Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
570
datasets available to search
ShareScore release 0.9.0
Dataset results
570 results for “mediality”
ECT Pulse Amplitude and Medial Temporal Lobe Engagement
ClinicalTrials.gov study NCT02999269. IPD Sharing: YES. Countries: 1. Publications: 2.
Adductor Canal Block for Medial Compartment Knee Arthroplasty
ClinicalTrials.gov study NCT01818531. IPD Sharing: Not stated. Countries: 1. Publications: 10.
Exercise and Markers of Medial Temporal Health in Youth At-risk for Psychosis
ClinicalTrials.gov study NCT02155699. IPD Sharing: Not stated. Countries: 1. Publications: 7.
Arthroscopy in the Treatment of Degenerative Medial Meniscus Tear
ClinicalTrials.gov study NCT00549172. IPD Sharing: Not stated. Countries: 1. Publications: 7.
iGABASnFR data from: Co-release of GABA and ACh from medial olivocochlear neurons as a fine regulatory mechanism of cochlear efferent inhibition
Open the record for dataset details and reuse information.
Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
Open the record for dataset details and reuse information.
Evaluation of the horizontal approach to the medial malleolar facet in sagittal talar fractures through dorsiflexion and plantarflexion positions
Open the record for dataset details and reuse information.
The amyloid precursor protein regulates synaptic transmission at medial perforant path synapses
Open the record for dataset details and reuse information.
Data from: Three-photon in vivo imaging of neurons and glia in the medial prefrontal cortex with sub-cellular resolution
Open the record for dataset details and reuse information.
Data for: Human subsystems of medial temporal lobes extend locally to amygdala nuclei and globally to an allostatic-interoceptive system
<p><strong>Description</strong></p> <p>Results from masked-ICA based on 20 components and dual regression at the local (medial temporal lobe including the amygdala: 'within-A-MTL', download mask here: <a href="https://osf.io/8j9ts/">https://osf.io/8j9ts/</a>) and global (whole brain) level in three different samples presented in the paper <a href="https://www.sciencedirect.com/science/article/pii/S1053811919309954?via%3Dihub">Human subsystems of medial temporal lobes extend locally to amygdala nuclei and globally to an allostatic-interoceptive system</a> (<a href="https://doi.org/10.1016/j.neuroimage.2019.116404">doi.org/10.1016/j.neuroimage.2019.116404</a>)</p> <p><strong>Content</strong></p> <ul> <li><strong>MaskedICA-Global_dual_regression_20_ICs_original</strong>: Twenty .nii files corresponding to 20 independent components (ICs) at the whole-brain level (hence, 'Global') after the 'dual regression' step, based on the 'original' sample data. See manuscript for IC numbering.</li> <li><strong>MaskedICA-Global_dual_regression_20_ICs_replication1</strong>: One .nii files containing all 20 ICs ('merged'), using the first replication (REP1) sample data.</li> <li><strong>MaskedICA-Global_dual_regression_20_ICs_replication2</strong>: Same as the previous one, but based on the second replication (REP2) sample data.</li> <li><strong>MaskedICA-Local_dual_regression_20_ICs_original</strong>: Twenty .nii files corresponding to 20 ICs at the level of the A-MTL (hence, 'Local') after dual regression, based on the original sample data.</li> <li><strong>MaskedICA-Local_dual_regression_20_ICs_replication1</strong>: One .nii (merged) file containing all ICs at the A-MTL level, using REP1 sample data.</li> <li><strong>MaskedICA-Local_dual_regression_20_ICs_replication2</strong>: Same as the previous one, but based on REP2 sample data.</li> <li><strong>MaskedICA-Peaks_20_ICs_original</strong>: Twenty .nii files; each file contains voxelwise t-values derived from the dual regression step in the original sample. These files allow finding the 'functional connectivity peak', i.e., the voxel with the highest t-value.</li> </ul>
Data from: Medial pith cells per meter in twigs as a proxy for mitotic growth rate (Phi/m) in the apical meristem
The Φ model for plant mating system evolution proposes a causal link between Φ, the number of mitoses that occur within a plant's lifetime from zygote to gamete production, and constraints on the evolution of inbreeding depression and thereby on the evolution of plant mating systems. Through its use of plant stature, the Φ model emphasizes the important role of morphology in creating developmental and genetic constraints on plant evolution. However, the estimation of Φ itself is likely to be extraordinarily complex. Here I describe a protocol for estimating Φ per meter linear growth by an apical meristem (Φ/m) using medial pith cells from mature internodes of twigs. While such cells are produced by the apical meristem, during internode elongation these pith cells also undergo further mitoses and thus their measurement can only approximate a 'true' Φ/m via the application of a multiplier (the adjustment ratio) that partially corrects for the occurrence of cell divisions and cell growth beyond the apical meristem. I apply this method to Delonix regia (Caesalpiniaceae) and derive several adjustment ratios from the literature. As variation in Φ/m can have profound evolutionary implications, I also examine interspecific and intraspecific variation as well as within-individual variation in Φ/m. Conifers apparently have lower Φ/m than angiosperms, while 20% of the total variance in Φ/m for D. regia was found among individual trees, with the remainder found within trees. Given the large differences in stature between 'high-Φ' plants such as trees and 'low-Φ' plants such as herbs, these results support the idea that the total per-generation mutation rate for high-Φ plants is likely to be many times higher than that for low-Φ plants.
FIGURE 3 in Pseudochromis erdmanni, a new species of dottyback with medially placed palatine teeth from Indonesia (Teleostei: Perciformes: Pseudochromidae)
FIGURE 3. Distribution records for Pseudochromis erdmanni (filled circles), P. howsoni (squares), P. m o o re i (triangles) and P. steenei (stars).
FIGURE 1 in Pseudochromis erdmanni, a new species of dottyback with medially placed palatine teeth from Indonesia (Teleostei: Perciformes: Pseudochromidae)
FIGURE 1. Pseudochromis erdmanni new species, female individual, ca. 60 mm SL, Pulau Taunalu, Loloda Selatan, Halmahera, North Maluku Province, Indonesia (photo by G.R. Allen).
FIGURE 2 in Pseudochromis erdmanni, a new species of dottyback with medially placed palatine teeth from Indonesia (Teleostei: Perciformes: Pseudochromidae)
FIGURE 2. Pseudochromis erdmanni new species, male holotype, NCIP 6344, 81.5 mm SL, Pulau Taunalu, Loloda Selatan, Halmahera, North Maluku Province, Indonesia (photo by G.R. Allen).
FIGURES 3–6. Eatoniana plumipes. Adult, female. 3. Palp, medial aspect. 4 in Abalakeus Southcott, 1994 is a junior synonym of " plume-footed " Eatoniana Cambridge, 1898 (Trombidiformes, Erythraeidae) — evidence from experimental rearing
FIGURES 3–6. Eatoniana plumipes. Adult, female. 3. Palp, medial aspect. 4. Crista metopica; A—socket of broken ASens. 5. Position of eye in relation to crista metopica (not to scale). 6. Dorsal seta.
FIGURES 40–41 in Six new Dinotrema species (Hymenoptera, Braconidae) from Spain, with prescutellar pit and medially sculptured propodeum
FIGURES 40–41. Dinotrema enanum sp. nov. (female). 40. Metasoma and ovipositor, lateral view. 41. Fore and hind wings.
FIGURES 26–27 in Six new Dinotrema species (Hymenoptera, Braconidae) from Spain, with prescutellar pit and medially sculptured propodeum
FIGURES 26–27. Dinotrema broadi sp. nov. (female). 26. Metasoma and ovipositor. 27. Fore and hind wings.
FIGURES 2–7 in Six new Dinotrema species (Hymenoptera, Braconidae) from Spain, with prescutellar pit and medially sculptured propodeum
FIGURES 2–7. Dinotrema achterbergi sp. nov. (female) 2. Habitus, lateral view. 3. Head, lateral view. 4. Mandible. 5. Antenna. 6. Head, dorsal view. 7. Mesosoma, lateral view.
FIGURES 60–65 in Six new Dinotrema species (Hymenoptera, Braconidae) from Spain, with prescutellar pit and medially sculptured propodeum
FIGURES 60–65. Dinotrema munki sp. nov. (female). 60. Head, dorsal view. 61. Mesosoma, lateral view. 62. Mesoscutum. 63. Propodeum. 64. Hind leg. 65. First metasomal tergite.
FIGURES 20–25 in Six new Dinotrema species (Hymenoptera, Braconidae) from Spain, with prescutellar pit and medially sculptured propodeum
FIGURES 20–25. Dinotrema broadi sp. nov. (female). 20. Head, dorsal view. 21. Mesosoma, lateral view. 22. Mesonotum. 23. Propodeum. 24. First metasomal tergite. 25. Hind leg.
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.