785 research outputs found

    Large Extra Dimensions at Linear Colliders

    Get PDF
    In this talk, I first present the motivation for theories wherein extra spacetime dimensions can be compactified to have large magnitudes. In particular, I discuss the Arkani-Hamed, Dimopoulos, Dvali (ADD) scenario. I present the constraints that have been derived on these models from current experiments and the expectations from future colliders. I concentrate particularly on the possibilities of probing these extra dimensions at future linear colliders.Comment: Talk given at the Third International Workshop on Electron-Electron Interactions at TeV Energies (e- e- 99), Santa Cruz, California, 10-12 Dec 1999. 7 pages, LaTeX, style files attache

    Spin configuration of top quark pair production with large extra dimensions at photon-photon colliders

    Get PDF
    Top quark pair production at photon-photon colliders is studied in low scale quantum gravity scenario. From the dependence of the cross sections on the spin configuration of the top quark and anti-quark, we introduce a new observable, top spin asymmetry. It is shown that there exists a special top spin basis where with the polarized parent electron beams the top spin asymmetry vanishes in the standard model but retains substantial values with the large extra dimension effects. We also present lower bounds of the quantum gravity scale MSM_S from total cross sections with various combinations of the laser, electron beam, and top quark pair polarizations. The measurements of the top spin state (t↑tˉ↓)(t_\uparrow\bar{t}_\downarrow) with unpolarized initial beams are shown to be most effective, enhancing by about 5% the MSM_S bounds with respect to totally unpolarized case.Comment: 18 pages, 4 figures, ReVTe

    Patients with refractory cytomegalovirus (CMV) infection following allogeneic haematopoietic stem cell transplantation are at high risk for CMV disease and non-relapse mortality

    Get PDF
    AbstractPre-emptive therapy is an effective approach for cytomegalovirus (CMV) control; however, refractory CMV still occurs in a considerable group of recipients after allogeneic haematopoietic stem cell transplantation (allo-HSCT). Until now, hardly any data have been available about the clinical characteristics and risk factors of refractory CMV, or its potential harmful impact on the clinical outcome following allo-HSCT. We studied transplant factors affecting refractory CMV in the 100 days after allo-HSCT, and the impact of refractory CMV on the risk of CMV disease and non-relapse mortality (NRM). We retrospectively studied 488 consecutive patients with CMV infection after allo-HSCT. Patients with refractory CMV in the 100 days after allo-HSCT had a higher incidence of CMV disease and NRM than those without refractory CMV (11.9% vs. 0.8% and 17.1% vs. 8.3%, respectively). Multivariate analysis showed that refractory CMV infection in the 100 days after allo-HSCT was an independent risk factor for CMV disease (hazard ratio (HR) 10.539, 95% CI 2.467–45.015, p 0.001), and that refractory CMV infection within 60–100 days after allo-HSCT was an independent risk factor for NRM (HR 8.435, 95% CI 1.511–47.099, p 0.015). Clinical factors impacting on the risk of refractory CMV infection included receiving transplants from human leukocyte antigen-mismatched family donors (HR 2.012, 95% CI 1.603–2.546, p <0.001) and acute graft-versus-host disease (HR 1.905, 95% CI 1.352–2.686, p <0.001). We conclude that patients with refractory CMV infection during the early stage after allo-HSCT are at high risk for both CMV disease and NRM

    Direct Signals for Large Extra Dimensions in the Production of Fermion Pairs at Linear Colliders

    Get PDF
    We analyze the potentiality of the new generation of e+e−e^+e^- linear colliders to search for large extra dimensions via the production of fermion pairs in association with Kaluza-Klein gravitons (G), i.e. e+e−←ffˉGe^+e^- \leftarrow f\bar{f}G. This process leads to a final state exhibiting a significant amount of missing energy in addition to acoplanar lepton or jet pairs. We study in detail this reaction using full tree level contibutions due to the graviton emission and the standard model backgrounds. After choosing the cuts to enhance the signal, we show that a linear collider with a center-of-mass energy of 500 GeV will be able to probe quantum gravity scales from 0.96(0.86) up to 4.1(3.3) TeV at 2(5)σ\sigma level, depending on the number of extra dimensions.Comment: 19 pages, 5 figures. Using RevTex, axodraw.sty. Discussion was extended. No changes in the results. Accepted for publication by Phys. Rev.

    Kaluza-Klein gravitino production with a single photon at e^+ e^- colliders

    Full text link
    In a supersymmetric large extra dimension scenario, the production of Kaluza-Klein gravitinos accompanied by a photino at e^+ e^- colliders is studied. We assume that a bulk supersymmetry is softly broken on our brane such that the low-energy theory resembles the MSSM. Low energy supersymmetry breaking is further assumed as in GMSB, leading to sub-eV mass shift in each KK mode of the gravitino from the corresponding graviton KK mode. Since the photino decays within a detector due to its sufficiently large inclusive decay rate into a photon and a gravitino, the process e^+ e^- -> photino + gravitino yields single photon events with missing energy. Even if the total cross section can be substantial at sqrt(s)=500 GeV, the KK graviton background of e^+ e^- -> photon + graviton is kinematically advantageous and thus much larger. It is shown that the observable, sigma(e^-_L)-sigma(e^-_R), can completely eliminate the KK graviton background but retain most of the KK gravitino signal, which provides a unique and robust method to probe the supersymmetric bulk.Comment: Reference added and typos correcte

    Testing the Nature of Kaluza-Klein Excitations at Future Lepton Colliders

    Get PDF
    With one extra dimension, current high precision electroweak data constrain the masses of the first Kaluza-Klein excitations of the Standard Model gauge fields to lie above ≃4\simeq 4 TeV. States with masses not much larger than this should be observable at the LHC. However, even for first excitation masses close to this lower bound, the second set of excitations will be too heavy to be produced thus eliminating the possibility of realizing the cleanest signature for KK scenarios. Previous studies of heavy Zâ€ČZ' and Wâ€ČW' production in this mass range at the LHC have demonstrated that very little information can be obtained about their couplings to the conventional fermions given the limited available statistics and imply that the LHC cannot distinguish an ordinary Zâ€ČZ' from the degenerate pair of the first KK excitations of the Îł\gamma and ZZ. In this paper we discuss the capability of lepton colliders with center of mass energies significantly below the excitation mass to resolve this ambiguity. In addition, we examine how direct measurements obtained on and near the top of the first excitation peak at lepton colliders can confirm these results. For more than one extra dimension we demonstrate that it is likely that the first KK excitation is too massive to be produced at the LHC.Comment: 38 pages, 10 Figs, LaTex, comments adde

    t→bWt \to b W in NonCommutative Standard Model

    Full text link
    We study the top quark decay to b quark and W boson in the NonCommutative Standard Model (NCSM). The lowest contribution to the decay comes from the terms quadratic in the matrix describing the noncommutative (NC) effects while the linear term is seen to identically vanish because of symmetry. The NC effects are found to be significant only for low values of the NC characteristic scale.Comment: 11 page Latex file containing 2 eps figures (redrawn). More discussion included. To appear in PR

    Modeling manufacturing processes using a genetic programming-based fuzzy regression with detection of outliers

    Get PDF
    Fuzzy regression (FR) been demonstrated as a promising technique for modeling manufacturing processes where availability of data is limited. FR can only yield linear type FR models which have a higher degree of fuzziness, but FR ignores higher order or interaction terms and the influence of outliers, all of which usually exist in the manufacturing process data. Genetic programming (GP), on the other hand, can be used to generate models with higher order and interaction terms but it cannot address the fuzziness of the manufacturing process data. In this paper, genetic programming-based fuzzy regression (GP-FR), which combines the advantages of the two approaches to overcome the deficiencies of the commonly used existing modeling methods, is proposed in order to model manufacturing processes. GP-FR uses GP to generate model structures based on tree representation which can represent interaction and higher order terms of models, and it uses an FR generator based on fuzzy regression to determine outliers in experimental data sets. It determines the contribution and fuzziness of each term in the model by using experimental data excluding the outliers. To evaluate the effectiveness of GP-FR in modeling manufacturing processes, it was used to model a non-linear system and an epoxy dispensing process. The results were compared with those based on two commonly used FR methods, Tanka's FR and Peters' FR. The prediction accuracy of the models developed based on GP-FR was shown to be better than that of models based on the other two FR methods

    Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma

    Get PDF
    Cutaneous squamous cell carcinoma (SCC) is one of the most common cancers in the United States. Previous genome-wide association studies (GWAS) have identified 14 single nucleotide polymorphisms (SNPs) associated with cutaneous SCC. Here, we report the largest cutaneous SCC meta-analysis to date, representing six international cohorts and totaling 19,149 SCC cases and 680,049 controls. We discover eight novel loci associated with SCC, confirm all previously associated loci, and perform fine mapping of causal variants. The novel SNPs occur within skin-specific regulatory elements and implicate loci involved in cancer development, immune regulation, and keratinocyte differentiation in SCC susceptibility
    • 

    corecore