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

The Efficacy of Selected Probiotic Strains and Their Combination to Inhibit the Interaction of Adherent-Invasive Escherichia coli (AIEC) with a Co-Culture of Caco-2:HT29-MTX Cells

Bradford, G., Asgari, B., Smit, B., Hatje, E., Kuballa, A., & Katouli, M. (2024) · Microorganisms · doi:10.3390/microorganisms12030502 · Cited by 13

Fecal Microbiota Transplantation (FMT) and Clinical Outcomes Among Inflammatory Bowel Disease (IBD) Patients: An Umbrella Review

Malik, S., Naqvi, S. A. A., Shadali, A. H., Khan, H., Christof, M., Niu, C., Schwartz, D. A., & Adler, D. G. (2025) · Digestive Diseases and Sciences · doi:10.1007/s10620-025-08946-8 · Cited by 12

Roxithromycin inhibits nuclear factor kappaB signaling and endoplasmic reticulum stress in intestinal epithelial cells and ameliorates experimental colitis in mice

Choi, Y., Koh, S., Lee, H. S., Kim, J. W., Kim, B. G., Lee, K. L., & Kim, J. S. (2015) · Experimental Biology and Medicine · doi:10.1177/1535370215591829 · Cited by 12

Impact of PepT1 deletion on microbiota composition and colitis requires multiple generations

Viennois, É., Pujada, A., Sung, J. J., Yang, C., Gewirtz, A. T., Chassaing, B., & Merlin, D. (2020) · npj Biofilms and Microbiomes · doi:10.1038/s41522-020-0137-y · Cited by 12

Specific IgG Response against Mycobacterium avium paratuberculosis in Children and Adults with Crohn’s Disease

Verdier, J., Deroche, L., Allez, M., Loy, C., Biet, F., Bodier, C. C., Bay, S., Ganneau, C., Matysiak‐Budnik, T., Reyrat, J. M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062780 · Cited by 12

Microbiote intestinal et développement des maladies inflammatoires chroniques de l’intestin

Rahmouni, O., Dubuquoy, L., Desreumaux, P., & Neut, C. (2016) · médecine/sciences · doi:10.1051/medsci/20163211012 · Cited by 11

Dasatinib-induced Crohn’s-like colitis

Grillo, F., Carlin, L., Remo, A., Fassan, M., Mescoli, C., Campora, M., Caserta, L., Mazza, F., & Mastracci, L. (2022) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2022-208340 · Cited by 11

Intratumoral microorganisms in tumors of the digestive system

Xuan, M., Gu, X., Liu, Y., Li, Y., Li, Y., Huang, D., Li, J., & Xue, C. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-023-01425-5 · Cited by 13

Environmental influences on the onset and clinical course of Crohn's disease-part 2: infections and medication use.

Berg, A. M., Dam, A. N., & Farraye, F. A. (2013) · Europe PMC (PubMed Central) · Cited by 11

A literature review on large intestinal hyperelastic constitutive modeling

Bhattarai, A., Kowalczyk, W., & Trần, T. N. (2021) · Clinical Biomechanics · doi:10.1016/j.clinbiomech.2021.105445 · Cited by 13

Trends of Medication Usage and Associated Outcomes for Taiwanese Patients with Inflammatory Bowel Disease from 2001 to 2015

Weng, M., Tung, C., Chang, Y., Leong, Y., Wang, Y., Wong, J., & Wei, S. (2018) · Journal of Clinical Medicine · doi:10.3390/jcm7110394 · Cited by 11

The absence of interleukin 10 affects the morphology, differentiation, granule content and the production of cryptidin-4 in Paneth cells in mice

Berkowitz, L., Pardo‐Roa, C., Ramírez, G., Vallejos, O. P., Sebastián, V. P., Riedel, C. A., Álvarez-Lobos, M., & Bueno, S. M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221618 · Cited by 11

Prebiotic Carbohydrates for Therapeutics

Basavaiah, R., & Gurudutt, P. S. (2020) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/1871530320666200929140522 · Cited by 10

Experimental Colitis Is Exacerbated by Concomitant Infection with Mycobacterium avium ssp. paratuberculosis

Suwandi, A., Bargen, I., Roy, B., Pils, M. C., Krey, M., Lage, S. Z., Basler, T., Rohde, M., Falk, C. S., Hornef, M. W., et al. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000157 · Cited by 10

Replication of Crohn’s Disease Mucosal E. coli Isolates inside Macrophages Correlates with Resistance to Superoxide and Is Dependent on Macrophage NF-kappa B Activation

Tawfik, A., Knight, P., Duckworth, C. A., Pritchard, D. M., Rhodes, J. M., & Campbell, B. J. (2019) · Pathogens · doi:10.3390/pathogens8020074 · Cited by 12

A Novel Grape-Derived Prebiotic Selectively Enhances Abundance and Metabolic Activity of Butyrate-Producing Bacteria in Faecal Samples

Oliver, L., Ramió‐Pujol, S., Amoedo, J., Malagón, M., Serrano, M., Bahí, A., Lluansí, A., Torrealba, L., Busquets, D., Pardo, L., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.639948 · Cited by 11

Gnotobiology and the Study of Complex Interactions between the Intestinal Microbiota, Probiotics, and the Host

Tlaskalová-Hogenová, H., Kverka, M., Verdu, E. F., & Wells, J. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00008-2 · Cited by 10

Role ofSalmonella entericaexposure in Chilean Crohn's disease patients

Álvarez-Lobos, M. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i35.5855 · Cited by 10

Colitis aggravated by Mrgprb2 knockout is associated with altered immune response, intestinal barrier function and gut microbiota

Shao, M., Liu, J., Liu, J., Yuan, F., & Deng, Y. (2022) · Experimental Physiology · doi:10.1113/ep090635 · Cited by 9

Impact of bread diet on intestinal dysbiosis and irritable bowel syndrome symptoms in quiescent ulcerative colitis: A pilot study

Lluansí, A., Llirós, M., Carreras‐Torres, R., Bahí, A., Capdevila, M., Feliu, A., Vilà-Quintana, L., Masiques, N. E., Cueva, E., Peries, L., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0297836 · Cited by 10

Why Are Omics Technologies Important to Understanding the Role of Nutrition in Inflammatory Bowel Diseases?

Ferguson, L. R., & Barnett, M. P. G. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17101763 · Cited by 9

Probiotics and gastrointestinal diseases

Dargenio, V. N., Castellaneta, S. P., PANICO, S., Papagni, M. E., Dargenio, C., SCHETTINI, F., Francavilla, R., & Cristofori, F. (2022) · Minerva Pediatrics · doi:10.23736/s2724-5276.22.07031-8 · Cited by 10

Probiotics: an update

Vandenplas, Y., Huys, G. R. B., & Daube, G. (2015) · Jornal de Pediatria (Versão em Português) · doi:10.1016/j.jpedp.2014.08.006 · Cited by 9

Working together: gut microbe-microbe interactions shape host inflammation

Lawing, A., & Bleich, R. M. (2025) · Infection and Immunity · doi:10.1128/iai.00512-24 · Cited by 8

Use of Probiotics to Prevent Celiac Disease and IBD in Pediatrics

Serena, G., & Fasano, A. (2018) · Advances in experimental medicine and biology · doi:10.1007/5584_2018_317 · Cited by 8

Microbes, Their Metabolites, and Effector Molecules: A Pharmacological Perspective for Host-Microbiota Interaction

Bhushan, B., Singh, B. P., Kumari, M., Mishra, V., Saini, K., & Singh, D. (2019) · Environmental chemistry for a sustainable world · doi:10.1007/978-3-030-04675-0_7 · Cited by 9

Effects of sialylated lactulose on the mouse intestinal microbiome using Illumina high-throughput sequencing

Song, M., Zeng, J., Jia, T., Gao, H., Zhang, R., Jiang, J., Li, G., & Su, T. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10169-7 · Cited by 8

The Emerging Role of CCL17 in the Immunologic Regulation of Inflammatory Bowel Disease

Zhang, C., Ouyang, Y., He, H., Su, P., & Li, Z. (2025) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.70005 · Cited by 7

Improvement of intestinal microbial structure in patients with cerebral infarction through in vitro fermentation of anthocyanins from Lycium ruthenicum Murray

Qiu, J. Q., Ye, B., & Feng, L. (2024) · Food Science & Nutrition · doi:10.1002/fsn3.4263 · Cited by 8

Faecal microbiota transplantation: looking beyond clostridium difficile infection at inflammatory bowel disease.

Patel, K., Patel, A. B., Hawes, D., Shah, J., & Shah, K. (2018) · Gastroenterology and hepatology from bed to bench. · Cited by 7

The Mechanism of Important Components in Canine Fecal Microbiota Transplantation

Li, K., Yang, J., Zhou, X., Wang, H., Ren, Y., Huang, Y., Liu, H., Zhong, Z., Peng, G., Zheng, C., et al. (2022) · Veterinary Sciences · doi:10.3390/vetsci9120695 · Cited by 11

Visualization of melanoma tumor with lectin-conjugated rare-earth doped fluoride nanocrystals

Dumych, T. I., Lutsyk, M. M., Bański, M., Yashchenko, А. М., Sojka, B., Horbay, R., Lutsyk, A. D., Stoika, R. S., Misiewicz, J., Podhorodecki, A., et al. (2014) · Croatian Medical Journal · doi:10.3325/cmj.2014.55.186 · Cited by 7

Alterations in programmed cell death mechanism and their role in the pathogenesis of inflammatory bowel diseases

Eder, P., Łykowska‐Szuber, L., Stawczyk‐Eder, K., Krela‐Kaźmierczak, I., & Linke, K. (2014) · Gastroenterology Review · doi:10.5114/pg.2014.46162 · Cited by 7

Current State of Knowledge on Implications of Gut Microbiome for Surgical Conditions

Chen, E. B., Cason, C. A., Gilbert, J. A., & Ho, K. J. (2018) · Journal of Gastrointestinal Surgery · doi:10.1007/s11605-018-3755-4 · Cited by 7

Local Mesenchymal Stem Cell Therapy in Experimentally Induced Colitis in the Rat

de la Portilla, F., Yuste, Y., Pereira, S., Olano, C., Maestre, M. V., & Ruiz, F. J. P. (2018) · International Journal of Stem Cells · doi:10.15283/ijsc17074 · Cited by 7

Dysbiosis in Inflammatory Bowel Disease and Spondyloarthritis: Still a Long Way to Go?

Bragazzi, M. C., Pianigiani, F., Venere, R., & Ridola, L. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13082237 · Cited by 6

Impact of Oral Probiotics in Amelioration of Immunological and Inflammatory Responses on Experimentally Induced Acute Diverticulitis

Soliman, M. G., Mansour, H. A., Hassan, W. A., & Shawky, E. (2022) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-022-09969-7 · Cited by 6

Beyond cancer: The potential application of CD47-based therapy in non-cancer diseases

Deng, W.-Q., Ye, Z.-H., Tang, Z.-H., Zhang, X., & Lu, J. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.11.018 · Cited by 7

Pathogenic or Therapeutic: The Mediating Role of Gut Microbiota in Non-Communicable Diseases

Bu, F., Yao, X., Lü, Z., Yuan, X., Chen, C., Li, L., Li, Y., Jiang, F., Zhu, L., Shi, G., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.906349 · Cited by 6

Protective effects of amoxicillin and probiotics on colon disorders in an experimental model of acute diverticulitis disease

Soliman, M. G., Mansour, H. A., Hassan, W. A., & Shawky, E. (2022) · Inflammopharmacology · doi:10.1007/s10787-022-01093-w · Cited by 6

Advances in the polysaccharide derivatives for the treatment of inflammatory bowel disease: A review

Zhang, L., Wang, S., Fu, X., Yang, Y., Zhang, Z., & Ju, J. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.144192 · Cited by 5

Analysis of the Preventive Effect of Lonicera caerulea Pomace and Its Isolated Components on Colitis in Mice Based on Gut Microbiota and Serum Metabolomics

Zhou, Z., Huang, X., & Zhang, B. (2024) · Antioxidants · doi:10.3390/antiox13121478 · Cited by 5

Colonic Phenotype of the Ileum in Crohnʼs Disease

Ascolani, M., Mescoli, C., Palmieri, G., Sica, G. S., Calabrese, E., Petruzziello, C., Onali, S., Albertoni, L., Lolli, E., Condino, G., et al. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000127 · Cited by 5

Caracterización, influencia y manipulación de la microbiota gastrointestinal en salud y enfermedad

García-Mazcorro, J. F., Garza‐González, E., Marroquín-Cardona, A. G., & Tamayo, J. L. (2015) · Gastroenterología y Hepatología · doi:10.1016/j.gastrohep.2015.01.004 · Cited by 5

Effects of GBT1118 , a voxelotor analog, on intestinal pathophysiology in sickle cell disease

Haroun, E., Dutta, D., & Lim, S. H. (2023) · British Journal of Haematology · doi:10.1111/bjh.18813 · Cited by 5

Human β-Defensin 2 Induces Extracellular Accumulation of Adenosine in Escherichia coli

Estrela, A. B., Rohde, M., Gutierrez, M. G., Molinari, G., & Abraham, W. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00820-13 · Cited by 5

IL-5-producing Group 2 innate lymphoid cells promote T cell-independent IgA production in cooperation with eosinophils

Yanagibashi, T., Ikutani, M., Nagai, T., Arita, M., Watanabe, Y., Nagai, Y., & Takatsu, K. (2024) · International Immunology · doi:10.1093/intimm/dxae070 · Cited by 5

Treatment of immune checkpoint inhibitor-related colitis: a narrative review

Wang, S., & Wang, H. (2024) · Translational Cancer Research · doi:10.21037/tcr-24-2150 · Cited by 4

Importance of Bacteria as Trigger in Inflammatory Bowel Disease

Denizot, J. (2012) · Journal of Gastrointestinal & Digestive System · doi:10.4172/2161-069x.s8-003 · Cited by 4

Enteropathogen-Induced Microbiota Biofilm Disruptions and Post-Infectious Intestinal Inflammatory Disorders

Buret, A. G. (2016) · Current Tropical Medicine Reports · doi:10.1007/s40475-016-0079-x · Cited by 4

Fungus fuels mucosal wounds in Crohn’s disease

Magnaye, K. M., & Lynch, S. V. (2021) · Immunity · doi:10.1016/j.immuni.2021.04.013 · Cited by 4

Adsorptive granulomonocytapheresis alters the gut bacterial microbiota in patients with active ulcerative colitis

Chen, X., Lou, L., Tang, H., Tan, X., Bi, J., Wu, H., Li, N., Wang, Y.-D., & Mao, J. (2021) · Journal of Clinical Apheresis · doi:10.1002/jca.21887 · Cited by 5

The Impact of Immune Dysregulation on the Development of Autoimmune Gastrointestinal and Liver Disease

Levine, J. J. (2014) · Current problems in pediatric and adolescent health care · doi:10.1016/j.cppeds.2014.10.001 · Cited by 4

Crohn’s Disease: a Role of Gut Microbiota and Nod2 Gene Polymorphisms in Disease Pathogenesis

Hrnčíř, T., Krejsek, J., Šplı́chal, I., & Hrnčíř, T. (2014) · Acta Medica (Hradec Kralove Czech Republic) · doi:10.14712/18059694.2014.46 · Cited by 4

Do Shared Exposures Link the Lungs and Gut? Association Between Asthma and Inflammatory Bowel Disease

Barnes, E. L., & Kappelman, M. D. (2017) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2017.04.030 · Cited by 4

Dysregulation of the engulfment pathway in the gut fuels Inflammatory Bowel DiseasePreprint

Suarez, K., Lim, E., Singh, S., Pereira, M. P., Joosen, L., Ibeawuchi, S., Dunkel, Y., Mittal, Y., Ho, S. B., Chattopadhyay, R., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/280172 · Cited by 4

Establishing the phenotypic basis of adherent-invasive Escherichia coli (AIEC) pathogenicity in intestinal inflammationPreprint

Kittana, H., Neto, J. C. G., Heck, K., Sughroue, J. A., Xian, Y., Mantz, S., Muñoz, R. R. S., Cody, L. A., Schmaltz, R. J., Anderson, C. L., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/772012 · Cited by 4

Anti-Inflammatory Effects of Amomum villosum Extract on Dextran Sodium Sulfate-Induced Colitis in Mice

Choi, H.-B., Kim, R. W., Bae, G., Jang, J. H., Kim, Y.-S., Park, B. O., & Kwon, K. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47060389 · Cited by 3

The differential alleviation of DSS-induced colitis in mice by black tea extracts of different origins via enhancing the gut barrier and gut microbiota modulation

Huang, Y., He, Y., Cai, Y., Chen, Y., Shi, X., He, J., Wu, K., & Wei, H. (2025) · Food & Function · doi:10.1039/d5fo02993g · Cited by 3

Microbiota-driven mechanisms in multisystem diseases: integrative evidence across cardiovascular, metabolic, neurological and autoimmune disorders

Ansari, S., Purohit, K. J., Shelke, A. B., Shah, M., Nkhoma, I. A., Navale, A. M., & Wakchaure, R. S. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02296-9 · Cited by 4

Herbal Medicines for the Management of Irritable Bowel Syndrome and Constipation Problem

Puppala, E. R., Prasad, N., Singh, M., Prakash, A. N., Abubakar, M., Adhikari, P., & Naidu, V. G. M. (2023) · Springer eBooks · doi:10.1007/978-981-99-7703-1_16 · Cited by 3

Bifidobacterial biofilms as next-generation probiotics and their role in intestinal microbiocenosis

Aziz, K., & Zaidi, A. (2024) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2024.2438119 · Cited by 3

Role of Food Additives and Intestinal Microflora in Colorectal Cancer

Soni, V. K., Amit, A., Chandra, V., Singh, P. K., Singh, P. K., Singh, R. P., Patel, G. K., & Singh, R. P. (2022) · Springer eBooks · doi:10.1007/978-3-030-72702-4_14 · Cited by 3

Intestinal mucosal and fecal microbiota profiles in Crohn's disease in Chinese children

Wu, P., Wu, B., Zhuang, Z., Liu, J., Hong, L., Ma, B., Lin, B., Wang, J., Lin, C., Chen, J., et al. (2022) · Medicine in Microecology · doi:10.1016/j.medmic.2022.100071 · Cited by 3

Probiotics to Prevent Celiac Disease and Inflammatory Bowel Diseases

Fasano, A., & Matera, M. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-58572-2_6 · Cited by 4

Diarrhoeal episodes in travellers suffering from IBD

Ellul, P., Fenech, V. A., Azzopardi, C., Callus, L., Delicata, N. P., Muscat, J., Azzopardi, N., & Vassallo, M. (2012) · Frontline Gastroenterology · doi:10.1136/flgastro-2012-100265 · Cited by 3

Infrared spectroscopy as a screening technique for colitis

Titus, J., Ghimire, H., Viennois, É., Merlin, D., & Perera, A. G. U. (2017) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2264462 · Cited by 3

Usefulness of Probiotics for Neonates?

Butel, M., Waligora‐Dupriet, A., & Aires, J. (2012) · InTech eBooks · doi:10.5772/51265 · Cited by 3

Gut dysbiosis and its epigenomic impact on disease

Odenwald, M. A., & Chapman, C. G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816843-1.00025-4 · Cited by 3

Sustainable Biomaterials: Turning Food Waste into Advanced Regenerative Technology

Dempsey, S. G., Young, D. A., Veale, R. W. F., & May, B. C. H. (2025) · Biomedical engineering · doi:10.5772/intechopen.1010994 · Cited by 2

Optimized TRIzol–silica column RNA extraction for DSS-colitis: resolving PCR inhibition

Lin, J., Zhang, J., Santiago, A. M., & Sun, Q. (2025) · Agricultural Products Processing and Storage · doi:10.1007/s44462-025-00030-8 · Cited by 2

Biomimetic priming of hMSC aggregates with cadherin-IL-1β synergistic microparticles enhances immune homeostasis in inflammatory bowel disease

Qian, M., Ge, M., Liu, S., Wen, X., Liu, N., Wang, Q., Cao, J., Jiang, X., Zhang, Y., Yang, J., et al. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.168570 · Cited by 2

Food and Intestinal Microorganisms: Factors in Pathogenesis, Prevention and Therapy of Ulcerative Colitis

Orel, R., & Urlep, D. (2011) · InTech eBooks · doi:10.5772/27798 · Cited by 2

Polymorphisms in Autophagy-Related Genes in Crohn’s Disease

Bringer, M.-A., Lapaquette, P., Nguyen, H. T. T., & Darfeuille–Michaud, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405529-2.00006-8 · Cited by 6

Implication de la flore fongique intestinale dans le développement de la maladie de Crohn

Hoarau, G., Colombel, J., Poulain, D., & Sendid, B. (2013) · médecine/sciences · doi:10.1051/medsci/2013298004 · Cited by 2

Effects of Taste Signaling Protein Abolishment on Gut Inflammation in an Inflammatory Bowel Disease Mouse Model

Du, Y.-W., Liu, Q., Luo, X., Zhao, D.-X., Xue, J., Feng, P., Margolskee, R. F., Wang, H., & Huang, L. (2018) · Journal of Visualized Experiments · doi:10.3791/58668-v · Cited by 2

Inflammatory bowel disease: factors involved in pathogenesis

Dudík, B., Sepová, H. K., & Bilková, A. (2018) · Česká a slovenská farmacie · doi:10.36290/csf.2018.013 · Cited by 2

Impact of oral administration of single strain Lactococcus lactis spp. cremoris on immune responses to keyhole limpet hemocyanin immunization and gut microbiota: A randomized placebo-controlled trial in healthy volunteers

Saghari, M., Gal, P., Grievink, H. W., Klaassen, E. S., Itano, A. A., McHale, D., & Moerland, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1009304 · Cited by 2

Adalimumab for maintenance of remission in Crohn's disease

Cepek, J., Abbass, M., Nguyen, T. M., Parker, C. E., MacDonald, J. K., Feagan, B. G., Jairath, V., & Khanna, R. (2017) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd012877 · Cited by 2

Molecular analysis of candidate probiotic effector molecules of Lactobacillus plantarum

Remus, D. M. (2012) · doi:10.18174/232424 · Cited by 2

Microbiota Alterations in Inflammatory Bowel Diseases: From Correlation to Causality

Chassaing, B. (2016) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2016.04.008 · Cited by 2

Ulcerative Colitis but Not Dextran Sodium Sulfate–Induced Colitis–Associated Microbiota Promotes Early Biomarkers of Colitis in Interleukin-10 −/− Mice

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In the labyrinths of pathogenesis: the environment and metamorphosis of IBD

Av, T., Сирекановна, М. Л., Евгеньевна, М. К., & Боханова, Е. Г. (2021) · South Russian Journal of Therapeutic Practice · doi:10.21886/2712-8156-2021-2-3-30-39 · Cited by 1

The Host Microbiota is Associated with the Occurrence and Development of Esophageal Squamous Cell Carcinoma

Zuo, J., Liu, Y., Lv, W., Wang, Y., Fan, Z., Wang, L., Li, F., Zhang, X., Han, J., & Ni, Z. (2022) · Protein & Cell · doi:10.1093/procel/pwac024 · Cited by 1

Inflammatory bowel disease and diet: Is there a place for probiotics?

Nikolova, D. (2023) · Galenika Medical Journal · doi:10.5937/galmed2305041n · Cited by 1

The Science Underlying the Probiotic Strain Bifidobacterium in Beneficial Effects on Immunological and Gastrointestinal Health

Ali, A., Islam, N., Fakir, N. I., Kabir, A., Sharmin, M., Islam, T., Rahman, M., Badal, F. A., & Taher, A. (2024) · International Journal of Immunology · doi:10.11648/j.iji.20241201.12 · Cited by 1

Prävention und Therapie von entzündlichen Magen‐/Darm‐Erkrankungen

Stein, J. M., & Dignass, A. U. (2012) · Pharmazie in unserer Zeit · doi:10.1002/pauz.201100460 · Cited by 1

Discordance between Patients and Parents Regarding the Perceived Causes of Clinical Relapse in Young Inflammatory Bowel Disease Patients

Kim, S. B., Kim, K. O., Jung, Y. S., Chung, H. H., Lee, S. H., & Jang, B. I. (2015) · Korean Journal of Gastroenterology · doi:10.4166/kjg.2015.65.2.99 · Cited by 1

Inflammatory bowel disease and the gut microbiota

Ding, N. S., & Hart, A. L. (2016) · Wiley eBooks · doi:10.1002/9781118982907.ch19 · Cited by 1

Etudes comparatives de lactobacillus delbrueckii sous-espèces lactis et bulgaricus : identification des déterminants du phénotype anti-inflammatoire

Kafsi, H. E. (2014) · theses.fr (ABES) · doi:10.70675/c3ef71e9z2564z4f3fza520z4e48023240b0 · Cited by 1

Modulation nutritionnelle du développement postnatal des fonctions neuro-digestives

Vanhaecke, T. (2016) · theses.fr (ABES) · doi:10.70675/314bdbdfz4219z4db8zacd3z796751145682 · Cited by 1

Ocena wpływu leczenia przeciwciałami anty-TNF-alfa na ekspresję wybranych receptorów oraz białek biorących udział w procesie apoptozy nabłonka i limfocytów blaszki właściwej jelita u pacjentów z chorobą Leśniowskiego-Crohna

Eder, P. (2012) · Biblioteka Uniwersytetu Medycznego w Poznaniu

Chronisch-entzündliche Erkrankungen des Kolorektums

Aust, D. E. (2013) · Springer eBooks · doi:10.1007/978-3-642-02322-4_27

The faecal flora: a source of healthcare-associated infections and antibiotic resistance

Samuelsson, A. (2013) · Linköping University Electronic Press eBooks · doi:10.3384/diss.diva-97709

Drug toxicity in inflammatory bowel disease

Juncadella, A. C., & Deshpande, A. R. (2014) · Clinical Practice · doi:10.2217/cpr.14.51

Dysbiosis of the Faecal Microbiota in Patients with Crohn's Disease and Their Unaffected Relatives (Gut 2011;60:631-637)

Kang, S. J., & Im, J. P. (2011) · Intestinal Research · doi:10.5217/ir.2011.9.2.166 · Cited by 1

Commensal gut microbiota, genetic and epigenetic factors and susceptibility to inflammatory bowel disease

Riordan, S. M. (2013) · Microbiology Australia · doi:10.1071/ma13050

Adherent-invasive Escherichia coli Biofilm Formation Assays

Chassaing, B., & Darfeuille–Michaud, A. (2013) · BIO-PROTOCOL · doi:10.21769/bioprotoc.982

SYSTEMS BIOLOGY OF MICROBIOTA METABOLITES AND ADIPOCYTE TRANSCRIPTION FACTOR NETWORK

Choi, K. (2013) · OakTrust (Texas A&M University Libraries)

The Roles of Inflammation, Nutrient Availability and the Commensal Microbiota in Enteric Pathogen Infection

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Microbial Influences in Inflammatory Bowel Diseases

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Dysbiosis in Inflammatory Bowel Disease: Pathogenic Role and Potential Therapeutic Targets

Santana, P. T., Rosas, S. L. B., Ribeiro, B. E., Marinho, Y., & de Souza, H. S. P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073464 · Cited by 359

Microbiome and Diseases: Inflammatory Bowel Diseases

Hildner, K., Waldschmitt, N., & Haller, D. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_11 · Cited by 3

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