1,146 research outputs found
T-duality and Actions for Non-BPS D-branes
We employ T-duality to restrict the tachyon dependence of effective actions
for non-BPS D-branes. For the Born-Infeld part the criteria of T-duality and
supersymmetry are satisfied by a simple extension of the D-brane Born-Infeld
action.Comment: Latex, 11 page
N=2 supergravity in five dimensions revisited
We construct matter-coupled N=2 supergravity in five dimensions, using the
superconformal approach. For the matter sector we take an arbitrary number of
vector-, tensor- and hyper-multiplets. By allowing off-diagonal vector-tensor
couplings we find more general results than currently known in the literature.
Our results provide the appropriate starting point for a systematic search for
BPS solutions, and for applications of M-theory compactifications on Calabi-Yau
manifolds with fluxes.Comment: 35 pages; v.2: A sign changed in a bilinear fermion term in (5.7
Species interactions: nextâlevel citizen science
We envisage a future research environment where digital data on species interactions are easily accessible and comprehensively cover all species, life stages and habitats. To achieve this goal, we need data from many sources, including the largely untapped potential of citizen science for mobilising and utilising existing information on species interactions. Traditionally volunteers contributing information on the occurrence of species have focused on single-species observations from within one target taxon. We make recommendations on how to improve the gathering of species interaction data through citizen science, which data should be collected and how it can be motivated. These recommendations include providing feedback in the form of network visualisations, leveraging a wide variety of other data sources and eliciting an emotional connection to the species in question. There are many uses for these data, but in the context of biological invasions, information on species interactions will increase understanding of the effects of invasive alien species on recipient communities and ecosystems. We believe that the inclusion of ecological networks as a concept within citizen science, not only for initiatives focussed on biological invasions but also across other ecological themes, will not only enrich scientific knowledge on species interactions but also deepen the experience and enjoyment of citizens themselves
Long-term Mortality in HIV-Positive Individuals Virally Suppressed for >3 Years With Incomplete CD4 Recovery
Virally suppressed HIV-positive individuals on combination antiretroviral therapy who do not achieve a CD4 count >200 cells/”L have substantially increased long-term mortality. The increased mortality was seen across different patient groups and for all causes of deat
Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B
Background Malformations of cortical development (MCDs) have been reported in a subset of patients with pathogenic heterozygous variants in GRIN1 or GRIN2B, genes which encode for subunits of the N-methyl-D-aspartate receptor (NMDAR). The aim of this study was to further define the phenotypic spectrum of NMDAR-related MCDs.
Methods We report the clinical, radiological and molecular features of 7 new patients and review data on 18 previously reported individuals with NMDAR-related MCDs. Neuropathological findings for two individuals with heterozygous variants in GRIN1 are presented. We report the clinical and neuropathological features of one additional individual with homozygous pathogenic variants in GRIN1.
Results Heterozygous variants in GRIN1 and GRIN2B were associated with overlapping severe clinical and imaging features, including global developmental delay, epilepsy, diffuse dysgyria, dysmorphic basal ganglia and hippocampi. Neuropathological examination in two fetuses with heterozygous GRIN1 variants suggests that proliferation as well as radial and tangential neuronal migration are impaired. In addition, we show that neuronal migration is also impaired by homozygous GRIN1 variants in an individual with microcephaly with simplified gyral pattern.
Conclusion These findings expand our understanding of the clinical and imaging features of the âNMDARopathyâ spectrum and contribute to our understanding of the likely underlying pathogenic mechanisms leading to MCD in these patients.
Data availability statement
Data are available upon reasonable request. All data relevant to the study are included in the article or uploaded as supplementary information. Anonymised data from this study will be shared by request from any qualified investigator
A roadmap to the efficient and robust characterization of temperate terrestrial planet atmospheres with JWST
Ultra-cool dwarf stars are abundant, long-lived, and uniquely suited to
enable the atmospheric study of transiting terrestrial companions with JWST.
Amongst them, the most prominent is the M8.5V star TRAPPIST-1 and its seven
planets, which have been the favored targets of eight JWST Cycle 1 programs.
While Cycle 1 observations have started to yield preliminary insights into the
planets, they have also revealed that their atmospheric exploration requires a
better understanding of their host star. Here, we propose a roadmap to
characterize the TRAPPIST-1 system -- and others like it -- in an efficient and
robust manner. We notably recommend that -- although more challenging to
schedule -- multi-transit windows be prioritized to constrain stellar
heterogeneities and gather up to 2 more transits per JWST hour spent.
We conclude that in such systems planets cannot be studied in isolation by
small programs, thus large-scale community-supported programs should be
supported to enable the efficient and robust exploration of terrestrial
exoplanets in the JWST era
A Phylogenetic Analysis of Human Immunodeficiency Virus Type 1 Sequences in Kiev: Findings Among Key Populations
Background: The human immunodeficiency virus (HIV) epidemic in Ukraine has been driven by a rapid rise among people who inject drugs, but recent studies have shown an increase through sexual transmission. Methods: Protease and reverse transcriptase sequences from 876 new HIV diagnoses (April 2013âMarch 2015) in Kiev were linked to demographic data. We constructed phylogenetic trees for 794 subtype A1 and 64 subtype B sequences and identified factors associated with transmission clustering. Clusters were defined as â„2 sequences, â„80% local branch support, and maximum genetic distance of all sequence pairs in the cluster â€2.5%. Recent infection was determined through the limiting antigen avidity enzyme immunoassay. Sequences were analyzed for transmitted drug resistance mutations. Results Thirty percent of subtype A1 and 66% of subtype B sequences clustered. Large clusters (maximum 11 sequences) contained mixed risk groups. In univariate analysis, clustering was significantly associated with subtype B compared to A1 (odds ratio [OR], 4.38 [95% confidence interval {CI}, 2.56â7.50]); risk group (OR, 5.65 [95% CI, 3.27â9.75]) for men who have sex with men compared to heterosexual males; recent, compared to long-standing, infection (OR, 2.72 [95% CI, 1.64â4.52]); reported sex work contact (OR, 1.93 [95% CI, 1.07â3.47]); and younger age groups compared with age â„36 years (OR, 1.83 [95% CI, 1.10â3.05] for age â€25 years). Females were associated with lower odds of clustering than heterosexual males (OR, 0.49 [95% CI, .31â.77]). In multivariate analysis, risk group, subtype, and age group were independently associated with clustering (P < .001, P = .007, and P = .033, respectively). Eighteen sequences (2.1%) indicated evidence of transmitted drug resistance. Conclusions Our findings suggest high levels of transmission and bridging between risk groups
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium
Extraversion is a relatively stable and heritable personality trait associated with numerous psychosocial, lifestyle and health outcomes. Despite its substantial heritability, no genetic variants have been detected in previous genome-wide association (GWA) studies, which may be due to relatively small sample sizes of those studies. Here, we report on a large meta-analysis of GWA studies for extraversion in 63,030 subjects in 29 cohorts. Extraversion item data from multiple personality inventories were harmonized across inventories and cohorts. No genome-wide significant associations were found at the single nucleotide polymorphism (SNP) level but there was one significant hit at the gene level for a long non-coding RNA site (LOC101928162). Genome-wide complex trait analysis in two large cohorts showed that the additive variance explained by common SNPs was not significantly different from zero, but polygenic risk scores, weighted using linkage information, significantly predicted extraversion scores in an independent cohort. These results show that extraversion is a highly polygenic personality trait, with an architecture possibly different from other complex human traits, including other personality traits. Future studies are required to further determine which genetic variants, by what modes of gene action, constitute the heritable nature of extraversion
The CMS Phase-1 pixel detector upgrade
The CMS detector at the CERN LHC features a silicon pixel detector as its innermost subdetector. The original CMS pixel detector has been replaced with an upgraded pixel system (CMS Phase-1 pixel detector) in the extended year-end technical stop of the LHC in 2016/2017. The upgraded CMS pixel detector is designed to cope with the higher instantaneous luminosities that have been achieved by the LHC after the upgrades to the accelerator during the first long shutdown in 2013â2014. Compared to the original pixel detector, the upgraded detector has a better tracking performance and lower mass with four barrel layers and three endcap disks on each side to provide hit coverage up to an absolute value of pseudorapidity of 2.5. This paper describes the design and construction of the CMS Phase-1 pixel detector as well as its performance from commissioning to early operation in collision data-taking.Peer reviewe
A large-scale genome-wide association study meta-analysis of cannabis use disorder
Summary Background Variation in liability to cannabis use disorder has a strong genetic component (estimated twin and family heritability about 50â70%) and is associated with negative outcomes, including increased risk of psychopathology. The aim of the study was to conduct a large genome-wide association study (GWAS) to identify novel genetic variants associated with cannabis use disorder. Methods To conduct this GWAS meta-analysis of cannabis use disorder and identify associations with genetic loci, we used samples from the Psychiatric Genomics Consortium Substance Use Disorders working group, iPSYCH, and deCODE (20â916 case samples, 363â116 control samples in total), contrasting cannabis use disorder cases with controls. To examine the genetic overlap between cannabis use disorder and 22 traits of interest (chosen because of previously published phenotypic correlations [eg, psychiatric disorders] or hypothesised associations [eg, chronotype] with cannabis use disorder), we used linkage disequilibrium score regression to calculate genetic correlations. Findings We identified two genome-wide significant loci: a novel chromosome 7 locus (FOXP2, lead single-nucleotide polymorphism [SNP] rs7783012; odds ratio [OR] 1·11, 95% CI 1·07â1·15, p=1·84âĂâ10â9) and the previously identified chromosome 8 locus (near CHRNA2 and EPHX2, lead SNP rs4732724; OR 0·89, 95% CI 0·86â0·93, p=6·46âĂâ10â9). Cannabis use disorder and cannabis use were genetically correlated (rg 0·50, p=1·50âĂâ10â21), but they showed significantly different genetic correlations with 12 of the 22 traits we tested, suggesting at least partially different genetic underpinnings of cannabis use and cannabis use disorder. Cannabis use disorder was positively genetically correlated with other psychopathology, including ADHD, major depression, and schizophrenia. Interpretation These findings support the theory that cannabis use disorder has shared genetic liability with other psychopathology, and there is a distinction between genetic liability to cannabis use and cannabis use disorder. Funding National Institute of Mental Health; National Institute on Alcohol Abuse and Alcoholism; National Institute on Drug Abuse; Center for Genomics and Personalized Medicine and the Centre for Integrative Sequencing; The European Commission, Horizon 2020; National Institute of Child Health and Human Development; Health Research Council of New Zealand; National Institute on Aging; Wellcome Trust Case Control Consortium; UK Research and Innovation Medical Research Council (UKRI MRC); The Brain & Behavior Research Foundation; National Institute on Deafness and Other Communication Disorders; Substance Abuse and Mental Health Services Administration (SAMHSA); National Institute of Biomedical Imaging and Bioengineering; National Health and Medical Research Council (NHMRC) Australia; Tobacco-Related Disease Research Program of the University of California; Families for Borderline Personality Disorder Research (Beth and Rob Elliott) 2018 NARSAD Young Investigator Grant; The National Child Health Research Foundation (Cure Kids); The Canterbury Medical Research Foundation; The New Zealand Lottery Grants Board; The University of Otago; The Carney Centre for Pharmacogenomics; The James Hume Bequest Fund; National Institutes of Health: Genes, Environment and Health Initiative; National Institutes of Health; National Cancer Institute; The William T Grant Foundation; Australian Research Council; The Virginia Tobacco Settlement Foundation; The VISN 1 and VISN 4 Mental Illness Research, Education, and Clinical Centers of the US Department of Veterans Affairs; The 5th Framework Programme (FP-5) GenomEUtwin Project; The Lundbeck Foundation; NIH-funded Shared Instrumentation Grant S10RR025141; Clinical Translational Sciences Award grants; National Institute of Neurological Disorders and Stroke; National Heart, Lung, and Blood Institute; National Institute of General Medical Sciences.Peer reviewe
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