Lepton flavor violation at linear collider experiments in supersymmetric grand unified theories

Lepton flavor violation at linear collider experiments is discussed. We show that detectable lepton flavor violation could occur through scalar lepton pair production and decay in the supersymmetric SU(5) grand unified theory in spite of the stringent present experimental constraints by rare process searches. Possible cross sections about 40fb for an e+e- collider and 280fb for an e-e- collider are illustrated.Comment: 12 pages, including 3 figures, REVTeX, eps

Characterization of scintillators for lost alpha diagnostics on burning plasma experiments

The characteristics of light output by ion beam irradiations under high ion fluxes have been measured for three kinds of scintillators: ZnS:Ag deposited on the glass plate, Y_3Al_5O_12:Ce powder stiffened with a binder, and Y_3Al_5O_12:Ce ceramics sintered at high temperature. The ion beam flux in the range from 10^12 to 10^13 ions/(cm^2 s) is irradiated to simulate the burning plasma experiments. The decrease of light output has been observed by long time ion irradiation. The deterioration of ZnS:Ag deposited scintillator is most serious. The deterioration has been improved for the scintillators of Y_3Al_5O_12:Ce with a binder and that sintered. Their applications to ITER lost alpha diagnostics are discussed

Slepton Oscillation at Large Hadron Collider

Measurement of Lepton-Flavor Violation (LFV) in the minimal SUSY Standard Model (MSSM) at Large Hadron Collider (LHC) is studied based on a realistic simulation. We consider the LFV decay of the second-lightest neutralino, $\tilde{\chi}^0_2 \to \tilde{l} l' \to l l' \tilde{\chi}^0_1$, in the case where the flavor mixing exists in the right-handed sleptons. We scan the parameter space of the minimal supergravity model (MSUGRA) and a more generic model in which we take the Higgsino mass $\mu$ as a free parameter. We find that the possibility of observing LFV at LHC is higher if $\mu$ is smaller than the MSUGRA prediction; the LFV search at LHC can cover the parameter range where the $\mu \to e \gamma$ decay can be suppressed by the cancellation among the diagrams for this case.Comment: 29 pages, 10 figure

The SUSY seesaw model and lepton-flavor violation at a future electron-positron linear collider

We study lepton-flavor violating slepton production and decay at a future e^+e^- linear collider in context with the seesaw mechanism in mSUGRA post-LEP benchmark scenarios. The present knowledge in the neutrino sector as well as improved future measurements are taken into account. We calculate the signal cross-sections \sigma(e^{+/-}e^- -> l_{\beta}^{+/-} l_{\alpha}^- \tilde{\chi}_b^0 \tilde{\chi}_a^0); l_{\delta}=e, \mu, \tau; \alpha =|= \beta and estimate the main background processes. Furthermore, we investigate the correlations of these signals with the corresponding lepton-flavor violating rare decays l_{\alpha} -> l_{\beta} \gamma. It is shown that these correlations are relatively weakly affected by uncertainties in the neutrino data, but very sensitive to the model parameters. Hence, they are particularly suited for probing the origin of lepton-flavor violation.Comment: 31 pages, 10 figures, version published in Phys. Rev.

Microarray-based global mapping of integration sites for the retrotransposon, intracisternal A-particle, in the mouse genome

Mammalian genomes contain numerous evolutionary harbored mobile elements, a part of which are still active and may cause genomic instability. Their movement and positional diversity occasionally result in phenotypic changes and variation by causing altered expression or disruption of neighboring host genes. Here, we describe a novel microarray-based method by which dispersed genomic locations of a type of retrotransposon in a mammalian genome can be identified. Using this method, we mapped the DNA elements for a mouse retrotransposon, intracisternal A-particle (IAP), within genomes of C3H/He and C57BL/6J inbred mouse strains; consequently we detected hundreds of probable IAP cDNA–integrated genomic regions, in which a considerable number of strain-specific putative insertions were included. In addition, by comparing genomic DNAs from radiation-induced myeloid leukemia cells and its reference normal tissue, we detected three genomic regions around which an IAP element was integrated. These results demonstrate the first successful genome-wide mapping of a retrotransposon type in a mammalian genome