The Commensal Microbiota and Enteropathogens in the Pathogenesis of Inflammatory Bowel Diseases

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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030

IL-17 and th17 cells

Korn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873

Metagenomic Analysis of the Human Distal Gut Microbiome

Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699

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

Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria

Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554

Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients

Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413

Unravelling the pathogenesis of inflammatory bowel disease

Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364

Impact of food additives on the gut-brain axis

Holder, M. K., & Chassaing, B. (2018) · Physiology & Behavior · doi:10.1016/j.physbeh.2018.02.025 · Cited by 43

Microbial Signature in Adipose Tissue of Crohn’s Disease Patients

Serena, C., Queipo‐Ortuño, M. I., Millán, M., Sánchez‐Alcoholado, L., Caro, A., Espina, B., Menacho, M., Bautista, M., Monfort-Ferré, D., Terrón‐Puig, M., et al. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9082448 · Cited by 38

The σ E Pathway Is Involved in Biofilm Formation by Crohn's Disease-Associated Adherent-Invasive Escherichia coli

Chassaing, B., & Darfeuille–Michaud, A. (2012) · Journal of Bacteriology · doi:10.1128/jb.01079-12 · Cited by 37

Gut microbiota, an emergent target to shape the efficiency of cancer therapy

Kouidhi, S., Zidi, O., Belkhiria, Z., Raïs, H., Ayadi, A., Ayed, F. B., Mosbah, A., Cherif, A., & Gaaied, A. B. A. E. (2023) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2023.00132 · Cited by 37

Neural networks in intestinal immunoregulation

Costes, L. M. M., Boeckxstaens, G. E., de Jonge, W. J., & Cailotto, C. (2013) · Organogenesis · doi:10.4161/org.25646 · Cited by 36

Has provoking microbiota aggression driven the obesity epidemic?

Chassaing, B., & Gewirtz, A. T. (2016) · BioEssays · doi:10.1002/bies.201500116 · Cited by 35

The effect of probiotics and polysaccharides on the gut microbiota composition and function of weaned rats

Wang, M., Chen, Y., Wang, Y., Li, Y., Zheng, H., Ma, F., Ma, C., Zhang, X., Lu, B., Xie, Z., et al. (2018) · Food & Function · doi:10.1039/c7fo01507k · Cited by 36

Invasive non-typhoidal Salmonella in sickle cell disease in Africa: is increased gut permeability the missing link?

Lim, S. H., Methé, B. A., Knoll, B. M., Morris, A., & Obaro, S. (2018) · Journal of Translational Medicine · doi:10.1186/s12967-018-1622-4 · Cited by 37

Pharmacological activation of ERβ by arctigenin maintains the integrity of intestinal epithelial barrier in inflammatory bowel diseases

Tao, Y., Yue, M., Lv, C., Yun, X., Qiao, S., Fang, Y., Wei, Z., Xia, Y., & Dai, Y. (2019) · The FASEB Journal · doi:10.1096/fj.201901638rr · Cited by 36

Computational Proteome-Wide Study for the Prediction of Escherichia coli Protein Targeting in Host Cell Organelles and Their Implication in Development of Colon Cancer

Khan, S., Zaidi, S., Alouffi, A., Hassan, I., Imran, A., & Khan, R. A. (2020) · ACS Omega · doi:10.1021/acsomega.9b04042 · Cited by 36

Multi-Omics Analysis of Gut Microbiota in Inflammatory Bowel Diseases: What Benefits for Diagnostic, Prognostic and Therapeutic Tools?

Lacroix, V., Cassard, A., Mas, E., & Barreau, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011255 · Cited by 36

Biomaterial-based strategies for immunomodulation in IBD: current and future scenarios

Jori, C., Chaudhary, A. A., Rashid, S., Ali, M. A. M., Alawam, A. S., Haouala, F., & Khan, R. (2023) · Journal of Materials Chemistry B · doi:10.1039/d3tb00276d · Cited by 35

Effect of a Probiotic Preparation (VSL#3) in Patients with Mild to Moderate Ulcerative Colitis

Lee, J. H., Moon, G., Kwon, H. J., Jung, W. J., Seo, P. J., Baec, T. Y., Lee, J. H., & Kim, H. S. (2012) · Korean Journal of Gastroenterology · doi:10.4166/kjg.2012.60.2.94 · Cited by 35

Identification of Commensal Species Positively Correlated with Early Stress Responses to a Compromised Mucus Barrier

Sovran, B., Lu, P., Loonen, L. M. P., Hugenholtz, F., Belzer, C., Stolte, E. H., Boekschoten, M. V., van Baarlen, P., Smidt, H., Kleerebezem, M., et al. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000688 · Cited by 34

Current Evidence for the Management of Inflammatory Bowel Diseases Using Fecal Microbiota Transplantation

Jeon, S. R., Chai, J., Kim, C., & Lee, C. (2018) · Current Infectious Disease Reports · doi:10.1007/s11908-018-0627-8 · Cited by 32

Enhanced E. coli LF82 Translocation through the Follicle-associated Epithelium in Crohn’s Disease is Dependent on Long Polar Fimbriae and CEACAM6 expression, and Increases Paracellular Permeability

Keita, Å. V., Alkaissi, L. Y., Holm, E. B., Heil, S. D. S., Chassaing, B., Darfeuille–Michaud, A., McKay, D. M., & Söderholm, J. D. (2019) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjz144 · Cited by 35

Mucosa‐attached bacterial community in Crohn's disease coheres with the clinical disease activity index

Schäffler, H., Herlemann, D. P. R., Alberts, C., Kaschitzki, A., Bodammer, P., Bannert, K., Köller, T., Warnke, P., Kreikemeyer, B., & Lamprecht, G. (2016) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12411 · Cited by 35

Mice harboring pathobiont-free microbiota do not develop intestinal inflammation that normally results from an innate immune deficiency

Chassaing, B., & Gewirtz, A. T. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195310 · Cited by 37

Gut microbiota and intestinal immunity interaction in ulcerative colitis and its application in treatment

Bu, F., Chen, K., Chen, S., & Jiang, Y. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1565082 · Cited by 39

Clinicopathological and Molecular Specificities of Inflammatory Bowel Disease–Related Colorectal Neoplastic Lesions: The Role of Inflammation

Svrcek, M., Borralho, P., Villanacci, V., Beaugerie, L., Rogler, G., Hertogh, G. D., Tripathi, M., Feakins, R. M., & H-ECCO group (2018) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjy132 · Cited by 34

Effects of oxidation-based tea processing on the characteristics of the derived polysaccharide conjugates and their regulation of intestinal homeostasis in DSS-induced colitis mice

Xu, A., Zhao, Y., Shi, Y., Zuo, X., Yang, Y., Wang, Y., & Xu, P. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.06.115 · Cited by 34

Colitis-associated intestinal microbiota regulates brain glycine and host behavior in mice

Morozova, M. V., Borisova, M. A., Snytnikova, O. A., Achasova, K. M., Litvinova, E. A., Tsentalovich, Y. P., & Kozhevnikova, E. N. (2022) · Scientific Reports · doi:10.1038/s41598-022-19219-z · Cited by 36

Use of antibiotics in the treatment of Crohn’s disease

Scribano, M. L. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i5.648 · Cited by 34

Genome analysis of E. coli isolated from Crohn’s disease patients

Rakitina, D. V., Manolov, A. I., Kanygina, A. V., Garushyants, S. K., Baikova, I. P., Alexeev, D. G., Ladygina, V. G., Kostryukova, E., Larin, A. K., Semashko, T. A., et al. (2017) · BMC Genomics · doi:10.1186/s12864-017-3917-x · Cited by 32

Bovine colostrum demonstrates anti-inflammatory and antibacterial activity in in vitro models of intestinal inflammation and infection

Chae, A., Aitchison, A., Day, A. S., & Keenan, J. I. (2016) · Journal of Functional Foods · doi:10.1016/j.jff.2016.11.016 · Cited by 33

NASPGHAN Clinical Report on the Evaluation and Treatment of Pediatric Patients With Internal Penetrating Crohn Disease

Pfefferkorn, M. D., Marshalleck, F. E., Saeed, S. A., Splawski, J. B., Linden, B. C., & Weston, B. F. (2013) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e31829ef850 · Cited by 32

Metagenomic Characterization of Microbial Communities In Situ Within the Deeper Layers of the Ileum in Crohn’s Disease

Pedamallu, C. S., Bhatt, A. S., Bullman, S., Fowler, S. A., Freeman, S. S., Durand, J., Jung, J., Duke, F. F., Manzo, V. E., Cai, D., et al. (2016) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2016.05.011 · Cited by 32

Total flavone of Abelmoschus Manihot improves colitis by promoting the growth of Akkermansia in mice

Bu, F., Ding, Y., Chen, T., Wang, Q., Wang, R., Zhou, J., Jiang, F., Zhang, D., Xu, M., Shi, G., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-00070-7 · Cited by 32

Appendix and Ulcerative Colitis: a Key to Explaining the Pathogenesis and Directing Novel Therapies?

Fard, N. A., Armstrong, H., Perry, T., & Wine, E. (2022) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izac106 · Cited by 31

Fecal Microbiota Transplantation and Its Potential Therapeutic Uses in Gastrointestinal Disorders

Heath, R. D. (2017) · Northern Clinics of Istanbul · doi:10.14744/nci.2017.10692 · Cited by 32

A critical review on the relationship of herbal medicine, Akkermansia muciniphila, and human health

Bu, F., Zhang, S., Duan, Z., Ding, Y., Chen, T., Wang, R., Feng, Z., Shi, G., Zhou, J., & Chen, Y. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110352 · Cited by 31

Anti-inflammatory and intestinal microbiota modulation properties of Ganoderma lucidum β-d-glucans with different molecular weight in an ulcerative colitis model

Liu, L., Feng, J., Jiang, S., Zhou, S., Yan, M., Zhang, Z., Wang, W., Liu, Y., & Zhang, J. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.126351 · Cited by 30

Neohesperidin Attenuates DSS-Induced Ulcerative Colitis by Inhibiting Inflammation, Reducing Intestinal Barrier Damage, and Modulating Intestinal Flora Composition

Ju, T., Song, Z., Qin, D., Cheng, J., Li, T., Hu, G., & Fu, S. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c04433 · Cited by 33

Gut Microbiota

Chaluvadi, S., Hotchkiss, A. T., & Yam, K. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802189-7.00036-8 · Cited by 30

Consenso mexicano para el diagnóstico y tratamiento de la colitis ulcerosa crónica idiopática

Yamamoto-Furusho, J. K., Gutiérrez-Grobe, Y., López-Gómez, J. G., Bosques‐Padilla, F., & Ramírez, J. L. R. (2018) · Revista de Gastroenterología de México · doi:10.1016/j.rgmx.2017.08.006 · Cited by 30

Different Dose of Sucrose Consumption Divergently Influences Gut Microbiota and PPAR-γ/MAPK/NF-κB Pathway in DSS-Induced Colitis Mice

Zhang, X., Zhang, B., Peng, B., Wang, J., Hu, Y., Wang, R., & Wang, S. (2022) · Nutrients · doi:10.3390/nu14132765 · Cited by 35

Knockout of Ste20-Like Proline/Alanine-Rich Kinase (SPAK) Attenuates Intestinal Inflammation in Mice

Zhang, Y., Viennois, É., Xiao, B., Baker, M. T., Yang, S., Okoro, I., & Yan, Y. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.01.028 · Cited by 30

Mucosal immunity and gut microbiota in dogs with chronic enteropathy

Eissa, N., Kittana, H., Neto, J. C. G., & Hussein, H. H. (2018) · Research in Veterinary Science · doi:10.1016/j.rvsc.2018.11.019 · Cited by 35

Immune‐mediated diseases and microbial exposure in early life

Bisgaard, H. F., Bønnelykke, K., & Stokholm, J. (2014) · Clinical & Experimental Allergy · doi:10.1111/cea.12291 · Cited by 29

A polymicrobial view of disease potential in Crohn's-associated adherent-invasive E. coli

Elhenawy, W., Oberc, A. M., & Coombes, B. K. (2017) · Gut Microbes · doi:10.1080/19490976.2017.1378291 · Cited by 29

Chronic Inflammatory Diseases: Are We Ready for Microbiota-based Dietary Intervention?

Viennois, É., Gewirtz, A. T., & Chassaing, B. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.02.008 · Cited by 31

Antibiotics and Inflammatory Bowel Diseases

Scribano, M. L., & Prantera, C. (2013) · Digestive Diseases · doi:10.1159/000354704 · Cited by 27

The Mexican consensus on the diagnosis and treatment of ulcerative colitis

Yamamoto-Furusho, J. K., Gutiérrez-Grobe, Y., López-Gómez, J. G., Bosques‐Padilla, F., & Ramírez, J. L. R. (2018) · Revista de Gastroenterología de México (English Edition) · doi:10.1016/j.rgmxen.2018.04.001 · Cited by 27

Inflammatory Bowel Diseases: The Role of Gut Microbiota

Musis, C. D., Granata, L., Dallio, M., Miranda, A., Gravina, A. G., & Romano, M. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200420144128 · Cited by 27

Analysis of the σ E Regulon in Crohn's Disease-Associated Escherichia coli Revealed Involvement of the waaWVL Operon in Biofilm Formation

Chassaing, B., Garénaux, E., Carrière, J., Rolhion, N., Guérardel, Y., Barnich, N., Bonnet, R., & Darfeuille–Michaud, A. (2015) · Journal of Bacteriology · doi:10.1128/jb.02499-14 · Cited by 26

Weight loss is a sufficient and economical single outcome measure of murine dextran sulfate sodium colitis

Britto, S. L., Krishna, M., & Kellermayer, R. (2019) · FASEB BioAdvances · doi:10.1096/fba.2019-00035 · Cited by 26

Meta-analysis of ciprofloxacin in treatment of Crohn's disease

Wu, X., Ji, H., & Wang, F. (2014) · Biomedical Reports · doi:10.3892/br.2014.368 · Cited by 26

The Prophylactic Use of Bovine Colostrum in a Murine Model of TNBS-Induced Colitis

Menchetti, L., Curone, G., Filipescu, I. E., Barbato, O., Leonardi, L., Guelfi, G., Traina, G., Proietti, P. C., Riva, F., Casano, A. B., et al. (2020) · Animals · doi:10.3390/ani10030492 · Cited by 27

Ribonucleotide Reductase NrdR as a Novel Regulator for Motility and Chemotaxis during Adherent-Invasive Escherichia coli Infection

Dreux, N., Cendra, M. D. M., Massier, S., Darfeuille–Michaud, A., Barnich, N., & Torrents, E. (2015) · Infection and Immunity · doi:10.1128/iai.02772-14 · Cited by 24

Oligomannose-Rich Membranes of Dying Intestinal Epithelial Cells Promote Host Colonization by Adherent-Invasive E. coli

Dumych, T. I., Yamakawa, N., Sivignon, A., Garénaux, E., Robakiewicz, S., Coddeville, B., Bongiovanni, A., Bray, F., Barnich, N., Szunerits, S., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00742 · Cited by 25

Inflammatory bowel disease and cancer response due to anti-CTLA-4: is it in the flora?

Carbonnel, F., Soularue, É., Coutzac, C., Chaput, N., Mateus, C., Lepage, P., & Robert, C. (2017) · Seminars in Immunopathology · doi:10.1007/s00281-016-0613-x · Cited by 26

Effects of quercitrin on bacterial translocation in a rat model of experimental colitis

Dönder, Y., Arıkan, T. B., Baykan, M., Akyüz, M., & Öz, B. (2018) · Asian Journal of Surgery · doi:10.1016/j.asjsur.2017.12.002 · Cited by 24

Probiotic Bacteria in the Prevention and the Treatment of Inflammatory Bowel Disease

Fedorak, R. N., & Demeria, D. D. (2012) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2012.08.003 · Cited by 24

Immunomodulatory effect of Syphacia obvelata in treatment of experimental DSS-induced colitis in mouse model

Taghipour, N., Mosaffa, N., Aghdaei, H. A., Rostami‐Nejad, M., Weinstock, J. V., Shahnavaz, S., & Zali, M. R. (2019) · Scientific Reports · doi:10.1038/s41598-019-55552-6 · Cited by 23

Exposure to antibiotics during pregnancy alters offspring outcomes

Qu, W., Liu, L., & Miao, L. (2021) · Expert Opinion on Drug Metabolism & Toxicology · doi:10.1080/17425255.2021.1974000 · Cited by 25

Ring1a protects against colitis through regulating mucosal immune system and colonic microbial ecology

Wang, Y., Li, Q., Zhang, J., Liu, P., Zheng, H., Chen, L., Wang, Z., Tan, C., Zhang, M., Zhang, H., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2251646 · Cited by 23

Associations of FUT2 and FUT3 gene polymorphisms with C rohn's disease in C hinese patients

Hu, D., Shao, X., Xu, C., Xia, S., Yu, L., Jiang, L., Jin, J., Lin, X., & Jiang, Y. (2014) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.12599 · Cited by 23

Clostridium difficile Infection

Roy, A., & Lichtiger, S. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000641 · Cited by 23

Protective effects of fermented rice extract on ulcerative colitis induced by dextran sodium sulfate in mice

Oh, W., Jung, J., Choi, Y., Mun, J., Ku, S., & Song, C. (2020) · Food Science & Nutrition · doi:10.1002/fsn3.1460 · Cited by 23

Anti-inflammatory effects of the Aralia elata and Cirsium japonicum in Raw264.7 cells and in vivo colitis model in mice and dogs

Kim, R., Islam, M. S., Yoo, Y.-J., Shin, H.-Y., Lee, J. H., Cho, J.-H., Park, Y.-G., Choi, J.-Y., Tae, H., & Park, B. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113186 · Cited by 21

Genetic Profiling in Inflammatory Bowel Disease: From Association to Bedside

Limbergen, J. V., Philpott, D. J., & Griffiths, A. M. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.09.018 · Cited by 20

Adalimumab for maintenance of remission in Crohn's disease

Townsend, C., Nguyen, T. M., Cepek, J., Abbass, M., Parker, C. E., MacDonald, J. K., Khanna, R., Jairath, V., & Feagan, B. G. (2020) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd012877.pub2 · Cited by 20

The Role of the Gut Microbiome in Health and Disease in the Elderly

Chen, L. A., & Boyle, K. (2024) · Current Gastroenterology Reports · doi:10.1007/s11894-024-00932-w · Cited by 22

Function, Regulation, and Pathophysiological Relevance of the POT Superfamily, Specifically PepT1 in Inflammatory Bowel Disease

Viennois, É., Pujada, A., Zen, J., & Merlin, D. (2018) · Comprehensive physiology · doi:10.1002/j.2040-4603.2018.tb00024.x · Cited by 19

Faecal bacterial composition in dairy cows shedding Mycobacterium avium subsp. paratuberculosis in faeces in comparison with nonshedding cows

Kaevska, M., Videnska, P., Sedlář, K., Bartejsova, I., Králová, A., & Slaná, I. (2016) · Canadian Journal of Microbiology · doi:10.1139/cjm-2015-0814 · Cited by 19

Effector triggered manipulation of host immune response elicited by different pathotypes of Escherichia coli

Jayamani, E., & Mylonakis, E. E. (2014) · Virulence · doi:10.4161/viru.29948 · Cited by 19

Clostridium difficileinfection aggravates colitis in interleukin 10-deficient mice

Kim, M. N. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i45.17084 · Cited by 19

Phage therapy in gut microbiome

Chen, X., Mendes, B. G., Alves, B. S., & Duan, Y. (2023) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2023.04.005 · Cited by 19

Computational prediction of Escherichia coli proteins host subcellular targeting and their implications in colorectal cancer etiology

Khan, A. A., Khan, Z., Malik, A., Shrivastava, A., Jain, S. K., & Alshamsan, A. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.04.024 · Cited by 18

Roles of lymphocyte Kv1.3-channels in gut mucosal immune system: Novel therapeutic implications for inflammatory bowel disease

Kazama, I. (2015) · Medical Hypotheses · doi:10.1016/j.mehy.2015.03.023 · Cited by 19

Friendly pathogens: prevent or provoke autoimmunity

Sathyabama, S., Khan, N., & Agrewala, J. N. (2013) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2013.787043 · Cited by 18

Anti-TNF Agents Restrict Adherent-invasive Escherichia coli Replication Within Macrophages Through Modulation of Chitinase 3-like 1 in Patients with Crohn’s Disease

Douadi, C., Vazeille, E., Chambon, C., Hébraud, M., Fargeas, M., Dodel, M., Çoban, D., Pereira, B., Birer, A., Sauvanet, P., et al. (2022) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjab236 · Cited by 23

Bifidobacterium breve CBT BR3 is effective at relieving intestinal inflammation by augmenting goblet cell regeneration

Park, I. S., Kim, J. H., Yu, J., Shin, Y., Kim, K., Kim, T. I., Kim, S. W., & Cheon, J. H. (2023) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.16209 · Cited by 17

Immune Diseases Associated with Aging: Molecular Mechanisms and Treatment Strategies

Kim, M. E., & Lee, J. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115584 · Cited by 20

Current Status and Prospects of Intestinal Microbiome Studies

Han, D. S. (2014) · Intestinal Research · doi:10.5217/ir.2014.12.3.178 · Cited by 17

Probiotics and IBD.

Greef, E. D., Vandenplas, Y., Hauser, B., Devreker, T., & Veereman‐Wauters, G. (2013) · PubMed · Cited by 17

Biotin sulfone tagged oligomannosides as immunogens for eliciting antibodies against specific mannan epitopes

Despras, G., Robert, R., Sendid, B., Machez, E., Poulain, D., & Mallet, J. (2012) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.12.048 · Cited by 17

Patterns of Antibiotic Exposure and Clinical Disease Activity in Inflammatory Bowel Disease

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The rectal mucosal but not fecal microbiota detects subclinical ulcerative colitis

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