18,914 research outputs found
Constructing topological models by symmetrization: A PEPS study
Symmetrization of topologically ordered wavefunctions is a powerful method
for constructing new topological models. Here, we study wavefunctions obtained
by symmetrizing quantum double models of a group in the Projected Entangled
Pair States (PEPS) formalism. We show that symmetrization naturally gives rise
to a larger symmetry group which is always non-abelian. We prove
that by symmetrizing on sufficiently large blocks, one can always construct
wavefunctions in the same phase as the double model of . In order to
understand the effect of symmetrization on smaller patches, we carry out
numerical studies for the toric code model, where we find strong evidence that
symmetrizing on individual spins gives rise to a critical model which is at the
phase transitions of two inequivalent toric codes, obtained by anyon
condensation from the double model of .Comment: 10 pages. v2: accepted versio
An equatorial ultra iron-poor star identified in BOSS
We report the discovery of SDSS J131326.89-001941.4, an ultra iron-poor red
giant star ([Fe/H] ~ -4.3) with a very high carbon abundance ([C/Fe]~ +2.5).
This object is the fifth star in this rare class, and the combination of a
fairly low effective temperature (Teff ~ 5300 K), which enhances line
absorption, with its brightness (g=16.9), makes it possible to measure the
abundances of calcium, carbon and iron using a low-resolution spectrum from the
Sloan Digital Sky Survey. We examine the carbon and iron abundance ratios in
this star and other similar objects in the light of predicted yields from
metal-free massive stars, and conclude that they are consistent. By way of
comparison, stars with similarly low iron abundances but lower carbon-to-iron
ratios deviate from the theoretical predictions.Comment: 6 pages, 4 figures, accepted for publication in A&
Deposition of SiNx : H thin films by the electron cyclotron resonance and its application to Al/SiNx : H/Si structures
We have analyzed the electrical properties and bonding characteristics of SiNx:H thin films deposited at 200 degrees C by the electron cyclotron resonance plasma method. The films show the presence of hydrogen bonded to silicon (at the films with the ratio N/Si<1.33) or to nitrogen (for films where the ratio N/Si is higher than 1.33). In the films with the N/Si ratio of 1.38, the hydrogen content is 6 at. %. For compositions which are comprised of between N/Si=1.1 and 1.4, hydrogen concentration remains below 10 at. %. The films with N/Si=1.38 exhibited the better values of the electrical properties (resistivity, 6x10(13) Omega cm; and electric breakdown field, 3 MV/cm). We have used these films to make metal-insulator-semiconductor (MIS) devices on n-type silicon wafers. C-V measurements accomplished on the structures indicate that the interface trap density is kept in the range (3 - 5) x 10(11) cm(-2) eV(-1) for films with the N/Si ratio below 1.38. For films where the N/Si ratio is higher than 1.3, the trap density suddenly increases, following the same trend of the concentration of N-H bonds in the SiNx:H films. The results are explained on the basis of the model recently reported by Lucovsky [J. Vac. Sci. Technol. B 14, 2832 (1996)] for the electrical behavior of (oxide-nitride-oxide)/Si structures. The model is additionally supported by deep level transient spectroscopy measurements, that show the presence of silicon dangling bonds at the insulator/semiconductor interface (the so-called P-bN0 center), The concentration of these centers follows the same trend with the film composition of the interface trap density and, as a consequence, with the concentration of N-H bonds. This result further supports the N-H bonds located at the insulator/semiconductor interface which act as a precursor site to the defect generation of the type . Si=Si-3, i.e., the P-bN0 centers. A close relation between interface trap density, P-bN0 centers and N-H bond density is established
Caveolin-1 is a risk factor for postsurgery metastasis in preclinical melanoma models
Melanomas are highly lethal skin tumours that are frequently treated by surgical resection. However, the efficacy of such procedures is often limited by tumour recurrence and metastasis. Caveolin-1 (CAV1) has been attributed roles as a tumour suppressor, although in late-stage tumours, its presence is associated with enhanced metastasis. The expression of this protein in human melanoma development and particularly how the presence of CAV1 affects metastasis after surgery has not been defined. CAV1 expression in human melanocytes and melanomas increases with disease progression and is highest in metastatic melanomas. The effect of increased CAV1 expression can then be evaluated using B16F10 murine melanoma cells injected into syngenic immunocompetent C57BL/6 mice or human A375 melanoma cells injected into immunodeficient B6Rag1−/− mice. Augmented CAV1 expression suppresses tumour formation upon a subcutaneous injection, but enhances lung metastasis of cells injected into the tail vein in both models. A procedure was initially developed using B16F10 melanoma cells in C57BL/6 mice to mimic better the situation in patients undergoing surgery. Subcutaneous tumours of a defined size were removed surgically and local tumour recurrence and lung metastasis were evaluated after another 14 days. In this postsurgery setting, CAV1 presence in B16F10 melanomas favoured metastasis to the lung, although tumour suppression at the initial site was still evident. Similar results were obtained when evaluating A375 cells in B6Rag1−/− mice. These results implicate CAV1 expression in melanomas as a marker of poor prognosis for patients undergoing surgery as CAV1 expression promotes experimental lung metastasis in two different preclinical models
Resolving galaxies in time and space: II: Uncertainties in the spectral synthesis of datacubes
In a companion paper we have presented many products derived from the
application of the spectral synthesis code STARLIGHT to datacubes from the
CALIFA survey, including 2D maps of stellar population properties and 1D
averages in the temporal and spatial dimensions. Here we evaluate the
uncertainties in these products. Uncertainties due to noise and spectral shape
calibration errors and to the synthesis method are investigated by means of a
suite of simulations based on 1638 CALIFA spectra for NGC 2916, with
perturbations amplitudes gauged in terms of the expected errors. A separate
study was conducted to assess uncertainties related to the choice of
evolutionary synthesis models. We compare results obtained with the Bruzual &
Charlot models, a preliminary update of them, and a combination of spectra
derived from the Granada and MILES models. About 100k CALIFA spectra are used
in this comparison.
Noise and shape-related errors at the level expected for CALIFA propagate to
0.10-0.15 dex uncertainties in stellar masses, mean ages and metallicities.
Uncertainties in A_V increase from 0.06 mag in the case of random noise to 0.16
mag for shape errors. Higher order products such as SFHs are more uncertain,
but still relatively stable. Due to the large number statistics of datacubes,
spatial averaging reduces uncertainties while preserving information on the
history and structure of stellar populations. Radial profiles of global
properties, as well as SFHs averaged over different regions are much more
stable than for individual spaxels. Uncertainties related to the choice of base
models are larger than those associated with data and method. Differences in
mean age, mass and metallicity are ~ 0.15 to 0.25 dex, and 0.1 mag in A_V.
Spectral residuals are ~ 1% on average, but with systematic features of up to
4%. The origin of these features is discussed. (Abridged)Comment: A&A, accepte
Limits on Associated Production of Visibly and Invisibly Decaying Higgs Bosons from Z Decays
Many extensions of the standard electroweak model Higgs sector suggest that
the main Higgs decay channel is "invisible", for example, where
denotes the majoron, a weakly interacting pseudoscalar Goldstone boson
associated to the spontaneous violation of lepton number. In many of these
models the Higgs boson may also be produced in association to a massive
pseudoscalar boson (HA), in addition to the standard Bjorken mechanism (HZ). We
describe a general strategy to determine limits from LEP data on the masses and
couplings of such Higgs bosons, using the existing data on acoplanar dijet
events as well as data on four and six jet event topologies. For the sake
of illustration, we present constraints that can be obtained for the ALEPH
data.Comment: FTUV/94-36, IFIC/94-31 TIFR/TH/94--25, 12 pages + 4 figures (included
as ps files at the end
Developing a comparative marine socio-economic framework for the European Atlantic Area
Availability and easy access to a wide range of natural and human-activity data on the oceans and coastal regions of Europe is the basis for strategic decision-making on coastal and marine policy. Strategies within Europe’s Integrated Maritime Policy, including the Maritime Strategy for the Atlantic Area, Blue Growth, Maritime Spatial Planning and Marine Data and Knowledge, require coherent and comparable socio-economic data across European countries. Similarly, the Marine Strategy Framework Directive requires member states to carry out economic and social analysis of their waters and the reformed Common Fisheries Policy includes a social dimension requiring socio-economic data. However, the availability of consistent, accessible marine socio-economic data for the European Atlantic Arc regions is limited. Ocean economy studies have been undertaken in some countries (for example, Ireland, France, and UK) but timescales and methodologies are not necessarily comparable. Marnet is an EU transnational co-operation project involving eight partners from five member states of the Atlantic Area (Ireland, Spain, UK, France and Portugal). Marnet has developed a methodology to collate comparable marine socio-economic data across the Atlantic regions. The comparative marine socio-economic information system developed by Marnet could provide a template for other European States to follow that could potentially facilitate the construction of a Europe-wide marine economic information system as envisaged under the EU Integrated Maritime Policy
New physics searches at near detectors of neutrino oscillation experiments
We systematically investigate the prospects of testing new physics with tau
sensitive near detectors at neutrino oscillation facilities. For neutrino beams
from pion decay, from the decay of radiative ions, as well as from the decays
of muons in a storage ring at a neutrino factory, we discuss which effective
operators can lead to new physics effects. Furthermore, we discuss the present
bounds on such operators set by other experimental data currently available.
For operators with two leptons and two quarks we present the first complete
analysis including all relevant operators simultaneously and performing a
Markov Chain Monte Carlo fit to the data. We find that these effects can induce
tau neutrino appearance probabilities as large as O(10^{-4}), which are within
reach of forthcoming experiments. We highlight to which kind of new physics a
tau sensitive near detector would be most sensitive.Comment: 20 pages, 2 figures, REVTeX
Association of single nucleotide polymorphisms in Pre-miR-27a, Pre-miR-196a2, Pre-miR-423, miR-608 and Pre-miR-618 with breast cancer susceptibility in a South American population
Indexación: Web of ScienceBackground
MicroRNAs (miRNAs) are a novel class of endogenous, non-coding, single-stranded RNAs capable of regulating gene expression by suppressing translation or degrading mRNAs. Single nucleotide polymorphisms (SNP) can alter miRNA expression, resulting in diverse functional consequences. Previous studies have examined the association of miRNA SNPs with breast cancer (BC) susceptibility. The contribution of miRNA gene variants to BC susceptibility in South American women had been unexplored. Our study evaluated the association of the SNPs rs895819 in pre-miR27a, rs11614913 in pre-miR-196a2, rs6505162 in pre-miR-423, rs4919510 in miR-608, and rs2682818 in pre-mir-618 with familial BC and early-onset non-familial BC in non-carriers of BRCA1/2 mutations from a South American population.
Results
We evaluated the association of five SNPs with BC risk in 440 cases and 807 controls. Our data do not support an association of rs11614913:C > T and rs4919510:C > G with BC risk. The rs6505162:C > A was significantly associated with increased risk of familial BC in persons with a strong family history of BC (OR = 1.7 [95 % CI 1.0–2.0] p = 0.05). The rs2682818:C > A genotype C/A is associated with an increased BC risk in non-familial early-onset BC. For the rs895819:A > G polymorphism, the genotype G/G is significantly associated with reduced BC risk in families with a moderate history of BC (OR = 0.3 [95 % CI 0.1–0.8] p = 0.01).
Conclusions
The contribution of variant miRNA genes to BC in South American women had been unexplored. Our findings support the following conclusions: a) rs6505162:C > A in pre-miR-423 increases risk of familial BC in families with a strong history of BC; b) the C/A genotype at rs2682818:C > A (pre-miR-618) increases BC risk in non-familial early-onset BC; and c) the G/G genotype at rs895819:A > G (miR-27a) reduces BC risk in families with a moderate history of BC.http://bmcgenet.biomedcentral.com/articles/10.1186/s12863-016-0415-
The Caveolin-1 Connection to Cell Death and Survival
Nunez, S (Nunez, S.)[ 1,4 ] 1. Fac Med, CEMC, Lab Comunicac Celulares, Santiago, Chile. 4. Univ Talca, Fac Hlth Sci, Talca, ChileCaveolins are a family of membrane proteins required for the formation of small plasma membrane invaginations called caveolae that are implicated in cellular trafficking processes. In addition to this structural role, these scaffolding proteins modulate numerous intracellular signaling pathways; often via direct interaction with specific binding partners. Caveolin-1 is particularly well-studied in this respect and has been attributed a large variety of functions. Thus, Caveolin-1 also represents the best-characterized isoform of this family with respect to its participation in cancer. Rather strikingly, available evidence indicates that Caveolin-1 belongs to a select group of proteins that function, depending on the cellular settings, both as tumor suppressor and promoter of cellular traits commonly associated with enhanced malignant behavior, such as metastasis and multi-drug resistance. The mechanisms underlying such ambiguity in Caveolin-1 function constitute an area of great interest. Here, we will focus on discussing how Caveolin-1 modulates cell death and survival pathways and how this may contribute to a better understanding of the ambiguous role this protein plays in cancer
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