16 research outputs found

    The Buckley-Coffin Crusade: Preaching the Gospel of Political Ideology to Yale and America in the 1960s

    Get PDF
    The story of William Sloane Coffin Jr. and William F. Buckley Jr. sheds some light on the complexity of student politics in the 1960s, challenging the simplistic historical analysis so often applied to the period. In large measure, liberal and conservative student movements evolved, like Buckley and Coffin, in conversation with one another in the 1960s, with roots that extended back to the beginning of the decade and before. These movements did not emerge organically on college campuses, in a sphere free of adult influences; many of these student visionaries found their mission with the encouragement and support of generational mentors. This paper uses the Buckley-Coffin story as a framework for examining the interplay between the New Left and the New Right in the 1960s among college students. It demonstrates how the campus climate was simultaneously an important part of and shaped by the larger conversation that was already happening on a national level: a debate over how America would respond to the challenges of the post-war decades and define itself for the future

    Perinatal and 2-year neurodevelopmental outcome in late preterm fetal compromise: the TRUFFLE 2 randomised trial protocol

    Get PDF
    Introduction: Following the detection of fetal growth restriction, there is no consensus about the criteria that should trigger delivery in the late preterm period. The consequences of inappropriate early or late delivery are potentially important yet practice varies widely around the world, with abnormal findings from fetal heart rate monitoring invariably leading to delivery. Indices derived from fetal cerebral Doppler examination may guide such decisions although there are few studies in this area. We propose a randomised, controlled trial to establish the optimum method of timing delivery between 32 weeks and 36 weeks 6 days of gestation. We hypothesise that delivery on evidence of cerebral blood flow redistribution reduces a composite of perinatal poor outcome, death and short-term hypoxia-related morbidity, with no worsening of neurodevelopmental outcome at 2 years. Methods and analysis: Women with non-anomalous singleton pregnancies 32+0 to 36+6 weeks of gestation in whom the estimated fetal weight or abdominal circumference is <10th percentile or has decreased by 50 percentiles since 18-32 weeks will be included for observational data collection. Participants will be randomised if cerebral blood flow redistribution is identified, based on umbilical to middle cerebral artery pulsatility index ratio values. Computerised cardiotocography (cCTG) must show normal fetal heart rate short term variation (≥4.5 msec) and absence of decelerations at randomisation. Randomisation will be 1:1 to immediate delivery or delayed delivery (based on cCTG abnormalities or other worsening fetal condition). The primary outcome is poor condition at birth and/or fetal or neonatal death and/or major neonatal morbidity, the secondary non-inferiority outcome is 2-year infant general health and neurodevelopmental outcome based on the Parent Report of Children's Abilities-Revised questionnaire. Ethics and dissemination: The Study Coordination Centre has obtained approval from London-Riverside Research Ethics Committee (REC) and Health Regulatory Authority (HRA). Publication will be in line with NIHR Open Access policy. Trial registration number: Main sponsor: Imperial College London, Reference: 19QC5491. Funders: NIHR HTA, Reference: 127 976. Study coordination centre: Imperial College Healthcare NHS Trust, Du Cane Road, London, W12 0HS with Centre for Trials Research, College of Biomedical & Life Sciences, Cardiff University. IRAS Project ID: 266 400. REC reference: 20/LO/0031. ISRCTN registry: 76 016 200

    Review of Molecular Technologies for Investigating Canine Cancer.

    Get PDF
    Genetic molecular testing is starting to gain traction as part of standard clinical practice for dogs with cancer due to its multi-faceted benefits, such as potentially being able to provide diagnostic, prognostic and/or therapeutic information. However, the benefits and ultimate success of genomic analysis in the clinical setting are reliant on the robustness of the tools used to generate the results, which continually expand as new technologies are developed. To this end, we review the different materials from which tumour cells, DNA, RNA and the relevant proteins can be isolated and what methods are available for interrogating their molecular profile, including analysis of the genetic alterations (both somatic and germline), transcriptional changes and epigenetic modifications (including DNA methylation/acetylation and microRNAs). We also look to the future and the tools that are currently being developed, such as using artificial intelligence (AI) to identify genetic mutations from histomorphological criteria. In summary, we find that the molecular genetic characterisation of canine neoplasms has made a promising start. As we understand more of the genetics underlying these tumours and more targeted therapies become available, it will no doubt become a mainstay in the delivery of precision veterinary care to dogs with cancer

    COVID-19 impact on adolescent mental health: A reassessment accounting for development

    No full text
    Background: We examine whether age-related change over 11-14 years accounts for the increase in depression and behavioural problems associated with the pandemic. Methods: Parents and adolescents in a UK-based birth cohort (Wirral Child Health and Development Study; WCHADS; N=737) reported on adolescent depression and behavioural problems pre-pandemic (February 2020), mid-pandemic (August 2020) and late-pandemic (August 2021). Analysis used repeated measures models for over-dispersed Poisson counts with a child-specific intercept with age as a time -varying covariate. Results: The pre-pandemic subsample (56% response) did not differ on socio-demographic or risk characteristics from the full sample, response was 87% at mid and 82% at late- pandemic. Maturational curves for girls, but not for boys, showed a significant increase in self-reported depression symptoms over ages 11-14 years. Behavioural problems decreased for both. After adjusting for age-related change, girls’ depression increased by only 13% (CI -1%, 27%) at mid-pandemic and returned to near pre-pandemic level at late-pandemic (mid versus late -12% CI -29%,6%), whereas boys’ depression increased by 31% (CI 10%,51%) and remained elevated (mid versus late 1%, CI -22%,+25%). Age-adjusted behavioural problems increased for both (girls 40%, CI 21%,60% and boys 41%, CI 20%,61%) and worsened from mid to late-pandemic (girls 33%, CI 1%, 65%; boys 18%, CI -12%,+48%). Conclusions: Initial reports of a pandemic related increase in depression in young adolescent girls could be explained by a natural maturational rise. In contrast, maturational decreases in boys’ depression and both boys’ and girls’ behavioural problems may mask an effect of the pandemic
    corecore