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Fig. 6 in A fold in the visor: formation of the bivalved shell in Berthelinia singaporensis Jensen, 2015 (Gastropoda: Heterobranchia: Sacoglossa), with notes on spawning and development
Fig. 6. Stages of shell metamorphosis in Berthelinia singaporensis. A, initial growth of visor-shaped shell (arrowhead); B–C, pedi-veligers on Caulerpa with increasing visor; in C veliger shell is tilted; D, first appearance of fold in visor (arrow) looking like notch.
Fig. 9 in A fold in the visor: formation of the bivalved shell in Berthelinia singaporensis Jensen, 2015 (Gastropoda: Heterobranchia: Sacoglossa), with notes on spawning and development
Fig. 9. Juvenile development of Berthelinia singaporensis (continued). A, two specimens on Caulerpa; smaller white one with many brown pigment spots, larger specimen completely green with some brown spots; B, close-up of protoconch area of larger specimen showing green contents of digestive gland extending into protoconch.
Text-fig. 52. Scanning electron microscope (SEM) images of tricolpate pollen of Samylinaea punctata gen. et sp. nov from a pollen clump; Torres Vedras locality, Portugal. a) Pollen clump (probable stamen fragment) that yielded the pollen in this Text-figure; b) Polar view of pollen grain showing two colpi, granular aperture membrane, and punctate tectum; c) Orbicule showing very finely granular surface; d) Pollen wall showing short columellae, well-developed punctate tectum and slightly thinner foot layer; e–h) Pollen grains showing punctate tectum and the folds associated with the irregular development of the colpi. Specimen, TV44-S174565 (holotype; a–h). Scale bars 300 Μm (a), 6 Μm (b, e–h), 3 Μm (c, d). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 52. Scanning electron microscope (SEM) images of tricolpate pollen of Samylinaea punctata gen. et sp. nov from a pollen clump; Torres Vedras locality, Portugal. a) Pollen clump (probable stamen fragment) that yielded the pollen in this Text-figure; b) Polar view of pollen grain showing two colpi, granular aperture membrane, and punctate tectum; c) Orbicule showing very finely granular surface; d) Pollen wall showing short columellae, well-developed punctate tectum and slightly thinner foot layer; e–h) Pollen grains showing punctate tectum and the folds associated with the irregular development of the colpi. Specimen, TV44-S174565 (holotype; a–h). Scale bars 300 Μm (a), 6 Μm (b, e–h), 3 Μm (c, d).
Text-fig. 51. Scanning electron microscope (SEM) images of tricolpate pollen of Mcdougallia irregularis gen. et sp. nov. from a stamen fragment; Torres Vedras locality, Portugal. a) Holotype; stamen fragment that yielded the pollen in this Text-figure; b) Polar view of tricolpate pollen grain showing the continuous psilate tectum in the apocolpium and the poorly developed discontinuous foveolate-reticulate tectum in the mesocolpial areas, note irregular fold in tectum wall (arrowhead); c) Equatorial view of pollen grain showing the discontinuous tectum in the mesocolpial areas; d) Pollen grains showing variably developed tectum, colpi with a finely granular aperture membrane and the folds (arrowheads) associated with the irregular development of the colpi; e) Orbicule showing faintly striate surface; f) Pollen wall showing very short columellae, thin tectum and thin foot layer. Specimen, TV44-S148215 (holotype). Scale bars 300 Μm (a), 6 Μm (b–d), 3 Μm (e, f). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 51. Scanning electron microscope (SEM) images of tricolpate pollen of Mcdougallia irregularis gen. et sp. nov. from a stamen fragment; Torres Vedras locality, Portugal. a) Holotype; stamen fragment that yielded the pollen in this Text-figure; b) Polar view of tricolpate pollen grain showing the continuous psilate tectum in the apocolpium and the poorly developed discontinuous foveolate-reticulate tectum in the mesocolpial areas, note irregular fold in tectum wall (arrowhead); c) Equatorial view of pollen grain showing the discontinuous tectum in the mesocolpial areas; d) Pollen grains showing variably developed tectum, colpi with a finely granular aperture membrane and the folds (arrowheads) associated with the irregular development of the colpi; e) Orbicule showing faintly striate surface; f) Pollen wall showing very short columellae, thin tectum and thin foot layer. Specimen, TV44-S148215 (holotype). Scale bars 300 Μm (a), 6 Μm (b–d), 3 Μm (e, f).
Text-fig. 27. Scanning electron microscope (SEM) images of monocolpate pollen grains of Goczania rugosa gen. et sp. nov. in situ in dithecate, tetrasporangiate stamens; Torres Vedras locality, Portugal. a, b) Stamens in apical view (holotype a) showing the paired pollen sacs; c) Pollen grain from stamen fragment in (b) showing short aperture and rugulate-microechinate surface; d–f) Pollen grains from stamen fragment in (a) showing a folded distal aperture and rugulate-microechinate surface; note the orbicules of different sizes. Specimens, TV44-S136688 (holotype; a, c–f), TV44-S136664 (b). Scale bars 300 Μm (a,b), 6 Μm (c–e), 3 Μm (f). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 27. Scanning electron microscope (SEM) images of monocolpate pollen grains of Goczania rugosa gen. et sp. nov. in situ in dithecate, tetrasporangiate stamens; Torres Vedras locality, Portugal. a, b) Stamens in apical view (holotype a) showing the paired pollen sacs; c) Pollen grain from stamen fragment in (b) showing short aperture and rugulate-microechinate surface; d–f) Pollen grains from stamen fragment in (a) showing a folded distal aperture and rugulate-microechinate surface; note the orbicules of different sizes. Specimens, TV44-S136688 (holotype; a, c–f), TV44-S136664 (b). Scale bars 300 Μm (a,b), 6 Μm (c–e), 3 Μm (f).
Text-fig. 8. Scanning electron microscope (SEM) images of spores from clumps of spores and sporangia with affinities to polypodiopsids (a–c) and of uncertain affinity (d–k); Torres Vedras locality, Portugal. a) Folded Cyathidites minor spores in proximal view showing trilete mark, from clump of spores; b) Cyathidites minor spores in proximal view showing trilete mark, from group of sporangia; c) Cyathidites australis spores in proximal view showing trilete mark, from group of sporangia; d–f) Linear group of spore masses (d; probable sporangial contents) composed of Taurocusporites segmentatus spores showing distal surface (e, middle) with concentric regions and proximal surface with segmented laesurae of elongated granules (e, right; f); in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 8. Scanning electron microscope (SEM) images of spores from clumps of spores and sporangia with affinities to polypodiopsids (a–c) and of uncertain affinity (d–k); Torres Vedras locality, Portugal. a) Folded Cyathidites minor spores in proximal view showing trilete mark, from clump of spores; b) Cyathidites minor spores in proximal view showing trilete mark, from group of sporangia; c) Cyathidites australis spores in proximal view showing trilete mark, from group of sporangia; d–f) Linear group of spore masses (d; probable sporangial contents) composed of Taurocusporites segmentatus spores showing distal surface (e, middle) with concentric regions and proximal surface with segmented laesurae of elongated granules (e, right; f);
Text-fig. 10. Scanning electron microscope (SEM) images of conifer seeds (a, b) and pollen (c) and monoporate pollen of unknown affinity (d–j); Torres Vedras locality, Portugal. a, b) Unnamed conifer seeds (conifer seed sp. 1); c) Clump of bisaccate pollen grains; d) Fragment with microsporangia that yielded the pollen in (e–j); e, f, h) Monoporate pollen grains folded in various ways, exposing the tiny pore (e, h, arrowheads) or resembling a monocolpate grain (f); g) Detail of pollen grain showing pore (arrowhead) and finely rugulate exine surface that reflects the reticulate infratectal layer beneath the thin tectum; i) Detail of pore showing very slightly thickened margin; j) Spherical orbicules on the surface of two grains. Specimens, TV44-S174594 (a), TV44-S174595 (b), TV44-S174573 (c), TV44-S137904 (d–j). Scale bars 1 mm (a, b), 300 Μm (d), 100 Μm (c), 6 Μm (e, f, h), 3 Μm (g, j), 1.5 Μm (i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 10. Scanning electron microscope (SEM) images of conifer seeds (a, b) and pollen (c) and monoporate pollen of unknown affinity (d–j); Torres Vedras locality, Portugal. a, b) Unnamed conifer seeds (conifer seed sp. 1); c) Clump of bisaccate pollen grains; d) Fragment with microsporangia that yielded the pollen in (e–j); e, f, h) Monoporate pollen grains folded in various ways, exposing the tiny pore (e, h, arrowheads) or resembling a monocolpate grain (f); g) Detail of pollen grain showing pore (arrowhead) and finely rugulate exine surface that reflects the reticulate infratectal layer beneath the thin tectum; i) Detail of pore showing very slightly thickened margin; j) Spherical orbicules on the surface of two grains. Specimens, TV44-S174594 (a), TV44-S174595 (b), TV44-S174573 (c), TV44-S137904 (d–j). Scale bars 1 mm (a, b), 300 Μm (d), 100 Μm (c), 6 Μm (e, f, h), 3 Μm (g, j), 1.5 Μm (i).
Fig. 2. Fin fold reabsorption during larvae-juvenile transition. A in The effect of rearing temperature in larval development of pejerrey, Odontesthes bonariensis - Morphological indicators of development
Fig. 2. Fin fold reabsorption during larvae-juvenile transition. A) The characteristic lobulated caudal fin showing the first fin rays (arrowhead) and the straight notochord (arrow); B) The second segment appeared (arrowhead) and the ray started to be aligned with the rostro-caudal axis (arrow); C) The ray aligned with the rostro-caudal axis (arrow); D) The forked homocercal caudal fin; E) Bifurcation of the central fin rays (arrowhead); F) The remnant fin-fold between the anus and the anal fin; G) The body shape acquires the adult conformation. A-F, bar = 0.5 mm; G = 1 mm.
Network of hotspot interactions cluster tau amyloid folds
<p>Datafiles associated with <strong>Network of hotspot interactions cluster tau amyloid folds.</strong></p> <p> </p> <p>The alascan files contain the averaged and raw outputs of the <em>in silico </em>alanine scan conducted on tau fibrils. The combo aggregation file contains ThT fluorescence data from the VQIVYK/VEVKSE alanine mutants and coaggregation experiments. The incorporation_vs_insilico file contains the results of the alanine scan top and bottom hits compared to the results of the incorporation experiment of alanine mutants on that position.</p> <p> </p> <p>Version 2: Files added providing data for how edge and center chains contribute to the total energetics, as well as a per-layer energy contribution to total deltaREU in the alanine scan of the PHF fibril.</p>
The ER folding sensor UGGT1 acts on TAPBPR-chaperoned peptide-free MHC I
<p>Adaptive immune responses are triggered by antigenic peptides presented on major histocompatibility complex class I (MHC I) at the surface of pathogen-infected or cancerous cells. Formation of stable peptide-MHC I complexes is facilitated by tapasin and TAPBPR, two related MHC I-specific chaperones that catalyze selective loading of suitable peptides onto MHC I in a process called peptide editing or proofreading. On their journey to the cell surface, MHC I complexes must pass a quality control step performed by UGGT1, which senses the folding status of the transiting N-linked glycoproteins in the endoplasmic reticulum (ER). UGGT1 reglucosylates non-native glycoproteins and thereby allows them to revisit the ER folding machinery. Here, we describe a reconstituted <em>in-vitro</em> system of purified human proteins that enabled us to delineate the function of TAPBPR during the UGGT1-catalyzed quality control and reglucosylation of MHC I. By combining glycoengineering with liquid chromatography-mass spectrometry, we show that TAPBPR promotes reglucosylation of peptide-free MHC I by UGGT1. Thus, UGGT1 cooperates with TAPBPR in fulfilling a crucial function in the quality control mechanisms of antigen processing and presentation.</p>
Text-fig. 12. Scanning electron microscope (SEM) images of isolated "Stamen fragment with Clavatipollenites-type pollen sp. 3"; Catefica locality, Portugal. a) Stamen fragment with pollen in situ; b, c) Pollen grains showing the semitectate-reticulate pollen wall and folds (c) indicating a possible monocolpate aperture; d) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation; e) Detail of pollen wall showing tiny, spherical, finely spiny orbicules. Specimen, Catefica 50-S170449 (a–e). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d, e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 12. Scanning electron microscope (SEM) images of isolated "Stamen fragment with Clavatipollenites-type pollen sp. 3"; Catefica locality, Portugal. a) Stamen fragment with pollen in situ; b, c) Pollen grains showing the semitectate-reticulate pollen wall and folds (c) indicating a possible monocolpate aperture; d) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation; e) Detail of pollen wall showing tiny, spherical, finely spiny orbicules. Specimen, Catefica 50-S170449 (a–e). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d, e).
Text-fig. 26. Scanning electron microscope (SEM) images of stamens and pollen grains of Elasmostemon paisii gen. et sp. nov. (a–c) and laminar stamens with monocolpate reticulate pollen sp. (d–g); Catefica locality, Portugal. a) Stamen fragment with basal portion missing showing two pairs of pollen sacs on one surface of the stamen close to the margin and separated by a broad connective, except near the apex where the thecae meet; note that the thecae are dehisced with the walls of the pollen sacs curled back; b) Pollen grains inside a dehisced pollen sac; note variation in size and development of the reticulum; c) Detail of (b) showing monocolpate, reticulate pollen with lumen of reticulum varying markedly in size but partly obscured by residual organic material; d) Stamen with apical and basal part of anther preserved showing two pairs of pollen sacs (asterisks) on the curved, perhaps ventral, surface close to the stamen margin; e) Detail of crack in the anther showing the inner anther wall with densely spaced spherical orbicules that vary greatly in size; f) Pollen exposed in the crack in the anther; note coarsely foveolate to coarsely reticulate pollen wall and densely spaced orbicules; g) Folded pollen grains with reticulate pollen wall and also showing the inner anther wall with densely spaced spherical orbicules that vary greatly in size. Specimens, Catefica 49-S172560 (a–c), Catefica 50- S170384 (d–g). Scale bars = 600 Μm (a, d), 20 Μm (b, e), 6 Μm (c, f, g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 26. Scanning electron microscope (SEM) images of stamens and pollen grains of Elasmostemon paisii gen. et sp. nov. (a–c) and laminar stamens with monocolpate reticulate pollen sp. (d–g); Catefica locality, Portugal. a) Stamen fragment with basal portion missing showing two pairs of pollen sacs on one surface of the stamen close to the margin and separated by a broad connective, except near the apex where the thecae meet; note that the thecae are dehisced with the walls of the pollen sacs curled back; b) Pollen grains inside a dehisced pollen sac; note variation in size and development of the reticulum; c) Detail of (b) showing monocolpate, reticulate pollen with lumen of reticulum varying markedly in size but partly obscured by residual organic material; d) Stamen with apical and basal part of anther preserved showing two pairs of pollen sacs (asterisks) on the curved, perhaps ventral, surface close to the stamen margin; e) Detail of crack in the anther showing the inner anther wall with densely spaced spherical orbicules that vary greatly in size; f) Pollen exposed in the crack in the anther; note coarsely foveolate to coarsely reticulate pollen wall and densely spaced orbicules; g) Folded pollen grains with reticulate pollen wall and also showing the inner anther wall with densely spaced spherical orbicules that vary greatly in size. Specimens, Catefica 49-S172560 (a–c), Catefica 50- S170384 (d–g). Scale bars = 600 Μm (a, d), 20 Μm (b, e), 6 Μm (c, f, g).
Text-fig. 2. Light micrographs of Pinus spp. cuticles prepared with the modified, gentle bleaching procedure. a: Cuticle 1, Pinus sp. 1. Nearly the entire width of the leaf has been preserved. Five parallel rows of stomata are visible. b: Cuticle 1, close-up of (a). Two guard cells are visible around each stoma. c: Cuticle 1, close-up of eight stomata. Two guard cells and eight subsidiary cells are visible around each stoma. d: Cuticle 2, Pinus sp. 2. Some folding of the cuticle occurred during preparation, but many parallel rows of stomata on both sides of a thin, central midvein are evident. e: Cuticle 2, close-up of (d). Pairs of guard cells surround each stoma. f: Cuticle 2, close-up of (e). Subsidiary and epithelial cells can be observed around the stomata. in A Modified, Step-By-Step Procedure For The Gentle Bleaching Of Delicate Fossil Leaf Cuticles
Text-fig. 2. Light micrographs of Pinus spp. cuticles prepared with the modified, gentle bleaching procedure. a: Cuticle 1, Pinus sp. 1. Nearly the entire width of the leaf has been preserved. Five parallel rows of stomata are visible. b: Cuticle 1, close-up of (a). Two guard cells are visible around each stoma. c: Cuticle 1, close-up of eight stomata. Two guard cells and eight subsidiary cells are visible around each stoma. d: Cuticle 2, Pinus sp. 2. Some folding of the cuticle occurred during preparation, but many parallel rows of stomata on both sides of a thin, central midvein are evident. e: Cuticle 2, close-up of (d). Pairs of guard cells surround each stoma. f: Cuticle 2, close-up of (e). Subsidiary and epithelial cells can be observed around the stomata.
PDMS-Polyimide transcutaneous blood gas collector with self-folding out-of-plane heater elements, dataset
<p>Recorded data and accompanying matlab code for the publication <em>PDMS-Polyimide transcutaneous blood gas collector with self-folding out-of-plane heater elements</em> accepted for publication in <em>Journal of Micromechanics and Microengineering</em>.</p>
Experimental characterization of TERIPHIC 4-fold and 8-fold InP photodiode arrays - Detection of 50Gbaud signals with NRZ and PAM-4 modulation formats
<p>The data sets refer to the results from the experimental characterization of the TERIPHIC 4-fold and 8-fold InP-photodiode arrays, which operate in the O-band. The experimental setup consisted of a commercially available off-the-shelf (COTS) laser source, a COTS Mach-Zehnder modulator, and the TERIPHIC PD arrays. For the purposes of the experiments, signals with NRZ and PAM-4 modulation formats and 50 Gbaud symbol rates were generated, transmitted, and detected by the TERIPHIC photodetectors. Two different subassemblies were evaluated. The first subassembly had four InP photodiodes and the second eight. The generated photocurrents were sampled by a real-time oscilloscope with a 256 Gbaud sample rate. The data sets are actually the samples extracted from the oscilloscope. The data sets have a filename in the format “Symbol rate#Modulation formats#PDn#Transmission length#version#Subassemblyn.bin”, where<br> Symbol rate = 50 Gbaud<br> PDn, for n= 1,2, ...,8<br> Transmission length = B2B (0 km), 2 km, and 10 km<br> Subassembly for n=1 and 2<br> <br> The data sets are parts of the Open data management plan of the TERIPHIC ICT project (GA No. 825502)</p>
Characterizing the Folding Transition State Ensembles in the Energy Landscape of an RNA Tetraloop - available data.
<p>Trajectory file and scripts necessary to generate an ELViM [Oliveira, A. B.; Yang, H.; Whitford, P. C.; Leite, V. B. P. JCTC, 2019, 15, p.6482] projection of the conformational space for the GCAA tetraloop.</p>
A THOUSAND-FOLD OFFERING RITUAL by Gser mo mtsho གསེར་མོ་མཚོ།
<p>A THOUSAND-FOLD OFFERING RITUAL by Gser mo mtsho གསེར་མོ་མཚོ།</p> <p>A Thousand-Fold Offering Ritual was held by monks at my home in Ban ser Community, Mgo mang (Guomaying) Township, Mang rdzong (Guinan) County, Mstho Lho (Hainan) Tibetan Autonomous Prefecture, Mstho sngon (Qinghai) Province, PR China on Thursday, May 25, 2023. This involved offering butter lamps, holy water, incense, prostrations, and circumambulation, with each activity being performed a thousand times. </p> <p>Stong mchod is an important spiritual practice helping practitioners overcome their fears and attachments, purify negative karma, and develop compassion and wisdom. The primary purpose of this ritual was to assist my sick grandmother, a devout Buddhist. Despite receiving medical treatment, her condition did not improve, so my family sought hope and healing from religious practice. My family invited 6 monks from Klu tshang Monastery to conduct the ritual. My family gave 300 RMB and offered <em>kha btags</em> 'a strip of silk'. The total cost of the ritual was approximately 4,000 RMB.</p> <p>TIBETAN TERMS</p> <p>ban ser བན་སེར།</p> <p>klu tshang ཀླུ་ཚང་།</p> <p>kha btags ཁ་བཏགས།</p> <p>mang rzong མང་རྫོང ་།</p> <p>mgo mang མགོ་མང ་།</p> <p>mtso lho མཚོ་ལྷོ །</p> <p>mtso sngon མཚོ་སྔོན །</p> <p>sha rgya ཤ་རྒྱ །</p> <p>stong mchod སྟོང་མཆོད །</p> <p>CHINESE TERMS</p> <p>Guinan 贵南</p> <p>Guomaying 过马营</p> <p>Hainan 海南</p>
Fig. 5. Folded 16S-23S in Newly recorded genera and species, Pantanalinema rosaneae and Alkalinema pantanalense (Leptolyngbyaceae, Cyanobacteria) isolated in Korea
Fig. 5. Folded 16S-23S rRNA ITS secondary structures of strains of (A) Pantanalinema rosaneae and (B) Alkalinema pantanalense.
Context-dependent perturbations in chromatin folding and the transcriptome by cohesin and related factors
<p>Cohesin plays vital roles in chromatin folding and gene expression regulation, cooperating with such factors as cohesin loaders, unloaders, and the insulation factor CTCF. Although models of regulation have been proposed (e.g., loop extrusion), how cohesin and related factors collectively or individually regulate the hierarchical chromatin structure and gene expression remains unclear. We have depleted cohesin and related factors and then conducted a comprehensive evaluation of the resulting 3D genome, transcriptome and epigenome data. We observed substantial variation in depletion effects among factors at topologically associating domain (TAD) boundaries and on interTAD interactions, which were related to epigenomic status. Gene expression changes were highly correlated with direct cohesin binding and gain of TAD boundaries than with the loss of boundaries. Moreover, cohesin was broadly enriched in active compartment A chromosomes, which were retained after CTCF depletion. Our results demonstrate context-specific roles of cohesin for gene expression and chromatin folding.</p>
PARALLEL G-QUADRUPLEX FOLDS VIA MULTIPLE PATHS INVOLVING G-TRACT STACKING AND STRUCTURING FROM COIL ENSEMBLE
<p>Data from all-atom molecular dynamics simulations of DNA G-quadruplex and various G-hairpins: input files (Gromacs and Amber), stripped trajectory files (reactive trajectories and reference replicas for G4, and reactive trajectories, and reference replicas for selected hairpin simulations), metadynamics bias files, and the ΔG_fold calculation protocol.</p>
ScienceDex guides
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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.