3,160 research outputs found

    Formation of antiwaves in gap-junction-coupled chains of neurons

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    Using network models consisting of gap junction coupled Wang-Buszaki neurons, we demonstrate that it is possible to obtain not only synchronous activity between neurons but also a variety of constant phase shifts between 0 and \pi. We call these phase shifts intermediate stable phaselocked states. These phase shifts can produce a large variety of wave-like activity patterns in one-dimensional chains and two-dimensional arrays of neurons, which can be studied by reducing the system of equations to a phase model. The 2\pi periodic coupling functions of these models are characterized by prominent higher order terms in their Fourier expansion, which can be varied by changing model parameters. We study how the relative contribution of the odd and even terms affect what solutions are possible, the basin of attraction of those solutions and their stability. These models may be applicable to the spinal central pattern generators of the dogfish and also to the developing neocortex of the neonatal rat

    Comparative DNA methylome analysis of endometrial carcinoma reveals complex and distinct deregulation of cancer promoters and enhancers

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    BACKGROUND: Aberrant DNA methylation is a hallmark of many cancers. Classically there are two types of endometrial cancer, endometrioid adenocarcinoma (EAC), or Type I, and uterine papillary serous carcinoma (UPSC), or Type II. However, the whole genome DNA methylation changes in these two classical types of endometrial cancer is still unknown. RESULTS: Here we described complete genome-wide DNA methylome maps of EAC, UPSC, and normal endometrium by applying a combined strategy of methylated DNA immunoprecipitation sequencing (MeDIP-seq) and methylation-sensitive restriction enzyme digestion sequencing (MRE-seq). We discovered distinct genome-wide DNA methylation patterns in EAC and UPSC: 27,009 and 15,676 recurrent differentially methylated regions (DMRs) were identified respectively, compared with normal endometrium. Over 80% of DMRs were in intergenic and intronic regions. The majority of these DMRs were not interrogated on the commonly used Infinium 450K array platform. Large-scale demethylation of chromosome X was detected in UPSC, accompanied by decreased XIST expression. Importantly, we discovered that the majority of the DMRs harbored promoter or enhancer functions and are specifically associated with genes related to uterine development and disease. Among these, abnormal methylation of transposable elements (TEs) may provide a novel mechanism to deregulate normal endometrium-specific enhancers derived from specific TEs. CONCLUSIONS: DNA methylation changes are an important signature of endometrial cancer and regulate gene expression by affecting not only proximal promoters but also distal enhancers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-868) contains supplementary material, which is available to authorized users

    Precision measurement of the branching fractions of J/psi -> pi+pi-pi0 and psi' -> pi+pi-pi0

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    We study the decays of the J/psi and psi' mesons to pi+pi-pi0 using data samples at both resonances collected with the BES III detector in 2009. We measure the corresponding branching fractions with unprecedented precision and provide mass spectra and Dalitz plots. The branching fraction for J/psi -> pi+pi-pi0 is determined to be (2.137 +- 0.004 (stat.) +0.058-0.056 (syst.) +0.027-0.026 (norm.))*10-2, and the branching fraction for psi' -> pi+pi-pi0 is measured as (2.14 +- 0.03 (stat.) +0.08-0.07 (syst.) +0.09-0.08 (norm.))*10-4. The J/psi decay is found to be dominated by an intermediate rho(770) state, whereas the psi' decay is dominated by di-pion masses around 2.2 GeV/c2, leading to strikingly different Dalitz distributions.Comment: 15 pages, 2 figure

    Study of J/ψppˉJ/\psi\to p\bar{p} and J/ψnnˉJ/\psi\to n\bar{n}

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    The decays J/ψppˉJ/\psi\to p\bar{p} and J/ψnnˉJ/\psi\to n\bar{n} have been investigated with a sample of 225.2 million J/ψJ/\psi events collected with the BESIII detector at the BEPCII e+ee^+e^- collider. The branching fractions are determined to be B(J/ψppˉ)=(2.112±0.004±0.031)×103\mathcal{B}(J/\psi\to p\bar{p})=(2.112\pm0.004\pm0.031)\times10^{-3} and B(J/ψnnˉ)=(2.07±0.01±0.17)×103\mathcal{B}(J/\psi\to n\bar{n})=(2.07\pm0.01\pm0.17)\times10^{-3}. Distributions of the angle θ\theta between the proton or anti-neutron and the beam direction are well described by the form 1+αcos2θ1+\alpha\cos^2\theta, and we find α=0.595±0.012±0.015\alpha=0.595\pm0.012\pm0.015 for J/ψppˉJ/\psi\to p\bar{p} and α=0.50±0.04±0.21\alpha=0.50\pm0.04\pm0.21 for J/ψnnˉJ/\psi\to n\bar{n}. Our branching-fraction results suggest a large phase angle between the strong and electromagnetic amplitudes describing the J/ψNNˉJ/\psi\to N\bar{N} decay.Comment: 16 pages, 13 figures, the 2nd version, submitted to PR

    First observation of the M1 transition ψ(3686)γηc(2S)\psi(3686)\to \gamma\eta_c(2S)

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    Using a sample of 106 million \psi(3686) events collected with the BESIII detector at the BEPCII storage ring, we have made the first measurement of the M1 transition between the radially excited charmonium S-wave spin-triplet and the radially excited S-wave spin-singlet states: \psi(3686)\to\gamma\eta_c(2S). Analyses of the processes \psi(2S)\to \gamma\eta_c(2S) with \eta_c(2S)\to \K_S^0 K\pi and K^+K^-\pi^0 gave an \eta_c(2S) signal with a statistical significance of greater than 10 standard deviations under a wide range of assumptions about the signal and background properties. The data are used to obtain measurements of the \eta_c(2S) mass (M(\eta_c(2S))=3637.6\pm 2.9_\mathrm{stat}\pm 1.6_\mathrm{sys} MeV/c^2), width (\Gamma(\eta_c(2S))=16.9\pm 6.4_\mathrm{stat}\pm 4.8_\mathrm{sys} MeV), and the product branching fraction (\BR(\psi(3686)\to \gamma\eta_c(2S))\times \BR(\eta_c(2S)\to K\bar K\pi) = (1.30\pm 0.20_\mathrm{stat}\pm 0.30_\mathrm{sys})\times 10^{-5}). Combining our result with a BaBar measurement of \BR(\eta_c(2S)\to K\bar K \pi), we find the branching fraction of the M1 transition to be \BR(\psi(3686)\to\gamma\eta_c(2S)) = (6.8\pm 1.1_\mathrm{stat}\pm 4.5_\mathrm{sys})\times 10^{-4}.Comment: 7 pages, 1 figure, 1 tabl

    Observation of a charged charmoniumlike structure in e+e(DDˉ)±πe^+e^- \to (D^{*} \bar{D}^{*})^{\pm} \pi^\mp at s=4.26\sqrt{s}=4.26GeV

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    We study the process e+e(DDˉ)±πe^+e^- \to (D^{*} \bar{D}^{*})^{\pm} \pi^\mp at a center-of-mass energy of 4.26GeV using a 827pb1^{-1} data sample obtained with the BESIII detector at the Beijing Electron Positron Collider. Based on a partial reconstruction technique, the Born cross section is measured to be (137±9±15)(137\pm9\pm15)pb. We observe a structure near the (DDˉ)±(D^{*} \bar{D}^{*})^{\pm} threshold in the π\pi^\mp recoil mass spectrum, which we denote as the Zc±(4025)Z^{\pm}_c(4025). The measured mass and width of the structure are (4026.3±2.6±3.7)(4026.3\pm2.6\pm3.7)MeV/c2^2 and (24.8±5.6±7.7)(24.8\pm5.6\pm7.7)MeV, respectively. Its production ratio σ(e+eZc±(4025)π(DDˉ)±π)σ(e+e(DDˉ)±π)\frac{\sigma(e^+e^-\to Z^{\pm}_c(4025)\pi^\mp \to (D^{*} \bar{D}^{*})^{\pm} \pi^\mp)}{\sigma(e^+e^-\to (D^{*} \bar{D}^{*})^{\pm} \pi^\mp)} is determined to be 0.65±0.09±0.060.65\pm0.09\pm0.06. The first uncertainties are statistical and the second are systematic.Comment: 7 pages, 4 figures, 1 table; version accepted to be published in PR

    Search for Baryonic Decays of \psi(3770) and \psi(4040)

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    By analyzing data samples of 2.9 fb^{-1} collected at \sqrt s=3.773 GeV, 482 pb^{-1} collected at \sqrt s=4.009 GeV and 67 pb^{-1} collected at \sqrt s=3.542, 3.554, 3.561, 3.600 and 3.650 GeV with the BESIII detector at the BEPCII storage ring, we search for \psi(3770) and \psi(4040) decay to baryonic final states, including \Lambda\bar\Lambda\pi^+\pi^-, \Lambda \bar\Lambda\pi^0, \Lambda\bar\Lambda\eta, \Sigma^+ \bar\Sigma^-, \Sigma^0 \bar\Sigma^0, \Xi^-\bar\Xi^+ and \Xi^0\bar\Xi^0 decays. None are observed, and upper limits are set at the 90% confidence level.Comment: 9 pages, 3 figure

    Observation of χc1\chi_{c1} decays into vector meson pairs ϕϕ\phi\phi, ωω\omega\omega, and ωϕ\omega\phi

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    Decays of χc1\chi_{c1} to vector meson pairs ϕϕ\phi\phi, ωω\omega\omega and ωϕ\omega\phi are observed for the first time using (106±4)×106(106\pm4)\times 10^6 \psip events accumulated at the BESIII detector at the BEPCII e+ee^+e^- collider. The branching fractions are measured to be (4.4±0.3±0.5)×104(4.4\pm 0.3\pm 0.5)\times 10^{-4}, (6.0±0.3±0.7)×104(6.0\pm 0.3\pm 0.7)\times 10^{-4}, and (2.2±0.6±0.2)×105(2.2\pm 0.6\pm 0.2)\times 10^{-5}, for χc1ϕϕ\chi_{c1}\to \phi\phi, ωω\omega\omega, and ωϕ\omega\phi, respectively. The observation of χc1\chi_{c1} decays into a pair of vector mesons ϕϕ\phi\phi, ωω\omega\omega and ωϕ\omega\phi indicates that the hadron helicity selection rule is significantly violated in χcJ\chi_{cJ} decays. In addition, the measurement of χcJωϕ\chi_{cJ}\to \omega\phi gives the rate of doubly OZI-suppressed decay. Branching fractions for χc0\chi_{c0} and χc2\chi_{c2} decays into other vector meson pairs are also measured with improved precision.Comment: 4 pages, 2 figure
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