28 research outputs found

    The anomalous magnetic moment of the muon in the Standard Model

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    194 pages, 103 figures, bib files for the citation references are available from: https://muon-gm2-theory.illinois.eduWe review the present status of the Standard Model calculation of the anomalous magnetic moment of the muon. This is performed in a perturbative expansion in the fine-structure constant α\alpha and is broken down into pure QED, electroweak, and hadronic contributions. The pure QED contribution is by far the largest and has been evaluated up to and including O(α5)\mathcal{O}(\alpha^5) with negligible numerical uncertainty. The electroweak contribution is suppressed by (mμ/MW)2(m_\mu/M_W)^2 and only shows up at the level of the seventh significant digit. It has been evaluated up to two loops and is known to better than one percent. Hadronic contributions are the most difficult to calculate and are responsible for almost all of the theoretical uncertainty. The leading hadronic contribution appears at O(α2)\mathcal{O}(\alpha^2) and is due to hadronic vacuum polarization, whereas at O(α3)\mathcal{O}(\alpha^3) the hadronic light-by-light scattering contribution appears. Given the low characteristic scale of this observable, these contributions have to be calculated with nonperturbative methods, in particular, dispersion relations and the lattice approach to QCD. The largest part of this review is dedicated to a detailed account of recent efforts to improve the calculation of these two contributions with either a data-driven, dispersive approach, or a first-principle, lattice-QCD approach. The final result reads aμSM=116591810(43)×1011a_\mu^\text{SM}=116\,591\,810(43)\times 10^{-11} and is smaller than the Brookhaven measurement by 3.7σ\sigma. The experimental uncertainty will soon be reduced by up to a factor four by the new experiment currently running at Fermilab, and also by the future J-PARC experiment. This and the prospects to further reduce the theoretical uncertainty in the near future-which are also discussed here-make this quantity one of the most promising places to look for evidence of new physics

    Safety and Optimization of Metabolic Labeling of Endothelial Progenitor Cells for Tracking

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    Metabolic labeling is one of the most powerful methods to label the live cell for in vitro and in vivo tracking. However, the cellular mechanisms by modified glycosylation due to metabolic agents are not fully understood. Therefore, metabolic labeling has not yet been widely used in EPC tracking and labeling. In this study, cell functional properties such as proliferation, migration and permeability and gene expression patterns of metabolic labeling agent-treated hUCB-EPCs were analyzed to demonstrate cellular effects of metabolic labeling agents. As the results, 10 mu M Ac4ManNAz treatment had no effects on cellular function or gene regulations, however, higher concentration of Ac4ManNAz (> 20 mu M) led to the inhibition of functional properties (proliferation rate, viability and rate of endocytosis) and down-regulation of genes related to cell adhesion, PI3K/AKT, FGF and EGFR signaling pathways. Interestingly, the new blood vessel formation and angiogenic potential of hUCB-EPCs were not affected by Ac4ManNAz concentration. Based on our results, we suggest 10 mu M as the optimal concentration of Ac4ManNAz for in vivo hUCB-EPC labeling and tracking. Additionally, we expect that our approach can be used for understanding the efficacy and safety of stem cell-based therapy in vivo

    The human cadherin 11 is a pro-apoptotic tumor suppressor modulating cell stemness through Wnt/β-catenin signaling and silenced in common carcinomas

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    Genetic alterations of 16q21-q22, the locus of a 6-cadherin cluster, are frequently involved in multiple tumors, suggesting the presence of critical tumor suppressor genes (TSGs). Using 1 Mb array comparative genomic hybridization (aCGH), we refined a small hemizygous deletion (1 Mb) at 16q21-22.1, which contains a single gene Cadherin-11 (CDH11, OB-cadherin). CDH11 was broadly expressed in human normal adult and fetal tissues, while its silencing and promoter CpG methylation were frequently detected in tumor cell lines, but not in immortalized normal epithelial cells. Aberrant methylation was also frequently detected in multiple primary tumors. CDH11 silencing could be reversed by pharmacologic or genetic demethylation, indicating an epigenetic mechanism. Ectopic expression of CDH11 strongly suppressed tumorigenecity and induced tumor cell apoptosis. Moreover, CDH11 was found to inhibit Wnt/beta-catenin and AKT/Rho A signaling, as well as actin stress fiber formation, thus further inhibiting tumor cell migration and invasion. CDH11 also inhibited epithelial-to-mesenchymal transition and downregulated stem cell markers. Thus, our work identifies CDH11 as a functional tumor suppressor and an important antagonist of Wnt/beta-catenin and AKT/Rho A signaling, with frequent epigenetic inactivation in common carcinomas.link_to_OA_fulltex

    Measurement of Gamma(eta -> pione+ pione- gamma)/Gamma(eta -> pione+ pione- pione0) with the KLOE Detector

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    The ratio R_η=Γ(η-> π^+π^-γ)/Γ(η-> π^+π^-π^0) has been measured by analyzing 22 million φ\to ηγdecays collected by the KLOE experiment at DA\PhiNE, corresponding to an integrated luminosity of 558 pb^{-1}. The η\to π^+π^-γproceeds both via the ρresonant contribution, and possibly a non-resonant direct term, connected to the box anomaly. Our result, R_η= 0.1856\pm 0.0005_{stat} \pm 0.0028_{syst}, points out a sizable contribution of the direct term to the total width. The di-pion invariant mass for the η-> π^+π^-γdecay could be described in a model-independent approach in terms of a single free parameter, α. The determined value of the parameter αis α= (1.32 \pm 0.08_{stat} +0.10/-0.09_{syst}\pm 0.02_{theo}) GeV^{-2

    Study of the resonance structures in the process e(+) e(-) -> pi(+) pi(-) J/psi

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    Using about 23 fb(-1) of data collected with the BESIII detector operating at the BEPCII storage ring, a precise measurement of the e(+) e(-) -> pi(+) pi(-) J/psi Born cross section is performed at center-of-mass energies from 3.7730 to 4.7008 GeV. Two structures, identified as the Y(4220) and the Y(4320) states, are observed in the energy-dependent cross section with a significance larger than 10 sigma. The masses and widths of the two structures are determined to be (M,(sic)) = (4221.4 +/- 1.5 +/- 2.0 MeV=c(2); 41.8 +/- 2.9 +/- 2.7 MeV) and (M,(sic)) = (4298 +/- 12 +/- 26 MeV=c(2); 127 +/- 17 +/- 10 MeV)respectively. A small enhancement around 4.5 GeV with a significance about 3s, compatible with the psi(4415), might also indicate the presence of an additional resonance in the spectrum. The inclusion of this additional contribution in the fit to the cross section affects the resonance parameters of the Y(4320) state
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