1,062 research outputs found
D=7 / D=6 Heterotic Supergravity with Gauged R-Symmetry
We construct a family of chiral anomaly-free supergravity theories in D=6
starting from D=7 supergravity with a gauged noncompact R-symmetry, employing a
Horava-Witten bulk-plus-boundary construction. The gauged noncompact R-symmetry
yields a positive (de Sitter sign) D=6 scalar field potential. Classical
anomaly inflow which is needed to cancel boundary-field loop anomalies requires
careful consideration of the gravitational, gauge, mixed and local
supersymmetry anomalies. Coupling of boundary hypermultiplets requires care
with the Sp(1) gauge connection required to obtain quaternionic Kahler target
manifolds in D=6. This class of gauged R-symmetry models may be of use as
starting points for further compactifications to D=4 that take advantage of the
positive scalar potential, such as those proposed in the scenario of
supersymmetry in large extra dimensions.Comment: 43 pages, plain Latex; Clarification of discussion and references
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Wilson Lines and a Canonical Basis of SU(4) Heterotic Standard Models
The spontaneous breaking of SU(4) heterotic standard models by Z_3 x Z_3
Wilson lines to the MSSM with three right-handed neutrino supermultiplets and
gauge group SU(3)_C x SU(2)_L x U(1) x U(1) is explored. The two-dimensional
subspace of the Spin(10) Lie algebra that commutes with su(3)_C + su(2)_L is
analyzed. It is shown that there is a unique basis for which the initial soft
supersymmetry breaking parameters are uncorrelated and for which the U(1) x
U(1) field strengths have no kinetic mixing at any scale. If the Wilson lines
"turn on" at different scales, there is an intermediate regime with either a
left-right or a Pati-Salam type model. We compute their spectra directly from
string theory, and adjust the associated mass parameter so that all gauge
parameters exactly unify. A detailed analysis of the running gauge couplings
and soft gaugino masses is presented.Comment: 59 pages, 9 figure
Heterotic Line Bundle Standard Models
In a previous publication, arXiv:1106.4804, we have found 200 models from
heterotic Calabi-Yau compactifications with line bundles, which lead to
standard models after taking appropriate quotients by a discrete symmetry and
introducing Wilson lines. In this paper, we construct the resulting standard
models explicitly, compute their spectrum including Higgs multiplets, and
analyze some of their basic properties. After removing redundancies we find
about 400 downstairs models, each with the precise matter spectrum of the
supersymmetric standard model, with one, two or three pairs of Higgs doublets
and no exotics of any kind. In addition to the standard model gauge group, up
to four Green-Schwarz anomalous U(1) symmetries are present in these models,
which constrain the allowed operators in the four-dimensional effective
supergravity. The vector bosons associated to these anomalous U(1) symmetries
are massive. We explicitly compute the spectrum of allowed operators for each
model and present the results, together with the defining data of the models,
in a database of standard models accessible at
http://www-thphys.physics.ox.ac.uk/projects/CalabiYau/linebundlemodels/index.html.
Based on these results we analyze elementary phenomenological properties. For
example, for about 200 models all dimension four and five proton decay
violating operators are forbidden by the additional U(1) symmetries.Comment: 55 pages, Latex, 3 pdf figure
Distributed autonomy and trade-offs in online multiobject k-coverage
In this article, we explore the online multiobject k-coverage problem in visual sensor networks. This problem combines k-coverage and the cooperative multirobot observation of multiple moving targets problem, and thereby captures key features of rapidly deployed camera networks, including redundancy and team-based tracking of evasive or unpredictable targets. The benefits of using mobile cameras are demonstrated and we explore the balance of autonomy between cameras generating new subgoals, and those responders able to fulfill them. We show that higher performance against global goals is achieved when decisions are delegated to potential responders who treat subgoals as optional, rather than as obligations that override existing goals without question. This is because responders have up-to-date knowledge of their own state and progress toward goals where they are situated, which is typically old or incomplete at locations remote from them. Examining the extent to which approaches overprovision or underprovision coverage, we find that being well suited for achieving 1-coverage does not imply good performance at k-coverage. Depending on the structure of the environment, the problems of 1-coverage and k-coverage are not necessarily aligned and that there is often a trade-off to be made between standard coverage maximization and achieving k-coverage
6-thioguanine treatment in inflammatory bowel disease: A critical appraisal by a European 6-TG working party
Recently, the suggestion to use 6-thioguanine (6-TG) as an alternative thiopurine in patients with inflammatory bowel disease (IBD) has been discarded due to reports about possible (hepato) toxicity. During meetings arranged in Vienna and Prague in 2004, European experts applying 6-TG further on in IBD patients presented data on safety and efficacy of 6-TG. After thorough evaluation of its risk-benefit ratio, the group consented that 6-TG may still be considered as a rescue drug in stringently defined indications in IBD, albeit restricted to a clinical research setting. As a potential indication for administering 6-TG, we delineated the requirement for maintenance therapy as well as intolerance and/or resistance to aminosalicylates, azathioprine, 6-mercaptopurine, methotrexate and infliximab. Furthermore, indications are preferred in which surgery is thought to be inappropriate. The standard 6-TG dosage should not exceed 25 mg daily. Routine laboratory controls are mandatory in short intervals. Liver biopsies should be performed after 6-12 months, three years and then three-yearly accompanied by gastroduodenoscopy, to monitor for potential hepatotoxicity, including nodular regenerative hyperplasia (NRH) and veno-occlusive disease (VOD). Treatment with 6-TG must be discontinued in case of overt or histologically proven hepatotoxicity. Copyright (c) 2006 S. Karger AG, Basel
Predicting cell types and genetic variations contributing to disease by combining GWAS and epigenetic data
Genome-wide association studies (GWASs) identify single nucleotide polymorphisms (SNPs) that are enriched in individuals suffering from a given disease. Most disease-associated SNPs fall into non-coding regions, so that it is not straightforward to infer phenotype or function; moreover, many SNPs are in tight genetic linkage, so that a SNP identified as associated with a particular disease may not itself be causal, but rather signify the presence of a linked SNP that is functionally relevant to disease pathogenesis. Here, we present an analysis method that takes advantage of the recent rapid accumulation of epigenomics data to address these problems for some SNPs. Using asthma as a prototypic example; we show that non-coding disease-associated SNPs are enriched in genomic regions that function as regulators of transcription, such as enhancers and promoters. Identifying enhancers based on the presence of the histone modification marks such as H3K4me1 in different cell types, we show that the location of enhancers is highly cell-type specific. We use these findings to predict which SNPs are likely to be directly contributing to disease based on their presence in regulatory regions, and in which cell types their effect is expected to be detectable. Moreover, we can also predict which cell types contribute to a disease based on overlap of the disease-associated SNPs with the locations of enhancers present in a given cell type. Finally, we suggest that it will be possible to re-analyze GWAS studies with much higher power by limiting the SNPs considered to those in coding or regulatory regions of cell types relevant to a given disease
Superpotential de-sequestering in string models
Non-perturbative superpotential cross-couplings between visible sector matter
and K\"ahler moduli can lead to significant flavour-changing neutral currents
in compactifications of type IIB string theory. Here, we compute corrections to
Yukawa couplings in orbifold models with chiral matter localised on D3-branes
and non-perturbative effects on distant D7-branes. By evaluating a threshold
correction to the D7-brane gauge coupling, we determine conditions under which
the non-perturbative corrections to the Yukawa couplings appear. The flavour
structure of the induced Yukawa coupling generically fails to be aligned with
the tree-flavour structure. We check our results by also evaluating a
correlation function of two D7-brane gauginos and a D3-brane Yukawa coupling.
Finally, by calculating a string amplitude between n hidden scalars and visible
matter we show how non-vanishing vacuum expectation values of distant D7-brane
scalars, if present, may correct visible Yukawa couplings with a flavour
structure that differs from the tree-level flavour structure.Comment: 37 pages + appendices, 8 figure
Loss of functional pRB is not a ubiquitous feature of B-cell malignancies
Human cancers frequently sustain genetic mutations that alter the function of their G1 cell cycle control check point. These include changes to the retinoblastoma gene and to the genes that regulate its phosphorylation, such as the cyclin-dependent kinase inhibitor p16(INK4a). Altered expression of retinoblastoma protein (pRb) is associated with non-Hodgkin's lymphoma, particularly centroblastic and Burkitt's lymphomas. pRb is expressed in normal B-cells and its regulatory phosphorylation pathway is activated in response to a variety of stimuli. Since human B-lymphoma-derived cell lines are often used as in vitro model systems to analyse the downstream effects of signal transduction, we examined the functional status of pRb in a panel of human B-cell lines. We identified eleven cell lines which express the hyperphosphorylated forms of pRb. Furthermore, we suggest that the pRb protein appears to be functional in these cell lines
Brane-World Gravity
The observable universe could be a 1+3-surface (the "brane") embedded in a
1+3+\textit{d}-dimensional spacetime (the "bulk"), with Standard Model
particles and fields trapped on the brane while gravity is free to access the
bulk. At least one of the \textit{d} extra spatial dimensions could be very
large relative to the Planck scale, which lowers the fundamental gravity scale,
possibly even down to the electroweak ( TeV) level. This revolutionary
picture arises in the framework of recent developments in M theory. The
1+10-dimensional M theory encompasses the known 1+9-dimensional superstring
theories, and is widely considered to be a promising potential route to quantum
gravity. At low energies, gravity is localized at the brane and general
relativity is recovered, but at high energies gravity "leaks" into the bulk,
behaving in a truly higher-dimensional way. This introduces significant changes
to gravitational dynamics and perturbations, with interesting and potentially
testable implications for high-energy astrophysics, black holes, and cosmology.
Brane-world models offer a phenomenological way to test some of the novel
predictions and corrections to general relativity that are implied by M theory.
This review analyzes the geometry, dynamics and perturbations of simple
brane-world models for cosmology and astrophysics, mainly focusing on warped
5-dimensional brane-worlds based on the Randall--Sundrum models. We also cover
the simplest brane-world models in which 4-dimensional gravity on the brane is
modified at \emph{low} energies -- the 5-dimensional Dvali--Gabadadze--Porrati
models. Then we discuss co-dimension two branes in 6-dimensional models.Comment: A major update of Living Reviews in Relativity 7:7 (2004)
"Brane-World Gravity", 119 pages, 28 figures, the update contains new
material on RS perturbations, including full numerical solutions of
gravitational waves and scalar perturbations, on DGP models, and also on 6D
models. A published version in Living Reviews in Relativit
Cyclin D1 expression in non-small-cell lung cancers: its association with altered p53 expression, cell proliferation and clinical outcome
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