36 research outputs found
The Nab Experiment: A Precision Measurement of Unpolarized Neutron Beta Decay
Neutron beta decay is one of the most fundamental processes in nuclear
physics and provides sensitive means to uncover the details of the weak
interaction. Neutron beta decay can evaluate the ratio of axial-vector to
vector coupling constants in the standard model, , through
multiple decay correlations. The Nab experiment will carry out measurements of
the electron-neutrino correlation parameter with a precision of and the Fierz interference term to
in unpolarized free neutron beta decay. These results, along with a more
precise measurement of the neutron lifetime, aim to deliver an independent
determination of the ratio with a precision of that will allow an evaluation of and sensitively
test CKM unitarity, independent of nuclear models. Nab utilizes a novel, long
asymmetric spectrometer that guides the decay electron and proton to two large
area silicon detectors in order to precisely determine the electron energy and
an estimation of the proton momentum from the proton time of flight. The Nab
spectrometer is being commissioned at the Fundamental Neutron Physics Beamline
at the Spallation Neutron Source at Oak Ridge National Lab. We present an
overview of the Nab experiment and recent updates on the spectrometer,
analysis, and systematic effects.Comment: Presented at PPNS201
Neutron Decay Correlations in the Nab Experiment
The Nab experiment will measure the correlation a between the momenta of the beta particle and antineutrino in neutron decay as well as the Fierz term b which distorts the beta spectrum
Wnt signaling and orthopedics, an overview
Wnt signaling is a ubiquitous system for intercellular communication, with multiple functions during development and in homeostasis of the body. It comprises several ligands, receptors, and inhibitors. Some molecules, such as sclerostin, appear to have bone-specific functions, and can be targeted by potential drugs. Now, ongoing clinical trials are testing these drugs as treatments for osteoporosis. Animal studies have also suggested that these drugs can accelerate fracture healing and implant fixation. This brief overview focuses on currently available information on the effects of manipulations of Wnt signaling on bone healing
A Missense Mutation in PPARD Causes a Major QTL Effect on Ear Size in Pigs
Chinese Erhualian is the most prolific pig breed in the world. The breed exhibits exceptionally large and floppy ears. To identify genes underlying this typical feature, we previously performed a genome scan in a large scale White Duroc × Erhualian cross and mapped a major QTL for ear size to a 2-cM region on chromosome 7. We herein performed an identical-by-descent analysis that defined the QTL within a 750-kb region. Historically, the large-ear feature has been selected for the ancient sacrificial culture in Erhualian pigs. By using a selective sweep analysis, we then refined the critical region to a 630-kb interval containing 9 annotated genes. Four of the 9 genes are expressed in ear tissues of piglets. Of the 4 genes, PPARD stood out as the strongest candidate gene for its established role in skin homeostasis, cartilage development, and fat metabolism. No differential expression of PPARD was found in ear tissues at different growth stages between large-eared Erhualian and small-eared Duroc pigs. We further screened coding sequence variants in the PPARD gene and identified only one missense mutation (G32E) in a conserved functionally important domain. The protein-altering mutation showed perfect concordance (100%) with the QTL genotypes of all 19 founder animals segregating in the White Duroc × Erhualian cross and occurred at high frequencies exclusively in Chinese large-eared breeds. Moreover, the mutation is of functional significance; it mediates down-regulation of β-catenin and its target gene expression that is crucial for fat deposition in skin. Furthermore, the mutation was significantly associated with ear size across the experimental cross and diverse outbred populations. A worldwide survey of haplotype diversity revealed that the mutation event is of Chinese origin, likely after domestication. Taken together, we provide evidence that PPARD G32E is the variation underlying this major QTL