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920 results for “Functional analysis”
The Early Functional Abilities-revised may bridge the gap between the disorder of consciousness and the functional independence scales: evidence from Rasch analysis
<p>Raw data associated with the scientific publication “The Early Functional Abilities-revised may bridge the gap between the disorder of consciousness and the functional independence scales: evidence from Rasch analysis”</p>
Supplementary material 1 from: Graupner N, Boenigk J, Bock C, Jensen M, Marks S, Rahmann S, Beisser D (2017) Functional and phylogenetic analysis of the core transcriptome of Ochromonadales. Metabarcoding and Metagenomics 1: e19862. https://doi.org/10.3897/mbmg.1.19862
KEGG orthologous genes of the core trancriptome of the herein investigated Ochromonadales (Poteriospumella lacustris strains JBC07, JBM10, JBNZ41; Poterioochromonas malhamensis DS; Spumella vulgaris 199hm; Pedospumella encystans JBMS11) used for phylogenetic analyses.
Biomechanical Analysis of Limits of Stability Using Computerized Posturography: Correlations with Functional Mobility in Elderly Individuals with Hip Osteoarthritis – A Cross-Sectional Study
<p>The study titled "Biomechanical Analysis of Limits of Stability Using Computerized Posturography: Correlations with Functional Mobility in Elderly Individuals with Hip Osteoarthritis – A Cross-Sectional Study" delves into the intricate relationship between postural stability and functional mobility in elderly patients suffering from hip osteoarthritis (OA). Utilizing advanced computerized posturography, the research quantitatively assesses the limits of stability (LOS) in various directional planes, providing a comprehensive biomechanical profile of the participants. The findings reveal significant discrepancies in LOS between hip OA patients and age-matched asymptomatic controls, underscoring the profound impact of hip OA on balance and stability. Additionally, the study examines the correlation between LOS measurements and functional mobility, as assessed by the Timed Up and Go (TUG) test. The results indicate a strong association, suggesting that diminished postural stability in hip OA patients contributes to impaired functional mobility. This cross-sectional analysis highlights the importance of targeted interventions to enhance stability and mobility in this population, aiming to mitigate the risk of falls and improve overall quality of life.</p>
Transcriptome analysis and functional study of phospholipase A2 in Galleria mellonella larvae lipid metabolism in response to envenomation by an ectoparasitoid, Iseropus kuwanae
<p>The file is the raw data of "Transcriptome analysis and functional study of phospholipase A2 in <em>Galleria mellonella</em> larvae lipid metabolism in response to envenomation by an ectoparasitoid, <em>Iseropus kuwanae</em>".</p>
Example Datasets for Functional Enrichment Analysis
<p>This dataset contains a set of example data for a functional enrichment tutorial.</p>
Fig. 4 in Functional morphology of the cave bear (Ursus spelaeus) mandible: a 3D geometric morphometric analysis
Fig. 4 PCAs on the regression residuals of all extant Ursidae and U. spelaeus after a regression analysis of the Procrustes coordinates onto log centroid size pooled per species (a, b) and on the regression residuals of the regression taking phylogeny into account (c, d). The colors indicate the
Fig. 6 in Functional morphology of the cave bear (Ursus spelaeus) mandible: a 3D geometric morphometric analysis
Fig. 6 Scatterplot of the PC1 scores versus the logarithm of the percentage of foliage in the diet. Linear regression lines were fitted with the 95 % confidence interval of the group mean and the mean scores of U. spelaeus (vertical line)
Fig. 2 in Functional morphology of the cave bear (Ursus spelaeus) mandible: a 3D geometric morphometric analysis
Fig. 2 Mandibles of Ursus spelaeus (a, b) and Tremarctos ornatus (c) and showing the position of the masseteric fossa (MF) and the premasseteric fossa (PMF). Positions of the landmarks on a mandible of Ursus spelaeus on the lingual side (a) and the labial side (b). The landmarks are described in Table 3. Not to scale. Part A of the figure also displays the biomechanics. The resistance (Fout) at the carnassial of the lower jaw depends on the muscular input force (Fin), the angle of insertion of the muscle onto the jaw (α) and the ratio of in-lever arm or moment arm (Li) to out-lever arm (Lo). Angle of insertion of jaw muscles changes during jaw closing and determines the moment arm of the muscular input force (Mi). Mass pertaining to the masseter, Temp pertaining to the temporalis. Li Mass and Mi Mass happen to be the same in this diagram
Fig. 5 2B in Functional morphology of the cave bear (Ursus spelaeus) mandible: a 3D geometric morphometric analysis
Fig. 5 2B-PLS on the regression residuals of all extant Ursidae and U. spelaeus after a regression analysis of the Procrustes coordinates onto log centroid size pooled per species. A phylogenetic overlay is shown in gray
Fig. 5 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 5. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal by standardized 1-g biomass of Canthon rutilans cyanescens, Deltochilum multicolor, Dichotomius sericeus, and Phanaeus splendidulus exposed to dog feces for two and seven days. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Fig. 4 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 4. Comparative analysis of dung removal and secondary dispersal of small and large seeds by single male/ female pair of Canthon rutilans cyanescens (Cr), Deltochilum multicolor (Dm), Dichotomius sericeus (Ds), and Phanaeus splendidulus (Ps) exposed to dog feces for two and seven days. Squares with the same letter and color are not significantly different (Tukey test, P> 0.05).
Fig. 3 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 3. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal and secondary seed dispersal by two paracoprid dung beetles as single male/female pair and three male/female pairs exposed to dog feces for two, seven, and 21 days. A) Dung removal capacity, B) Small seed dispersal, and C) Large seed dispersal by Dichotomius sericeus. D) Dung removal capacity, E) Small seed dispersal, and F) Large seed dispersal by Phanaeus splendidulus. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Fig. 1 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 1. Arenas for the study of dung removal and secondary seed dispersal by dung beetles. A) Arena for telecoprids with 30 g of dyed feces divided into three portions of 10 g each with a variable number of artificial seeds, B) Closed arena covered with veil-type fabric, C) Arena protected from rain. D, E, and F show the same sequence for the arenas for paracoprids.
Fig. 2 in Comparative Analysis of the Ecological Functions of Dung Removal and Seed Dispersal among Two Telecoprid and Two Paracoprid Dung Beetles (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 2. Box plots of the median, first, and third quartile, and lower and upper limits of dung removal and secondary seed dispersal by two telecoprid dung beetles as single male/female pair and three male/female pairs exposed to dog feces for two, seven, and 21 days. A) Dung removal capacity, B) Small seed dispersal, and C) Large seed dispersal by Canthon rutilans cyanescens. D) Dung removal capacity, E) Small seed dispersal, and F) Large seed dispersal by Deltochilum multicolor. Plots with the same letter are not significantly different (Tukey test, P> 0.05).
Identification of genetic loci and functional analysis of candidate gene, OsCycB1;5 associated with seed callus induction in rice (Oryza sativa L.)
Open the record for dataset details and reuse information.
Ice recrystallization inhibitors enable efficient cryopreservation of induced pluripotent stem cells: A functional and transcriptomic analysis
<p><span>The successful use of human induced pluripotent stem cells (iPSCs) for research or clinical applications requires the development of robust, efficient, and reproducible cryopreservation protocols. After cryopreservation, the survival rate of iPSCs is suboptimal and cell line dependent. We assessed the use of ice recrystallization inhibitors (IRIs) for cryopreservation of human iPSCs<span>. A toxicity screening study was performed to assess specific small-molecule carbohydrate-based IRI and concentrations for further evaluation.</span> Then, a cryopreservation study compared the cryoprotective efficiency of 15 mM IRIs in 5 % or 10 % DMSO-containing solutions and with CryoStor® CS10. Three iPSC lines were cryopreserved as single-cell suspensions in the cryopreservation solutions and post-thaw characteristics, including pluripotency and differential gene expression, were assessed. </span><span>W</span><span>e demonstrate the fitness-for-purpose of 15 mM IRI in 5 % DMSO as an efficient cryoprotective solution for iPSCs in terms of post-thaw recovery, viability, pluripotency, and transcriptomic changes. Given that this dataset is the first report where mRNA sequencing has been used to identify expression changes resulting from iPSCs cryopreservation, it has the potential to be used for molecular mechanism analysis relating to cryopreservation. IRIs can reduce DMSO concentrations, thereby improving the utility, effectiveness, and efficiency of cryopreservation. </span></p>
Transcriptomic analysis demonstrates the expression, origin and function of lncRNAs in multiple skin diseases
<p>Transcriptomic analysis demonstrates the expression, origin and function of lncRNAs in multiple skin diseases</p>
dataset for "A location and dispersion effects-based ridge analysis method using desirability functions for multi-response optimization"
<p>dataset and code for “A location and dispersion effects-based ridge analysis method using desirability functions for multi-response optimization”</p>
FIGURE. Results of discriminant function analysis (DFA) for C. repens and their putative parental species. Characters abbreviated as in Table 2. A. Carex brizoides (br), C. repens (re) and C. disticha (di). Loadings for the first axis (only absolute values>0.50 are given): IL = -0.50. Loadings for the second axis (only absolute values>0.50 are given): CLW = 0.61, IL = -0.71, SN = 0.74. B. Carex arenaria (ar), C. repens (re) and C. disticha (di). Loadings for the first axis (only absolute values>0.50 are given): CL = 0.89, IL = -0.63, SN = 0.51. Loadings for the second axis: CLW = 0.83, IL = -0.70, SN = 0.59. C. Carex arenaria (ar), C. repens (re) and C. brizoides (br). Loadings for the first axis (only absolute values> 0.50 are given): CL = -0.83. Loadings for the second axis: CL = -0.61. in Carex section Ammoglochin (Cyperaceae) in Poland
FIGURE. Results of discriminant function analysis (DFA) for C. repens and their putative parental species. Characters abbreviated as in Table 2. A. Carex brizoides (br), C. repens (re) and C. disticha (di). Loadings for the first axis (only absolute values>0.50 are given): IL = -0.50. Loadings for the second axis (only absolute values>0.50 are given): CLW = 0.61, IL = -0.71, SN = 0.74. B. Carex arenaria (ar), C. repens (re) and C. disticha (di). Loadings for the first axis (only absolute values>0.50 are given): CL = 0.89, IL = -0.63, SN = 0.51. Loadings for the second axis: CLW = 0.83, IL = -0.70, SN = 0.59. C. Carex arenaria (ar), C. repens (re) and C. brizoides (br). Loadings for the first axis (only absolute values> 0.50 are given): CL = -0.83. Loadings for the second axis: CL = -0.61.
FIGURE. Results of discriminant function analysis (DFA) for C. arenaria (ar), C. colchica (co) and C. praecox (pr). Characters abbreviated as in Table 2. A. Reproductive characters. Loadings for the first axis (only absolute values>0.50 are given): LW = -0.53, LN = -1.53, WN = 2.40, LN/WN = 2.13. Loadings for the second axis: LN = -0.56. B. Vegetative characters. Loadings for the first axis (only absolute values>0.50 are given): IL = 0.62. Loadings for the second axis: CW = 0.86, CLL = 0.78, CLW = -0.65. in Carex section Ammoglochin (Cyperaceae) in Poland
FIGURE. Results of discriminant function analysis (DFA) for C. arenaria (ar), C. colchica (co) and C. praecox (pr). Characters abbreviated as in Table 2. A. Reproductive characters. Loadings for the first axis (only absolute values>0.50 are given): LW = -0.53, LN = -1.53, WN = 2.40, LN/WN = 2.13. Loadings for the second axis: LN = -0.56. B. Vegetative characters. Loadings for the first axis (only absolute values>0.50 are given): IL = 0.62. Loadings for the second axis: CW = 0.86, CLL = 0.78, CLW = -0.65.
ScienceDex guides
Understand access before you commit
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.