1,886 research outputs found

    Next-to-leading order QCD corrections to the single top quark production via model-independent t-q-g flavor-changing neutral-current couplings at hadron colliders

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    We present the calculations of the complete next-to-leading order (NLO) QCD effects on the single top productions induced by model-independent tqgtqg flavor-changing neutral-current couplings at hadron colliders. Our results show that, for the tcgtcg coupling the NLO QCD corrections can enhance the total cross sections by about 60% and 30%, and for the tugtug coupling by about 50% and 20% at the Tevatron and LHC, respectively, which means that the NLO corrections can increase the experimental sensitivity to the FCNC couplings by about 10%-30%. Moreover, the NLO corrections reduce the dependence of the total cross sections on the renormalization or factorization scale significantly, which lead to increased confidence on the theoretical predictions. Besides, we also evaluate the NLO corrections to several important kinematic distributions, and find that for most of them the NLO corrections are almost the same and do not change the shape of the distributions.Comment: minor changes, version published in PR

    Threshold Resummation Effects in Neutral Higgs Boson Production by Bottom Quark Fusion at the CERN Large Hadron Collider

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    We investigate the QCD effects in the production of neutral Higgs bosons via bottom quark fusion in both the standard model and the minimal supersymmetric standard model at the CERN Large Hadron Collider. We include the next-to-leading order (NLO) QCD corrections (including supersymmetric QCD) and the threshold resummation effects. We use the soft-collinear effective theory to resum the large logarithms near threshold from soft gluon emission. Our results show that the resummation effects can enhance the total cross sections by about 5% compared with the NLO results.Comment: 29pages, 14 figures, version to appear in Physical Review

    Next-to-leading order QCD corrections to the top quark decay via the Flavor-Changing Neutral-Current operators with mixing effects

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    In this paper detailed calculations of the complete O(αs)\mathcal{O}(\alpha_s) corrections to top quark decay widths Γ(tq+V)\Gamma(t\to q+V) are presented (V=g,γ,ZV=g,\gamma,Z). Besides describing in detail the calculations in our previous paper (arXiv:0810.3889), we also include the mixing effects of the Flavor-Changing Neutral-Current (FCNC) operators for tq+γt\to q+\gamma and tq+Zt\to q+Z, which were not considered in our previous paper. The results for tq+gt\to q+g are the same as in our previous paper. But the mixing effects can either be large or small, and increase or decrease the branching ratios for tq+γt\to q+\gamma and tq+Zt\to q+Z, depending on the values of the anomalous couplings (κtqg,γ,Z/Λ\kappa^{g,\gamma,Z}_{\mathrm{tq}}/\Lambda, ftqg,γ,Zf^{g,\gamma,Z}_{\mathrm{tq}} and htqg,γ,Zh^{g,\gamma,Z}_{\mathrm{tq}}).Comment: 21 pages, 12 figure

    Threshold Resummation Effects in Neutral Higgs Boson Production by Bottom Quark Fusion at the CERN Large Hadron Collider

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    We investigate the QCD effects in the production of neutral Higgs bosons via bottom quark fusion in both the standard model and the minimal supersymmetric standard model at the CERN Large Hadron Collider. We include the next-to-leading order (NLO) QCD corrections (including supersymmetric QCD) and the threshold resummation effects. We use the soft-collinear effective theory to resum the large logarithms near threshold from soft gluon emission. Our results show that the resummation effects can enhance the total cross sections by about 5% compared with the NLO results.Comment: 29pages, 14 figures, version to appear in Physical Review

    Icariin accelerates Bone Regeneration By inducing Osteogenesis-Angiogenesis Coupling in Rats With Type 1 Diabetes Mellitus

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    BACKGROUND: Icariin (ICA), a natural flavonoid compound monomer, has multiple pharmacological activities. However, its effect on bone defect in the context of type 1 diabetes mellitus (T1DM) has not yet been examined. AIM: to explore the role and potential mechanism of ICA on bone defect in the context of T1DM. METHODS: The effects of ICA on osteogenesis and angiogenesis were evaluated by alkaline phosphatase staining, alizarin red S staining, quantitative real-time polymerase chain reaction, Western blot, and immunofluorescence. Angiogenesis-related assays were conducted to investigate the relationship between osteogenesis and angiogenesis. A bone defect model was established in T1DM rats. The model rats were then treated with ICA or placebo and micron-scale computed tomography, histomorphometry, histology, and sequential fluorescent labeling were used to evaluate the effect of ICA on bone formation in the defect area. RESULTS: ICA promoted bone marrow mesenchymal stem cell (BMSC) proliferation and osteogenic differentiation. The ICA treated-BMSCs showed higher expression levels of osteogenesis-related markers (alkaline phosphatase and osteocalcin) and angiogenesis-related markers (vascular endothelial growth factor A and platelet endothelial cell adhesion molecule 1) compared to the untreated group. ICA was also found to induce osteogenesis-angiogenesis coupling of BMSCs. In the bone defect model T1DM rats, ICA facilitated bone formation and CD31 CONCLUSION: ICA was able to accelerate bone regeneration in a T1DM rat model by inducing osteogenesis-angiogenesis coupling of BMSCs

    Identification and target prediction of miRNAs specifically expressed in rat neural tissue

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    <p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a large group of RNAs that play important roles in regulating gene expression and protein translation. Several studies have indicated that some miRNAs are specifically expressed in human, mouse and zebrafish tissues. For example, miR-1 and miR-133 are specifically expressed in muscles. Tissue-specific miRNAs may have particular functions. Although previous studies have reported the presence of human, mouse and zebrafish tissue-specific miRNAs, there have been no detailed reports of rat tissue-specific miRNAs. In this study, Home-made rat miRNA microarrays which established in our previous study were used to investigate rat neural tissue-specific miRNAs, and mapped their target genes in rat tissues. This study will provide information for the functional analysis of these miRNAs.</p> <p>Results</p> <p>In order to obtain as complete a picture of specific miRNA expression in rat neural tissues as possible, customized miRNA microarrays with 152 selected miRNAs from miRBase were used to detect miRNA expression in 14 rat tissues. After a general clustering analysis, 14 rat tissues could be clearly classified into neural and non-neural tissues based on the obtained expression profiles with p values < 0.05. The results indicated that the miRNA profiles were different in neural and non-neural tissues. In total, we found 30 miRNAs that were specifically expressed in neural tissues. For example, miR-199a was specifically expressed in neural tissues. Of these, the expression patterns of four miRNAs were comparable with those of Landgraf et al., Bak et al., and Kapsimani et al. Thirty neural tissue-specific miRNAs were chosen to predict target genes. A total of 1,475 target mRNA were predicted based on the intersection of three public databases, and target mRNA's pathway, function, and regulatory network analysis were performed. We focused on target enrichments of the dorsal root ganglion (DRG) and olfactory bulb. There were four Gene Ontology (GO) functions and five KEGG pathways significantly enriched in DRG. Only one GO function was significantly enriched in the olfactory bulb. These targets are all predictions and have not been experimentally validated.</p> <p>Conclusion</p> <p>Our work provides a global view of rat neural tissue-specific miRNA profiles and a target map of miRNAs, which is expected to contribute to future investigations of miRNA regulatory mechanisms in neural systems.</p

    A Close-in Substellar Object Orbiting the sdOB-type Eclipsing-Binary System NSVS14256825

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    NSVS 14256825 is the second sdOB + dM eclipsing binary systems with anorbital period of 2.65 hours. The special binary was reported to contain circumbinary planets or brown dwarfs by using the timing method. However, different results were derived by different authors because of the insufficient coverage of eclipse timings. Since 2008, we have monitored this binary for about 10 years by using several telescopes and 84 new times of light minimum in high precision were obtained. It is found that the O-C curve is increasing recently and it shows a cyclic variation with a period of 8.83 years and amplitude of 46.31 seconds. The cyclic change cannot be explained by magnetic activity cycles of the red-dwarf component because the required energy is much larger than that radiated by this component in one whole period. This cyclic change detected in NSVS1425 could be explained by the light-travel time effect via the presence of a third body. The lowest mass of the third body is determined as 14.15 Mjup that is in the transition between planets and brown dwarfs. The substellar object is orbiting around this evolved binary at an orbital separation around 3 AU with an eccentricity of 0.12. These results indicate that NSVS 14256825 is the first sdOB-type eclipsing binary consisting of a hierarchical substellar object. The detection of a close-in substellar companion to NSVS 14256825 will provide some insights on the formation and evolution of sdOB-type binaries and their companions.Fil: Zhu, Li-Ying. Yunnan Observatories, Chinese Academy Of Sciences; ChinaFil: Qian, Sheng Bang. Yunnan Observatories, Chinese Academy Of Sciences; ChinaFil: Fernandez Lajus, Eduardo Eusebio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Astrofísica La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Astronómicas y Geofísicas. Instituto de Astrofísica La Plata; ArgentinaFil: Wang, Zhi Hua. Yunnan Observatories, Chinese Academy Of Sciences; ChinaFil: Li, Lin Jia. Yunnan Observatories, Chinese Academy Of Sciences; Chin
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