The DOI matches its Crossref record; 166 of the 166 references it cites were found in a registry or an index.
Gut microbiota functions: metabolism of nutrients and other food components
Open accessAbstract
The diverse microbial community that inhabits the human gut has an extensive metabolic repertoire that is distinct from, but complements the activity of mammalian enzymes in the liver and gut mucosa and includes functions essential for host digestion. As such, the gut microbiota is a key factor in shaping the biochemical profile of the diet and, therefore, its impact on host health and disease. The important role that the gut microbiota appears to play in human metabolism and health has stimulated research into the identification of specific microorganisms involved in different processes, and the elucidation of metabolic pathways, particularly those associated with metabolism of dietary components and some host-generated substances. In the first part of the review, we discuss the main gut microorganisms, particularly bacteria, and microbial pathways associated with the metabolism of dietary carbohydrates (to short chain fatty acids and gases), proteins, plant polyphenols, bile acids, and vitamins. The second part of the review focuses on the methodologies, existing and novel, that can be employed to explore gut microbial pathways of metabolism. These include mathematical models, omics techniques, isolated microbes, and enzyme assays.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The intricate role of the gut microbiota in breaking down complex carbohydrates, proteins, and lipids enhances the digestive process, facilitating the absorption of essential nutrients.”
From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [15]
Experimental — accuracy not yet measuredIn the citing paper
“The gut microbiota is an important factor that shapes both energy harvest and storage through metabolism of proteins and production of several metabolites including SCFAs, ammonia, sulfur-containing metabolites such as hydrogen sulfide and methanethiol, and neuroactive compounds such as tryptamine, serotonin, phenethylamine, tryptophan, and histamine [137, 138].”
From The athletic gut microbiota (2020) · cites this paper as [138]
In the citing paper
“It is well appreciated that the gut microbiota can synthesize certain vitamins, most notably vitamin K and B-group vitamins [e.g., cobalamin (B 12 ), folate, and riboflavin (144, 145)], some of which might be directly absorbed.”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [145]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Kaoutari, A. E., Armougom, F., Leroy, Q., Vialettes, B., Million, M., Raoult, D., & Henrissat, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084033 · Cited by 56
RetractedPolyphenols: Food sources and bioavailability
Manach, C., Scalbert, A., Morand, C., Rémésy, C., & Jiménez, L. (2004) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.5.727 · Cited by 8,175
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease
Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597
Host-gut microbiota metabolic interactions
Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760
Self-citationCirculating mitochondrial DAMPs cause inflammatory responses to injury
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812
Formation of propionate and butyrate by the human colonic microbiota
Louis, P., & Flint, H. J. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13589 · Cited by 3,028
The gut microbiota, bacterial metabolites and colorectal cancer
Louis, P., Hold, G. L., & Flint, H. J. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3344 · Cited by 2,925
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
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Brown, A. J., Goldsworthy, S. M., Barnes, A. A., Eilert, M. M., Tcheang, L., Daniels, D., Muir, A. I., Wigglesworth, M. J., Kinghorn, I., Fraser, N. J., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211609200 · Cited by 2,409
The gut microbiota and host health: a new clinical frontier
Marchesi, J. R., Adams, D. H., Fava, F., Hermes, G. D. A., Hirschfield, G. M., Hold, G., Quraishi, M. N., Kinross, J., Smidt, H., Tuohy, K. M., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309990 · Cited by 2,302 · cited 1×
“More recently evidence has been accumulating that the microbiota may also be involved in obesity and diabetes [4, 5].”
BackgroundBile 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
Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits
De Vadder, F., Kovatcheva-Datchary, P., Goncalves, D., Vinera, J., Zitoun, C., Duchampt, A., Bäckhed, F., & Mithieux, G. (2014) · Cell · doi:10.1016/j.cell.2013.12.016 · Cited by 2,200
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
The interaction between bacteria and bile
Begley, M., Gahan, C. G. M., & Hill, C. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2004.09.003 · Cited by 1,776
The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism
Frost, G., Sleeth, M. L., Sahuri-Arisoylu, M., Lizarbe, B., Cerdan, S., Brody, L., Anastasovska, J., Ghourab, S., Hankir, M., Zhang, S., et al. (2014) · Nature Communications · doi:10.1038/ncomms4611 · Cited by 1,771
Dominant and diet-responsive groups of bacteria within the human colonic microbiota
Walker, A. W., Ince, J., Duncan, S. H., Webster, L. M., Holtrop, G., Ze, X., Brown, D., Stares, M. D., Scott, P., Bergerat, A., et al. (2011) · The ISME Journal · doi:10.1038/ismej.2010.118 · Cited by 1,632
Bacteria as vitamin suppliers to their host: A gut microbiota perspective
LeBlanc, J. G., Milani, C., de Giori, G. S., Sesma, F., van Sinderen, D., & Ventura, M. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.08.005 · Cited by 1,613 · cited 1×
“[55] explored the metabolic potential of gut microbial sequences from two subjects and found that their microbiomes were enriched for a variety of clustered orthologous groups (COGs) involved in the synthesis of deoxyxylulose-5-phosphate, a precursor of thiamine and pyridoxal.”
BackgroundThe control and consequences of bacterial fermentation in the human colon
Cummings, J. H., & Macfarlane, G. T. (1991) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1991.tb02739.x · Cited by 1,499
Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1c
渡辺, 光., Houten, S. M., Wang, L., Moschetta, A., Mangelsdorf, D. J., Heyman, R. A., Moore, D. D., & Auwerx, J. H. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21025 · Cited by 1,425
Reichardt, N., Duncan, S. H., Young, P., Belenguer, Á., Leitch, E. C. M., Scott, K. P., Flint, H. J., & Louis, P. (2014) · The ISME Journal · doi:10.1038/ismej.2014.14 · Cited by 1,327
Trygg, J., Holmes, E. C., & Lundstedt, T. (2006) · Journal of Proteome Research · doi:10.1021/pr060594q · Cited by 1,276
Revealing the Bacterial Butyrate Synthesis Pathways by Analyzing (Meta)genomic Data
Vital, M., Howe, A. C., & Tiedje, J. M. (2014) · mBio · doi:10.1128/mbio.00889-14 · Cited by 1,189
The first 1000 cultured species of the human gastrointestinal microbiota
Rajilić-Stojanović, M., & de Vos, W. M. (2014) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12075 · Cited by 1,182
Jones, B. V., Begley, M., Hill, C., Gahan, C. G. M., & Marchesi, J. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804437105 · Cited by 1,098
Duncan, S. H., Belenguer, A., Holtrop, G., Johnstone, A. M., Flint, H. J., & Lobley, G. E. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.02340-06 · Cited by 941
Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes
Magnúsdóttir, S., Ravcheev, D., de Crécy-Lagard, V., & Thiele, I. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00148 · Cited by 876
Belenguer, A., Duncan, S. H., Calder, A. G., Holtrop, G., Louis, P., Lobley, G. E., & Flint, H. J. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.5.3593-3599.2006 · Cited by 856
Constraint-based models predict metabolic and associated cellular functions
Bordbar, A., Monk, J. M., King, Z. A., & Palsson, B. Ø. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3643 · Cited by 844
Greenblum, S., Turnbaugh, P. J., & Borenstein, E. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116053109 · Cited by 821
Louis, P., Young, P., Holtrop, G., & Flint, H. J. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.02066.x · Cited by 804
Bioavailability of Dietary Polyphenols and Gut Microbiota Metabolism: Antimicrobial Properties
Marín, L., Miguélez, E. M., Villar, C. J., & Lombó, F. (2015) · BioMed Research International · doi:10.1155/2015/905215 · Cited by 802
Katsuma, S., Hirasawa, A., & Tsujimoto, G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.01.139 · Cited by 789
Constraining the metabolic genotype–phenotype relationship using a phylogeny of in silico methods
Lewis, N. E., Nagarajan, H., & Palsson, B. O. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2737 · Cited by 779
Sequencing and beyond: integrating molecular 'omics' for microbial community profiling
Franzosa, E. A., Hsu, T. Y., Sirota‐Madi, A., Shafquat, A., Abu-Ali, G., Morgan, X. C., & Huttenhower, C. (2015) · Nature Reviews Microbiology · doi:10.1038/nrmicro3451 · Cited by 761
Analytical Methods in Untargeted Metabolomics: State of the Art in 2015
Alonso, A., Marsal, S., & Julià, A. (2015) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2015.00023 · Cited by 727
Systems biology properties of reconstructed networks
Palsson, B. Ø. (2006) · Cited by 684
Diets that differ in their FODMAP content alter the colonic luminal microenvironment
Halmos, E. P., Christophersen, C. T., Bird, A. R., Shepherd, S. J., Gibson, P. R., & Muir, J. G. (2015) · Gut · doi:10.1136/gutjnl-2014-307264 · Cited by 681
Comparison of fermentation reactions in different regions of the human colon
Macfarlane, G. T., Gibson, G. R., & Cummings, J. H. (1992) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1992.tb04882.x · Cited by 676
Emwas, A.-H. M. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2377-9_13 · Cited by 669
Systems Biology: Properties of Reconstructed Networks
Palsson, B. Ø. (2006) · doi:10.1017/cbo9780511790515 · Cited by 617
Regulation of host weight gain and lipid metabolism by bacterial bile acid modification in the gut
Joyce, S. A., MacSharry, J., Casey, P. G., Kinsella, M., Murphy, E. F., Shanahan, F., Hill, C., & Gahan, C. G. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323599111 · Cited by 604
Interaction of dietary compounds, especially polyphenols, with the intestinal microbiota: a review
Duda-Chodak, A., Tarko, T., Satora, P., & Sroka, P. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0852-y · Cited by 599
Endocrine functions of bile acids
Houten, S. M., 渡辺, 光., & Auwerx, J. H. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601049 · Cited by 595
Chemometrics in metabolomics—A review in human disease diagnosis
Madsen, R., Lundstedt, T., & Trygg, J. (2009) · Analytica Chimica Acta · doi:10.1016/j.aca.2009.11.042 · Cited by 574
Intestinal flora and endogenous vitamin synthesis
Hill, M. J. (1997) · European Journal of Cancer Prevention · doi:10.1097/00008469-199703001-00009 · Cited by 551
Intestinal luminal nitrogen metabolism: Role of the gut microbiota and consequences for the host
Davila, A.-M., Blachier, F., Gotteland, M., Andriamihaja, M., Benetti, P.-H., Sanz, Y., & Tomé, D. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2012.11.005 · Cited by 548
Analytical Strategies in Metabonomics
Lenz, E. M., & Wilson, I. D. (2006) · Journal of Proteome Research · doi:10.1021/pr0605217 · Cited by 544
Shotgun metaproteomics of the human distal gut microbiota
VerBerkmoes, N. C., Russell, A. L., Shah, M. B., Godzik, A., Rosenquist, M., Halfvarson, J., Lefsrud, M. G., Apajalahti, J., Tysk, C., Hettich, R. L., et al. (2008) · The ISME Journal · doi:10.1038/ismej.2008.108 · Cited by 544
Bacterial species involved in the conversion of dietary flavonoids in the human gut
Braune, A., & Blaut, M. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1158395 · Cited by 527
Louis, P., Duncan, S. H., McCrae, S. I., Millar, J., Jackson, M. S., & Flint, H. J. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.7.2099-2106.2004 · Cited by 517
Colonic metabolism of dietary polyphenols: influence of structure on microbial fermentation products
Rechner, A. R., Smith, M. A., Kuhnle, G., Gibson, G. R., Debnam, E. S., Srai, S. K., Moore, K. P., & Rice-Evans, C. A. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.09.022 · Cited by 512
Hooper, L. V., Xu, J., Falk, P. G., Midtvedt, T., & Gordon, J. I. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.17.9833 · Cited by 500
Smith, E. A., & Macfarlane, G. T. (1996) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1996.tb04331.x · Cited by 481
Tomás‐Barberán, F. A., González‐Sarrías, A., García‐Villalba, R., Núñez‐Sánchez, M. A., Selma, M. V., García‐Conesa, M. T., & Espín, J. C. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500901 · Cited by 465
Protein Degradation by Human Intestinal Bacteria
Macfarlane, G. T., Cummings, J. H., & Allison, C. (1986) · Microbiology · doi:10.1099/00221287-132-6-1647 · Cited by 455
Contribution of acetate to butyrate formation by human faecal bacteria
Duncan, S. H., Holtrop, G., Lobley, G. E., Calder, A. G., Stewart, C. S., & Flint, H. J. (2004) · British Journal of Nutrition · doi:10.1079/bjn20041150 · Cited by 449
Dietary intake of 337 polyphenols in French adults
Pérez‐Jiménez, J., Fezeu, L., Touvier, M., Arnault, N., Manach, C., Herçberg, S., Galan, P., & Scalbert, A. (2011) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.110.007096 · Cited by 435
Application of metagenomics in the human gut microbiome
Wang, W., Xu, S., Ren, Z., Tao, L., Jiang, J., & Zheng, S. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i3.803 · Cited by 419
Tomás-Barberán, F. A., García-Villalba, R., González-Sarrías, A., Selma, M. V., & Espín, J. C. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf5024615 · Cited by 419
Russell, W. R., Duncan, S. H., Scobbie, L., Duncan, G., Cantlay, L., Calder, A. G., Anderson, S. E., & Flint, H. J. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200594 · Cited by 417
Dietary requirements of “nutritionally non-essential amino acids” by animals and humans
Wu, G., Wu, Z., Dai, Z., Yang, Y., Wang, W., Liu, C., Wang, B., Wang, J., & Yin, Y. (2012) · Amino Acids · doi:10.1007/s00726-012-1444-2 · Cited by 408
Roles of short-chain fatty acids receptors, GPR41 and GPR43 on colonic functions.
Tazoe, H., Otomo, Y., Kaji, I., Tanaka, R., Si, K., & Kuwahara, A. (2008) · PubMed · Cited by 406
Bioavailability of phyto-oestrogens
Rowland, I. R., Faughnan, M. S., Hoey, L., Wähälä, K., Williamson, G., & Cassidy, A. (2003) · British Journal Of Nutrition · doi:10.1079/bjn2002796 · Cited by 397
Metatranscriptomic Approach to Analyze the Functional Human Gut Microbiota
Gosalbes, M. J., Durbán, A., Pignatelli, M., Abellan, J. J., Jiménez‐Hernández, N., Pérez‐Cobas, A. E., Latorre, A., & Moyá, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017447 · Cited by 395
Mechanism of growth inhibition by free bile acids in lactobacilli and bifidobacteria
Kurdi, P., Kawanishi, K., Mizutani, K., & Yokota, A. (2006) · Journal of Bacteriology · doi:10.1128/jb.188.5.1979-1986.2006 · Cited by 364
Falony, G., Vlachou, A., Verbrugghe, K., & Vuyst, L. D. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01296-06 · Cited by 362
Dabek, M., McCrae, S. I., Stevens, V. J., Duncan, S. H., & Louis, P. (2008) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2008.00520.x · Cited by 332
Taurocholic acid metabolism by gut microbes and colon cancer
Ridlon, J. M., Wolf, P. G., & Gaskins, H. R. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1150414 · Cited by 327
Isolation and characterization of human colonic bacteria able to hydrolyse chlorogenic acid
Couteau, D., McCartney, A. L., Gibson, G. R., Williamson, G., & Faulds, C. B. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01316.x · Cited by 305
Selma, M. V., Beltrán, D., García-Villalba, R., Espín, J. C., & Tomás-Barberán, F. A. (2014) · Food Funct. · doi:10.1039/c4fo00092g · Cited by 304
Production, metabolism, and excretion of hydrogen in the large intestine
Christl, S. U., Murgatroyd, P. R., Gibson, G. R., & Cummings, J. H. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)90765-q · Cited by 300
Regulation of Carbohydrate Metabolism by the Farnesoid X Receptor
Stayrook, K. R., Bramlett, K. S., Savkur, R. S., FICORILLI, J. V., Cook, T. G., Christe, M. E., Michael, L. F., & Burris, T. P. (2004) · Endocrinology · doi:10.1210/en.2004-0965 · Cited by 294
Gibson, G. R., Cummings, J. H., & Macfarlane, G. T. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.11.2750-2755.1988 · Cited by 286
Scott, K. P., Martin, J. C., Campbell, G. P., Mayer, C., & Flint, H. J. (2006) · Journal of Bacteriology · doi:10.1128/jb.00137-06 · Cited by 282
García‐Cañaveras, J. C., Donato, M. T., Castell, J. V., & Lahoz, A. (2012) · Journal of Lipid Research · doi:10.1194/jlr.d028803 · Cited by 276
Functional metagenomics to mine the human gut microbiome for dietary fiber catabolic enzymesPreprint
Tasse, L., Bercovici, J., Pizzut‐Serin, S., Robe, P., Tap, J., Klopp, C., Cantarel, B. L., Coutinho, P. M., Henrissat, B., Leclerc, M., et al. (2010) · Genome Research · doi:10.1101/gr.108332.110 · Cited by 276
Detoxification of Lithocholic Acid, A Toxic Bile Acid: Relevance to Drug Hepatotoxicity
Hofmann, A. F. (2004) · Drug Metabolism Reviews · doi:10.1081/dmr-200033475 · Cited by 269
Utilization of amino acids by bacteria from the pig small intestine
Dai, Z.-L., Zhang, J., Wu, G., & Zhu, W.-Y. (2010) · Amino Acids · doi:10.1007/s00726-010-0556-9 · Cited by 246
Functional Metabolic Map of Faecalibacterium prausnitzii, a Beneficial Human Gut Microbe
Heinken, A., Khan, M. T., Paglia, G., Rodionov, D. A., Harmsen, H. J. M., & Thiele, I. (2014) · Journal of Bacteriology · doi:10.1128/jb.01780-14 · Cited by 244
Bjerrum, J. T., Wang, Y., Hao, F., Coskun, M., Ludwig, C., Günther, U. L., & Nielsen, O. H. (2014) · Metabolomics · doi:10.1007/s11306-014-0677-3 · Cited by 241
Physiology and ecology of the sulphate‐reducing bacteria
Gibson, G. R. (1990) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1990.tb01575.x · Cited by 234
Decroos, K., Vanhemmens, S., Cattoir, S., Boon, N., & Verstraete, W. (2004) · Archives of Microbiology · doi:10.1007/s00203-004-0747-4 · Cited by 234
Corona, G., Tzounis, X., Dessì, M., Deiana, M., Debnam, E. S., Visioli, F., & Spencer, J. P. E. (2006) · Free Radical Research · doi:10.1080/10715760500373000 · Cited by 231
Systems-level characterization of a host-microbe metabolic symbiosis in the mammalian gut
Heinken, A., Sahoo, S., Fleming, R. M. T., & Thiele, I. (2013) · Gut Microbes · doi:10.4161/gmic.22370 · Cited by 225
Synthetic Ecology of Microbes: Mathematical Models and Applications
Zomorrodi, A. R., & Segrè, D. (2015) · Journal of Molecular Biology · doi:10.1016/j.jmb.2015.10.019 · Cited by 221
Noecker, C. A., Eng, A., Srinivasan, S., Theriot, C. M., Young, V. B., Jansson, J. K., Fredricks, D. N., & Borenstein, E. (2016) · mSystems · doi:10.1128/msystems.00013-15 · Cited by 217
Clavel, T., Henderson, G., Engst, W., Dore, J. M., & Blaut, M. (2006) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2005.00057.x · Cited by 209
Butyrate Histone Deacetylase Inhibitors
Steliou, K., Boosalis, M. S., Perrine, S. P., Sangerman, J., & Faller, D. V. (2012) · BioResearch open access · doi:10.1089/biores.2012.0223 · Cited by 208
Dehydroepiandrosterone Sulfotransferase Gene Induction by Bile Acid Activated Farnesoid X Receptor
Song, C. S., Echchgadda, I., Baek, B. S., Ahn, S., Oh, T., Roy, A. K., & Chatterjee, B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107557200 · Cited by 208
Bioactivation of Phytoestrogens: Intestinal Bacteria and Health
Landete, J. M., Arqués, J. L., Médina, M., Gaya, P., Rivas, B. D. L., & Múñoz, R. (2015) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2013.789823 · Cited by 204
In vitro transformation of chlorogenic acid by human gut microbiota
Tomás-Barberán, F. A., Garcı́a-Villalba, R., Quartieri, A., Raimondi, S., Amaretti, A., Leonardi, A., & Rossi, M. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201300441 · Cited by 202
Sulphate-reducing bacteria and hydrogen sulphide in the aetiology of ulcerative colitis
Rowan, F. E., Docherty, N. G., Coffey, J. C., & O'Connell, P. R. (2009) · British Journal of Surgery · doi:10.1002/bjs.6454 · Cited by 201
Kolmeder, C. A., de Been, M., Nikkilä, J., Ritamo, I., Mättö, J., Valmu, L., Salojärvi, J., Palva, A., Salonen, A., & de Vos, W. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029913 · Cited by 200
Volume, Composition, and Source of Intestinal Gas
Levitt, M. D., & Bond, J. H. (1970) · Gastroenterology · doi:10.1016/s0016-5085(19)33654-6 · Cited by 199
Farnesoid X Receptor Regulates Bile Acid-Amino Acid Conjugation
Pircher, P. C., Kitto, J. L., Petrowski, M. L., Tangirala, R. K., Bischoff, E. D., Schulman, I. G., & Westin, S. K. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302128200 · Cited by 197
Microbial regulation of host hydrogen sulfide bioavailability and metabolism
Shen, X., Carlström, M., Borniquel, S., Jädert, C., Kevil, C. G., & Lundberg, J. O. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.02.024 · Cited by 194
Hirokane, H., Nakahara, M., Tachibana, S., Shimizu, M., & Sato, R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m404255200 · Cited by 189
Dose response and minimal daily requirement for vitamin K in man.
Frick, P. G., Riedler, G., & Brögli, H. (1967) · Journal of Applied Physiology · doi:10.1152/jappl.1967.23.3.387 · Cited by 184
Muñoz‐Tamayo, R., Laroche, B., Walter, É., Dore, J. M., Duncan, S. H., Flint, H. J., & Leclerc, M. (2011) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2011.01085.x · Cited by 174
Isolation of a human intestinal bacterium capable of daidzein and genistein conversion
Matthies, A., Blaut, M., & Braune, A. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01795-08 · Cited by 161
Gut Bacteria and Hydrogen Sulfide: The New Old Players in Circulatory System Homeostasis
Tomášová, L., Konopelski, P., & Ufnal, M. (2016) · Molecules · doi:10.3390/molecules21111558 · Cited by 161
Wei, X., Yan, X., Zou, D., Yang, Z., Wang, X., Liu, W., Wang, S., Li, X., Han, J., Huang, L., et al. (2013) · BMC Gastroenterology · doi:10.1186/1471-230x-13-175 · Cited by 160
Is equol the key to the efficacy of soy foods?
Lampe, J. W. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.26736t · Cited by 158
H2metabolism is widespread and diverse among human colonic microbes
Wolf, P. G., Biswas, A., Morales, S. E., Greening, C., & Gaskins, H. R. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1182288 · Cited by 156
Modelling the emergent dynamics and major metabolites of the human colonic microbiota
Kettle, H., Louis, P., Holtrop, G., Duncan, S. H., & Flint, H. J. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12599 · Cited by 149
Significance of microflora in proteolysis in the colon
Gibson, S. A., McFarlan, C., Hay, S., & Macfarlane, G. T. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.3.679-683.1989 · Cited by 147
Transformation of Flavonoids by Intestinal Microorganisms
Blaut, M., Schoefer, & Braune, A. (2003) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831.73.2.79 · Cited by 146
Clavel, T., Lippman, R., Gavini, F., Dore, J. M., & Blaut, M. (2006) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2006.02.003 · Cited by 145
François, I., Lescroart, O., Veraverbeke, W. S., Marzorati, M., Possemiers, S., Evenepoel, P., Hamer, H. M., Houben, E., Windey, K., Welling, G. W., et al. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512000372 · Cited by 144
Insights into human colonic physiology obtained from the study of flatus composition
Suarez, F. L., Furne, J. K., Springfield, J. R., & Levitt, M. D. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.272.5.g1028 · Cited by 141
The Bioavailability of Apigenin-7-Glucoside Is Influenced by Human Intestinal Microbiota in Rats
Hanske, L., Loh, G., Sczesny, S., Blaut, M., & Braune, A. (2009) · Journal of Nutrition · doi:10.3945/jn.108.102814 · Cited by 140
Bernstein, H. (1999) · Toxicology Letters · doi:10.1016/s0378-4274(99)00113-7 · Cited by 137
Matthies, A., Loh, G., Blaut, M., & Braune, A. (2011) · Journal of Nutrition · doi:10.3945/jn.111.148247 · Cited by 137
Acetate production from hydrogen and [13C]carbon dioxide by the microflora of human feces
Lajoie, S. F., Bank, S., Miller, T. L., & Wolin, M. J. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.11.2723-2727.1988 · Cited by 136
Xiong, W., Abraham, P. E., Li, Z., Pan, C., & Hettich, R. L. (2015) · PROTEOMICS · doi:10.1002/pmic.201400571 · Cited by 136
l-Glutamine regulates amino acid utilization by intestinal bacteria
Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2012) · Amino Acids · doi:10.1007/s00726-012-1264-4 · Cited by 135
McIntosh, F. M., Maison, N., Holtrop, G., Young, P., Stevens, V. J., Ince, J., Johnstone, A. M., Lobley, G. E., Flint, H. J., & Louis, P. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02711.x · Cited by 132
Inference of Network Dynamics and Metabolic Interactions in the Gut Microbiome
Steinway, S. N., Biggs, M. B., Loughran, T. P., Papin, J. A., & Albert, R. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004338 · Cited by 130
Swann, J. R., Tuohy, K. M., Lindfors, P., Brown, D. T., Gibson, G. R., Wilson, I. D., Sidaway, J. E., Nicholson, J. K., & Holmes, E. C. (2011) · Journal of Proteome Research · doi:10.1021/pr200243t · Cited by 125
Metabolic network modeling of microbial communities
Biggs, M. B., Medlock, G. L., Kolling, G. L., & Papin, J. A. (2015) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1308 · Cited by 124
Anoxic Conditions Promote Species-Specific Mutualism between Gut Microbes In Silico
Heinken, A., & Thiele, I. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00101-15 · Cited by 123 · cited 3×
“The model predicted that the need to regenerate reducing equivalents enforced mutualism in certain pairs under anoxic conditions [153].”
BackgroundMethodInfluentialPossemiers, S., Rabot, S., Espı́n, J. C., Bruneau, A., Philippe, C., González‐Sarrías, A., Heyerick, A., Tomás-Barberán, F. A., Keukeleire, D. D., & Verstraete, W. (2008) · Journal of Nutrition · doi:10.1093/jn/138.7.1310 · Cited by 120
Kandell, R. L., & Bernstein, C. (1991) · Nutrition and Cancer · doi:10.1080/01635589109514161 · Cited by 120
The Role of FXR in Disorders of Bile Acid Homeostasis
Eloranta, J. J., & Kullak-Ublick, G. A. (2008) · Physiology · doi:10.1152/physiol.00020.2008 · Cited by 120
Wang, Y., Liu, S., Yuanjia, H., Li, P., & Wan, J. (2015) · RSC Advances · doi:10.1039/c5ra14058g · Cited by 112
Kolmeder, C. A., & de Vos, W. M. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.05.018 · Cited by 110
Heinken, A., & Thiele, I. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1023494 · Cited by 107
Hanske, L., Engst, W., Loh, G., Sczesny, S., Blaut, M., & Braune, A. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512003376 · Cited by 105
Gustafsson, B. E., Daft, F. S., McDaniel, E. G., Smith, J. C., & FITZGERALD, R. J. (1962) · Journal of Nutrition · doi:10.1093/jn/78.4.461 · Cited by 102
Systems-based approaches to unravel multi-species microbial community functioning
Abram, F. (2014) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2014.11.009 · Cited by 101
Systems biology of host–microbe metabolomics
Heinken, A., & Thiele, I. (2015) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1301 · Cited by 99
A biomolecular isolation framework for eco-systems biology
Roume, H., Muller, E. E. L., Cordes, T., Renaut, J., Hiller, K., & Wilmes, P. (2012) · The ISME Journal · doi:10.1038/ismej.2012.72 · Cited by 98
Said, H. M. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00231.2013 · Cited by 97
Mallonee, D. H., & Hylemon, P. B. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.24.7053-7058.1996 · Cited by 97
Lockyer, S., Corona, G., Yaqoob, P., Spencer, J. P. E., & Rowland, I. R. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515001269 · Cited by 90
Cole, C. B., Fuller, R., Mallet, A., & Rowland, I. R. (1985) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1985.tb03359.x · Cited by 88
Hussaini, S. H., Pereira, S. P., Murphy, G. M., & Dowling, R. H. (1995) · Hepatology · doi:10.1002/hep.1840220619 · Cited by 87
Impaired hydrogen metabolism in pneumatosis cystoides intestinalis
Christl, S. U., Gibson, G. R., Murgatroyd, P. R., Scheppach, W. M., & Cummings, J. H. (1993) · Gastroenterology · doi:10.1016/0016-5085(93)90406-3 · Cited by 86
Anti-Inflammatory Implications of the Microbial Transformation of Dietary Phenolic Compounds
Russell, W. R., Scobbie, L., Chesson, A., Richardson, A. J., Stewart, C. S., Duncan, S. H., Drew, J. E., & Duthie, G. G. (2008) · Nutrition and Cancer · doi:10.1080/01635580801987498 · Cited by 86
Tauroconjugation of cholic acid stimulates 7 alpha-dehydroxylation by fecal bacteria
Eldere, J. V., Celis, P., Pauw, G. D., Lesaffre, E., & Eyssen, H. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.2.656-661.1996 · Cited by 86
Manor, O., Levy, R., & Borenstein, E. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.07.021 · Cited by 84
Amino Acids in Human and Animal Nutrition
Karau, A., & Grayson, I. (2014) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2014_269 · Cited by 83
Ziemer, C. J. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.03016-13 · Cited by 82
Intestinal colonization: How key microbial players become established in this dynamic process
Aidy, S. E., den Abbeele, P. V., de Wiele, T. V., Louis, P., & Kleerebezem, M. (2013) · BioEssays · doi:10.1002/bies.201300073 · Cited by 74
Braune, A., Engst, W., & Blaut, M. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12864 · Cited by 64
Detection of novel metabolites of flaxseed lignans in vitro and in vivo
Quartieri, A., Garcı́a-Villalba, R., Amaretti, A., Raimondi, S., Leonardi, A., Rossi, M., & Tomás-Barberán, F. A. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500773 · Cited by 64
Human lymphocyte repertoires in ageing
Boyd, S. D., Liu, Y., Wang, C., Martin, V., & Dunn‐Walters, D. K. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.07.007 · Cited by 61
Profiling of Phenols in Human Fecal Water after Raspberry Supplementation
Gill, C. I. R., McDougall, G. J., Glidewell, S. M., Stewart, D., Shen, Q., Tuohy, K. M., Dobbin, A., Boyd, A., Brown, E. M., Haldar, S., et al. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf1017143 · Cited by 61
Young, J. C., Pan, C., Adams, R. M., Brooks, B., Banfield, J. F., Morowitz, M. J., & Hettich, R. L. (2015) · PROTEOMICS · doi:10.1002/pmic.201400563 · Cited by 61
Agent Based Modeling of Human Gut Microbiome Interactions and Perturbations
Shashkova, T., Popenko, A., Tyakht, A., Peskov, K. V., Kosinsky, Y., Bogolubsky, L. I., Raigorodskii, A. M., Ischenko, D. S., Alexeev, D. G., & Govorun, V. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148386 · Cited by 56
Bauer, E., Laczny, C. C., Magnúsdóttir, S., Wilmes, P., & Thiele, I. (2015) · Microbiome · doi:10.1186/s40168-015-0121-6 · Cited by 46
Kok, M. G. M., Ruijken, M., Swann, J. R., Wilson, I. D., Somsen, G. W., & de Jong, G. J. (2013) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-012-6701-4 · Cited by 42
Tannock, G. W., Lawley, B., Munro, K., Sims, I. M., Lee, J., Butts, C. A., & Roy, N. C. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.03799-13 · Cited by 39
Mohammed, A., & Guda, C. (2015) · BMC Genomics · doi:10.1186/1471-2164-16-s7-s16 · Cited by 37
Gustafsson, B. E., Angelin, B., Einarsson, K., & Gustafsson, J.-Α. (1977) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)41589-5 · Cited by 34
Effect of ursodeoxycholic acid on cholesterol absorption and metabolism in humans
Woollett, L. A., Buckley, D. D., Yao, L., Jones, P. J. H., Granholm, N. A., Tolley, E. A., & Heubi, J. E. (2003) · Journal of Lipid Research · doi:10.1194/jlr.m200478-jlr200 · Cited by 33
Microbiological aspects of enterohepatic neutral sterol and bile acid metabolism.
Kellogg, T. F. (1972) · PubMed · Cited by 33
Metabolome progression during early gut microbial colonization of gnotobiotic mice
Marcobal, A. M., Yusufaly, T., Higginbottom, S. K., Snyder, M. P., Sonnenburg, J. L., & Mias, G. I. (2015) · Scientific Reports · doi:10.1038/srep11589 · Cited by 31
Bastos, F. S., Bessa, J., Pacheco, C. C., Marco, P. D., Castro, P. M. L., SILVA, M. N. A., & Jorge, R. F. (2002) · Biodegradation · doi:10.1023/a:1020834603785 · Cited by 27
Bacterial Enzymes: Their Role in the Formation of Mutagens and Carcinogens in the Intestine
Mallett, A. K., & Rowland, I. R. (2008) · Digestive Diseases · doi:10.1159/000171241 · Cited by 22
Hermanussen, M., Gonder, U., Jakobs, C., Stegemann, D., & Hoffmann, G. F. (2009) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2009.116 · Cited by 17
pH feedback and phenotypic diversity within bacterial functional groups of the human gut
Kettle, H., Donnelly, R., Flint, H. J., & Marion, G. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.10.015 · Cited by 13
Methane excretion and experimental colonic carcinogenesis
Flick, J. A., Hamilton, S. R., Rosales, F. J., & Perman, J. A. (1990) · Digestive Diseases and Sciences · doi:10.1007/bf01536766 · Cited by 9
[Clinical significance of sulfate-reducing bacteria for ulcerative colitis].
Watanabe, K., Mikamo, H., & Tanaka, K. Y. (2007) · PubMed · Cited by 4
Flagged first, then by citations
Research works printed but not linked: 1
- Walker AW, Duncan SH, Louis P, Flint HJ (2014) Phylogeny, culturing, and metagenomics of the approaches to unravel multi-species microbial community functioning. Comput Struct. Biotechnol J 13:24–32
Cited by
Sorted by citations
Probiotics and prebiotics in intestinal health and disease: from biology to the clinic
Sanders, M. E., Merenstein, D. J., Reid, G., Gibson, G. R., & Rastall, R. A. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0173-3 · Cited by 2,059
Stojanov, S., Berlec, A., & Štrukelj, B. (2020) · Microorganisms · doi:10.3390/microorganisms8111715 · Cited by 1,967
Flavonoids as Anticancer Agents
Kopustinskienė, D. M., Jakštas, V., Savickas, A., & Bernatonienė, J. (2020) · Nutrients · doi:10.3390/nu12020457 · Cited by 1,420
Fassarella, M., Blaak, E. E., Penders, J., Nauta, A., Smidt, H., & Zoetendal, E. G. (2020) · Gut · doi:10.1136/gutjnl-2020-321747 · Cited by 818
Human gut microbiota in health and disease: Unveiling the relationship
Afzaal, M., Saeed, F., Shah, Y. A., Hussain, M., Rabail, R., Socol, C. T., Hassoun, A., Pateiro, M., Lorenzo, J. M., Rusu, A. V., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.999001 · Cited by 762
Metadata
- Authors
- Rowland, I., Gibson, G., Heinken, A., Scott, K., Swann, J., Thiele, I., & Tuohy, K.
- Affiliations
- University of Reading (GB)
- University of Luxembourg (LU)
- University of Aberdeen (GB)
- Imperial College London (GB)
- Fondazione Edmund Mach (IT)
- Corresponding author
- Rowland, Ian
- Venue
- European Journal of Nutrition
- Published
- 2017-04-09
- Volume
- 57
- Issue
- 1
- Pages
- 1-24
- ISSN
- 1436-6207 (ISSN-L)
- 1436-6215
- PMC
- PMC5847071
- OpenAlex
- W2604323123
- Cited by
- 2,878
- References
- 166
- Citations by year
- 2026: 317 · 2025: 393 · 2024: 431 · 2023: 382 · 2022: 424 · 2021: 365 · 2020: 305 · 2019: 173 · 2018: 65 · 2017: 17
- FWCI
- 14.34
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- European Journal of Nutrition (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- CentAUR (University of Reading) (acceptedVersion, other-oa)
- ePrints Soton (University of Southampton) (acceptedVersion)
- Aberdeen University Research Archive (Aberdeen University) (submittedVersion, other-oa)
- CINECA IRIS Institutional Research Information System (Fondazione Edmund Mach) (submittedVersion, cc-by)
- Open Repository and Bibliography (University of Luxembourg) (submittedVersion, cc-by-nc-sa)
- Spiral (Imperial College London) (submittedVersion, cc-by)
- Funders
- International Life Sciences Institute Europe
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Keywords
- gut microbiota, host-microbe interactions, nutrient metabolism, dietary carbohydrates, short-chain fatty acids, protein metabolism, plant polyphenols, bile acids, vitamin metabolism, microbial metabolic pathways, enzyme activity assay
- MeSH terms
- Gastrointestinal Microbiome, Bacteria, Bile Acids and Salts, Diet, Dietary Carbohydrates, Dietary Proteins, Fatty Acids, Food, Health Promotion, Humans, Models, Theoretical, Plants, Edible, Vitamins, Proteomics, Metagenomics, Polyphenols, Phytochemicals
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review