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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.
Genotype and individual data for genetic structure in Louisiana Iris species reveals patterns of recent and historical admixture
<p><b><span>Premise: </span></b><span>When divergent lineages come into secondary contact reproductive isolation may be incomplete, thus providing an opportunity to investigate how speciation is manifested in the genome. The Louisiana Irises (<i>Iris</i>, series <i>Hexagonae</i>) comprise a group of three or more ecologically and reproductively divergent lineages that can produce hybrids where they come into contact. In this study we sought to estimate standing genetic variation to understand the current distribution of population structure in the Louisiana Irises.</span></p> <p><b><span>Methods:</span></b><span> We used genotyping-by-sequencing techniques to sample the genomes of Louisiana Iris species across their ranges. Twenty populations were sampled (total n=632) across 11,249 loci. Population genetic data were assessed using ENTROPY and PCA models. </span></p> <p><b><span>Results: </span></b><span>We discovered evidence for interspecific gene flow in parts of the range and revealed patterns of population structure at odds with widely accepted nominal taxonomy. Undescribed hybrid populations were discovered that were designated as belonging to the <i>I. brevicaulis</i> lineage. <i>Iris nelsonii </i>shared significant ancestry with only one of the purported parent species, <i>I. fulva, </i>evidence inconsistent with a hybrid origin.</span></p> <p><b><span>Conclusions: </span></b><span>This study provides several key findings important to the investigation of standing genetic variation in the Louisiana Iris species complex. <i>Iris brevicaulis</i> has a large amount of genetic diversity within it relative to the other nominal species. In addition, this study has discovered a previously unknown hybrid zone between <i>I. brevicaulis </i>and <i>I. hexagona</i> along the Texas coast. Finally, <i>I. nelsonii</i> does not appear to have mixed ancestry from three parental taxa as has been the longstanding hypothesis. </span></p>
Trajectory Based Classification of Recovery In Sensorimotor Complete Traumatic Cervical Spinal Cord Injury – Individual Recovery Trajectory Data
<p><b>Objective</b></p> <p>To test the hypothesis that sensorimotor complete traumatic cervical spinal cord injury is a heterogenous clinical entity comprising several subpopulations that follow fundamentally different trajectories of neurological recovery.</p> <p><b>Methods</b></p> <p>We analyzed demographic and injury data from 655 patients who were pooled from four prospective longitudinal multicenter studies. Group based trajectory modeling was applied to model neurological recovery trajectories over the initial 12-months postinjury and to identify predictors of recovery trajectories. Neurological outcomes included: Upper Extremity Motor Score, Total Motor Scores and AIS grade improvement.</p> <p><b>Results </b></p> <p>The analysis identified three distinct trajectories of neurological recovery. These clinical courses included: (1) Marginal recovery trajectory: characterized by minimal or no improvement in motor strength or change in AIS grade status (remained grade A); (2) Moderate recovery trajectory: characterized by low baseline motor scores that improved approximately 13 points; or AIS conversion of one grade point; (3) Good recovery trajectory: characterized by baseline motor scores in the upper quartile that improved to near maximum values within three months of injury. Patients following the moderate or good recovery trajectories were of younger age, had more caudally located injuries, a higher degree of preserved motor and sensory function at baseline examination and exhibited a greater extent of motor and sensory function in the zone of partial preservation.</p> <p><b>Conclusion</b></p> <p>Cervical complete SCI can be classified into one of three distinct subpopulations with fundamentally different trajectories of neurological recovery. This study defines unique clinical phenotypes based on potential for recovery, rather than baseline severity of injury alone. This approach may prove beneficial in clinical prognostication and in the design and interpretation of clinical trials in SCI.</p>
Repeatable individual variation in migration timing in two anadromous salmonids and ecological consequences
<p>Consistent individual differences in behaviour has been demonstrated for many animals, but there are few studies of consequences of such repeated behaviour in the wild. We tested consistency in migration timing to and from the sea among anadromous Arctic char (<i>Salvelinus alpinus</i>) and brown trout (<i>Salmo trutta</i>), using data from a study period of about 25 years, including more than 27,000 uniquely Carlin-tagged individuals that migrated to sea for feeding in the spring and returned to the river in late summer for up to 13 successive years. Consistency was found between individuals across time in timing of the seaward migration. Individuals migrating early during their first migration tended to migrate early the following years, and late migrants tended to migrate late. The same pattern was found also at ascent to freshwater. Hence, this study demonstrated that individual fish in nature can differ in behaviour related to migration timing, and that these differences can be consistent during their life time. Early migrants increased their mass more than late migrants, and had a higher specific growth rate. Early migrating Arctic char, but not brown trout, experienced a longer life after the first migration to sea than late migrants. In both species, maturity occurred earlier in individuals that migrated early. For brown trout, but not for Arctic char, fecundity was significantly correlated to the timing of smolt migration. Hence, the repeatable individual variation in migration timing seemed to have ecological and fitness consequences in terms of growth, longevity, timing of maturity, and life-time fecundity.</p>
INDIVIDUAL RESPONSES FROM THE DUBOWITZ NEUROLOGICAL EXAMINATION AND DEMOGRAPHIC QUESTIONNAIRE
<p>INDIVIDUAL RESPONSES FROM THE DUBOWITZ NEUROLOGICAL EXAMINATION AND DEMOGRAPHIC QUESTIONNAIRE</p>
Text-fig. 5. Aerial view showing location of individual 'Cenoceras Islands' (marked by red pins) at Helwell Bay, Doniford. in 'Cenoceras Islands' In The Blue Lias Formation (Lower Jurassic) Of West Somerset, Uk: Nautilid Dominance And Influence On Benthic Faunas
Text-fig. 5. Aerial view showing location of individual 'Cenoceras Islands' (marked by red pins) at Helwell Bay, Doniford.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.