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3,472 results for “Balance”

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zenodo28/100

Relationship between Cognitive Function, Fear of Falling, and Balance in Community-Dwelling Elderly: Cross-Sectional Study.

Open the record for dataset details and reuse information.

opencc-by-4.0Oct 2024View details →
zenodo28/100

Mass-balance model inputs for the Kaskawulsh River headwaters

<p>This dataset contains the input files necessary to run the mass-balance model (see Young et al. (2021), Robinson et al. (2024)) for the Kaskawulsh River headwaters from 1980&ndash;2022. Downscaled/bias corrected temperature/precipitation inputs will be uploaded separately due to the large file sizes.</p> <p><strong>Downscaling &gt; CoarseNARR_KRH</strong></p> <p>This folder contains the coarse North American Regional Reanalysis (NARR) data that were downscaled to obtain the temperature/precipitation inputs used to drive the Kaskawulsh River headwaters mass-balance model (see Robinson, 2024).&nbsp;</p> <p>All files contain an array of 6 x 6 gridcells, centered on the Kaskawulsh Glacier, Yukon, Canada. The bottom left corner of the grid has coordinates 502592 E, 6624579 N and is located over Yakutat Bay, Alaska.&nbsp;</p> <p>Variables:&nbsp;</p> <ul> <li> <p>air: NARR 3-hourly multi-level air temperatures</p> </li> <li> <p>hgt: NARR 3-hourly multi-level geopotential height</p> </li> <li> <p>apcp: NARR daily total surface precipitation</p> </li> <li> <p>KRH_CE.nc: Time-invariant elevation of NARR gricells</p> </li> </ul> <p><strong>Input_geometry &gt; KRH</strong></p> <p>This folder contains the input geometries needed to run the model for the Kaskawulsh River headwaters.</p> <p>KRH_Xgrid.txt / KRH_Ygrid.txt - contains the Easting/Northing (UTM 7N) of each gridcell in the model domain.&nbsp;</p> <p>Zgrids - a folder containing the annual surface elevation grids (m a.s.l.) for 1979&ndash;2022 (see Robinson et al. (2024) for details on how these were derived.</p> <p>KRH_SfcType.txt - a value of 0 indicates the gridcell is glacierized terrain, a value of 1 indicates that the gridcell is non-glacierized terrain.&nbsp;</p> <p>KRH_Tributaries.txt - gridcell value indicates which portion of the Kaskawulsh Glacier the gridcell belongs to (1 = South Arm, 2 = Stairway Glacier, 3 = Central Arm, 4 = North Arm, 5 = Trunk).&nbsp;</p> <p><strong>Solar</strong></p> <p>Contains one file per year with the 3-hourly potential direct clear-sky solar radiation, calculated using the shading program from the Hock (1999) Distributed Enhanced Temperature-Index Model (DETIM). For details see Hock (1999).</p> <p><strong>Debris</strong></p> <p>&lsquo;KRH_debrismap.txt&rsquo; is a text file with dimensions &nbsp;x,y = 230 gridcells x 329 grid cells. Gridcells are 200 m x 200 m. Each gridcell contains either a value representing the estimated debris thickness (in meters), or NaN if the gridcell is not debris covered. Debris thicknesses are from the Rounce et al. (2021) global debris thickness dataset, interpolated to the Kaskawulsh River headwaters 200 m domain by Robinson (2024).</p> <p>For details on the debris thickness estimate, see Rounce et al. (2021).&nbsp;For details on the interpolation of the original debris thickness estimate to the gridcell size of the model, see Robinson (2024).</p> <p><strong>Tuning &gt; parameters</strong></p> <p>This directory contains a folder &lsquo;initial_params&rsquo; with all the original values of a_ice, a_snow, and MF used to tune all the mass-balance models in Robinson et al. (2024) (in groups of 10,000 param combinations).&nbsp;</p> <p>Each additional directory contains the final 100 parameter combinations tuned for each model presented in Robinson et al. (2024), including:</p> <ol> <li> <p>The reference model.</p> </li> <li> <p>The debris-free model.</p> </li> <li> <p>The model with sub-debris melt-scaling from Rounce et al. (2021).</p> </li> <li> <p>The model with uncorrected accumulation.</p> </li> <li> <p>The model with accumulation bias corrected with precipitation gauge data.</p> </li> </ol> <p><strong>Tuning &gt; snowlines</strong></p> <p>Contains 53 .npy files with the rasterized versions of observed snow cover on the Kaskawulsh Glacier delineated from satellite images (see Robinson, 2024). These rasters are used in the second stage of tuning&nbsp; to compare modelled and observed snowlines.&nbsp;</p>

opencc-by-4.0Oct 2024View details →
dryad28/100

Data from: Neighbor effects on tree architecture: functional trade-offs balancing crown competitiveness with wind resistance

1. The architecture of trees is the result of constrained, morphologically plastic growth—constrained by an underlying architectural model embedded in their genome, the structure of which can be significantly altered during growth to match the changing environmental conditions to which the tree is exposed. Here, we examined the hypothesis that crowding from neighbors should cause trees to optimize traits for light competition at the expense of wind resistance, with the reverse being true for trees lacking neighbors. Previous studies have examined the influence of light competition or wind resistance on shaping tree architecture, but few, if any, have simultaneously addressed tradeoffs for optimizing these traits in response to crowding from neighboring trees in forests, as compared to open-grown conditions. 2. We studied the response of tree- and branch-level architectural traits of temperate, broad-leaved, deciduous tree species of differing shade tolerance and wood strength from multiple locations across the northeastern United States. Trees ranged in size (4 to 83 cm diameter at 1.3 m) and crowding conditions (open-grown and forests) and occupied different canopy positions. The open-grown trees represented a null condition, where the lack of neighboring trees to shape architectural traits could be contrasted with the influence of different levels of crowding in forests. 3. Our results show strong evidence for a tree neighborhood-induced convergence of architectural traits across species and conditions, even when trees are growing in urban rather than natural forest conditions. After accounting for crowding, the effects of species and sample location contributed very little to explaining variation in architectural traits. One exception was crown dimensions, for which species-specific differences explained about 15% of the residual variation. 4. Under open-grown conditions, alleviation of light competition caused trees to develop relatively large crowns and branches and a squat growth form suitable to resist greater wind exposure. By contrast, increasing shading from neighboring trees caused forest-grown trees to become increasingly more spindly in the main stem, with slender branches sparsely distributed over a disproportionately large crown volume—presumably to maximize light capture. Though the latter is an intrinsically less wind-stable form, it can be adopted to increase light capture, because neighboring trees reduce exposure to the wind, which should greatly reduce the likelihood of stem breakage or uprooting under critical wind pressures.

opencc-zeroDec 2016View details →
dryad28/100

Data from: Effect of H. pylori infection on cytokine profiles and oxidative balance in subjects with chronic alcohol ingestion

Different amounts of ingested alcohol can have distinct effects on the human body. However, there is limited research on chronic alcohol consumption with Helicobacter pylori infection. We sought to investigate the relationship between the cytokine profile, oxidative balance and H. pylori infection in subjects with chronic alcohol consumption. A total of 142 subjects were divided into three groups: 59 subjects with chronic alcohol ingestion and H. pylori infection (group A); 53 subjects with chronic alcohol ingestion without H. pylori infection (group B); and 30 control subjects (group C). The serum levels of CagA, interleukin (IL)-10, E-selectin, TNF-α, malondialdehyde (MDA) and superoxide dismutase (SOD) activity were measured by enzyme-linked immunosorbent assay (ELISA). We found that the ages and serum H. pylori CagA levels among the three groups, as well as both the mean drinking age and the mean daily alcohol consumption between groups A and B, were matched and comparable. Comparing the BMIs among the three groups, the BMI differences were found to be statistically significant (F=3.921, P&lt;0.05). Compared with group C, the BMIs in groups A and B were significantly higher (P&lt;0.001 and P&lt;0.01, respectively); however, the BMI differences between group A and group B were not statistically significant (P&gt;0.05). Additionally, no differences in the serum CagA levels were found in comparisons among the groups (all P&gt;0.05). The serum IL-10 and E-selectin levels in group A were significantly lower than those in group B (serum IL-10: P&lt;0.05; E-selectin: P&lt;0.05). The serum IL-10 in group A was significantly higher than that in group C (P&lt;0.01); the serum E-selectin levels in group A did not significantly differ compared with those in group C (P&gt;0.05). Furthermore, the serum IL-10 and E-selectin levels in group B were significantly higher than those in group C (serum IL-10: P&lt;0.001; E-selectin: P&lt;0.05); however, the serum TNF-α levels did not differ among groups (all P&gt;0.05). Although the serum levels of MDA and SOD in groups A and B were slightly lower than those in group C, there were no significant differences among groups (all P&gt;0.05). In conclusion, we believe that H. pylori infection might cause a significant inhibition of certain cytokine profiles in subjects with chronic alcohol ingestion. Moreover, chronically ingested alcohol may exert an adjusted inflammatory effect, but there was no association between H. pylori infection, chronic alcohol consumption and oxidative balance.

opencc-zeroDec 2014View details →
zenodo28/100

Output from the Glacier Energy and Mass Balance (GEMB v1.0) forced with 3-hourly RACMO fields, Greenland and Antarctica 1979-2014

<p>These model output are those presented in the manuscript that provides&nbsp;the first description of version 1.0 of the open-source Glacier Energy and Mass Balance model. GEMB is a column model of ice sheet and glacier surface-atmospheric energy and mass exchange as well as&nbsp;firn state. GEMB has been integrated into the open-source Ice-Sheet and Sea-level System Model which can be downloaded at&nbsp;https://issm.jpl.nasa.gov/.&nbsp; Here, GEMB is forced with 3-hourly RACMO output from 1979-2014.&nbsp;&nbsp;</p>

opencc-by-4.0Jul 2022View details →
zenodo28/100

Replication package for the paper - "Balanced Knowledge Distribution among Software Development Teams - Observations from Open-Source and Closed-Source Software Development"

<p>Replication package for the&nbsp;paper - &quot;Balanced Knowledge Distribution among Software Development Teams - Observations from Open-Source and Closed-Source Software Development&quot;.</p>

opencc-by-4.0Mar 2022View details →
ClinicalTrials.gov28/100

Replacing Canes With an Elasticated Orthosis in Chronic Stroke Patients: The Influence on Gait and Balance. A Series of N-of-1 Trials

ClinicalTrials.gov study NCT03642444. IPD Sharing: NO. Countries: 0. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

Group Lifestyle Balance Adapted for Individuals With Impaired Mobility (GLB-AIM)

ClinicalTrials.gov study NCT03307187. IPD Sharing: UNDECIDED. Countries: 0. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov28/100

Effects of Calisthenics and Life Kinetics on Reaction Time, Balance, and Swimming in Male Swimmers

ClinicalTrials.gov study NCT07089563. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

A Radiolabeled Mass Balance Study of [14C]-Ertugliflozin (PF04971729, MK-8835) In Healthy Male Participants (MK-8835-038)

ClinicalTrials.gov study NCT01127308. IPD Sharing: Not stated. Countries: 0. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov28/100

Automatic Prosthetic Foot Stiffness Modulation to Improve Balance

ClinicalTrials.gov study NCT06711588. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov28/100

Exploring How Exercise Frequency Impacts Muscle Resistance and Balance in Institutionalized Seniors

ClinicalTrials.gov study NCT07060729. IPD Sharing: YES. Countries: 0. Publications: 4.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov28/100

EMG Biofeedback Training to Improve Balance in Individuals with Multiple Sclerosis

ClinicalTrials.gov study NCT06461741. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

The Effects of Cognitive Rehabilitation on Motor Performance, Balance and Fear of Falling in Stroke Patients

ClinicalTrials.gov study NCT05490628. IPD Sharing: NO. Countries: 0. Publications: 4.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

Ezetimibe-Ursodiol Combination Therapy on Biomarkers of Liver Function and Sterol Balance in Subjects With NAFLD

ClinicalTrials.gov study NCT02244944. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov28/100

Copper and Molybdenum Balance in Participants With Wilson Disease Treated With ALXN1840

ClinicalTrials.gov study NCT04573309. IPD Sharing: NO. Countries: 3. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

Cerebellar tDCS and Balance Training in PwMS

ClinicalTrials.gov study NCT04391023. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov28/100

Evaluation of Group Lifestyle Balance Maintenance Strategies

ClinicalTrials.gov study NCT00869609. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

Perioperative Fluid Therapy With Balanced Crystalloids

ClinicalTrials.gov study NCT02691676. IPD Sharing: NO. Countries: 0. Publications: 13.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

NM Balance Regulation With ULLS and Loss of Sleep

ClinicalTrials.gov study NCT05956964. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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Allen Brain Atlas

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allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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