131 research outputs found
Electroweak Gauge-Boson Production at Small q_T: Infrared Safety from the Collinear Anomaly
Using methods from effective field theory, we develop a novel, systematic
framework for the calculation of the cross sections for electroweak gauge-boson
production at small and very small transverse momentum q_T, in which large
logarithms of the scale ratio M_V/q_T are resummed to all orders. These cross
sections receive logarithmically enhanced corrections from two sources: the
running of the hard matching coefficient and the collinear factorization
anomaly. The anomaly leads to the dynamical generation of a non-perturbative
scale q_* ~ M_V e^{-const/\alpha_s(M_V)}, which protects the processes from
receiving large long-distance hadronic contributions. Expanding the cross
sections in either \alpha_s or q_T generates strongly divergent series, which
must be resummed. As a by-product, we obtain an explicit non-perturbative
expression for the intercept of the cross sections at q_T=0, including the
normalization and first-order \alpha_s(q_*) correction. We perform a detailed
numerical comparison of our predictions with the available data on the
transverse-momentum distribution in Z-boson production at the Tevatron and LHC.Comment: 34 pages, 9 figure
Probing the low transverse momentum domain of Z production with novel variables
The measurement of the low transverse momentum region of vector boson
production in Drell-Yan processes has long been invaluable to testing our
knowledge of QCD dynamics both beyond fixed-order in perturbation theory as
well as in the non-perturbative region. Recently the D\O\ collaboration have
introduced novel variables which lead to improved measurements compared to the
case of the standard QT variable. To complement this improvement on the
experimental side, we develop here a complete phenomenological study dedicated
in particular to the new \phi* variable. We compare our study, which contains
the state-of-the-art next-to-next-to-leading resummation of large logarithms
and a smooth matching to the full next-to-leading order result, to the
experimental data and find excellent agreement over essentially the entire
range of \phi*, even without direct inclusion of non-perturbative effects. We
comment on our findings and on the potential for future studies to constrain
non-perturbative behaviour.Comment: 20 pages, 7 figures. Version accepted for publication in JHEP. A
figure with comparison to RESBOS has been adde
Lateral specialization in unilateral spatial neglect : a cognitive robotics model
In this paper, we present the experimental results of an embodied cognitive robotic approach for modelling the human cognitive deficit known as unilateral spatial neglect (USN). To this end, we introduce an artificial neural network architecture designed and trained to control the spatial attentional focus of the iCub robotic platform. Like the human brain, the architecture is divided into two hemispheres and it incorporates bio-inspired plasticity mechanisms, which allow the development of the phenomenon of the specialization of the right hemisphere for spatial attention. In this study, we validate the model by replicating a previous experiment with human patients affected by the USN and numerical results show that the robot mimics the behaviours previously exhibited by humans. We also simulated recovery after the damage to compare the performance of each of the two hemispheres as additional validation of the model. Finally, we highlight some possible advantages of modelling cognitive dysfunctions of the human brain by means of robotic platforms, which can supplement traditional approaches for studying spatial impairments in humans
The electroretinogram:a useful tool for evaluating age-related macular disease?
With an ageing population, the number of age-related macular disease (ARMD) cases will inevitably rise. This gives greater impetus for the need to identify the disease earlier and assess treatments to slow disease progression. Differing electroretinogram (ERG) modalities have been reviewed in relation to the objective assessment of retinal function in ARMD and for monitoring the effectiveness of clinical interventions. Conflicting results have been found with regard to the efficacy of ERG findings in the investigation of ARMD in previous years. The newer multifocal ERG paradigm provides spatial topographical information about retinal function in ARMD. It has shown promising results in monitoring effectiveness of clinical interventions and studies are continuing in this area. Better knowledge of retinal function in ARMD may lead to enhanced treatments at each phase of the disease
Bessel-Weighted Asymmetries in Semi Inclusive Deep Inelastic Scattering
The concept of weighted asymmetries is revisited for semi-inclusive deep
inelastic scattering. We consider the cross section in Fourier space, conjugate
to the outgoing hadron's transverse momentum, where convolutions of transverse
momentum dependent parton distribution functions and fragmentation functions
become simple products. Individual asymmetric terms in the cross section can be
projected out by means of a generalized set of weights involving Bessel
functions. Advantages of employing these Bessel weights are that they suppress
(divergent) contributions from high transverse momentum and that soft factors
cancel in (Bessel-) weighted asymmetries. Also, the resulting compact
expressions immediately connect to previous work on evolution equations for
transverse momentum dependent parton distribution and fragmentation functions
and to quantities accessible in lattice QCD. Bessel weighted asymmetries are
thus model independent observables that augment the description and our
understanding of correlations of spin and momentum in nucleon structure.Comment: Matches published version, JHEP style, 36 pages and 2 figures, minor
correction
Targeted Inactivation of Cerberus Like-2 Leads to Left Ventricular Cardiac Hyperplasia and Systolic Dysfunction in the Mouse
Previous analysis of the Cerberus like 2 knockout (Cerl2(-/-)) mouse revealed a significant mortality during the first day after birth, mostly due to cardiac defects apparently associated with randomization of the left-right axis. We have however, identified Cerl2-associated cardiac defects, particularly a large increase in the left ventricular myocardial wall in neonates that cannot be explained by laterality abnormalities. Therefore, in order to access the endogenous role of Cerl2 in cardiogenesis, we analyzed the embryonic and neonatal hearts of Cerl2 null mutants that did not display a laterality phenotype. Neonatal mutants obtained from the compound mouse line Cer2(-/-)Fundacao para a Ciencia e Tecnologia (FCT); IBB/CBME [PEst-OE/EQB/LA0023/2011]; FCT [SFRH/BD/62081/2009]info:eu-repo/semantics/publishedVersio
Autosomal recessive cerebellar ataxias
Autosomal recessive cerebellar ataxias (ARCA) are a heterogeneous group of rare neurological disorders involving both central and peripheral nervous system, and in some case other systems and organs, and characterized by degeneration or abnormal development of cerebellum and spinal cord, autosomal recessive inheritance and, in most cases, early onset occurring before the age of 20 years. This group encompasses a large number of rare diseases, the most frequent in Caucasian population being Friedreich ataxia (estimated prevalence 2–4/100,000), ataxia-telangiectasia (1–2.5/100,000) and early onset cerebellar ataxia with retained tendon reflexes (1/100,000). Other forms ARCA are much less common. Based on clinicogenetic criteria, five main types ARCA can be distinguished: congenital ataxias (developmental disorder), ataxias associated with metabolic disorders, ataxias with a DNA repair defect, degenerative ataxias, and ataxia associated with other features. These diseases are due to mutations in specific genes, some of which have been identified, such as frataxin in Friedreich ataxia, α-tocopherol transfer protein in ataxia with vitamin E deficiency (AVED), aprataxin in ataxia with oculomotor apraxia (AOA1), and senataxin in ataxia with oculomotor apraxia (AOA2). Clinical diagnosis is confirmed by ancillary tests such as neuroimaging (magnetic resonance imaging, scanning), electrophysiological examination, and mutation analysis when the causative gene is identified. Correct clinical and genetic diagnosis is important for appropriate genetic counseling and prognosis and, in some instances, pharmacological treatment. Due to autosomal recessive inheritance, previous familial history of affected individuals is unlikely. For most ARCA there is no specific drug treatment except for coenzyme Q10 deficiency and abetalipoproteinemia
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