43 research outputs found
Effective Dark Matter Model: Relic density, CDMS II, Fermi LAT and LHC
The Cryogenic Dark Matter Search recently announced the observation of two
signal events with a 77% confidence level. Although statistically inconclusive,
it is nevertheless suggestive. In this work we present a model-independent
analysis on the implication of a positive signal in dark matter scattering off
nuclei. Assuming the interaction between (scalar, fermion or vector) dark
matter and the standard model induced by unknown new physics at the scale
, we examine various dimension-6 tree-level induced operators and
constrain them using the current experimental data, e.g. the WMAP data of the
relic abundance, CDMS II direct detection of the spin-independent scattering,
and indirect detection data (Fermi LAT cosmic gamma-ray), etc. Finally, the LHC
reach is also explored
Minimal Supersymmetric Inverse Seesaw: Neutrino masses, lepton flavour violation and LHC phenomenology
We study neutrino masses in the framework of the supersymmetric inverse
seesaw model. Different from the non-supersymmetric version a minimal
realization with just one pair of singlets is sufficient to explain all
neutrino data. We compute the neutrino mass matrix up to 1-loop order and show
how neutrino data can be described in terms of the model parameters. We then
calculate rates for lepton flavour violating (LFV) processes, such as , and chargino decays to singlet scalar neutrinos. The latter decays
are potentially observable at the LHC and show a characteristic decay pattern
dictated by the same parameters which generate the observed large neutrino
angles.Comment: 26 pages, 4 figures; added explanatory comments, final version for
publicatio
Sneutrino dark matter in low-scale seesaw scenarios
We consider supersymmetric models in which sneutrinos are viable dark matter candidates. These are either simple extensions of the Minimal Supersymmetric Standard Model with additional singlet superfields, such as the inverse or linear seesaw, or a model with an additional U(1) group. All of these models can accomodate the observed small neutrino masses and large mixings. We investigate the properties of sneutrinos as dark matter candidates in these scenarios. We check for phenomenological bounds, such as correct relic abundance, consistency with direct detection cross section limits and laboratory constraints, among others lepton flavour violating (LFV) charged lepton decays. While inverse and linear seesaw lead to different results for LFV, both models have very similar dark matter phenomenology, consistent with all experimental bounds. The extended gauge model shows some additional and peculiar features due to the presence of an extra gauge boson Z' and an additional light Higgs. Specifically, we point out that for sneutrino LSPs there is a strong constraint on the mass of the Z' due to the experimental bounds on the direct detection scattering cross section
A4 Flavor Models in Split Seesaw Mechanism
A seesaw mechanism in an extra-dimension, known as the split seesaw
mechanism, provides a natural way to realize a splitting mass spectrum of
right-handed neutrinos. It leads to one keV sterile neutrino as a dark matter
candidate and two heavy right-handed neutrinos being responsible for
leptogenesis to explain the observed baryon asymmetry of the Universe. We study
models based on flavor symmetry in the context of the split seesaw
mechanism. It is pointed out that most of known flavor models with three
right-handed neutrinos being triplet suffer from a degeneracy problem for
the bulk mass terms, which disturbs the split mechanism for right-handed
neutrino mass spectrum. Then we construct a new flavor model to work in
the split seesaw mechanism. In the model, the experimentally observed neutrino
masses and mixing angles can be realized from both type I+II seesaw
contributions. The model predicts the symmetry in the neutrino mass
matrix at the leading order, resulting in the vanishing and
maximal . The flavor symmetry is broken via the flavon
vacuum alignment which can be obtained from the orbifold compactification. The
model can be consistent with all data of neutrino oscillation experiments,
cosmological discussions of dark matter abundance, leptogenesis, and recent
astrophysical data.Comment: 21 pages, 1 figure, version to appear in JHE
Prader–Willi syndrome and autism spectrum disorders: an evolving story
Prader–Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11–q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums, irritability, hyperphagia, and increased risks of obesity. Many individuals also have co-occurring autism spectrum disorders (ASDs), psychosis, and mood disorders. Although the PWS 15q11–q13 region confers risks for autism, relatively few studies have assessed autism symptoms in PWS or directly compared social, behavioral, and cognitive functioning across groups with autism or PWS. This article identifies areas of phenotypic overlap and difference between PWS and ASD in core autism symptoms and in such comorbidities as psychiatric disorders, and dysregulated sleep and eating. Though future studies are needed, PWS provides a promising alternative lens into specific symptoms and comorbidities of autism
Backbending, seniority, and Pauli blocking of pairing correlations at high rotational frequencies in rapidly rotating nuclei
Garrett et al. systematically investigated band-crossing frequencies resulting from the rotational alignment of the first pair of i13/2 neutrons (AB) in rare-earth nuclei. In that study, evidence was found for an odd-even neutron number dependence attributed to changes in the strength of neutron pairing correlations. The present paper carries out a similar investigation at higher rotational frequencies for the second pair of aligning i13/2 neutrons (BC). Again, a systematic difference in band-crossing frequencies is observed between odd-N and even-N Er, Yb, Hf, and W nuclei, but in the BC case, it is opposite to the AB neutron-number dependence. These results are discussed in terms of a reduction of neutron pairing correlations at high rotational frequencies and of the effects of Pauli blocking on the pairing field by higher-seniority configurations. Also playing a significant role are the changes in deformation with proton and neutron numbers, the changes in location of single-particle orbitals as a function of quadrupole deformation, and the position of the Fermi surface with regard to the various ω components of the neutron i13/2 shell
Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease
BackgroundLow-grade alimentary lymphoma (LGAL) is characterised by the infiltration of neoplastic T-lymphocytes, typically in the small intestine. The incidence of LGAL has increased over the last ten years and it is now the most frequent digestive neoplasia in cats and comprises 60 to 75% of gastrointestinal lymphoma cases. Given that LGAL shares common clinical, paraclinical and ultrasonographic features with inflammatory bowel diseases, establishing a diagnosis is challenging. A review was designed to summarise current knowledge of the pathogenesis, diagnosis, prognosis and treatment of feline LGAL. Electronic searches of PubMed and Science Direct were carried out without date or language restrictions.ResultsA total of 176 peer-reviewed documents were identified and most of which were published in the last twenty years. 130 studies were found from the veterinary literature and 46 from the human medicine literature. Heterogeneity of study designs and outcome measures made meta-analysis inappropriate. The pathophysiology of feline LGAL still needs to be elucidated, not least the putative roles of infectious agents, environmental factors as well as genetic events. The most common therapeutic strategy is combination treatment with prednisolone and chlorambucil, and prolonged remission can often be achieved. Developments in immunohistochemical analysis and clonality testing have improved the confidence of clinicians in obtaining a correct diagnosis between LGAL and IBD. The condition shares similarities with some diseases in humans, especially human indolent T-cell lymphoproliferative disorder of the gastrointestinal tract.ConclusionsThe pathophysiology of feline LGAL still needs to be elucidated and prospective studies as well as standardisation of therapeutic strategies are needed. A combination of conventional histopathology and immunohistochemistry remains the current gold-standard test, but clinicians should be cautious about reclassifying cats previously diagnosed with IBD to lymphoma on the basis of clonality testing. Importantly, feline LGAL could be considered to be a potential animal model for indolent digestive T-cell lymphoproliferative disorder, a rare condition in human medicine
