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164 results for “relative position”
Effect of Shoe Cushioning Position and Properties on Running-related Injury Risk
ClinicalTrials.gov study NCT06384872. IPD Sharing: NO. Countries: 1. Publications: 3.
SAR408701 Versus Docetaxel in Previously Treated, Carcinoembryonic Antigen-related Cell Adhesion Molecule 5 (CEACAM5) Positive Metastatic Non-squamous Non-small-cell Lung Cancer Patients
ClinicalTrials.gov study NCT04154956. IPD Sharing: YES. Countries: 26. Publications: 0.
Data from: Lesser snow goose helminths show recurring and positive parasite infection-diversity relations
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Data from: Selfing ability and dispersal are positively related, but not affected by range position, across multiple species of southern African Asteraceae
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Data for: Recent changes in thermal niche position and breadth of bird assemblages in Spain in relation to increasing temperatures
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Data from: A transcriptome screen for positive selection in domesticated breadfruit and its wild relatives (Artocarpus spp.)
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Social network connections are positively related to temperature in winter flocks of black-capped chickadees
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Megafruit and megafauna diversity are positively associated, while megafruit traits are related to abiotic factors, in Tropical Asia
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Adequate vitamin A liver stores estimated by the Modified-Relative Dose Response test are positively associated with breastfeeding but not vitamin A supplementation in Senegalese urban children 9-23 months old: a comparative cross-sectional study
<p><span><span><span><span><span><span><span><span><span><span><span>Vitamin A supplementation (VAS) in 6-59 month old children is recommended but its sustainability is currently questioned. In Senegal, data suggest that VAS should be maintained, but geographic and age-related specificities need to be addressed by gathering more evidence on the impact of this program. The objective of this comparative cross-sectional study, conducted in urban settings of Dakar, was to evaluate the effectiveness of VAS on vitamin A liver stores (VALS) among 9-23 month old children. The supplemented group (n = 119) received VAS (either 100 000 UI or 200 000 UI) 2 to 6 months before evaluation while the non-supplemented group (n = 110) had not received VAS during the past 6 months. VALS were assessed using the modified-relative dose response (MRDR) test. Serum retinol concentrations (SR) and biomarkers of subclinical inflammation were measured. Children's health-related data and feeding patterns were collected. Mean MRDR values (VAS: 0.030 ± 0.017, non-VAS: 0.028 ± 0.016, P = 0.39) and inflammation-adjusted SR (VAS: 1.34 ± 0.37, non-VAS: 1.3 ± 0.35, P = 0.51) of children were adequate. Low prevalence of VALS (VAS: 5.2%, non-VAS: 5.4%) and inflammation-adjusted VAD (VAS: 2.6%, non-VAS: 0.9%) were detected despite high presence of infections and inflammation. Children were mostly still being breastfed (VAS: 85.7%, non-VAS: 77.3%) and complementary feeding indicators were similar in both groups. Only breastfeeding was associated with VALS (adjusted OR = 0.24, 95% CI: 0.07-0.8, P = 0.02). Based on MRDR values, VAS was not related to improved VALS and SR as well as VAD reduction among these children with adequate VALS. Reinforcing breastfeeding advocacy and morbidity prevention/control are essential in this setting. Scaling-back VAS in this subpopulation should be examined regarding the risk of hypervitaminosis A. However, an evaluation of dietary VA intake sufficiency and a more quantitative assessment of VALS should be prior considered.</span></span></span></span></span></span></span></span></span></span></span></p>
SuperDARN convection data used in the study of "Relation between Magnetopause Position and Reconnection Rate under Quasi-Steady Solar Wind Dynamic Pressure"
<p>Convection velocity data is available in the netCDF file format.</p>
Table 2 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 2. Diagnostic character state combinations shown by exemplars of Hololeius ceylanicus and Hololeius cyaneus.</p><table><tbody><tr><th>No.</th><th>Characters</th><th>Hololeius ceylanicus</th><th>Hololeius cyaneus</th></tr></tbody><tbody><tr><td>01</td><td>Pubescence of integument</td><td>partly pubescent</td><td>glabrous</td></tr><tr><td>02</td><td>Punctuation of integument</td><td>punctate (Figs 1-3)</td><td>impunctate (Figs 13-16)</td></tr><tr><td>03</td><td>Antennomere 3</td><td>with a few short and scattered setae</td><td>glabrous</td></tr><tr><td>04</td><td>Mentum tooth form anteriorly</td><td>truncate</td><td>rounded</td></tr><tr><td>05</td><td>PW/PL</td><td>1.14-1.15 (Fig. 1)</td><td>1.24-1.37 (Fig. 13)</td></tr><tr><td>06</td><td>Basal margin of pronotum at posterior angles</td><td>oblique (Fig. 1)</td><td>gradually rounded (Fig. 13)</td></tr><tr><td>07</td><td>Pronotum</td><td>bordered laterally and lateroapically, not bordered medioapically and basally (Fig. 1)</td><td>bordered throughout (Fig. 13)</td></tr><tr><td>08</td><td>Elytral striae 1-8</td><td>1-7 punctate, 8 impunctate (Fig. 2)</td><td>impunctate (Fig. 14)</td></tr><tr><td>09</td><td>Stria 8</td><td>not or hardly deeper than other striae (Figs 2-3)</td><td>evidently deeper than other striae (Figs 14-16)</td></tr><tr><td>10</td><td>Elytral intervals</td><td>punctate (Figs 2-3)</td><td>impunctate (Figs 14-16)</td></tr><tr><td>11</td><td>Interval 9</td><td>distinct throughout</td><td>transformed into marginal gutter along anterior 2/5 of elytra, distinct in posterior 3/5</td></tr><tr><td>12</td><td>Number of umbilicate pores</td><td>23-25</td><td>15-16</td></tr><tr><td>13</td><td>Mesocoxa lateral margin</td><td>with one long seta</td><td>without seta</td></tr><tr><td>14</td><td>Joins of claws</td><td>opposite, distantly situated from each other</td><td>nearly parallel, closely situated to each other (Figs 14-15)</td></tr><tr><td>15</td><td>Number of pores on last sternum in female</td><td>four pores</td><td>two pores</td></tr><tr><td>16</td><td>Apical stylomere of ovipositor</td><td>subtriangular, as wide as basal stylomere, with 36 long ensiform setae at dorsomedial, dorsolateral and ventral position, and with nematiform setae, shorter than ensiform setae (Figs 10-11)</td><td>subelongate, nearly twice as narrow as basal stylomere, with 11 short ensiform setae at dorsomedial and dorsolateral position, and with nematiform setae, nearly twice as long as ensiform setae (Figs 17-18)</td></tr></tbody></table>
Table 1 in Two new related oodine genera in the Oriental Region, with remarks on the systematic position of the genera Hololeius and Holosoma (Coleoptera, Carabidae)
<p>Table 1. List of the Oriental genera of Oodini, their species number and distribution.</p><table><tbody><tr><th>Genera</th><th>Species</th><th>Distribution (incl. unpublished data)</th></tr></tbody><tbody><tr><td>Anatrichis LeConte, 1853</td><td>3</td><td>Indian subcontinent, Myanmar, Philippines</td></tr><tr><td>Bamaroodes B. Guéorguiev, gen. n.</td><td>1</td><td>Myanmar, Thailand</td></tr><tr><td>Brachyodes Jeannel, 1949</td><td>4</td><td>whole region</td></tr><tr><td>Holcocoleus Chaudoir in Oberthur, 1883</td><td>2</td><td>India (Tamil Nadu), Ceylon</td></tr><tr><td>" Holosoma boettcheri Jedlička, 1936 "</td><td>1</td><td>Philippines</td></tr><tr><td>Megaloodes Lesne, 1896</td><td>1</td><td>SE Thailand, E Cambodia</td></tr><tr><td>Miltodes Andrewes, 1922</td><td>1</td><td>India, Thailand, Sumatra</td></tr><tr><td>Nanodiodes Bousquet, 1996</td><td>3</td><td>Ceylon, SE Asia, Indonesia, Philippines</td></tr><tr><td>Oodes Bonelli, 1810</td><td>16</td><td>whole region</td></tr><tr><td>Oodinus Motschulsky, 1864</td><td>1</td><td>Vietnam, Sumatra, Moluccas, Philippines</td></tr><tr><td>Pseudosphaerodes Jeannel, 1949</td><td>2</td><td>Myanmar, Philippines</td></tr><tr><td>Simous Chaudoir, 1882</td><td>9</td><td>whole region east of Bengal</td></tr><tr><td>Systolocranius Chaudoir, 1857</td><td>1</td><td>“Bengal”: MNHUB; "Ind. or.": NMW</td></tr><tr><td>Thaioodes B. Guéorguiev, gen. n.</td><td>1</td><td>Thailand</td></tr></tbody></table>
Dataset related to article: "Fluoxetine increases brain MeCP2 immuno-positive cells in a female Mecp2 heterozygous mouse model of Rett syndrome through endogenous serotonin. "
<pre>Dataset related to article: "Fluoxetine increases brain MeCP2 immuno-positive cells in a female Mecp2 heterozygous mouse model of Rett syndrome through endogenous serotonin." </pre>
Two new species of the Lycophyte Genus Selaginella (Selaginellaceae) from China, with notes on phylogenetic position of related species
<p>Two new species of lycophytes, <em>Selaginella obovata</em> and <em>S. zhangii</em>, were discovered in southeastern Yunnan, China. <em>Selaginella obovata</em> is characterized by the prostrate habit and relatively small size of plant, obovate median leaves, and short, dorsiventral strobili, and is not apparently similar to any known species. Phylogenetic analyses of plastid sequences (<em>rbcL</em>, <em>atpI</em>, <em>psbA</em>) indicated that <em>S. obovata</em> is closely allied to <em>S. bisulcata</em>, which is also supported by spore morphology, and that these two taxa together with <em>S. pennata</em> constitute a well-supported monophyletic group. <em>Selaginella zhangii</em> is comparable to <em>S. rolandi-principis</em> in their broad stems (including leaves) and shape and arrangement of vegetative leaves; but the former differs from the latter in its prostrate habit and dorsiventral strobili. The result of phylogenetic analyses showed indicate that <em>S. zhangii</em> is allied to <em>S. heterostachys</em> in the <em>S. heterostachys–S. ciliaris</em> clade, while <em>S. rolandi-principis</em> is distantly placed in the <em>S. doederleinii–S. involvens</em> clade. Finally, we provide comprehensive descriptions, photographs of living plants, line drawings, and scanning electron micrographs of spores to facilitate their recognition.</p>
Figure S1: SARS-CoV-2-specific neutralization activity at days 1 and 8 relative to enrollment in exposed seronegative nasal SIgA positive and infected participants.
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Supplementary material 2 from: Pérez Santa-Rita JV, Baixeras J (2018) Two new species of Brusqeulia Razowski & Becker, 2000 from the Neotropics, with comments on the systematic position of the genus in relation to the Apolychrosis Amsel, 1962 group of genera (Lepidoptera, Tortricidae, Cochylini). ZooKeys 770: 193-210. https://doi.org/10.3897/zookeys.770.24281
Character matrix : Explanation note: Data matrix for phylogenetic analysis.
Supplementary material 1 from: Pérez Santa-Rita JV, Baixeras J (2018) Two new species of Brusqeulia Razowski & Becker, 2000 from the Neotropics, with comments on the systematic position of the genus in relation to the Apolychrosis Amsel, 1962 group of genera (Lepidoptera, Tortricidae, Cochylini). ZooKeys 770: 193-210. https://doi.org/10.3897/zookeys.770.24281
Material examined : Explanation note: Collection data of the voucher material examined.
Figure 5 from: Pérez Santa-Rita JV, Baixeras J (2018) Two new species of Brusqeulia Razowski & Becker, 2000 from the Neotropics, with comments on the systematic position of the genus in relation to the Apolychrosis Amsel, 1962 group of genera (Lepidoptera, Tortricidae, Cochylini). ZooKeys 770: 193-210. https://doi.org/10.3897/zookeys.770.24281
Figure 5 Hypothesis of phylogenetic relationships in the Apolychrosis group. Brusqeulia is positioned as sister group of the Apolychrosis group. The P. niphastra group has been excluded from the analysis.
Figure 2 from: Pérez Santa-Rita JV, Baixeras J (2018) Two new species of Brusqeulia Razowski & Becker, 2000 from the Neotropics, with comments on the systematic position of the genus in relation to the Apolychrosis Amsel, 1962 group of genera (Lepidoptera, Tortricidae, Cochylini). ZooKeys 770: 193-210. https://doi.org/10.3897/zookeys.770.24281
Figure 2 Morphological characters of Brusqeulia yunkensis sp. n. A habitus (Paratype, male, Bolivia, Santa Cruz, Pampagrande, 25 January 2011, ICBiBE) B male genitalia, phallus removed (GS JBA20728, z = 161 µm) C male genitalia left valva completely extended (GS JBA20684, z = 83 µm) D phallus with everted vesica (caecum removed, GS JBA20844) E phallus uneverted (GS JBA20728, same scale as D) F female genitalia (GS JBA20727). Abbreviations. ds: ductus seminalis connection to the bursa; la, lamella antevaginalis; lp, sclerite on the lamella postvaginalis; lt, lateral pocket; sf, ventral spinous field of segment 8. Scale bars: 2 mm (A); 200 µm (B, C, D, F).
Figure 4 from: Pérez Santa-Rita JV, Baixeras J (2018) Two new species of Brusqeulia Razowski & Becker, 2000 from the Neotropics, with comments on the systematic position of the genus in relation to the Apolychrosis Amsel, 1962 group of genera (Lepidoptera, Tortricidae, Cochylini). ZooKeys 770: 193-210. https://doi.org/10.3897/zookeys.770.24281
Figure 4 Female terminalia of Brusqeulia yunkensis and B. araguensis, ventral view, under scanning electron microscopy. A B. yunkensis B B. araguensis C subpapillar sclerite of B. yunkensis D same in B. araguensis. Abbreviations; la, lamella antevaginalis; lp, lamella postvaginalis; sf, ventral spinous field of segment 8; sp, subpapillar sclerite. Scale bars 100 µm.
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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.