Target Design for XUV Probing of Radiative Shock Experiments

Radiative shocks are strong shocks characterized by plasma at a high temperature emitting an important fraction of its energy as radiation. Radiative shocks are commonly found in many astrophysical systems and are templates of radiative hydrodynamic flows, which can be studied experimentally using high-power lasers. This is not only important in the context of laboratory astrophysics but also to benchmark numerical studies. We present details on the design of experiments on radiative shocks in xenon gas performed at the kJ scale PALS laser facility. It includes technical specifications for the tube targets design and numerical studies with the 1-D radiative hydrodynamics code MULTI. Emphasis is given to the technical feasibility of an XUV imaging diagnostic with a 21 nm (~58 eV) probing beam, which allows to probe simultaneously the post-shock and the precursor region ahead of the shock. The novel design of the target together with the improved X-ray optics and XUV source allow to show both the dense post-shock structure and the precursor of the radiative shock.Comment: 12 pages, 4 figure

The decay Z -> neutrino antineutrino photon in the Standard Model

A complete study of the one-loop induced decay Z -> neutrino antineutrino photon is presented within the framework of the Standard Model. The advantages of using a nonlinear gauge are stressed. We have found that the main contributions come from the electric dipole and the magnetic dipole transitions of the Z gauge boson and the neutrino, respectively. We obtain a branching ratio B=7.16E-10, which is about four orders of magnitude smaller than the bound recentely obtained by the L3 collaboration and thus it leaves open a window to search for new physics effects in single-photon decays of the Z boson.Comment: REVTEX,15 pp, 5 eps figures, Approved for publication in Physical Review

Signatures of the anomalous ZγZ\gamma and ZZ production at the lepton and hadron Colliders

The possible form of New Physics (NP) interactions affecting the ZZZ, $ZZ \gamma$ and $Z\gamma \gamma$ vertices, is critically examined. Their signatures and the possibilities to study them, through ZZ and $Z\gamma$ production, at the e^-e^+ Colliders LEP and LC and at the hadronic Colliders Tevatron and LHC, are investigated. Experimental limits obtained or expected on each coupling are collected. A simple theoretical model based on virtual effects due to some heavy fermions is used for acquiring some guidance on the plausible forms of these NP vertices. In such a case specific relations among the various neutral couplings are predicted, which can be experimentally tested and possibly used to constrain the form of the responsible NP structure.Comment: 17 pages and 9 figures, version to appear in Phys. ReV. e-mail: [email protected]

Production of the neutral toppion at the e gamma colliders

In the framework of topcolor-assisted technicolor(TC2) model, we study a neutral toppion production process $e^{-}\gamma\to e^{-}\Pi^{0}_{t}$ in this paper. Our results show that the production cross section of $e^{-}\gamma\to e^{-}\Pi^{0}_{t}$ can reach the level of several tens fb, and over $10^{3}$ neutral toppion events can be produced in the planned $e^+e^-$ linear colliders each year. Therefore, such a toppion production process provides us a unique chance to detect toppion events and test the TC2 model. On the other hand, the cross section of $e^{-}\gamma\to e^{-}\Pi^{0}_{t}$ is about one order of magnitude larger than those of some similar processes in SM and MSSM(i.e., $e^{-}\gamma\to e^{-}H$ in SM and $e^{-}\gamma\to e^{-}H^{0}(A^0,h^0)$ in MSSM). So, we can easily distinguish the neutral toppion from other neutral Higgs bosons in SM and MSSM.Comment: 12 pages, 4 figures, The paper has been accepted by Phys.Rev.

Probing the charged Higgs boson at the LHC in the CP-violating type-II 2HDM

We present a phenomenological study of a CP-violating two-Higgs-doublet Model with type-II Yukawa couplings at the Large Hadron Collider (LHC). In the light of recent LHC data, we focus on the parameter space that survives the current and past experimental constraints as well as theoretical bounds on the model. Once the phenomenological scenario is set, we analyse the scope of the LHC in exploring this model through the discovery of a charged Higgs boson produced in association with a W boson, with the former decaying into the lightest neutral Higgs and a second W state, altogether yielding a b\bar b W^+W^- signature, of which we exploit the W^+W^- semileptonic decays.Comment: 37 pages, 16 figures; v2 updated treatment of LHC constraint

Very light CP-odd scalar in the Two-Higgs-Doublet Model

We show that a general two-Higgs-doublet model (THDM) with a very light CP-odd scalar (A) can be compatible with the rho parameter, Br(b --> s\gamma), R_b, A_b, (g-2) of muon, Br(Upsilon --> A gamma), and the direct search via the Yukawa process at LEP. For its mass around 0.2 GeV, the muon (g-2) and Br(Upsilon --> A \gamma) data require tan(beta) to be about 1. Consequently, A can behave like a fermiophobic CP-odd scalar and predominantly decay into a photon pair ("gamma gamma"), which registers in detectors of high energy collider experiments as a single photon signature when the momentum of A is large. We compute the partial decay width of Z --> A A A and the production rate of f \bar{f} --> Z A A --> Z +"gamma gamma", f^' {\bar f} --> W^{\pm} A A --> W^\pm + "gamma gamma" and f \bar f --> H^+ H^- --> W^+ W^- A A --> W^+ W^- + "gamma gamma" at high energy colliders such as LEP, Tevatron, LHC, and future Linear Colliders. Other production mechanisms of a light A, such as gg --> h --> AA --> "gamma gamma", are also discussed.Comment: Some improvementes, references updated, 3 new figures, one new appendix, abstract and conclusions unchaged. Version to appear in Physical Review

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.

To identify genetic loci influencing central obesity and fat distribution, we performed a meta-analysis of 16 genome-wide association studies (GWAS, N = 38,580) informative for adult waist circumference (WC) and waist-hip ratio (WHR). We selected 26 SNPs for follow-up, for which the evidence of association with measures of central adiposity (WC and/or WHR) was strong and disproportionate to that for overall adiposity or height. Follow-up studies in a maximum of 70,689 individuals identified two loci strongly associated with measures of central adiposity; these map near TFAP2B (WC, P = 1.9x10(-11)) and MSRA (WC, P = 8.9x10(-9)). A third locus, near LYPLAL1, was associated with WHR in women only (P = 2.6x10(-8)). The variants near TFAP2B appear to influence central adiposity through an effect on overall obesity/fat-mass, whereas LYPLAL1 displays a strong female-only association with fat distribution. By focusing on anthropometric measures of central obesity and fat distribution, we have identified three loci implicated in the regulation of human adiposity

Anti-HIV-1 activity of cellulose acetate phthalate: Synergy with soluble CD4 and induction of "dead-end" gp41 six-helix bundles

BACKGROUND: Cellulose acetate phthalate (CAP), a promising candidate microbicide for prevention of sexual transmission of the human immunodeficiency virus type 1 (HIV-1) and other sexually transmitted disease (STD) pathogens, was shown to inactivate HIV-1 and to block the coreceptor binding site on the virus envelope glycoprotein gp120. It did not interfere with virus binding to CD4. Since CD4 is the primary cellular receptor for HIV-1, it was of interest to study CAP binding to HIV-1 complexes with soluble CD4 (sCD4) and its consequences, including changes in the conformation of the envelope glycoprotein gp41 within virus particles. METHODS: Enzyme-linked immunosorbent assays (ELISA) were used to study CAP binding to HIV-1-sCD4 complexes and to detect gp41 six-helix bundles accessible on virus particles using antibodies specific for the α-helical core domain of gp41. RESULTS: 1) Pretreatment of HIV-1 with sCD4 augments subsequent binding of CAP; 2) there is synergism between CAP and sCD4 for inhibition of HIV-1 infection; 3) treatment of HIV-1 with CAP induced the formation of gp41 six-helix bundles. CONCLUSIONS: CAP and sCD4 bind to distinct sites on HIV-1 IIIB and BaL virions and their simultaneous binding has profound effects on virus structure and infectivity. The formation of gp41 six-helical bundles, induced by CAP, is known to render the virus incompetent for fusion with target cells thus preventing infection

Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways

OBJECTIVE Glycated hemoglobin (HbA1c), used to monitor and diagnose diabetes, is influenced by average glycemia over a 2- to 3-month period. Genetic factors affecting expression, turnover, and abnormal glycation of hemoglobin could also be associated with increased levels of HbA1c. We aimed to identify such genetic factors and investigate the extent to which they influence diabetes classification based on HbA1c levels. RESEARCH DESIGN AND METHODS We studied associations with HbA1c in up to 46,368 nondiabetic adults of European descent from 23 genome-wide association studies (GWAS) and 8 cohorts with de novo genotyped single nucleotide polymorphisms (SNPs). We combined studies using inverse-variance meta-analysis and tested mediation by glycemia using conditional analyses. We estimated the global effect of HbA1c loci using a multilocus risk score, and used net reclassification to estimate genetic effects on diabetes screening. RESULTS Ten loci reached genome-wide significant association with HbA1c, including six new loci near FN3K (lead SNP/P value, rs1046896/P = 1.6 × 10−26), HFE (rs1800562/P = 2.6 × 10−20), TMPRSS6 (rs855791/P = 2.7 × 10−14), ANK1 (rs4737009/P = 6.1 × 10−12), SPTA1 (rs2779116/P = 2.8 × 10−9) and ATP11A/TUBGCP3 (rs7998202/P = 5.2 × 10−9), and four known HbA1c loci: HK1 (rs16926246/P = 3.1 × 10−54), MTNR1B (rs1387153/P = 4.0 × 10−11), GCK (rs1799884/P = 1.5 × 10−20) and G6PC2/ABCB11 (rs552976/P = 8.2 × 10−18). We show that associations with HbA1c are partly a function of hyperglycemia associated with 3 of the 10 loci (GCK, G6PC2 and MTNR1B). The seven nonglycemic loci accounted for a 0.19 (% HbA1c) difference between the extreme 10% tails of the risk score, and would reclassify ∼2% of a general white population screened for diabetes with HbA1c. CONCLUSIONS GWAS identified 10 genetic loci reproducibly associated with HbA1c. Six are novel and seven map to loci where rarer variants cause hereditary anemias and iron storage disorders. Common variants at these loci likely influence HbA1c levels via erythrocyte biology, and confer a small but detectable reclassification of diabetes diagnosis by HbA1c