Glycan Foraging in Vivo by an Intestine-Adapted Bacterial Symbiont

The gut microbiota as an environmental factor that regulates fat storage

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Biodiversity and ecosystem productivity in a fluctuating environment: The insurance hypothesis

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MICROBIAL ECOLOGY OF THE GASTROINTESTINAL TRACT

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Molecular Analysis of Commensal Host-Microbial Relationships in the Intestine

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H OW H OST -M ICROBIAL I NTERACTIONS S HAPE THE N UTRIENT E NVIRONMENT OF THE M AMMALIAN I NTESTINE

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A Genomic View of the Human- Bacteroides thetaiotaomicron Symbiosis

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Human Fecal Flora: The Normal Flora of 20 Japanese-Hawaiians

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Honor thy symbionts

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A Model of Host-Microbial Interactions in an Open Mammalian Ecosystem

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Carbon nutrition of Escherichia coli in the mouse intestine

Chang, D., Smalley, D. J., Tucker, D. L., Leatham, M. P., Norris, W. E., Stevenson, S. J., Anderson, A. B., Grissom, J. E., Laux, D. C., Cohen, P. S., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307888101 · Cited by 513

Dynamics in gut microbiota diversity, composition, and assembly reveal the adaptability of invasive snail Pomacea canaliculata during hibernation in rice fields

Yao, F., Li, C., Chen, Y., Zhang, J., Shi, Z., & Qin, Z. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1616681 · Cited by 5

Identification of strain-specific cues that regulate biofilm formation in Bacteroides thetaiotaomicron

Glowacki, R. W. P., Engelhart, M. J., Till, J. M., Kadam, A., Nemet, I., Sangwan, N., & Ahern, P. P. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.03419-24 · Cited by 5

From gut dysbiosis to eubiosis: understanding microbiome recovery as an ecological process

Kennedy, M. S., & Chang, E. B. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2649448 · Cited by 5

Functional Genomic Examinations Of Interactions Between Common Members Of The Human Gut Microbiota

Mahowald, M. A. (2010) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7fn1470 · Cited by 5

Variation in spatial organization of the gut microbiota along the longitudinal and transverse axes of the intestines

Fox, E. A., & Lyte, M. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-02952-4 · Cited by 5

Depletion of essential mycobacterial gene glmM reduces pathogen survival and induces host-protective immune responses against tuberculosis

Agarwal, M., Bhaskar, A., Singha, B., Mukhopadhyay, S., Pahuja, I., Singh, A., Chaturvedi, S., Agarwal, N., Dwivedi, V. P., & Nandicoori, V. K. (2024) · Communications Biology · doi:10.1038/s42003-024-06620-9 · Cited by 5

Oat bran fiber protects against radiation-induced disruption of gut barrier dynamics and mucosal damage

Patel, P., Jin, C., Nookaew, I., Robeson, M. S., Malipatlolla, D. K., Devarakonda, S., Rascón, A., NYMAN, M. E., Karlsson, N. G., Wold, A. E., et al. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00759-x · Cited by 5

Comparative analysis of the fecal microbiome and metabolomics of healthy versus captive South China tigers with mild diarrhea

Yuan, Y., Wu, H., & Pan, H. (2022) · Canadian Journal of Microbiology · doi:10.1139/cjm-2022-0115 · Cited by 5

Fucosylated TLR4 mediates communication between mutualist fucotrophic microbiota and mammalian gut mucosa

Nanthakumar, N. N., Meng, D., & Newburg, D. S. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1070734 · Cited by 5

Differences in Faecal Microbiome Taxonomy, Diversity and Functional Potential in a Bovine Cohort Experimentally Challenged with Mycobacterium avium subsp. paratuberculosis (MAP)

Matthews, C., Walsh, A. M., Gordon, S. V., Markey, B. K., Cotter, P. D., & Mahony, J. O. (2023) · Animals · doi:10.3390/ani13101652 · Cited by 5

Microbial gene expression during hibernation in arctic ground squirrels: greater differences across gut sections than in response to pre-hibernation dietary protein content

Grond, K., Buck, C. L., & Duddleston, K. N. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1210143 · Cited by 5

Moniezia benedeni drives CD3+ T cells residence in the sheep intestinal mucosal effector sites

Chai, W., Yao, W., Pan, J., Huang, Z., Wang, B., Xu, B., Fan, X., He, W., Wang, W., & Zhang, W. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1342169 · Cited by 5

QM/MM investigation on the catalytic mechanism of Bacteroides thetaiotaomicron α-glucosidase BtGH97a

Wang, J., Sheng, X., Zhao, Y. D., Liu, Y., & Liu, C. (2012) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2012.03.005 · Cited by 5

Nutrition and Immunity

Kussmann, M. (2010) · Royal Society of Chemistry eBooks · doi:10.1039/9781849730921-00268 · Cited by 5

Causality in Biological Transmission: Forces and Energies

Baquero, F. (2018) · Microbiology Spectrum · doi:10.1128/microbiolspec.mtbp-0018-2016 · Cited by 5

Alteration of Intestinal Microbiome of Clostridioides difficile-Infected Hamsters during the Treatment with Specific Cow Antibodies

Heidebrecht, H.-J., Lagkouvardos, I., Reitmeier, S., Hengst, C., Kulozik, U., & Pfaffl, M. W. (2021) · Antibiotics · doi:10.3390/antibiotics10060724 · Cited by 5

Functional foods for health promotion: microbes and health Extended abstracts from the 11th Annual Conference on Functional Foods for Health Promotion, April 2008

Walker, W. A., Martens, E. C., Sherman, P. M., Lampe, J. W., Hullar, M. A. J., & Wu, C. D. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2008.00135.x · Cited by 5

Recovery of the Gut Microbiota after Antibiotics Depends on Host Diet and Environmental ReservoirsPreprint

Ng, K. M., Aranda-Díaz, A., Tropini, C., Frankel, M. R., Treuren, W. V., O’Laughlin, C., Merrill, B. D., Yu, F. B., Pruss, K. M., Oliveira, R. A., et al. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3325029 · Cited by 5

Tetracycline Antibiotics Induce Biosynthesis of Pro-Inflammatory Metabolites in the Immunobiotic Bacteroides dorei

Han, E. J., Ganley, J. G., Winner, C. B., An, J. S., & Seyedsayamdost, M. R. (2025) · ACS Central Science · doi:10.1021/acscentsci.5c00969 · Cited by 4

Immunology and treatments of fatty liver disease

Tang, S., Wu, S., Zhang, W., Ma, L., Zuo, L., & Wang, H. (2024) · Archives of Toxicology · doi:10.1007/s00204-024-03920-1 · Cited by 6

Proteomics of Bacterial and Mouse Extracellular Vesicles Released in the Gastrointestinal Tracts of Nutrient-Stressed Animals Reveals an Interplay Between Microbial Serine Proteases and Mammalian Serine Protease Inhibitors

Stentz, R., Jones, E. J., Gul, L., Latousakis, D., Parker, A., Brion, A., Goldson, A. J., Gotts, K., & Carding, S. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094080 · Cited by 5

Carbohydrates and the oxidative branch of the pentose phosphate pathway modify Bacteroides thetaiotaomicron phage resistance by phase-variable S-layers

Fuentes, J. J., Singh, S., Pudlo, N. A., Heaver, S. L., Ley, R. E., & Martens, E. C. (2025) · Journal of Bacteriology · doi:10.1128/jb.00178-25 · Cited by 4

When guests turn hostile

Ley, R. E. (2013) · Nature · doi:10.1038/494437a · Cited by 4

Gut Microbiota, Obesity and Metabolic Dysfunction

Meiliana, A., & Wijaya, A. (2011) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v3i3.147 · Cited by 4

Impact of Microplastics in Human Health

Fournier, E., Etienne‐Mesmin, L., Blanquet‐Diot, S., & Mercier‐Bonin, M. (2022) · Springer eBooks · doi:10.1007/978-3-030-39041-9_48 · Cited by 4

Transcriptional Profiling of the Small Intestine and the Colon Reveals Modulation of Gut Infection with Citrobacter rodentium According to the Vitamin A Status

Chai, Z., Lyu, Y., Chen, Q., Wei, C., Snyder, L. M., Weaver, V. C., Sebastian, A., Albert, I. U., Li, Q., Cantorna, M. T., et al. (2022) · Nutrients · doi:10.3390/nu14081563 · Cited by 4

Interactions of Pathogenic Escherichia coli with Gut Microbiota

Miliwebsky, E. S., Jure, M. Á., Farfán, M. J., & Palermo, M. S. (2023) · Springer eBooks · doi:10.1007/978-3-031-29882-0_12 · Cited by 4

Intestinal Microbiome in Health and Disease: Introduction

Haller, D. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_1 · Cited by 6

Enteric Pathogens Exploit the Microbiota-generated Nutritional Environment of the Gut

Pacheco, A. R., & Sperandio, V. (2015) · ASM Press eBooks · doi:10.1128/9781555818883.ch13 · Cited by 4

Structure and Properties of Mucins

Berry, M., & Corfield, A. P. (2014) · Wiley eBooks · doi:10.1002/9781118794203.ch06 · Cited by 4

Investigating the Potential of Plant-derived Antimicrobials and Probiotic Bacteria for Controlling Listeria monocytogenes

Upadhyay, A. (2014) · OpenCommons at University of Connecticut (University of Connecticut) · Cited by 4

Diet Leaves a Genetic Signature in a Keystone Member of the Gut MicrobiotaPreprint

Đapa, T., Pedro, M. F., Ramiro, R. S., Gordo, I., & Xavier, K. B. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3907580 · Cited by 4

Transcription Factor‐Based Biosensors and Their Application in Microbiome Engineering

Kim, S. K., Woo, S. G., Kim, T. H., Park, S. H., Lee, J. J., Park, A.-H., Oh, S. H., Bak, S. K., Lee, S., & Lee, D. (2022) · Wiley eBooks · doi:10.1002/9783527825462.ch10 · Cited by 4

The Adaptive Alternation of Intestinal Microbiota and Regulation of Host Genes Jointly Promote Pigs to Digest Appropriate High-Fiber Diets

Zhang, Y., Li, H., Li, B., He, J., Chen, P., Xie, Y., Huang, G., Zhao, P., & Wang, Z. (2024) · Animals · doi:10.3390/ani14142076 · Cited by 3

Comparison of microbiota in different intestinal regions between hibernating and active Daurian ground squirrels

Zheng, Y.-H., Lin, X. K., Pan, X. Y., Ma, X. M., Ju, X., & Wang, J. (2025) · The European Zoological Journal · doi:10.1080/24750263.2025.2583787 · Cited by 3

Bacterial constipation: Mucin-degrading intestinal commensal bacteria cause constipation

Hamaguchi, T., Gibo, N., Ohara, M., Ito, M., Ogura, T., Takeda, J.-I., Nishiwaki, H., Zhao, F., Kinoshita-Daitoku, R., Hattori, M., et al. (2026) · Gut Microbes · doi:10.1080/19490976.2025.2596809 · Cited by 3

Pollen Polysaccharides Drive the Strain‐Level Assembly and Competitive Dynamics of Bifidobacterium in the Honeybee Gut

Li, Y., Ye, F., Wu, J., Meng, Y., Lang, H., Meng, S., Li, F., Wang, X., Zhang, X., Zheng, H., et al. (2026) · Integrative Zoology · doi:10.1111/1749-4877.70147 · Cited by 3

Genome sequence and annotation of Bacteroides sp aff. Thetaiotaomicron strain isolated from blood

Wu, Z. C., Wu, L., Zhang, M., & Zhou, W. (2021) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2021.104816 · Cited by 3

Seasonal changes in gut microbiota of sea cucumber over natural aestivation cycle

Zhao, Y., Wang, H., Wang, H., Zhang, L., Sun, H., & Zhang, Y. (2024) · Journal of Oceanology and Limnology · doi:10.1007/s00343-023-3077-6 · Cited by 3

A commensal bacterium secretes effector proteins to establish population heterogeneity in the gut

Zagieboylo, A. P., Mo, R., Lim, B., & Goodman, A. L. (2025) · Cell Host & Microbe · doi:10.1016/j.chom.2025.11.009 · Cited by 3

MCSPACE: inferring microbiome spatiotemporal dynamics from high-throughput co-localization data

Uppal, G., Urtecho, G., Richardson, M., Comba, I. Y., Lee, J., Moody, T. U., Wang, H. H., & Gerber, G. K. (2025) · Microbiome · doi:10.1186/s40168-025-02279-4 · Cited by 3

Secretory Defense Response in the Bird’s Gastro-Intestinal Tract and Nutritional Strategies to Modulate It

Gómez-Osorio, L.-M., Jiang, Z., Zhang, Q., Yan, H., Villegas, A.-M., & Applegate, T. J. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95952 · Cited by 3

Impact of Microplastics in Human Health

Fournier, E., Etienne‐Mesmin, L., Blanquet‐Diot, S., & Mercier‐Bonin, M. (2021) · Springer eBooks · doi:10.1007/978-3-030-10618-8_48-1 · Cited by 4

Causality in Biological Transmission: Forces and Energies

Baquero, F. (2019) · ASM Press eBooks · doi:10.1128/9781555819743.ch2 · Cited by 3

Analysis of the galactomannan binding ability of β-mannosidases, BtMan2A and CmMan5A, regarding their activity and synergism with a β-mannanase

Malgas, S., Thoresen, M., Moses, V., Prinsloo, E., van Dyk, J. S., & Pletschke, B. I. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.06.038 · Cited by 3

Role of mushroom polysaccharides in improving gut health and associated diseases

Yadav, D., & Negi, P. S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822238-6.00013-3 · Cited by 3

Metabolism of Dietary Substrates by Intestinal Bacteria and Consequences for the Host Intestine

Blachier, F. (2023) · Springer eBooks · doi:10.1007/978-3-031-26322-4_3 · Cited by 4

Evaluating Gut Microbiota Modification as a Next-Generation Therapy for Obesity and Diabetes

Hossain, M. I., Akash, S. R., Faruk, M. O., Mimi, S. I., Chowdhury, I. H., Islam, M. S., Alam, M. M., & Ali, M. S. (2023) · Current Diabetes Reviews · doi:10.2174/1573399820666230515115307 · Cited by 7

Validation of collection and anaerobic fermentation techniques for measuring prebiotic impact on gut microbiota

Thorman, A. W., Morrow, A. L., Groeneveld, A., Nauta, A., & Newburg, D. S. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107169 · Cited by 3

Characterization of the response of Escherichia coli to l ‐fucose in bacterial swimming motility

Li, J., Chen, J., Wang, L., Lin, Y., Zhang, X., Liu, J., & Wang, F. (2022) · Journal of Basic Microbiology · doi:10.1002/jobm.202200054 · Cited by 3

Non-redundant functionality of Lactiplantibacillus plantarum phospho-β-glucosidases revealed by carbohydrate utilization signatures associated to pbg2 and pbg4 gene mutants

Plaza‐Vinuesa, L., Sánchez-Arroyo, A., de Felipe, F. L., Rivas, B. D. L., & Múñoz, R. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxad077 · Cited by 3

Gut microbial ecology

Flint, H. J., Duncan, S. H., & Louis, P. (2009) · Elsevier eBooks · doi:10.1533/9781845696603.1.38 · Cited by 4

Draft Genome Sequence of Bacteroides faecis MAJ27T, a Strain Isolated from Human Feces

Kim, M., Whon, T. W., Roh, S. W., Shin, N.-R., & Bae, J. (2011) · Journal of Bacteriology · doi:10.1128/jb.06210-11 · Cited by 3

Microbiota: Current Research and Emerging Trends

Salazar, N., González Solares, S., Nogacka, A., Rios-Covián, D., Arboleya, S., Fernández, M. G., & González de los Reyes-Gavilán, C. (2018) · Caister Academic Press eBooks · doi:10.21775/9781910190937 · Cited by 3

The MUC2 mucin -A network in the intestinal protective mucus

Johansson, M. (2009) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 3

the role of soluble and insoluble fibers during fermentation of Chicory root pulp

Ramasamy, U. S. (2014) · doi:10.18174/303260 · Cited by 3

Microbiome Management for the 21st Century and Beyond

Hryckowian, A. J. (2021) · mSystems · doi:10.1128/msystems.00760-21 · Cited by 3

The Microbiome, Metabolism, and Networks in Precision Nutrition

Mensah, G. E., Maseng, M. G., Allard, S., & Gilbert, J. A. (2024) · Precision Nutrition · doi:10.1016/b978-0-443-15315-0.00011-0 · Cited by 2

Gut microbiota in professional and amateur athletes: the impact of physical activity on microbiota - what do we know? A literature review

Szopa, S., & Szymonik, J. (2024) · Quality in Sport · doi:10.12775/qs.2023.15.002 · Cited by 2

Microbiota and B-1 B cell repertoire development in mice

New, J. S., King, R. G., Foote, J. B., & Kearney, J. F. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102452 · Cited by 2

Metaproteomics-based stable isotope fingerprinting links intestinal bacteria to their carbon source and captures diet-induced substrate switching

Mordant, A. L., Blakeley‐Ruiz, J. A., & Kleiner, M. (2025) · The ISME Journal · doi:10.1093/ismejo/wraf127 · Cited by 2

Gut Microbiome Genes Involved in Plant and Mucin Breakdown Correlate with Diet and Gastrointestinal Inflammation in Healthy United States Adults

Blecksmith, S. E., Oliver, A. S., Alkan, Z., & Lemay, D. G. (2025) · Journal of Nutrition · doi:10.1016/j.tjnut.2025.08.027 · Cited by 2

Structural and evolutionary constraints shape adaptive landscapes of immune-related genes across mammalian phylogeny

Li, Z., Hassan, M., Ahmad, H. I., Ashraf, M. A., Asif, A. R., Qadeer, I., Shahzad, A. H., Abbas, S., Sajid, M., Mateen, A., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0332734 · Cited by 2

Effects of dietary N-carbamylglutamate (NCG) supplementation on arginine biosynthesis, metabolism, digestion and mTOR signaling pathway gene expression in Eriocheir sinensis

Liu, Z., Sun, J., Shi, A., Weng, C., Xiang, A., Hou, M., Zhao, M., Chen, Z., Cheng, Y., & Yang, X. (2025) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2025.111178 · Cited by 2

An electron transport complex required in the gut sensitizes Bacteroides to a pore-forming type VI secretion toxin

Ratner, H. K., Duong, B. D., Miao, P., Bertolli, S. K., Shen, B. A., Mitchell, U., Gallagher, L. A., Radey, M. C., Peterson, S. B., & Mougous, J. D. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2523503122 · Cited by 2

Genetic toolbox development for engineering Bacteroides and other bacterial species

Yeh, Y.-H., & Sirk, S. J. (2026) · Current Opinion in Microbiology · doi:10.1016/j.mib.2026.102709 · Cited by 4

Engineered commensal Bacteroides thetaiotaomicron enables targeted drug delivery to colorectal tumors

Jia, X., Xu, Y., Liu, X., Ye, M., Wang, F., Yang, X., Gao, X., Yu, J., & Liu, W. (2026) · Journal of Controlled Release · doi:10.1016/j.jconrel.2026.114945 · Cited by 2

Changes of Colon Flora and Antitoxic Effect Induced by Zearalenone in Mice

Zhang, J., Wang, X., Zhao, Y., Jin, Y., Zhou, Y., Wang, J., Fu, Y., Wang, R., Li, R., Fang, H., et al. (2020) · Pakistan Journal of Zoology · doi:10.17582/journal.pjz/20190115060153 · Cited by 2

How Gut Micro-organisms Make Use of Available Carbohydrates

Flint, H. J. (2020) · Fascinating life sciences · doi:10.1007/978-3-030-43246-1_7 · Cited by 2

Farmen i tarmen DEL 1 AV 2

Bøhn, S. K. (2017) · Norsk tidsskrift for ernæring · doi:10.18261/ntfe.15.1.3 · Cited by 2

Association of calcium supplementation with fat excretion, changes in body weight, and gut enterobacteriales in obese, and non-obese mice

Ripon, M. A. R., Rahman, R., Amin, M. T., AHMED, F., & Hossain, M. S. (2023) · Journal of Research in Pharmacy · doi:10.29228/jrp.317 · Cited by 2

Fate, uptake and gut toxicity of two colloidal silver products in mice: how micro X-ray fluorescence, micro X-ray absorption spectroscopy and near-infrared spectroscopy provide new insights in food nanotoxicology

Gillois, K., Rivard, C., Levasseur‐Garcia, C., Bézirard, V., Terrisse, H., Leonard, R., Masselot, C. R., Maguin, E., Richard, M. L., Théodorou, V., et al. (2023) · Environmental Science Nano · doi:10.1039/d2en01135b · Cited by 2

Metagenome-derived SusD-homologs affiliated with Bacteroidota bind to synthetic polymers

Silvério, M. P., Neumann, T., Schaubruch, K., Heermann, R., Pérez-García, P., Chow, J., & Streit, W. R. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.00933-24 · Cited by 2

Hologenomics: The Interaction Between Host, Microbiome and Diet

Marsh, A. J., & Azcárate-Peril, M. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-08-100596-5.22701-7 · Cited by 2

A novel mutant with triple the dietary fiber content in white rice

Nishimura, M., Kobayashi, A., Morita, R., Idesawa, Y., Sakuma, Y., Otosaka, I., & Tomita, K. (2021) · Ikushugaku zasshi · doi:10.1270/jsbbs.20140 · Cited by 2

Single-molecule dynamics of surface lipoproteins in bacteroides indicate similarities and cooperativity

Geffroy, L., Brown, H. A., DeVeaux, A. L., Koropatkin, N. M., & Biteen, J. S. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.10.024 · Cited by 2

Mechanisms of Probiotic Regulation of Host Homeostasis

Yan, F., & Polk, D. B. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-289-6_5 · Cited by 2

The Influence of Diet on the Mammalian Gut Microbiome

Muegge, B. D. (2013) · PubMed · doi:10.7936/k7gf0rhw · Cited by 2

Iron as Nutrient: Strategies for Iron Acquisition and Usage by Pathogenic Microorganisms

Massé, É., & Pawelek, P. D. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-462-9_4 · Cited by 2

The Gut Microbiome: Current Understanding and Future Perspectives

Yu, Z., & Morrison, M. (2014) · ASM Press eBooks · doi:10.1128/9781555815479.ch2 · Cited by 2

The Microbiota: A New Player in the Etiology of Colorectal Cancer

Levy, M., Thaiss, C. A., & Elinav, E. (2013) · Current Colorectal Cancer Reports · doi:10.1007/s11888-013-0196-z · Cited by 3

Influence of the Gut Microbiota with Ageing

Murphy, E., Murphy, C., & O’Mahony, L. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-327-1_8 · Cited by 2

Intestinales Mikrobiom

Blaut, M. (2016) · Der Diabetologe · doi:10.1007/s11428-016-0129-y · Cited by 2

Knowledge, Attitudes and Practices of the Health Personnel of the Pediatric and Gynecology-Obstetrics Departments of the Bouaké University Hospital Center (CHU) regarding the Intestinal Microbiota and the First 1000 Days of Life

Azagoh-Kouadio, R., Christian, Y. K., Hélène, A.-T. K. A., Christelle, S.-A., Roland, Y. K., Sahi, G. J. L., Romeo, A. L., Iburaima, A., Alexise, A., & Vincent, A. K. (2021) · Open Journal of Pediatrics · doi:10.4236/ojped.2021.111003 · Cited by 2

Impact of different shades of light-emitting diode on fecal microbiota and gut health in broiler chickens

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Prebiotics, Probiotics, and Synbiotics

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