20,387 research outputs found
A New Light Particle in B Decays?
We investigate the possibility whether the tensions with SM expectations
observed in several b -> sll transitions, including hints for lepton flavour
non-universality, could be due to the decay of B into a new light resonance. We
find that qualitative agreement with the data can be obtained with a light
vector resonance dominantly decaying invisibly. This scenario predicts a shift
in the muon anomalous magnetic moment that could explain the long-standing
discrepancy. The most stringent constraint comes from searches for B decays
with missing energy. A striking prediction is a strong q^2 dependence of the
lepton flavour universality ratios R_K and R_K* that should allow to clearly
confirm or rule out this possibility experimentally. We also comment on the
possible connection of the invisible decay product with Dark Matter.Comment: 5 pages, 2 figures. v2: typos corrected, references and
clarifications adde
A Discrete Logarithm-based Approach to Compute Low-Weight Multiples of Binary Polynomials
Being able to compute efficiently a low-weight multiple of a given binary
polynomial is often a key ingredient of correlation attacks to LFSR-based
stream ciphers. The best known general purpose algorithm is based on the
generalized birthday problem. We describe an alternative approach which is
based on discrete logarithms and has much lower memory complexity requirements
with a comparable time complexity.Comment: 12 page
Identification and pharmacological inactivation of the MYCN gene network as a therapeutic strategy for neuroblastic tumor cells
This research was originally published in Journal of Biological Chemistry. Olesya Chayka, Cosimo Walter D’Acunto, Odette Middleton, Maryam Arab, and Arturo Sala. Identification and Pharmacological Inactivation of the MYCN Gene Network as a Therapeutic Strategy for Neuroblastic Tumor Cells. Journal of Biological Chemistry. 2015; Vol 290 (4) :pp. 2198 - 2212. © the American Society for Biochemistry and Molecular Biology.This article has been made available through the Brunel Open Access Publishing Fund.The MYC family of transcription factors consists of three well characterized members, c-MYC, L-MYC, and MYCN, deregulated in the majority of human cancers. In neuronal tumors such as neuroblastoma, MYCN is frequently activated by gene amplification, and reducing its expression by RNA interference has been shown to promote growth arrest and apoptosis of tumor cells. From a clinical perspective, RNA interference is not yet a viable option, and small molecule inhibitors of transcription factors are difficult to develop. We therefore planned to identify, at the global level, the genes interacting functionally with MYCN required to promote fitness of tumor cells facing oncogenic stress. To find genes whose inactivation is synthetically lethal to MYCN, we implemented a genome-wide approach in which we carried out a drop-out shRNA screen using a whole genome library that was delivered into isogenic neuroblastoma cell lines expressing or not expressing MYCN. After the screen, we selected for in-depth analysis four shRNAs targeting AHCY, BLM, PKMYT1, and CKS1B. These genes were chosen because they are directly regulated by MYC proteins, associated with poor prognosis of neuroblastoma patients, and inhibited by small molecule compounds. Mechanistically, we found that BLM and PKMYT1 are required to limit oncogenic stress and promote stabilization of the MYCN protein. Cocktails of small molecule inhibitors of CKS1B, AHCY, BLM, and PKMYT1 profoundly affected the growth of all neuroblastoma cell lines but selectively caused death of MYCN-amplified cells. Our findings suggest that drugging the MYCN network is a promising avenue for the treatment of high risk, neuroblastic cancers.SPARKS and the Neuroblastoma Society
Physical Connectivity Between the NE Atlantic Seamounts
Within the Portuguese Exclusive Economic Zone, the Great Meteor and Madeira-Tore complexes are highly productive areas, which are likely to be classified as marine protected areas (MPAs) due to their ecological vulnerability. This was the main focus of the BIOMETORE project and, framed on it, the aim of the present study was to investigate the physical connectivity between both seamount complexes. Using the HYbrid Coordinate Ocean Model coupled with the Connectivity Modeling System (CMS) (a Lagrangian tool), a series of experiments was conducted in order to determine the influence of the main oceanographic phenomena governing the area in: (i) the origin of the particles that reach each complex, (ii) their capacity to capture and retain incoming particles, and (iii) the physical connectivity between them as well as the intra-connectivity within each seamount system. Due to the geographical location of both groups of seamounts, the Azores Current (AzC) and its associated eddies were identified as the main transport pathways, its influence being stronger at intermediate waters and decreasing with depth. Notwithstanding, the Great Meteor and the MadeiraTore were mainly affected by the AzC southward and eastward branches, respectively, resulting in a non-significant connectivity between the two groups. Meanwhile, the inter-connectivity between seamounts slightly varied with depth at the Great Meteor complex while increasing at Madeira-Tore. In addition, the Plateau, Irving, and Cruiser (PIC) seamounts from the Great Meteor complex and Gorringe and Coral from the Madeira-Tore complex proved to incorporate the regional connectivity routes. Although containing the three smallest seamounts, Madeira-Tore showed the higher capturing capacity per square kilometer, highlighting the influence of the "sticky water effect." In the Great Meteor complex, the "seamount effect" seems to be the main phenomenon responsible for the greater retention and self-recruitment abilities of these seamounts. The presented results provide valuable information for the design of a MPA to preserve these vulnerable habitat
Advanced Exergy Analysis in the Dynamic Framework for Assessing Building Thermal Systems
This work applies the Dynamic Advanced Exergy Analysis (DAEA) to a heating and domestic hot water (DHW) facility supplied by a Stirling engine and a condensing boiler. For the first time, an advanced exergy analysis using dynamic conditions is applied to a building energy system. DAEA provides insights on the components’ exergy destruction (ED) by distinguishing the inefficiencies that can be prevented by improving the quality (avoidable ED) and the ones constrained because of technical limitations (unavoidable ED). ED is related to the inherent inefficiencies of the considered element (endogenous ED) and those coming from the interconnections (exogenous ED). That information cannot be obtained by any other approach. A dynamic calculation within the experimental facility has been performed after a component characterization driven by a new grey-box modelling technique, through TRNSYS and MATLAB. Novel solutions and terms of ED are assessed for the rational implementation of the DAEA in building energy installations. The influence of each component and their interconnections are valuated in terms of exergy destruction for further diagnosis and optimization purposes.BMWi, 03ET1218B, Anwendung exergiebasierter Methoden zur Verbesserung von Gebäudeenergiesysteme
The interaction-strength interpolation method for main-group chemistry: benchmarking, limitations, and perspectives
We have tested the original interaction-strength-interpolation (ISI)
exchange-correlation functional for main group chemistry. The ISI functional is
based on an interpolation between the weak and strong coupling limits and
includes exact-exchange as well as the G\"orling-Levy second-order energy. We
have analyzed in detail the basis-set dependence of the ISI functional, its
dependence on the ground-state orbitals, and the influence of the
size-consistency problem. We show and explain some of the expected limitations
of the ISI functional (i.e. for atomization energies), but also unexpected
results, such as the good performance for the interaction energy of
dispersion-bonded complexes when the ISI correlation is used as a correction to
Hartree-Fock.Comment: 20 pages, 20 figure
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