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Systematic review: bile acids and intestinal inflammation‐luminal aggressors or regulators of mucosal defence?
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bjs.1800570710openalex-snapshot
Experimental gastric ulcers in the rat: The separate and combined effects of vagotomy and bile-duct implantation into the stomach
inferredcites →https://doi.org/10.1002/bjs.1800631011openalex-snapshot
Endotoxin, bile salts and renal function in obstructive jaundice
inferredcites →https://doi.org/10.1002/bjs.1800780425openalex-snapshot
Prevention of postoperative renal dysfunction in patients with obstructive jaundice: A multicentre study of bile salts and lactulose
inferredcites →https://doi.org/10.1002/bjs.1800820514openalex-snapshot
Bile acid absorption from ileoanal pouches using enema scintigraphy
inferredcites →https://doi.org/10.1002/hep.1840040416openalex-snapshot
Influence of Hydroxylation and Conjugation of Bile Salts on Their Membrane-Damaging Properties-Studies on Isolated Hepatocytes and Lipid Membrane Vesicles†
inferredcites →https://doi.org/10.1002/hep.22789openalex-snapshot
Bile acids: Trying to understand their chemistry and biology with the hope of helping patients #
inferredcites →https://doi.org/10.1002/hep.24525openalex-snapshot
The G-Protein-coupled bile acid receptor, Gpbar1 (TGR5), negatively regulates hepatic inflammatory response through antagonizing nuclear factor kappa light-chain enhancer of activated B cells (NF-κB) in mice
inferredcites →https://doi.org/10.1002/hep.510230616openalex-snapshot
Biochemical Epidemiology of Gallbladder Cancer
inferredcites →https://doi.org/10.1002/ibd.20736openalex-snapshot
Lactobacillus casei downregulates commensalsʼ inflammatory signals in Crohnʼs disease mucosa
inferredcites →https://doi.org/10.1002/ibd.21339openalex-snapshot
Disease phenotype and genotype are associated with shifts in intestinal-associated microbiota in inflammatory bowel diseases
inferredcites →https://doi.org/10.1002/ibd.21562openalex-snapshot
Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease
inferredcites →https://doi.org/10.1002/ibd.21585openalex-snapshot
Prevalence and epidemiology of overweight and obesity in children with inflammatory bowel disease 12
inferredcites →https://doi.org/10.1002/ibd.22966openalex-snapshot
Associations Between Vitamin D Receptor Polymorphisms and Susceptibility to Ulcerative Colitis and Crohnʼs Disease
inferredcites →https://doi.org/10.1002/jcp.1040670117openalex-snapshot
The effect of bile salts on oxygen consumption, oxidative phosphorylation and ATP‐ase activity of mucosal homogenates from rat Jejunum and Ileum
inferredcites →https://doi.org/10.1007/bf01536791openalex-snapshot
Bile acids reversible effects on small intestinal permeability
inferredcites →https://doi.org/10.1007/bf01540406openalex-snapshot
Bile salt-induced increases in duodenal brush-border membrane proton permeability, fluidity, and fragility
inferredcites →https://doi.org/10.1007/bf02010727openalex-snapshot
Gastrointestinal ulcerations induced by anti-inflammatory drugs in rats
inferredcites →https://doi.org/10.1007/s00018-008-7568-6openalex-snapshot
Bile Acids: Chemistry, Pathochemistry, Biology, Pathobiology, and Therapeutics
inferredcites →https://doi.org/10.1016/0005-2736(85)90072-0openalex-snapshot
Bile salt damage of egg phosphatidylcholine liposomes
inferredcites →https://doi.org/10.1016/0006-2952(75)90450-5openalex-snapshot
Enterohepatic circulation of indomethacin and its role in intestinal irritation
inferredcites →https://doi.org/10.1016/0016-5085(82)90177-9openalex-snapshot
Role of Food in Gastrointestinal Ulceration Produced by Indomethacin in the Rat
inferredcites →https://doi.org/10.1016/0016-5085(87)90909-7openalex-snapshot
Nonsteroidal antiinflammatory drug-induced intestinal inflammation in humans
inferredcites →https://doi.org/10.1016/0016-5085(95)90599-5openalex-snapshot
Experimental models of inflammatory bowel disease
inferredcites →https://doi.org/10.1016/0041-008x(70)90036-0openalex-snapshot
Indomethacin-induced intestinal lesions in the rat
inferredcites →https://doi.org/10.1016/1357-2725(95)00125-5openalex-snapshot
Bile acid-induced alterations of mucin production in differentiated human colon cancer cell lines
inferredcites →https://doi.org/10.1016/j.bbadis.2011.04.005openalex-snapshot
Activation of bile salt nuclear receptor FXR is repressed by pro-inflammatory cytokines activating NF-κB signaling in the intestine
inferredcites →https://doi.org/10.1016/j.biochi.2012.09.004openalex-snapshot
Shotgun cholanomics of ileal fluid
inferredcites →https://doi.org/10.1016/j.cgh.2009.04.024openalex-snapshot
A New Mechanism for Bile Acid Diarrhea: Defective Feedback Inhibition of Bile Acid Biosynthesis
inferredcites →https://doi.org/10.1016/j.cgh.2013.07.001openalex-snapshot
Intestinal Permeability Defects: Is It Time to Treat?
inferredcites →https://doi.org/10.1016/j.chom.2014.02.005openalex-snapshot
The Treatment-Naive Microbiome in New-Onset Crohn’s Disease
inferredcites →https://doi.org/10.1016/j.clinre.2011.10.007openalex-snapshot
PSC, AIH and overlap syndrome in inflammatory bowel disease
inferredcites →https://doi.org/10.1016/j.clnu.2012.02.009openalex-snapshot
Intestinal permeability parameters in obese patients are correlated with metabolic syndrome risk factors
inferredcites →https://doi.org/10.1016/j.cmet.2011.11.006openalex-snapshot
TGR5 Activation Inhibits Atherosclerosis by Reducing Macrophage Inflammation and Lipid Loading
inferredcites →https://doi.org/10.1016/j.cmet.2013.01.003openalex-snapshot
Gut Microbiota Regulates Bile Acid Metabolism by Reducing the Levels of Tauro-beta-muricholic Acid, a Naturally Occurring FXR Antagonist
inferredcites →https://doi.org/10.1016/j.dld.2013.10.021openalex-snapshot
The bile acid TGR5 membrane receptor: From basic research to clinical application
inferredcites →https://doi.org/10.1016/j.ejps.2014.01.007openalex-snapshot
Pregnane X receptor agonists enhance intestinal epithelial wound healing and repair of the intestinal barrier following the induction of experimental colitis
inferredcites →https://doi.org/10.1016/j.jamcollsurg.2004.01.019openalex-snapshot
Bile salts affect epithelial restitution
inferredcites →https://doi.org/10.1016/j.jhep.2013.01.003openalex-snapshot
Modulation of the fecal bile acid profile by gut microbiota in cirrhosis
inferredcites →https://doi.org/10.1016/j.surg.2003.08.025openalex-snapshot
Taurodeoxycholate increases intestinal epithelial cell proliferation through c-myc expression
inferredcites →https://doi.org/10.1016/j.tips.2012.03.003openalex-snapshot
Pregnane X receptor as a target for treatment of inflammatory bowel disorders
inferredcites →https://doi.org/10.1016/s0016-5085(03)80515-2openalex-snapshot
Human ileal bile acid transporter gene ASBT (SLC10A2) is transactivated by the glucocorticoid receptor
inferredcites →https://doi.org/10.1016/s0016-5085(19)32592-2openalex-snapshot
In Vivo Effect of Bile Salts and Cholestyramine on Intestinal Anaerobic Bacteria
inferredcites →https://doi.org/10.1016/s0016-5085(19)33393-1openalex-snapshot
A Controlled Clinical Trial of Cholestyramine in the Treatment of Gastric Ulcer
inferredcites →https://doi.org/10.1016/s0016-5085(19)33593-0openalex-snapshot
Bile Damage to the Gastric Mucosal Barrier: The Influence of pH and Bile Acid Concentration
inferredcites →https://doi.org/10.1016/s0016-5085(19)33602-9openalex-snapshot
Bile Acid inhibition of the intestinal microflora—A function for simple bile acids?
inferredcites →https://doi.org/10.1016/s0016-5085(67)80140-9openalex-snapshot
The Syndrome of Ileal Disease and the Broken Enterohepatic Circulation: Cholerheic Enteropathy
inferredcites →https://doi.org/10.1016/s0016-5085(68)80001-0openalex-snapshot
Destruction of the Gastric Mucosal Barrier by Detergents and Urea
inferredcites →https://doi.org/10.1016/s0016-5085(70)80149-4openalex-snapshot
Relationship of the Enterohepatic Cycle to Ulcerogenesis in the Rat Small Bowel with Flufenamic Acid
inferredcites →https://doi.org/10.1016/s0016-5085(75)80133-8openalex-snapshot
Failure of Cholestyramine to Prevent Bile Salt Injury to Mouse Gastric Mucosa
inferredcites →https://doi.org/10.1016/s0016-5085(83)80167-xopenalex-snapshot
Evaluation of Ileal Function Using 23-Selena-25-Homotaurocholate, a γ-Labeled Conjugated Bile Acid
inferredcites →https://doi.org/10.1016/s0016-5085(98)70026-5openalex-snapshot
Diclofenac acyl glucuronide, a major biliary metabolite, is directly involved in small intestinal injury in rats
inferredcites →https://doi.org/10.1016/s0022-2143(96)90166-3openalex-snapshot
Tauroursodeoxycholic acid protects in vitro models of human colonic cancer cells from cytotoxic effects of hydrophobic bile acids
inferredcites →https://doi.org/10.1016/s0140-6736(73)90131-1openalex-snapshot
ROLE OF THE COLON IN ILEAL-RESECTION DIARRHŒA
inferredcites →https://doi.org/10.1016/s1072-7515(03)00720-8openalex-snapshot
Bile salts regulate intestinal epithelial cell migration by nuclear factor–κB–induced expression of transforming growth factor–β
inferredcites →https://doi.org/10.1023/a:1026644418142openalex-snapshot
Bile Acid Concentrations, Cytotoxicity, and pH of Fecal Water from Patients with Colorectal Adenomas
inferredcites →https://doi.org/10.1023/b:ddas.0000043365.39251.6eopenalex-snapshot
Ursodeoxycholic Acid Ameliorates Experimental Ileitis Counteracting Intestinal Barrier Dysfunction and Oxidative Stress
inferredcites →https://doi.org/10.1038/ijo.2012.38openalex-snapshot
Faecal calprotectin levels before and after weight loss in obese and overweight subjects
inferredcites →https://doi.org/10.1038/nature08529openalex-snapshot
Uptake through glycoprotein 2 of FimH+ bacteria by M cells initiates mucosal immune response
inferredcites →https://doi.org/10.1038/nature11225openalex-snapshot
Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10−/− mice
inferredcites →https://doi.org/10.1038/nature12331openalex-snapshot
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota
inferredcites →https://doi.org/10.1038/nature13135openalex-snapshot
FXR is a molecular target for the effects of vertical sleeve gastrectomy
inferredcites →https://doi.org/10.1038/nature13828openalex-snapshot
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile
inferredcites →https://doi.org/10.1038/nature14232openalex-snapshot
Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome
inferredcites →https://doi.org/10.1038/ncb1500openalex-snapshot
Maintenance of colonic homeostasis by distinctive apical TLR9 signalling in intestinal epithelial cells
inferredcites →https://doi.org/10.1038/ncomms5573openalex-snapshot
PPARα-UGT axis activation represses intestinal FXR-FGF15 feedback signalling and exacerbates experimental colitis
inferredcites →https://doi.org/10.1038/nrgastro.2013.151openalex-snapshot
Bile acid receptors as targets for drug development
inferredcites →https://doi.org/10.1038/nri2448openalex-snapshot
Exploring the full spectrum of macrophage activation
inferredcites →https://doi.org/10.1038/nrmicro2164openalex-snapshot
Clostridium difficile infection: new developments in epidemiology and pathogenesis
inferredcites →https://doi.org/10.1042/0264-6021:3560481openalex-snapshot
Bile acid hydrophobicity is correlated with induction of apoptosis and/or growth arrest in HCT116 cells
inferredcites →https://doi.org/10.1046/j.1365-2036.1999.00665.xopenalex-snapshot
Ursodeoxycholic acid has no influence on function after restorative proctocolectomy in ulcerative colitis
inferredcites →https://doi.org/10.1046/j.1365-2036.2003.01529.xopenalex-snapshot
Bile composition in inflammatory bowel disease: ileal disease and colectomy, but not colitis, induce lithogenic bile
inferredcites →https://doi.org/10.1053/gast.2002.33647openalex-snapshot
COX-1 and 2, intestinal integrity, and pathogenesis of nonsteroidal anti-inflammatory drug enteropathy in mice
inferredcites →https://doi.org/10.1053/gast.2002.37055openalex-snapshot
Inflammatory-mediated repression of the rat ileal sodium-dependent bile acid transporter by c-fos nuclear translocation
inferredcites →https://doi.org/10.1053/j.gastro.2004.04.061openalex-snapshot
High prevalence of adherent-invasive Escherichia coli associated with ileal mucosa in Crohn’s disease
inferredcites →https://doi.org/10.1053/j.gastro.2005.07.060openalex-snapshot
Inhibition of Hydrogen Sulfide Generation Contributes to Gastric Injury Caused by Anti-Inflammatory Nonsteroidal Drugs
inferredcites →https://doi.org/10.1053/j.gastro.2006.05.002openalex-snapshot
c-Fos Is a Critical Mediator of Inflammatory-Mediated Repression of the Apical Sodium-Dependent Bile Acid Transporter
inferredcites →https://doi.org/10.1054/clnu.2001.0503openalex-snapshot
Crohn's disease clinical course and severity in obese patients
inferredcites →https://doi.org/10.1056/nejmoa013136openalex-snapshot
Epidermal Growth Factor Enemas with Oral Mesalamine for Mild-to-Moderate Left-Sided Ulcerative Colitis or Proctitis
inferredcites →https://doi.org/10.1073/pnas.0509592103openalex-snapshot
Regulation of antibacterial defense in the small intestine by the nuclear bile acid receptor
inferredcites →https://doi.org/10.1073/pnas.0808700106openalex-snapshot
Failure of T cell homing, reduced CD4/CD8αα intraepithelial lymphocytes, and inflammation in the gut of vitamin D receptor KO mice
inferredcites →https://doi.org/10.1080/003655201750153430openalex-snapshot
Hydrophilic and Hydrophobic Bile Acids Exhibit Different Cytotoxicities Through Cytolysis, Interleukin-8 Synthesis and Apoptosis in the Intestinal Epithelial Cell Lines. IEC-6 and Caco-2 cells
inferredcites →https://doi.org/10.1080/00365520701320463openalex-snapshot
Dihydroxy bile acids increase mucosal permeability and bacterial uptake in human colon biopsies
inferredcites →https://doi.org/10.1080/01635589809514689openalex-snapshot
Different bile acids exhibit distinct biological effects: The tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation
inferredcites →https://doi.org/10.1081/dmr-200033475openalex-snapshot
Detoxification of Lithocholic Acid, A Toxic Bile Acid: Relevance to Drug Hepatotoxicity
inferredcites →https://doi.org/10.1093/ecco-jcc/jju020openalex-snapshot
Cholestyramine Treats Primary Sclerosing Cholangitis-Associated Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1093/infdis/141.1.92openalex-snapshot
Binding of Clostridium difficile Cytotoxin and Vancomycin by Anion-Exchange Resins
inferredcites →https://doi.org/10.1097/meg.0b013e328306078copenalex-snapshot
Medical management of patients with ileal pouch anal anastomosis after restorative procto-colectomy
inferredcites →https://doi.org/10.1097/mib.0000000000000283openalex-snapshot
Measures of Obesity and Risk of Crohnʼs Disease and Ulcerative Colitis
inferredcites →https://doi.org/10.1097/mog.0000000000000057openalex-snapshot
Bile acids and the gut microbiome
inferredcites →https://doi.org/10.1111/apt.12500openalex-snapshot
Review article: evidence‐based dietary advice for patients with inflammatory bowel disease
inferredcites →https://doi.org/10.1111/apt.12999openalex-snapshot
The response of patients with bile acid diarrhoea to the farnesoid X receptor agonist obeticholic acid
inferredcites →https://doi.org/10.1111/imm.12045openalex-snapshot
TGR 5 signalling inhibits the production of pro‐inflammatory cytokines by in vitro differentiated inflammatory and intestinal macrophages in Crohn's disease
inferredcites →https://doi.org/10.1111/j.1348-0421.1996.tb01108.xopenalex-snapshot
Role of Intestinal Bacteria in Ileal Ulcer Formation in Rats Treated with a Nonsteroidal Antiinflammatory Drug
inferredcites →https://doi.org/10.1111/j.1365-2036.2006.03168.xopenalex-snapshot
Budesonide treatment is associated with increased bile acid absorption in collagenous colitis
inferredcites →https://doi.org/10.1111/j.1365-2036.2011.04611.xopenalex-snapshot
Low levels of bile acids increase bacterial uptake in colonic biopsies from patients with collagenous colitis in remission
inferredcites →https://doi.org/10.1111/j.1365-2362.1982.tb00950.xopenalex-snapshot
Kinetics of primary bile acids in patients with non‐operated Crohn's disease
inferredcites →https://doi.org/10.1111/j.1365-2982.2010.01487.xopenalex-snapshot
Expression and function of the bile acid receptor GpBAR1 (TGR5) in the murine enteric nervous system
inferredcites →https://doi.org/10.1111/j.1462-2920.2012.02824.xopenalex-snapshot
Bile salts induce long polar fimbriae expression favouring Crohn's disease‐associated adherent‐invasive Escherichia coli interaction with Peyer's patches
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00868.xopenalex-snapshot
Adherent-invasive Escherichia coli isolated from Crohn's disease patients induce granulomas in vitro
inferredcites →https://doi.org/10.1111/j.1476-5381.2011.01481.xopenalex-snapshot
Activation of the farnesoid-X receptor protects against gastrointestinal injury caused by non-steroidal anti-inflammatory drugs in mice
inferredcites →https://doi.org/10.1111/j.1476-5381.2012.02128.xopenalex-snapshot
Activation of the bile acid receptor GPBAR 1 protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs and aspirin in mice
inferredcites →https://doi.org/10.1111/j.1478-3231.2011.02677.xopenalex-snapshot
The impact of inflammatory bowel disease post‐liver transplantation for primary sclerosing cholangitis
inferredcites →https://doi.org/10.1111/j.1749-6632.1966.tb52394.xopenalex-snapshot
PHYSICAL ASPECTS OF REVERSIBLE INACTIVATION OF ENDOTOXIN*
inferredcites →https://doi.org/10.1111/j.2042-7158.2011.01406.xopenalex-snapshot
NSAIDs: take with food or after fasting?
inferredcites →https://doi.org/10.1126/science.1070477openalex-snapshot
Vitamin D Receptor As an Intestinal Bile Acid Sensor
inferredcites →https://doi.org/10.1126/science.284.5418.1362openalex-snapshot
Identification of a Nuclear Receptor for Bile Acids
inferredcites →https://doi.org/10.1126/science.284.5418.1365openalex-snapshot
Bile Acids: Natural Ligands for an Orphan Nuclear Receptor
inferredcites →https://doi.org/10.1128/iai.69.9.5529-5537.2001openalex-snapshot
Adherent Invasive Escherichia coli Strains from Patients with Crohn's Disease Survive and Replicate within Macrophages without Inducing Host Cell Death
inferredcites →https://doi.org/10.1128/jb.01260-08openalex-snapshot
Chenodeoxycholate Is an Inhibitor of Clostridium difficile Spore Germination
inferredcites →https://doi.org/10.1128/jb.01765-07openalex-snapshot
Bile Salts and Glycine as Cogerminants for Clostridium difficile Spores
inferredcites →https://doi.org/10.1128/jb.100.1.220-223.1969openalex-snapshot
Effect of Bile Acids on the Intestinal Absorption of Endotoxin in Rats
inferredcites →https://doi.org/10.1128/jcm.15.3.443-446.1982openalex-snapshot
Use of sodium taurocholate to enhance spore recovery on a medium selective for Clostridium difficile
inferredcites →https://doi.org/10.1136/bmj.2.6049.1415openalex-snapshot
Endotoxaemia and renal failure in cirrhosis and obstructive jaundice.
inferredcites →https://doi.org/10.1136/gut.12.8.632openalex-snapshot
The role of bile salts in diarrhoea of patients with ulcerative colitis
inferredcites →https://doi.org/10.1136/gut.18.9.730openalex-snapshot
Bile acid studies in uncomplicated Crohn's disease.
inferredcites →https://doi.org/10.1136/gut.20.12.1072openalex-snapshot
Bile acid studies in patients with Crohn's colitis.
inferredcites →https://doi.org/10.1136/gut.2007.125955openalex-snapshot
Chronic subclinical bowel inflammation may explain increased risk of colorectal cancer in obese people: Figure 1
inferredcites →https://doi.org/10.1136/gut.2010.212159openalex-snapshot
Farnesoid X receptor activation inhibits inflammation and preserves the intestinal barrier in inflammatory bowel disease
inferredcites →https://doi.org/10.1136/gut.22.11.948openalex-snapshot
Ileal dysfunction in Crohn's disease assessed by the postprandial serum bile acid response.
inferredcites →https://doi.org/10.1136/gut.23.9.751openalex-snapshot
Bile acid absorption kinetics in Crohn's disease on elemental diet after oral administration of a stable-isotope tracer with chenodeoxycholic-11, 12-d2 acid.
inferredcites →https://doi.org/10.1136/gut.28.12.1577openalex-snapshot
Healthy controls have as much bile reflux as gastric ulcer patients.
inferredcites →https://doi.org/10.1136/gut.30.spec_no.22openalex-snapshot
Intestinal permeability, non-steroidal anti-inflammatory drug enteropathy and inflammatory bowel disease: an overview.
inferredcites →https://doi.org/10.1136/gut.32.12.1488openalex-snapshot
Effects of ileal resection on biliary lipids and bile acid composition in patients with Crohn's disease.
inferredcites →https://doi.org/10.1136/gut.33.9.1204openalex-snapshot
Metronidazole reduces intestinal inflammation and blood loss in non-steroidal anti-inflammatory drug induced enteropathy.
inferredcites →https://doi.org/10.1136/gut.35.1.90openalex-snapshot
Bile acid malabsorption in Crohn's disease and indications for its assessment using SeHCAT.
inferredcites →https://doi.org/10.1136/gut.38.5.724openalex-snapshot
Pathogenesis of aphthoid ulcers in Crohn's disease: correlative findings by magnifying colonoscopy, electron microscopy, and immunohistochemistry.
inferredcites →https://doi.org/10.1136/gut.41.3.344openalex-snapshot
Mitochondrial damage: a possible mechanism of the “topical” phase of NSAID induced injury to the rat intestine
inferredcites →https://doi.org/10.1136/gut.53.1.78openalex-snapshot
Human ileal bile acid transporter gene ASBT ( SLC10A2 ) is transactivated by the glucocorticoid receptor
inferredcites →https://doi.org/10.1136/gutjnl-2012-302578openalex-snapshot
Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel diseases
inferredcites →https://doi.org/10.1136/gutjnl-2012-304119openalex-snapshot
Western diet induces dysbiosis with increased E coli in CEABAC10 mice , alters host barrier function favouring AIEC colonisation
inferredcites →https://doi.org/10.1136/gutjnl-2013-304739openalex-snapshot
Colonic mucosa-associated diffusely adherent afaC+ Escherichia coli expressing lpfA and pks are increased in inflammatory bowel disease and colon cancer
inferredcites →https://doi.org/10.1152/ajpgi.00043.2007openalex-snapshot
Bile acids modulate tight junction structure and barrier function of Caco-2 monolayers via EGFR activation
inferredcites →https://doi.org/10.1152/ajpgi.00315.2013openalex-snapshot
Colonic inflammation and secondary bile acids in alcoholic cirrhosis
inferredcites →https://doi.org/10.1152/ajpgi.00387.2009openalex-snapshot
Effect of indomethacin on bile acid-phospholipid interactions: implication for small intestinal injury induced by nonsteroidal anti-inflammatory drugs
inferredcites →https://doi.org/10.1152/ajpgi.00398.2007openalex-snapshot
Novel role of the vitamin D receptor in maintaining the integrity of the intestinal mucosal barrier
inferredcites →https://doi.org/10.1152/ajpgi.00528.2006openalex-snapshot
Pregnane X receptor activation ameliorates DSS-induced inflammatory bowel disease via inhibition of NF-κB target gene expression
inferredcites →https://doi.org/10.1152/ajpgi.1997.272.5.g1249openalex-snapshot
Taurochenodeoxycholic acid ameliorates and ursodeoxycholic acid exacerbates small intestinal inflammation
inferredcites →https://doi.org/10.1152/ajpgi.90313.2008openalex-snapshot
Epidermal growth factor receptor is involved in enterocyte anoikis through the dismantling of E-cadherin-mediated junctions
inferredcites →https://doi.org/10.1155/1988/42486openalex-snapshot
Prevention of Endotoxaemia in Obstructive Jaundice — A Comparative Study of Bile Salts
inferredcites →https://doi.org/10.1158/1055-9965.epi-03-0160openalex-snapshot
Bowel Inflammation as Measured by Fecal Calprotectin
inferredcites →https://doi.org/10.1159/000200498openalex-snapshot
Comparison of Bile Salt Perturbation of Duodenal and Jejunal Isolated Brush-Border Membranes
inferredcites →https://doi.org/10.1172/jci105722openalex-snapshot
Bile salt malabsorption in regional ileitis, ileal resection, and mannitol-induced diarrhea
inferredcites →https://doi.org/10.1172/jci44632openalex-snapshot
Crohn disease–associated adherent-invasive E. coli bacteria target mouse and human Peyer’s patches via long polar fimbriae
inferredcites →https://doi.org/10.1172/jci65842openalex-snapshot
Intestinal epithelial vitamin D receptor signaling inhibits experimental colitis
inferredcites →https://doi.org/10.1177/1535370214523890openalex-snapshot
Vitamin D, immune regulation, the microbiota, and inflammatory bowel disease
inferredcites →https://doi.org/10.1186/1756-0500-5-461openalex-snapshot
Association of genetic variation in the NR1H4 gene, encoding the nuclear bile acid receptor FXR, with inflammatory bowel disease
inferredcites →https://doi.org/10.1186/1824-7288-36-66openalex-snapshot
Relationship between severe obesity and gut inflammation in children: what's next?
inferredcites →https://doi.org/10.1186/gb-2012-13-9-r79openalex-snapshot
Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment
inferredcites →https://doi.org/10.1189/jlb.0812396openalex-snapshot
Bile acids PKA-dependently induce a switch of the IL-10/IL-12 ratio and reduce proinflammatory capability of human macrophages
inferredcites →https://doi.org/10.1194/jlr.d047506openalex-snapshot
A simple and accurate HPLC method for fecal bile acid profile in healthy and cirrhotic subjects: validation by GC-MS and LC-MS
inferredcites →https://doi.org/10.1194/jlr.r049437openalex-snapshot
Key discoveries in bile acid chemistry and biology and their clinical applications: history of the last eight decades
inferredcites →https://doi.org/10.1194/jlr.r500013-jlr200openalex-snapshot
Bile salt biotransformations by human intestinal bacteria
inferredcites →https://doi.org/10.1194/jlr.r800026-jlr200openalex-snapshot
Fifty years of advances in bile acid synthesis and metabolism
inferredcites →https://doi.org/10.1210/jc.2012-3736openalex-snapshot
Weight Loss Induced by Roux-en-Y Gastric Bypass But Not Laparoscopic Adjustable Gastric Banding Increases Circulating Bile Acids
inferredcites →https://doi.org/10.1258/acb.2010.010040openalex-snapshot
Postprandial plasma bile acid responses in normal weight and obese subjects
inferredcites →https://doi.org/10.1371/journal.pone.0006386openalex-snapshot
Metabolomics Reveals Metabolic Biomarkers of Crohn's Disease
inferredcites →https://doi.org/10.1371/journal.pone.0016952openalex-snapshot
Characterization of Bacteria in Biopsies of Colon and Stools by High Throughput Sequencing of the V2 Region of Bacterial 16S rRNA Gene in Human
inferredcites →https://doi.org/10.1371/journal.pone.0023745openalex-snapshot
Farnesoid X Receptor (FXR) Activation and FXR Genetic Variation in Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1371/journal.pone.0025637openalex-snapshot
The Bile Acid Receptor GPBAR-1 (TGR5) Modulates Integrity of Intestinal Barrier and Immune Response to Experimental Colitis
inferredcites →https://doi.org/10.1371/journal.pone.0037160openalex-snapshot
Circulating Zonulin, a Marker of Intestinal Permeability, Is Increased in Association with Obesity-Associated Insulin Resistance
inferredcites →https://doi.org/10.1371/journal.pone.0049706openalex-snapshot
Pharmacological Activation of the Bile Acid Nuclear Farnesoid X Receptor Is Feasible in Patients with Quiescent Crohn's Colitis
inferredcites →https://doi.org/10.1371/journal.pone.0054472openalex-snapshot
The Bile Acid Sensor FXR Is Required for Immune-Regulatory Activities of TLR-9 in Intestinal Inflammation
inferredcites →https://doi.org/10.1517/17425255.2012.685237openalex-snapshot
Role of CAR and PXR in xenobiotic sensing and metabolism
inferredcites →https://doi.org/10.3109/00365521.2013.833647openalex-snapshot
Enhanced fasting and post-prandial plasma bile acid responses after Roux-en-Y gastric bypass surgery
inferredcites →https://doi.org/10.3109/00365521.2014.898326openalex-snapshot
Surface area of the digestive tract – revisited
inferredcites →https://doi.org/10.3109/00365528209181058openalex-snapshot
Postprandial Serum Bile Acids in Resected and Non-Resected Patients with Crohn's Disease
inferredcites →https://doi.org/10.3109/00365528309181619openalex-snapshot
Fasting and Postprandial Serum Concentrations of Glycine- and Taurine-Conjugated Bile Acids in Crohn's Disease
inferredcites →https://doi.org/10.3109/00365529509093280openalex-snapshot
Review: The Biochemical Basis of Non-Steroidal Anti-Inflammatory Drug-Induced Damage to the Gastrointestinal Tract: A Review and a Hypothesis
inferredcites →https://doi.org/10.3748/wjg.15.3134openalex-snapshot
Serum bile acid profiling reflects enterohepatic detoxification state and intestinal barrier function in inflammatory bowel disease
inferredcites →https://doi.org/10.4049/jimmunol.0803978openalex-snapshot
The Bile Acid Receptor FXR Is a Modulator of Intestinal Innate Immunity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Gut microbiome dysbiosis is associated with elevated toxic bile acids in Parkinson’s disease
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Review article: the gut microbiome as a therapeutic target in the pathogenesis and treatment of chronic liver disease
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Systematic review: human gut dysbiosis induced by non‐antibiotic prescription medications
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Influence of the bile acid/microbiota axis in ileal surgery: a systematic review
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inferred← citeshttps://doi.org/10.1126/scisignal.adl1786openalex-snapshot
Bile acid–induced metabolic changes in the colon promote Enterobacteriaceae expansion and associate with dysbiosis in Crohn’s disease
inferred← citeshttps://doi.org/10.1126/scitranslmed.abn7491openalex-snapshot
A gut-restricted glutamate carboxypeptidase II inhibitor reduces monocytic inflammation and improves preclinical colitis
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inferred← citeshttps://doi.org/10.1155/2022/8416578openalex-snapshot
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inferred← citeshttps://doi.org/10.1177/2050640617708953openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12866-026-05224-zopenalex-snapshot
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The Current and Future State of Microbiome Therapeutics in Liver Disease
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The Yin and Yang of bile acid action on tight junctions in a model colonic epithelium
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Repression of intestinal transporters and FXR-FGF15 signaling explains bile acids dysregulation in experimental colitis-associated colon cancer
inferred← citeshttps://doi.org/10.2147/dmso.s286430openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/0929867324666170619104105openalex-snapshot
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inferred← citeshttps://doi.org/10.2302/kjm.2020-0006-oaopenalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fcimb.2022.945368openalex-snapshot
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The Role of OmpR in Bile Tolerance and Pathogenesis of Adherent-Invasive Escherichia coli
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Farnesoid-X receptor as a therapeutic target for inflammatory bowel disease and colorectal cancer
inferred← citeshttps://doi.org/10.3389/fphys.2020.00564openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ani11061560openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antiox14010045openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antiox15070856openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biom12070877openalex-snapshot
Reduced Cytokine Tumour Necrosis Factor by Pharmacological Intervention in a Preclinical Study
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inferred← citeshttps://doi.org/10.3390/cells9091949openalex-snapshot
IL-13 as Target to Reduce Cholestasis and Dysbiosis in Abcb4 Knockout Mice
inferred← citeshttps://doi.org/10.3390/cimb45070351openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/diseases12050103openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/diseases8020013openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms22031397openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25021311openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jcm12103368openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jcm12134442openalex-snapshot
Microscopic Colitis: Pathogenesis and Diagnosis
inferred← citeshttps://doi.org/10.3390/jcm14062040openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/life12050723openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/life15071098openalex-snapshot
Non-Celiac Villous Atrophy—A Problem Still Underestimated
inferred← citeshttps://doi.org/10.3390/metabo11010029openalex-snapshot
Gut Microbiota Dysbiosis Is Associated with Elevated Bile Acids in Parkinson’s Disease
inferred← citeshttps://doi.org/10.3390/molecules30020281openalex-snapshot
Comparative Analysis of γ-Cyclodextrin, Perilla Oil, and Their Inclusion Complexes on Liver Injury and Dyslipidemia Associated with Elevated Gastrointestinal 12-Hydroxylated Bile Acid Levels
inferred← citeshttps://doi.org/10.3390/nu10050537openalex-snapshot
Enteral Nutrition in the Management of Pediatric and Adult Crohn’s Disease
inferred← citeshttps://doi.org/10.3390/nu12051434openalex-snapshot
Connecting the Dots Between Inflammatory Bowel Disease and Metabolic Syndrome: A Focus on Gut-Derived Metabolites
inferred← citeshttps://doi.org/10.3390/nu13113818openalex-snapshot
Dietary Fat Effect on the Gut Microbiome, and Its Role in the Modulation of Gastrointestinal Disorders in Children with Autism Spectrum Disorder
inferred← citeshttps://doi.org/10.3390/nu14122522openalex-snapshot
Long-Term Dietary Patterns Are Reflected in the Plasma Inflammatory Proteome of Patients with Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.3410/f.736551116.793573749openalex-snapshot
Faculty Opinions recommendation of Antibiotics-Driven Gut Microbiome Perturbation Alters Immunity to Vaccines in Humans.
inferred← citeshttps://doi.org/10.3748/wjg.v24.i37.4217openalex-snapshot
Focus on the gut-brain axis: Multiple sclerosis, the intestinal barrier and the microbiome
inferred← citeshttps://doi.org/10.3748/wjg.v29.i27.4252openalex-snapshot
Bile acids and their receptors: Potential therapeutic targets in inflammatory bowel disease
inferred← citeshttps://doi.org/10.4414/smw.2016.14293openalex-snapshot
Gastro-intestinal tract: The leading role of mucosal immunity
inferred← citeshttps://doi.org/10.5005/imcr-11021-0014openalex-snapshot
Yoga Therapy as an Add-on Treatment in the Management of Patients with Functional Dyspepsia: A Case Report
inferred← citeshttps://doi.org/10.7759/cureus.47150openalex-snapshot
Microscopic Colitis: A Review Article
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Science and Advanced Computing — runs a structured editorial panel for researchers
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