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Dataset results
601 results for “crossovers”
Four Way Crossover Closed Loop With Exercise Detection
ClinicalTrials.gov study NCT02862730. IPD Sharing: NO. Countries: 1. Publications: 1.
Three Way Crossover Closed Loop Study With Xeris Glucagon
ClinicalTrials.gov study NCT03424044. IPD Sharing: Not stated. Countries: 1. Publications: 1.
A Randomized, Double Blind, Placebo Controlled, Incomplete Block, Crossover, Dose Ranging Study to Evaluate the Dose Response of GSK573719 Administered Once or Twice Daily Over 7 Days in Patients With
ClinicalTrials.gov study NCT01372410. IPD Sharing: YES. Countries: 1. Publications: 1.
Data from: Combined fluorescent and electron microscopic imaging unveils the specific properties of two classes of meiotic crossovers
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Data from: High-resolution crossover maps for each bivalent of Zea mays using recombination nodules
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Data from: Carrier density crossover and quasiparticle mass enhancement in a doped 5d Mott insulator
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Protocol, case report(s), ethics approvals, informed consent, inclusion and exclusion criteria underlying: The effect of morning versus evening administration of empagliflozin on its pharmacokinetics and pharmacodynamics characteristics in healthy adults: a two-way crossover, non-randomised trial
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Variants and QTL associated with variation in genome-wide crossover number
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Sixty-minute inhalation of molecular hydrogen decreases blood oxygen saturation but does not alter autonomic cardiac regulation at rest in healthy females: A randomized, double-blind, placebo-controlled crossover study
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Data from: Use of the lung flute ECO to assist in sputum collection for tuberculosis testing: a randomized crossover trial
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Pharmacokinetics parameters, bioanalytical method underlying the manuscript: The effect of morning versus evening administration of empagliflozin on its pharmacokinetics and pharmacodynamics characteristics in healthy adults: a two-way crossover non-randomised trial
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Pharmacodynamics parameters underlying the manuscript: The effect of morning versus evening administration of empagliflozin on its pharmacokinetics and pharmacodynamics characteristics in healthy adults: a two-way crossover, non-randomised trial
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Data from: Gardner-like crossover from variable to persistent force contacts in granular crystals
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Data from: BCI training to move a virtual hand reduces phantom limb pain: a randomized crossover trial
<p>Objective: To determine whether training with a brain–computer interface (BCI) to control an image of a phantom hand, which moves based on cortical currents estimated from magnetoencephalographic signals, reduces phantom limb pain.</p> <p>Methods: Twelve patients with chronic phantom limb pain of the upper limb due to amputation or brachial plexus root avulsion participated in a randomized single-blinded crossover trial. Patients were trained to move the virtual hand image controlled by the BCI with a real decoder, which was constructed to classify intact hand movements from motor cortical currents, by moving their phantom hands for 3 days ("real training"). Pain was evaluated using a visual analogue scale (VAS) before and after training, and at follow-up for an additional 16 days. As a control, patients engaged in the training with the same hand image controlled by randomly changing values ("random training"). The two trainings were randomly assigned to the patients. This trial is registered at UMIN-CTR (UMIN000013608).</p> <p>Results: VAS at day 4 was significantly reduced from the baseline after real training (45.3 [24.2] to 30.9 [20.6], 1/100mm, mean [SDs]; P=0.009<0.025), but not after random training (P=0.047>0.025). Compared to VAS at day 1, VAS at days 4 and 8 was significantly reduced by 32% and 36%, respectively, after real training and was significantly lower than VAS after random training (P<0.01).</p> <p>Conclusion: Three-day training to move the hand images controlled by BCI significantly reduced pain for one week.<br> Classification of evidence: This study provides Class &#8546; evidence that BCI reduces phantom limb pain.</p> <p> </p>
Data from: The effect of meal frequency in a reduced-energy regimen on the gastrointestinal and appetite hormones in patients with type 2 diabetes: a randomised crossover study
Background: Appetite and gastrointestinal hormones (GIHs) participate in energy homeostasis, feeding behavior and regulation of body weight. We demonstrated previously the superior effect of a hypocaloric diet regimen with lower meal frequency (B2) on body weight, hepatic fat content, insulin sensitivity and feelings of hunger compared to the same diet divided into six smaller meals a day (A6).Studies with isoenergetic diet regimens indicate that lower meal frequency should also have an effect on fasting and postprandial responses of GIHs.The aim of this secondary analysis was to explore the effect of two hypocaloric diet regimens on fasting levels of appetite and GIHs and on their postprandial responses after a standard meal. It was hypothesized that lower meal frequency in a reduced-energy regimen leading to greater body weight reduction and reduced hunger would be associated with decreased plasma concentrations of GIHs: gastric inhibitory peptide (GIP), glucagon-like peptide-1(GLP-1), peptide YY(PYY), pancreatic polypeptide (PP) and leptin and increased plasma concentration of ghrelin. The postprandial response of satiety hormones (GLP-1, PYY and PP) and postprandial suppression of ghrelin will be improved. Methods: In a randomized crossover study, 54 patients suffering from type 2 diabetes (T2D) underwent both regimens.The concentrations of GLP-1, GIP, PP, PYY, amylin, leptin and ghrelin were determined using multiplex immunoanalyses. Results: Fasting leptin and GIP decreased in response to both regimens with no difference between the treatments (p=0.37 and p=0.83, respectively). Fasting ghrelin decreased in A6 and increased in B2 (with difference between regimens p=0.023). Fasting PP increased in B2with no significant difference between regimens (p=0.17). Neither GLP-1 nor PYY did change in either regimen. The decrease in body weight correlated negatively with changes in fasting ghrelin (r=-0.4, p<0.043) and the postprandial reduction of ghrelin correlated positively with its fasting level (r=0.9, p<0.001). The postprandial responses of GIHs and appetite hormones were similar after both diet regimens. Conclusions: Both hypocaloric diet regimens reduced fasting leptin and GIP and postprandial response of GIP comparably. The postprandial responses of GIHs and appetite hormones were similar after both diet regimens. Eating only breakfast and lunch increased fasting plasma ghrelin more than the same caloric restriction split into six meals. The changes in fasting ghrelin correlated negatively with the decrease in body weight. These results suggest that for type 2 diabetic patients on a hypocaloric diet, eating larger breakfast and lunch may be more efficient than six smaller meals during the day.
Data used for submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover"
<p>Datasets generated and presented in the submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover".</p>
Data used for submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover".
<p>Datasets generated and presented in the submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover". Includes the results of statistical analysis.</p>
Data used for submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover".
<p>Datasets generated and presented in the submission entitled "Critical Mutation Rate has an Exponential Dependence on Population Size for Eukaryotic-length Genomes with Crossover". Includes the results of statistical analysis.</p>
Impact of Probiotic Veillonella atypica FB0054 Supplementation on Anaerobic Capacity and Lactate Changes: A Randomized, Crossover Pilot
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The Positional Bias might not Influence Cartesian Genetic Programming with Crossover
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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.