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555 results for “upper extremity”
Effect of Vojta Therapy on Upper Extremity Function of Children With Cerebral Palsy
ClinicalTrials.gov study NCT06203366. IPD Sharing: YES. Countries: 1. Publications: 6.
Effects of Post-Stroke Upper Extremity Assistance
ClinicalTrials.gov study NCT05036642. IPD Sharing: NO. Countries: 1. Publications: 1.
Brain Machine Interface Control of an Robotic Exoskeleton in Training Upper Extremity Functions in Stroke
ClinicalTrials.gov study NCT01948739. IPD Sharing: NO. Countries: 1. Publications: 5.
Effectiveness of Virtual Reality Gaming Therapy Versus CI Therapy for Upper Extremity Rehabilitation
ClinicalTrials.gov study NCT02631850. IPD Sharing: YES. Countries: 1. Publications: 5.
Data from: Hormonal and metabolic responses to upper temperature extremes in divergent life-history ecotypes of a garter snake
Extreme temperatures constrain organismal physiology and impose both acute and chronic effects. Additionally, temperature-induced hormone-mediated stress response pathways and energetic trade-offs are important drivers of life-history variation. This study employs an integrative approach to quantify acute physiological responses to high temperatures in divergent life-history ecotypes of the western terrestrial garter snake (Thamnophis elegans). Using wild-caught animals, we measured oxygen consumption rate and physiological markers of hormonal stress response, energy availability, and anaerobic respiration in blood plasma across five ecologically relevant temperatures (24, 28, 32, 35, and 38° C; 3-hour exposure). Corticosterone, insulin, and glucose concentrations all increased with temperature, but with different thermal response curves, suggesting that high temperatures differently affect energy-regulation pathways. Additionally, oxygen consumption rate increased without plateau and lactate concentration did not increase with temperature, challenging the recent hypothesis that oxygen limitation sets upper thermal tolerance limits. Finally, animals had similar physiological thermal responses to high-temperature exposure regardless of genetic background, suggesting that local adaptation has not resulted in fixed differences between ecotypes. Together, these results identify some of the mechanisms by which higher temperatures alter hormonal-mediated energy balance in reptiles and potential limits to the flexibility of this response.
Distribution. Upper Amazon in S Colombia, W Brazil, E Peru, and N Bolivia, from the Rio Caqueta in Colombia, S through the Peruvian Amazon and the extreme W Brazilian Amazon into the Pando region of Bolivia. in Callitrichiade
Distribution. Upper Amazon in S Colombia, W Brazil, E Peru, and N Bolivia, from the Rio Caqueta in Colombia, S through the Peruvian Amazon and the extreme W Brazilian Amazon into the Pando region of Bolivia.
Subspecies and Distribution. T. s. bakeri S. L. Williams, Willig & Reid, 1995 — from extreme SE Mexico (LLacandon Forest, Chiapas) E to Honduras; then, distribution is apparently disjunct and continues S from Nicaragua into South America through N Colombia, NW Ecuador, and NW & N Venezuela (N of Cordillera de Mérida). T.s. maresi S. L. Williams, Willig & Reid, 1995 — Venezuela (E & S of Cordillera de Mérida), the Guianas, N & E Brazil, and along upper Amazon Basin in Colombia, W Brazil, Ecuador, Peru, and Bolivia; also on Trinidad I. in Phyllostomidae
Subspecies and Distribution. T. s. bakeri S. L. Williams, Willig & Reid, 1995 — from extreme SE Mexico (LLacandon Forest, Chiapas) E to Honduras; then, distribution is apparently disjunct and continues S from Nicaragua into South America through N Colombia, NW Ecuador, and NW & N Venezuela (N of Cordillera de Mérida). T.s. maresi S. L. Williams, Willig & Reid, 1995 — Venezuela (E & S of Cordillera de Mérida), the Guianas, N & E Brazil, and along upper Amazon Basin in Colombia, W Brazil, Ecuador, Peru, and Bolivia; also on Trinidad I.
Distribution. Amazon Basin of the upper Orinoco and Casiquiare rivers of extreme E Colombia and S Venezuela; it might occur in adjacent N Brazil. in Echimyidae
Distribution. Amazon Basin of the upper Orinoco and Casiquiare rivers of extreme E Colombia and S Venezuela; it might occur in adjacent N Brazil.
Code and data for An Upper Bound for Extreme Temperatures over Midlatitude Land
<p>This .zip file contains data and Jupyter Notebooks to reproduce the results in "An Upper Bound for Extreme Temperatures over Midlatitude Land" by Zhang and Boos.</p>
Data from: Evolutionary process of extremely twisted heteromorph ammonites from the Upper Cretaceous in Japan
<p><span>The heteromorph ammonite </span><em><span>Pravitoceras sigmoidale</span></em><span> with extremely twisted retroversal hook and its probable ancestors, </span><em><span>Didymoceras awajiense</span></em><span> and </span><em><span>D</span><span>. </span><span>morozumii</span></em><span>, occur mainly in the Upper Cretaceous Izumi and Sotoizumi groups in southwest Japan. Their morphological characteristics were investigated in this study. Morphotypes I–II were recognized in </span><em><span>D. morozumii</span></em><span>. Morphotypes III–V were recognized in </span><em><span>D. awajiense</span></em><span>. Morphotypes VI–VIII were recognized in </span><em><span>P. sigmoidale</span></em><span>. Moreover, all morphotypes were recognized in both the dextral and sinistral forms of these three species. Based on the morphological and stratigraphic relationships, it is considered that the evolutionary process of these species is divided into three steps: (1) shift from morphotypes I–II to III; (2) increase in variation from morphotypes III to III–V; and (3) shift from morphotypes III–V to VI–VIII. By comparing these morphotypes based on the 'growing tube model' belonging to the moving frame analysis, it is seen that there are no significant gaps of coiling patterns in the evolutionary processes of this lineage. Meanwhile, morphotypes III–V of </span><em><span>D. awajiense</span></em><span> have a larger morphological variation than morphotypes I–II of </span><em><span>D</span><span>. </span><span>morozumii</span></em><span><em> </em>and morphotypes VI–VIII of </span><em><span>P. sigmoidale</span></em><span>. These results, and the radiometric ages from previous studies, suggest that </span><em><span>D. awajiense</span></em><span>, with considerable variation between ancestor and descendant species, existed in a short interval. It seems that </span><em><span>P. sigmoidale</span></em><span> occurred after the continuous but rapid and drastic morphological evolution from </span><em><span>D. morozumii</span></em><span><em> </em>via<em> </em></span><em><span>D. awajiense</span></em><span>.</span></p>
Upper Extremity Function, Shoulder Position Sense and Disability Level İn Patients With Multiple Sclerosis
ClinicalTrials.gov study NCT03846336. IPD Sharing: Not stated. Countries: 1. Publications: 1.
The Effects Of Upper Extremity Robotic Rehabilitation On Upper Extremity Functions And Gait Parameters
ClinicalTrials.gov study NCT05136612. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Upper Extremity Stability and Balance in Youth Basketball Players
ClinicalTrials.gov study NCT06907940. IPD Sharing: NO. Countries: 1. Publications: 1.
Effect of mCIMT on Upper Extremity Functions of Stroke Patients With Right/Left Hemiplegia
ClinicalTrials.gov study NCT04013750. IPD Sharing: NO. Countries: 1. Publications: 1.
PNF Strengthening and De-lorme and Watkins Exercises on Upper Extremity Function and Strength in Stroke Patients
ClinicalTrials.gov study NCT05904795. IPD Sharing: NO. Countries: 1. Publications: 7.
Conditioning Neural Circuits to Improve Upper Extremity Function
ClinicalTrials.gov study NCT02611375. IPD Sharing: NO. Countries: 1. Publications: 13.
Physiotherapy Applications in Upper Extremity Lipedema
ClinicalTrials.gov study NCT04643392. IPD Sharing: NO. Countries: 1. Publications: 1.
Synchronous Telerehabilitation vs Face to Face Method for Upper Extremity Functions in Children With Hemiparetic CP
ClinicalTrials.gov study NCT05522452. IPD Sharing: NO. Countries: 1. Publications: 1.
Musculoskeletal Health of the Upper Extremity in Emerging Health Professionals
ClinicalTrials.gov study NCT02587897. IPD Sharing: YES. Countries: 1. Publications: 13.
Brachial Plexus Block vs. General Anesthesia for Anesthesia Anxiety Before Orthopedic Upper Extremity Surgery
ClinicalTrials.gov study NCT05476198. IPD Sharing: YES. Countries: 1. Publications: 4.
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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.