Vulvar Cancer: Facing a Rare Disease

“We must never be afraid to go too far, for truth lies beyond [...

Non-perturbative renormalisation and running of BSM four-quark operators in Nf=2 QCD

We perform a non-perturbative study of the scale-dependent renormalisation factors of a complete set of dimension-six four-fermion operators without power subtractions. The renormalisation-group (RG) running is determined in the continuum limit for a specific Schrödinger Functional (SF) renormalisation scheme in the framework of lattice QCD with two dynamical flavours (Nf= 2). The theory is regularised on a lattice with a plaquette Wilson action and O(a)-improved Wilson fermions. For one of these operators, the computation had been performed in Dimopoulos et al. (JHEP 0805, 065 (2008). arXiv:0712.2429); the present work completes the study for the rest of the operator basis, on the same simulations (configuration ensembles). The related weak matrix elements arise in several operator product expansions; in Δ F= 2 transitions they contain the QCD long-distance effects, including contributions from beyond-Standard Model (BSM) processes. Some of these operators mix under renormalisation and their RG-running is governed by anomalous dimension matrices. In Papinutto et al. (Eur Phys J C 77(6), 376 (2017). arXiv:1612.06461) the RG formalism for the operator basis has been worked out in full generality and the anomalous dimension matrix has been calculated in NLO perturbation theory. Here the discussion is extended to the matrix step-scaling functions, which are used in finite-size recursive techniques. We rely on these matrix-SSFs to obtain non-perturbative estimates of the operator anomalous dimensions for scales ranging from O(Λ QCD) to O(MW)

Quark-antiquark potential in defect conformal field theory

We consider antiparallel Wilson lines in N = 4 super Yang-Mills in the presence of a codimension-1 defect. We compute the Wilson lines’ expectation value both at weak coupling, in the gauge theory, and at strong coupling, by finding the string configurations which are dual to this operator. These configurations display a Gross-Ooguri transition between a connected, U-shaped string phase and a phase in which the string breaks into two disconnected surfaces. We analyze in detail the critical configurations separating the two phases and compare the string result with the gauge theory one in a certain double scaling limit

Negative Prognostic Effect of Baseline Antipsychotic Exposure in Clinical High Risk for Psychosis (CHR-P): Is Pre-Test Risk Enrichment the Hidden Culprit?

INTRODUCTION: Sample enrichment is a key factor in contemporary early-detection strategies aimed at the identification of help-seekers at increased risk of imminent transition to psychosis. We undertook a meta-analytic investigation to ascertain the role of sample enrichment in the recently highlighted negative prognostic effect of baseline antipsychotic (AP) exposure in clinical high-risk (CHR-P) of psychosis individuals. METHODS: Systematic review and meta-analysis of all published studies on CHR-P were identified according to a validated diagnostic procedure. The outcome was the proportion of transition to psychosis, which was calculated according to the Freeman‐Tukey double arcsine transformation. RESULTS: Thirty-three eligible studies were identified, including 16 samples with details on AP exposure at baseline and 17 samples with baseline AP exposure as exclusion criterion for enrollment. Those with baseline exposure to AP (n = 395) had higher transition rates (29.9%; 95% CI: 25.1%–34.8%) than those without baseline exposure to AP in the same study (n = 1289; 17.2%; 15.1%–19.4%) and those coming from samples that did not include people who were exposed to AP at baseline (n = 2073; 16.2%; 14.6%–17.8%; P < .05 in both the fixed-effects and the random-effects models). Heterogeneity within studies was substantial, with values above 75% in all comparisons. CONCLUSIONS: Sample enrichment is not a plausible explanation for the higher risk of transition to psychosis of CHR-P individuals who were already exposed to AP at the enrollment in specialized early-detection programs. Baseline exposure to AP at CHR-P assessment is a major index of enhanced, imminent risk of psychosis

Eukaryotic snoRNAs: a paradigm for gene expression flexibility.

AbstractSmall nucleolar RNAs (snoRNAs) are one of the most ancient and numerous families of non-protein-coding RNAs (ncRNAs). The main function of snoRNAs – to guide site-specific rRNA modification – is the same in Archaea and all eukaryotic lineages. In contrast, as revealed by recent genomic and RNomic studies, their genomic organization and expression strategies are the most varied. Seemingly snoRNA coding units have adopted, in the course of evolution, all the possible ways of being transcribed, thus providing a unique paradigm of gene expression flexibility. By focusing on representative fungal, plant and animal genomes, we review here all the documented types of snoRNA gene organization and expression, and we provide a comprehensive account of snoRNA expressional freedom by precisely estimating the frequency, in each genome, of each type of genomic organization. We finally discuss the relevance of snoRNA genomic studies for our general understanding of ncRNA family evolution and expression in eukaryotes

GABAergic neuroactive steroids: A new frontier in bipolar disorders?

Neurosteroids are synthesized in the brain and modulate brain excitability. There is increasing evidence of their sedative, anesthetic and antiseizure properties, as well as their influence on mood. Currently neurosteroids are classified as pregnane neurosteroids (allopregnanolone and allotetrahydrodeoxycorticosterone), androstane neurosteroids (androstanediol and etiocholanone) or sulfated neurosteroids (pregnenolone sulfate and dehydroepiandrosterone sulfate). Both preclinical and clinical findings indicate that progesterone derivative neurosteroids such as allopregnanolone and allotetrahydrodeoxycorticosterone play a role in mood disorders. Clozapine and olanzapine, which were shown to be effective in stabilizing bipolar disorder, elevate pregnenolone levels in rat hippocampus, cerebral cortex, and serum. In lithium-treated mice, the blood levels of allopregnanolone and pregnenolone were elevated compared to control levels. Women diagnosed with bipolar disorder typically show symptomatic exacerbation in relation to the menstrual cycle, and show vulnerability to the onset or recurrence of mood disorders immediately after giving birth, when the levels of neurosteroid derivatives of progesterone drop. Whereas in women who had recovered from bipolar disorder, the plasma concentration of allopregnanolone was elevated compared to either healthy controls or women with major depressive disorder during the premenstrual period. During depressive episodes, blood level of allopregnanolone is low. Treatment with fluoxetine tends to stabilize the levels of neurosteroids in depression. These findings converge to suggest that these steroids have significant mood-stabilizing effect. This hypothesis is consistent with the observation that a number of anticonvulsants are effective therapies for bipolar disorder, a finding also consistent with the antiseizure properties of neurosteroids. Further exploration of action of neuroactive steroids is likely to open new frontiers in the investigation of the etiology and treatment of mood disorders, particularly bipolar disorders

Regge spectroscopy of higher twist states in N=4\mathcal{N}=4 supersymmetric Yang-Mills theory

We study a family of higher-twist Regge trajectories in $\mathcal{N}=4$ supersymmetric Yang-Mills theory using the Quantum Spectral Curve. We explore the many-sheeted Riemann surface connecting the different trajectories and show the interplay between the degenerate non-local operators known as horizontal trajectories. We resolve their degeneracy analytically by computing the first non-trivial order of the Regge intercept at weak coupling, which exhibits new behaviour: it depends linearly on the coupling. This is consistent with our numerics, which interpolate all the way to strong coupling.Comment: main text: 6 pages, 5 figures; supplemental material: 17 pages, 3 figures, 3 table