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The Asterolecaniidae (Hemiptera: Coccomorpha), known as pit scales, are currently represented by 11 genera and 52 species in the Neotropical region, and by five species in Argentina. The goal of this study is to review and update the information currently known about the biodiversity of Asterolecaniidae in Argentina. We describe Argenta Granara de Willink new genus, Argenta eduardoi Granara de Willink new species, Mycetococcus ligae Granara de Willink new species, and Sclerosococcus williamsi Granara de Willink new species; an illustration of Pollinia pollini (Costa) is also included; the species Asterolecanium puteanum Russell and Russellaspis pustulans (Cockerell) are noted for the first time in Argentina. Dichotomous keys to the genera of Asterolecaniidae and the species of Asterolecanium Targioni-Tozzetti, Mycetococcus Ferris, and Sclerosococcus McKenzie in Argentina are presented. This work increases the number of known species in Argentina to ten.
ZooBank registration. urn:lsid:zoobank.org:pub:2A1FB016-1B67-4861-BB8B-2011B26679F1
Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p = 1.0 × 10(-5)) and an increase in affected subjects carrying exonic pathogenic CNVs overlapping known loci associated with dominant or X-linked ASD and intellectual disability (odds ratio = 12.62, p = 2.7 × 10(-15), ∼3% of ASD subjects). Pathogenic CNVs, often showing variable expressivity, included rare de novo and inherited events at 36 loci, implicating ASD-associated genes (CHD2, HDAC4, and GDI1) previously linked to other neurodevelopmental disorders, as well as other genes such as SETD5, MIR137, and HDAC9. Consistent with hypothesized gender-specific modulators, females with ASD were more likely to have highly penetrant CNVs (p = 0.017) and were also overrepresented among subjects with fragile X syndrome protein targets (p = 0.02). Genes affected by de novo CNVs and/or loss-of-function single-nucleotide variants converged on networks related to neuronal signaling and development, synapse function, and chromatin regulation.
The results from the STAR Collaboration on directed flow (v1), elliptic flow (v2), and the fourth harmonic (v4) in the anisotropic azimuthal distribution of particles from Au+Au collisions at sqrt[sNN]=200GeV are summarized and compared with results from other experiments and theoretical models. Results for identified particles are presented and fit with a blast-wave model. Different anisotropic flow analysis methods are compared and nonflow effects are extracted from the data. For v2, scaling with the number of constituent quarks and parton coalescence are discussed. For v4, scaling with v22 and quark coalescence are discussed.