20 research outputs found

    The Conformal Anomaly and the Neutral Currents Sector of the Standard Model

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    We elaborate on the structure of the graviton-gauge-gauge vertex in the electroweak theory, obtained by the insertion of the complete energy-momentum tensor (TT) on 2-point functions of neutral gauge currents (VV′VV'). The vertex defines the leading contribution to the effective action which accounts for the conformal anomaly and related interaction between the Standard Model and gravity. The energy momentum tensor is derived from the curved spacetime Lagrangian in the linearized gravitational limit, and with the inclusion of the term of improvement of a conformally coupled Higgs sector. As in the previous cases of QED and QCD, we find that the conformal anomaly induces an effective massless scalar interaction between gravity and the neutral currents in each gauge invariant component of the vertex. This is described by the exchange of an anomaly pole. We show that for a spontaneously broken theory the anomaly can be entirely attributed to the poles only for a conformally coupled Higgs scalar. In the exchange of a graviton, the trace part of the corresponding interaction can be interpreted as due to an effective dilaton, using a local version of the effective action. We discuss the implications of the anomalous Ward identity for the TVV′TVV' correlator for the structure of the gauge/gauge/ effective dilaton vertex in the effective action. The analogy between these effective interactions and those related to the radion in theories with large extra dimensions is pointed out.Comment: 19 pages, 10 figures. Extended version, To appear in Phys. Lett.

    Dilaton Interactions and the Anomalous Breaking of Scale Invariance of the Standard Model

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    We discuss the main features of dilaton interactions for fundamental and effective dilaton fields. In particular, we elaborate on the various ways in which dilatons can couple to the Standard Model and on the role played by the conformal anomaly as a way to characterize their interactions. In the case of a dilaton derived from a metric compactification (graviscalar), we present the structure of the radiative corrections to its decay into two photons, a photon and a ZZ, two ZZ gauge bosons and two gluons, together with their renormalization properties. We prove that, in the electroweak sector, the renormalization of the theory is guaranteed only if the Higgs is conformally coupled. For such a dilaton, its coupling to the trace anomaly is quite general, and determines, for instance, an enhancement of its decay rates into two photons and two gluons. We then turn our attention to theories containing a non-gravitational (effective) dilaton, which, in our perturbative analysis, manifests as a pseudo-Nambu Goldstone mode of the dilatation current (JDJ_D). The infrared coupling of such a state to the two-photons and to the two-gluons sector, and the corresponding anomaly enhancements of its decay rates in these channels, is critically analyzed.Comment: Revised version, 42 pages, 5 figure

    Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review

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    IntroductionSLC6A1 pathogenic variants have been associated with epilepsy and neurodevelopmental disorders. The clinical phenotype includes different seizure types, intellectual disability, and psychiatric symptoms affecting mood and behavior. Few data regarding neuropsychological features have been described, and details on cognitive profiles are often missing due to the lack of standardized tests.MethodsWe retrospectively reviewed the neuropsychological assessments of five subjects carrying heterozygous missense genetic variants in SLC6A1. We also collected data on epileptic features, EEGs, and brain MRIs. Additionally, we reviewed neuropsychological data from 204 previously reported patients with SLC6A1 pathogenic variants.ResultsIn our series, at the last evaluation (median 12.6 years), three patients had borderline intellectual functioning, one patient had mild cognitive impairment, and one patient presented with a moderate cognitive disability. Three out of five patients underwent at least two neuropsychological evaluations, which revealed a worsening of cognitive functions over time. We detected attention deficits in all patients. In addition, we observed anxiety, disruptive behavior disorder, emotional instability, and hetero aggressiveness. We also performed a literature review that highlighted that most of the patients with SLC6A1 pathogenic variants have mild-to-moderate intellectual disability and that one-third of cases have autistic traits.DiscussionBased on the literature review and the detailed description of our cases, we conclude that patients with SLC6A1-related epilepsy mostly present with mild-to-moderate intellectual disability, often associated with attention disorders. Such symptoms may worsen over time. Periodic standardized neuropsychological tests may be useful tools to follow development over time, and patient-specific rehabilitation programs could be tailored consistently

    Progettazione di un ponte strallato ciclopedonale sul fiume Arno tra Riglione e Cisanello

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    La tesi riguarda la progettazione strutturale ed architettonica di un ponte ciclopedonale, che colleghi gli itinerari ciclabili su due lati del fiume Arno a Pisa, presso gli abitati di Riglione e di Cisanello. L’opera programmata all’interno della “ciclopista dell’Arno” diverrebbe, inoltre una infrastruttura a servizio del policlinico cittadino che negli ultimi anni ha subito una eccezionale trasformazione ed un progressivo ampliamento. La soluzione adottata prevede la realizzazione di un ponte strallato in carpenteria metallica senza appoggi intermedi che prosegue con un viadotto in grado di consentire il superamento dell’ampia area golenale presente sulla sponda destra del fiume. A seguito della creazione di un modello FEM tridimensionale è stata valutata la sicurezza strutturale e geotecnica secondo le normative europee e italiane e sono stati infine studiati i fenomeni relativi alle vibrazioni indotte dai pedoni per mezzo di analisi dinamiche non lineari (time history)

    F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency: Results from a genotype-phenotype study

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    Congenital factor VII (FVII) deficiency is a rare bleeding disorder caused by mutations in F7 gene with autosomal recessive inheritance. A clinical heterogeneity with poor correlation with FVII:C levels has been described. It was the objective of this study to identify genetic defects and to evaluate their relationships with phenotype in a large cohort of patients with FVII:C<50 %. One hundred twenty-three probands were genotyped for F7 mutations and three polymorphic variants and classified according to recently published clinical scores. Forty out of 123 patients (33 %) were symptomatic (43 bleedings). A severe bleeding tendency was observed only in patients with FVII:C<0.10 %. Epistaxis (11 %) and menorrhagia (32 % of females in fertile age) were the most frequent bleedings. Molecular analysis detected 48 mutations, 20 not reported in the F7 international databases. Most mutations (62 %) were missense, large deletions were 6.2 %. Compound heterozygotes/homozygotes for mutations presented lower FVII:C levels compared to the other classes (Chi2=43.709, p<0,001). The polymorphisms distribution was significantly different among the three F7 genotypic groups (Chi2=72.289, p<0,001). The presence of truncating mutations was associated with lowest FVII:C levels (Chi2=21.351, p=0.002). This study confirms the clinical and molecular variability of the disease and the type of symptoms. It shows a good correlation between the type of F7 mutation and/or polymorphisms and FVII:C levels, without a direct link between FVII:C and bleeding tendency. The results suggest that large deletions are underestimated and that they represent a common mechanism of F7 gene inactivation which should always be investigated in the diagnostic testing for FVII deficiency

    Narrow-bandwidth picosecond pulses by spectral compression of femtosecond pulses in second-order nonlinear crystals

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    We introduce a simple approach for the efficient generation of tunable narrow-bandwidth picosecond pulses synchronized to broadband femtosecond ones. Second harmonic generation in the presence of large group velocity mismatch between the interacting pulses transfers a large fraction of the energy of a broadband fundamental frequency pulse into a narrowband second harmonic one. Using a periodically poled stoichiometric lithium tantalate crystal coupled to an infrared optical parametric amplifier, we generated 200-nJ pulses with spectral width lower than 8.5 cm-1 and tunability from 720 to 890 nm. Energy scaling and extension of the tuning range are straightforward
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