Bile acids as regulatory molecules

International Union of Pharmacology: Approaches to the Nomenclature of Voltage-Gated Ion Channels

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SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver

Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15593 · Cited by 4,794

SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver

Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215593 · Cited by 4,092

Bile salt biotransformations by human intestinal bacteria

Ridlon, J. M., Kang, D.-J., & Hylemon, P. B. (2006) · Journal of Lipid Research · doi:10.1194/jlr.r500013-jlr200 · Cited by 2,829

Identification of a nuclear receptor for bile acids

Makishima, M., Okamoto, A. Y., Repa, J. J., Tu, H., Learned, R. M., Luk, A., Hull, M. V., Lustig, K. D., Mangelsdorf, D. J., & Shan, B. (1999) · Science · doi:10.1126/science.284.5418.1362 · Cited by 2,714

Bile Acids: Natural Ligands for an Orphan Nuclear Receptor

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Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation

Watanabe, M., Houten, S. M., Mataki, C., Christoffolete, M. A., Kim, B. W., Sato, H., Messaddeq, N., Harney, J. W., Ezaki, O., Kodama, T., et al. (2006) · Nature · doi:10.1038/nature04330 · Cited by 2,220

The Enzymes, Regulation, and Genetics of Bile Acid Synthesis

Russell, D. W. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161712 · Cited by 2,069

A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis

Goodwin, B., Jones, S. A., Price, R. R., Watson, M. A., McKee, D. D., Moore, L. B., Galardi, C., Wilson, J. G., Lewis, M. C., Roth, M. E., et al. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00051-4 · Cited by 1,940

Ostα−/−mice exhibit altered expression of intestinal lipid absorption genes, resistance to age-related weight gain, and modestly improved insulin sensitivity

Wheeler, S. G., Hammond, C. L., Jornayvaz, F. R., Samuel, V. T., Shulman, G. I., Soroka, C. J., Boyer, J. L., Hinkle, P. M., & Ballatori, N. (2014) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00368.2013 · Cited by 16

Xenobiotics Targeting Cardiolipin Metabolism to Promote Thrombosis in Zebrafish

Liu, H., Cui, H., Huang, Y., Gao, S., Tao, S., Hu, J., & Wan, Y. (2021) · Environmental Science & Technology · doi:10.1021/acs.est.0c08068 · Cited by 15

Bile acid disorders and intestinal barrier dysfunction are involved in the development of fatty liver in laying hens

Zhao, L., Jiang, Q., Lei, J., Cui, J., Pan, X., Yuan, Y., & Zhang, B. (2024) · Poultry Science · doi:10.1016/j.psj.2024.104422 · Cited by 18

Gut microbiota in non-alcoholic fatty liver disease: Pathophysiology, diagnosis, and therapeutics

Pandey, H., Goel, P., Srinivasan, V. M., Tang, D. W. T., Wong, S. H., & Lal, D. (2025) · World Journal of Hepatology · doi:10.4254/wjh.v17.i6.106849 · Cited by 20

The role of intestinal microbiota in the pathogenesis of metabolic diseases

Węgielska, I., & Suliburska, J. (2016) · Acta Scientiarum Polonorum Technologia Alimentaria · doi:10.17306/j.afs.2016.2.20 · Cited by 15

Metabolomics in Bariatric Surgery: Towards Identification of Mechanisms and Biomarkers of Metabolic Outcomes

Ha, J., Kwon, Y., & Park, S. S. (2021) · Obesity Surgery · doi:10.1007/s11695-021-05566-9 · Cited by 16

Population pharmacokinetic model to generate mechanistic insights in bile acid homeostasis and drug-induced cholestasis

de Bruijn, V. M. P., Rietjens, I. M. C. M., & Bouwmeester, H. (2022) · Archives of Toxicology · doi:10.1007/s00204-022-03345-8 · Cited by 15

Paeoniae Radix Rubra can enhance fatty acid β-oxidation and alleviate gut microbiota disorder in α-naphthyl isothiocyanate induced cholestatic model rats

Xu, J., Xu, F., Wang, W., Wang, P.-P., Xian, J., Han, X., Shang, M., Liu, G., Wang, X., & Cai, S. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1002922 · Cited by 18

Gut Microbiome and Bile Acid Interactions

Wu, N., Bayatpour, S., Hylemon, P. B., Aseem, S. O., Brindley, P. J., & Zhou, H. (2024) · American Journal Of Pathology · doi:10.1016/j.ajpath.2024.11.004 · Cited by 15

Effects of preventative application of metformin on bile acid metabolism in high fat-fed/streptozotocin-diabetic rats.

Ding, L., Qu, Z., Chi, J., Shi, R., Wang, L., Hou, L., Wang, Y., & Pang, S. (2015) · PubMed · Cited by 15

Analysis of serum bile acids by isotope dilution-mass spectrometry to assess the performance of routine total bile acid methods

Ducroq, D., Morton, M. S., Shadi, N., Fraser, H. L., Strevens, C., Morris, J., & Thomas, M. A. (2010) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1258/acb.2010.010154 · Cited by 15

Bile Acid Metabolism

Chiang, J. Y. L. (2010) · Molecular pathology library · doi:10.1007/978-1-4419-7107-4_12 · Cited by 15

Exogenous Players in Mitochondria-Related CNS Disorders: Viral Pathogens and Unbalanced Microbiota in the Gut-Brain Axis

Righetto, I., Gasparotto, M., Casalino, L., Vacca, M., & Filippini, F. (2023) · Biomolecules · doi:10.3390/biom13010169 · Cited by 14

Alterations in the gut microbiota and serum metabolomics of spontaneous cholestasis caused by loss of FXR signal in mice

Wei, S., He, T., Zhao, X., Jing, M., Li, H., Chen, L., Zheng, R., & Zhao, Y. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1197847 · Cited by 14

Untargeted metabolomics in the aqueous humor reveals the involvement of TAAR pathway in glaucoma

Gowtham, L., Halder, N., Angmo, D., Singh, S. B., Jayasundar, R., Dada, T., & Velpandian, T. (2023) · Experimental Eye Research · doi:10.1016/j.exer.2023.109592 · Cited by 14

Biopolymer-based sequestrants for lowering cholesterol: Structures, in vitro bile acid anion binding effects, and interaction mechanisms

Li, M.-Z., Wang, L., Chen, G.-J., & Chen, Z. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106002 · Cited by 14

Bile acids and coronavirus disease 2019

Huang, X., Liu, X., & Li, Z. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.02.011 · Cited by 15

Bile acids inhibit Na+/H+ exchanger and Cl−/HCO3 − exchanger activities via cellular energy breakdown and Ca2+ overload in human colonic crypts

Kunstár, É. P., Farkas, K., Maléth, J., Rakonczay, Z., Nagy, F. T., Molnár, T., Szepes, Z., Venglovecz, V., Lonovics, J., Rázga, Z., et al. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1560-9 · Cited by 14

Long-term virus-induced alterations of CYP3A-mediated drug metabolism: a look at the virology, immunology and molecular biology of a multi-faceted problem

Croyle, M. A. (2009) · Expert Opinion on Drug Metabolism & Toxicology · doi:10.1517/17425250903136748 · Cited by 14

Separation and determination of structurally related free bile acids by pressurized capillary electrochromatography coupled to laser induced fluorescence detection

Wu, Y., Wang, X., Wu, Q., Wu, X., Lin, X., & Xie, Z. (2010) · Analytical Methods · doi:10.1039/c0ay00309c · Cited by 14

Quantification of multiple bile acids in uninephrectomized rats using ultra-performance liquid chromatography-tandem mass spectrometry

Penno, C. A., Arsenijevic, D., Cunha, T. D., Kullak-Ublick, G. A., Montani, J., & Odermatt, A. (2013) · Analytical Methods · doi:10.1039/c3ay26520j · Cited by 14

The Gut Microbiota–Metabolic Axis: Emerging Insights from Human and Experimental Studies on Type 2 Diabetes Mellitus—A Narrative Review

Alqahtani, M. S. (2025) · Medicina · doi:10.3390/medicina61112017 · Cited by 24

Secondary bile acids and the biliary epithelia: The good and the bad

Lenci, I., Milana, M., Signorello, A., Grassi, G. B., & Baiocchi, L. (2023) · World Journal of Gastroenterology · doi:10.3748/wjg.v29.i2.357 · Cited by 13

The relative abundance of fecal bacterial species belonging to the Firmicutes and Bacteroidetes phyla is related to plasma levels of bile acids in young adults

Osuna‐Prieto, F. J., Xu, H., Ortiz-Alvarez, L., Di, X., Köhler, I., Jurado‐Fasoli, L., Rubio‐López, J., Plaza‐Díaz, J., Vilchez‐Vargas, R., Link, A., et al. (2023) · Metabolomics · doi:10.1007/s11306-023-02016-8 · Cited by 14

Gpbar-1/cAMP/PKA signaling mitigates macrophage-mediated acute cholestatic liver injury via antagonizing NLRP3-ASC inflammasome

Zhuang, L., Jia, N., Zhang, L., Zhang, Q., Antwi, S. O., Sartorius, K., Wu, K., Sun, D., Xi, D., & Lu, Y. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167266 · Cited by 13

EP4 emerges as a novel regulator of bile acid synthesis and its activation protects against hypercholesterolemia

Fan, Y., Cai, Y., Wong, H. K., Chen, X. Y., Huang, I. B., Vanhoutte, P. M., Xia, Z., Xu, A., & Tang, E. H. C. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2018.06.003 · Cited by 14

A novel voltammetric approach to the detection of primary bile acids in serum samples

Klouda, J., Nesměrák, K., Kočovský, P., Barek, J., & Schwarzová‐Pecková, K. (2020) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2020.107539 · Cited by 13

Role of mitochondria in regulating immune response during bacterial infection

Khan, S., Basu, S., Raj, D., & Lahiri, A. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.10.004 · Cited by 13

The Human Microbiome and Its Role in Musculoskeletal Disorders

Aboushaala, K. A., Wong, A. Y. L., Barajas, J. N., Lim, P., Al‐Harthi, L., Chee, A., Forsyth, C. B., Oh, C., Toro, S. J., Williams, F. M. K., et al. (2023) · Genes · doi:10.3390/genes14101937 · Cited by 13

Bile Acid Metabolism

Dawson, P. A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-444-63438-2.00012-2 · Cited by 13

Dietary Regulation of Mouse Intestinal P450 Expression and Drug Metabolism

Zhang, P., Jia, K., Fang, C., Zhou, X., Ding, X., & Zhang, Q. (2012) · Drug Metabolism and Disposition · doi:10.1124/dmd.112.049403 · Cited by 13

Oral health status of children with syndromic craniosynostosis.

Dalben, G. D. S., Costa, B., & Gomide, M. R. (2006) · PubMed · Cited by 13

Bile acids target proteolipid nano-assemblies of EGFR and phosphatidic acid in the plasma membrane for stimulation of MAPK signaling

Hong, L., Estes, M. K., Zhang, H., Du, G., & Zhou, Y. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198983 · Cited by 13

siRNA-mediated gene silencing for non-alcoholic fatty liver disease: A comprehensive review of molecular targets

Mahmoudi, A. A., Rostami, M., Hajihasani, M. M., Sukhorukov, V. N., Kesharwani, P., & Sahebkar, A. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.112866 · Cited by 12

Regulation of Mitochondrial and Peroxisomal Metabolism in Female Obesity and Type 2 Diabetes

Antelo-Cea, D. A., Martínez-Rojas, L., Cabrerizo-Ibáñez, I., Rashtabady, A. R., & Hernández‐Álvarez, M. I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011237 · Cited by 13

Gut microbial metabolites: The bridge connecting diet and atherosclerosis, and next-generation targets for dietary interventions

Zhang, L., Yin, Y., & Jin, S. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.128037 · Cited by 14

Regulation of Intestinal Cytochrome P450 Expression by Hepatic Cytochrome P450: Possible Involvement of Fibroblast Growth Factor 15 and Impact on Systemic Drug Exposure

Zhu, Y., Ding, X., Fang, C., & Zhang, Q.-Y. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.088914 · Cited by 12

Interspecies Chemical Signals Released into the Environment may Create Xenohormetic, Hormetic and Cytostatic Selective Forces that Drive the Ecosystemic Evolution of Longevity Regulation Mechanisms

Burstein, M. T., Beach, A., Richard, V. R., Koupaki, O., Gomez-Perez, A., Goldberg, A. A., Kyryakov, P., Bourque, S. D., Glebov, A., & Titorenko, V. I. (2011) · Dose-Response · doi:10.2203/dose-response.11-011.titorenko · Cited by 12

Fitness for purpose of stabilized stool samples for bile acid metabolite analyses

Neuberger-Castillo, L., Ammerlaan, W., & Betsou, F. (2021) · Scientific Reports · doi:10.1038/s41598-021-86784-0 · Cited by 12

Nutritional implications in the mechanistic link between the intestinal microbiome, renin-angiotensin system, and the development of obesity and metabolic syndrome

Guimarães, V. H. D., Marinho, B. M., Motta‐Santos, D., Mendes, G. D. R. L., & Santos, S. H. S. (2022) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.109252 · Cited by 15

Microbiota–Liver Diseases Interactions

Capparelli, R., Cuomo, P., Gentile, A., & Iannelli, D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043883 · Cited by 12

Metabolic adaptation allows Amacr-deficient mice to remain symptom-free despite low levels of mature bile acids

Selkälä, E. M., Kuusisto, S. M., Salonurmi, T., Savolainen, M. J., Jauhiainen, M., Pirilä, P., Kvist, A.-P., Conzelmann, E., Schmitz, W., Alexson, S. E. H., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2013.05.002 · Cited by 12

Fibroblast growth factor receptor 4 Gly388Arg polymorphism associated with severity of gallstone disease in a Chinese population.

Chen, Q.-P., Li, W.-J., Wan, Y.-Y., Yu, C.-D., & Li, W.-G. (2012) · Genetics and Molecular Research · doi:10.4238/2012.march.8.3 · Cited by 10

Liver Transcriptome Changes of Hyla Rabbit in Response to Chronic Heat Stress

Wu, Z., Yang, X., Chen, S., Deng, F., Jia, X., Hu, S., Wang, J., & Lai, S. (2019) · Animals · doi:10.3390/ani9121141 · Cited by 12

Nerve growth factor induced farnesoid X receptor upregulation modulates autophagy flux and protects hepatocytes in cholestatic livers

Tsai, M., Lee, H.-M., Huang, S.-C., Sun, C., Chiu, T.-C., Chen, P., Lin, Y., Hung, T., Lee, P., & Kao, Y. H. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108281 · Cited by 12

Unravelling the potential of gut microbiota in sustaining brain health and their current prospective towards development of neurotherapeutics

Banerjee, A., Pradhan, L. K., Sahoo, P. K., Jena, K. K., Chauhan, N. R., Chauhan, S., & Das, S. K. (2021) · Archives of Microbiology · doi:10.1007/s00203-021-02276-9 · Cited by 13

Modulation of Disordered Bile Acid Homeostasis and Hepatic Tight Junctions Using Salidroside against Hepatocyte Apoptosis in Furan-Induced Mice

Wang, Z., Liu, H., Li, L., Li, Y., Yan, H., & Yuan, Y. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c04654 · Cited by 11

Emerging roles of lipid and metabolic sensing in the neuroendocrine control of body weight and reproduction

Rodríguez-Vázquez, E., Torrecillas, Á. A., López-Sancho, M., Castellano, J. M., & Tena‐Sempere, M. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1454874 · Cited by 12

Transcription of the human microsomal epoxide hydrolase gene (EPHX1) is regulated by an HNF-4α/CAR/RXR/PSF complex

Peng, H., Zhu, Q., Zhong, S., & Levy, D. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.05.003 · Cited by 11

Empirical Validation of a Hypothesis of the Hormetic Selective Forces Driving the Evolution of Longevity Regulation Mechanisms

Gomez-Perez, A., Kyryakov, P., Burstein, M. T., Asbah, N., Noohi, F., Iouk, T., & Titorenko, V. I. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00216 · Cited by 11

Hydroxytyrosol-Rich Olive Extract for Plasma Cholesterol Control

Cicero, A. F. G., Fogacci, F., Micoli, A. D., Veronesi, M., Grandi, E., & Borghi, C. (2022) · Applied Sciences · doi:10.3390/app121910086 · Cited by 11

The Biliary System, Second Edition

Wang, D. Q. ‐., Neuschwander‐Tetri, B. A., & Portincasa, P. (2016) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00147ed2v01y201611isp071 · Cited by 10

Anti-inflammatory activity of polyamide dendrimers bearing bile acid termini synthesized via SPAAC

Porras, A. M. G., Bertuzzi, D. L., Lucas, K., & Ornelas, C. (2019) · Journal of Nanoparticle Research · doi:10.1007/s11051-019-4672-5 · Cited by 11

Proteome, Bioinformatic, and Functional Analyses Reveal a Distinct and Conserved Metabolic Pathway for Bile Salt Degradation in the Sphingomonadaceae

Feller, F. M., Wöhlbrand, L., Holert, J., Schnaars, V., Elsner, L., Mohn, W. W., Rabus, R., & Philipp, B. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.00987-21 · Cited by 12

Renal Farnesoid X Receptor improves high fructose-induced salt-sensitive hypertension in mice by inhibiting DNM3 to promote nitro oxide production

Zhu, Y., Tao, Y., Wu, C.-Y., Zeng, Y., Du, H., Xiang, Q., Chen, Y., Zhu, Q., & Wang, L. (2022) · Journal of Hypertension · doi:10.1097/hjh.0000000000003189 · Cited by 11

Investigation of vitamin B6 inadequacy, induced by exposure to the anti-B6 factor 1-amino d-proline, on plasma lipophilic metabolites of rats: a metabolomics approach

Mayengbam, S., House, J. D., & Aliani, M. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0934-x · Cited by 11

Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism

Dias, V., & Ribeiro, V. (2011) · Journal of Pharmacy And Bioallied Sciences · doi:10.4103/0975-7406.84465 · Cited by 11

The effects of taurochenodeoxycholic acid in preventing pulmonary fibrosis in mice.

Zhou, C., Shi, Y., Li, J., Zhang, W., Wang, Y., Liu, Y., & Liu, J. (2013) · PubMed · Cited by 11

Do Therapeutic Bile Acids Hit the Sweet Spot of Glucose Metabolism in NAFLD?

Karpen, S. J. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.07.017 · Cited by 11

The interplay between bile acids and mucosal adaptive immunity

Mohammed, A. D., Ball, R. A. W., & Kubinak, J. L. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011356 · Cited by 10

Probiotics Enhance Coilia nasus Growth Performance and Nutritional Value by Regulating Glucolipid Metabolism via the Gut–Liver Axis

Mang, Q., Gao, J., Li, Q., Sun, Y., Xu, G., & Xu, P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212196 · Cited by 10

Managing Type 2 Diabetes Mellitus via the Regulation of Gut Microbiota: A Chinese Medicine Perspective

Ng, C. Y. J., Zhong, L. L. D., Ng, H. S., Goh, K. S., & Zhao, Y. X. (2024) · Nutrients · doi:10.3390/nu16223935 · Cited by 11

Lipidomics-based natural products for chronic kidney disease treatment

Zhang, R., Wang, J., Wu, C., Wang, L., Liu, P., & Li, P. (2025) · Heliyon · doi:10.1016/j.heliyon.2024.e41620 · Cited by 10

Microbiome and gut-liver interactions: From mechanisms to therapies

Anis, M. A., Shahid, Y., Majeed, A. A., & Abid, S. (2025) · World Journal of Gastroenterology · doi:10.3748/wjg.v31.i40.111409 · Cited by 12

The Use of Stable and Radioactive Sterol Tracers as a Tool to Investigate Cholesterol Degradation to Bile Acids in Humans in Vivo

Bertolotti, M., Crosignani, A., & Puppo, M. D. (2012) · Molecules · doi:10.3390/molecules17021939 · Cited by 10

Bile Acids in Control of the Gut-Liver-Axis

Hild, B., Heinzow, H. S., Schmidt, H., & Maschmeier, M. (2021) · Zeitschrift für Gastroenterologie · doi:10.1055/a-1330-9644 · Cited by 10

Exploration of the underlying mechanisms of isoniazid/rifampicin‐induced liver injury in mice using an integrated proteomics and metabolomics approach

Song, Y., Qu, X., Tao, L., Gao, H., Zhang, Y., Zhai, J., Gong, J., & Hu, T. (2022) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.23217 · Cited by 12

Secretion and Function of Gastrointestinal Hormones after Bariatric Surgery: Their Role in Type 2 Diabetes

Shukla, A. P., & Rubino, F. (2011) · Canadian Journal of Diabetes · doi:10.1016/s1499-2671(11)52008-8 · Cited by 10

Molecular aspects of cholangiocarcinoma

Kiguchi, K. (2014) · Journal of Hepato-Biliary-Pancreatic Sciences · doi:10.1002/jhbp.66 · Cited by 10

An association between post-meal bile acid response and bone resorption in normal subjects

Ewang-Emukowhate, M., Alaghband-Zadeh, J., Vincent, R. P., Sherwood, R., & Cf, M. (2013) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1177/0004563213482891 · Cited by 10

CLA-Enriched Diet Containing t10,c12- CLA Alters Bile Acid Homeostasis and Increases the Risk of Cholelithiasis in Mice

Zabala‐Letona, A., Niot, I., Laugerette, F., Athias, A., Monnot, M.-C., Portillo, M. P., Besnard, P., & Poirier, H. (2011) · Journal of Nutrition · doi:10.3945/jn.110.136168 · Cited by 10

Non-Alcoholic Fatty Liver Disease: The Effect of Bile Acids and Farnesoid X Receptor Agonists on Pathophysiology and Treatment

Khalid, Q., Bailey, I., & Patel, V. B. (2015) · Liver Research - Open Journal · doi:10.17140/lroj-1-106 · Cited by 10

Bile Acids, Chaperones, and Mammalian Longevity

Krøll, J. (2012) · Rejuvenation Research · doi:10.1089/rej.2011.1286 · Cited by 10

An Edge Selection Mechanism for Chirally Selective Solubilization of Binaphthyl Atropisomeric Guests by Cholate and Deoxycholate Micelles

Eckenroad, K. W., Manley, G. A., Yehl, J., Pirnie, R. T., Strein, T. G., & Rovnyak, D. (2016) · Chirality · doi:10.1002/chir.22609 · Cited by 10

Improved infrared spectroscopic discrimination between gall bladder (GB) polyps and GB cancer using component-descriptive spectral features of separated phases from bile

Jang, E., Jeong, J., Yim, J.-H., Kim, Y., Lee, C., Choi, D., & Chung, H. (2019) · The Analyst · doi:10.1039/c9an00878k · Cited by 10

Metabolomics profiling in acute liver transplant rejection in a pediatric population

Frediani, J. K., Beyh, Y. S., Gupta, N. A., Westbrook, A. L., Cleeton, R. L., Cordero, M., Hernández, A., Tran, V., Jones, D. P., & Vos, M. B. (2022) · Scientific Reports · doi:10.1038/s41598-022-18957-4 · Cited by 9

Conformational properties of cholic acid, a lead compound at the crossroads of bile acid inspired drug discovery

Gioiello, A., Venturoni, F., Tamimi, S., Custodi, C., Pellicciari, R., & Macchiarulo, A. (2014) · MedChemComm · doi:10.1039/c4md00024b · Cited by 9

Alterations in the gut microbiome and metabolome profiles of septic rats treated with aminophylline

Li, Y., Zhao, H., Sun, G., Duan, Y., Guo, Y., Xie, L., & Ding, X. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03280-3 · Cited by 9

Human microbiome and cardiovascular diseases

Alam, J., Puppala, V., Uppulapu, S. K., Das, B., & Banerjee, S. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.07.012 · Cited by 11

Impact of cholecystectomy on acute coronary syndrome according to metabolic condition: a nationwide population-based cohort study

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Bile deficiency induces changes in intestinal Cl − and HCO 3− secretions in mice

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