4,065 research outputs found
Recommended from our members
Long distance chiral corrections in beta meson amplitudes
We discuss the chiral corrections to fB and BB with particular emphasis on determining the portion of the correction that arises from long distance physics. For very small pion and kaon masses all of the usual corrections are truly long distance, while for larger masses the long distance portion decreases. These chiral corrections have been used to extrapolate lattice calculations towards the physical region of lighter masses. We show in particular that the chiral extrapolation is better behaved if only the long distance portion of the correction is used. We also display the long distance portions of the infrared enhanced chiral logarithms that appear in partially quenched chiral perturbation theory
Long-term Tracking in the Wild: A Benchmark
We introduce the OxUvA dataset and benchmark for evaluating single-object
tracking algorithms. Benchmarks have enabled great strides in the field of
object tracking by defining standardized evaluations on large sets of diverse
videos. However, these works have focused exclusively on sequences that are
just tens of seconds in length and in which the target is always visible.
Consequently, most researchers have designed methods tailored to this
"short-term" scenario, which is poorly representative of practitioners' needs.
Aiming to address this disparity, we compile a long-term, large-scale tracking
dataset of sequences with average length greater than two minutes and with
frequent target object disappearance. The OxUvA dataset is much larger than the
object tracking datasets of recent years: it comprises 366 sequences spanning
14 hours of video. We assess the performance of several algorithms, considering
both the ability to locate the target and to determine whether it is present or
absent. Our goal is to offer the community a large and diverse benchmark to
enable the design and evaluation of tracking methods ready to be used "in the
wild". The project website is http://oxuva.netComment: To appear at ECCV 201
A Protein‐Based Pentavalent Inhibitor of the Cholera Toxin B‐Subunit
Protein toxins produced by bacteria are the cause of many life-threatening diarrheal diseases. Many of these toxins, including cholera toxin (CT), enter the cell by first binding to glycolipids in the cell membrane. Inhibiting these multivalent protein/carbohydrate interactions would prevent the toxin from entering cells and causing diarrhea. Here we demonstrate that the site-specific modification of a protein scaffold, which is perfectly matched in both size and valency to the target toxin, provides a convenient route to an effective multivalent inhibitor. The resulting pentavalent neoglycoprotein displays an inhibition potency (IC50) of 104 pM for the CT B-subunit (CTB), which is the most potent pentavalent inhibitor for this target reported thus far. Complexation of the inhibitor and CTB resulted in a protein heterodimer. This inhibition strategy can potentially be applied to many multivalent receptors and also opens up new possibilities for protein assembly strategies
Variable order Mittag-Leffler fractional operators on isolated time scales and application to the calculus of variations
We introduce new fractional operators of variable order on isolated time
scales with Mittag-Leffler kernels. This allows a general formulation of a
class of fractional variational problems involving variable-order difference
operators. Main results give fractional integration by parts formulas and
necessary optimality conditions of Euler-Lagrange type.Comment: This is a preprint of a paper whose final and definite form is with
Springe
Vaccination with DNA plasmids expressing Gn coupled to C3d or alphavirus replicons expressing Gn protects mice against rift valley fever virus
Background: Rift Valley fever (RVF) is an arthropod-borne viral zoonosis. Rift Valley fever virus (RVFV) is an important biological threat with the potential to spread to new susceptible areas. In addition, it is a potential biowarfare agent. Methodology/Principal Findings: We developed two potential vaccines, DNA plasmids and alphavirus replicons, expressing the Gn glycoprotein of RVFV alone or fused to three copies of complement protein, C3d. Each vaccine was administered to mice in an all DNA, all replicon, or a DNA prime/replicon boost strategy and both the humoral and cellular responses were assessed. DNA plasmids expressing Gn-C3d and alphavirus replicons expressing Gn elicited high titer neutralizing antibodies that were similar to titers elicited by the live-attenuated MP12 virus. Mice vaccinated with an inactivated form of MP12 did elicit high titer antibodies, but these antibodies were unable to neutralize RVFV infection. However, only vaccine strategies incorporating alphavirus replicons elicited cellular responses to Gn. Both vaccines strategies completely prevented weight loss and morbidity and protected against lethal RVFV challenge. Passive transfer of antisera from vaccinated mice into naïve mice showed that both DNA plasmids expressing Gn-C3d and alphavirus replicons expressing Gn elicited antibodies that protected mice as well as sera from mice immunized with MP12. Conclusion/Significance: These results show that both DNA plasmids expressing Gn-C3d and alphavirus replicons expressing Gn administered alone or in a DNA prime/replicon boost strategy are effective RVFV vaccines. These vaccine strategies provide safer alternatives to using live-attenuated RVFV vaccines for human use. © 2010 Bhardwaj et al
LHC Searches for Non-Chiral Weakly Charged Multiplets
Because the TeV-scale to be probed at the Large Hadron Collider should shed
light on the naturalness, hierarchy, and dark matter problems, most searches to
date have focused on new physics signatures motivated by possible solutions to
these puzzles. In this paper, we consider some candidates for new states that
although not well-motivated from this standpoint are obvious possibilities that
current search strategies would miss. In particular we consider vector
representations of fermions in multiplets of with a lightest neutral
state. Standard search strategies would fail to find such particles because of
the expected small one-loop-level splitting between charged and neutral states.Comment: 16 pages, 9 figure
Ultraviolet Completion of Flavour Models
Effective Flavour Models do not address questions related to the nature of
the fundamental renormalisable theory at high energies. We study the
ultraviolet completion of Flavour Models, which in general has the advantage of
improving the predictivity of the effective models. In order to illustrate the
important features we provide minimal completions for two known A4 models. We
discuss the phenomenological implications of the explicit completions, such as
lepton flavour violating contributions that arise through the exchange of
messenger fields.Comment: 18 pages, 8 figure
Opportunities for topical antimicrobial therapy: permeation of canine skin by fusidic acid
BACKGROUND: Staphylococcal infection of the canine epidermis and hair follicle is amongst the commonest reasons for antimicrobial prescribing in small animal veterinary practice. Topical therapy with fusidic acid (FA) is an attractive alternative to systemic therapy based on low minimum inhibitory concentrations (MICs, commonly <0.03 mg/l) documented in canine pathogenic staphylococci, including strains of MRSA and MRSP (methicillin-resistant Staphylococcus aureus and S. pseudintermedius). However, permeation of canine skin by FA has not been evaluated in detail. This study aimed to define the degree and extent of FA permeation in canine skin in vitro from two sites with different hair follicle density following application of a licensed ophthalmic formulation that shares the same vehicle as an FA-betamethasone combination product approved for dermal application in dogs. Topical FA application was modelled using skin held in Franz-type diffusion cells. Concentrations of FA in surface swabs, receptor fluid, and transverse skin sections of defined anatomical depth were determined using high-performance liquid chromatography and ultraviolet (HPLC-UV) analysis. RESULTS: The majority of FA was recovered by surface swabs after 24 h, as expected (mean ± SEM: 76.0 ± 17.0%). FA was detected within 424/470 (90%) groups of serial sections of transversely cryotomed skin containing follicular infundibula, but never in 48/48 (100%) groups of sections containing only deeper follicular structures, nor in receptor fluid, suggesting that FA does not permeate beyond the infundibulum. The FA concentration (mean ± SEM) in the most superficial 240 μm of skin was 2000 ± 815 μg/g. CONCLUSIONS: Topically applied FA can greatly exceed MICs for canine pathogenic staphylococci at the most common sites of infection. Topical FA therapy should now be evaluated using available formulations in vivo as an alternative to systemic therapy for canine superficial bacterial folliculitis.Peer reviewedFinal Published versio
- …