853 research outputs found

    Thioamides. XI. The Preparation of 5-Bromo-2-thiofuramides

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    A number of 5-bromo-2-furamides, obtained from 5-bromo- 2-furoyl chloride and ammonia or various amines, have been converted to corresponding thioamides by thiation with phosphorus pentasulfide in dry dioxane

    Thioamides. XI. The Preparation of 5-Bromo-2-thiofuramides

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    A number of 5-bromo-2-furamides, obtained from 5-bromo- 2-furoyl chloride and ammonia or various amines, have been converted to corresponding thioamides by thiation with phosphorus pentasulfide in dry dioxane

    Molecular diagnostic and genetic characterization of highly pathogenic viruses: application during Crimean–Congo haemorrhagic fever virus outbreaks in Eastern Europe and the Middle East

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    AbstractSeveral haemorrhagic fevers are caused by highly pathogenic viruses that must be handled in Biosafety level 4 (BSL–4) containment. These zoonotic infections have an important impact on public health and the development of a rapid and differential diagnosis in case of outbreak in risk areas represents a critical priority. We have demonstrated the potential of a DNA resequencing microarray (PathogenID v2.0) for this purpose. The microarray was first validated in vitro using supernatants of cells infected with prototype strains from five different families of BSL-4 viruses (e.g. families Arenaviridae, Bunyaviridae, Filoviridae, Flaviviridae and Paramyxoviridae). RNA was amplified based on isothermal amplification by Phi29 polymerase before hybridization. We were able to detect and characterize Nipah virus and Crimean–Congo haemorrhagic fever virus (CCHFV) in the brains of experimentally infected animals. CCHFV was finally used as a paradigm for epidemics because of recent outbreaks in Turkey, Kosovo and Iran. Viral variants present in human sera were characterized by BLASTN analysis. Sensitivity was estimated to be 105–106 PFU/mL of hybridized cDNA. Detection specificity was limited to viral sequences having ˜13–14% of global divergence with the tiled sequence, or stretches of ˜20 identical nucleotides. These results highlight the benefits of using the PathogenID v2.0 resequencing microarray to characterize geographical variants in the follow-up of haemorrhagic fever epidemics; to manage patients and protect communities; and in cases of bioterrorism

    Observation of D0ρ0γD^0\to \rho^0\gamma and search for CPCP violation in radiative charm decays

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    We report the first observation of the radiative charm decay D0ρ0γD^0 \to \rho^0 \gamma and the first search for CPCP violation in decays D0ρ0γD^0 \to \rho^0 \gamma, ϕγ\phi\gamma, and K0γ\overline{K}{}^{*0} \gamma, using a data sample of 943 fb1^{-1} collected with the Belle detector at the KEKB asymmetric-energy e+ee^+e^- collider. The branching fraction is measured to be B(D0ρ0γ)=(1.77±0.30±0.07)×105\mathcal{B}(D^0 \to \rho^0 \gamma)=(1.77 \pm 0.30 \pm 0.07) \times 10^{-5}, where the first uncertainty is statistical and the second is systematic. The obtained CPCP asymmetries, ACP(D0ρ0γ)=+0.056±0.152±0.006\mathcal{A}_{CP}(D^0 \to \rho^0 \gamma)=+0.056 \pm 0.152 \pm 0.006, ACP(D0ϕγ)=0.094±0.066±0.001\mathcal{A}_{CP}(D^0 \to \phi \gamma)=-0.094 \pm 0.066 \pm 0.001, and ACP(D0K0γ)=0.003±0.020±0.000\mathcal{A}_{CP}(D^0 \to \overline{K}{}^{*0} \gamma)=-0.003 \pm 0.020 \pm 0.000, are consistent with no CPCP violation. We also present an improved measurement of the branching fractions B(D0ϕγ)=(2.76±0.19±0.10)×105\mathcal{B}(D^0 \to \phi \gamma)=(2.76 \pm 0.19 \pm 0.10) \times 10^{-5} and B(D0K0γ)=(4.66±0.21±0.21)×104\mathcal{B}(D^0 \to \overline{K}{}^{*0} \gamma)=(4.66 \pm 0.21 \pm 0.21) \times 10^{-4}

    Evidence for B- -> Ds+ K- l- nubar and search for B- -> Ds*+ K- l- nubar

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    We report measurements of the decays B- -> Ds(*)+ K- l- nubar in a data sample containing 657x10^6 BBbar pairs collected with the Belle detector at the KEKB asymmetric-energy e+e- collider. We observe a signal with a significance of 6 sigma for the combined Ds and Ds* modes and find the first evidence of the B- -> Ds+ K- l- nubar decay with a significance of 3.4 sigma. We measure the following branching fractions: BF(B- -> Ds+ K- l nubar) = (0.30 +/- 0.09(stat) +0.11 -0.08(syst)) x 10^-3 and BF(B- -> Ds*+ K- l- nubar) = (0.59 +/- 0.12(stat) +/- 0.15(syst)) x 10^-3 and set an upper limit BF(B- -> Ds*+ K- l- nubar) < 0.56 x 10^-3 at the 90% confidence level. We also present the first measurement of the Ds+K- invariant mass distribution in these decays, which is dominated by a prominent peak around 2.6 GeV/c^2.Comment: Submitted to Phys. Rev.

    Observation of D0Dˉ0D^0-\bar{D}^0 Mixing in e+ee^+e^- Collisions

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    We observe D0Dˉ0D^0-\bar{D}^0 mixing in the decay D0K+πD^0\rightarrow K^+\pi^- using a data sample of integrated luminosity 976 fb1^{-1} collected with the Belle detector at the KEKB e+ee^+e^- asymmetric-energy collider. We measure the mixing parameters x2=(0.09±0.22)×103{x'}^2 = (0.09\pm0.22)\times 10^{-3} and y=(4.6±3.4)×103y' = (4.6\pm3.4)\times 10^{-3} and the ratio of doubly Cabibbo-suppressed to Cabibbo-favored decay rates RD=(3.53±0.13)×103R_D = (3.53\pm0.13)\times 10^{-3}, where the uncertainties are statistical and systematic combined. Our measurement excludes the no-mixing hypothesis at the 5.1 standard deviation level.Comment: 6 pages, 4 figure

    Energy scan of the e+ehb(nP)π+πe^+e^- \to h_b(nP)\pi^+\pi^- (n=1,2)(n=1,2) cross sections and evidence for Υ(11020)\Upsilon(11020) decays into charged bottomonium-like states

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    Using data collected with the Belle detector at the KEKB asymmetric-energy e+ee^+e^- collider, we measure the energy dependence of the e+ehb(nP)π+πe^+e^- \to h_b(nP)\pi^+\pi^- (n=1,2)(n=1,2) cross sections from thresholds up to 11.0211.02\,GeV. We find clear Υ(10860)\Upsilon(10860) and Υ(11020)\Upsilon(11020) peaks with little or no continuum contribution. We study the resonant substructure of the Υ(11020)hb(nP)π+π\Upsilon(11020) \to h_b(nP)\pi^+\pi^- transitions and find evidence that they proceed entirely via the intermediate isovector states Zb(10610)Z_b(10610) and Zb(10650)Z_b(10650). The relative fraction of these states is loosely constrained by the current data: the hypothesis that only Zb(10610)Z_b(10610) is produced is excluded at the level of 3.3 standard deviations, while the hypothesis that only Zb(10650)Z_b(10650) is produced is not excluded at a significant level.Comment: 8 pages, 4 figures, submitted to Physical Review Letter

    Arthroscopic removal of an osteoid osteoma of the acetabulum

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    In this case report, we describe the arthroscopic removal of an osteoid osteoma from the acetabulum in a young adolescent. After identifying the osteoid osteoma close to the cartilage with MRI and CT investigations, we decided that in this case, arthroscopic removal was the best treatment. In the case of an osteoid osteoma in the acetabulum close to the cartilage, arthroscopic removal should be considered as one can treat the associated osteochondritic lesion during this procedure
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