Role of the normal gut microbiota

Structure, function and diversity of the healthy human microbiome

The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726

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

Diet rapidly and reproducibly alters the human gut microbiome

David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100

Pattern Recognition Receptors and Inflammation

Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895

Human gut microbes associated with obesity

Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815

Enterotypes of the human gut microbiome

MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548

Changes of Intestinal Functions in Liver Cirrhosis

Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820

Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa

De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579

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

Local and Systemic Effects of Bioactive Food Ingredients: Is There a Role for Functional Foods to Prime the Gut for Resilience?

Jacquier, E. F., van de Wouw, M., Nekrasov, E., Contractor, N., Kassis, A. N., & Marcu, D. E. (2024) · Foods · doi:10.3390/foods13050739 · Cited by 42

Life at the borderlands: microbiomes of interfaces critical to One Health

Law, S. R., Mathes, F., Paten, A. M., Alexandre, P. A., Regmi, R., Reid, C. J., Safarchi, A., Shaktivesh, S., Wang, Y., Wilson, A., et al. (2024) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuae008 · Cited by 39

Human intestinal microbiome: Role in health and disease

Cantón, R., Ramos, P. D. L., Botella, A. G., García‐Lledó, A., Hernández‐Sampelayo, T., Gómez‐Pavón, J., del Castillo, J. M. G., Martín-Delgado, M. C., Martín‐Sánchez, F. J., Martínez‐Sellés, M., et al. (2024) · Revista Española de Quimioterapia · doi:10.37201/req/056.2024 · Cited by 36

Glucoraphanin conversion into sulforaphane and related compounds by gut microbiota

Dmytriv, T. R., Lushchak, O. V., & Lushchak, V. I. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1497566 · Cited by 37

Melatonin: An important anticancer agent in colorectal cancer

Mirza‐Aghazadeh‐Attari, M., Mohammadzadeh, A., Mostavafi, S., Mihanfar, A., Darband, S. G., Sadighparvar, S., Gholamzadeh, S., Majidinia, M., & Yousefi, B. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29049 · Cited by 38

Microbiome as an Immunological Modifier

Kumar, M., Singh, P., Murugesan, S., Vétizou, M., McCulloch, J. A., Badger, J. H., Trinchieri, G., & Khodor, S. A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9773-2_27 · Cited by 36

Immune modulatory capacity of probiotic lactic acid bacteria and applications in vaccine development

Mojgani, N., Shahali, Y., & Dadar, M. (2020) · Beneficial Microbes · doi:10.3920/bm2019.0121 · Cited by 35

Spatial Organization of Cell Wall-Anchored Proteins at the Surface of Gram-Positive Bacteria

Dramsi, S., & Bierne, H. (2016) · Current Topics in Microbiology and Immunology · doi:10.1007/82_2016_4 · Cited by 36

Antimicrobial peptide production in response to gut microbiota imbalance

Cardoso, M. H. E. S., Meneguetti, B. T., Oliveira-Júnior, N. G., Macedo, M. L. R., & Franco, O. L. (2022) · Peptides · doi:10.1016/j.peptides.2022.170865 · Cited by 37

Changes in gut microbial community upon chronic kidney disease

Liu, W., Huang, J., Liu, T., Hu, Y., Shi, K., Zhou, Y., & Zhang, N. (2023) · PLoS ONE · doi:10.1371/journal.pone.0283389 · Cited by 34

“Cross-talk” between gut microbiome dysbiosis and osteoarthritis progression: a systematic review

Liu, S., Li, G., Xu, H., Wang, Q., Wei, Y., Yang, Q., Xiong, A., Yu, F., Weng, J., & Zeng, H. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1150572 · Cited by 40

Comprehensive insights from composition to functional microbe-based biodiversity of the infant human gut microbiota

Lugli, G. A., Mancabelli, L., Milani, C., Fontana, F., Tarracchini, C., Alessandri, G., van Sinderen, D., Turroni, F., & Ventura, M. (2023) · npj Biofilms and Microbiomes · doi:10.1038/s41522-023-00392-6 · Cited by 36

Effect of the gut microbiota and their metabolites on postoperative intestinal motility and its underlying mechanisms

Ma, T., Xue, X., Tian, H., Zhou, X., Wang, J.-K., Zhao, Z., Wang, M., Song, J., Feng, R., Li, L., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04215-2 · Cited by 41

Gut microbiota and intestinal immunity—A crosstalk in irritable bowel syndrome

Chen, Y., Feng, S., Li, Y., Zhang, C., Chao, G., & Zhang, S. (2024) · Immunology · doi:10.1111/imm.13749 · Cited by 36

Dietary polyphenols represent a phytotherapeutic alternative for gut dysbiosis associated neurodegeneration: A systematic review

Chatterjee, A., Kumar, S., Sarkar, S. R., Halder, R., Kumari, R., Banerjee, S., & Sarkar, B. (2024) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2024.109622 · Cited by 36

Exploring the Gut Microbiome’s Role in Inflammatory Bowel Disease: Insights and Interventions

Gyriki, D., Nikolaidis, C. G., Stavropoulou, E., Bezirtzoglou, I., Tsigalou, C., Vradelis, S., & Bezirtzoglou, E. (2024) · Journal of Personalized Medicine · doi:10.3390/jpm14050507 · Cited by 40

Dietary Patterns, Gut Microbiota and Sports Performance in Athletes: A Narrative Review

Chen, Y., Yang, K., Xu, M., Zhang, Y., Weng, X., Luo, J., Li, Y., & Mao, Y.-H. (2024) · Nutrients · doi:10.3390/nu16111634 · Cited by 46

The potential influence and intervention measures of gut microbiota on sperm: it is time to focus on testis-gut microbiota axis

Chen, W., Zou, H., Xu, H., Cao, R., Zhang, H., Zhang, Y., & Zhao, J. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1478082 · Cited by 42

A role for microglia in mediating the microbiota–gut–brain axis

Keane, L., Clarke, G. A., & Cryan, J. F. (2025) · Nature reviews. Immunology · doi:10.1038/s41577-025-01188-9 · Cited by 43

Gut–brain axis in the executive function of austism spectrum disorder

Román, P., Rueda‐Ruzafa, L., Cardona, D., & Cortés‐Rodríguez, A. E. (2018) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000428 · Cited by 36

‘Inside Out’– a dialogue between mitochondria and bacteria

Han, B., Lin, C.-C., Hu, G., & Wang, M. C. (2018) · FEBS Journal · doi:10.1111/febs.14692 · Cited by 37

Gut microbial modulation in the treatment of chemotherapy-induced diarrhea with Shenzhu Capsule

Wang, J., Feng, W., Zhang, S., Chen, L., Tang, F., Sheng, Y., Ao, H., & Peng, C. Y. (2019) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-019-2548-y · Cited by 34

Exploring Clinical Outcomes and Feasibility of Blended Tube Feeds in Children

Chandrasekar, N., Dehlsen, K., Leach, S. T., & Krishnan, U. (2020) · Journal of Parenteral and Enteral Nutrition · doi:10.1002/jpen.2062 · Cited by 36

Gut Microbiota and Human Body Interactions; Its Impact on Health: A Review

Hajiagha, M. N., Taghizadeh, S., Asgharzadeh, M., Dao, S., Ganbarov, K., Köse, Ş., & Kafil, H. S. (2021) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201022666210104115836 · Cited by 36

Gastrodin attenuates perfluorooctanoic acid-induced liver injury by regulating gut microbiota composition in mice

Ma, S., Sun, Y., Zheng, X., & Yang, Y. (2021) · Bioengineered · doi:10.1080/21655979.2021.2009966 · Cited by 35

Evaluating the effects of a standardized polyphenol mixture extracted from poplar-type propolis on healthy and diseased human gut microbiota

Garzarella, E. U., Navajas-Porras, B., Pérez-Burillo, S., Ullah, H., Esposito, C., Santarcangelo, C., Hinojosa-Nogueira, D., Pastoriza, S., Zaccaria, V., Xiao, J., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.112759 · Cited by 35

Exploring the Association between Gut and Urine Microbiota and Prostatic Disease including Benign Prostatic Hyperplasia and Prostate Cancer Using 16S rRNA Sequencing

Tsai, K.-Y., Wu, D., Wu, W., Wang, J., Juan, Y., Li, C., Liu, C., & Lee, H. (2022) · Biomedicines · doi:10.3390/biomedicines10112676 · Cited by 35

The modulatory effect of encapsulated bioactives and probiotics on gut microbiota: improving health status through functional food

Estrada, K. B., Sandoval-Cuellar, C. E., Rojas-Muñoz, Y. V., & Quintanilla‐Carvajal, M. X. (2022) · Food & Function · doi:10.1039/d2fo02723b · Cited by 36

On the Search to Elucidate the Role of Microbiota in the Genesis of Cancer: The Cases of Gastrointestinal and Cervical Cancer

Avilés‐Jiménez, F., Yu, G., Torres-Poveda, K., Madrid‐Marina, V., & Torres, J. (2017) · Archives of Medical Research · doi:10.1016/j.arcmed.2017.11.008 · Cited by 34

Characterization of the semen, gut, and urine microbiota in patients with different semen abnormalities

Cao, T., Wang, S., Pan, Y., Guo, F., Wu, B., Zhang, Y., Wang, Y., Tian, J., Xing, Q., & Liu, X. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1182320 · Cited by 36

Impacts of gut microbiota alteration on age-related chronic liver diseases

Adhikary, S., Esmeeta, A., Dey, A., Banerjee, A., Saha, B., Gopan, P., Duttaroy, A. K., & Pathak, S. (2023) · Digestive and Liver Disease · doi:10.1016/j.dld.2023.06.017 · Cited by 36

Factors Influencing Neonatal Gut Microbiome and Health with a Focus on Necrotizing Enterocolitis

Beharry, K. D. A., Latkowska, M., Valencia, A. M., Allana, A., Soto, J., Cai, C. L., GOLOMBEK, S. G., Hand, I. L., & Aranda, J. V. (2023) · Microorganisms · doi:10.3390/microorganisms11102528 · Cited by 39

Electrophilic Compounds in the Human Diet and Their Role in the Induction of the Transcription Factor NRF2

Andrés, C. M. C., de la Lastra, J. M. P., Munguira, E. B., Andrés, C., Plou, F. J., & Lebeña, E. P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063521 · Cited by 34

Unraveling the Microbiome–Human Body Axis: A Comprehensive Examination of Therapeutic Strategies, Interactions and Implications

Olteanu, G., Pană, M.-A., Busnatu, Ș., Lupuliasa, D., Neacșu, S. M., Mititelu, M., Musuc, A. M., Ioniță-Mîndrican, C.-B., & Boroghină, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105561 · Cited by 36

Gut microbiota immune cross-talk in amyotrophic lateral sclerosis

Kaul, M., Mukherjee, D., Weiner, H. L., & Cox, L. M. (2024) · Neurotherapeutics · doi:10.1016/j.neurot.2024.e00469 · Cited by 36

Unraveling the Gut–Liver–Brain Axis: Microbiome, Inflammation, and Emerging Therapeutic Approaches

Aghara, H., Patel, M., Chadha, P., Parwani, K., Chaturvedi, R., & Mandal, P. (2025) · Mediators of Inflammation · doi:10.1155/mi/6733477 · Cited by 39

The Role of Gut Microbiota in Gastrointestinal Immune Homeostasis and Inflammation: Implications for Inflammatory Bowel Disease

Bretto, E., Caviglia, G. P., Saracco, G. M., Bugianesi, E., & Ribaldone, D. G. (2025) · Biomedicines · doi:10.3390/biomedicines13081807 · Cited by 41

Harnessing the Power of Microbiome Assessment Tools as Part of Neuroprotective Nutrition and Lifestyle Medicine Interventions

Toribio-Mateas, M. A. (2018) · Microorganisms · doi:10.3390/microorganisms6020035 · Cited by 37

The effects of high doses of vitamin D on the composition of the gut microbiome of adolescent girls

Tabatabaeizadeh, S., Fazeli, M., Meshkat, Z., Khodashenas, E., Esmaily, H., Mazloum, S., Ferns, G. A., Abdizadeh, M. F., & Ghayour‐Mobarhan, M. (2019) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2019.10.020 · Cited by 34

Protective effects and mechanisms of Rehmannia glutinosa leaves total glycoside on early kidney injury in db/db mice

Xu, Z., Dai, X., Zhang, Q., Su, S., Yan, H., Zhu, K. Y., Shang, E., Qian, D., & Duan, J. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.109926 · Cited by 34

Dairy product intake modifies gut microbiota composition among hyperinsulinemic individuals

Khorraminezhad, L., Leclercq, M., O'Connor, S. E., Julien, P., Weisnagel, S. J., Gagnon, C., Droit, A., & Rudkowska, I. (2020) · European Journal of Nutrition · doi:10.1007/s00394-020-02226-z · Cited by 37

Understanding the effects of dietary components on the gut microbiome and human health

Rackerby, B., Kim, H. J., Dallas, D. C., & Park, S. H. (2020) · Food Science and Biotechnology · doi:10.1007/s10068-020-00811-w · Cited by 37

Gut Microbiota and Environment in Coronary Artery Disease

Piccioni, A., de Cunzo, T., Valletta, F., Covino, M., Rinninella, E., Raoul, P. C., Zanza, C., Mele, M. C., & Franceschi, F. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18084242 · Cited by 34

Gut Microbiota Dynamics, Growth Performance, and Gut Morphology in Broiler Chickens Fed Diets Varying in Energy Density with or without Bacitracin Methylene Disalicylate (BMD)

Adewole, D. I., & Akinyemi, F. T. (2021) · Microorganisms · doi:10.3390/microorganisms9040787 · Cited by 36

The gut microbiome in pancreatogenic diabetes differs from that of Type 1 and Type 2 diabetes

Talukdar, R., Sarkar, P., Jakkampudi, A., Sarkar, S., Aslam, M., Jandhyala, M., Gujjarlapudi, D., Unnisa, M., & Reddy, D. N. (2021) · Scientific Reports · doi:10.1038/s41598-021-90024-w · Cited by 33

Association of Gut Microbiome Dysbiosis with Neurodegeneration: Can Gut Microbe-Modifying Diet Prevent or Alleviate the Symptoms of Neurodegenerative Diseases?

Tan, L. Y., Yeo, X. Y., Bae, H., Lee, D. P. S., Ho, R., Kim, J. E., Jo, D., & Jung, S. (2021) · Life · doi:10.3390/life11070698 · Cited by 35

Host Genetics and Gut Microbiome: Perspectives for Multiple Sclerosis

Maglione, A., Zuccalà, M., Tosi, M., Clerico, M., & Rolla, S. (2021) · Genes · doi:10.3390/genes12081181 · Cited by 34

Type 3 resistant starch from Canna edulis modulates obesity and obesity-related low-grade systemic inflammation in mice by regulating gut microbiota composition and metabolism

Wu, J., Qiu, M., Zhang, C., Zhang, C., Wang, N., Zhao, F., Liqiao, L. V., Li, J., Lyu-Bu, A. G. A., Wang, T., et al. (2021) · Food & Function · doi:10.1039/d1fo02208c · Cited by 36

Panax notoginseng saponins alleviate damage to the intestinal barrier and regulate levels of intestinal microbes in a rat model of chronic kidney disease

Xie, J., Ma, X., Zheng, Y., Mao, N., Ren, S., & Fan, J. (2022) · Renal Failure · doi:10.1080/0886022x.2022.2143378 · Cited by 35

Fecal transplantation: digestive and extradigestive clinical applications

Filip, M., Tzaneva, V., & Dumitrascu, D. L. (2017) · Medicine and Pharmacy Reports · doi:10.15386/cjmed-946 · Cited by 35

Role of Probiotics in Diabetes: A Review of Their Rationale and Efficacy

Shah, N. J., & Swami, O. C. (2017) · EMJ Diabetes · doi:10.33590/emjdiabet/10310327 · Cited by 34

Biofilms associated with poultry processing equipment.

Lindsay, D., Geornaras, I., & von Holy, A. (1996) · PubMed · Cited by 34

Beneficial effect and mechanism of natural resourced polysaccharides on regulating bone metabolism through intestinal flora: A review

Zhou, Y., Sheng, Y. J., Li, C. Y., Zou, L., Tong, C. Y., Zhang, Y., Cao, G., & Shou, D. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127428 · Cited by 34

Gut microbiota influences the efficiency of immune checkpoint inhibitors by modulating the immune system (Review)

Jiang, H., & Zhang, Q. (2024) · Oncology Letters · doi:10.3892/ol.2024.14221 · Cited by 34

Association of dietary live microbe intake with frailty in US adults: evidence from NHANES

Huo, X., Jia, S., Sun, L., Yao, Y., Liao, H., & Chen, X. (2024) · The journal of nutrition health & aging · doi:10.1016/j.jnha.2024.100171 · Cited by 33

Unveiling the gut-eye axis: how microbial metabolites influence ocular health and disease

Nguyen, Y., Manis, J. R. Z., Ronczkowski, N. M., Bui, T., Oxenrider, A., Jadeja, R. N., & Thounaojam, M. C. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1377186 · Cited by 33

The effects of gut microbiota on metabolic outcomes in pregnant women and their offspring

Lv, Y., Yan, Z., Zhao, X. Y., Gang, X., He, G., Sun, L., Li, Z., & Wang, G. (2018) · Food & Function · doi:10.1039/c8fo00601f · Cited by 36

Response of the gut microbiome of Megalobrama amblycephala to crowding stress

Du, F., Li, Y., Tang, Y., Su, S., Yu, J., Yu, F. D., Li, J., Li, H., Wang, M., & Xu, P. (2018) · Aquaculture · doi:10.1016/j.aquaculture.2018.10.067 · Cited by 33

Intestinal Microbiota in Common Chronic Inflammatory Disorders Affecting Children

Torun, A., Hupalowska, A., Trzonkowski, P., Kierkuś, J., & Pyrzyńska, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.642166 · Cited by 40

Impact of Fat Intake on Blood Glucose Control and Cardiovascular Risk Factors in Children and Adolescents with Type 1 Diabetes

Garonzi, C., Forsander, G., & Maffeis, C. (2021) · Nutrients · doi:10.3390/nu13082625 · Cited by 35

Microbiome and Gestational Diabetes: Interactions with Pregnancy Outcome and Long-Term Infant Health

Neri, C., Serafino, E., Morlando, M., & Familiari, A. (2021) · Journal of Diabetes Research · doi:10.1155/2021/9994734 · Cited by 37

Exposed to Sulfamethoxazole induced hepatic lipid metabolism disorder and intestinal microbiota changes on zebrafish (Danio rerio)

Zheng, Y., Wang, Y., Zheng, M., Wang, G., & Zhao, H. (2021) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2021.109245 · Cited by 33

Altered gut microbiota patterns in COVID-19: Markers for inflammation and disease severity

Chakraborty, C., Sharma, A. R., Bhattacharya, M., Dhama, K., & Lee, S. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i25.2802 · Cited by 35

N-3 Polyunsaturated Fatty Acids and Gut Microbiota

Lim, S., & Jayapala, H. P. S. (2022) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207325666220701121025 · Cited by 36

Modulation of Gut Microbiota by Essential Oils and Inorganic Nanoparticles: Impact in Nutrition and Health

Lazăr, V., Holban, A. M., Curuțiu, C., & Diţu, L.-M. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.920413 · Cited by 37

Gut microbiota interactions with anti-diabetic medications and pathogenesis of type 2 diabetes mellitus

Kant, R., Chandra, L., Verma, V. K., Nain, P., Bello, D., Patel, S., Ala, S., Chandra, R., & Antony, M. A. (2022) · World Journal of Methodology · doi:10.5662/wjm.v12.i4.246 · Cited by 37

Antibiotic-induced dysbiosis of gut microbiota impairs corneal development in postnatal mice by affecting CCR2 negative macrophage distribution

Wu, M., Liu, J., Li, F., Huang, S., He, J., Xue, Y., Fu, T., Feng, S., & Li, Z. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0193-x · Cited by 32

Prevalent Human Gut Bacteria Hydrolyse and Metabolise Important Food-Derived Mycotoxins and Masked Mycotoxins

Daud, N., Currie, V., Duncan, G., Farquharson, F. M., Yoshinari, T., Louis, P., & Gratz, S. W. (2020) · Toxins · doi:10.3390/toxins12100654 · Cited by 33

Modulation of the Intestinal Barrier Integrity and Repair by Microbiota Extracellular Vesicles through the Differential Regulation of Trefoil Factor 3 in LS174T Goblet Cells

Olivo-Martínez, Y., Bosch, M., Badía, J., & Baldomà, L. (2023) · Nutrients · doi:10.3390/nu15112437 · Cited by 33

Indole-3-acetamide from gut microbiota activated hepatic AhR and mediated the remission effect of Lactiplantibacillus plantarum P101 on alcoholic liver injury in mice

Wang, M., Feng, X., Zhao, Y., Lan, Y., & Xu, H. (2023) · Food & Function · doi:10.1039/d3fo03585a · Cited by 35

Gut-spine axis: a possible correlation between gut microbiota and spinal degenerative diseases

Morimoto, T., Kobayashi, T., Kakiuchi, T., Esaki, M., Tsukamoto, M., Yoshihara, T., Hirata, H., Yabuki, S., & Mawatari, M. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1290858 · Cited by 32

In Vitro Models for Investigating Intestinal Host–Pathogen Interactions

McCoy, R. S. A., Oldroyd, S., Yang, W., Wang, K., Hoven, D., Bulmer, D. C., Zilbauer, M., & Owens, R. M. (2023) · Advanced Science · doi:10.1002/advs.202306727 · Cited by 34

Gut microbiome in alcohol use disorder: Implications for health outcomes and therapeutic strategies-a literature review

Koutromanos, I., Legaki, E., Gazouli, M., Vasilopoulos, E., Kouzoupis, A. V., & Tzavellas, E. (2024) · World Journal of Methodology · doi:10.5662/wjm.v14.i1.88519 · Cited by 35

Antioxidant Role of Probiotics in Inflammation-Induced Colorectal Cancer

Hamamah, S., Lobiuc, A., & Covașă, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25169026 · Cited by 33

Intestinal Microbiota Dysbiosis Role and Bacterial Translocation as a Factor for Septic Risk

Charitos, I. A., Scacco, S., Cotoia, A., Castellaneta, F., Castellana, G., Pasqualotto, F., Venneri, M. G., Ferrulli, A., Aliani, M., Santacroce, L., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26052028 · Cited by 36

IUPHAR review: Microbiota-gut-brain axis and its role in neuropsychiatric disorders

Lee, S.-H., Han, C., & Shin, C. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107749 · Cited by 38

Applying fecal microbiota transplantation (FMT) to treat recurrent Clostridium difficile infections (rCDI) in children

Fareed, S., Sarode, N., Stewart, F. J., Malik, A., Laghaie, E., Khizer, S., Yan, F., Pratte, Z. A., Lewis, J. D., & Immergluck, L. C. (2018) · PeerJ · doi:10.7717/peerj.4663 · Cited by 32

In Vitro Evaluation of Apoptotic Induction of Butyric Acid Derivatives in Colorectal Carcinoma Cells

PATTAYIL, L., & BALAKRISHNAN-SARASWATHI, H.-T. (2019) · Anticancer Research · doi:10.21873/anticanres.13528 · Cited by 32

Transcriptomic microRNA Profiling of Dendritic Cells in Response to Gut Microbiota-Secreted Vesicles

Díaz‐Garrido, N., Bonnin, S., Riera, M., Gíménez, R., Badı́a, J., & Baldomà, L. (2020) · Cells · doi:10.3390/cells9061534 · Cited by 33

Gastrointestinal stress as innate defence against microbial attack

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