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Figure 2 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2-methoxyethanol
Figure 2. Treatment group: 2- ME + Resveratrol Standard (10 x10).
Figure 1 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2-methoxyethanol
Figure 1. Control Group (10 x10).
Table 4 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2 - methoxyethanol
<p><b>Table 4.</b> Cytotoxic effect of various concentrations of Resveratrol and 2-Methoxyethanol Against Primary Neuron cell viability in MTT assay (570 nm).</p><table><tbody><tr><th><b>% Inhibition</b></th></tr></tbody><tbody><tr><th><b>Concentration of 2-Methoxyethanol</b></th><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td></tr><tr><th><b>and Resveratrol</b></th><td><b>Resveratrol (Standard)</b></td><td><b>Resveratrol (Tempeh)</b></td><td><b>Resveratrol (Soybean Seed Coat)</b></td></tr><tr><th>IC50</th><td>(17.38 ± 0.99 µg/mL)</td><td>(31.14 ± 0.02 µg/mL)</td><td>(13.40 ± 0.30 µg/mL)</td></tr><tr><th>1.4 (µg/mL)</th><td>12.57</td><td>0</td><td>11.98</td></tr><tr><th>2.8 (µg/mL)</th><td>4.59</td><td>1.75</td><td>17.03</td></tr><tr><th>4.2 (µg/mL)</th><td>0</td><td>0</td><td>0</td></tr></tbody></table>
Table 3 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2 - methoxyethanol
<p><b>Table 3.</b> Cytotoxic effect of various concentrations of Resveratrol and 2-Methoxyethanol Against Primary Neuron cell viability in MTT assay (540 nm).</p><table><tbody><tr><th><b>% Inhibition</b></th></tr></tbody><tbody><tr><th><b>Concentration of 2-Methoxyethanol</b></th><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td></tr><tr><th><b>and Resveratrol</b></th><td><b>Resveratrol (Standard)</b></td><td><b>Resveratrol (Tempeh)</b></td><td><b>Resveratrol (Soybean Seed Coat)</b></td></tr><tr><th>IC50</th><td>(17.64 ± 0.99 µg/mL)</td><td>(32.22 ± 1.18 µg/mL)</td><td>(17.43 ± 0.16 µg/mL)</td></tr><tr><th>1.4 (µg/mL)</th><td>11.8</td><td>0</td><td>7.95</td></tr><tr><th>2.8 (µg/mL)</th><td>5.27</td><td>0</td><td>14.41</td></tr><tr><th>4.2 (µg/mL)</th><td>0</td><td>0</td><td>0</td></tr></tbody></table>
Table 2 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2 - methoxyethanol
<p><b>Table 2.</b> Effect of Various concentrations of Resveratrol and 2-Methoxyethanol against Primary Neuron cell viability (570 nm).</p><table><tbody><tr><th><b>% Cell Viability</b></th></tr></tbody><tbody><tr><th><b>Concentration of 2-Methoxyethanol</b></th><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td></tr><tr><th><b>and Resveratrol</b></th><td><b>Resveratrol (Standard)</b></td><td><b>Resveratrol (Tempeh)</b></td><td><b>Resveratrol (Soybean Seed Coat)</b></td></tr><tr><th>1.4 (µg/mL)</th><td>87.43</td><td>100</td><td>88.02</td></tr><tr><th>2.8 (µg/mL)</th><td>95.41</td><td>98.25</td><td>82.97</td></tr><tr><th>4.2 (µg/mL)</th><td>100</td><td>100</td><td>100</td></tr></tbody></table>
Table 1 in Potential neuroprotective of trans-resveratrol a promising agent tempeh and soybean seed coats-derived against beta-amyloid neurotoxicity on primary culture of nerve cells induced by 2 - methoxyethanol
<p><b>Table 1.</b> Effect of Various concentrations of Resveratrol and 2-Methoxyethanol against Primary Neuron cell viability (540 nm).</p><table><tbody><tr><th><b>% Cell Viability</b></th></tr></tbody><tbody><tr><th><b>Concentration of 2-Methoxyethanol</b></th><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td><td><b>2-ME (10mM)</b></td></tr><tr><th><b>and Resveratrol</b></th><td><b>Resveratrol (Standard)</b></td><td><b>Resveratrol (Tempeh)</b></td><td><b>Resveratrol (Soybean Seed Coat)</b></td></tr><tr><th>1.4 (µg/mL)</th><td>88.2</td><td>100</td><td>92.05</td></tr><tr><th>2.8 (µg/mL)</th><td>94.73</td><td>100</td><td>85.59</td></tr><tr><th>4.2 (µg/mL)</th><td>100</td><td>100</td><td>100</td></tr></tbody></table>
Rawdata for publication: An Efficient and Stable Polarizing Agent for In-Cell Magic-Angle Spinning Dynamic Nuclear Polarization NMR Spectroscopy
<p>This is the raw dataset for the publication: An Efficient and Stable Polarizing Agent for In-Cell Magic-Angle Spinning Dynamic Nuclear Polarization NMR Spectroscopy. It contains the EPR and NMR data used in this publication. DOI of this pubcliation: 10.1021/acs.jpclett.4c02709</p>
Agent-based simulation
<p>This datasaet comprises the results of the agent-based simulation study described in: Mazurkiewicz, Bartosz and Kattenbeck, Markus and Giannopoulos, Ioannis, <strong>Navigating Your Way! Increasing the Freedom of Choice during Wayfinding, </strong>11th International Conference on Geographic Information Science (GIScience 2021) - Part II</p>
Figure 3 Alhagi maurorum, plant with typical Aceria alhagi n in A new Aceria species (Acari:Trombidiformes: Eriophyoidea) from West Asia, a potential biological control agent for the invasive weed camelthorn, Alhagi maurorum Medik. (Leguminosae)
Figure 3 Alhagi maurorum, plant with typical Aceria alhagi n. sp. symptoms where the shoot tips
Transposable prophages in leptospira : an ancient, now diverse, group predominant in causative agents of Weil's disease
<p>The virome associated to the corkscrew shaped bacterium leptospira, responsible for the Weil disease, is scarcely known and genetic tools available for these bacteria remain limited. To reduce these two issues, potential transposable prophages were searched in <em>Leptospiraceae</em> genomes. The 236 predicted transposable prophages are particularly abundant in the most pathogenic leptospiral clade, being potentially involved in the acquisition of virulent traits. According to genomic similarities and phylogenies, these prophages are distantly related to known transposable phages and are organized into six groups, one of them encompassing prophages with unusual TA-TA ends. Interestingly, structural and transposition proteins reconstruct different relationships between groups, suggesting ancestral recombinations. Based on the baseplate phylogeny, two large clades emerge, with specific gene-contents and high sequence divergence reflecting their ancient origin. Despite their high divergence, the size and overall genomic organization of all prophages are very conserved, a testimony of the highly constrained nature of their genomes. Finally, similarities between these prophages and the three known non-transposable phages infecting <em>L. biflexa</em>, suggest gene transfer between different Caudovirales inside their leptospiral host, and the possibility to use some of the transposable prophages in that model strain.</p>
Data - Attack of the clones: population genetics reveals clonality of Colletotrichum lupini, the causal agent of lupin anthracnose
<p><em>Colletotrichum lupini</em>, causing lupin anthracnose, is one of the worst pathogens to lupin cultivation worldwide. Understanding its population structure and evolutionary potential is crucial to design successful disease management strategies. The objective of this study was to employ population genetics to investigate the genetic diversity, evolutionary dynamics and molecular basis of host-speciation of this notorious lupin pathogen. A collection of globally representative <em>C. lupini </em>isolates was genotyped through triple digest restriction-site associated DNA sequencing (3D-RADseq), resulting in a dataset of unparalleled resolution. Phylogenetic and structural analysis could distinguish four (I – IV) independent lineages. The strong population structure, low recombination rate and slow linkage decay strongly indicate that <em>C. lupini</em> reproduces clonally. Different morphologies and virulence patterns on white and Andean lupin were observed between and within clonal lineages. Lineage II isolates were shown to have a mini chromosome which was also partly present in lineage III and IV, but not in lineage I isolates. Variation in the presence of this mini-chromosome could indicate a function related to virulence or host-speciation. All four lineages were present in the South American Andes region, which is concluded to be the center of origin of this species. Only members of lineage II have been found outside South America since the 1990s, indicating it as the current pandemic population. As a seed-borne pathogen, <em>C. lupini</em> has mainly spread through infected but symptomless seeds, stressing the importance of phytosanitary measures to prevent future outbreaks of strains that are yet confined to South America.</p>
When should bees be flower constant? An agent-based model highlights the importance of social information and foraging conditions
<p>1. Many bee species show flower constancy, i.e. a tendency to visit flowers of one type during a foraging trip. Flower constancy is important for plant reproduction, but the benefits of constancy to bees are unclear. Social bees, which often use communication about food sources, show particularly strong flower constancy.</p> <p>2. We aimed to better understand the benefits of flower constancy in social bees and how these benefits depend on foraging conditions. We hypothesised that sharing social information increases the benefits of flower constancy because social foragers share information selectively about high-quality food sources, thereby reducing the need to sample alternatives.</p> <p>3. We developed an agent-based model that allowed us to simulate bee colonies with and without communication and flower constancy in different foraging environments. By varying key environmental parameters, such as food source numbers and reward size, we explored how the costs and benefits of flower constancy depend on the foraging landscape.</p> <p>4. Flower constancy alone performed poorly in all environments, while indiscriminate flower choice was often the most successful strategy. However, communication improved the performance of flower constant colonies considerably in most environments. This combination was particularly successful when high-quality food sources were abundant and competition was weak.</p> <p>5. Our findings help explain why social bees tend to be more flower constant than solitary bees and suggest that flower constancy can be an adaptive strategy in social bees. Simulations suggest that anthropogenic changes of foraging landscapes will have different effects on the foraging performance of bees that vary in flower constancy.</p>
Dataset for: Buckling of lipidic ultrasound contrast agents under quasi-static load
<p>Collapse of lipidic ultrasound contrast agents under high-frequency compressive load has been historically interpreted by the vanishing of surface tension. By contrast, buckling of elastic shells is known to occur when costly compressible stress is released through bending. Through quasi-static compression experiments on lipidic shells, we analyze the buckling events in the framework of classical elastic buckling theory and deduce the mechanical characteristics of these shells. They are then compared to that obtained through acoustic characterization.</p>
Spielbücher, Prognostiken und Textamulette als 'manuscript agents'?
<p>Marco Heiles, Spielbücher, Prognostiken und Textamulette als ‚manuscript agents‘?. Videoaufzeichnung des Vortrags auf der Tagung ‚Was ist historische Wissens- und Gebrauchsliteratur? Theoretische Grundlagen und Parameter der Korpusbildung‘ des Netzwerks Historische Wissens- und Gebrauchsliteratur e.V., Herzog August Bibliothek Wolfenbüttel, 30.08.2022.</p> <p>Schnitt: Melinda Michel (Rheinische Friedrich-Wilhelms-Universität Bonn)</p> <p> </p> <p>Präsentation des Vortrags: </p> <p><a href="https://doi.org/10.5281/zenodo.7515437">https://doi.org/10.5281/zenodo.7515437</a></p> <p> </p> <p>Programm der Tagung: </p> <p>Kathrin Chlench-Priber, Marco Heiles, Sven Limbeck und Simone Schultz-Balluff, Was ist historische Wissens- und Gebrauchsliteratur? Tagungskonzept und Programm, in: Netzwerk Historische Wissensund Gebrauchsliteratur, zuerst Veröffentlicht am 13.06.2022, aktualisierte Version vom 07.11.2022, <a href="https://hwgl.hypotheses.org/1801">https://hwgl.hypotheses.org/1801</a> (PDF: <a href="https://doi.org/10.5281/zenodo.7515385">https://doi.org/10.5281/zenodo.7515385</a>).</p>
Wildlife response to disturbances in agent-based models: synthesis on current development and challenges (Systematic Review)
<p>This dataset was obtained from a systematic screening of 124 articles presenting agent-based models of wildlife response to disturbances. It is part of a manuscript for submission to the journal Methods in Ecology and Evolution. The manuscript is entitled: Wildlife response to disturbances in agent-based models: synthesis on current development and challenges.</p>
Multi-agent multi-mode composite task allocation problem (MACTA) instances
<p><strong>Contents</strong></p> <p>This repository contains all the instances of Multi-agent multi-mode composite task allocation problem (MACTA) used in the AAMAS paper [Picard, 2023].</p> <p>Instances are provided as json files (one per instance), following the provided schema (see <code>macta_schema.json</code>). Files are contained in subdirectories following the <code><n>_modes/<m>_requests_per_user/instance_<i>.json</code> pattern, where <code><n></code> is the number of modes per requests (1 or 5), <code><m></code> is the number of requests per user (between 2 and 30 by step of 2), and <code><i></code> is the instance number.</p> <p><strong>Acknowledgements</strong></p> <p>This work has been performed with the support of the French government in the context of the "Programme d'Invertissements d'Avenir", namely by the BPI PSPC LiChIE project (Lion Chaine Image Elargie), coordinated by Airbus Defence and Space.</p> <p><strong>References</strong></p> <p>Picard, G. (2023). Multi-agent consensus-based bundle allocation for multi-mode composite tasks. In <em>International Conference on Autonomous Agents and Multiagent Systems (AAMAS-23)</em>. IFAAMAS.</p>
Bacterial predation of a fungal wheat pathogen: Prelude to experimental evolution of enhanced biocontrol agents
<p><span>Research to identify appropriate biological agents for controlling pathogens might exploit experimental evolution to select for enhanced antagonism against pathogens. We report development of an experimental regime facilitating this approach featuring the broad-spectrum bacterial predator <em>Myxococcus</em> <em>xanthus</em> and the fungal wheat pathogen <em>Zymoseptoria</em> <em>tritici</em>. We demonstrate that <em>Z. tritici</em>, a major cause of crop loss and fungicide use worldwide, both fuels growth of and is killed by <em>M. xanthus</em> on wheat straw, a likely source of vernal seedling infection. <em>M. xanthus</em> is first found capable of density-dependent growth on moistened straw alone, unaided by <em>Z. tritici</em> as prey, growth that also depends on how long straw was moistened before <em>M. xanthus</em> inoculation. Such growth of non-cellulolytic myxobacteria on plant detritus may have implications for understanding their roles in nutrient cycling. However, straw with <em>Z. tritici </em>is found to fuel greater <em>M. xanthus </em>growth than straw alone under many conditions. After shorter moistening, growth by low-density <em>M. xanthus</em> populations is found to be fully dependent on <em>Z. tritici</em>. Such pathogen-dependent <em>M. xanthus</em> populations could be sustained with population replacement over five one-week growth cycles, indicating feasibility of conducting long-term experimental evolution with this system. Further, <em>M. xanthus</em> is found to kill majorities of <em>Z. tritici</em> populations on both buffered agar and straw. Our results suggest that myxobacteria may serve as effective biocontrol agents of <em>Z. tritici</em> and are amenable to long-term experimental selection for enhanced killing of this pathogen, an approach broadly applicable to many potential biocontrol agents and target pathogens.</span></p>
Supplementary material for AAMAS 2023 paper : Trusting Artificial Agents: Communication Trumps Performance
<p>This is the supplementary material for AAMAS 2023 full paper "Trusting Artificial Agents: Communication Trumps Performance". It includes a video of the conditions encountered by each group and details about how the study was led as well as statistical detailed analyses.</p>
Neural-logic Multi-agent System for flood event detection
<p>This repository contains the source code for the paper "Neural-logic Multi-agent System for flood event detection". The code implements a multi-agent system (MAS) designed to detect flooding events.</p>
Hyperpolarized [15N]nitrate as a potential long lived hyperpolarized contrast agent for MRI
<p>Primary data for DOI: <a href="https://doi.org/10.1016/j.jmr.2019.01.001">10.1016/j.jmr.2019.01.001</a></p> <p>Title: Hyperpolarized [<sup>15</sup>N]nitrate as a potential long lived hyperpolarized contrast agent for MRI</p> <p>Authors: Ayelet Gamliel, Sivaranjan Uppala, Gal Sapir, Talia Harris, Atara Nardi-Schreiber, David Shaul, Jacob Sosna, J. Moshe Gomori, Rachel Katz-Brull</p> <p>Description:</p> <p>The primary datasets in this archive contain data presented in the above publication and consist of <sup>15</sup>N-NMR spectra in solutions.</p> <p>Please consult the Archive Guide.</p>
ScienceDex guides
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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.