The small intestine microbiota, nutritional modulation and relevance for health

Diversity, stability and resilience of the human gut microbiota

Lozupone, C. A., Stombaugh, J. I., Gordon, J. I., Jansson, J. K., & Knight, R. (2012) · Nature · doi:10.1038/nature11550 · Cited by 5,533 · 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

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 · see citing works

Functional interactions between the gut microbiota and host metabolism

Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387 · see citing works

Gut microbiota in health and disease

Sekirov, I., Russell, S. L., Antunes, L. C. M., & Finlay, B. B. (2010) · Physiological Reviews · doi:10.1152/physrev.00045.2009 · Cited by 4,182 · see citing works

Induction of Colonic Regulatory T Cells by Indigenous <i>Clostridium</i> Species

Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752 · see citing works

The gut microbiota--masters of host development and physiology

Sommer, F., & Bäckhed, F. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro2974 · Cited by 3,681 · see citing works

Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders

Hsiao, E. Y., McBride, S. W., Hsien, S., Sharon, G., Hyde, E. R., McCue, T., Codelli, J. A., Chow, J., Reisman, S. E., Petrosino, J. F., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.024 · Cited by 3,283 · see citing works

The Treatment-Naive Microbiome in New-Onset Crohn’s Disease

Gevers, D., Kugathasan, S., Denson, L. A., Vázquez-Baeza, Y., Van Treuren, W., Ren, B., Schwager, E., Knights, D., Song, S. J., Yassour, M., et al. (2014) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2014.02.005 · Cited by 3,220 · see citing works

Transfer of intestinal microbiota from lean donors increases insulin sensitivity in individuals with metabolic syndrome

Vrieze, A., Van Nood, E., Holleman, F., Salojärvi, J., Kootte, R. S., Bartelsman, J. F. W. M., Dallinga–Thie, G. M., Ackermans, M. T., Serlie, M. J., Oozeer, R., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.06.031 · Cited by 2,913 · see citing works

Genetics and pathogenesis of inflammatory bowel disease

Khor, B., Gardet, A., & Xavier, R. J. (2011) · Nature · doi:10.1038/nature10209 · Cited by 2,630 · see citing works

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 · 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

Gut immune maturation depends on colonization with a host-specific microbiota

Chung, H., Pamp, S. J., Hill, J. A., Surana, N. K., Edelman, S. M., Troy, E. B., Reading, N. C., Villablanca, E. J., Wang, S., Mora, J. R., et al. (2012) · Cell · doi:10.1016/j.cell.2012.04.037 · Cited by 1,241 · see citing works

Differential Adaptation of Human Gut Microbiota to Bariatric Surgery–Induced Weight Loss

Furet, J.-P., Kong, L.-C., Tap, J., Poitou, C., Basdevant, A., Bouillot, J.-L., Mariat, D., Corthier, G., Doré, J., Henegar, C., et al. (2010) · Diabetes · doi:10.2337/db10-0253 · Cited by 1,173 · see citing works

FXR is a molecular target for the effects of vertical sleeve gastrectomy

Ryan, K. K., Tremaroli, V., Clemmensen, C., Kovatcheva-Datchary, P., Myronovych, A., Karns, R., Wilson-Pérez, H. E., Sandoval, D. A., Kohli, R., Bäckhed, F., et al. (2014) · Nature · doi:10.1038/nature13135 · Cited by 931 · see citing works

Lymphoid tissue inducer–like cells are an innate source of IL-17 and IL-22

Takatori, H., Kanno, Y., Watford, W. T., Tato, C. M., Weiss, G. E., Ivanov, I. I., Littman, D. R., & O’Shea, J. J. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072713 · Cited by 737 · see citing works

The human small intestinal microbiota is driven by rapid uptake and conversion of simple carbohydrates

Zoetendal, E. G., Raes, J., van den Bogert, B., Arumugam, M., Booijink, C. C. G. M., Troost, F. J., Bork, P., Wels, M., de Vos, W. M., & Kleerebezem, M. (2012) · The ISME Journal · doi:10.1038/ismej.2011.212 · Cited by 722 · see citing works

Multi-Faceted Functions of Secretory IgA at Mucosal Surfaces

Corthésy, B. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00185 · Cited by 678 · see citing works

Impact of diet and individual variation on intestinal microbiota composition and fermentation products in obese men

Salonen, A., Lahti, L., Salojärvi, J., Holtrop, G., Korpela, K., Duncan, S. H., Date, P., Farquharson, F., Johnstone, A. M., Lobley, G. E., et al. (2014) · The ISME Journal · doi:10.1038/ismej.2014.63 · Cited by 626 · see citing works

Increased Adipocyte O2 Consumption Triggers HIF-1α, Causing Inflammation and Insulin Resistance in Obesity

Lee, Y. S., Kim, J.-W., Osborne, O., Oh, D. Y., Sasik, R., Schenk, S., Chen, A., Chung, H., Murphy, A., Watkins, S. M., et al. (2014) · Cell · doi:10.1016/j.cell.2014.05.012 · Cited by 598 · see citing works

Exploring host–microbiota interactions in animal models and humansPreprint

Kostic, A. D., Howitt, M. R., & Garrett, W. S. (2013) · Genes & Development · doi:10.1101/gad.212522.112 · Cited by 491 · see citing works

Development and application of the human intestinal tract chip, a phylogenetic microarray: analysis of universally conserved phylotypes in the abundant microbiota of young and elderly adults

Rajilić‐Stojanović, M., Heilig, H. G. H. J., Molenaar, D., Kajander, K., Surakka, A., Smidt, H., & De Vos, W. M. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.01900.x · Cited by 484 · see citing works

Role of the intestinal microbiome in health and disease: from correlation to causation

de Vos, W. M., & de Vos, E. A. (2012) · Nutrition Reviews · doi:10.1111/j.1753-4887.2012.00505.x · Cited by 440 · see citing works

Modulation of the Intestinal Microbiota Alters Colitis-Associated Colorectal Cancer Susceptibility

Uronis, J. M., Mühlbauer, M., Herfarth, H. H., Rubinas, T. C., Jones, G. S., & Jobin, C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006026 · Cited by 425 · see citing works

Immune Responses to the Microbiota at the Intestinal Mucosal Surface

Duerkop, B. A., Vaishnava, S., & Hooper, L. V. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.009 · Cited by 424 · see citing works

Studies of mucus in mouse stomach, small intestine, and colon. I. Gastrointestinal mucus layers have different properties depending on location as well as over the Peyer's patches

Ermund, A., Schutte, A. H., Johansson, M., Gustafsson, J. K., & Hansson, G. C. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00046.2013 · Cited by 392 · see citing works

Differential NF-κB pathways induction by Lactobacillus plantarum in the duodenum of healthy humans correlating with immune tolerance

van Baarlen, P., Troost, F. J., van Hemert, S., van Kraaij, C., de Vos, W. M., de Groot, P. J., Hooiveld, G. J. E. J., Brummer, R. J., & Kleerebezem, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809919106 · Cited by 384 · see citing works

Gut microbiota, enteroendocrine functions and metabolism

Cani, P. D., Everard, A., & Duparc, T. (2013) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2013.09.008 · Cited by 378 · see citing works

Segmented Filamentous Bacterium Uses Secondary and Tertiary Lymphoid Tissues to Induce Gut IgA and Specific T Helper 17 Cell Responses

Lécuyer, E., Rakotobé, S., Garnier‐Lengliné, H., Lebreton, C., Picard, M., Juste, C., Fritzen, R., Eberl, G., McCoy, K. D., Macpherson, A. J., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.03.009 · Cited by 364 · see citing works

Human mucosal in vivo transcriptome responses to three lactobacilli indicate how probiotics may modulate human cellular pathways

van Baarlen, P., Troost, F. J., van Kraaij, C., Hooiveld, G. J. E. J., Boekschoten, M. V., Brummer, R. J., & Kleerebezem, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000079107 · Cited by 336 · see citing works

Dendritic cells in intestinal homeostasis and disease

Rescigno, M., & Sabatino, A. D. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39134 · Cited by 327 · see citing works

High temporal and inter‐individual variation detected in the human ileal microbiota

Booijink, C. C. G. M., El‐Aidy, S., Rajilić‐Stojanović, M., Heilig, H. G. H. J., Troost, F. J., Smidt, H., Kleerebezem, M., De Vos, W. M., & Zoetendal, E. G. (2010) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02294.x · Cited by 324 · see citing works

Patterns of Early Gut Colonization Shape Future Immune Responses of the Host

Hansen, C. H. F., Nielsen, D. S., Kverka, M., Zakostelska, Z. J., Kostovcikova, K., Hudcovic, T., Tlaskalová‐Hogenová, H., & Hansen, A. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034043 · Cited by 310 · see citing works

Better living through microbial action: the benefits of the mammalian gastrointestinal microbiota on the host

Leser, T. D., & Mølbak, L. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.01941.x · Cited by 304 · see citing works

Microbiota, Disease, and Back to Health: A Metastable Journey

Blumberg, R. S., & Powrie, F. M. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004184 · Cited by 279 · see citing works

Perspective: Alpha-Bugs, Their Microbial Partners, and the Link to Colon Cancer

Sears, C. L., & Pardoll, D. M. (2011) · The Journal of Infectious Diseases · doi:10.1093/jinfdis/jiq061 · Cited by 259 · see citing works

Temporal and spatial interplay of microbiota and intestinal mucosa drive establishment of immune homeostasis in conventionalized mice

Aidy, S. E., van Baarlen, P., Derrien, M., Lindenbergh-Kortleve, D. J., Hooiveld, G. J. E. J., Levenez, F., Dore, J. M., Dekker, J. P., Samsom, J. N., Nieuwenhuis, E. E. S., et al. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.32 · Cited by 247 · see citing works

Short-Chain Fatty Acid Receptor and Its Contribution to Glucagon-Like Peptide-1 Release

Kaji, I., Karaki, S.-I., & Kuwahara, A. (2014) · Digestion · doi:10.1159/000356211 · Cited by 177 · see citing works

Diversity of human small intestinal Streptococcus and Veillonella populations

van den Bogert, B., Erkuş, O., Boekhorst, J., de Goffau, M. C., Smid, E. J., Zoetendal, E. G., & Kleerebezem, M. (2013) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12127 · Cited by 172 · see citing works

Microbial Communities in the Human Small Intestine: Coupling Diversity to Metagenomics

Booijink, C. C., Zoetendal, E. G., Kleerebezem, M., & de Vos, W. M. (2007) · Future Microbiology · doi:10.2217/17460913.2.3.285 · Cited by 164 · see citing works

The gut microbiota elicits a profound metabolic reorientation in the mouse jejunal mucosa during conventionalisation

Aidy, S. E., Merrifield, C. A., Derrien, M., van Baarlen, P., Hooiveld, G. J. E. J., Levenez, F., Dore, J. M., Dekker, J. P., Holmes, E. C., Claus, S. P., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-301955 · Cited by 134 · see citing works

A novel ingestible electronic drug delivery and monitoring device

Schaar, P. J. V. D., Dijksman, J., Gast, H. S. B.-D., Shimizu, J., van Lelyveld, N., Zou, H., Iordanov, V. P., Wanke, C., & Siersema, P. D. (2013) · Gastrointestinal Endoscopy · doi:10.1016/j.gie.2013.03.170 · Cited by 119 · see citing works

Roux-en-Y gastric bypass surgery in rats alters gut microbiota profile along the intestine

Osto, M., Abegg, K., Bueter, M., le Roux, C. W., Cani, P. D., & Lutz, T. A. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.06.008 · Cited by 85 · see citing works

Transient inflammatory-like state and microbial dysbiosis are pivotal in establishment of mucosal homeostasis during colonisation of germ-free mice

Aidy, S. E., Derrien, M., Aardema, R., Hooiveld, G. J. E. J., Richards, S. E., Dane, A. D., Dekker, J. P., Vreeken, R. J., Levenez, F., Dore, J. M., et al. (2013) · Beneficial Microbes · doi:10.3920/bm2013.0018 · Cited by 82 · see citing works

Comparative Genomics Analysis of Streptococcus Isolates from the Human Small Intestine Reveals their Adaptation to a Highly Dynamic Ecosystem

van den Bogert, B., Boekhorst, J., Herrmann, R., Smid, E. J., Zoetendal, E. G., & Kleerebezem, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083418 · Cited by 74 · see citing works

Increased Hepatic Insulin Clearance After Roux-en-Y Gastric Bypass

Bojsen-Møller, K. N., Dirksen, C., Jørgensen, N. B., Jacobsen, S. H., Hansen, D. L., Worm, D., Naver, L., Kristiansen, V. B., Holst, J. J., & Madsbad, S. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-1286 · Cited by 69 · see citing works

T lymphocytes control microbial composition by regulating the abundance of Vibrio in the zebrafish gut

Brugman, S., Schneeberger, K., Witte, M., Klein, M. R., van den Bogert, B., Boekhorst, J., Timmerman, H. M., Boes, M. L., Kleerebezem, M., & Nieuwenhuis, E. E. S. (2014) · Gut Microbes · doi:10.4161/19490976.2014.972228 · Cited by 67 · see citing works

Are stool samples suitable for studying the link between gut microbiota and obesity?

Raoult, D., & Henrissat, B. (2014) · European Journal of Epidemiology · doi:10.1007/s10654-014-9905-4 · Cited by 66 · see citing works

Nod/Ripk2 signaling in dendritic cells activates IL-17A–secreting innate lymphoid cells and drives colitis in T-bet −/− .Rag2 −/− (TRUC) mice

Ermann, J., Staton, T. L., Glickman, J. N., Malefyt, R. D. W., & Glimcher, L. H. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1408540111 · Cited by 66 · see citing works

GI Microbiota and Regulation of the Immune System

Huffnagle, G. B., & Noverr, M. C. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-09550-9 · Cited by 56 · see citing works

Effects of Microbiota on GI Health: Gnotobiotic Research

Wagner, R. D. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-09550-9_4 · Cited by 48 · see citing works

Small intestine and microbiota

Cotter, P. D. (2010) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e328341dc67 · Cited by 46 · see citing works

FXR: the key to benefits in bariatric surgery?

Kuipers, F., & Groen, A. K. (2014) · Nature Medicine · doi:10.1038/nm.3525 · Cited by 33 · see citing works

Human buccal epithelium acquires microbial hyporesponsiveness at birth, a role for secretory leukocyte protease inhibitor

Menckeberg, C. L., Hol, J., Simons-Oosterhuis, Y., Raatgeep, H. C., de Ruiter, L. F., Lindenbergh-Kortleve, D. J., Male, A. M. K.-V., Aidy, S. E., van Lierop, P. P. E., Kleerebezem, M., et al. (2014) · Gut · doi:10.1136/gutjnl-2013-306149 · Cited by 29 · see citing works

Microbial Learning Lessons: SFB Educate the Immune System

Lee, Y. K., & Mazmanian, S. K. (2014) · Immunity · doi:10.1016/j.immuni.2014.04.002 · Cited by 24 · see citing works

Functional Intestinal Metagenomics

van den Bogert, B., Leimena, M. M., de Vos, W. M., Zoetendal, E. G., & Kleerebezem, M. (2011) · doi:10.1002/9781118010549.ch18 · Cited by 13 · see citing works

Handbook of Molecular Microbial Ecology

Zhang, W. (2012) · Food Microbiology · doi:10.1016/j.fm.2012.01.003 · Cited by 13 · see citing works

Draft Genome Sequence of Veillonella parvula HSIVP1, Isolated from the Human Small Intestine

van den Bogert, B., Boekhorst, J., Smid, E. J., Zoetendal, E. G., & Kleerebezem, M. (2013) · Genome Announcements · doi:10.1128/genomea.00977-13 · Cited by 12 · see citing works

Microbiota in health and diseases

Hou, K., Wu, Z.-X., Chen, X.-Y., Wang, J.-Q., Zhang, D., Xiao, C., Zhu, D., Koya, J. B., Wei, L., Li, J., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00974-4 · Cited by 3,171 · see citing works

An insight into gut microbiota and its functionalities

Adak, A., & Khan, M. R. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2943-4 · Cited by 1,485 · see citing works

Fate, activity, and impact of ingested bacteria within the human gut microbiota

Derrien, M., & van Hylckama Vlieg, J. E. T. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.03.002 · Cited by 605 · see citing works

Advances in Oral Drug Delivery for Regional Targeting in the Gastrointestinal Tract - Influence of Physiological, Pathophysiological and Pharmaceutical Factors

Hua, S. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00524 · Cited by 565 · see citing works

Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease

van Kessel, S. P., Frye, A. K., El-Gendy, A. O., Castejon, M., Keshavarzian, A., van Dijk, G., & El Aidy, S. (2019) · Nature Communications · doi:10.1038/s41467-019-08294-y · Cited by 521 · see citing works

The role of the intestinal microbiota in type 1 diabetes mellitus

Knip, M., & Siljander, H. (2016) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.218 · Cited by 434 · see citing works

Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system

Chevalier, G., Siopi, E., Guenin‐Macé, L., Pascal, M., Laval, T., Rifflet, A., Boneca, I. G., Demangel, C., Colsch, B., Pruvost, A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19931-2 · Cited by 324 · see citing works

Gut reactions: Breaking down xenobiotic–microbiome interactions

Clarke, G., Sandhu, K. V., Griffin, B. T., Dinan, T. G., Cryan, J. F., & Hyland, N. P. (2019) · Pharmacological Reviews · doi:10.1124/pr.118.015768 · Cited by 319 · see citing works

Small intestinal microbial dysbiosis underlies symptoms associated with functional gastrointestinal disorders

Saffouri, G. B., Shields‐Cutler, R. R., Chen, J., Yang, Y., Lekatz, H. R., Hale, V. L., Cho, J. M., Battaglioli, E. J., Bhattarai, Y., Thompson, K. J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09964-7 · Cited by 309 · see citing works

The food-gut axis: lactic acid bacteria and their link to food, the gut microbiome and human health

De Filippis, F., Pasolli, E., & Ercolini, D. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa015 · Cited by 303 · see citing works

Microbes vs. chemistry in the origin of the anaerobic gut lumen

Friedman, E. S., Bittinger, K. L., Esipova, T. V., Hou, L., Chau, L., Jiang, J., Mesaros, C., Lund, P. J., Liang, X., FitzGerald, G. A., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1718635115 · Cited by 272 · see citing works

Gut-on-a-chip: Current progress and future opportunities

Ashammakhi, N. A., Nasiri, R., de Barros, N. R., Tebon, P. J., Thakor, J., Goudie, M. J., Shamloo, A., Martín, M. G., & Khademhosseini, A. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120196 · Cited by 244 · see citing works

The Effects of Nutrition on the Gastrointestinal Microbiome of Cats and Dogs: Impact on Health and Disease

Wernimont, S. M., Radosevich, J., Jackson, M. I., Ephraim, E., Badri, D. V., MacLeay, J. M., Jewell, D. E., & Suchodolski, J. S. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01266 · Cited by 220 · see citing works

Adhesion Properties of Lactic Acid Bacteria on Intestinal Mucin

Nishiyama, K., Sugiyama, M., & Mukai, T. (2016) · Microorganisms · doi:10.3390/microorganisms4030034 · Cited by 170 · see citing works

Age and the aging process significantly alter the small bowel microbiome

Leite, G., Pimentel, M., Barlow, G. M., Chang, C. Y.-Y., Hosseini, A., Wang, J., Parodi, G., Sedighi, R., Rezaie, A. R., & Mathur, R. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109765 · Cited by 158 · see citing works

Microbiota at the crossroads of autoimmunity

Shamriz, O., Mizrahi, H., Werbner, M., Shoenfeld, Y., Avni, O., & Koren, O. (2016) · Autoimmunity Reviews · doi:10.1016/j.autrev.2016.07.012 · Cited by 151 · see citing works

Gut microbiota modulates drug pharmacokinetics

Zhang, J., Zhang, J., & Wang, R. (2018) · Drug Metabolism Reviews · doi:10.1080/03602532.2018.1497647 · Cited by 151 · see citing works

Diversity of Duodenal and Rectal Microbiota in Biopsy Tissues and Luminal Contents in Healthy Volunteers

Li, G., Yang, M. J., Zhou, K., Zhang, L., Tian, L., Lv, S., Jin, Y. T., Qian, W., Xiong, H., Lin, R., et al. (2015) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1412.12047 · Cited by 141 · see citing works

Environmental Enteropathy: Elusive but Significant Subclinical Abnormalities in Developing Countries

Watanabe, K., & Petri, W. A. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.07.030 · Cited by 139 · see citing works

The Impact of the Gut Microbiota on Drug Metabolism and Clinical Outcome.

Enright, E. F., Gahan, C. G. M., Joyce, S. A., & Griffin, B. T. (2016) · PubMed Central · Cited by 139 · see citing works

Comparative Analysis of the Gut Microbiota Composition between Captive and Wild Forest Musk Deer

Li, Y., Hu, X., Yang, S., Zhou, J., Zhang, T., Qi, L., Sun, X., Fan, M., Xu, S., Cha, M., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01705 · Cited by 137 · see citing works

Safety of Probiotics: Functional Fruit Beverages and Nutraceuticals

Žuntar, I., Petrić, Z., Kovačević, D. B., & Putnik, P. (2020) · Foods · doi:10.3390/foods9070947 · Cited by 142 · see citing works

Diarrhea Predominant-Irritable Bowel Syndrome (IBS-D): Effects of Different Nutritional Patterns on Intestinal Dysbiosis and Symptoms

Altomare, A., Rosa, C. D., Imperia, E., Emerenziani, S., Cicala, M., & Guarino, M. P. L. (2021) · Nutrients · doi:10.3390/nu13051506 · Cited by 132 · see citing works

Understanding dysbiosis and resilience in the human gut microbiome: biomarkers, interventions, and challenges

Safarchi, A., Al-Qadami, G. H., Tran, C. D., & Conlon, M. A. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1559521 · Cited by 133 · see citing works

Gut Microbiota Are Disease-Modifying Factors After Traumatic Spinal Cord Injury

Kigerl, K. A., Mostacada, K., & Popovich, P. G. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0583-2 · Cited by 124 · see citing works

Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment

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Xylitol’s Health Benefits beyond Dental Health: A Comprehensive Review

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The Impact of Epicatechin on Human Cognition: The Role of Cerebral Blood Flow

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Gut Microbiota in NSAID Enteropathy: New Insights From Inside

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Gut Microbiota and Clostridium difficile: What We Know and the New Frontiers

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Hepatocellular Carcinoma: How the Gut Microbiota Contributes to Pathogenesis, Diagnosis, and Therapy

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Presence and Germination of the Probiotic Bacillus subtilis DE111® in the Human Small Intestinal Tract: A Randomized, Crossover, Double-Blind, and Placebo-Controlled Study

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Milk Bioactive Compounds and Gut Microbiota Modulation: The Role of Whey Proteins and Milk Oligosaccharides

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Inulin Improves Postprandial Hypertriglyceridemia by Modulating Gene Expression in the Small Intestine

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mTOR Signaling Pathway and Gut Microbiota in Various Disorders: Mechanisms and Potential Drugs in Pharmacotherapy

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From clinical uncertainties to precision medicine: the emerging role of the gut barrier and microbiome in small bowel functional diseases

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An Insight on Novel Approaches & Perspectives for Gastro-Retentive Drug Delivery Systems

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Exploiting the Metabolism of the Gut Microbiome as a Vehicle for Targeted Drug Delivery to the Colon

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