Ethnicity, disadvantage and other variables in the analysis of Birmingham longitudinal school attainment datasets

Explaining and responding to inequalities in attainment are significant educational policy challenges in England as elsewhere. Data on four cohorts of Birmingham Local Education Authority (LEA) pupils, each approximately 13,000, were analysed by ethnicity, deprivation, gender and other relevant individual pupil variables. For the four successive cohorts of children, aged five in 1997–2001, analysis shows the attainment trajectory of each ethnic group from Baseline/Foundation Stage Profile (age 5) to GCSE (age 16). The relative constancy over time, the changes from one key stage to the next and the differences within broad ethnic categories argue against simplistic explanations. The ethnicity variable accounts for a relatively small amount of variance in pupil achievement, with the same ethnic subgroups recurrently low attainers. Considering explanatory perspectives on educational inequalities and ethnicity in the light of these data, we conclude that a structuralist perspective offers the best explanation recognising economic exploitation, dominance and oppression at the national and local levels. Notions of institutional racism and Critical Race Theory (CRT) are considered to be inadequate and counter-productive, in part shown by their inability to accommodate the range of attainment levels and educational experience of different ethnic groups. More tellingly, they lack causal explanations relevant to the United Kingdom and deflect attention from the need for sustained effort to reduce poverty and disadvantage as it affects children

Virtual reality in pediatric psychology

Copyright © 2017 by the American Academy of Pediatrics. Virtual reality (VR) technologies allow for controlled simulations of affectively engaging background narratives. These virtual environments offer promise for enhancing emotionally relevant experiences and social interactions. Within this context, VR can allow instructors, therapists, neuropsychologists, and service providers to offer safe, repeatable, and diversifiable interventions that can benefit assessments and learning in both typically developing children and children with disabilities. Research has also pointed to VR's capacity to reduce children's experience of aversive stimuli and reduce anxiety levels. Although there are a number of purported advantages of VR technologies, challenges have emerged. One challenge for this field of study is the lack of consensus on how to do trials. A related issue is the need for establishing the psychometric properties of VR assessments and interventions. This review investigates the advantages and challenges inherent in the application of VR technologies to pediatric assessments and interventions

The human papillomavirus E7 proteins associate with p190RhoGAP and alter its function

Using mass spectrometry, we identified p190RhoGAP (p190) as a binding partner of human papillomavirus 16 (HPV16) E7. p190 belongs to the GTPase activating protein (GAP) family and is one of the primary GAPs for RhoA. GAPs stimulate the intrinsic GTPase activity of the Rho proteins, leading to Rho inactivation and influencing numerous biological processes. RhoA is one of the best-characterized Rho proteins and is specifically involved in formation of focal adhesions and stress fibers, thereby regulating cell migration and cell spreading. Since this is the first report that E7 associates with p190, we carried out detailed interaction studies. We show that E7 proteins from other HPV types also bind p190. Furthermore, we found that conserved region 3 (CR3) of E7 and the middle domain of p190 are important for this interaction. More specifically, we identified two residues in CR3 of E7 that are necessary for p190 binding and used mutants of E7 with mutations of these residues to determine the biological consequences of the E7-p190 interaction. Our data suggest that the interaction of E7 with p190 dysregulates this GAP and alters the actin cytoskeleton. We also found that this interaction negatively regulates cell spreading on a fibronectin substrate and therefore likely contributes to important aspects of the HPV life cycle or HPV-induced tumorigenesis. © 2014, American Society for Microbiology

Elective affinities of the Protestant ethic : Weber and the chemistry of capitalism

Peer reviewedPostprin

Magnetic resonance imaging of the spinal epidural space

Spinalni epiduralni prostor smješten je između dure mater i vertebralne kolumne i proteže se od foramen magnuma do nivoa S2/S3 spinalnog kanala. Podijeljen je u prednji i stražnji odjeljak. Zbog izvrsnog razlučivanja mekih tkiva, magnetska rezonancija metoda je izbora za otkrivanje i karakterizaciju patoloških promjena spinalnog epiduralnog prostora koje su etiološki različitog podrijetla. Mnoge lezije proizlaze iz samog epiduralnog prostora ili se šire iz okolnih struktura, a ovaj je prostor često sijelo metastatskih depozita. Zbog mogućnosti širenja patoloških procesa prema korijenima spinalnih živaca ili leđnoj moždini, lezije epiduralnog prostora mogu se prezentirati simptomima radikulopatije ili mijelopatije.The spinal epidural space is located between the spinal dura mater and the vertebral column and extends from the foramen magnum to the sacral canal at the level of S2/S3. It is divided into anterior and posterior compartment. Due to its excellent soft tissue contrast magnetic resonance imaging is the gold standard for imaging and diagnosis of pathological processes of the spinal epidural space which differ in etiology. Many processes origin in the spinal epidural space or extend from adjacent structures and epidural space is a frequent location for metastatic processes. Due to the possibility of spreadingof the pathological processes along spinal nerves and the spinal cord, they may present with symptoms of radiculopathy or myelopathy

Medulloblastoma Exome Sequencing Uncovers Subtype-Specific Somatic Mutations

Medulloblastomas are the most common malignant brain tumors in children1. Identifying and understanding the genetic events that drive these tumors is critical for the development of more effective diagnostic, prognostic and therapeutic strategies. Recently, our group and others described distinct molecular subtypes of medulloblastoma based on transcriptional and copy number profiles2–5. Here, we utilized whole exome hybrid capture and deep sequencing to identify somatic mutations across the coding regions of 92 primary medulloblastoma/normal pairs. Overall, medulloblastomas exhibit low mutation rates consistent with other pediatric tumors, with a median of 0.35 non-silent mutations per megabase. We identified twelve genes mutated at statistically significant frequencies, including previously known mutated genes in medulloblastoma such as CTNNB1, PTCH1, MLL2, SMARCA4 and TP53. Recurrent somatic mutations were identified in an RNA helicase gene, DDX3X, often concurrent with CTNNB1 mutations, and in the nuclear co-repressor (N-CoR) complex genes GPS2, BCOR, and LDB1, novel findings in medulloblastoma. We show that mutant DDX3X potentiates transactivation of a TCF promoter and enhances cell viability in combination with mutant but not wild type beta-catenin. Together, our study reveals the alteration of Wnt, Hedgehog, histone methyltransferase and now N-CoR pathways across medulloblastomas and within specific subtypes of this disease, and nominates the RNA helicase DDX3X as a component of pathogenic beta-catenin signaling in medulloblastoma

A Modular BAM Complex in the Outer Membrane of the α-Proteobacterium Caulobacter crescentus

Mitochondria are organelles derived from an intracellular α-proteobacterium. The biogenesis of mitochondria relies on the assembly of β-barrel proteins into the mitochondrial outer membrane, a process inherited from the bacterial ancestor. Caulobacter crescentus is an α-proteobacterium, and the BAM (β-barrel assembly machinery) complex was purified and characterized from this model organism. Like the mitochondrial sorting and assembly machinery complex, we find the BAM complex to be modular in nature. A ∼150 kDa core BAM complex containing BamA, BamB, BamD, and BamE associates with additional modules in the outer membrane. One of these modules, Pal, is a lipoprotein that provides a means for anchorage to the peptidoglycan layer of the cell wall. We suggest the modular design of the BAM complex facilitates access to substrates from the protein translocase in the inner membrane

First light with HiPERCAM on the GTC

HiPERCAM is a quintuple-beam imager that saw first light on the 4.2 m William Herschel Telescope (WHT) in October 2017 and on the 10.4 m Gran Telescopio Canarias (GTC) in February 2018. The instrument uses re- imaging optics and 4 dichroic beamsplitters to record ugriz (300–1000 nm) images simultaneously on its five CCD cameras. The detectors in HiPERCAM are frame-transfer devices cooled thermo-electrically to 90°C, thereby allowing both long-exposure, deep imaging of faint targets, as well as high-speed (over 1000 windowed frames per second) imaging of rapidly varying targets. In this paper, we report on the as-built design of HiPERCAM, its first-light performance on the GTC, and some of the planned future enhancements