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Guts and Gall: Bile Acids in Regulation of Intestinal Epithelial Function in Health and Disease
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1 of the 200 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1007/s13277-014-2342-x (notice 2017-04-20).
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Bacteria and the etiology of colonic cancer
inferredcites →https://doi.org/10.1002/1097-0142(197512)36:6<2401::aid-cncr2820360619>3.0.co;2-oopenalex-snapshot
Role of bile metabolites in colon carcinogenesis. Animal models
inferredcites →https://doi.org/10.1002/1097-0142(19820801)50:3<543::aid-cncr2820500326>3.0.co;2-kopenalex-snapshot
Effect of bile acids on 1,2-dimethylhydrazine-induced colon cancer in rats
inferredcites →https://doi.org/10.1002/9781118512074.ch24openalex-snapshot
Electrolyte Secretion and Absorption in the Small Intestine and Colon
inferredcites →https://doi.org/10.1002/bies.201400071openalex-snapshot
Is eating behavior manipulated by the gastrointestinal microbiota? Evolutionary pressures and potential mechanisms
inferredcites →https://doi.org/10.1002/bjs.18003815005openalex-snapshot
Chronic peptic ulcerz of the œophagus and ‘œsophagitis’
inferredcites →https://doi.org/10.1002/cncr.21015openalex-snapshot
Bile acids induce MUC2 overexpression in human colon carcinoma cells
inferredcites →https://doi.org/10.1002/cncr.25796openalex-snapshot
Induction of MUC5AC mucin by conjugated bile acids in the esophagus involves the phosphatidylinositol 3‐kinase/protein kinase C/activator protein‐1 pathway
inferredcites →https://doi.org/10.1002/cncr.27910openalex-snapshot
Inhibition of farnesoid X receptor controls esophageal cancer cell growth in vitro and in nude mouse xenografts
inferredcites →https://doi.org/10.1002/hep.1840040813openalex-snapshot
Effect of Nuclear Hydroxy Substituents on Aqueous Solubility and Acidic Strength of Bile Acids
inferredcites →https://doi.org/10.1002/hep.22627openalex-snapshot
Bile acids activate fibroblast growth factor 19 signaling in human hepatocytes to inhibit cholesterol 7α‐hydroxylase gene expression†
inferredcites →https://doi.org/10.1002/hep.23032openalex-snapshot
The membrane-bound bile acid receptor TGR5 is localized in the epithelium of human gallbladders #
inferredcites →https://doi.org/10.1002/hep.26333openalex-snapshot
Taurolithocholate-induced MRP2 retrieval involves MARCKS phosphorylation by protein kinase Cε in HUH-NTCP Cells
inferredcites →https://doi.org/10.1002/hep.27240openalex-snapshot
Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype
inferredcites →https://doi.org/10.1002/hep.27677openalex-snapshot
Farnesoid X receptor–induced lysine‐specific histone demethylase reduces hepatic bile acid levels and protects the liver against bile acid toxicity
inferredcites →https://doi.org/10.1002/ibd.20109openalex-snapshot
Lipoxins and resolvins in inflammatory bowel disease
inferredcites →https://doi.org/10.1002/ibd.21191openalex-snapshot
Cell death in the colonic epithelium during inflammatory bowel diseases
inferredcites →https://doi.org/10.1002/ijc.26293openalex-snapshot
Expression of the nuclear bile acid receptor/farnesoid X receptor is reduced in human colon carcinoma compared to nonneoplastic mucosa independent from site and may be associated with adverse prognosis
inferredcites →https://doi.org/10.1002/ijc.2910600322openalex-snapshot
Apoptosis in colorectal tumour cells: Induction by the short chain fatty acids butyrate, propionate and acetate and by the bile salt deoxycholate
inferredcites →https://doi.org/10.1002/jcb.24172openalex-snapshot
Inhibition of butyrate uptake by the primary bile salt chenodeoxycholic acid in intestinal epithelial cells
inferredcites →https://doi.org/10.1002/mnfr.201700403openalex-snapshot
Evaluation of the hypocholesterolemic effect and prebiotic activity of a lentil (Lens culinaris Medik) extract
inferredcites →https://doi.org/10.1002/prp2.155openalex-snapshot
Pharmacology and physiology of gastrointestinal enteroendocrine cells
inferredcites →https://doi.org/10.1006/bbrc.2000.2899openalex-snapshot
Bile Acids Reduce the Apoptosis-Inducing Effects of Sodium Butyrate on Human Colon Adenoma (AA/C1) Cells: Implications for Colon Carcinogenesis
inferredcites →https://doi.org/10.1007/978-3-319-20215-0_5openalex-snapshot
Interactions Between Bacteria and the Gut Mucosa: Do Enteric Neurotransmitters Acting on the Mucosal Epithelium Influence Intestinal Colonization or Infection?
inferredcites →https://doi.org/10.1007/978-3-642-14541-4_4openalex-snapshot
Role of the Intestinal Bile Acid Transporters in Bile Acid and Drug Disposition
inferredcites →https://doi.org/10.1007/978-3-662-43492-5_1openalex-snapshot
IL-10 in Humans: Lessons from the Gut, IL-10/IL-10 Receptor Deficiencies, and IL-10 Polymorphisms
inferredcites →https://doi.org/10.1007/bf00580794openalex-snapshot
Influence of osmolality, short chain fatty acids and deoxycholic acid on mucus secretion in the rat colon
inferredcites →https://doi.org/10.1007/bf01395507openalex-snapshot
Dose-related effects of chenodeoxycholic acid in the rabbit colon
inferredcites →https://doi.org/10.1007/bf01536765openalex-snapshot
Modulation of human colonic lamina propria lymphocyte proliferation
inferredcites →https://doi.org/10.1007/bf01560694openalex-snapshot
Prostanoid generation in early stages of acute pancreatitis: A role for nitric oxide
inferredcites →https://doi.org/10.1007/bf02087427openalex-snapshot
Bile salts determine leukotriene B4 synthesis in a human intestinal cell line (CaCo-2)
inferredcites →https://doi.org/10.1007/s00109-013-1106-1openalex-snapshot
Role of macrophages in bile acid-induced inflammatory response of fetal lung during maternal cholestasis
inferredcites →https://doi.org/10.1007/s00134-008-1321-3openalex-snapshot
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration
inferredcites →https://doi.org/10.1007/s00384-004-0616-2openalex-snapshot
Bile salt-induced apoptosis in human colon cancer cell lines involves the mitochondrial transmembrane potential but not the CD95 (Fas/Apo-1) receptor
inferredcites →https://doi.org/10.1007/s00424-013-1364-3openalex-snapshot
FXR-induced secretion of FGF15/19 inhibits CYP27 expression in cholangiocytes through p38 kinase pathway
inferredcites →https://doi.org/10.1007/s00424-014-1560-9openalex-snapshot
Bile acids inhibit Na+/H+ exchanger and Cl−/HCO3 − exchanger activities via cellular energy breakdown and Ca2+ overload in human colonic crypts
inferredcites →https://doi.org/10.1007/s004240050974openalex-snapshot
Deoxycholic acid (DOC) affects the transport properties of distal colon
inferredcites →https://doi.org/10.1007/s00535-013-0833-yopenalex-snapshot
Ursodeoxycholic acid stabilizes the bile salt export pump in the apical membrane in MDCK II cells
inferredcites →https://doi.org/10.1007/s005350300001openalex-snapshot
Aberrant expression of CDX2 in Barrett's epithelium and inflammatory esophageal mucosa
inferredcites →https://doi.org/10.1007/s10495-011-0633-xopenalex-snapshot
Deoxycholic and chenodeoxycholic bile acids induce apoptosis via oxidative stress in human colon adenocarcinoma cells
inferredcites →https://doi.org/10.1007/s10620-006-9090-8openalex-snapshot
Taurodeoxycholate Modulates Apical Cl−/OH− Exchange Activity in Caco2 Cells
inferredcites →https://doi.org/10.1007/s10620-013-2975-4openalex-snapshot
Cyclooxygenase-2 and Inflammation Mediators Have a Crucial Role in Reflux-Related Esophageal Histological Changes and Barrett’s Esophagus
inferredcites →https://doi.org/10.1007/s10620-015-3634-8openalex-snapshot
Transgenic Expression of Vitamin D Receptor in Gut Epithelial Cells Ameliorates Spontaneous Colitis Caused by Interleukin-10 Deficiency
inferredcites →https://doi.org/10.1007/s10620-017-4510-5openalex-snapshot
Epidemiology of Recurrent Acute and Chronic Pancreatitis: Similarities and Differences
inferredcites →https://doi.org/10.1007/s10620-017-4602-2openalex-snapshot
Chronic Pancreatitis: Current Status and Challenges for Prevention and Treatment
inferredcites →https://doi.org/10.1007/s11605-008-0720-7openalex-snapshot
Bile Acid Alone, or in Combination with Acid, Induces CDX2 Expression Through Activation of the Epidermal Growth Factor Receptor (EGFR)
inferredcites →https://doi.org/10.1007/s11605-015-3062-2openalex-snapshot
Bile Salts at Low pH Cause Dilation of Intercellular Spaces in In Vitro Stratified Primary Esophageal Cells, Possibly by Modulating Wnt Signaling
inferredcites →https://doi.org/10.1007/s11894-016-0527-8openalex-snapshot
Nutritional Strategies in the Management of Adult Patients with Inflammatory Bowel Disease: Dietary Considerations from Active Disease to Disease Remission
inferredcites →https://doi.org/10.1007/s12072-015-9656-7openalex-snapshot
Bile acids: emerging role in management of liver diseases
inferredcites →https://doi.org/10.1007/s13277-014-2342-xopenalex-snapshot
MicroRNA-92 promotes gastric cancer cell proliferation and invasion through targeting FXR
inferredcites →https://doi.org/10.1016/0016-5085(79)90292-0openalex-snapshot
Rudolf Schindler, pioneer endoscopist
inferredcites →https://doi.org/10.1016/0016-5085(83)90137-3openalex-snapshot
Effects of small bowel transection, resection, or bypass in 1,2-dimethylhydrazine-induced rat intestinal neoplasia
inferredcites →https://doi.org/10.1016/0016-5085(91)90024-fopenalex-snapshot
Activation of mast cells by bile acids
inferredcites →https://doi.org/10.1016/0016-5085(93)90752-xopenalex-snapshot
Hepatic transport and bile secretion: Physiology and pathophysiology
inferredcites →https://doi.org/10.1016/0092-8674(95)90530-8openalex-snapshot
Identification of a nuclear receptor that is activated by farnesol metabolites
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.acthis.2007.08.001openalex-snapshot
Immunolocalization of farnesoid X receptor (FXR) in mouse tissues using tissue microarray
inferredcites →https://doi.org/10.1016/j.ajpath.2014.10.009openalex-snapshot
The FXR Agonist Obeticholic Acid Prevents Gut Barrier Dysfunction and Bacterial Translocation in Cholestatic Rats
inferredcites →https://doi.org/10.1016/j.bbadis.2010.11.011openalex-snapshot
Regulation of FXR transcriptional activity in health and disease: Emerging roles of FXR cofactors and post-translational modifications
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.bbagen.2016.09.024openalex-snapshot
Molecular features of bile salt hydrolases and relevance in human health
inferredcites →https://doi.org/10.1016/j.bbalip.2005.04.006openalex-snapshot
Bile acid induces hydrophobicity-dependent membrane alterations
inferredcites →https://doi.org/10.1016/j.bbalip.2016.04.006openalex-snapshot
Deoxycholic acid mediates non-canonical EGFR-MAPK activation through the induction of calcium signaling in colon cancer cells
inferredcites →https://doi.org/10.1016/j.bbamem.2013.05.007openalex-snapshot
Progressive stages of mitochondrial destruction caused by cell toxic bile salts
inferredcites →https://doi.org/10.1016/j.bbrc.2005.01.139openalex-snapshot
Bile acids promote glucagon-like peptide-1 secretion through TGR5 in a murine enteroendocrine cell line STC-1
inferredcites →https://doi.org/10.1016/j.bbrc.2006.12.168openalex-snapshot
Involvement of membrane-type bile acid receptor M-BAR/TGR5 in bile acid-induced activation of epidermal growth factor receptor and mitogen-activated protein kinases in gastric carcinoma cells
inferredcites →https://doi.org/10.1016/j.bbrc.2010.08.121openalex-snapshot
Ursodeoxycholic acid modulates the ubiquitin-proteasome degradation pathway of p53
inferredcites →https://doi.org/10.1016/j.bcp.2005.07.023openalex-snapshot
Bile acid-induced proliferation of a human colon cancer cell line is mediated by transactivation of epidermal growth factor receptors
inferredcites →https://doi.org/10.1016/j.bcp.2006.11.028openalex-snapshot
Matrix metalloproteinase-7-catalyzed release of HB-EGF mediates deoxycholyltaurine-induced proliferation of a human colon cancer cell line
inferredcites →https://doi.org/10.1016/j.bpg.2010.08.008openalex-snapshot
The integrity of the esophageal mucosa. Balance between offensive and defensive mechanisms
inferredcites →https://doi.org/10.1016/j.cellsig.2008.06.014openalex-snapshot
Bile acids and signal transduction: Role in glucose homeostasis
inferredcites →https://doi.org/10.1016/j.celrep.2014.02.032openalex-snapshot
Microbiota Modification with Probiotics Induces Hepatic Bile Acid Synthesis via Downregulation of the Fxr-Fgf15 Axis in Mice
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.2013.04.020openalex-snapshot
Bowel Functions, Fecal Unconjugated Primary and Secondary Bile Acids, and Colonic Transit in Patients With Irritable Bowel Syndrome
inferredcites →https://doi.org/10.1016/j.cgh.2016.11.012openalex-snapshot
Colonic Transit and Bile Acid Synthesis or Excretion in Patients With Irritable Bowel Syndrome–Diarrhea Without Bile Acid Malabsorption
inferredcites →https://doi.org/10.1016/j.cgh.2016.11.025openalex-snapshot
Incidence, Risk Factors, and Outcomes of Colorectal Cancer in Patients With Ulcerative Colitis With Low-Grade Dysplasia: A Systematic Review and Meta-analysis
inferredcites →https://doi.org/10.1016/j.cgh.2017.06.039openalex-snapshot
Bile Acid Deficiency in a Subgroup of Patients With Irritable Bowel Syndrome With Constipation Based on Biomarkers in Serum and Fecal Samples
inferredcites →https://doi.org/10.1016/j.clinre.2012.06.001openalex-snapshot
Aberrant expression of Wnt and Notch signal pathways in Barrett's esophagus
inferredcites →https://doi.org/10.1016/j.coph.2013.10.001openalex-snapshot
Gastrointestinal HCO3− transport and epithelial protection in the gut: new techniques, transport pathways and regulatory pathways
inferredcites →https://doi.org/10.1016/j.crohns.2013.05.006openalex-snapshot
Human colonic mucus is a reservoir for antimicrobial peptides
inferredcites →https://doi.org/10.1016/j.crohns.2014.02.027openalex-snapshot
Bile acid malabsorption assessed by 7 alpha-hydroxy-4-cholesten-3-one in pediatric inflammatory bowel disease: Correlation to clinical and laboratory findings
inferredcites →https://doi.org/10.1016/j.cub.2009.07.072openalex-snapshot
Ribosome-free Terminals of Rough ER Allow Formation of STIM1 Puncta and Segregation of STIM1 from IP3 Receptors
inferredcites →https://doi.org/10.1016/j.devcel.2009.02.010openalex-snapshot
Establishment of Intestinal Identity and Epithelial-Mesenchymal Signaling by Cdx2
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.drudis.2012.05.012openalex-snapshot
Farnesoid X receptor targeting to treat nonalcoholic steatohepatitis
inferredcites →https://doi.org/10.1016/j.ejca.2005.06.015openalex-snapshot
Ursodeoxycholic acid inhibits translocation of protein kinase C in human colonic cancer cell lines
inferredcites →https://doi.org/10.1016/j.ejphar.2011.06.058openalex-snapshot
Inhibition of NF-κB by a PXR-dependent pathway mediates counter-regulatory activities of rifaximin on innate immunity in intestinal epithelial cells
inferredcites →https://doi.org/10.1016/j.ejphar.2013.06.036openalex-snapshot
Ileal apical sodium-dependent bile acid transporter protein levels are down-regulated through ubiquitin-dependent protein degradation induced by bile acids
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.freeradbiomed.2005.04.026openalex-snapshot
Bile acid modulates transepithelial permeability via the generation of reactive oxygen species in the Caco-2 cell line
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2012.04.027openalex-snapshot
Glycochenodeoxycholate induces rat alveolar epithelial type II cell death and inhibits surfactant secretion in vitro
inferredcites →https://doi.org/10.1016/j.ijcard.2016.10.011openalex-snapshot
The effects of bile acid sequestrants on lipid profile and blood glucose concentrations: A systematic review and meta-analysis of randomized controlled trials
inferredcites →https://doi.org/10.1016/j.intimp.2012.11.017openalex-snapshot
Dose-dependent antiinflammatory effect of ursodeoxycholic acid in experimental colitis
inferredcites →https://doi.org/10.1016/j.intimp.2016.04.037openalex-snapshot
Tauroursodeoxycholate improves 2,4,6-trinitrobenzenesulfonic acid-induced experimental acute ulcerative colitis in mice
inferredcites →https://doi.org/10.1016/j.jcmgh.2016.08.004openalex-snapshot
The Farnesoid X Receptor: Good for BAD
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.jhep.2015.12.010openalex-snapshot
Obeticholic acid reduces bacterial translocation and inhibits intestinal inflammation in cirrhotic rats
inferredcites →https://doi.org/10.1016/j.jpsychores.2016.06.001openalex-snapshot
Depression and anxiety in patients with Inflammatory Bowel Disease: A systematic review
inferredcites →https://doi.org/10.1016/j.jsbmb.2015.01.011openalex-snapshot
Critical roles of intestinal epithelial vitamin D receptor signaling in controlling gut mucosal inflammation
inferredcites →https://doi.org/10.1016/j.jsbmb.2017.01.010openalex-snapshot
Anti-fibrotic effects of chronic treatment with the selective FXR agonist obeticholic acid in the bleomycin-induced rat model of pulmonary fibrosis
inferredcites →https://doi.org/10.1016/j.jtcvs.2004.10.035openalex-snapshot
Bile acid aspiration and the development of bronchiolitis obliterans after lung transplantation
inferredcites →https://doi.org/10.1016/j.mam.2017.06.002openalex-snapshot
Interactions between gut bacteria and bile in health and disease
inferredcites →https://doi.org/10.1016/j.mce.2012.05.004openalex-snapshot
FXR signaling in the enterohepatic system
inferredcites →https://doi.org/10.1016/j.molimm.2008.06.020openalex-snapshot
PU.1 and bacterial metabolites regulate the human gene CAMP encoding antimicrobial peptide LL-37 in colon epithelial cells
inferredcites →https://doi.org/10.1016/j.molmed.2015.06.003openalex-snapshot
Three cheers for the goblet cell: maintaining homeostasis in mucosal epithelia
inferredcites →https://doi.org/10.1016/j.pan.2013.05.011openalex-snapshot
Intraductal acidosis in acute biliary pancreatitis
inferredcites →https://doi.org/10.1016/j.pharep.2014.12.018openalex-snapshot
Effect of chenodeoxycholic acid and sodium hydrogen sulfide in dinitro benzene sulfonic acid (DNBS) – Induced ulcerative colitis in rats
inferredcites →https://doi.org/10.1016/j.physbeh.2017.02.039openalex-snapshot
Signalling in the gut endocrine axis
inferredcites →https://doi.org/10.1016/j.semcdb.2014.09.022openalex-snapshot
The role of molecular remodeling in differential regulation of tight junction permeability
inferredcites →https://doi.org/10.1016/j.steroids.2011.10.001openalex-snapshot
Identification of S-acyl glutathione conjugates of bile acids in human bile by means of LC/ESI-MS
inferredcites →https://doi.org/10.1016/j.surg.2005.06.030openalex-snapshot
Ligand-dependent activation of the epidermal growth factor receptor by secondary bile acids in polarizing colon cancer cells
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/j.tips.2015.08.002openalex-snapshot
TGR5 and Immunometabolism: Insights from Physiology and Pharmacology
inferredcites →https://doi.org/10.1016/j.tiv.2012.12.020openalex-snapshot
Bile acids in the colon, from healthy to cytotoxic molecules
inferredcites →https://doi.org/10.1016/j.toxlet.2006.06.006openalex-snapshot
Involvement of endoplasmic reticulum in glycochenodeoxycholic acid-induced apoptosis in rat hepatocytes
inferredcites →https://doi.org/10.1016/j.yexcr.2008.11.003openalex-snapshot
RETRACTED: Akt-dependent NF-κB activation is required for bile acids to rescue colon cancer cells from stress-induced apoptosis
inferredcites →https://doi.org/10.1016/s0002-9440(10)65211-xopenalex-snapshot
Activation of Pancreatic Stellate Cells in Human and Experimental Pancreatic Fibrosis
inferredcites →https://doi.org/10.1016/s0003-4975(10)65257-5openalex-snapshot
The Role of Bile and Acid in the Production of Esophagitis and the Motor Defect of Esophagitis
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/s0016-5085(00)70254-xopenalex-snapshot
Cyclooxygenase 2 expression in Barrett's esophagus and adenocarcinoma: Ex vivo induction by bile salts and acid exposure
inferredcites →https://doi.org/10.1016/s0016-5085(17)31403-8openalex-snapshot
Successful Therapy of Clostridium Difficile Infection with Fecal Microbiota Transplantation
inferredcites →https://doi.org/10.1016/s0016-5085(19)32637-xopenalex-snapshot
Metabolism of Lithocholate in Healthy Man
inferredcites →https://doi.org/10.1016/s0016-5085(19)33798-9openalex-snapshot
Perfusion of the Canine Colon with Unconjugated Bile Acids
inferredcites →https://doi.org/10.1016/s0016-5085(72)80178-1openalex-snapshot
Perfusion of the Hamster Jejunum with Conjugated and Unconjugated Bile Acids: Inhibition of Water Absorption and Effects on Morphology
inferredcites →https://doi.org/10.1016/s0016-5085(75)80239-3openalex-snapshot
Morphological and Functional Effects of Bile Salts on Rat Colon
inferredcites →https://doi.org/10.1016/s0016-5085(79)80007-4openalex-snapshot
Structure of Bile Acids Associated with Secretion in the Rat Cecum
inferredcites →https://doi.org/10.1016/s0022-2275(20)31482-6openalex-snapshot
Regulation of cholesterol-7α-hydroxylase: BAREly missing a SHP
inferredcites →https://doi.org/10.1016/s0022-2275(20)41426-9openalex-snapshot
Bile acid solubility and precipitation in vitro and in vivo: the role of conjugation, pH, and Ca2+ ions.
inferredcites →https://doi.org/10.1016/s0022-2275(20)41624-4openalex-snapshot
A proposed nomenclature for bile acids.
inferredcites →https://doi.org/10.1016/s0092-8674(00)00062-3openalex-snapshot
Targeted Disruption of the Nuclear Receptor FXR/BAR Impairs Bile Acid and Lipid Homeostasis
inferredcites →https://doi.org/10.1016/s0248-4900(03)00011-xopenalex-snapshot
Basolateral Ca2+‐dependent K+‐channels play a key role in Cl—secretion induced by taurodeoxycholate from colon mucosa
inferredcites →https://doi.org/10.1016/s0378-1119(02)00557-7openalex-snapshot
Generation of multiple farnesoid-X-receptor isoforms through the use of alternative promoters
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/10.1016/s1097-2765(00)00050-2openalex-snapshot
Molecular Basis for Feedback Regulation of Bile Acid Synthesis by Nuclear Receptors
inferredcites →https://doi.org/10.1016/s1097-2765(00)00051-4openalex-snapshot
A Regulatory Cascade of the Nuclear Receptors FXR, SHP-1, and LRH-1 Represses Bile Acid Biosynthesis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80348-2openalex-snapshot
Endogenous Bile Acids Are Ligands for the Nuclear Receptor FXR/BAR
inferredcites →https://doi.org/10.1016/s1097-2765(03)00112-6openalex-snapshot
Structural Basis for Bile Acid Binding and Activation of the Nuclear Receptor FXR
inferredcites →https://doi.org/10.1016/s1471-4892(02)00215-1openalex-snapshot
Neuroimmune and epithelial interactions in intestinal inflammation
inferredcites →https://doi.org/10.1016/s2210-7401(12)70018-9openalex-snapshot
Progressive familial intrahepatic cholestasis
inferredcites →https://doi.org/10.1016/s2213-8587(16)30155-3openalex-snapshot
Clinical relevance of the bile acid receptor TGR5 in metabolism
inferredcites →https://doi.org/10.1017/s0007114511004703openalex-snapshot
Cholesterol-lowering efficacy of a microencapsulated bile salt hydrolase-activeLactobacillus reuteriNCIMB 30242 yoghurt formulation in hypercholesterolaemic adults
inferredcites →https://doi.org/10.1017/s0029665116002834openalex-snapshot
Intestinal bile acid receptors are key regulators of glucose homeostasis
inferredcites →https://doi.org/10.1021/acs.jmedchem.7b00295openalex-snapshot
Synthesis and Biological Evaluation of Bile Acid Analogues Inhibitory to Clostridium difficile Spore Germination
inferredcites →https://doi.org/10.1021/jm901390popenalex-snapshot
Discovery of 6α-Ethyl-23( S )-methylcholic Acid ( S -EMCA, INT-777) as a Potent and Selective Agonist for the TGR5 Receptor, a Novel Target for Diabesity
inferredcites →https://doi.org/10.1023/a:1010607127822openalex-snapshot
Effect of Bile Salts on Colonic Mucus Secretion in Isolated Vascularly Perfused Rat Colon
inferredcites →https://doi.org/10.1023/a:1023307206125openalex-snapshot
Expression of Nuclear Receptors and Apo E Secretion During the Differentiation of Monocytic THP-1 cells into Macrophages
inferredcites →https://doi.org/10.1023/b:ddas.0000034558.78747.98openalex-snapshot
The Bile Acid Nuclear Receptor FXR and the Bile Acid Binding Protein IBABP Are Differently Expressed in Colon Cancer
inferredcites →https://doi.org/10.1038/ajg.2011.156openalex-snapshot
High-Dose Ursodeoxycholic Acid Is Associated With the Development of Colorectal Neoplasia in Patients With Ulcerative Colitis and Primary Sclerosing Cholangitis
inferredcites →https://doi.org/10.1038/ajg.2011.162openalex-snapshot
A Randomized Placebo-Controlled Phase IIb Trial of A3309, A Bile Acid Transporter Inhibitor, for Chronic Idiopathic Constipation
inferredcites →https://doi.org/10.1038/ajg.2011.285openalex-snapshot
Effects of A3309, an Ileal Bile Acid Transporter Inhibitor, on Colonic Transit and Symptoms in Females With Functional Constipation
inferredcites →https://doi.org/10.1038/ajg.2015.233openalex-snapshot
Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE): Determining Therapeutic Goals for Treat-to-Target
inferredcites →https://doi.org/10.1038/ajg.2015.424openalex-snapshot
Characterizing Factors Associated With Differences in FGF19 Blood Levels and Synthesis in Patients With Primary Bile Acid Diarrhea
inferredcites →https://doi.org/10.1038/bjc.2011.37openalex-snapshot
Farnesoid X receptor, overexpressed in pancreatic cancer with lymph node metastasis promotes cell migration and invasion
inferredcites →https://doi.org/10.1038/labinvest.2014.117openalex-snapshot
Tauroursodeoxycholic acid inhibits experimental colitis by preventing early intestinal epithelial cell death
inferredcites →https://doi.org/10.1038/labinvest.2015.137openalex-snapshot
Bile acids induce Delta-like 1 expression via Cdx2-dependent pathway in the development of Barrett's esophagus
inferredcites →https://doi.org/10.1038/labinvest.2017.6openalex-snapshot
Tauroursodeoxycholic acid protects bile acid homeostasis under inflammatory conditions and dampens Crohn's disease-like ileitis
inferredcites →https://doi.org/10.1038/mi.2011.41openalex-snapshot
Secretory IgA's complex roles in immunity and mucosal homeostasis in the gut
inferredcites →https://doi.org/10.1038/nature04330openalex-snapshot
Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation
inferredcites →https://doi.org/10.1038/nature11319openalex-snapshot
Gut microbiota composition correlates with diet and health in the elderly
inferredcites →https://doi.org/10.1038/nature12820openalex-snapshot
Diet rapidly and reproducibly alters the human gut microbiome
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/ncomms7342openalex-snapshot
Fat, fibre and cancer risk in African Americans and rural Africans
inferredcites →https://doi.org/10.1038/ncomms8629openalex-snapshot
Farnesoid X receptor inhibits glucagon-like peptide-1 production by enteroendocrine L cells
inferredcites →https://doi.org/10.1038/ni.3123openalex-snapshot
Control of adaptive immunity by the innate immune system
inferredcites →https://doi.org/10.1038/npp.2014.224openalex-snapshot
More than a Gut Feeling: the Microbiota Regulates Neurodevelopment and Behavior
inferredcites →https://doi.org/10.1038/nprot.2009.243openalex-snapshot
Experimental acute biliary pancreatitis induced by retrograde infusion of bile acids into the mouse pancreatic duct
inferredcites →https://doi.org/10.1038/nrendo.2014.60openalex-snapshot
Beyond intestinal soap—bile acids in metabolic control
inferredcites →https://doi.org/10.1038/nrgastro.2013.151openalex-snapshot
Bile acid receptors as targets for drug development
inferredcites →https://doi.org/10.1038/nrgastro.2014.32openalex-snapshot
Bile acid diarrhoea and FGF19: new views on diagnosis, pathogenesis and therapy
inferredcites →https://doi.org/10.1038/nrgastro.2015.12openalex-snapshot
Novel therapeutic targets in primary biliary cirrhosis
inferredcites →https://doi.org/10.1038/nrgastro.2015.150openalex-snapshot
The global burden of IBD: from 2015 to 2025
inferredcites →https://doi.org/10.1038/nrgastro.2015.186openalex-snapshot
Immunopathogenesis of IBD: current state of the art
inferredcites →https://doi.org/10.1038/nrgastro.2016.165openalex-snapshot
Diet, microorganisms and their metabolites, and colon cancer
inferredcites →https://doi.org/10.1038/nrgastro.2016.98openalex-snapshot
Understanding the mechanisms of faecal microbiota transplantation
inferredcites →https://doi.org/10.1038/nri.2015.17openalex-snapshot
Mucosal immunity to pathogenic intestinal bacteria
inferredcites →https://doi.org/10.1038/onc.2011.124openalex-snapshot
Farnesoid X receptor inhibits tamoxifen-resistant MCF-7 breast cancer cell growth through downregulation of HER2 expression
inferredcites →https://doi.org/10.1038/sj.bjp.0702615openalex-snapshot
Involvement of serotonin and calcium channels in the intestinal fluid secretion evoked by bile salt and cholera toxin
inferredcites →https://doi.org/10.1038/srep31538openalex-snapshot
Bile acid receptor TGR5, NADPH Oxidase NOX5-S and CREB Mediate Bile Acid-Induced DNA Damage In Barrett’s Esophageal Adenocarcinoma Cells
inferredcites →https://doi.org/10.1039/c5fo01276gopenalex-snapshot
Diet, microbiota, and dysbiosis: a ‘recipe’ for colorectal cancer
inferredcites →https://doi.org/10.1039/c6fo01207hopenalex-snapshot
Medium-chain fatty acids reduce serum cholesterol by regulating the metabolism of bile acid in C57BL/6J mice
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/10.1042/bsr20160124openalex-snapshot
Controlled bile acid exposure to oesophageal mucosa causes up-regulation of nuclear γ-H2AX possibly via iNOS induction
inferredcites →https://doi.org/10.1042/bst0380364openalex-snapshot
The role of Cdx2 in Barrett's metaplasia
inferredcites →https://doi.org/10.1042/cs20160926openalex-snapshot
Chronic microaspiration of bile acids induces lung fibrosis through multiple mechanisms in rats
inferredcites →https://doi.org/10.1046/j.1440-1746.1998.01784.xopenalex-snapshot
Bile acids inhibit tumour necrosis factor α-induced interleukin-8 production in human colon epithelial cells
inferredcites →https://doi.org/10.1053/gast.2002.33617openalex-snapshot
Transporter-mediated bile acid uptake causes Ca2+-dependent cell death in rat pancreatic acinar cells
inferredcites →https://doi.org/10.1053/j.gastro.2005.12.032openalex-snapshot
Bile Acids Induce Ectopic Expression of Intestinal Guanylyl Cyclase C Through Nuclear Factor-κB and Cdx2 in Human Esophageal Cells
inferredcites →https://doi.org/10.1053/j.gastro.2008.12.040openalex-snapshot
Bile Salts Control the Antimicrobial Peptide Cathelicidin Through Nuclear Receptors in the Human Biliary Epithelium
inferredcites →https://doi.org/10.1053/j.gastro.2009.07.055openalex-snapshot
Gastroesophageal Reflux Might Cause Esophagitis Through a Cytokine-Mediated Mechanism Rather Than Caustic Acid Injury
inferredcites →https://doi.org/10.1053/j.gastro.2009.10.052openalex-snapshot
Biliary Acute Pancreatitis in Mice is Mediated by the G-Protein−Coupled Cell Surface Bile Acid Receptor Gpbar1
inferredcites →https://doi.org/10.1053/j.gastro.2009.12.012openalex-snapshot
The Role of Bile Acids in Gallstone-Induced Pancreatitis
inferredcites →https://doi.org/10.1053/j.gastro.2010.01.037openalex-snapshot
Dynamic Changes in Cytosolic and Mitochondrial ATP Levels in Pancreatic Acinar Cells
inferredcites →https://doi.org/10.1053/j.gastro.2010.03.035openalex-snapshot
Acid and Bile Salt–Induced CDX2 Expression Differs in Esophageal Squamous Cells From Patients With and Without Barrett's Esophagus
inferredcites →https://doi.org/10.1053/j.gastro.2010.07.052openalex-snapshot
Chenodeoxycholate in Females With Irritable Bowel Syndrome-Constipation: A Pharmacodynamic and Pharmacogenetic Analysis
inferredcites →https://doi.org/10.1053/j.gastro.2011.02.054openalex-snapshot
Reactive Oxygen Species Induced by Bile Acid Induce Apoptosis and Protect Against Necrosis in Pancreatic Acinar Cells
inferredcites →https://doi.org/10.1053/j.gastro.2011.08.039openalex-snapshot
Trypsin Reduces Pancreatic Ductal Bicarbonate Secretion by Inhibiting CFTR Cl− Channels and Luminal Anion Exchangers
inferredcites →https://doi.org/10.1053/j.gastro.2012.06.011openalex-snapshot
Effects of Ethanol Metabolites on Exocytosis of Pancreatic Acinar Cells in Rats
showing the first 200 of 513 · page through all 513
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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High Soybean Meal Diet Inclusion of Lithospermum Erythrorhizon Mitigates Soybean-Induced Enteritis in Pearl Gentian Grouper (Epinephelus Fuscoguttatus ♀ × E. Lanceolatus ♂)
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Ileal bile acid transporter inhibitors in Alagille syndrome and Progressive Familial Intrahepatic Cholestasis: A systematic review into dose–response
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A perfusion host‐microbe bioreactor (HMB) system that captures dynamic interactions of secreted metabolites between epithelial cells cocultured with a human gut anaerobe
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Phosphatidylcholine in bile‐derived small extracellular vesicles as a novel biomarker of cholangiocarcinoma
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Targeting the Four Pillars of Enterohepatic Bile Salt Cycling; Lessons From Genetics and Pharmacology
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The immunologic changes during different phases of intestinal anastomotic healing
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Gut microbiota dysbiosis in functional gastrointestinal disorders: Underpinning the symptoms and pathophysiology
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Spatial distribution of gut microbiota in mice during the occurrence and remission of hyperuricemia
inferred← citeshttps://doi.org/10.1002/jsfa.70884openalex-snapshot
Haematococcus pluvialis peptides ameliorated cyclophosphamide‐induced immunodeficiency in mice by regulating intestinal barrier function
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SLC10A2 deficiency‐induced congenital chronic bile acid diarrhea and stunting
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Bile Acid Derivatives Effectively Prevented High‐Fat Diet‐Induced Colonic Barrier Dysfunction
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Microbial Metabolites and Intestinal Stem Cells Tune Intestinal Homeostasis
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Resveratrol inhibits bile acid‐induced gastric intestinal metaplasia via the PI3K / AKT / p‐FoxO4 signalling pathway
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Plasma Markers of Cholestasis in Critical Illness
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Plasma Markers of Cholestasis in Critical Illness
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Impacts of liver macrophages, gut microbiota, and bile acid metabolism on the differences in iHFC diet-induced MASH progression between TSNO and TSOD mice
inferred← citeshttps://doi.org/10.1007/s00210-023-02455-zopenalex-snapshot
Alleviation of cholestatic liver injury and intestinal permeability by lubiprostone treatment in bile duct ligated rats: role of intestinal FXR and tight junction proteins claudin-1, claudin-2, and occludin
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Defecation status, intestinal microbiota, and habitual diet are associated with the fecal bile acid composition: a cross-sectional study in community-dwelling young participants
inferred← citeshttps://doi.org/10.1007/s00604-025-07120-1openalex-snapshot
Design and application of graphene oxide-based molecularly imprinted covalent organic framework for simultaneous and precise recognition of bile acid metabolites
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Effect of bile salts on intestinal epithelial function in gilthead seabream (Sparus aurata)
inferred← citeshttps://doi.org/10.1007/s10753-025-02294-5openalex-snapshot
Critical Role of Cholic Acid in the Development of iHFC Diet-induced MASH in TSNO Mice
inferred← citeshttps://doi.org/10.1007/s10863-021-09927-yopenalex-snapshot
Gualou Xiebai Decoction ameliorates increased Caco-2 monolayer permeability induced by bile acids via tight junction regulation, oxidative stress suppression and apoptosis reduction
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Copper-mediated shifts in transcriptomic responses of intestines in Bufo gargarizans tadpoles to lead stress
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Targeting the Gut-Liver Mitochondria Axis in MASLD: Mechanisms and Therapeutic Perspectives
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Maldigestion Versus Malabsorption in the Elderly
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Getting the BS out of Irritable Bowel Syndrome with Diarrhea (IBS-D): Let’s Make a Diagnosis
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Decoding Abdominal Pain in Constipation-predominant Irritable Bowel Syndrome and Functional Constipation: Mechanisms and Managements
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Ileal bile acid transporter inhibition as an anticholestatic therapeutic target in biliary atresia and other cholestatic disorders
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Digestive Tract and Salivary Glands
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Cholesterol transport in blood, lipoproteins, and cholesterol metabolism
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Arsenic through the gastrointestinal tract
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Microbiome influences on neuro-immune interactions in neurodegenerative disease
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Extraction and quantitative determination of bile acids in feces
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Microbial bile acid metabolite ameliorates mycophenolate mofetil-induced gastrointestinal toxicity through vitamin D3 receptor
inferred← citeshttps://doi.org/10.1016/j.anifeedsci.2021.114926openalex-snapshot
Acid versus crude oils for broiler chicken diets: In vitro lipid digestion and bioaccessibility
inferred← citeshttps://doi.org/10.1016/j.aninu.2025.05.013openalex-snapshot
Integrating bile acid metabolism into precision nutrition strategies for improved swine performance
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741752openalex-snapshot
Comparative analysis of Seabuckthorn and its significant component in enhancing fish mucosal immunity
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Dietary bile acids supplementation improves the growth performance, glycolipid metabolism and bile acids homeostasis of blunt snout bream (Megalobrama amblycephala) fed a high-carbohydrate diet
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Turnover of bile acids in liver, serum and caecal content by high-fat diet feeding affects hepatic steatosis in rats
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The live biotherapeutic Blautia stercoris MRx0006 attenuates social deficits, repetitive behaviour, and anxiety-like behaviour in a mouse model relevant to autism
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A comprehensive time course and correlation analysis of indomethacin-induced inflammation, bile acid alterations and dysbiosis in the rat small intestine
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Bile acid metabolism in health and ageing-related diseases
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Slippery dopamine–fluoropolymer hybrid surface for improving biliary stent longevity
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Visualizing enterohepatic circulation in vivo by sensitive 19F MRI with a fluorinated ferrous chelate-based small molecule probe
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Membrane receptor TGR5 upregulates IP3R-induced calcium overload: Key mechanism of bile acid-induced acute pancreatitis
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Gut Goo: Physiology, Diet, and Therapy of Intestinal Mucus and Biofilms in Gastrointestinal Health and Disease
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Dachaihu decoction inhibits hypernutrition-induced liver metastasis from colorectal cancer by maintaining the gut vascular barrier
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Taurocholate uptake by Caco-2 cells is inhibited by pro-inflammatory cytokines and butyrate
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Bile acids supplementation improves colonic mucosal barrier via alteration of bile acids metabolism and gut microbiota composition in goats with subacute ruminal acidosis (SARA)
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120842openalex-snapshot
An unintended consequence of sub-NOAEL triazole fungicides exposure: Bile acids disturbance mediated drug absorption perturbation
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.172992openalex-snapshot
Hesperetin ameliorates DSS-induced colitis by maintaining the epithelial barrier via blocking RIPK3/MLKL necroptosis signaling
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Contrary effects of the gut metabolites deoxycholate and butyrate on the acetylcholine-evoked calcium response in an enteroendocrine cell model
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128813openalex-snapshot
Lambda-cyhalothrin exposure disrupts microbiota-associated bile acid metabolism and enterohepatic feedback in mice
inferred← citeshttps://doi.org/10.1016/j.fct.2022.113136openalex-snapshot
Taurocholic acid, a primary 12α-hydroxylated bile acid, induces leakiness in the distal small intestine in rats
inferred← citeshttps://doi.org/10.1016/j.foodres.2024.114317openalex-snapshot
Exploring lipid digestion discrepancies between preterm formula and human milk: Insights from in vitro gastrointestinal digestion and the impact of added milk fat
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.117172openalex-snapshot
Regulatory effect of Chinese Baijiu on gut microbiota and host metabolism
inferred← citeshttps://doi.org/10.1016/j.foodres.2026.118599openalex-snapshot
Modulation of intestinal microbiota and metabolites mediates the improvement of cyclophosphamide-induced immunodeficiency in mice by Monopterus albus slime protein
inferred← citeshttps://doi.org/10.1016/j.fsi.2022.10.049openalex-snapshot
Bile components affect the functions and transcriptome of the rainbow trout intestinal epithelial cell line RTgutGC
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.01.209openalex-snapshot
Disorder-to-helix conformational conversion of the human immunomodulatory peptide LL-37 induced by antiinflammatory drugs, food dyes and some metabolites
inferred← citeshttps://doi.org/10.1016/j.ijpx.2025.100444openalex-snapshot
Boosting buccal drug absorption: Mechanistic insights into bilosome-mediated delivery
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EGCG alleviates colitis in inflammatory bowel disease via gut microbiota-derived LCA and inhibition of NLRP3 inflammasome
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Probiotic Lactobacillus plantarum 299v supplementation in patients with major depression in a double-blind, randomized, placebo-controlled trial: A metabolomics study
inferred← citeshttps://doi.org/10.1016/j.japr.2026.100674openalex-snapshot
Effects of dietary Rhus coriaria L. powder on growth performance, antioxidant status, and immune competence of broiler chickens under high-density rearing conditions
inferred← citeshttps://doi.org/10.1016/j.jare.2025.08.053openalex-snapshot
The therapeutic value of “Bile Transfer” for complications of acute pancreatitis: A retrospective clinical study
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Pentacyclic triterpenes modulate farnesoid X receptor expression in colonic epithelial cells: Implications for colonic secretory function
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2021.12.017openalex-snapshot
LKB1 in Intestinal Epithelial Cells Regulates Bile Acid Metabolism by Modulating FGF15/19 Production
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2025.101504openalex-snapshot
Obese Adipose Tissue Extracellular Vesicles Activate Mitochondrial Fatty Acid β-oxidation to Drive Colonic Stemness
inferred← citeshttps://doi.org/10.1016/j.jcrc.2020.08.004openalex-snapshot
Diarrhea and elevation of plasma markers of cholestasis are common and often occur concomitantly in critically ill patients
inferred← citeshttps://doi.org/10.1016/j.jep.2026.121486openalex-snapshot
Yanxiao Di’naer decoction attenuates metabolic dysfunction-associated steatohepatitis through the regulation of gut microbiota and the metabolism of bile acid
inferred← citeshttps://doi.org/10.1016/j.jff.2024.106337openalex-snapshot
Unveiling the role of functional foods with emphasis on prebiotics and probiotics in human health: A review
inferred← citeshttps://doi.org/10.1016/j.jhep.2020.05.007openalex-snapshot
FGF15 improves outcomes after brain dead donor liver transplantation with steatotic and non-steatotic grafts in rats
inferred← citeshttps://doi.org/10.1016/j.jhepr.2021.100344openalex-snapshot
Ablation of liver Fxr results in an increased colonic mucus barrier in mice
inferred← citeshttps://doi.org/10.1016/j.jhip.2026.02.002openalex-snapshot
Mechanistic insights into the preventive efficacy of 21-day prefeeding with β-galactosidase hydrolyzed milk in DSS-induced ulcerative colitis mice
inferred← citeshttps://doi.org/10.1016/j.jlr.2022.100275openalex-snapshot
Characterization of long-chain fatty acid-linked bile acids: a major conjugation form of 3β-hydroxy bile acids in feces
inferred← citeshttps://doi.org/10.1016/j.jlr.2023.100340openalex-snapshot
Combining ASBT inhibitor and FGF15 treatments enhances therapeutic efficacy against cholangiopathy in female but not male Cyp2c70 KO mice
inferred← citeshttps://doi.org/10.1016/j.jpha.2021.10.003openalex-snapshot
Interactions between gut microbiota and berberine, a necessary procedure to understand the mechanisms of berberine
inferred← citeshttps://doi.org/10.1016/j.kint.2020.03.020openalex-snapshot
The absorbing life of bile acids
inferred← citeshttps://doi.org/10.1016/j.livres.2023.09.002openalex-snapshot
Microbial transformations of bile acids and their receptors in the regulation of metabolic dysfunction-associated steatotic liver disease
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2023.105403openalex-snapshot
Mitochondria of intestinal epithelial cells in depression: Are they at a crossroads of gut-brain communication?
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N-(4-[18F]fluorobenzyl)cholylglycine, a potential tracer for positron emission tomography of enterohepatic circulation and drug-induced inhibition of ileal bile acid transport. A proof-of-concept PET/CT study in pigs
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2019.107396openalex-snapshot
Ursodeoxycholic acid and cancer: From chemoprevention to chemotherapy
inferred← citeshttps://doi.org/10.1016/j.plipres.2022.101210openalex-snapshot
Bile acids and their receptors in regulation of gut health and diseases
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.160849openalex-snapshot
Lead and copper influenced bile acid metabolism by changing intestinal microbiota and activating farnesoid X receptor in Bufo gargarizans
inferred← citeshttps://doi.org/10.1016/j.snb.2023.135181openalex-snapshot
An intestinal-targeting near-infrared probe for imaging nitroreductase in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.stem.2022.08.008openalex-snapshot
Hepatic cytochrome P450 8B1 and cholic acid potentiate intestinal epithelial injury in colitis by suppressing intestinal stem cell renewal
inferred← citeshttps://doi.org/10.1016/j.steroids.2019.108461openalex-snapshot
Ursodeoxycholic acid inhibits ENaC and Na/K pump activity to restore airway surface liquid height in cystic fibrosis bronchial epithelial cells
inferred← citeshttps://doi.org/10.1016/j.steroids.2021.108879openalex-snapshot
Research progress in the application of bile acid-drug conjugates: A “trojan horse” strategy
inferred← citeshttps://doi.org/10.1016/j.yexcr.2023.113670openalex-snapshot
Bile salts and proinflammatory cytokines inhibit MCT1-mediated cellular uptake of butyrate and interfere with its antiproliferative properties
inferred← citeshttps://doi.org/10.1016/s2468-1253(22)00093-0openalex-snapshot
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial
inferred← citeshttps://doi.org/10.1016/s2468-1253(22)00436-8openalex-snapshot
Lessons from a trial of colesevelam for bile acid diarrhoea
inferred← citeshttps://doi.org/10.1016/s2468-1253(24)00074-8openalex-snapshot
Efficacy and safety of odevixibat in patients with Alagille syndrome (ASSERT): a phase 3, double-blind, randomised, placebo-controlled trial
inferred← citeshttps://doi.org/10.1017/s0954422421000172openalex-snapshot
Modulation of intestinal stem cell homeostasis by nutrients: a novel therapeutic option for intestinal diseases
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.4c00539openalex-snapshot
Synthesis and Biological Evaluation of Bile Acid–Triclosan Conjugates: A Study on Antibacterial, Antibiofilm, and Molecular Docking
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b03173openalex-snapshot
Chenodeoxycholic Acid (CDCA) Protects against the Lipopolysaccharide-Induced Impairment of the Intestinal Epithelial Barrier Function via the FXR-MLCK Pathway
inferred← citeshttps://doi.org/10.1038/s41374-021-00628-zopenalex-snapshot
Bile acid-induced tissue factor activity in hepatocytes correlates with activation of farnesoid X receptor
inferred← citeshttps://doi.org/10.1038/s41467-022-28126-wopenalex-snapshot
Defective humoral immunity disrupts bile acid homeostasis which promotes inflammatory disease of the small bowel
inferred← citeshttps://doi.org/10.1038/s41467-024-53673-9openalex-snapshot
Exposing 24-hour cycles in bile acids of male humans
inferred← citeshttps://doi.org/10.1038/s41586-023-06906-8openalex-snapshot
Reverse metabolomics for the discovery of chemical structures from humans
inferred← citeshttps://doi.org/10.1038/s41598-020-77374-7openalex-snapshot
The Pathophysiology of Bile Acid Diarrhoea: Differences in the Colonic Microbiome, Metabolome and Bile Acids
inferred← citeshttps://doi.org/10.1038/s41598-021-89542-4openalex-snapshot
Chorioamnionitis induces hepatic inflammation and time-dependent changes of the enterohepatic circulation in the ovine fetus
inferred← citeshttps://doi.org/10.1038/s41598-026-63156-0openalex-snapshot
Loss of TGR5-activating bile acids is associated with disease activity in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1038/s42003-025-09346-4openalex-snapshot
Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance
inferred← citeshttps://doi.org/10.1038/s42255-022-00559-zopenalex-snapshot
Metabolic Messengers: bile acids
inferred← citeshttps://doi.org/10.1038/s42255-025-01262-5openalex-snapshot
Alterations in intestinal bile acid transport provide a therapeutic target in patients with post-bariatric hypoglycaemia
inferred← citeshttps://doi.org/10.1039/d3fo01044aopenalex-snapshot
Dietary berberine supplementation improves growth performance and alleviates gut injury in weaned piglets by modulating ileal microbiota and metabolites
inferred← citeshttps://doi.org/10.1039/d5lc00937eopenalex-snapshot
A microfluidic chip recapitulating the human neurovascular unit with a functional blood–brain barrier for modeling gut–brain interactions
inferred← citeshttps://doi.org/10.1053/j.gastro.2021.06.024openalex-snapshot
Mucosal Biofilms Are an Endoscopic Feature of Irritable Bowel Syndrome and Ulcerative Colitis
inferred← citeshttps://doi.org/10.1053/j.gastro.2023.03.226openalex-snapshot
Odevixibat Treatment Induces Biliary Bile Acid Secretion in Responsive Patients With Bile Salt Export Pump Deficiency
inferred← citeshttps://doi.org/10.1055/s-0042-1748037openalex-snapshot
Intestinal Barrier Dysfunction in Fatty Liver Disease: Roles of Microbiota, Mucosal Immune System, and Bile Acids
inferred← citeshttps://doi.org/10.1080/10837450.2021.1916032openalex-snapshot
Bile acids as novel enhancers of CNS targeting antitumor drugs: a comprehensive review
inferred← citeshttps://doi.org/10.1080/13543784.2022.2151890openalex-snapshot
Odevixibat: an investigational inhibitor of the ileal bile acid transporter (IBAT) for the treatment of biliary atresia
inferred← citeshttps://doi.org/10.1080/17425247.2020.1743677openalex-snapshot
The impact of endogenous gastrointestinal molecules on the dissolution and precipitation of orally delivered hydrophobic APIs
inferred← citeshttps://doi.org/10.1080/17474124.2019.1561274openalex-snapshot
Perspectives on the interlinked nature of systemic sclerosis and reflux disease
inferred← citeshttps://doi.org/10.1080/17474124.2024.2402353openalex-snapshot
Managing bile acid diarrhea: aspects of contention
inferred← citeshttps://doi.org/10.1080/17474124.2025.2549381openalex-snapshot
The evolution of irritable bowel syndrome as a group of organic diseases: a narrative review
inferred← citeshttps://doi.org/10.1080/19490976.2020.1840766openalex-snapshot
Host miRNA-21 promotes liver dysfunction by targeting small intestinal Lactobacillus in mice
inferred← citeshttps://doi.org/10.1080/19490976.2024.2353399openalex-snapshot
Host-microbiota interaction in intestinal stem cell homeostasis
inferred← citeshttps://doi.org/10.1080/19490976.2024.2382336openalex-snapshot
Gut microbiota-derived fatty acid and sterol metabolites: biotransformation and immunomodulatory functions
inferred← citeshttps://doi.org/10.1080/19490976.2024.2421623openalex-snapshot
Giardia antagonizes beneficial functions of indigenous and therapeutic intestinal bacteria during protein deficiency
inferred← citeshttps://doi.org/10.1080/19490976.2024.2423040openalex-snapshot
B. vulgatus ameliorates high-fat diet-induced obesity through modulating intestinal serotonin synthesis and lipid absorption in mice
inferred← citeshttps://doi.org/10.1080/19490976.2025.2496437openalex-snapshot
Gut microbiota regulates hepatic ketogenesis and lipid accumulation in ketogenic diet-induced hyperketonemia by disrupting bile acid metabolism
inferred← citeshttps://doi.org/10.1093/bbb/zbad030openalex-snapshot
Skatole-induced p38 and JNK activation coordinately upregulates, whereas AhR activation partially attenuates TNFα expression in intestinal epithelial cells
inferred← citeshttps://doi.org/10.1093/jn/nxac161openalex-snapshot
The Fecal Metabolome Links Diet Composition, Foacidic positive ion conditions, chromatographicallyod Processing, and the Gut Microbiota to Gastrointestinal Health in a Randomized Trial of Adults Consuming a Processed Diet
inferred← citeshttps://doi.org/10.1096/fba.2024-00044openalex-snapshot
Bile acids differentially regulate longitudinal smooth muscle contractility in everted mouse ileum
inferred← citeshttps://doi.org/10.1096/fj.201902687ropenalex-snapshot
Western diet‐induced increase in colonic bile acids compromises epithelial barrier in nonalcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1096/fj.202000042ropenalex-snapshot
The early life microbiota protects neonatal mice from pathological small intestinal epithelial cell shedding
inferred← citeshttps://doi.org/10.1097/hep.0000000000001430openalex-snapshot
Pretreatment serum bile acid composition and predictability of subsequent response to odevixibat in patients with bile salt export pump (BSEP) deficiency
inferred← citeshttps://doi.org/10.1097/mpa.0000000000001175openalex-snapshot
Accelerating the Drug Delivery Pipeline for Acute and Chronic Pancreatitis
inferred← citeshttps://doi.org/10.1097/mpa.0000000000001706openalex-snapshot
Role of Bile Acids and Bile Salts in Acute Pancreatitis
inferred← citeshttps://doi.org/10.1097/mpg.0000000000002645openalex-snapshot
Rapid Postnatal Upregulation of Intestinal Farnesoid X Receptor‐Fibroblast Growth Factor 19 Signaling in Premature Pigs
inferred← citeshttps://doi.org/10.1097/nrl.0000000000000626openalex-snapshot
Stroke-Associated Pneumonia and the Brain-Gut-Lung Axis
inferred← citeshttps://doi.org/10.1101/2020.09.26.279851openalex-snapshot
Gut microbiome dysbiosis is associated with elevated toxic bile acids in Parkinson’s disease
inferred← citeshttps://doi.org/10.1101/2020.11.21.392837openalex-snapshot
Salicylate, Bile Acids and Extreme Acid Cause Fitness Tradeoffs for Multidrug Pumps in Escherichia coli K-12
inferred← citeshttps://doi.org/10.1101/2024.01.22.575921openalex-snapshot
Giardia Antagonizes Beneficial Functions of Indigenous and Therapeutic Intestinal Bacteria during Malnutrition
inferred← citeshttps://doi.org/10.1111/apt.17739openalex-snapshot
Prospective comparison of diagnostic tests for bile acid diarrhoea
inferred← citeshttps://doi.org/10.1111/apt.70666openalex-snapshot
Review Article: Ileal Bile Acid Transport ( IBAT ) Inhibitors as an Emerging Treatment for Cholestatic Liver Disease
inferred← citeshttps://doi.org/10.1111/febs.17200openalex-snapshot
The role of the gut microbiome in disorders of gut–brain interaction
inferred← citeshttps://doi.org/10.1111/gtc.13134openalex-snapshot
Antibiotic effects on gut microbiota modulate diet‐induced metabolic dysfunction‐associated steatohepatitis development in C57BL/6 mice
inferred← citeshttps://doi.org/10.1111/jcmm.15881openalex-snapshot
A novel role for farnesoid X receptor in the bile acid‐mediated intestinal glucose homeostasis
inferred← citeshttps://doi.org/10.1111/jgh.15032openalex-snapshot
Marshall and Warren Lecture 2019: A paradigm shift in pathophysiological basis of irritable bowel syndrome and its implication on treatment
inferred← citeshttps://doi.org/10.1111/jgh.15676openalex-snapshot
Deoxycholic acid delays the wound healing of colonic epithelial cells via transmembrane G‐protein‐coupled receptor 5
inferred← citeshttps://doi.org/10.1111/jpn.13969openalex-snapshot
Effects of bile acid metabolism on intestinal health of livestock and poultry
inferred← citeshttps://doi.org/10.1111/liv.14553openalex-snapshot
Potential of ileal bile acid transporter inhibition as a therapeutic target in Alagille syndrome and progressive familial intrahepatic cholestasis
inferred← citeshttps://doi.org/10.1111/nmo.13854openalex-snapshot
Duodenal bile acids as determinants of intestinal mucosal homeostasis and disease
inferred← citeshttps://doi.org/10.1111/nmo.13943openalex-snapshot
Synthetic G protein‐coupled bile acid receptor agonists and bile acids act via basolateral receptors in ileal and colonic mucosa
inferred← citeshttps://doi.org/10.1113/ep092451openalex-snapshot
The mood stabilizers lithium and valproate disrupt hepatic and intestinal farnesoid X receptor signalling and increase bile synthesis in the rat
inferred← citeshttps://doi.org/10.1113/jp281620openalex-snapshot
Physiological mechanisms of unexplained (functional) gastrointestinal disorders
inferred← citeshttps://doi.org/10.1113/jp281727openalex-snapshot
Bile acids, bioactive signalling molecules in interoceptive gut‐to‐brain communication
inferred← citeshttps://doi.org/10.1113/jp291470openalex-snapshot
Increasing gut short‐chain fatty acids protects intestinal barrier function but does not spare muscle glycogen or impact aerobic performance
inferred← citeshttps://doi.org/10.1126/sciadv.abo2794openalex-snapshot
Inhibition of microbial deconjugation of micellar bile acids protects against intestinal permeability and liver injury
inferred← citeshttps://doi.org/10.1126/science.aav0173openalex-snapshot
Tumor metastasis to lymph nodes requires YAP-dependent metabolic adaptation
inferred← citeshttps://doi.org/10.1128/aem.00724-21openalex-snapshot
Extreme Acid Modulates Fitness Trade-Offs of Multidrug Efflux Pumps MdtEF-TolC and AcrAB-TolC in Escherichia coli K-12
inferred← citeshttps://doi.org/10.1128/msphere.00669-21openalex-snapshot
Fecal Microbiota Transplantation Increases Colonic IL-25 and Dampens Tissue Inflammation in Patients with Recurrent Clostridioides difficile
inferred← citeshttps://doi.org/10.1136/bmjgast-2023-001340openalex-snapshot
Risk of cancer in patients with bile acid diarrhoea: a Danish nationwide matched cohort study
inferred← citeshttps://doi.org/10.1146/annurev-nutr-122221-103916openalex-snapshot
Babies, Bugs, and Barriers: Dietary Modulation of Intestinal Barrier Function in Early Life
inferred← citeshttps://doi.org/10.1152/ajpcell.00523.2022openalex-snapshot
SLC26A3 (DRA) is stimulated in a synergistic, intracellular Ca 2+ -dependent manner by cAMP and ATP in intestinal epithelial cells
inferred← citeshttps://doi.org/10.1152/ajpgi.00011.2022openalex-snapshot
Bile acid detergency: permeability, inflammation, and effects of sulfation
inferred← citeshttps://doi.org/10.1152/ajpgi.00016.2019openalex-snapshot
Deoxycholic acid activates colonic afferent nerves via 5-HT3 receptor-dependent and -independent mechanisms
inferred← citeshttps://doi.org/10.1152/ajpgi.00063.2024openalex-snapshot
FXR deletion attenuates intestinal barrier dysfunction in murine acute intestinal inflammation
inferred← citeshttps://doi.org/10.1152/ajpgi.00079.2025openalex-snapshot
Host-microbial interactions in the esophagus
inferred← citeshttps://doi.org/10.1152/ajpgi.00086.2025openalex-snapshot
Farnesoid X receptor inhibits proinflammatory cytokine-induced epithelial necroptosis in vitro: implications for preservation of intestinal barrier function
inferred← citeshttps://doi.org/10.1152/ajpgi.00091.2021openalex-snapshot
Fecal microbiome and bile acid metabolome in adult short bowel syndrome
inferred← citeshttps://doi.org/10.1152/ajpgi.00163.2019openalex-snapshot
Ursodeoxycholic acid: a promising therapeutic target for inflammatory bowel diseases?
inferred← citeshttps://doi.org/10.1152/ajpgi.00178.2021openalex-snapshot
A systems-level analysis of bile acids effects on rat colon epithelial cells
inferred← citeshttps://doi.org/10.1152/physrev.00018.2018openalex-snapshot
The Microbiota-Gut-Brain Axis
inferred← citeshttps://doi.org/10.1152/physrev.00049.2019openalex-snapshot
Molecular physiology of bile acid signaling in health, disease, and aging
inferred← citeshttps://doi.org/10.1155/2020/1805418openalex-snapshot
An Integrated Fecal Microbiome and Metabolomics in T2DM Rats Reveal Antidiabetes Effects from Host-Microbial Metabolic Axis of EtOAc Extract from Sophora flavescens
inferred← citeshttps://doi.org/10.1155/2020/2389312openalex-snapshot
An Inverse Correlation of Serum Fibroblast Growth Factor 19 with Abdominal Pain and Inflammatory Markers in Patients with Ulcerative Colitis
inferred← citeshttps://doi.org/10.1155/2022/3589525openalex-snapshot
Farnesoid X Receptor Deficiency Induces Hepatic Lipid and Glucose Metabolism Disorder via Regulation of Pyruvate Dehydrogenase Kinase 4
inferred← citeshttps://doi.org/10.11569/wcjd.v28.i2.65openalex-snapshot
Relationship between gastroesophageal reflux disease and Helicobacter pylori infection
inferred← citeshttps://doi.org/10.1161/strokeaha.123.042755openalex-snapshot
Poststroke Lung Infection by Opportunistic Commensal Bacteria Is Not Mediated by Their Expansion in the Gut Microbiota
inferred← citeshttps://doi.org/10.1172/jci.insight.132055openalex-snapshot
A human-origin probiotic cocktail ameliorates aging-related leaky gut and inflammation via modulating the microbiota/taurine/tight junction axis
inferred← citeshttps://doi.org/10.1186/s10020-026-01578-2openalex-snapshot
A TRIM15–CDX2 loop drives bile acid-induced gastric intestinal metaplasia
inferred← citeshttps://doi.org/10.1186/s12889-020-09124-3openalex-snapshot
The study protocol for a pseudo-randomised pre-post designed controlled intervention trial to study the effects of a 7-week cooking program on self-efficacy and biomarkers of health: the ECU lifestyle and biomarkers get connected study (ECULABJMOF) including the Jamie’s Ministry of Food WA…
inferred← citeshttps://doi.org/10.1186/s12957-020-01861-4openalex-snapshot
Evaluating the distribution of the locations of colorectal cancer after appendectomy and cholecystectomy
inferred← citeshttps://doi.org/10.1186/s40104-019-0402-1openalex-snapshot
Clostridium species as probiotics: potentials and challenges
inferred← citeshttps://doi.org/10.1186/s40104-026-01441-8openalex-snapshot
Bidirectional regulation of gut microbiota and young ruminant host: implications for intestinal development and mucosal immunity
inferred← citeshttps://doi.org/10.1194/jlr.m094508openalex-snapshot
FXR overexpression alters adipose tissue architecture in mice and limits its storage capacity leading to metabolic derangements
inferred← citeshttps://doi.org/10.1210/endocr/bqab063openalex-snapshot
Deletion of Intestinal SHP Impairs Short-term Response to Cholic Acid Challenge in Male Mice
inferred← citeshttps://doi.org/10.12775/jehs.2023.30.01.009openalex-snapshot
The role of the gut microbiota in understanding functional gastrointestinal disorders
inferred← citeshttps://doi.org/10.1371/journal.pone.0268445openalex-snapshot
The protective effects of HIF-1α activation on sepsis induced intestinal mucosal barrier injury in rats model of sepsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0328000openalex-snapshot
Chenodeoxycholic acid triggers gastric mucosal injury by inducing apoptosis and FXR activation
inferred← citeshttps://doi.org/10.1371/journal.ppat.1011356openalex-snapshot
The interplay between bile acids and mucosal adaptive immunity
inferred← citeshttps://doi.org/10.14218/jcth.2022.00136openalex-snapshot
The Gut Microbiome and Ferroptosis in MAFLD
inferred← citeshttps://doi.org/10.14232/phd.10329openalex-snapshot
Important therapeutic targets in acute pancreatitis
inferred← citeshttps://doi.org/10.14309/ajg.0000000000000637openalex-snapshot
Fecal Bile Acid Testing in Assessing Patients With Chronic Unexplained Diarrhea: Implications for Healthcare Utilization
inferred← citeshttps://doi.org/10.14309/crj.0000000000002162openalex-snapshot
Ileal Bile Acid Transporter Inhibitors for Symptomatic Cholestasis due to Vanishing Bile Duct Syndrome in Adults
inferred← citeshttps://doi.org/10.14309/ctg.0000000000000229openalex-snapshot
Controlled Delivery of Bile Acids to the Colon
inferred← citeshttps://doi.org/10.15389/agrobiology.2022.6.1217engopenalex-snapshot
CORRELATION INTERACTION OF TOTAL BILE ACIDS WITH BASIC BLOOD BIOCHEMICAL INDICATORS IN MINKS (Mustela vison Schreber, 1777)
inferred← citeshttps://doi.org/10.15389/agrobiology.2022.6.1217rusopenalex-snapshot
КОРРЕЛЯЦИОННЫЕ ВЗАИМОЗАВИСИМОСТИ МЕЖДУ СОДЕРЖАНИЕМ ОБЩИХ ЖЕЛЧНЫХ КИСЛОТ И ОСНОВНЫМИ БИОХИМИЧЕСКИМИ ПОКАЗАТЕЛЯМИ КРОВИ У НОРОК (Mustela vison Schreber, 1777)
inferred← citeshttps://doi.org/10.1631/jzus.b1900158openalex-snapshot
Bile-ology: from bench to bedside
inferred← citeshttps://doi.org/10.18174/549523openalex-snapshot
Breaking down the barriers : The effects of aging, gut microbiota and bile acids on intestinal health
inferred← citeshttps://doi.org/10.20996/1819-6446-2020-04-02openalex-snapshot
Gut Microbiota Composition and Metabolites as the new Determinants of Cardiovascular Pathology Development
inferred← citeshttps://doi.org/10.21147/j.issn.1000-9604.2021.04.07openalex-snapshot
Features of colorectal cancer in China stratified by anatomic sites: A hospital-based study conducted in university-affiliated hospitals from 2014 to 2018
inferred← citeshttps://doi.org/10.2139/ssrn.5064083openalex-snapshot
The Therapeutic Value of 'Bile Transfer' for Complications of Acute Pancreatitis: A Real-World Study
inferred← citeshttps://doi.org/10.2174/0109298673274040231121113410openalex-snapshot
Bile Acid-conjugate as a Promising Anticancer Agent: Recent Progress
inferred← citeshttps://doi.org/10.2174/2589977515666230308125238openalex-snapshot
Odevixibat: A Review of a Bioactive Compound for the Treatment of Pruritus Approved by the FDA
inferred← citeshttps://doi.org/10.22141/2308-2097.57.2.2023.540openalex-snapshot
Efficacy of bile salt hydrolase synthesizing probiotic bacteria in the treatment of irritable bowel syndrome with diarrhea
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