72 research outputs found
Constraints on supersymmetry with light third family from LHC data
We present a re-interpretation of the recent ATLAS limits on supersymmetry in
channels with jets (with and without b-tags) and missing energy, in the context
of light third family squarks, while the first two squark families are
inaccessible at the 7 TeV run of the Large Hadron Collider (LHC). In contrast
to interpretations in terms of the high-scale based constrained minimal
supersymmetric standard model (CMSSM), we primarily use the low-scale
parametrisation of the phenomenological MSSM (pMSSM), and translate the limits
in terms of physical masses of the third family squarks. Side by side, we also
investigate the limits in terms of high-scale scalar non-universality, both
with and without low-mass sleptons. Our conclusion is that the limits based on
0-lepton channels are not altered by the mass-scale of sleptons, and can be
considered more or less model-independent.Comment: 20 pages, 8 figures, 2 tables. Version published in JHE
Bigger, Better, Faster, More at the LHC
Multijet plus missing energy searches provide universal coverage for theories
that have new colored particles that decay into a dark matter candidate and
jets. These signals appear at the LHC further out on the missing energy tail
than two-to-two scattering indicates. The simplicity of the searches at the LHC
contrasts sharply with the Tevatron where more elaborate searches are necessary
to separate signal from background. The searches presented in this article
effectively distinguish signal from background for any theory where the LSP is
a daughter or granddaughter of the pair-produced colored parent particle
without ever having to consider missing energies less than 400 GeV.Comment: 26 pages, 8 Figures. Minor textual changes, typos fixed and
references adde
Phenomenological Implications of Deflected Mirage Mediation: Comparison with Mirage Mediation
We compare the collider phenomenology of mirage mediation and deflected
mirage mediation, which are two recently proposed "mixed" supersymmetry
breaking scenarios motivated from string compactifications. The scenarios
differ in that deflected mirage mediation includes contributions from gauge
mediation in addition to the contributions from gravity mediation and anomaly
mediation also present in mirage mediation. The threshold effects from gauge
mediation can drastically alter the low energy spectrum from that of pure
mirage mediation models, resulting in some cases in a squeezed gaugino spectrum
and a gluino that is much lighter than other colored superpartners. We provide
several benchmark deflected mirage mediation models and construct model lines
as a function of the gauge mediation contributions, and discuss their discovery
potential at the LHC.Comment: 29 pages, 9 figure
Where the Sidewalk Ends: Jets and Missing Energy Search Strategies for the 7 TeV LHC
This work explores the potential reach of the 7 TeV LHC to new colored states
in the context of simplified models and addresses the issue of which search
regions are necessary to cover an extensive set of event topologies and
kinematic regimes. This article demonstrates that if searches are designed to
focus on specific regions of phase space, then new physics may be missed if it
lies in unexpected corners. Simple multiregion search strategies can be
designed to cover all of kinematic possibilities. A set of benchmark models are
created that cover the qualitatively different signatures and a benchmark
multiregion search strategy is presented that covers these models.Comment: 30 pages, 8 Figures, 3 Tables. Version accepted at JHEP. Minor
changes. Added figur
Heavy Squarks at the LHC
The LHC, with its seven-fold increase in energy over the Tevatron, is capable
of probing regions of SUSY parameter space exhibiting qualitatively new
collider phenomenology. Here we investigate one such region in which first
generation squarks are very heavy compared to the other superpartners. We find
that the production of these squarks, which is dominantly associative, only
becomes rate-limited at mSquark > 4(5) TeV for L~10(100) fb-1. However,
discovery of this scenario is complicated because heavy squarks decay primarily
into a jet and boosted gluino, yielding a dijet-like topology with missing
energy (MET) pointing along the direction of the second hardest jet. The result
is that many signal events are removed by standard jet/MET anti-alignment cuts
designed to guard against jet mismeasurement errors. We suggest replacing these
anti-alignment cuts with a measurement of jet substructure that can
significantly extend the reach of this channel while still removing much of the
background. We study a selection of benchmark points in detail, demonstrating
that mSquark= 4(5) TeV first generation squarks can be discovered at the LHC
with L~10(100)fb-1
Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis
Vertical and horizontal interactions between membrane constituents account for integrity, strength and deformability of the
erythrocyte. Disruption of vertical interactions caused by membrane
protein deficiencies in hereditary spherocytosis (HS), favor membrane
vesiculation with development of spherocytic cells. Our aim was to evaluate the hematological and clinical presentation of HS according to the type and amount of protein deficiency. We studied 81 Portuguese
individuals, 71 belonging to 21 families plus 10 unrelated subjects, and found that 51 of them were HS patients. Patients were classified as presenting mild, typical or severe HS, according to laboratory results
and clinical follow-up. We performed screening tests and the standardized
electrophoretic membrane protein analysis to identify and quantify protein deficiencies. We found band 3 and ankyrin deficiencies
as the major causes for HS. The ratios between the value of the primary and/or secondary protein deficiencies showed significantly different values according to the severity of HS, and a significant inverse correlation with the severity of HS was observed. In mild HS, the ratios
between protein deficiencies reflected equivalent protein deficiencies,
while an unbalance was observed in typical HS, which was enhanced in severe HS. Our data suggest that the relative quantification of each major membrane protein and of the ratios between the values of protein deficiencies may be helpful in providing additional data about the
clinical outcome of HS
MFV Reductions of MSSM Parameter Space
The 100+ free parameters of the minimal supersymmetric standard model (MSSM)
make it computationally difficult to compare systematically with data,
motivating the study of specific parameter reductions such as the cMSSM and
pMSSM. Here we instead study the reductions of parameter space implied by using
minimal flavour violation (MFV) to organise the R-parity conserving MSSM, with
a view towards systematically building in constraints on flavour-violating
physics. Within this framework the space of parameters is reduced by expanding
soft supersymmetry-breaking terms in powers of the Cabibbo angle, leading to a
24-, 30- or 42-parameter framework (which we call MSSM-24, MSSM-30, and MSSM-42
respectively), depending on the order kept in the expansion. We provide a
Bayesian global fit to data of the MSSM-30 parameter set to show that this is
manageable with current tools. We compare the MFV reductions to the
19-parameter pMSSM choice and show that the pMSSM is not contained as a subset.
The MSSM-30 analysis favours a relatively lighter TeV-scale pseudoscalar Higgs
boson and with multi-TeV sparticles.Comment: 2nd version, minor comments and references added, accepted for
publication in JHE
Interpreting LHC SUSY searches in the phenomenological MSSM
We interpret within the phenomenological MSSM (pMSSM) the results of SUSY
searches published by the CMS collaboration based on the first ~1 fb^-1 of data
taken during the 2011 LHC run at 7 TeV. The pMSSM is a 19-dimensional
parametrization of the MSSM that captures most of its phenomenological
features. It encompasses, and goes beyond, a broad range of more constrained
SUSY models. Performing a global Bayesian analysis, we obtain posterior
probability densities of parameters, masses and derived observables. In
contrast to constraints derived for particular SUSY breaking schemes, such as
the CMSSM, our results provide more generic conclusions on how the current data
constrain the MSSM.Comment: 15 pages, 7 figures; minor revision, some references and a comment on
prior dependence added; version accepted by JHE
BALB/c Mice Infected with Antimony Treatment Refractory Isolate of Leishmania braziliensis Present Severe Lesions due to IL-4 Production
Leishmaniasis is a neglected disease that affects more than 12 million people worldwide. In Brazil, the cutaneous disease is more prevalent with about 28,000 new cases reported each year, and L. braziliensis is the main causative agent. The interesting data about the infection with this parasite is the wide variety of clinical manifestations that ranges from single ulcerated lesions to mucocutaneous and disseminated disease. However, experimental models to study the infection with this parasite are difficult to develop due to high resistance of most mouse strains to the infection, and the mechanisms underlying the distinct manifestations remain poorly understood. Here, the authors use a mouse experimental model of infection with different L. braziliensis isolates, known to induce diseases with distinct severity in the human hosts, to elucidate immune mechanisms that may be involved in the different manifestations. They showed that distinct parasite isolates may modulate host response, and increased IL-4 production and Arg I expression was related to more severe disease, resulting in longer length of disease with larger lesions and reduced parasite clearance. These findings may be useful in the identification of immunological targets to control L. braziliensis infection and potential clinical markers of disease progression
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcome.
The first described patients with pyridox(am)ine 5'-phosphate oxidase deficiency all had neonatal onset seizures that did not respond to treatment with pyridoxine but responded to treatment with pyridoxal 5'-phosphate. Our data suggest, however, that the clinical spectrum of pyridox(am)ine 5'-phosphate oxidase deficiency is much broader than has been reported in the literature. Sequencing of the PNPO gene was undertaken for a cohort of 82 individuals who had shown a reduction in frequency and severity of seizures in response to pyridoxine or pyridoxal 5'-phosphate. Novel sequence changes were studied using a new cell-free expression system and a mass spectrometry-based assay for pyridoxamine phosphate oxidase. Three groups of patients with PNPO mutations that had reduced enzyme activity were identified: (i) patients with neonatal onset seizures responding to pyridoxal 5'-phosphate (n = 6); (ii) a patient with infantile spasms (onset 5 months) responsive to pyridoxal 5'-phosphate (n = 1); and (iii) patients with seizures starting under 3 months of age responding to pyridoxine (n = 8). Data suggest that certain genotypes (R225H/C and D33V) are more likely to result in seizures that to respond to treatment with pyridoxine. Other mutations seem to be associated with infertility, miscarriage and prematurity. However, the situation is clearly complex with the same combination of mutations being seen in patients who responded and did not respond to pyridoxine. It is possible that pyridoxine responsiveness in PNPO deficiency is affected by prematurity and age at the time of the therapeutic trial. Other additional factors that are likely to influence treatment response and outcome include riboflavin status and how well the foetus has been supplied with vitamin B6 by the mother. For some patients there was a worsening of symptoms on changing from pyridoxine to pyridoxal 5'-phosphate. Many of the mutations in PNPO affected residues involved in binding flavin mononucleotide or pyridoxal 5'-phosphate and many of them showed residual enzyme activity. One sequence change (R116Q), predicted to affect flavin mononucleotide binding and binding of the two PNPO dimers, and with high residual activity was found in Groups (ii) and (iii). This sequence change has been reported in the 1000 Genomes project suggesting it could be a polymorphism but alternatively it could be a common mutation, perhaps responsible for the susceptibility locus for genetic generalized epilepsy on 17q21.32 (close to rs72823592). We believe the reduction in PNPO activity and B6-responsive epilepsy in the patients reported here indicates that it contributes to the pathogenesis of epilepsy
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