Linking the Microbiota, Chronic Disease, and the Immune System

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444 · see citing works

A human gut microbial gene catalogue established by metagenomic sequencing

MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624 · see citing works

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762 · see citing works

Metabolic Endotoxemia Initiates Obesity and Insulin Resistance

Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., Neyrinck, A. M., Fava, F., Tuohy, K. M., Chabo, C., et al. (2007) · Diabetes · doi:10.2337/db06-1491 · Cited by 6,638 · see citing works

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 · see citing works

Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549 · see citing works

The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T _reg Cell Homeostasis

Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413 · see citing works

Role of the microbiota in immunity and inflammation.

Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385 · see citing works

Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation

Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838 · see citing works

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662 · see citing works

Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases

Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611 · see citing works

Cross-talk between <i>Akkermansia muciniphila</i> and intestinal epithelium controls diet-induced obesity

Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511 · see citing works

Macrophages in Tissue Repair, Regeneration, and Fibrosis

Wynn, T. A., & Vannella, K. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.015 · Cited by 4,481 · see citing works

Intestinal microbiota metabolism of l-carnitine, a nutrient in red meat, promotes atherosclerosis

Koeth, R. A., Wang, Z., Levison, B. S., Buffa, J. A., Org, E., Sheehy, B. T., Britt, E. B., Fu, X., Wu, Y., Li, L., et al. (2013) · Nature Medicine · doi:10.1038/nm.3145 · Cited by 4,386 · see citing works

Interactions Between the Microbiota and the Immune System

Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173 · see citing works

Gut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice

Ridaura, V. K., Faith, J. J., Rey, F. E., Cheng, J., Duncan, A. E., Kau, A. L., Griffin, N. W., Lombard, V., Henrissat, B., Bain, J. R., et al. (2013) · Science · doi:10.1126/science.1241214 · Cited by 3,788 · see citing works

Inflammatory Mechanisms in Obesity

Gregor, M. F., & Hotamisligil, G. S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101322 · Cited by 3,754 · see citing works

Microbial translocation is a cause of systemic immune activation in chronic HIV infection

Brenchley, J. M., Price, D. A., Schacker, T. W., Asher, T. E., Silvestri, G., Rao, S., Kazzaz, Z., Bornstein, E., Lambotte, O., Altmann, D., et al. (2006) · Nature Medicine · doi:10.1038/nm1511 · Cited by 3,559 · see citing works

Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human

Wu, J., Boström, P., Sparks, L. M., Li, Y., Choi, J. H., Giang, A.-H., Khandekar, M. J., Virtanen, K. A., Nuutila, P., Schaart, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.016 · Cited by 3,299 · see citing works

Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43

Maslowski, K. M., Vieira, A. T., Ng, A., Kranich, J., Sierro, F., Yu, D., Schilter, H. C., Rolph, M. S., Mackay, F., Artis, D., et al. (2009) · Nature · doi:10.1038/nature08530 · Cited by 3,241 · see citing works

Personalized nutrition by prediction of glycemic responses

Zeevi, D., Korem, T., Zmora, N., Israeli, D., Rothschild, D., Weinberger, A., Ben-Yacov, O., Lador, D., Avnit-Sagi, T., Lotan-Pompan, M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.001 · Cited by 2,929 · see citing works

Diet-Induced Obesity Is Linked to Marked but Reversible Alterations in the Mouse Distal Gut Microbiome

Turnbaugh, P. J., Bäckhed, F., Fulton, L., & Gordon, J. I. (2008) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2008.02.015 · Cited by 2,915 · see citing works

An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System

Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910 · see citing works

Intestinal Crosstalk between Bile Acids and Microbiota and Its Impact on Host Metabolism

Wahlstrom, A. M., Sayin, S. I., Marschall, H., & Bäckhed, F. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.005 · Cited by 2,903 · see citing works

Inflammasome-mediated dysbiosis regulates progression of NAFLD and obesity

Henao-Mejia, J., Elinav, E., Jin, C., Hao, L., Mehal, W. Z., Strowig, T., Thaiss, C. A., Kau, A. L., Eisenbarth, S. C., Jurczak, M. J., et al. (2012) · Nature · doi:10.1038/nature10809 · Cited by 2,435 · see citing works

Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota

MetaHIT consortium, Forslund, K., Hildebrand, F., Nielsen, T., Falony, G., Le Chatelier, E., Sunagawa, S., Prifti, E., Vieira-Silva, S., Gudmundsdottir, V., et al. (2015) · Nature · doi:10.1038/nature15766 · Cited by 2,116 · see citing works

Metabolic Syndrome and Altered Gut Microbiota in Mice Lacking Toll-Like Receptor 5

Vijay-Kumar, M., Aitken, J. D., Carvalho, F. A., Cullender, T. C., Mwangi, S., Srinivasan, S., Sitaraman, S. V., Knight, R., Ley, R. E., & Gewirtz, A. T. (2010) · Science · doi:10.1126/science.1179721 · Cited by 2,068 · see citing works

NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis

Elinav, E., Strowig, T., Kau, A. L., Henao-Mejia, J., Thaiss, C. A., Booth, C. J., Peaper, D. R., Bertin, J., Eisenbarth, S. C., Gordon, J. I., et al. (2011) · Cell · doi:10.1016/j.cell.2011.04.022 · Cited by 2,024 · see citing works

Variations in the Prevalence of Obesity Among European Countries, and a Consideration of Possible Causes

Blundell, J. E., Baker, J. L., Boyland, E. J., Blaak, E. E., Charzewska, J., Henauw, S. D., Frühbeck, G., González‐Gross, M., Hebebrand, J., Holm, L., et al. (2017) · Obesity Facts · doi:10.1159/000455952 · Cited by 1,980 · see citing works

Gut Microbial Metabolite TMAO Enhances Platelet Hyperreactivity and Thrombosis Risk

Zhu, W., Gregory, J. C., Org, E., Buffa, J. A., Gupta, N., Wang, Z., Li, L., Fu, X., Wu, Y., Mehrabian, M., et al. (2016) · Cell · doi:10.1016/j.cell.2016.02.011 · Cited by 1,968 · see citing works

Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice

Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B. (2012) · Nature · doi:10.1038/nature11225 · Cited by 1,904 · see citing works

Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile

Buffie, C. G., Bucci, V., Stein, R. R., McKenney, P. T., Ling, L., Gobourne, A., No, D., Liu, H., Kinnebrew, M., Viale, A., et al. (2015) · Nature · doi:10.1038/nature13828 · Cited by 1,872 · see citing works

Altering the intestinal microbiota during a critical developmental window has lasting metabolic consequences

Cox, L. M., Yamanishi, S., Sohn, J., Alekseyenko, A. V., Leung, J. M., Cho, I., Kim, S. G., Li, H., Gao, Z., Mahana, D., et al. (2014) · Cell · doi:10.1016/j.cell.2014.05.052 · Cited by 1,859 · see citing works

Dietary intervention impact on gut microbial gene richness

Cotillard, A., Kennedy, S. P., Kong, L. C., Prifti, E., Pons, N., Le Chatelier, E., Almeida, M., Quinquis, B., Levenez, F., Galleron, N., et al. (2013) · Nature · doi:10.1038/nature12480 · Cited by 1,832 · see citing works

Inflammatory bowel disease

Kaser, A., Zeissig, S., & Blumberg, R. S. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101225 · Cited by 1,806 · see citing works

Polysaccharide utilization by gut bacteria: potential for new insights from genomic analysis

Flint, H. J., Bayer, E. A., Rincón, M. T., Lamed, R., & White, B. A. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1817 · Cited by 1,710 · see citing works

Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function

Olszak, T., An, D., Zeissig, S., Vera, M. P., Richter, J., Franke, A., Glickman, J. N., Siebert, R., Baron, R. M., Kasper, D. L., et al. (2012) · Science · doi:10.1126/science.1219328 · Cited by 1,661 · see citing works

The global burden of diarrhoeal disease, as estimated from studies published between 1992 and 2000.

Kosek, M. N., Bern, C., & Guerrant, R. L. (2003) · Europe PMC (PubMed Central) · Cited by 1,617 · see citing works

Antibiotics in early life alter the murine colonic microbiome and adiposity

Cho, I., Yamanishi, S., Cox, L., Methé, B. A., Zavadil, J., Li, K., Gao, Z., Mahana, D., Raju, K., Teitler, I., et al. (2012) · Nature · doi:10.1038/nature11400 · Cited by 1,613 · see citing works

Fecal Microbiota Transplantation Induces Remission in Patients With Active Ulcerative Colitis in a Randomized Controlled Trial

Moayyedi, P., Surette, M. G., Kim, P. T., Libertucci, J., Wolfe, M., Onischi, C., Armstrong, D., Marshall, J. K., Kassam, Z., Reinisch, W., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.04.001 · Cited by 1,499 · see citing works

Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasome

Macia, L., Tan, J., Vieira, A. T., Leach, K., Stanley, D., Luong, S., Maruya, M., Ian McKenzie, C., Hijikata, A., Wong, C., et al. (2015) · Nature Communications · doi:10.1038/ncomms7734 · Cited by 1,439 · see citing works

Exercise and associated dietary extremes impact on gut microbial diversity

Clarke, S. F., Murphy, E. F., O'Sullivan, O., Lucey, A. J., Humphreys, M., Hogan, A., Hayes, P., O'Reilly, M., Jeffery, I. B., Wood-Martin, R., et al. (2014) · Gut · doi:10.1136/gutjnl-2013-306541 · Cited by 1,439 · see citing works

Host-Mediated Inflammation Disrupts the Intestinal Microbiota and Promotes the Overgrowth of Enterobacteriaceae

Lupp, C., Robertson, M. L., Wickham, M. E., Sekirov, I., Champion, O. L., Gaynor, E. C., & Finlay, B. B. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.06.010 · Cited by 1,310 · see citing works

Immunoglobulin A Coating Identifies Colitogenic Bacteria in Inflammatory Bowel Disease

Palm, N. W., de Zoete, M. R., Cullen, T. W., Barry, N. A., Stefanowski, J., Hao, L., Degnan, P. H., Hu, J., Peter, I., Zhang, W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.006 · Cited by 1,286 · see citing works

Low counts of Faecalibacterium prausnitzii in colitis microbiota

Sokol, H., Seksik, P., Furet, J. P., Firmesse, O., Nion-Larmurier, I., Beaugerie, L., Cosnes, J., Corthier, G., Marteau, P., & Doré, J. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20903 · Cited by 1,275 · see citing works

Human oral, gut, and plaque microbiota in patients with atherosclerosis

Koren, O., Spor, A., Felin, J., Fåk, F., Stombaugh, J., Tremaroli, V., Behre, C. J., Knight, R., Fagerberg, B., Ley, R. E., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011383107 · Cited by 1,196 · see citing works

The Global Burden of Disease Study 2010: Interpretation and Implications for the Neglected Tropical Diseases

Hotez, P. J., Alvarado, M., Basáñez, M.-G., Bolliger, I. W., Bourne, R., Boussinesq, M., Brooker, S. J., Brown, A. S., Buckle, G. C., Budke, C. M., et al. (2014) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0002865 · Cited by 1,089 · see citing works

Atopic dermatitis: a disease of altered skin barrier and immune dysregulation

Boguniewicz, M., & Leung, D. Y. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01027.x · Cited by 1,081 · see citing works

Host-Derived Nitrate Boosts Growth of <i>E. coli</i> in the Inflamed Gut

Winter, S. E., Winter, M. G., Xavier, M. N., Thiennimitr, P., Poon, V., Keestra, A. M., Laughlin, R. C., Gomez, G., Wu, J., Lawhon, S. D., et al. (2013) · Science · doi:10.1126/science.1232467 · Cited by 1,019 · see citing works

Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity

Brestoff, J. R., Kim, B. S., Saenz, S. A., Stine, R. R., Monticelli, L. A., Sonnenberg, G. F., Thome, J. J., Farber, D. L., Lutfy, K., Seale, P., et al. (2015) · Nature · doi:10.1038/nature14115 · Cited by 968 · see citing works

Microbiota-modulated metabolites shape the intestinal microenvironment by regulating NLRP6 inflammasome signaling

Levy, M., Thaiss, C. A., Zeevi, D., Dohnalová, L., Zilberman-Schapira, G., Mahdi, J. A., David, E., Savidor, A., Korem, T., Herzig, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2015.10.048 · Cited by 960 · see citing works

Findings From a Randomized Controlled Trial of Fecal Transplantation for Patients With Ulcerative Colitis

Rossen, N. G., Fuentes, S., van der Spek, M. J., Tijssen, J. G., Hartman, J. H. A., Duflou, A., Löwenberg, M., van den Brink, G. R., Mathus-Vliegen, E. M. H., de Vos, W. M., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.03.045 · Cited by 921 · see citing works

Virus-Plus-Susceptibility Gene Interaction Determines Crohn's Disease Gene Atg16L1 Phenotypes in Intestine

Cadwell, K., Patel, K., Maloney, N. S., Liu, T., Ng, A., Storer, C. E., Head, R. D., Xavier, R. J., Stappenbeck, T. S., & Virgin, H. W. (2010) · Cell · doi:10.1016/j.cell.2010.05.009 · Cited by 897 · see citing works

Starving our Microbial Self: The Deleterious Consequences of a Diet Deficient in Microbiota-Accessible Carbohydrates

Sonnenburg, E. D., & Sonnenburg, J. L. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.07.003 · Cited by 871 · see citing works

Eosinophils and Type 2 Cytokine Signaling in Macrophages Orchestrate Development of Functional Beige Fat

Qiu, Y., Nguyen, K. D., Odegaard, J. I., Cui, X., Tian, X., Locksley, R. M., Palmiter, R. D., & Chawla, A. (2014) · Cell · doi:10.1016/j.cell.2014.03.066 · Cited by 869 · see citing works

What are the consequences of the disappearing human microbiota?

Blaser, M. J., & Falkow, S. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2245 · Cited by 859 · see citing works

Intestinal mucosal adherence and translocation of commensal bacteria at the early onset of type 2 diabetes: molecular mechanisms and probiotic treatment

Amar, J., Chabo, C., Waget, A., Klopp, P., Vachoux, C., Bermúdez‐Humarán, L. G., Smirnova, N. F., Bergé, M., Sulpice, T., Lahtinen, S. J., et al. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201100159 · Cited by 837 · see citing works

Diversity and dialogue in immunity to helminths

Allen, J. E., & Maizels, R. M. (2011) · Nature reviews. Immunology · doi:10.1038/nri2992 · Cited by 831 · see citing works

Gut Microbiota Orchestrates Energy Homeostasis during Cold

Chevalier, C., Stojanović, O., Colin, D. J., Suarez-Zamorano, N., Tarallo, V., Veyrat-Durebex, C., Rigo, D., Fabbiano, S., Stevanović, A., Hagemann, S., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.004 · Cited by 829 · see citing works

Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice

Schneeberger, M., Everard, A., Gómez-Valadés, A. G., Matamoros, S., Ramírez, S., Delzenne, N. M., Gomis, R., Claret, M., & Cani, P. D. (2015) · Scientific Reports · doi:10.1038/srep16643 · Cited by 798 · see citing works

Enterobacteriaceae Act in Concert with the Gut Microbiota to Induce Spontaneous and Maternally Transmitted Colitis

Garrett, W. S., Gallini, C. A., Yatsunenko, T., Michaud, M., DuBois, A., Delaney, M. L., Punit, S., Karlsson, M., Bry, L., Glickman, J. N., et al. (2010) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2010.08.004 · Cited by 788 · see citing works

Dysbiosis of the Gut Microbiota Is Associated with HIV Disease Progression and Tryptophan Catabolism

Vujkovic-Cvijin, I., Dunham, R. M., Iwai, S., Maher, M. C., Albright, R. G., Broadhurst, M. J., Hernandez, R. D., Lederman, M. M., Huang, Y., Somsouk, M., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3006438 · Cited by 734 · see citing works

Macrophages, Immunity, and Metabolic Disease

McNelis, J., & Olefsky, J. M. (2014) · Immunity · doi:10.1016/j.immuni.2014.05.010 · Cited by 728 · see citing works

Stress, Inflammation, and Defense of Homeostasis

Chovatiya, R., & Medzhitov, R. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.03.030 · Cited by 704 · see citing works

Regulated virulence controls the ability of a pathogen to compete with the gut microbiota

Kamada, N., Kim, Y.-G., Sham, H. P., Vallance, B. A., Puente, J. L., Martens, E. C., & Núñez, G. (2012) · Science · doi:10.1126/science.1222195 · Cited by 682 · see citing works

Prognostic Value of Elevated Levels of Intestinal Microbe-Generated Metabolite Trimethylamine-N-Oxide in Patients With Heart Failure

Tang, W. H. W., Wang, Z., Fan, Y., Levison, B., Hazen, J. E., Donahue, L. M., Wu, Y., & Hazen, S. L. (2014) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2014.02.617 · Cited by 681 · see citing works

Activated Type 2 Innate Lymphoid Cells Regulate Beige Fat Biogenesis

Lee, M.-W., Odegaard, J. I., Mukundan, L., Qiu, Y., Molofsky, A. B., Nussbaum, J. C., Yun, K. M., Locksley, R. M., & Chawla, A. (2014) · Cell · doi:10.1016/j.cell.2014.12.011 · Cited by 680 · see citing works

The oral microbiome and the immunobiology of periodontal disease and caries

Costalonga, M., & Herzberg, M. C. (2014) · Immunology Letters · doi:10.1016/j.imlet.2014.08.017 · Cited by 645 · see citing works

Sphingolipids from a Symbiotic Microbe Regulate Homeostasis of Host Intestinal Natural Killer T Cells

An, D., Oh, S. F., Olszak, T., Neves, J. F., Avci, F. Y., Erturk-Hasdemir, D., Lu, X., Zeissig, S., Blumberg, R. S., & Kasper, D. L. (2014) · Cell · doi:10.1016/j.cell.2013.11.042 · Cited by 643 · see citing works

Industrial Food Animal Production, Antimicrobial Resistance, and Human Health

Silbergeld, E. K., Graham, J. P., & Price, L. B. (2008) · Annual Review of Public Health · doi:10.1146/annurev.publhealth.29.020907.090904 · Cited by 636 · see citing works

The Role of Retinoic Acid in Tolerance and Immunity

Hall, J. A., Grainger, J. R., Spencer, S. P., & Belkaid, Y. (2011) · Immunity · doi:10.1016/j.immuni.2011.07.002 · Cited by 556 · see citing works

Transient Inability to Manage Proteobacteria Promotes Chronic Gut Inflammation in TLR5-Deficient Mice

Carvalho, F. A., Koren, O., Goodrich, J. K., Johansson, M. E. V., Nalbantoglu, I., Aitken, J. D., Su, Y., Chassaing, B., Walters, W. A., González, A., et al. (2012) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2012.07.004 · Cited by 548 · see citing works

Western diet induces dysbiosis with increased <i>E coli</i> in CEABAC10 mice <i>,</i> alters host barrier function favouring AIEC colonisation

Martinez-Medina, M., Denizot, J., Dreux, N., Robin, F., Billard, E., Bonnet, R., Darfeuille-Michaud, A., & Barnich, N. (2014) · Gut · doi:10.1136/gutjnl-2012-304119 · Cited by 539 · see citing works

Rapid fucosylation of intestinal epithelium sustains host–commensal symbiosis in sickness

Pickard, J. M., Maurice, C. F., Kinnebrew, M. A., Abt, M. C., Schenten, D., Golovkina, T. V., Bogatyrev, S. R., Ismagilov, R. F., Pamer, E. G., Turnbaugh, P. J., et al. (2014) · Nature · doi:10.1038/nature13823 · Cited by 535 · see citing works

An altered intestinal mucosal microbiome in HIV-1 infection is associated with mucosal and systemic immune activation and endotoxemia

Dillon, S. M., Lee, E. J., Kotter, C. V., Austin, G. L., Dong, Z. M., Hecht, D. K., Gianella, S., Siewe, B. T., Smith, D. M., LANDAY, A. L., et al. (2014) · Mucosal Immunology · doi:10.1038/mi.2013.116 · Cited by 533 · see citing works

Foxp3+ T Cells Regulate Immunoglobulin A Selection and Facilitate Diversification of Bacterial Species Responsible for Immune Homeostasis

Kawamoto, S., Maruya, M., Kato, L. M., Suda, W., Atarashi, K., Doi, Y., Tsutsui, Y., Qin, H., Honda, K., Okada, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.05.016 · Cited by 531 · see citing works

Intestinal Microbiota, Microbial Translocation, and Systemic Inflammation in Chronic HIV Infection

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Gut inflammation can boost horizontal gene transfer between pathogenic and commensal <i>Enterobacteriaceae</i>

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The gut microbiota, environmental factors, and links to the development of food allergy

Lee, K. H., Song, Y., Wu, W., Yu, K., & Zhang, G. (2020) · Clinical and Molecular Allergy · doi:10.1186/s12948-020-00120-x · Cited by 121 · see citing works

The gut microbiome derived from anorexia nervosa patients impairs weight gain and behavioral performance in female mice

Hata, T., Miyata, N., Takakura, S., Yoshihara, K., Asano, Y., Kimura-Todani, T., Yamashita, M., Zhang, X.-T., Watanabe, N., Mikami, K., et al. (2019) · Endocrinology · doi:10.1210/en.2019-00408 · Cited by 116 · see citing works

Gut Microbiome as a Potential Factor for Modulating Resistance to Cancer Immunotherapy

Shui, L., Yang, X., Li, J., Yi, C., Sun, Q., & Zhu, H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02989 · Cited by 115 · see citing works

Blood Microbiome Profile in CKD

Shah, N. B., Allegretti, A. S., Nigwekar, S. U., Kalim, S., Zhao, S. J., Lelouvier, B., Servant, F., Serena, G., Thadhani, R., Raj, D. S., et al. (2019) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.12161018 · Cited by 115 · see citing works

Intestinal flora imbalance affects bile acid metabolism and is associated with gallstone formation

Wang, Q., Hao, C., Yao, W., Zhu, D., Lu, H., Li, L., Ma, B., Sun, B., Xue, D., & Zhang, W. (2020) · BMC Gastroenterology · doi:10.1186/s12876-020-01195-1 · Cited by 113 · see citing works

Mechanisms by Which the Gut Microbiota Influences Cytokine Production and Modulates Host Inflammatory Responses

de Almeida, V. M., Galvão, I., & Vieira, A. T. (2019) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2019.0011 · Cited by 108 · see citing works

Gut microbiome and bone

Ibáñez, L., Rouleau, M., Wakkach, A., & Blin-Wakkach, C. (2019) · Joint Bone Spine · doi:10.1016/j.jbspin.2018.02.008 · Cited by 103 · see citing works

The neuropsychiatric manifestations of COVID-19: Interactions with psychiatric illness and pharmacological treatment

van Vuren, E. J., Steyn, S. F., Brink, C. B., Möller, M., Viljoen, F. P., & Harvey, B. H. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111200 · Cited by 105 · see citing works

Microalgae—Sustainable Source for Alternative Proteins and Functional Ingredients Promoting Gut and Liver Health

Eilam, Y., Khattib, H., Pintel, N., & Avni, D. (2023) · Global Challenges · doi:10.1002/gch2.202200177 · Cited by 101 · see citing works

Impact of probiotics and prebiotics targeting metabolic syndrome

Xavier-Santos, D., Bedani, R., Lima, E. D., & Saad, S. M. I. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.103666 · Cited by 96 · see citing works

Human Microbiota Flagellins Drive Adaptive Immune Responses in Crohn’s Disease

Alexander, K. L., Zhao, Q. S., Reif, M. S., Rosenberg, A. F., Mannon, P., Duck, L. W., & Elson, C. O. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.03.064 · Cited by 96 · see citing works

A randomised trial of probiotics to reduce severity of physiological and microbial disorders induced by partial gastrectomy for patients with gastric cancer

Zheng, C., Chen, T., Wang, Y., Gao, Y., Kong, Y., Liu, Z., & Deng, X. (2019) · Journal of Cancer · doi:10.7150/jca.29072 · Cited by 93 · see citing works

Allergic Diseases: A Comprehensive Review on Risk Factors, Immunological Mechanisms, Link with COVID-19, Potential Treatments, and Role of Allergen Bioinformatics

Aldakheel, F. M. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph182212105 · Cited by 94 · see citing works

The effects of dietary fibers from rice bran and wheat bran on gut microbiota: An overview

Yao, W., Gong, Y., Li, C., Hu, X., & You, L. (2022) · Food Chemistry X · doi:10.1016/j.fochx.2022.100252 · Cited by 90 · see citing works

Metformin: An old drug against old age and associated morbidities

Salvatore, T., Pafundi, P. C., Morgillo, F., Liello, R. D., Galiero, R., Nevola, R., Marfella, R., Monaco, L., Rinaldi, L., Adinolfi, L. E., et al. (2020) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2020.108025 · Cited by 87 · see citing works

Do an Altered Gut Microbiota and an Associated Leaky Gut Affect COVID-19 Severity?

Kim, H. S. (2021) · mBio · doi:10.1128/mbio.03022-20 · Cited by 82 · see citing works

Insights Into a Possible Influence on Gut Microbiota and Intestinal Barrier Function During Chronic Exposure of Mice to Imazalil

Jin, C., Xia, J., Wu, S., Tu, W., Pan, Z., Fu, Z., Wang, Y., & Jin, Y. (2017) · Toxicological Sciences · doi:10.1093/toxsci/kfx227 · Cited by 84 · see citing works

Long-term human spaceflight and inflammaging: Does it promote aging?

Capri, M., Conte, M., Ciurca, E., Pirazzini, C., Garagnani, P., Santoro, A., Longo, F., Salvioli, S., Lau, P., Moeller, R., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101909 · Cited by 85 · see citing works

Immunophenotypic Profiles in Polycystic Ovary Syndrome

Hu, C., Pang, B., Ma, Z., & Yi, H. (2020) · Mediators of Inflammation · doi:10.1155/2020/5894768 · Cited by 81 · see citing works

The systemic anti-microbiota IgG repertoire can identify gut bacteria that translocate across gut barrier surfaces

Vujkovic-Cvijin, I., Welles, H. C., Ha, C. W. Y., Huq, L., Mistry, S., Brenchley, J. M., Trinchieri, G., Devkota, S., & Belkaid, Y. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abl3927 · Cited by 79 · see citing works

Beneficial effects of three brown seaweed polysaccharides on gut microbiota and their structural characteristics: An overview

You, L., Gong, Y., Li, C., Hu, X., Brennan, C. S., & Kulikouskaya, V. I. (2019) · International Journal of Food Science & Technology · doi:10.1111/ijfs.14408 · Cited by 75 · see citing works

Gut microbiota-dependent modulation of innate immunity and lymph node remodeling affects cardiac allograft outcomes

Bromberg, J. S., Hittle, L., Xiong, Y., Saxena, V., Smyth, E. M., Li, L., Zhang, T., Wagner, C., Fricke, W. F., Simon, T., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.121045 · Cited by 73 · see citing works

Gut microbiota determines the social behavior of mice and induces metabolic and inflammatory changes in their adipose tissue

Agranyoni, O., Meninger-Mordechay, S., Uzan-Yulzari, A., Oren, Z., Salmon‐Divon, M., Rodin, D., Raz, O., Koman, I. E., Koren, O., Pinhasov, A., et al. (2021) · npj Biofilms and Microbiomes · doi:10.1038/s41522-021-00193-9 · Cited by 73 · see citing works

Infant Feeding Alters the Longitudinal Impact of Birth Mode on the Development of the Gut Microbiota in the First Year of Life

Coker, M. O., Laue, H. E., Hoen, A. G., Hilliard, M. A., Dade, E. F., Li, Z., Palys, T. J., Morrison, H. G., Baker, E., Karagas, M. R., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.642197 · Cited by 75 · see citing works

Environmental enteric dysfunction induces regulatory T cells that inhibit local CD4+ T cell responses and impair oral vaccine efficacy

Bhattacharjee, A., Burr, A. B. P., Overacre-Delgoffe, A. E., Tometich, J. T., Yang, D., Huckestein, B. R., Linehan, J. L., Spencer, S. P., Hall, J. A., Harrison, O. J., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.07.005 · Cited by 75 · see citing works

Dietary Influences on the Microbiota–Gut–Brain Axis

Barber, T. M., Valsamakis, G., Mastorakos, G. P., Hanson, P., Kyrou, I., Randeva, H. S., & Weickert, M. O. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073502 · Cited by 74 · see citing works

Fructooligosaccharides protect against OVA-induced food allergy in mice by regulating the Th17/Treg cell balance using tryptophan metabolites

Yan, X., Yan, J., Xiang, Q., Wang, F., Dai, H., Huang, K., Fang, L., Yao, H., Wang, L., & Zhang, W. (2021) · Food & Function · doi:10.1039/d0fo03371e · Cited by 72 · see citing works

Gut microbiome modulation by probiotics, prebiotics, synbiotics and postbiotics: a novel strategy in food allergy prevention and treatment

Shi, J., Wang, Y., Cheng, L., Wang, J., & Raghavan, V. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2160962 · Cited by 70 · see citing works

Gut microbiota and sleep: Interaction mechanisms and therapeutic prospects

Lin, Z., Jiang, T., Chen, M., Ji, X., & Wang, Y. (2024) · Open Life Sciences · doi:10.1515/biol-2022-0910 · Cited by 68 · see citing works

Protective effects of iridoid glycosides on acute colitis via inhibition of the inflammatory response mediated by the STAT3/NF-кB pathway

Yuan, J., Cheng, W., Zhang, G., Ma, Q., Li, X., Zhang, B., Hu, T., & Song, G. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106240 · Cited by 60 · see citing works

Wheat Consumption Aggravates Colitis in Mice via Amylase Trypsin Inhibitor–mediated Dysbiosis

Pickert, G., Wirtz, S. J., Matzner, J., Ashfaq–Khan, M., Heck, R., Rosigkeit, S., Thies, D., Surabattula, R., Ehmann, D., Wehkamp, J., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.03.064 · Cited by 59 · see citing works

Therapy of Sinonasal Microbiome in CRS: A Critical Approach

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Prevalence of Blastocystis and its association with Firmicutes/Bacteroidetes ratio in clinically healthy and metabolically ill subjects

Muñoz-Yáñez, C., Hernández, A. M., Martínez-Sandoval, A., Domínguez, M. A. M., Muñiz, S. A. Z., & Guangorena-Gómez, J. O. (2021) · BMC Microbiology · doi:10.1186/s12866-021-02402-z · Cited by 58 · see citing works

Gold nanoparticles exhibit anti-osteoarthritic effects via modulating interaction of the “microbiota-gut-joint” axis

Deng, Z.-H., Yang, C., Xiang, T.-W., Dou, C., Sun, D., Dai, Q.-J., Ling, Z.-G., Xu, J.-Z., Luo, F., & Chen, Y.-Q. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02447-y · Cited by 53 · see citing works

The microbiota: a key regulator of health, productivity, and reproductive success in mammals

Khan, I. M., Nassar, N., Chang, H., Khan, S., Cheng, M., Wang, Z., & Xiang, X. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1480811 · Cited by 59 · see citing works

Applications of the Soil, Plant and Rumen Microbiomes in Pastoral Agriculture

Attwood, G. T., Wakelin, S. A., Leahy, S. C., Rowe, S. J., Clarke, S., Chapman, D. F., Muirhead, R. W., & Jacobs, J. M. E. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00107 · Cited by 55 · see citing works

Microbiota-gut-brain axis and nutritional strategy under heat stress

Wen, C., Wei, S., Zong, X., Wang, Y., & Jin, M. (2021) · Animal nutrition · doi:10.1016/j.aninu.2021.09.008 · Cited by 54 · see citing works

Antioxidant Activity, Metal Chelating Ability and DNA Protective Effect of the Hydroethanolic Extracts of Crocus sativus Stigmas, Tepals and Leaves

Ouahhoud, S., Khoulati, A., Kadda, S., Bencheikh, N., Mamri, S., Ziani, A., Baddaoui, S., Eddabbeh, F.-E., Lahmass, I., Benabbes, R., et al. (2022) · Antioxidants · doi:10.3390/antiox11050932 · Cited by 53 · see citing works

An Overview of Chronic Kidney Disease Pathophysiology: The Impact of Gut Dysbiosis and Oral Disease

Altamura, S., Pietropaoli, D., Lombardi, F., Pinto, R. D., & Ferri, C. (2023) · Biomedicines · doi:10.3390/biomedicines11113033 · Cited by 58 · see citing works

Tegumentary leishmaniasis and coinfections other than HIV

Martínez, D. Y., Verdonck, K., Kaye, P. M., Adaui, V., Polman, K., Llanos‐Cuentas, A., Dujardin, J., & Boelaert, M. (2018) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006125 · Cited by 51 · see citing works

Results of the Seventh Scientific Workshop of ECCO: Precision Medicine in IBD—What, Why, and How

Fiocchi, C., Dragoni, G., Iliopoulos, D., Katsanos, K. H., Hernández, V., Suzuki, K., Verstockt, B., Fiocchi, C., Torres, J., & Scharl, M. M. (2021) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjab051 · Cited by 52 · see citing works

Gut Microbiota Modulation as a Potential Target for the Treatment of Lung Infections

Cruz, C. S., Ricci, M. F., & Vieira, A. T. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.724033 · Cited by 53 · see citing works

Effect of Electroacupuncture on Gut Microbiota in Participants With Knee Osteoarthritis

Wang, T., Li, L., Tan, C.-X., Yang, J., Shi, G., Wang, L., Hu, H., Liu, Z., Wang, J., Wang, T., et al. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.597431 · Cited by 50 · see citing works

Differential Transcriptomic Profiles Following Stimulation with Lipopolysaccharide in Intestinal Organoids from Dogs with Inflammatory Bowel Disease and Intestinal Mast Cell Tumor

Sahoo, D. K., Borcherding, D. C., Chandra, L. C., Jergens, A. E., Atherly, T. A., Bourgois‐Mochel, A., Severin, A. J., Ellinwood, M., Snella, E., Martin, M., et al. (2022) · Cancers · doi:10.3390/cancers14143525 · Cited by 49 · see citing works

Associations between Diet, the Gut Microbiome, and Short-Chain Fatty Acid Production among Older Caribbean Latino Adults

Maldonado‐Contreras, A., Noel, S. E., Ward, D. V., Velez, M., & Mangano, K. M. (2020) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2020.04.018 · Cited by 51 · see citing works

Gut Microbiome-Mediated Alteration of Immunity, Inflammation, and Metabolism Involved in the Regulation of Non-alcoholic Fatty Liver Disease

He, L., Yao, D.-H., Wang, L., Zhang, L., & Bai, X. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.761836 · Cited by 48 · see citing works

Living probiotic biomaterials for osteoporosis therapy

Chen, Z., Cai, Z., Zhuang, P., Li, F., Cui, W., & Li, Z. (2022) · Biomedical Technology · doi:10.1016/j.bmt.2022.11.007 · Cited by 49 · see citing works

Identification of commensal gut microbiota signatures as predictors of clinical severity and disease progression in multiple sclerosis

Montgomery, T. L., Wang, Q., Mirza, A., Dwyer, D., Wu, Q., Dowling, C. A., Martens, J. W. S., Yang, J., Krementsov, D. N., & Mao‐Draayer, Y. (2024) · Scientific Reports · doi:10.1038/s41598-024-64369-x · Cited by 48 · see citing works

Nutritional Modulation of the Microbiome and Immune Response

Burr, A. B. P., Bhattacharjee, A., & Hand, T. W. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000419 · Cited by 49 · see citing works

Total Flavones of Abelmoschus manihot Remodels Gut Microbiota and Inhibits Microinflammation in Chronic Renal Failure Progression by Targeting Autophagy-Mediated Macrophage Polarization

Tu, Y., Fang, Q., Sun, W., Liu, B.-H., Liu, Y., Wu, W., Yee, H.-Y., Yuan, C., Wang, M., Wan, Z.-Y., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.566611 · Cited by 46 · see citing works

The Bufei Jianpi Formula Improves Mucosal Immune Function by Remodeling Gut Microbiota Through the SCFAs/GPR43/NLRP3 Pathway in Chronic Obstructive Pulmonary Disease Rats

Mao, J., Li, Y., Bian, Q., Xuan, Y., Li, J., Wang, Z., Feng, S., Liu, X., Tian, Y., & Li, S. (2022) · International Journal of COPD · doi:10.2147/copd.s359428 · Cited by 45 · see citing works

Host genetics and microbiome associations through the lens of genome wide association studies

Weissbrod, O., Rothschild, D., Barkan, E., & Segal, E. (2018) · Current Opinion in Microbiology · doi:10.1016/j.mib.2018.05.003 · Cited by 43 · see citing works

Fabrication of a soluble crosslinked corn bran arabinoxylan matrix supports a shift to butyrogenic gut bacteria

Zhang, X., Chen, T., Lim, J., Xie, J., Zhang, B., Yao, T., & Hamaker, B. R. (2019) · Food & Function · doi:10.1039/c8fo02575d · Cited by 44 · see citing works

Probiotics can really cure an autoimmune disease?

Yousefi, B., Eslami, M., Ghasemian, A., Kokhaei, P., & Sadeghnejhad, A. (2019) · Gene Reports · doi:10.1016/j.genrep.2019.100364 · Cited by 43 · see citing works

Emerging Approaches for Validating and Managing Multiple Sclerosis Relapse

Mills, E. A., Mirza, A., & Mao‐Draayer, Y. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00116 · Cited by 41 · see citing works

The Gut Microbiome in Psychosis From Mice to Men: A Systematic Review of Preclinical and Clinical Studies

Kraeuter, A.-K., Phillips, R., & Sarnyai, Z. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00799 · Cited by 43 · see citing works

Aronia berry polyphenols have matrix-dependent effects on the gut microbiota

Liu, X., Martin, D., Valdez, J. C., Sudakaran, S., Rey, F. E., & Bolling, B. W. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.129831 · Cited by 41 · see citing works

Probiotics ameliorate chronic low-grade inflammation and fat accumulation with gut microbiota composition change in diet-induced obese mice models

Joung, H., Chu, J., Kim, B.-K., Choi, I.-S., Kim, W., & Park, T. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-11060-6 · Cited by 41 · see citing works

Inflammatory Bowel Disease: Complexity and Variability Need Integration

Fiocchi, C. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00075 · Cited by 39 · see citing works

Microbes: possible link between modern lifestyle transition and the rise of metabolic syndrome

Moossavi, S., & Bishehsari, F. (2018) · Obesity Reviews · doi:10.1111/obr.12784 · Cited by 37 · see citing works

The interactions of CAP and LYN with the insulin signaling transducer CBL play an important role in polycystic ovary syndrome

Shen, H., Xu, X. L., Fu, Z., Xu, C., & Wang, Y. (2022) · Metabolism · doi:10.1016/j.metabol.2022.155164 · Cited by 37 · see citing works

Regulation of tissue-resident memory T cells by the Microbiota

Overacre-Delgoffe, A. E., & Hand, T. W. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00491-1 · Cited by 37 · see citing works

Lactobacillus rhamnosus Modulates Lung Inflammation and Mitigates Gut Dysbiosis in a Murine Model of Asthma-COPD Overlap Syndrome

Vasconcelos, J. A., Mota, A., Olimpio, F. R. D. S., Rosa, P. C., Damaceno‐Rodrigues, N. R., Vieira, R. P., Taddei, C. R., & Aimbire, F. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10167-2 · Cited by 33 · see citing works

Characterization of markers, functional properties, and microbiome composition in human gut-derived bacterial extracellular vesicles

Li, C.-C., Hsu, W.-F., Chiang, P.-C., Kuo, M., Wo, A. M., & Tseng, Y. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2288200 · Cited by 33 · see citing works

Metabolic syndrome during female midlife: what are the risks?

Chedraui, P. A., & Pérez-López, F. R. (2019) · Climacteric · doi:10.1080/13697137.2018.1561666 · Cited by 33 · see citing works

EEN Yesterday and Today … CDED Today and Tomorrow

Herrador‐López, M., Martín‐Masot, R., & Navas‐López, V. M. (2020) · Nutrients · doi:10.3390/nu12123793 · Cited by 33 · see citing works

The Role of Gut Microbiota in the Etiopathogenesis of Multiple Chronic Diseases

Pires, L., Paramás, A. M. G., Heleno, S. A., & Calhelha, R. C. (2024) · Antibiotics · doi:10.3390/antibiotics13050392 · Cited by 33 · see citing works

Corynebacterium accolens inhibits Staphylococcus aureus induced mucosal barrier disruption

Huang, S., Hon, K., Bennett, C. A., Hu, H., Menberu, M. A., Wormald, P., Zhao, Y., Vreugde, S., & Liu, S. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.984741 · Cited by 31 · see citing works

Colonization and immunoregulation of Lactobacillus plantarum BF_15, a novel probiotic strain from the feces of breast-fed infants

Zhang, N., Li, C., Niu, Z., Kang, H., Wang, M., Zhang, B., & Tian, H. (2020) · Food & Function · doi:10.1039/c9fo02745a · Cited by 31 · see citing works

Optimization extraction and characterization of Artemisia ordosica polysaccharide and its beneficial effects on antioxidant function and gut microbiota in rats

Xing, Y. Y., Xu, Y., Jin, X., Shi, L., Guo, S., Yan, S., & Shi, B. (2020) · RSC Advances · doi:10.1039/d0ra05063f · Cited by 31 · see citing works

The First Report of Differences in Gut Microbiota Composition between Obese and Normal Weight Iranian Subjects

Marvasti, F. E., Moshiri, A., Taghavi, M., Riazi, S., Taati, M., Sadati, S. F., Ghaheri, A., Masoomi, M., Vaziri, F., Fateh, A., et al. (2020) · Iranian Biomedical Journal · doi:10.29252/ibj.24.3.148 · Cited by 30 · see citing works

In search for interplay between stool microRNAs, microbiota and short chain fatty acids in Crohn’s disease - a preliminary study

Ambrożkiewicz, F., Karczmarski, J., Kulecka, M., Paziewska, A., Niemira, M., Żeber‐Lubecka, N., Zagórowicz, E., Kretowski, A. J., & Ostrowski, J. (2020) · BMC Gastroenterology · doi:10.1186/s12876-020-01444-3 · Cited by 30 · see citing works

Multidetector CT of the solitary pulmonary nodule

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Gut microbiota-derived metabolites and chronic inflammatory diseases

Vargas, A., Robinson, B. L., Houston, K. V., Sangay, A. R. V., Saadeh, M., D'Souza, S. M., & Johnson, D. A. (2025) · Exploration of Medicine · doi:10.37349/emed.2025.1001275 · Cited by 18 · see citing works

The Involvement of Human Gut Microbiota in Chronic Systemic Inflammation

Kashtanova, D. A., Egshatyan, L. V., & Tkacheva, O. N. (2015) · DOAJ (DOAJ: Directory of Open Access Journals)

Gut Microbiota, Low‐Grade Inflammation, and Metabolic Syndrome

Gewirtz, A. T. (2015) · The FASEB Journal · doi:10.1096/fasebj.29.1_supplement.368.2 · Cited by 3 · see citing works

The Central Role of the Gut Microbiota in Chronic Inflammatory Diseases

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