Searching for the squark flavor mixing in CP violations of Bs -> K+ K- and K0bar K0 decays

We study CP violations in the B_s-> K+K- and Bs->K0K0 decays in order to find the contribution of the supersymmetry, which comes from the gluino-squark mediated flavor changing current. We obtain the allowed region of the squark flavor mixing parameters by putting the experimental data, the mass difference Delta M_Bs, the CP violating phase phi_s in Bs to J/psi phi decay and the b to s gamma branching ratio. In addition to these data, we take into account the constraint from the asymmetry of B0->K+pi because the Bs->K+K- decay is related with the B0->K+pi- decay by replacing the spectator s with d. Under these constraints, we predict the magnitudes of the CP violation in the Bs->K+K- and Bs->K0K0 decays. The predicted region of the CP violation C_{K+K-} is strongly cut from the direct CP violation of barB0 to K-pi+, therefore, the deviation from the SM prediction of C_{K+K-} is not found. On the other hand, the CP violation S_{K+K-} is possibly deviated from the SM prediction considerably, in the region of 0.1- 0.5. Since the standard model predictions of C_{K0bar K0} and S_{K0bar K0} are very small, the squark contribution can be detectable in C_{K0bar K0} and S_{K0bar K0}. These magnitudes are expected in the region C_{K0bar K0}=-0.06-0.06 and S_{K0bar K0}=-0.5-0.3. More precise data of these CP violations provide us a crucial test for the gluino-squark mediated flavor changing current.Comment: 20 pages, 10 figures, discussions added, references added. arXiv admin note: substantial text overlap with arXiv:1307.037

Electrophysiological analysis of mammalian cells expressing hERG using automated 384-well-patch-clamp

BACKGROUND: An in vitro electrophysiological assay system, which can assess compound effects and thus show cardiotoxicity including arrhythmia risks of test drugs, is an essential method in the field of drug development and toxicology. METHODS: In this study, high-throughput electrophysiological recordings of human embryonic kidney (HEK 293) cells and Chinese hamster ovary (CHO) cells stably expressing human ether-a-go-go related gene (hERG) were performed utilizing an automated 384-well-patch-clamp system, which records up to 384 cells simultaneously. hERG channel inhibition, which is closely related to a drug-induced QT prolongation and is increasing the risk of sudden cardiac death, was investigated in the high-throughput screening patch-clamp system. RESULTS: In the automated patch-clamp measurements performed here, K(v) currents were investigated with high efficiency. Various hERG channel blockers showed concentration-dependent inhibition, the 50 % inhibitory concentrations (IC(50)) of those blockers were in good agreement with previous reports. CONCLUSIONS: The high-throughput patch-clamp system has a high potential in the field of pharmacology, toxicology, and cardiac physiology, and will contribute to the acceleration of pharmaceutical drug development and drug safety testing

Pctaire1/Cdk16 promotes skeletal myogenesis by inducing myoblast migration and fusion

AbstractThe Cdk-related protein kinase Pctaire1/Cdk16 is abundantly expressed in brain, testis and skeletal muscle. Functional roles of Pctaire1 such as regulation of neuron migration and neurite outgrowth thus far have been mainly elucidated in the field of nervous system development. Although these regulations based on cytoskeletal rearrangements evoke a possible role of Pctaire1 in the development of skeletal muscle, little is known in this regard. In this study, we demonstrated that myogenic differentiation and subsequent fusion is promoted in Pctaire1 overexpressing cells, and conversely, is inhibited in the knockdown cells. Furthermore, our findings suggest that Pctaire1 exerts promyogenic effects by regulating myoblast migration and process formation during skeletal myogenesis

Remarks on theta series

In this note we prove two propositions about theta series. The field of real numbers will be denoted by R, the field of complex numbers by C, and Siegel upper half domain of degree n by Hn. ..

b tagging in ATLAS and CMS

Many physics signals presently studied at the high energy collision experiments lead to final states with jets originating from heavy flavor quarks. This report reviews the algorithms for heavy flavor jets identification developed by the ATLAS and CMS Collaborations in view of the Run2 data taking period at the Large Hadron Collider. The improvements of the algorithms used in 2015 and 2016 data analyses with respect to previous data taking periods are discussed, as well as the ongoing developments in view of the next years of data taking. The measurements of the performance of the algorithms on data as well as the dedicated techniques for the identification of heavy flavor jets in events with boosted topologies are also presented. Finally, the effectiveness of heavy flavor jet identification in the complex environment expected during the high luminosity LHC phase is discussed.Comment: 6 pages, Proceeding for the Fifth Annual Large Hadron Collider Physics (LHCP2017) conferenc