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4,215 results for “high risk”
FIGURES 93–94 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURES 93–94. Geographical distributions of Parasthetops species.
FIGURE 69 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 69. Mesoceration curvosum, dorsal and lateral habitus of holotype.
FIGURE 68 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 68. Mesoceration natalensis, dorsal and lateral habitus of holotype.
FIGURE 51 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 51. Mesoceration barriotum, dorsal and lateral habitus of holotype.
FIGURES 91–92 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURES 91–92. Geographical distributions of Parasthetops species.
FIGURE 39 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 39. Mesoceration reticulatum, dorsal and lateral habitus of holotype.
FIGURE 16 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 16. Parasthetops pampinus, dorsal and lateral habitus of holotype.
FIGURE 36 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 36. Mesoceration disjunctum, dorsal and lateral habitus of holotype.
FIGURE 37 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 37. Mesoceration repandum, dorsal and lateral habitus of holotype.
FIGURE 17 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 17. Parasthetops lemniscus, dorsal and lateral habitus of holotype.
FIGURE 15 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 15. Parasthetops semiplanus, dorsal and lateral habitus of holotype.
FIGURE 9 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 9. Parasthetops unicornus, dorsal and lateral habitus of holotype.
FIGURE 10 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 10. Parasthetops buunicornus, dorsal and lateral habitus of holotype.
FIGURE 8 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 8. Parasthetops propitius, dorsal and lateral habitus of holotype.
FIGURE 7 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 7. Parasthetops sebastiani, dorsal and lateral habitus of holotype.
FIGURE 2 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 2. Pterosthetops hawequas, dorsal and lateral habitus of holotype.
FIGURE 1 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 1. Prosthetops gladiator, dorsal and lateral habitus of holotype.
The influence of maternal glucocorticoids on offspring phenotype in high- and low-risk environments
<p><span><span><span><span><span><span><span><span><span><span><span>Elevated maternal glucocorticoid levels during gestation can lead to phenotypic changes in offspring via maternal effects. Although such effects have traditionally been considered maladaptive, maternally derived glucocorticoids may adaptively prepare offspring for their future environment depending upon the correlation between maternal and offspring environments. Nevertheless, relatively few studies test the effects of prenatal glucocorticoid exposure across multiple environments. We tested the potential for ecologically relevant increases in maternal glucocorticoids in the eastern fence lizard (<i>Sceloporus undulatus</i>) to induce adaptive phenotypic changes in offspring exposed to high or low densities of an invasive fire ant predator. Maternal treatment had limited effects on offspring morphology and behaviour at hatching, but by 10 days of age, we found maternal treatment interacted with offspring environment to alter anti-predator behaviours. We did not detect differences in early-life survival based on maternal treatment or offspring environment. Opposing selection on anti-predator behaviours from historic and novel invasive predators may confound the potential of maternal glucocorticoids to adaptively influence offspring behaviour. Our test of the phenotypic outcomes of transgenerational glucocorticoid effects across risk environments provides important insight into the context-specific nature of this phenomenon and the importance of understanding both current and historic evolutionary pressures.</span></span></span></span></span></span></span></span></span></span></span></p>
The Safety and Efficacy of Combined Microwave Ablation During Limb-sparing Surgery in High-risk Soft Tissue Sarcoma Patients
ClinicalTrials.gov study NCT06802510. IPD Sharing: NO. Countries: 1. Publications: 0.
The Effect of PRP on Wound Healing in High Risk Patients Undergoing Abdominal Hysterectomy
ClinicalTrials.gov study NCT06298110. IPD Sharing: Not stated. Countries: 0. Publications: 8.
ScienceDex guides
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.