On the public citation graph

Jejunum: The understudied meeting place of dietary lipids and the microbiota

https://doi.org/10.1016/j.biochi.2020.09.007
0 signed · 213 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.2015.5941openalex-snapshot
The 2015 US Dietary Guidelines
inferredcites →https://doi.org/10.1002/jcp.20173openalex-snapshot
Lipid micelles stimulate the secretion of triglyceride‐enriched apolipoprotein B48‐containing lipoproteins by Caco‐2 cells
inferredcites →https://doi.org/10.1002/jcp.25402openalex-snapshot
Metabolic Adaptation of the Small Intestine to Short- and Medium-Term High-Fat Diet Exposure
inferredcites →https://doi.org/10.1002/mnfr.201600252openalex-snapshot
Gut microbiota, diet, and obesity‐related disorders—The good, the bad, and the future challenges
inferredcites →https://doi.org/10.1002/path.5134openalex-snapshot
Increased jejunal permeability in human obesity is revealed by a lipid challenge and is linked to inflammation and type 2 diabetes
inferredcites →https://doi.org/10.1007/s00253-004-1568-8openalex-snapshot
Bacterial lipases: an overview of production, purification and biochemical properties
inferredcites →https://doi.org/10.1007/s00253-016-8006-6openalex-snapshot
Interaction of gut microbiota with bile acid metabolism and its influence on disease states
inferredcites →https://doi.org/10.1007/s002530000330openalex-snapshot
Protective effect of the bile salt hydrolase-active Lactobacillus reuteri against bile salt cytotoxicity
inferredcites →https://doi.org/10.1007/s10654-014-9905-4openalex-snapshot
Are stool samples suitable for studying the link between gut microbiota and obesity?
inferredcites →https://doi.org/10.1007/s11894-015-0436-2openalex-snapshot
Small Intestinal Fungal Overgrowth
inferredcites →https://doi.org/10.1007/s12223-010-0061-2openalex-snapshot
Development of gut microflora in obese and lean rats
inferredcites →https://doi.org/10.1016/0002-9610(79)90309-xopenalex-snapshot
Microflora of the human small intestine
inferredcites →https://doi.org/10.1016/0005-2760(72)90019-7openalex-snapshot
Adaptive changes of the rat small intestine in response to a high fat diet
inferredcites →https://doi.org/10.1016/j.anaerobe.2015.10.016openalex-snapshot
A whole new ball game: Stem cell-derived epithelia in the study of host–microbe interactions
inferredcites →https://doi.org/10.1016/j.bbalip.2016.04.012openalex-snapshot
Recent discoveries on absorption of dietary fat: Presence, synthesis, and metabolism of cytoplasmic lipid droplets within enterocytes
inferredcites →https://doi.org/10.1016/j.biochi.2013.07.009openalex-snapshot
Triglyceride-rich lipoproteins and cytosolic lipid droplets in enterocytes: Key players in intestinal physiology and metabolic disorders
inferredcites →https://doi.org/10.1016/j.biochi.2015.06.020openalex-snapshot
Metabolic endotoxemia with obesity: Is it real and is it relevant?
inferredcites →https://doi.org/10.1016/j.ceb.2019.03.018openalex-snapshot
Lipid droplet biogenesis
inferredcites →https://doi.org/10.1016/j.celrep.2017.10.087openalex-snapshot
Mucus Detachment by Host Metalloprotease Meprin β Requires Shedding of Its Inactive Pro-form, which Is Abrogated by the Pathogenic Protease RgpB
inferredcites →https://doi.org/10.1016/j.celrep.2019.01.108openalex-snapshot
Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
inferredcites →https://doi.org/10.1016/j.chom.2017.10.013openalex-snapshot
Commensal Fungi Recapitulate the Protective Benefits of Intestinal Bacteria
inferredcites →https://doi.org/10.1016/j.chom.2018.03.011openalex-snapshot
Small Intestine Microbiota Regulate Host Digestive and Absorptive Adaptive Responses to Dietary Lipids
inferredcites →https://doi.org/10.1016/j.chom.2019.06.013openalex-snapshot
Meta-Analysis Reveals Reproducible Gut Microbiome Alterations in Response to a High-Fat Diet
inferredcites →https://doi.org/10.1016/j.chom.2019.08.011openalex-snapshot
Regional Diversity of the Gastrointestinal Microbiome
inferredcites →https://doi.org/10.1016/j.chom.2020.01.028openalex-snapshot
Fermentation Products of Commensal Bacteria Alter Enterocyte Lipid Metabolism
inferredcites →https://doi.org/10.1016/j.chom.2020.02.009openalex-snapshot
Feeling the Burn: Intestinal Epithelial Cells Modify Their Lipid Metabolism in Response to Bacterial Fermentation Products
inferredcites →https://doi.org/10.1016/j.clinmicnews.2008.01.006openalex-snapshot
Lactobacillus: a Review
inferredcites →https://doi.org/10.1016/j.cmet.2013.03.013openalex-snapshot
Pleiotropic Roles of Bile Acids in Metabolism
inferredcites →https://doi.org/10.1016/j.cmet.2016.05.005openalex-snapshot
Intestinal Crosstalk between Bile Acids and Microbiota and Its Impact on Host Metabolism
inferredcites →https://doi.org/10.1016/j.cmet.2017.12.016openalex-snapshot
The Small Intestine Converts Dietary Fructose into Glucose and Organic Acids
inferredcites →https://doi.org/10.1016/j.copbio.2014.09.005openalex-snapshot
The small intestine microbiota, nutritional modulation and relevance for health
inferredcites →https://doi.org/10.1016/j.devcel.2019.05.003openalex-snapshot
Membrane Asymmetry Imposes Directionality on Lipid Droplet Emergence from the ER
inferredcites →https://doi.org/10.1016/j.femsre.2004.09.003openalex-snapshot
The interaction between bacteria and bile
inferredcites →https://doi.org/10.1016/j.ijantimicag.2013.12.008openalex-snapshot
In vitro activity of rifaximin against isolates from patients with small intestinal bacterial overgrowth
inferredcites →https://doi.org/10.1016/j.it.2004.09.005openalex-snapshot
Let's go mucosal: communication on slippery ground
inferredcites →https://doi.org/10.1016/j.it.2004.11.009openalex-snapshot
Let's go mucosal: communication on slippery ground
inferredcites →https://doi.org/10.1016/j.it.2015.06.006openalex-snapshot
The bilateral responsiveness between intestinal microbes and IgA
inferredcites →https://doi.org/10.1016/j.jcmgh.2019.07.006openalex-snapshot
The Structure and Function of the Human Small Intestinal Microbiota: Current Understanding and Future Directions
inferredcites →https://doi.org/10.1016/j.jhep.2006.03.006openalex-snapshot
The expanding role of the bile acid receptor FXR in the small intestine
inferredcites →https://doi.org/10.1016/j.micpath.2016.03.006openalex-snapshot
Metabolic role of lactobacilli in weight modification in humans and animals
inferredcites →https://doi.org/10.1016/j.molmet.2016.06.002openalex-snapshot
Causality of small and large intestinal microbiota in weight regulation and insulin resistance
inferredcites →https://doi.org/10.1016/j.phrs.2015.12.007openalex-snapshot
Pharmacology of bile acid receptors: Evolution of bile acids from simple detergents to complex signaling molecules
inferredcites →https://doi.org/10.1016/j.plipres.2009.01.001openalex-snapshot
Intestinal absorption of long-chain fatty acids: Evidence and uncertainties
inferredcites →https://doi.org/10.1016/j.tem.2017.12.001openalex-snapshot
Recent Advances in Triacylglycerol Mobilization by the Gut
inferredcites →https://doi.org/10.1016/j.tibtech.2012.08.001openalex-snapshot
Relevance and challenges in modeling human gastric and small intestinal digestion
inferredcites →https://doi.org/10.1016/j.yexcr.2015.09.018openalex-snapshot
Characteristics and functions of lipid droplets and associated proteins in enterocytes
inferredcites →https://doi.org/10.1016/s0006-291x(02)02550-0openalex-snapshot
Identification of membrane-type receptor for bile acids (M-BAR)
inferredcites →https://doi.org/10.1016/s0140-6736(66)91744-2openalex-snapshot
JEJUNAL BACTERIOLOGY AND BILE-SALT METABOLISM IN PATIENTS WITH INTESTINAL MALABSORPTION
inferredcites →https://doi.org/10.1016/s0163-7827(03)00050-xopenalex-snapshot
The digestion of dietary triacylglycerols
inferredcites →https://doi.org/10.1016/s1286-4579(01)01460-5openalex-snapshot
IgA responses in the intestinal mucosa against pathogenic and non-pathogenic microorganisms
inferredcites →https://doi.org/10.1017/s0007114512001444openalex-snapshot
Recommended dietary reference intakes, nutritional goals and dietary guidelines for fat and fatty acids: a systematic review
inferredcites →https://doi.org/10.1021/pr500833vopenalex-snapshot
The Impact of High-Fat Diet on Metabolism and Immune Defense in Small Intestine Mucosa
inferredcites →https://doi.org/10.1038/cr.2008.289openalex-snapshot
FXR: a metabolic regulator and cell protector
inferredcites →https://doi.org/10.1038/ismej.2011.212openalex-snapshot
The human small intestinal microbiota is driven by rapid uptake and conversion of simple carbohydrates
inferredcites →https://doi.org/10.1038/ismej.2014.45openalex-snapshot
Microbiome of prebiotic-treated mice reveals novel targets involved in host response during obesity
inferredcites →https://doi.org/10.1038/nature07935openalex-snapshot
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
inferredcites →https://doi.org/10.1038/nature18849openalex-snapshot
Interactions between the microbiota and pathogenic bacteria in the gut
inferredcites →https://doi.org/10.1038/nature21673openalex-snapshot
Interplay between metabolic identities in the intestinal crypt supports stem cell function
inferredcites →https://doi.org/10.1038/nrgastro.2013.35openalex-snapshot
The gastrointestinal mucus system in health and disease
inferredcites →https://doi.org/10.1038/nrgastro.2017.119openalex-snapshot
Bile acid–microbiota crosstalk in gastrointestinal inflammation and carcinogenesis
inferredcites →https://doi.org/10.1038/nrmicro2114openalex-snapshot
Do symbiotic bacteria subvert host immunity?
inferredcites →https://doi.org/10.1038/nrmicro3552openalex-snapshot
Gut biogeography of the bacterial microbiota
inferredcites →https://doi.org/10.1038/nutd.2014.6openalex-snapshot
Comparative genomics analysis of Lactobacillus species associated with weight gain or weight protection
inferredcites →https://doi.org/10.1038/oby.2008.435openalex-snapshot
Developmental Changes of Gut Microflora and Enzyme Activity in Rat Pups Exposed to Fat‐rich Diet
inferredcites →https://doi.org/10.1038/s41575-018-0061-2openalex-snapshot
You are what you eat: diet, health and the gut microbiota
inferredcites →https://doi.org/10.1038/s41575-019-0250-7openalex-snapshot
Regulation of intestinal lipid metabolism: current concepts and relevance to disease
inferredcites →https://doi.org/10.1038/s41575-019-0258-zopenalex-snapshot
Gut microbiota-derived metabolites as key actors in inflammatory bowel disease
inferredcites →https://doi.org/10.1038/sj.embor.7400731openalex-snapshot
The gut flora as a forgotten organ
inferredcites →https://doi.org/10.1042/bj20051359openalex-snapshot
Adaptation of enterocytic Caco-2 cells to glucose modulates triacylglycerol-rich lipoprotein secretion through triacylglycerol targeting into the endoplasmic reticulum lumen
inferredcites →https://doi.org/10.1053/j.gastro.2011.07.050openalex-snapshot
Long-term Expansion of Epithelial Organoids From Human Colon, Adenoma, Adenocarcinoma, and Barrett's Epithelium
inferredcites →https://doi.org/10.1053/j.gastro.2016.07.009openalex-snapshot
Antibiotics Suppress Activation of Intestinal Mucosal Mast Cells and Reduce Dietary Lipid Absorption in Sprague-Dawley Rats
inferredcites →https://doi.org/10.1073/pnas.0600780103openalex-snapshot
How bile acids confer gut mucosal protection against bacteria
inferredcites →https://doi.org/10.1073/pnas.1407597111openalex-snapshot
Microbial-induced meprin β cleavage in MUC2 mucin and a functional CFTR channel are required to release anchored small intestinal mucus
inferredcites →https://doi.org/10.1073/pnas.1612559113openalex-snapshot
High-fat diet modifies the PPAR-γ pathway leading to disruption of microbial and physiological ecosystem in murine small intestine
inferredcites →https://doi.org/10.1080/19490976.2015.1127483openalex-snapshot
Consequences of bile salt biotransformations by intestinal bacteria
inferredcites →https://doi.org/10.1080/19490976.2018.1502539openalex-snapshot
Small intestinal microbiota: the neglected stepchild needed for fat digestion and absorption
inferredcites →https://doi.org/10.1093/chemse/bjs095openalex-snapshot
Evidence for Presence of Nonesterified Fatty Acids as Potential Gustatory Signaling Molecules in Humans
inferredcites →https://doi.org/10.1093/femsec/fiz096openalex-snapshot
Microbial communities in a dynamic in vitro model for the human ileum resemble the human ileal microbiota
inferredcites →https://doi.org/10.1093/infdis/137.1.1openalex-snapshot
Bacterial Flora of the Small Bowel Before and After Bypass Procedure for Morbid Obesity
inferredcites →https://doi.org/10.1096/fj.10-164921openalex-snapshot
Germ-free C57BL/6J mice are resistant to high-fat-diet-induced insulin resistance and have altered cholesterol metabolism
inferredcites →https://doi.org/10.1097/mog.0000000000000057openalex-snapshot
Bile acids and the gut microbiome
inferredcites →https://doi.org/10.1097/mol.0000000000000084openalex-snapshot
Intestinal lipid absorption and lipoprotein formation
inferredcites →https://doi.org/10.1098/rstb.2015.0504openalex-snapshot
When pathogenic bacteria meet the intestinal microbiota
inferredcites →https://doi.org/10.1099/jmm.0.45935-0openalex-snapshot
Molecular analysis of jejunal, ileal, caecal and recto-sigmoidal human colonic microbiota using 16S rRNA gene libraries and terminal restriction fragment length polymorphism
inferredcites →https://doi.org/10.1111/1574-6941.12127openalex-snapshot
Diversity of human small intestinal Streptococcus and Veillonella populations
inferredcites →https://doi.org/10.1111/apt.12304openalex-snapshot
Dysmotility and proton pump inhibitor use are independent risk factors for small intestinal bacterial and/or fungal overgrowth
inferredcites →https://doi.org/10.1111/j.1365-2362.1992.tb01464.xopenalex-snapshot
Glucagon‐like peptide‐1 cells in the gastrointestinal tract and pancreas of rat, pig and man
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02294.xopenalex-snapshot
High temporal and inter‐individual variation detected in the human ileal microbiota
inferredcites →https://doi.org/10.1126/science.284.5418.1365openalex-snapshot
Bile Acids: Natural Ligands for an Orphan Nuclear Receptor
inferredcites →https://doi.org/10.1126/science.291.5505.881openalex-snapshot
Molecular Analysis of Commensal Host-Microbial Relationships in the Intestine
inferredcites →https://doi.org/10.1126/scitranslmed.3000322openalex-snapshot
The Effect of Diet on the Human Gut Microbiome: A Metagenomic Analysis in Humanized Gnotobiotic Mice
inferredcites →https://doi.org/10.1128/aem.02519-12openalex-snapshot
Identification and Characterization of a Bile Salt Hydrolase from Lactobacillus salivarius for Development of Novel Alternatives to Antibiotic Growth Promoters
inferredcites →https://doi.org/10.1128/aem.71.8.4925-4929.2005openalex-snapshot
Genetic Analysis of Two Bile Salt Hydrolase Activities in Lactobacillus acidophilus NCFM
inferredcites →https://doi.org/10.1128/cmr.13.1.122openalex-snapshot
Potential Role of Phospholipases in Virulence and Fungal Pathogenesis
inferredcites →https://doi.org/10.1128/iai.00282-18openalex-snapshot
Modeling Host-Pathogen Interactions in the Context of the Microenvironment: Three-Dimensional Cell Culture Comes of Age
inferredcites →https://doi.org/10.1128/jb.180.17.4344-4349.1998openalex-snapshot
Identification of Genes Encoding Conjugated Bile Salt Hydrolase and Transport in Lactobacillus johnsonii 100-100
inferredcites →https://doi.org/10.1128/mbio.01493-18openalex-snapshot
Disentangling Host-Microbiota Regulation of Lipid Secretion by Enterocytes: Insights from Commensals Lactobacillus paracasei and Escherichia coli
inferredcites →https://doi.org/10.1128/msphere.00126-19openalex-snapshot
Spatial and Temporal Analysis of the Stomach and Small-Intestinal Microbiota in Fasted Healthy Humans
inferredcites →https://doi.org/10.1128/msystems.00407-19openalex-snapshot
Rapid and Concomitant Gut Microbiota and Endocannabinoidome Response to Diet-Induced Obesity in Mice
inferredcites →https://doi.org/10.1136/gut.14.7.513openalex-snapshot
Postprandial concentrations of free and conjugated bile acids down the length of the normal human small intestine
inferredcites →https://doi.org/10.1136/gut.21.9.793openalex-snapshot
Role of anaerobic bacteria in the metabolic welfare of the colonic mucosa in man.
inferredcites →https://doi.org/10.1146/annurev-immunol-071219-125715openalex-snapshot
Microbiota Metabolites in Health and Disease
inferredcites →https://doi.org/10.1146/annurev-nutr-011720-122203openalex-snapshot
Short Bowel Syndrome: A Paradigm for Intestinal Adaptation to Nutrition?
inferredcites →https://doi.org/10.1152/ajpgi.00017.2016openalex-snapshot
Insights into the pathogenesis of ulcerative colitis from a murine model of stasis-induced dysbiosis, colonic metaplasia, and genetic susceptibility
inferredcites →https://doi.org/10.1152/ajpgi.00046.2013openalex-snapshot
Studies of mucus in mouse stomach, small intestine, and colon. I. Gastrointestinal mucus layers have different properties depending on location as well as over the Peyer's patches
inferredcites →https://doi.org/10.1152/ajpgi.2001.280.5.g922openalex-snapshot
The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo
inferredcites →https://doi.org/10.1152/physrev.00045.2009openalex-snapshot
Gut Microbiota in Health and Disease
inferredcites →https://doi.org/10.1155/2017/9474896openalex-snapshot
High Fat Diet Alters Gut Microbiota and the Expression of Paneth Cell-Antimicrobial Peptides Preceding Changes of Circulating Inflammatory Cytokines
inferredcites →https://doi.org/10.1159/000364794openalex-snapshot
The Pathophysiology of Malabsorption
inferredcites →https://doi.org/10.1177/026119299502300205openalex-snapshot
A Multicompartmental Dynamic Computer-controlled Model Simulating the Stomach and Small Intestine
inferredcites →https://doi.org/10.1177/0884533613485882openalex-snapshot
Diagnosis and Management of Small Intestinal Bacterial Overgrowth
inferredcites →https://doi.org/10.1186/1755-8794-1-14openalex-snapshot
The role of the small intestine in the development of dietary fat-induced obesity and insulin resistance in C57BL/6J mice
inferredcites →https://doi.org/10.1186/s12866-017-1059-6openalex-snapshot
The human jejunum has an endogenous microbiota that differs from those in the oral cavity and colon
inferredcites →https://doi.org/10.1194/jlr.m046029openalex-snapshot
The role of lipolysis in human orosensory fat perception
inferredcites →https://doi.org/10.1194/jlr.m600283-jlr200openalex-snapshot
Chronic high-fat diet affects intestinal fat absorption and postprandial triglyceride levels in the mouse
inferredcites →https://doi.org/10.12938/bmfh.18-027openalex-snapshot
High-fat diet reduces the level of secretory immunoglobulin A coating of commensal gut microbiota
inferredcites →https://doi.org/10.1371/journal.pone.0074957openalex-snapshot
Bacterial Community Mapping of the Mouse Gastrointestinal Tract
inferredcites →https://doi.org/10.20524/aog.2018.0239openalex-snapshot
Role of bile acids in inflammatory bowel disease
inferredcites →https://doi.org/10.2337/db06-1491openalex-snapshot
Metabolic Endotoxemia Initiates Obesity and Insulin Resistance
inferredcites →https://doi.org/10.2337/db13-0035openalex-snapshot
Overnutrition Stimulates Intestinal Epithelium Proliferation Through β-Catenin Signaling in Obese Mice
inferredcites →https://doi.org/10.3109/00365521.2014.898326openalex-snapshot
Surface area of the digestive tract – revisited
inferredcites →https://doi.org/10.3389/fcimb.2020.00151openalex-snapshot
Current Sampling Methods for Gut Microbiota: A Call for More Precise Devices
inferredcites →https://doi.org/10.3389/fendo.2017.00047openalex-snapshot
Cholecystokinin—From Local Gut Hormone to Ubiquitous Messenger
inferredcites →https://doi.org/10.3389/fimmu.2013.00185openalex-snapshot
Multi-Faceted Functions of Secretory IgA at Mucosal Surfaces
inferredcites →https://doi.org/10.3389/fmicb.2018.00151openalex-snapshot
Gut Microbiota: An Integral Moderator in Health and Disease
inferredcites →https://doi.org/10.3389/fphys.2018.01584openalex-snapshot
Intestinal in vitro and ex vivo Models to Study Host-Microbiome Interactions and Acute Stressors
inferredcites →https://doi.org/10.3389/fphys.2020.00797openalex-snapshot
Selective Regional Alteration of the Gut Microbiota by Diet and Antibiotics
inferredcites →https://doi.org/10.3390/jcm8122227openalex-snapshot
The Role of the Gut Microbiota in Lipid and Lipoprotein Metabolism

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4670255openalex-extracted
The Digestion Profiles of Lipids with Different Unsaturated Levels Under the Treatment of Different Intestinal Microbiota
inferred← citeshttps://doi.org/10.1002/mnfr.202300535openalex-snapshot
Novel Lauric Acid‐Butyric Structural Lipid Inhibits Inflammation: Small Intestinal Microbes May Be Important Mediators
inferred← citeshttps://doi.org/10.1007/978-981-19-4492-5_2openalex-snapshot
Gut Microbiome in Health and Gastrointestinal Cancer
inferred← citeshttps://doi.org/10.1007/978-981-96-5099-6_3openalex-snapshot
Implications of Metabolic and Bariatric Operations on Nutrient Absorption
inferred← citeshttps://doi.org/10.1007/s00068-026-03145-0openalex-snapshot
Multifaceted intestinal defense following experimental blunt abdominal trauma
inferred← citeshttps://doi.org/10.1007/s11306-025-02288-2openalex-snapshot
Untargeted and semi-targeted metabolomics approach for profiling small intestinal and fecal metabolome using high-resolution mass spectrometry
inferred← citeshttps://doi.org/10.1007/s11695-022-06401-5openalex-snapshot
Efficacy and Safety of One Anastomosis Gastric Bypass Versus Roux-en-Y Gastric Bypass for Obesity: a Meta-analysis and Systematic Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-823371-9.00006-xopenalex-snapshot
Dietary oxidized lipids
inferred← citeshttps://doi.org/10.1016/b978-0-443-13195-0.00018-1openalex-snapshot
Gut microbiota and diabetes: Exploring the intricate connection
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2021.737655openalex-snapshot
The effects of different lipid sources on the growth, intestinal health, and lipid metabolism of the pacific white shrimp (Litopenaeus vannamei)
inferred← citeshttps://doi.org/10.1016/j.bbalip.2022.159154openalex-snapshot
Postprandial consequences of lipid absorption in the onset of obesity: Role of intestinal CD36
inferred← citeshttps://doi.org/10.1016/j.fbio.2023.102944openalex-snapshot
Butyric-lauric acid structural lipid relieves liver inflammation and small intestinal microbial disturbance: In obese male C57BL/6 mice
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.104158openalex-snapshot
The digestion profiles of lipids with different unsaturated levels under the treatment of different intestinal bacteria
inferred← citeshttps://doi.org/10.1016/j.foodres.2022.112143openalex-snapshot
Bioaccessibility and uptake/epithelial transport of vitamin E: Discoveries and challenges of in vitro and ex vivo assays
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.116207openalex-snapshot
Fu brick tea supplementation ameliorates non-alcoholic fatty liver disease and associated endotoxemia via maintaining intestinal homeostasis and remodeling hepatic immune microenvironment
inferred← citeshttps://doi.org/10.1016/j.foodres.2026.120049openalex-snapshot
High-fat diet primes vulnerability to polyethylene terephthalate nanoplastic toxicity via the gut microbiota-metabolism axis
inferred← citeshttps://doi.org/10.1016/j.gastha.2022.11.008openalex-snapshot
AGA-PancreasFest Joint Symposium on Exocrine Pancreatic Insufficiency
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e22116openalex-snapshot
Alterations of ileal mucosa-associated microbiota in hypercholesterolemia patients
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.141543openalex-snapshot
Oat β-glucan prevents high fat diet induced obesity by targeting ileal Farnesoid X receptor-fibroblast growth factor 15 signaling
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2022.04.009openalex-snapshot
A Planar Culture Model of Human Absorptive Enterocytes Reveals Metformin Increases Fatty Acid Oxidation and Export
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118904openalex-snapshot
Renalase is localized to the small intestine crypt and expressed upon the activation of NF-κB p65 in mice model of fasting-induced oxidative stress
inferred← citeshttps://doi.org/10.1016/j.micres.2025.128053openalex-snapshot
Akkermansia muciniphila inhibits jejunal lipid absorption and regulates jejunal core bacteria
inferred← citeshttps://doi.org/10.1016/j.molmet.2024.101958openalex-snapshot
A novel fatty acid mimetic with pan-PPAR partial agonist activity inhibits diet-induced obesity and metabolic dysfunction-associated steatotic liver disease
inferred← citeshttps://doi.org/10.1016/j.nfs.2025.100213openalex-snapshot
Development of an in vitro triculture model of intestine inflammation to assess the immunomodulatory properties of cassava and roselle, two African green leafy vegetables
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105067openalex-snapshot
From gut microbiota to host genes: A dual-regulatory pathway driving body weight variation in dagu chicken (Gallus gallus domesticus)
inferred← citeshttps://doi.org/10.1016/j.psj.2025.106212openalex-snapshot
The impact of embryonic thermal manipulation on the microbiome of the jejunum and cecum in response to post-hatch acute heat stress
inferred← citeshttps://doi.org/10.1016/j.tifs.2022.05.017openalex-snapshot
Glycerol monolaurate beyond an emulsifier: Synthesis, in vivo fate, food quality benefits and health efficacies
inferred← citeshttps://doi.org/10.1016/j.tim.2024.02.013openalex-snapshot
Small intestinal microbiota: from taxonomic composition to metabolism
inferred← citeshttps://doi.org/10.1016/j.tjnut.2024.03.001openalex-snapshot
Dietary α-Ketoglutarate Alleviates Escherichia coli LPS-Induced Intestinal Barrier Injury by Modulating the Endoplasmic Reticulum-Mitochondrial System Pathway in Piglets
inferred← citeshttps://doi.org/10.1038/s41467-022-35579-6openalex-snapshot
Chemical reaction-mediated covalent localization of bacteria
inferred← citeshttps://doi.org/10.1038/s41598-022-05723-9openalex-snapshot
Investigating the human jejunal microbiota
inferred← citeshttps://doi.org/10.1038/s41598-023-33522-3openalex-snapshot
Music-based interventions in the feeding environment on the gut microbiota of mice
inferred← citeshttps://doi.org/10.1039/d4fo00991fopenalex-snapshot
In vivo evaluations of Lactobacillus -fermented Eucheuma spinosum polysaccharides on alleviating food allergy activity
inferred← citeshttps://doi.org/10.1080/10408398.2024.2382942openalex-snapshot
Functional foods lipids: unraveling their role in the immune response in obesity
inferred← citeshttps://doi.org/10.1080/10408398.2024.2434961openalex-snapshot
Site-specific impact of polyphenols on the gastrointestinal microbiome
inferred← citeshttps://doi.org/10.1080/1745039x.2023.2202591openalex-snapshot
Combination of emulsifier and xylanase in triticale-based broiler chickens diets
inferred← citeshttps://doi.org/10.1080/19490976.2025.2540483openalex-snapshot
Portal bile acid composition and microbiota along the murine intestinal tract exhibit sex differences in physiology
inferred← citeshttps://doi.org/10.1093/femsre/fuad022openalex-snapshot
The small intestine: dining table of host–microbiota meetings
inferred← citeshttps://doi.org/10.1093/femsre/fuag016openalex-snapshot
Small intestinal microbiome, the underrated maestro of SIMO disease
inferred← citeshttps://doi.org/10.1093/ismeco/ycaf224openalex-snapshot
Exploring the human small intestinal luminal microbiome via a newly developed ingestible sampling device
inferred← citeshttps://doi.org/10.1101/2022.01.24.477515openalex-snapshot
Transcriptomics informs design of a planar human enterocyte culture system that reveals metformin enhances fatty acid export
inferred← citeshttps://doi.org/10.1101/2025.04.18.25326056openalex-snapshot
Profiling the human luminal small intestinal microbiome using a novel ingestible medical device
inferred← citeshttps://doi.org/10.1136/gutjnl-2021-326789openalex-snapshot
Gut microbiome and health: mechanistic insights
inferred← citeshttps://doi.org/10.1136/gutjnl-2024-332602openalex-snapshot
Multiomics of the intestine-liver-adipose axis in multiple studies unveils a consistent link of the gut microbiota and the antiviral response with systemic glucose metabolism
inferred← citeshttps://doi.org/10.1186/s13071-022-05340-5openalex-snapshot
Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis
inferred← citeshttps://doi.org/10.1186/s13578-025-01385-yopenalex-snapshot
Distribution of gut microbiota across intestinal segments and their impact on human physiological and pathological processes
inferred← citeshttps://doi.org/10.1186/s40168-023-01468-3openalex-snapshot
Core-predominant gut fungus Kazachstania slooffiae promotes intestinal epithelial glycolysis via lysine desuccinylation in pigs
inferred← citeshttps://doi.org/10.1186/s42523-021-00117-0openalex-snapshot
Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.1242/dev.202529openalex-snapshot
RFX6 regulates human intestinal patterning and function upstream of PDX1
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1638131/v1openalex-snapshot
Copper sulfate and cupric citrate supplementation improves growth performance, nutrient utilization, antioxidant capacity and intestinal microbiota of broilers
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3103766/v1openalex-snapshot
Copper sulfate and cupric citrate supplementation improves growth performance, nutrient utilization, antioxidant capacity and intestinal microbiota of broilers Cupric citrate addition on performance in broilers
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7956394/v1openalex-snapshot
Inhibition of oxygen-mediated opportunistic bacteria overgrowth in the ileum alleviates excessive fatty acid absorption against a high-fat diet
inferred← citeshttps://doi.org/10.2147/ijgm.s399812openalex-snapshot
Small Intestinal Bacterial Overgrowth in Patients with Gallbladder Polyps: A Cross-Sectional Study
inferred← citeshttps://doi.org/10.2147/jir.s530054openalex-snapshot
Multiple Roles of Palmitic Acid in Cardiovascular Diseases
inferred← citeshttps://doi.org/10.23889/suthesis.66312openalex-snapshot
Controlling the Public and Animal Health Threat from Campylobacter Infection in Broiler Chickens by Improving Gut Health and Reducing Inflammation
inferred← citeshttps://doi.org/10.31146/1682-8658-ecg-211-3-61-68openalex-snapshot
Videocapsular endoscopy in the diagnosis of gastrointestinal diseases
inferred← citeshttps://doi.org/10.31146/1682-8658-ecg-213-5-92-99openalex-snapshot
Clinical significance of capsule endoscopy in the study of the functional state and endoscopic anatomy of the gastroduodenal junction
inferred← citeshttps://doi.org/10.33545/26174693.2025.v9.i8sc.5116openalex-snapshot
Microscopic and micrometric analysis of jejunal development in Japanese quail
inferred← citeshttps://doi.org/10.3389/fcell.2022.983031openalex-snapshot
The phenotype of the gut region is more stably retained than developmental stage in piglet intestinal organoids
inferred← citeshttps://doi.org/10.3389/fendo.2022.795371openalex-snapshot
Perturbation on gut microbiota impedes the onset of obesity in high fat diet-induced mice
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1242242openalex-snapshot
Diversity of the microbiota communities found in the various regions of the intestinal tract in healthy individuals and inflammatory bowel diseases
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1536694openalex-snapshot
Transcriptomics and microbiome insights reveal the protective mechanism of mulberry-derived postbiotics against inflammation in LPS-induced mice
inferred← citeshttps://doi.org/10.3389/fmicb.2021.710940openalex-snapshot
Mucosa-Associated Microbial Profile Is Altered in Small Intestinal Bacterial Overgrowth
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1051200openalex-snapshot
Characteristics of intestinal microbiota in C57BL/6 mice with non-alcoholic fatty liver induced by high-fat diet
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1065668openalex-snapshot
Gut microbiota contributes to the methionine metabolism in host
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1441143openalex-snapshot
Different lysine-to-methionine ratios in a low-protein diet affect the microbiome and metabolome, influencing the jejunal barrier function in Tibetan sheep
inferred← citeshttps://doi.org/10.3389/fnut.2021.806646openalex-snapshot
Gastrointestinal Tract and Dietary Fiber Driven Alterations of Gut Microbiota and Metabolites in Durco × Bamei Crossbred Pigs
inferred← citeshttps://doi.org/10.3389/fvets.2024.1436282openalex-snapshot
Effects of taurine on the growth performance, diarrhea, oxidative stress and intestinal barrier function of weanling piglets
inferred← citeshttps://doi.org/10.3389/fvets.2026.1772556openalex-snapshot
Comparative analysis of jejunal morphology, antioxidant capacity and barrier function between Dahe pigs and Dahe black pigs
inferred← citeshttps://doi.org/10.3390/ani13060976openalex-snapshot
Bovine Colostrum Supplementation Modulates the Intestinal Microbial Community in Rabbits
inferred← citeshttps://doi.org/10.3390/ani15050753openalex-snapshot
Gut Metagenome Reveals the Microbiome Signatures in Tibetan and Black Pigs
inferred← citeshttps://doi.org/10.3390/antiox14101145openalex-snapshot
Shikimic Acid Mitigates Deoxynivalenol-Induced Jejunal Barrier Injury in Mice via Activation of the Nrf-2/HO-1/NQO1 Pathway and Modulation of Gut Microbiota
inferred← citeshttps://doi.org/10.3390/foods13121794openalex-snapshot
Silicon as a Functional Meat Ingredient Improves Jejunal and Hepatic Cholesterol Homeostasis in a Late-Stage Type 2 Diabetes Mellitus Rat Model
inferred← citeshttps://doi.org/10.3390/life15111764openalex-snapshot
The Vicious Circle of Metabolic Dysfunction-Associated Steatotic Liver Disease When Micronutrient Deficiency Drives Microbial Imbalance and Liver Injury
inferred← citeshttps://doi.org/10.3390/parasitologia1040024openalex-snapshot
Infection with Leishmania (Leishmania) infantum Changes the Morphology and Myenteric Neurons of the Jejunum of Golden Hamsters
inferred← citeshttps://doi.org/10.3390/vaccines11030595openalex-snapshot
The Development of Gut Microbiota and Its Changes Following C. jejuni Infection in Broilers
inferred← citeshttps://doi.org/10.4081/ejh.2021.3310openalex-snapshot
Distribution of α-synuclein in normal human jejunum and its relations with the chemosensory and neuroendocrine system
inferred← citeshttps://doi.org/10.5414/alx02400eopenalex-snapshot
Vegan diets from an allergy point of view – Position paper of the DGAKI working group on food allergy
inferred← citeshttps://doi.org/10.5713/ab.24.0382openalex-snapshot
Cupric citrate supplementation improves growth performance, nutrient utilization, antioxidant capacity, and intestinal microbiota of broilers
inferred← citeshttps://doi.org/10.6084/m9.figshare.15178460openalex-snapshot
Additional file 1 of Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.6084/m9.figshare.15178463openalex-snapshot
Additional file 2 of Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.6084/m9.figshare.15178466openalex-snapshot
Additional file 3 of Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.6084/m9.figshare.15178469openalex-snapshot
Additional file 4 of Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.6084/m9.figshare.15178472openalex-snapshot
Additional file 5 of Gut microbiome is affected by gut region but robust to host physiological changes in captive active-season ground squirrels
inferred← citeshttps://doi.org/10.70675/5e2f8221z1d95z45acz9e89z3bc81dc0ad9aopenalex-snapshot
Prévention de l’inflammation chronique associée aux cancers intestinaux par l’action du TGF-β sur les lymphocytes T RORγtpos
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.