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315 results for “human intestine”

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dryad36/100

Distribution and activity of nitrate and nitrite reductases in the microbiota of the human intestinal tract

Open the record for dataset details and reuse information.

publicOct 2025View details →
dryad36/100

Single cell RNA sequencing of human tissue along the stomach-intestinal tract

Open the record for dataset details and reuse information.

publicOct 2024View details →
dryad32/100

Data from: Tipping elements in the human intestinal ecosystem

The microbial communities living in the human intestine can have profound impact on our well-being and health. However, we have limited understanding of the mechanisms that control this complex ecosystem. Here, based on a deep phylogenetic analysis of the intestinal microbiota in a thousand western adults, we identify groups of bacteria that exhibit robust bistable abundance distributions. These bacteria are either abundant or nearly absent in most individuals, and exhibit decreased temporal stability at the intermediate abundance range. The abundances of these bimodally distributed bacteria vary independently, and their abundance distributions are not affected by short-term dietary interventions. However, their contrasting alternative states are associated with host factors such as ageing and overweight. We propose that the bistable groups reflect tipping elements of the intestinal microbiota, whose critical transitions may have profound health implications and diagnostic potential.

opencc-zeroDec 2013View details →
zenodo32/100

OMAP-15 Human Intestine with CODEX

<p>Datasets are CODEX experiments performed on TMA ffpe sections (composed of human duodenum, proximal jejunum, 3 mid jejunum samples, ileum, ascending colon, and sigmoid colon samples) labeled with nuclear marker DAPI and anitbodies directed against the indicated markers in OMAP-15. Images were acquired with the Akoya Phenocycler.&nbsp;</p> <p>Markers not included in OMAP-15 are not representative images.</p> <p>See "S16-0513-B13-TMA_Scan1.qptiff" for all markers except SPIB. See "S7-B017-011624_Scan1.qptiff" for SPIB.</p>

opencc-by-4.0Apr 2024View details →
dryad32/100

Data from: Epidemiological interactions between urogenital and intestinal human schistosomiasis in the context of praziquantel treatment across three West African countries

Background: In many parts of sub-Saharan Africa, urogenital and intestinal schistosomiasis co-occur, and mixed species infections containing both Schistosoma haematobium and S. mansoni can be common. During co-infection, interactions between these two species are possible, yet the extent to which such interactions influence disease dynamics or the outcome of control efforts remains poorly understood. Methodology/Principal Findings: Here we analyse epidemiological data from three West African countries co-endemic for urogenital and intestinal schistosomiasis (Senegal, Niger and Mali) to test whether the impact of praziquantel (PZQ) treatment, subsequent levels of re-infection or long-term infection dynamics are altered by co-infection. In all countries, positive associations between the two species prevailed at baseline: infection by one species tended to predict infection intensity for the other, with the strength of association varying across sites. Encouragingly, we found little evidence that co-infection influenced PZQ efficacy: species-specific egg reduction rates (ERR) and cure rates (CR) did not differ significantly with co-infection, and variation in treatment success was largely geographical. In Senegal, despite positive associations at baseline, children with S. mansoni co-infection at the time of treatment were less intensely re-infected by S. haematobium than those with single infections, suggesting competition between the species may occur post-treatment. Furthermore, the proportion of schistosome infections attributable to S. mansoni increased over time in all three countries examined. Conclusions/Significance: These findings suggest that while co-infection between urinary and intestinal schistosomes may not directly affect PZQ treatment efficacy, competitive interspecific interactions may influence epidemiological patterns of re-infection post-treatment. While re-infection patterns differed most strongly according to geographic location, interspecific interactions also seem to play a role, and could cause the community composition in mixed species settings to shift as disease control efforts intensify, a situation with implications for future disease management in this multi-species system.

opencc-zeroDec 2014View details →
zenodo32/100

Single cell atlas of the human neonatal small intestine affected by necrotizing enterocolitis

<p>Codes and single cell data for &quot;<strong>Single cell atlas of the human neonatal small intestine affected by necrotizing enterocolitis</strong>&quot; paper.</p> <p><strong>File: Tunel_Lyve1_Data.xlsx </strong>&ndash; quantifications of Tunel+Lyve1+ cells for n=4 NECs and n=4 neonatal samples.</p> <p><strong>Folder: Cell_ranger_output</strong></p> <p>Data produced using 10x sequencing.</p> <p>This folder contains&nbsp;all the Cell Ranger output raw files from all 11 subjects used for single cell RNA sequencing (5x Neonatal- S1056, S1127, S1212, S1214, S1082, 6x NECs- S1021, S1074, S1095, S1109, S1155, S1193).</p> <p>The neonatal subjects had two 10X runs (except subject 1082) - one done on CD45 negatively selected small intestinal cells and the other on non-selected small intestinal cells.</p> <p>The NEC subjects had one run each (subject 1074 was sequenced twice) with no selection due to low yield in the selected runs.</p> <p><strong>Folder: Seurat_pipeline</strong></p> <p>Done with Seurat package version 3.2.2</p> <p>This folder contains R scripts for Seurat analysis and script for background (BG) subtraction of the data.</p> <ol> <li>BG_subtraction_before_seurat.R - Script that creates a BG subtracted matrix for each CellRanger output before Seurat analysis.</li> <li>seurat_pipline_all_cells_NEC.R - Script for Seurat analysis for the full atlas.</li> <li>Final_seurat_obj_after_filtration_all_cells.rds &ndash; rds file of final Seurat object of all cells after pipeline filtration</li> <li>Files description in &ldquo;RDS_files_for_seurat_pipeline&rdquo; folder: <ol> <li>list_UMIs_after_BG_subtruction.rds &ndash; rds file containing a list of all 10x runs used in the study after background subtraction. Used as input file for &ldquo;seurat_pipline_all_cells_NEC.R&rdquo; script.</li> <li>list_metadata_after_BG_subtruction.rds &ndash; rds file containing a list of metadata for all 10x runs used in the study after background subtraction. Used as input file for &ldquo;seurat_pipline_all_cells_NEC.R&rdquo; script.</li> </ol> </li> </ol> <p><strong>Folder: Deconvolution_analysis</strong></p> <p>Done on Matlab R2019b</p> <p>This folder contains the script for deconvolution analysis and its input files.</p> <ol> <li>Deconvolution_parsing_NEC_for_zenodo.m - Matlab script to create box plots of deconvolution results and their q- values.</li> <li>Files description: <ol> <li>deconvolution_original8_clusters.mat &ndash; structure of deconvolution results. Signature cells were split into the 8 major cell type groups shown in figure 1.</li> <li>cellanneal_split_clust_results.mat &ndash; structure of deconvolution results. Signature cells were split into sub groups for each cell type group.</li> </ol> </li> </ol> <p><strong>Folder: Ligand-receptor_interaction_analysis</strong></p> <p>This folder contains matlab and R scripts for ligand-receptor interaction analysis.</p> <ol> <li>run_permutations_for_lig_rec_ratio_tensor_Zenodo.m &ndash; main script to run ligand-receptor analysis.</li> <li>calculate_ratio_ligand_receptor.m &ndash; function used by the main script.</li> <li>Interactions_visualizations_heatmaps.R &ndash; R script for heatmap visualization.</li> <li>Files description in &ldquo;Mat_files_for_analysis&rdquo; folder: <ol> <li>all_cells_split_for_interactions.mat &ndash; single cell structure of all cells. Cells are split into subgroups for ligand receptor analysis.</li> <li>ramilowsky.mat &ndash; ligand-receptor lists taken from Ramilowski et al. 2015 to use in main script and function.</li> <li>tensor_real_q100permutations.mat &ndash; output mat file of the interactions ratio, q values and ligand-receptor names for heatmaps visualization in R (input file for &ldquo;Interactions_visualizations_heatmaps.R&rdquo;).</li> </ol> </li> </ol>

opencc-by-4.0Mar 2023View details →
zenodo32/100

Fig. 8 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR

Fig. 8. (A) The 3D structure and hydrogen bond interaction of compound 18 with FXR at the 50th ns MD stimulation. (B) The agonistic activity of compound 18 against the wild-type, mutant R341V, or S342V FXR. Data were shown as the mean ± SD, n = 4 (*p &lt;0.05, **p &lt;0.01, ***p &lt;0.001 compared to the Ctrl group; #p &lt;0.05, ##p &lt;0.01, ###p &lt;0.001 compared to the WT group).

opennotspecifiedJan 2022View details →
zenodo32/100

Fig. 7 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR

Fig. 7. The RMSD (A) and RMSF (B) of compound 18 with FXR in 50 ns MD stimulation. (C) The volume of pock for a complex of compound 18 and FXR in 50 ns MD stimulation. (D–F) The energy of the complex (D), energy of contribution (E), and hydrogen bond number (F) of compound 18 with FXR in the 50 ns MD stimulation. (G) The distance of compound 18 with amino acid residues Val325, Met328, and Phe329. (H) The distance of compound 18 with amino acid residues Ser332 and Tyr369.

opennotspecifiedJan 2022View details →
zenodo32/100

Fig. 5 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR

Fig. 5. (A) Effects of compound 18 (2 μM) towards FXR, SHP1, and BSEP mRNA levels. (B) Effects of compound 18 (2 μM) towards FXR, SHP1, FGF, and BSEP expression levels. (C) Quantitative analysis of FXR, SHP1, FGF, and BSEP expression levels. Data were shown as the mean ± SD, n = 3 (*p &lt;0.05, **p &lt;0.01, ***p &lt;0.001 compared to the Ctrl group). CDCA (80 μM) was used as the positive control.

opennotspecifiedJan 2022View details →
zenodo32/100

Fig. 4 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR

Fig. 4. Experimental and calculated ECD spectra of 1 (A) and 5–7 (B–D) at the CAM-B3LYP/def-tzvp level.

opennotspecifiedJan 2022View details →
zenodo32/100

Fig. 3 in Microbial transformation of capsaicin by several human intestinal fungi and their inhibitory effects against lysine-specific demethylase 1

Fig. 3. The metabolites of capsaicin transformed by Rhizopus oryzae R2701 and its hypothetical biotransformation pathway.

opennotspecifiedOct 2022View details →
zenodo32/100

Fig. 1 in Microbial transformation of capsaicin by several human intestinal fungi and their inhibitory effects against lysine-specific demethylase 1

Fig. 1. The metabolites of capsaicin transformed by Aspergillus fumigatus PB4204, Aspergillus japonicus Y4009A, and the hypothetical biotransformation pathway.

opennotspecifiedOct 2022View details →
zenodo32/100

Ceftriaxone and Cefotaxime Have Similar Effects on the Intestinal Microbiota in Human Volunteers

<p><strong>Pour ce TP, nous allons d&eacute;terminer l&rsquo;impact d&rsquo;un traitement &agrave; la ceftriaxone sur la flore intestinale (<a href="https://aac.asm.org/content/63/6/e02244-18.abstract">https://aac.asm.org/content/63/6/e02244-18.abstract</a>). 22 volontaires sains ont re&ccedil;u par intraveineuse de la ceftriaxone (1g / 24 h) ou de la cefotaxime ( 1g / 8h) pendant 3 jours. Le consortium CEREMI a collect&eacute; des &eacute;chantillons de selles de ces volontaires et r&eacute;alis&eacute; une &eacute;tude de m&eacute;tag&eacute;nomique cibl&eacute;e sur le g&egrave;ne 16S rRNA. En raison des limitations de vos machines, nous allons analyser les &eacute;chantillons du groupe B uniquement &agrave; 2 temps: Jm1 (un jour avant le traitement) et J4</strong></p>

opencc-by-4.0Aug 2023View details →
ClinicalTrials.gov32/100

Establishment of the Human Intestinal and Salivary Microbiota Biobank - Kidney Diseases

ClinicalTrials.gov study NCT04689074. IPD Sharing: NO. Countries: 1. Publications: 5.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Establishment of the Human Intestinal and Salivary Microbiota Biobank - Gastrointestinal Diseases

ClinicalTrials.gov study NCT04698148. IPD Sharing: NO. Countries: 1. Publications: 5.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Human Milk and Infant Intestinal Microbiome Study

ClinicalTrials.gov study NCT03181269. IPD Sharing: NO. Countries: 1. Publications: 11.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Calibrated Diets and Human Intestinal Microflora

ClinicalTrials.gov study NCT00639561. IPD Sharing: Not stated. Countries: 1. Publications: 7.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Investigation of the Ability of a Supplement to Increase Good Bacteria in the Human Intestine and Blood Sugar Levels

ClinicalTrials.gov study NCT01944904. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Establishment of the Human Intestinal and Salivary Microbiota Biobank - Oncologic Diseases

ClinicalTrials.gov study NCT04698161. IPD Sharing: NO. Countries: 1. Publications: 5.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Intestinal Glucagon-like Peptide-1 (GLP-1) and the Physiological Role in Eating in Humans

ClinicalTrials.gov study NCT01900340. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →

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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.

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

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.

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