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111,170 results for “cell”
Bulk and single-cell gene expression profiling of SARS-CoV-2 infected human cell lines identifies molecular targets for therapeutic intervention
<p>Single cell RNA seq datasets used for analysis in the Bulk and single-cell gene expression profiling of SARS-CoV-2 infected human cell lines identifies molecular targets for therapeutic intervention</p>
Supplementary data to accompany Information flow, cell types and stereotypy in a full olfactory connectome
<p>Supplemental file 1</p> <p>Layers assigned by the probabilistic graph traversal model. bodyId refers to neurons’ unique ID in ne- uPrint. layer mean contains the mean layer after 10,000 iterations of the main model (Figure 2). layer - olf mean and layer th mean contain the mean layers from running the traversal model with ORNs and THN/HRNs, respectively (Figure S2).</p> <p>S1 hemibrain neuron layers.csv</p> <p>Supplemental file 2</p> <p>Sensory meta-information related to each glomerulus. Columns: glomerulus (canonical name for one of the 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli), laterality (whether the glomerulus receives bilateral or only unilateral innervation from ALRNs), expected cit (a citation that describes the expected number of RNs in this glomerulus), expected RN female 1h (number of expected RNs in one hemi- sphere), expected RN female SD (standard deviation in the expected number of RNs), missing (qualitative assessment of glomeruli truncation), RN frag (if the RNs in that glomerulus are fragmented), receptor (the OR or IR expressed by cognate ALRNs (Bates et al., 2020; Task et al., 2020)), odour scenes (the general ‘odour scene(s)’ which this glomerulus may help signal (Mansourian and Stensmyr, 2015; Bates et al., 2020)), key ligand(the ligand that excites the cognate ALLRN or receptor the most, based on pooled data from multiple studies (Mu ̈nch and Galizia, 2016)), valence (the presumed valence of this odour chan- nel (Badel et al., 2016)). Exists as hemibrain glomeruli summary in our R package hemibrainr.</p> <p>S2 hemibrain olfactory information.csv</p> <p>Supplemental file 3</p> <p>File listing all identified antennal lobe receptor neurons (ALRNs) in the hemibrain, including information shown in neuPrint. See above for column explanations. Exists as rn.info in our R package hemibrainr.</p> <p>S3 hemibrain ALRN meta.csv</p> <p>Supplemental file 4</p> <p>All the hemibrain neurons we have classed as antennal lobe local neurons (ALLNs). See above for column explanations. Exists as alln.info in our R package hemibrainr.</p> <p>S4 hemibrain ALLN meta.csv</p> <p>Supplemental file 5</p> <p>All the hemibrain neurons we have classed as antennal lobe projection neurons (ALPNs). See above for column explanations. In addition, across dataset cluster refers to the clustering with left and right FAFB PNs; is canonical indicates whether that ALPN is one of the well studied “canonical” uPNs. Exists as pn.info in our R package hemibrainr.</p> <p>40</p> <p>S5 hemibrain ALPN meta.csv</p> <p>Supplemental file 6</p> <p>All the hemibrain neurons we have classed as third-order olfactory neurons (TOONs) including lateral horn neurons (LHNs), as well as wedge projection neurons (WEDPNs), lateral horn centrifugal neurons (LHCENT) and other projection neuron classes (Figure 1). See above for column explanations. Exists as ton.info in our R package hemibrainr.</p> <p>S6 hemibrain TOON meta.csv</p> <p>Supplemental file 7</p> <p>All the hemibrain neurons we have classed as neurons that descend to the ventral nervous system (DNs). See above for column explanations. Exists as dn.info in our R package hemibrainr.</p> <p>S8 hemibrain DN meta.csv</p> <p>Supplemental file 8</p> <p>The root point in hemibrain voxel space, for each hemibrain neuron. This is either the location of the soma, or the tip of a severed cell body fibre tract, where possible. Exists as hemibrain somas in our R package hemibrainr.</p> <p>S8 hemibrain root points.csv</p> <p>Supplemental file 9</p> <p>The start points for different neuron compartments. Nodes downstream of this position in the 3D structure of the neuron indicated with bodyid, belong to the compartment type designated by Label. A product of running flow centrality on hemibrain neurons, exists as hemibrain splitpoints in our R package hemi- brainr.</p> <p>S9 hemibrain compartment startpoints.csv</p> <p>Supplemental file 10</p> <p>3D triangle mesh for the hemibrain surface as a .obj file. This mesh was generated by first merging individual ROI meshes from neuPrint and then filling the gaps in between in a semi-manual process. It also exists as hemibrain.surf in our R package hemibrainr.</p> <p>S10 hemibrain raw.obj</p> <p>Supplemental file 11</p> <p>3D meshes of 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli for the hemibrain volume, generated from ALRN presynapses.</p> <p>41</p> <p>Note that hemibrain coordinate system has the anterior-posterior axis aligned with the Y axis (rather than the Z axis, which is more commonly observed).</p> <p>S11 hemibrain AL glomeruli meshes RN-based.zip</p> <p>Supplemental file 12</p> <p>3D meshes of 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli for the hemibrain volume, generated from ALPN presynapses.</p> <p>Note that hemibrain coordinate system has the anterior-posterior axis aligned with the Y axis (rather than the Z axis, which is more commonly observed).</p> <p>These meshes are also available as hemibrain al.surf in our R package hemibrainr. S12 hemibrain AL glomeruli meshes PN-based.zip</p>
Comparative proteomics analysis of whole-cell catalyst of K. rhizophila strain SA117 catabolism of SMX
<p><span>Sulfamethoxazole (SMX), an oral sulfonamide antibiotic, presents significant environmental challenges due to its persistence and potential role in promoting antibiotic resistance. The bacterial strain <em><span>Kocuria rhizophila</span></em> SA117, isolated from polluted soils, has demonstrated a remarkable capability to metabolize SMX. Proteomic analysis revealed the presence of various enzymes and metabolic pathways that may contribute to SMX degradation, including those involved in para-aminobenzoate condensation and protocatechuate metabolism. Notably, the genome of SA117 harbors eight monooxygenase genes, including those related to antibiotic biosynthesis and flavin family monooxygenases. Additionally, several cytochrome c-encoding genes, known for their role in respiratory versatility and potential application in bioremediation, were identified. Genes associated with sulfur metabolism, including an iron-sulfur cluster gene cluster (SufB, C, D, R, E) linked to oxidative stress response, were also found. A comparative proteomic study under SMX exposure highlighted significant upregulation of stress-related proteins. These findings underscore the metabolic adaptability of <em><span>Kocuria rhizophila</span></em> SA117 and its potential application in the bioremediation of SMX-contaminated environments.</span></p>
scRNA-seq atlases for 3 Caenorhabditis species - annotated cell datasets
<p>Annotated datasets (monocle3 objects) of scRNA-seq data for <em>C. elegans</em>, <em>C. briggsae</em> and <em>C. tropicalis</em> L2 nematodes. The datasets are published together with the manuscript "Divergence in neuronal signaling pathways despite conserved neuronal identity among <em>Caenorhabditis</em> species".</p> <p><a href="https://doi.org/10.1016/j.cub.2025.05.036" target="_blank" rel="noopener">https://doi.org/10.1016/j.cub.2025.05.036</a></p> <p>Files deposited include cell datasets for all sequenced cells ("all_cds") and datasets for all cells annotated as neurons ("neu_cds"). </p> <p><em>C. elegans</em> strain - N2.</p> <p><em>C. briggsae</em> strain - AF16.</p> <p><em>C. tropicalis</em> strain - NIC203.</p>
Data for Cell-type-specific inhibitory circuitry from a connectomic census of mouse visual cortex
<p>Data for the paper: Cell-type-specific inhibitory circuitry from a connectomic census of mouse visual cortex, Nature 640, 2025</p> <p>In brief, this data archive includes information about the skeleton morphology and synaptic features of neurons whose cell bodies fell within a 100 micron by 100 micron column spanning all layers of mouse visual cortex. See <a href="https://www.microns-explorer.org/cortical-mm3">MICrONs-Explorer</a> for a full description of the broader volume and how it was collected.</p> <p>The data here include both data tables of cell locations, neuronal features, synapse lists, and more, as well as files containing morphological descriptions of all neurons used for the analysis in the initial version of the preprint. See the README.md file for more complete information about the individual files.</p> <p>Note: Data has been updated with post-publication files.</p>
Enhanced Biosafety of the Sleeping Beauty Transposon System by Using mRNA as Source of Transposase to Efficiently and Stably Transfect Retinal Pigment Epithelial Cells
<p>Raw data of the publication "Enhanced Biosafety of the Sleeping Beauty Transposon System by Using mRNA as Source of Transposase to Efficiently and Stably Transfect Retinal Pigment Epithelial Cells".</p> <p>Abstract: Neovascular age-related macular degeneration (nvAMD) is characterized by choroidal<br> neovascularization (CNV), which leads to retinal pigment epithelial (RPE) cell and photoreceptor<br> degeneration and blindness if untreated. Since blood vessel growth is mediated by endothelial cell<br> growth factors, including vascular endothelial growth factor (VEGF), treatment consists of repeated,<br> often monthly, intravitreal injections of anti-angiogenic biopharmaceuticals. Frequent injections are<br> costly and present logistic difficulties; therefore, our laboratories are developing a cell-based gene<br> therapy based on autologous RPE cells transfected ex vivo with the pigment epithelium derived factor<br> (PEDF), which is the most potent natural antagonist of VEGF. Gene delivery and long-term expression<br> of the transgene are enabled by the use of the non-viral Sleeping Beauty (SB100X) transposon system<br> that is introduced into the cells by electroporation. The transposase may have a cytotoxic effect and a<br> low risk of remobilization of the transposon if supplied in the form of DNA. Here, we investigated<br> the use of the SB100X transposase delivered as mRNA and showed that ARPE-19 cells as well as<br> primary human RPE cells were successfully transfected with the Venus or the PEDF gene, followed<br> by stable transgene expression. In human RPE cells, secretion of recombinant PEDF could be detected<br> in cell culture up to one year. Non-viral ex vivo transfection using SB100X-mRNA in combination<br> with electroporation increases the biosafety of our gene therapeutic approach to treat nvAMD while<br> ensuring high transfection efficiency and long-term transgene expression in RPE cells.</p>
Characterization of a loss-offunction NSF attachment protein beta mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived and CRISPR-corrected induced pluripotent stem cell lines
<p>RNA-seq data of matured cortical neurons (8-weeks old) derived from the induced pluripoent stem cells (iPSC) of control parents (CtrlF and CtrlM) and corrected proband. There are three replicates (Rep1, Rep2, Rep3) for each sample with Forwad read (R1_001.fastq.gz)</p> <p>CtrlF: Control Father sample</p> <p>CtrlM: Control mother sample</p> <p>NDD_01_Corr_Het: Heterozygous correction of NAPB mutation (c.354+2T>G) in NDD_01 proband</p> <p>NDD_05_Corr_Hom: Homozygous correction of NAPB mutation (c.354+2T>G) in NDD_05 proband</p>
Data from: An implicit, conservative electrostatic particle-in-cell algorithm for paraxial magnetic nozzles
<p><strong> Data from: An implicit, conservative electrostatic particle-in-cell algorithm for paraxial magnetic nozzles</strong></p> <p>- Authors: Pedro Jimenez, Luis Chacon, Mario Merino</p> <p>- Contact email: pejimene@ing.uc3m.es</p> <p>- Date: 2024-02-09</p> <p>- Keywords: electric propulsion, plasma simulation, magnetic nozzles, implicit particle-in-cell (PIC)</p> <p>- Version: 1.2</p> <p>- Digital Object Identifier (DOI): 10.5281/zenodo.8081962</p> <p>- License: This dataset is made available under the <a href="http://opendatacommons.org/licenses/by/1.0">Open Data Commons Attribution License</a></p> <p><strong>Abstract</strong></p> <p>This dataset contains the data found in the plots of the journal article:</p> <p><a href="https://www.sciencedirect.com/science/article/pii/S0021999124000755?via%3Dihub">Pedro Jimenez, Luis Chacon, Mario Merino, "An implicit, conservative electrostatic particle-in-cell algorithm for paraxial magnetic nozzles"</a></p> <p>The data in this repository are the results of kinetic plasma simulations as described in the reference. For further information on the setup for the simulation please refer to the article.</p> <p><strong>Data Files</strong></p> <p>The data files are in .csv format. They were produced in Julia using <a href="http://csv.juliadata.org/stable/)">CSV.jl</a> and <a href="https://dataframes.juliadata.org/stable/">DataFrames.jl</a> libraries.</p> <p>The files are organised following the order of the figures in the article. All the plots are 1D series, the first column corresponding to the x-axis data. Y-axis data is presented in the following columns, the total number of additional columns is equal to the number of line series. The title of each series is found in the first row of the .csv files. Please find below some specificalities in certain figures:</p> <p>- The columns for the time evolution in <strong>fig6_left.csv</strong> and<strong> fig6_right.csv </strong>(corresponding to the actual left and right columns in the figure i.e. cases A and B) contain a field tag followed by the corresponding time step (e.g. phi_500).</p> <p>- Due to the different number of nodes, steady state fields for cases A and B are saved in <strong>fig8_a-f.csv</strong> while cases AF and BF are saved in <strong>fig8_a-f_fine.csv</strong>.</p> <p>The rest of the data files should be self descripting</p> <p><strong>Citation</strong></p> <p>Any works using this dataset or any part of it in any form shall cite it as follows:</p> <p>The prefered means of citation is to reference the publication asociated to the jounal article with DOI: <a href="https://doi.org/10.1016/j.jcp.2024.112826">10.1016/j.jcp.2024.112826</a></p> <p>The BibTex is also provided for the sake of convinience:</p> <pre>@article{jimenez2024implicit, title={An implicit, conservative electrostatic particle-in-cell algorithm for paraxial magnetic nozzles}, author={Jim{\'e}nez, Pedro and Chac{\'o}n, Luis and Merino, Mario}, journal={Journal of Computational Physics}, pages={112826}, year={2024}, publisher={Elsevier} }</pre> <p>Optionally the dataset can be cited by referencing the corresponding DOI:</p> <p><a href="https://doi.org/10.5281/zenodo.8081962">https://doi.org/10.5281/zenodo.8081962</a></p> <p><strong>Acknowledgments</strong></p> <p>This dataset was created by the [ERC-ZARATHUSTRA project](https://erc-zarathustra.uc3m.es/).</p> <p>The ERC-ZARATHUSTRA project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement No 950466).</p>
The evolution of genomic, transcriptomic, and single-cell protein markers of metastatic upper tract urothelial carcinoma
<p>The molecular characteristics of metastatic upper tract urothelial carcinoma (UTUC) are unknown. The genomic and transcriptomic differences between primary and metastatic UTUC is not well described either. We combined whole-exome sequencing, RNA-sequencing, and Imaging Mass Cytometry<sup>TM</sup> (IMC<sup>TM</sup>) of 44 tumor samples from 28 patients with high-grade primary and metastatic UTUC. IMC enables spatially resolved single-cell analyses to examine the evolution of cancer cell, immune cell, and stromal cell markers using mass cytometry with lanthanide metal-conjugated antibodies. We discovered that actionable genomic alterations are frequently discordant between primary and metastatic UTUC tumors in the same patient. In contrast, molecular subtype membership and immune depletion signature were stable across primary and matched metastatic UTUC. Molecular and immune subtypes were consistent between bulk RNA-sequencing and mass cytometry of protein markers from 340,798 single-cells. Molecular subtyping at the single cell level was highly conserved between primary and metastatic UTUC tumors within the same patient.</p>
Dataset of "Capabilities of a novel electrochemical cell for operando XAS and SAXS investigations for PEM fuel cells and water electrolysers"
<p>With this work we present a reversible electrochemical cell and introduce a valuable approach, suitable for being used either for in operando X-Ray Absorption Spectroscopy (XAS) and Small Angle X-Ray Scattering (SAXS). The reversible electrochemical cell was used to depict the time-resolved degradation of a Pt/C catalyst material for Proton Exchange Membrane Fuel Cells (PEMFC). The evolution of the specific electrochemical active surface area (ECSA) was coupled to the evolution of morphological parameters, supported by the analysis of Pt oxidation state. As a result, we obtain a coherent picture in which: the increase of particle (and particle cluster) size is connected to the diminishing of ECSA and to the changes in the fraction of metallic Pt, detailing as the evolution develops in the first 2000 cycles, as previously observed on catalyst model systems. Finally, we introduce some preliminary results underlying the change in Ir oxidation state for a commercial Ir/IrO X catalyst material for PEM water electrolysers and showing as this change is not sufficient to induce any remarkable morphological variations within 500 cycles of accelerated stress tests.</p>
CAbiNet: Joint clustering and visualization of cells and genes for single-cell transcriptomics
<p>We here provide the data sets to reproduce the results in our manuscript "CAbiNet: Joint clustering and visualization of cells and genes for single-cell transcriptomics". Our package "CAbiNet" can be downloaded from https://github.com/VingronLab/CAbiNet. The scripts to reproduce the results in our manuscript can be found from https://github.com/VingronLab/CAbiNet_paper.</p><p>You can find the description of folders in 'Data.zip' in the README.md file.</p>
Transcriptomic atlas reveals organ-specific disease tolerance in sickle cell mice: dataset bone marrow HbAA mice injected or not with heme
<p>The objective of this experiment was to explore the transcriptome of the HbSS Townes mouse model of sickle cell disease. Townes model mice carry several human hemoglobin knock-in genes replacing the endogenous mouse genes and may be useful in studying sickle cell disease. All mice were genotyped, age- and sex-matched littermates. All HbAA (control, normal human hemoglobin) vs HbSS (sickle cell disease, mutated human hemoglobin) mice were used for experimentations at 6-8 weeks of age, to limit intra-group heterogeneity. Hemin (Ferriprotoporphyrin IX) was purchased from Frontiers Scientific and injected intravenously (iv.) in a retroorbital sinus at a concentration of 24 µmol/kg. Control mice received PBS instead. Mice were anesthetized with isoflurane 2-3% for injections, blood collection and sacrifice. All mice were sacrificed by cervical dislocation, 4 hours after injection.</p> <p>This dataset contains the results of the HbAA mice with and without heme.</p> <p>The corresponding HbSS mice with and without heme are deposited under number 10.5281/zenodo.10962782</p> <p>Bone marrow RNA was extracted by Macherey Nagel kit, according to the manufacturer’s instructions. The quality and quantity of mRNA were evaluated using a 2100<br>bioanalyzer with TNA 6000 NanoKits (all Agilent Technologies, Palo Alto, CA, USA). RNA Integrity Numbers superior to 7 were eligible for subsequent reverse transcription into cDNA. RNAseq was performed at the GenomIC plateform Cochin Institute INSERM U1016. After RNA extraction, RNA quality (RNA integrity number) was estimated. 1μg of high-quality total RNA sample (RIN &gt;7) was processed to build up the libraries, using TruSeq Stranded mRNA kit (Illumina) according to manufacturer instructions. Briefly, purified poly-A containing mRNA molecules were fragmented and reverse-transcribed using random primers. Replacement of dTTP by dUTP during second strand synthesis allowed us to achieve strand specificity. Addition of a single A base to the cDNA was followed by ligation of Illumina adapters.<br>Libraries were quantified by qPCR using KAPA Library Quantification Kits for Illumina Libraries (KapaBiosystems, Wilmington, MA). Library profiles were assessed using DNA High Sensitivity LabChip kits on an Agilent Bioanalyzer. Libraries were sequenced on an Illumina Nextseq 500 instrument using 75 base-lengths read V2 chemistry in a paired-end mode. After sequencing, primary analysis based on AOZAN software (ENS, Paris), was applied to demultiplex and control the quality of the raw data (based of FastQC modules / version 0.11.5).</p> <p>The dataset here represents 4 groups of mice, 4 mice per group as follows: HbAA PBS, HbAA heme, HbSS PBS, HbSS heme. </p> <p> </p>
PM_035469_B_Celles
<u>File Name</u>: PM_035469_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035464_B_Celles
<u>File Name</u>: PM_035464_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail A chicken (?) <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035467_B_Celles
<u>File Name</u>: PM_035467_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035463_B_Celles
<u>File Name</u>: PM_035463_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035462_B_Celles
<u>File Name</u>: PM_035462_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035461_B_Celles
<u>File Name</u>: PM_035461_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail A chicken (?) <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035460_B_Celles
<u>File Name</u>: PM_035460_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
PM_035453_B_Celles
<u>File Name</u>: PM_035453_B_Celles.jpg <br><u>Sublocation</u>: Celles-les-Dinant, Eglise Saint-Hadelin <br><u>Location</u>: Houyet <br><u>Province</u>: Namur <br><u>Country</u>: Belgium <br><u>Header</u>: Intérieur, les stalles du choeur, détail <br><u>Description</u>: Parish church (Eglise Saint-Hadelin) Interior The choir Seating 13th century Wood Detail A chicken (?) <br><u>Keywords</u>: Belgium, Celles-les-Dinant (Houyet), Cultural heritage, Europe, Furniture/accessory furnishing, Houyet, Namur, Thematic <br><br><u>Author</u>: Photo: Paul M.R. Maeyaert <br><u>Copyright</u>: Paul M.R. Maeyaert <br>
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.