257 research outputs found

    Inclusive double-quarkonium production at the Large Hadron Collider

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    Based on the nonrelativistic QCD (NRQCD) factorization formalism, we investigate inclusive productions of two spin-triplet S-wave quarkonia pp->2J/psi+X, 2Upsilon+X, and J/psi+Upsilon+X at the CERN Large Hadron Collider. The total production rates integrated over the rapidity (y) and transverse-momentum (p_T) ranges |y|<2.4 and p_T<50 GGeV are predicted to be sigma[pp->2J/psi+X] = 22 (35) nb, sigma[pp->2Upsilon+X] = 24 (49) pb, and sigma[pp->J/psi+Upsilon+X] = 7 (13) pb at the center-of-momentum energy sqrt{s} = 7 (14) TeV. In order to provide predictions that can be useful in both small- and large-p_T regions, we do not employ the fragmentation approximation and we include the spin-triplet S-wave color-singlet and color-octet channels for each quarkonium final state at leading order in the strong coupling. The p_T distributions of pp->2J/psi+X and 2Upsilon+X in the low-p_T region are dominated by the color-singlet contributions. At leading order in the strong coupling, the color-singlet channel is absent for pp->J/psi+Upsilon+X. Therefore, the process pp->J/psi+Upsilon+X may provide a useful probe to the color-octet mechanism of NRQCD.Comment: 26 pages, 7 figures, 3 tables, version published in JHE

    P-wave Quarkonium Decays to Meson Pairs

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    The processes of P-wave Quarkonium exclusive decays to two mesons are investigated, in which the final state vector mesons with various polarizations are considered separately. In the calculation, the initial heavy quarkonia are treated in the framework of non-relativistic quantum chromodynamics, whereas for light mesons, the light cone distribution amplitudes up to twist-3 are employed. It turns out that the higher twist contribution is significant and provides a possible explanation for the observation of the hadron helicity selection rule violated processes χc1ϕϕ,ωω\chi_{c1}\rightarrow \phi\phi,\omega\omega by the BESIII collaboration in recently. We also evaluate the χb1J/ψJ/ψ\chi_{b1}\to J/\psi J/\psi process and find that its branching ratio is big enough to be measured at the B-factories.Comment: more results and discussions adde

    The NLO QCD Corrections to BcB_c Meson Production in Z0Z^0 Decays

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    The decay width of Z0Z^0 to BcB_c meson is evaluated at the next-to-leading order(NLO) accuracy in strong interaction. Numerical calculation shows that the NLO correction to this process is remarkable. The quantum chromodynamics(QCD)renormalization scale dependence of the results is obviously depressed, and hence the uncertainties lying in the leading order calculation are reduced.Comment: 14 pages, 7 figures; references added; expressions and typos ammende

    QCD corrections to J/ψJ/\psi plus Z0Z^0-boson production at the LHC

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    The J/ψ+Z0J/\psi+Z^0 associated production at the LHC is an important process in investigating the color-octet mechanism of non-relativistic QCD in describing the processes involving heavy quarkonium. We calculate the next-to-leading order (NLO) QCD corrections to the J/ψ+Z0J/\psi +Z^0 associated production at the LHC within the factorization formalism of nonrelativistic QCD, and provide the theoretical predictions for the distribution of the J/ψJ/\psi transverse momentum. Our results show that the differential cross section at the leading-order is significantly enhanced by the NLO QCD corrections. We conclude that the LHC has the potential to verify the color-octet mechanism by measuring the J/ψ+Z0J/\psi+Z^0 production events.Comment: 14 page revtex, 5 eps figures, to appear in JHEP. fig5 and the corresponding analysis are correcte

    O(αs)O(\alpha_s) corrections to J/ψ+χcJJ/\psi+\chi_{cJ} production at BB factories

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    We investigate the O(αs){\cal O}(\alpha_s) corrections to e+eJ/ψ(ψ)+χcJe^+e^-\to J/\psi(\psi')+\chi_{cJ} (J=0,1,2J=0,1,2) in the NRQCD factorization approach. These next-to-leading order (NLO) corrections are calculated at the level of helicity amplitude. We have made a detailed analysis for both polarized and unpolarized cross sections, and compared our predictions with the measurements at the BB factories. We also derive the asymptotic expressions for each of the NLO helicity amplitudes, and confirm the earlier speculation that at NLO in αs\alpha_s, the double logarithm of type ln2(s/mc2)\ln^2 (s/m_c^2) appearing in the NRQCD short-distance coefficient is always associated with the helicity-suppressed channels.Comment: v3, 18+3 pages, 6 figures, 3 tables; some formulas corrected, erratum adde

    Neuronal circuitry for pain processing in the dorsal horn

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    Neurons in the spinal dorsal horn process sensory information, which is then transmitted to several brain regions, including those responsible for pain perception. The dorsal horn provides numerous potential targets for the development of novel analgesics and is thought to undergo changes that contribute to the exaggerated pain felt after nerve injury and inflammation. Despite its obvious importance, we still know little about the neuronal circuits that process sensory information, mainly because of the heterogeneity of the various neuronal components that make up these circuits. Recent studies have begun to shed light on the neuronal organization and circuitry of this complex region

    Glycine insertion makes yellow fluorescent protein sensitive to hydrostatic pressure

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    Fluorescent protein-based indicators for intracellular environment conditions such as pH and ion concentrations are commonly used to study the status and dynamics of living cells. Despite being an important factor in many biological processes, the development of an indicator for the physicochemical state of water, such as pressure, viscosity and temperature, however, has been neglected. We here found a novel mutation that dramatically enhances the pressure dependency of the yellow fluorescent protein (YFP) by inserting several glycines into it. The crystal structure of the mutant showed that the tyrosine near the chromophore flipped toward the outside of the β-can structure, resulting in the entry of a few water molecules near the chromophore. In response to changes in hydrostatic pressure, a spectrum shift and an intensity change of the fluorescence were observed. By measuring the fluorescence of the YFP mutant, we succeeded in measuring the intracellular pressure change in living cell. This study shows a new strategy of design to engineer fluorescent protein indicators to sense hydrostatic pressure

    Glomerular angiotensinogen protein is enhanced in pediatric IgA nephropathy

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    Enhanced intrarenal renin-angiotensin system (RAS) is implicated in the development and progression of renal injury. To investigate whether angiotensinogen (AGT) expression is involved in glomerular RAS activity and glomerular injury, we examined glomerular AGT expression and its correlation with expression of other RAS components, and levels of glomerular injury in samples from patients with immunoglobulin A nephropathy (IgAN) (23) and minor glomerular abnormalities (MGA) (8). Immunohistochemistry showed that AGT protein was highly expressed by glomerular endothelial cells (GEC) and mesangial cells in nephritic glomeruli of IgAN compared with glomeruli of MGA. Levels of glomerular AGT protein were well correlated with levels of glomerular angiotensin II (ang II), transforming growth factor-β (TGF-β), α-smooth-muscle actin, glomerular cell number, and glomerulosclerosis score but not with those of glomerular angiotensin-converting enzyme and ang II type 1 receptor. Real-time polymerase chain reaction (RT-PCR) and Western blot analyses using cultured human GEC indicated that ang II upregulated AGT messenger ribonucleic acid (mRNA) and protein expression in a dose- and time-dependent manner. These data suggest that activated glomerular AGT expression is likely involved in elevated local ang II production and, thereby, may contribute to increased TGF-β production and development of glomerular injury in IgAN. Augmentation of GEC-AGT production with ang II stimulation might drive further glomerular injury in a positive-feedback loop
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