy, potential predictive biomarkers and proposed mechanisms of resistance, including paradoxical effects such as enhanced tumour aggressiveness. In terms of future directions, we discuss the need to delineate further the complexities of tumour vascularisation if we are to develop more effective and personalised anti-angiogenic therapies. © 2014 The Author(s)

    MSSM Electroweak Baryogenesis and LHC Data

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    Electroweak baryogenesis is an attractive scenario for the generation of the baryon asymmetry of the universe as its realization depends on the presence at the weak scale of new particles which may be searched for at high energy colliders. In the MSSM it may only be realized in the presence of light stops, and with moderate or small mixing between the left- and right-handed components. Consistency with the observed Higgs mass around 125 GeV demands the heavier stop mass to be much larger than the weak scale. Moreover the lighter stop leads to an increase of the gluon-gluon fusion Higgs production cross section which seems to be in contradiction with indications from current LHC data. We show that this tension may be considerably relaxed in the presence of a light neutralino with a mass lower than about 60 GeV, satisfying all present experimental constraints. In such a case the Higgs may have a significant invisible decay width and the stop decays through a three or four body decay channel, including a bottom quark and the lightest neutralino in the final state. All these properties make this scenario testable at a high luminosity LHC.Comment: 28 pages, 18 figures; v2) Discussion on point C removed for conciseness, minor changes in the text to match the published versio

    EBV Promotes Human CD8+ NKT Cell Development

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    The reports on the origin of human CD8+ Vα24+ T-cell receptor (TCR) natural killer T (NKT) cells are controversial. The underlying mechanism that controls human CD4 versus CD8 NKT cell development is not well-characterized. In the present study, we have studied total 177 eligible patients and subjects including 128 healthy latent Epstein-Barr-virus(EBV)-infected subjects, 17 newly-onset acute infectious mononucleosis patients, 16 newly-diagnosed EBV-associated Hodgkin lymphoma patients, and 16 EBV-negative normal control subjects. We have established human-thymus/liver-SCID chimera, reaggregated thymic organ culture, and fetal thymic organ culture. We here show that the average frequency of total and CD8+ NKT cells in PBMCs from 128 healthy latent EBV-infected subjects is significantly higher than in 17 acute EBV infectious mononucleosis patients, 16 EBV-associated Hodgkin lymphoma patients, and 16 EBV-negative normal control subjects. However, the frequency of total and CD8+ NKT cells is remarkably increased in the acute EBV infectious mononucleosis patients at year 1 post-onset. EBV-challenge promotes CD8+ NKT cell development in the thymus of human-thymus/liver-SCID chimeras. The frequency of total (3% of thymic cells) and CD8+ NKT cells (∼25% of NKT cells) is significantly increased in EBV-challenged chimeras, compared to those in the unchallenged chimeras (<0.01% of thymic cells, CD8+ NKT cells undetectable, respectively). The EBV-induced increase in thymic NKT cells is also reflected in the periphery, where there is an increase in total and CD8+ NKT cells in liver and peripheral blood in EBV-challenged chimeras. EBV-induced thymic CD8+ NKT cells display an activated memory phenotype (CD69+CD45ROhiCD161+CD62Llo). After EBV-challenge, a proportion of NKT precursors diverges from DP thymocytes, develops and differentiates into mature CD8+ NKT cells in thymus in EBV-challenged human-thymus/liver-SCID chimeras or reaggregated thymic organ cultures. Thymic antigen-presenting EBV-infected dendritic cells are required for this process. IL-7, produced mainly by thymic dendritic cells, is a major and essential factor for CD8+ NKT cell differentiation in EBV-challenged human-thymus/liver-SCID chimeras and fetal thymic organ cultures. Additionally, these EBV-induced CD8+ NKT cells produce remarkably more perforin than that in counterpart CD4+ NKT cells, and predominately express CD8αα homodimer in their co-receptor. Thus, upon interaction with certain viruses, CD8 lineage-specific NKT cells are developed, differentiated and matured intrathymically, a finding with potential therapeutic importance against viral infections and tumors
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