Multi-lepton signatures of vector-like leptons with flavor

We investigate collider signatures of standard model extensions featuring vector-like leptons and a flavor- ful scalar sector. Such a framework arises naturally within asymptotically safe model building, which tames the UV behavior of the standard model towards the Planck scale and beyond. We focus on values of Yukawa couplings and masses which allow to explain the present data on the muon and electron anomalous magnetic moments. Using a CMS search based on 77.4 fb−1 at the √s = 13 TeV LHC we find that flavorful vector-like leptons are excluded for masses below around 300 GeV if they are singlets under SU (2)L , and around 800 GeV if they are doublets. Exploiting the flavor-violating-like decays of the scalars, we design novel null test observables based on opposite sign opposite flavor invariant masses. These multi-lepton distributions allow to signal new physics and to extract mass hierarchies in reach of near-future searches at the LHC and the HL-LHC

Model building from asymptotic safety with Higgs and flavor portals

We perform a comprehensive search for Standard Model extensions inspired by asymptotic safety. Our models feature a singlet matrix scalar field, three generations of vectorlike leptons, and direct links to the Higgs and flavor sectors via new Yukawa and portal couplings. A novel feature is that the enlarged scalar sector may spontaneously break lepton flavor universality. We provide a complete two-loop renormalization group analysis of the running gauge, Yukawa, and quartic couplings to find ultraviolet fixed points and the critical surface of parameters, i.e., the set of boundary conditions at the TeV scale for which models remain well-behaved and predictive up to the Planck scale without encountering Landau poles or instabilities. This includes templates for asymptotically safe Standard Model extensions that match the measured values of gauge couplings and the Higgs, top, and bottom masses. We further detail the phenomenology of our models covering production, decay, fermion mixing, anomalous magnetic moments, effects from scalar mixing and chiral enhancement, and constraints on model parameters from data. Signatures at proton-proton and lepton colliders, such as lepton flavor violation and displaced vertices, and the prospect for electric dipole moments or charged lepton-flavor-violating type processes are also indicated

Anomalous magnetic moments from asymptotic safety

The measurements of the muon and electron anomalous magnetic moments hint at physics beyond the standard model. We show why and how models inspired by asymptotic safety can explain deviations from standard model predictions naturally. Our setup features an enlarged scalar sector and Yukawa couplings between leptons and new vectorlike fermions. Using the complete two-loop running of couplings, we observe a well-behaved high-energy limit of models including a stabilization of the Higgs. We find that a manifest breaking of lepton universality beyond standard model Yukawas is not necessary to explain the muon and electron anomalies. We further predict the tau anomalous magnetic moment and new particles in the TeV energy range, whose signatures at colliders are indicated. With small CP phases, the electron EDM can be as large as the present bound

Phenotyping in the era of genomics: MaTrics—a digital character matrix to document mammalian phenotypic traits

A new and uniquely structured matrix of mammalian phenotypes, MaTrics (Mammalian Traits for Comparative Genomics) in a digital form is presented. By focussing on mammalian species for which genome assemblies are available, MaTrics provides an interface between mammalogy and comparative genomics. MaTrics was developed within a project aimed to find genetic causes of phenotypic traits of mammals using Forward Genomics. This approach requires genomes and comprehensive and recorded information on homologous phenotypes that are coded as discrete categories in a matrix. MaTrics is an evolving online resource providing information on phenotypic traits in numeric code; traits are coded either as absent/present or with several states as multistate. The state record for each species is linked to at least one reference (e.g., literature, photographs, histological sections, CT scans, or museum specimens) and so MaTrics contributes to digitalization of museum collections. Currently, MaTrics covers 147 mammalian species and includes 231 characters related to structure, morphology, physiology, ecology, and ethology and available in a machine actionable NEXUS-format*. Filling MaTrics revealed substantial knowledge gaps, highlighting the need for phenotyping efforts. Studies based on selected data from MaTrics and using Forward Genomics identified associations between genes and certain phenotypes ranging from lifestyles (e.g., aquatic) to dietary specializations (e.g., herbivory, carnivory). These findings motivate the expansion of phenotyping in MaTrics by filling research gaps and by adding taxa and traits. Only databases like MaTrics will provide machine actionable information on phenotypic traits, an important limitation to genomics. MaTrics is available within the data repository Morph·D·Base (www.morphdbase.de)

Immune Evasion by Yersinia enterocolitica: Differential Targeting of Dendritic Cell Subpopulations In Vivo

CD4+ T cells are essential for the control of Yersinia enterocolitica (Ye) infection in mice. Ye can inhibit dendritic cell (DC) antigen uptake and degradation, maturation and subsequently T-cell activation in vitro. Here we investigated the effects of Ye infection on splenic DCs and T-cell proliferation in an experimental mouse infection model. We found that OVA-specific CD4+ T cells had a reduced potential to proliferate when stimulated with OVA after infection with Ye compared to control mice. Additionally, proliferation of OVA-specific CD4+ T cells was markedly reduced when cultured with splenic CD8α+ DCs from Ye infected mice in the presence of OVA. In contrast, T-cell proliferation was not impaired in cultures with CD4+ or CD4−CD8α− DCs isolated from Ye infected mice. However, OVA uptake and degradation as well as cytokine production were impaired in CD8α+ DCs, but not in CD4+ and CD4−CD8α− DCs after Ye infection. Pathogenicity factors (Yops) from Ye were most frequently injected into CD8α+ DCs, resulting in less MHC class II and CD86 expression than on non-injected CD8α+ DCs. Three days post infection with Ye the number of splenic CD8α+ and CD4+ DCs was reduced by 50% and 90%, respectively. The decreased number of DC subsets, which was dependent on TLR4 and TRIF signaling, was the result of a faster proliferation and suppressed de novo DC generation. Together, we show that Ye infection negatively regulates the stimulatory capacity of some but not all splenic DC subpopulations in vivo. This leads to differential antigen uptake and degradation, cytokine production, cell loss, and cell death rates in various DC subpopulations. The data suggest that these effects might be caused directly by injection of Yops into DCs and indirectly by affecting the homeostasis of CD4+ and CD8α+ DCs. These events may contribute to reduced T-cell proliferation and immune evasion of Ye

Search for dark matter produced in association with bottom or top quarks in √s = 13 TeV pp collisions with the ATLAS detector

A search for weakly interacting massive particle dark matter produced in association with bottom or top quarks is presented. Final states containing third-generation quarks and miss- ing transverse momentum are considered. The analysis uses 36.1 fb−1 of proton–proton collision data recorded by the ATLAS experiment at √s = 13 TeV in 2015 and 2016. No significant excess of events above the estimated backgrounds is observed. The results are in- terpreted in the framework of simplified models of spin-0 dark-matter mediators. For colour- neutral spin-0 mediators produced in association with top quarks and decaying into a pair of dark-matter particles, mediator masses below 50 GeV are excluded assuming a dark-matter candidate mass of 1 GeV and unitary couplings. For scalar and pseudoscalar mediators produced in association with bottom quarks, the search sets limits on the production cross- section of 300 times the predicted rate for mediators with masses between 10 and 50 GeV and assuming a dark-matter mass of 1 GeV and unitary coupling. Constraints on colour- charged scalar simplified models are also presented. Assuming a dark-matter particle mass of 35 GeV, mediator particles with mass below 1.1 TeV are excluded for couplings yielding a dark-matter relic density consistent with measurements

Genome-wide association study of germline variants and breast cancer-specific mortality

BACKGROUND: We examined the associations between germline variants and breast cancer mortality using a large meta-analysis of women of European ancestry. METHODS: Meta-analyses included summary estimates based on Cox models of twelve datasets using ~10