267 research outputs found
PEN: a low energy test of lepton universality
Allowed charged meson decays are characterized by simple dynamics, few
available decay channels, mainly into leptons, and extremely well controlled
radiative and loop corrections. In that sense, pion decays represent a
veritable triumph of the standard model (SM) of elementary particles and
interactions. This relative theoretical simplicity makes charged pion decays a
sensitive means for testing the underlying symmetries and the universality of
weak fermion couplings, as well as for studying pion structure and chiral
dynamics. Even after considerable recent improvements, experimental precision
is lagging far behind that of the theoretical description for pion decays. We
review the current state of experimental study of the pion electronic decay
, or , where the
indicates inclusion and explicit treatment of radiative decay events. We
briefly review the limits on non-SM processes arising from the present level of
experimental precision in decays. Focusing on the PEN
experiment at the Paul Scherrer Institute (PSI), Switzerland, we examine the
prospects for further improvement in the near term.Comment: 11 pages, 5 figures; paper presented at the XIII International
Conference on Heavy Quarks and Leptons, 22-27 May 2016, Blacksburg, Virginia,
US
PEN experiment: a precise measurement of the pi+ -> e+ nu decay branching fraction
A new measurement of , the decay
branching ratio, is currently under way at the Paul Scherrer Institute. The
present experimental result on constitutes the most accurate test
of lepton universality available. The accuracy, however, still lags behind the
theoretical precision by over an order of magnitude. Because of the large
helicity suppression of the decay, its branching ratio is
susceptible to significant contributions from new physics, making this decay a
particularly suitable subject of study.Comment: 4 pages, 3 figures, talk given at the Tenth Conference on the
Intersections of Particle and Nuclear Physics (CIPANP 2009), La Jolla/San
Diego, CA, 26-31 May 2009; to appear in Proceedings to be published by the
American Institute of Physic
Role of Polyamine-Induced Dimerization of Antizyme in Its Cellular Functions
Funding: This work was supported by grants from the Russian Science Foundation (grant # 17-74-20049—synthesis of C-methylated Spd analogues, ITC studies of dimerization of OAZ1, and frameshifting experiments), the Russian Science Foundation (grant # 19-74-10086—isolation of OAZ1, electrophoresis studies of dimerization of OAZ1), and the Academy of Finland (grants # 292574 and # 315487). Acknowledgments: The authors thank A. Karppinen, A. Korhonen, T. Reponen, M. Salminkoski, and S.D. Negrya for their skillful technical assistance.Peer reviewedPublisher PD
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