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565 results for “ESCAPE”
Determinants of gastric cancer immune escape identified from non-coding immune-landscape quantitative trait loci
GEO Series GSE261709. Homo sapiens. 7 samples. Type: Other.
Megadomains and superloops form dynamically during X-chromosome inactivation but are dispensable for silencing and escape
GEO Series GSE116649. Mus musculus. 65 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
Supplementary data for: "The Venusian atmospheric oxygen ion escape: Extrapolation to the early Solar System"
<p>Supplementary data for paper "The Venusian atmospheric oxygen ion escape: Extrapolation to the early Solar System", submitted to Journal of Geophysical Research: Planets. See README file for description of the data in each file.</p>
Data for "Learning the language of viral evolution and escape"
<p>Training data from:</p> <ul> <li>Influenza A HA protein sequences from the NIAID Influenza Research Database (IRD) (<a href="http://www.fludb.org">http://www.fludb.org</a>)</li> <li>HIV-1 Env protein sequences from the Los Alamos National Laboratory (LANL) HIV database (<a href="https://www.hiv.lanl.gov">https://www.hiv.lanl.gov</a>)</li> <li><em>Coronavidae</em> spike protein sequences from the Virus Pathogen Resource (ViPR) database (<a href="https://www.viprbrc.org/brc/home.spg?decorator=corona">https://www.viprbrc.org/brc/home.spg?decorator=corona</a>)</li> <li>SARS-CoV-2 Spike protein sequences from NCBI Virus (<a href="https://www.ncbi.nlm.nih.gov/labs/virus/vssi/">https://www.ncbi.nlm.nih.gov/labs/virus/vssi/</a>)</li> <li>SARS-CoV-2 Spike and other Betacoronavirus spike protein sequences from GISAID (<a href="https://www.gisaid.org/">https://www.gisaid.org/</a>)</li> </ul> <p>Datasets for fitness and escape validation:</p> <ul> <li>Fitness single-residue DMS of HA H1 WSN33 from Doud and Bloom (2016)</li> <li>Fitness combinatorial DMS of antigenic site B in six HA H3 strains from Wu et al. (2020)</li> <li>Fitness single-residue DMS of Env BF520 and BG505 from Haddox et al. (2018)</li> <li>ACE2 binding affinity combinatorial DMS of Spike from Starr et al. (2020)</li> <li>Escape single-residue DMS of HA H1 WSN33 from Doud et al. (2018)</li> <li>Escape single-residue DMS of HA H3 Perth09 from Lee et al. (2019)</li> <li>Escape single-residue DMS of Env BG505 from Dingens et al. (2019)</li> <li>Escape mutations of Spike from Baum et al. (2020)</li> <li>Escape single-residue DMS of Spike from Greaney et al. (2020)</li> </ul>
Chum salmon escapement on Bonanza River in Norton Sound, Alaska
<p>Bonanza River flows 40 rkm south from the Kigluaik Mountains and drains into Safety Sound approximately 39 km northeast of Nome, Alaska. Chum, pink, and coho salmon are the predominant species that return to the Bonanza River. A fixed-picket weir was installed approximately 11 rkm above the Bonanza Bridge on the Nome-Council Highway (GPS coordinates 64°32.964ʹN, 164°35.812ʹW). The Bonanza River weir enumerated chum salmon for three seasons from 2018 to 2020. Chum salmon escapements were 7,903 in 2018; 8,824 in 2019; and 2,471 in 2020. In 2018 and 2019, high water delayed installation of the weir and therefore the beginning of the run may have been missed. Additionally, in 2019 high water forced weir operations to stop before the proposed end date, so it is likely the end of the chum salmon run was missed. In 2020, the weir went in according to schedule and counted the beginning of the run, but personnel issues, exacerbated by COVID-19 protocols, resulted in early termination of the project, and likely caused missed counting at the end of the run. High water that hindered counting on Bonanza River in 2018 and 2019 also hindered counting operations on other Subdistrict 1 rivers, and as a result aspects of Objectives 1 and 2 could not be completed for all project years. Age, sex, and length data were collected from chum salmon passing through the weir in all three years. Minimum sample size requirements to evaluate Objective 3 were met in 2018 and 2020, but not in 2019. In 2018, chum salmon were predominantly 4 years old and in 2020 chum salmon were predominantly 5 years old. This project indicated that using existing methods, such as weirs and aerial surveys, to estimate Bonanza River's contribution to chum salmon abundance in Subdistrict 1 provide a reasonable approximation of chum salmon escapement in the absence of an enumeration project on Bonanza River.</p>
Data from: Too important to tamper with: predation risk affects body mass and escape behaviour but not escape ability
1. Escaping from a predator is a matter of life or death, and prey are expected to adaptively alter their physiology under chronic predation risk in ways that may affect escape. Theoretical models assume that escape performance is mass-dependent whereby scared prey strategically maintain an optimal body mass to enhance escape. Experiments testing the mass-dependent predation risk (MDPR) hypothesis have demonstrated that prior experience of predation risk can affect body mass, and the behavioural decisions about evasive actions to take. Other studies on natural changes in body mass indicate that mass can affect escape. No single experiment has tested if all of these components are indeed linked, which is a critical necessary condition underpinning the MDPR. 2. We tested all components of the MDPR in a repeated-measures experiment by presenting predator and non-predator cues to brown-headed cowbirds housed in semi-natural conditions. Exposure to predator cues affected body mass, fat, pectoral muscle thickness, and evasive actions (take-off angle and speed), but not the physiological capacity to escape, as measured by flying ability. Examining individual variation revealed that flying ability was unrelated to mass loss in either sex, unrelated to mass gain in males, and only females that gained a very large amount of mass flew poorly. 3. We next conducted a body mass manipulation in the lab to rigorously test whether small to large perturbations in mass can ever affect flying ability. We induced either no change in mass (control), a moderate reduction of <10%, and a more extreme reduction of >10% which the literature suggests should enhance flight. Flying ability was maintained regardless of treatment. Examining individual variation revealed the same precise patterns as in the first experiment. 4. We conclude that prey may alter their mass and evasive actions in response to predation risk, but their escape ability remains robust and inelastic, presumably because dis-abling oneself is likely to lead to disastrous consequences. We suggest that animals may only face a mass-dependant predation risk trade-off in a narrow set of circumstances linked to life history stages that require large amounts of mass gain, e.g. parturition and migration.
Fig 1 from: Kuga T, Kasuya E (2024) Factors related to sound production by the Chinese grasshopper Acrida cinerea during escape. Journal of Orthoptera Research 33(1): 13-19. https://doi.org/10.3897/jor.33.100865
Fig 1 Photos of male A. cinerea (A) and its habitat where field experiments were conducted (B).
Enhanced ion escape rate during IMF rotation under weak intrinsic magnetic field conditions on a Mars-like planet
<p>This dataset contains the simulation results used for figures in the paper "Enhanced ion escape rate during CME-like IMF rotation under weak intrinsic magnetic field conditions on a Mars-like planet" submitted to Journal of Geophysical Research: Space Physics. Detailed information about the dataset can be found in "README.txt".</p>
Pasagshak River Sockeye Salmon (Oncorhynchus nerka) Escapement Monitoring 2019–2021
<p>Since 2011, sockeye salmon (<em>Oncorhynchus nerka)</em> escapement through the Pasagshak River into Lake Rose Teed on the Kodiak Island road system has been estimated with a weir. A continuation of funding from the Alaska Sustainable Salmon Fund (AKSSF, Project #52009) allowed the Alaska Department of Fish and Game (ADF&G), Division of Commercial Fisheries to operate a PVC floating weir near the mouth of Lake Rose Teed during the 2019 through 2021 seasons. This data set includes the number and species of fish counted through the weir, and the age, sex, and length (ASL) information gathered from sockeye salmon captured and sampled at the weir.</p>
Data from: Extensive hybridization following a large escape of domesticated Atlantic salmon in the Northwest Atlantic
[No abstract entered]
Replication Package for: Private Sector Provision as an Escape Valve: The Mexico Diabetes Experiment
<p>Bronsoler, A., Gruber, J., & Seira, E. (2023). <em>Private Sector Provision as an “Escape Valve”: The Mexico Diabetes Experiment .</em></p> <p><em>Replication package for tables and figures. Includes publically available data and de-identified experimental data.</em></p>
Fire Escape
The popular New york building fire escape. Made this for a project in blender. also added array modifier so it can be repeated however many times you want. Source: Objaverse 1.0 / Sketchfab
Natural Killer Cells Functions, Tumoral Escape to Immune System and Regulation of Natural Cytotoxixity Receptors in Haematological Malignancies
ClinicalTrials.gov study NCT01915992. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Escape Room Game in Oncology Nursing
ClinicalTrials.gov study NCT06181058. IPD Sharing: NO. Countries: 1. Publications: 0.
Example of Escape Room in Nursing Student Education
ClinicalTrials.gov study NCT05830526. IPD Sharing: NO. Countries: 1. Publications: 0.
Virtual Escape Room Game About Medical Device in Nurses
ClinicalTrials.gov study NCT07081490. IPD Sharing: NO. Countries: 1. Publications: 0.
Comparison of the Escape Room and Storytelling Methods in Learning the Stress Response
ClinicalTrials.gov study NCT05865509. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effectiveness of Digital Escape Room Game-Based Disaster Midwifery Training: MERCI Model
ClinicalTrials.gov study NCT07090642. IPD Sharing: NO. Countries: 1. Publications: 0.
ESCAPE Study : Validation of a Specific Tool Scoring Residents at Risk of Escaping/Elopement From Nursing Homes (ESCAPE)
ClinicalTrials.gov study NCT03662464. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effect of Tyrosine on Behavioral, Physiological and Nutritional Status During Survive, Evade, Resist, Escape (SERE) School
ClinicalTrials.gov study NCT01823276. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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.