Stressor Exposure Disrupts Commensal Microbial Populations in the Intestines and Leads to Increased Colonization by Citrobacter rodentium

A core gut microbiome in obese and lean twins

Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823

The Ribosomal Database Project: improved alignments and new tools for rRNA analysis

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Metagenomic Analysis of the Human Distal Gut Microbiome

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The gut flora as a forgotten organ

O'Hara, A. M., & Shanahan, F. (2006) · The EMBO Reports · doi:10.1038/sj.embor.7400731 · Cited by 2,791

Early, postnatal experience alters hypothalamic corticotropin-releasing factor (CRF) mRNA, median eminence CRF content and stress-induced release in adult rats

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Host-Mediated Inflammation Disrupts the Intestinal Microbiota and Promotes the Overgrowth of Enterobacteriaceae

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Evaluation of the bacterial diversity in the feces of cattle using 16S rDNA bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP)

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The Fecal Microbiota of Irritable Bowel Syndrome Patients Differs Significantly From That of Healthy Subjects

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Colonization resistance of the digestive tract in conventional and antibiotic-treated mice

van der Waaij, D., Vries, J. M. B.-D., & der Wees, J. E. C. L.-V. (1971) · Journal of Hygiene · doi:10.1017/s0022172400021653 · Cited by 907

Reproducible Community Dynamics of the Gastrointestinal Microbiota following Antibiotic Perturbation

Antonopoulos, D. A., Huse, S. M., Morrison, H. G., Schmidt, T. M., Sogin, M. L., & Young, V. B. (2009) · Infection and Immunity · doi:10.1128/iai.01520-08 · Cited by 564

Supplementary Materials and Methods

Groenendijk, F. H., Zwart, W. T., Floore, A. N., Akbari, S., & Bernards, R. (2013) · Cited by 22

Analysis of microbiota in stable patients with chronic obstructive pulmonary disease

Aguirre, E., Galiana, A., Mira, Á., Guardiola, R., Sánchez-Guillén, L., García-Pachón, E., Santibáñez, M., Royo, G., & Rodrı́guez, J. C. (2015) · Apmis · doi:10.1111/apm.12363 · Cited by 21

Campylobacter concisus and exotoxin 9 levels in paediatric patients with Crohn’s disease and their association with the intestinal microbiota

Kaakoush, N. O., Castaño‐Rodríguez, N., Day, A. S., Lemberg, D. A., Leach, S. T., & Mitchell, H. M. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.067231-0 · Cited by 21

Chronic restraint stress induced changes in colonic homeostasis-related indexes and tryptophan-kynurenine metabolism in rats

Li, C., Gan, L., Tan, Y. Y., Yan, M., Liu, X., Chang, Q., & Pan, R. (2021) · Journal of Proteomics · doi:10.1016/j.jprot.2021.104190 · Cited by 22

The roles of hormones in the modulation of growth and virulence genes’ expressions in UPEC strains

Gümüş, D., Yüksek, F. K., Sefer, Ö., Yörük, E., Uz, G., & Küçüker, M. A. (2019) · Microbial Pathogenesis · doi:10.1016/j.micpath.2019.05.019 · Cited by 19

Relationship between psychosocial stress-induced prefrontal cortex activity and gut microbiota in healthy participants-a functional near-infrared spectroscopy study

Yamaoka, K., Uotsu, N., & Hoshino, E. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100479 · Cited by 18

Disturbance in the mucosa-associated commensal bacteria is associated with the exacerbation of chronic colitis by repeated psychological stress; is that the new target of probiotics

Arase, S., Watanabe, Y., Setoyama, H., Nagaoka, N., Kawai, M., & Matsumoto, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160736 · Cited by 18

Impact of a Model Used to Simulate Chronic Socio-Environmental Stressors Encountered during Spaceflight on Murine Intestinal Microbiota

Alauzet, C., Cunat, L., Wack, M., Lanfumey, L., Legrand-Frossi, C., Lozniewski, A., Agrinier, N., Cailliez‐Grimal, C., & Frippiat, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217863 · Cited by 19

Individual Nutrition Is Associated with Altered Gut Microbiome Composition for Adults with Food Insecurity

Bixby, M., Gennings, C., Malecki, K. M. C., Sethi, A. K., Safdar, N., Peppard, P. E., & Eggers, S. I. (2022) · Nutrients · doi:10.3390/nu14163407 · Cited by 20

Concurrent psychological stress and infectious colitis is key to sustaining enhanced peripheral sensory signaling

Spreadbury, I., Ochoa‐Cortés, F., Ibeakanma, C. O., Martin, N., Hurlbut, D. J., & Vanner, S. J. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12497 · Cited by 20

MEAT SCIENCE AND MUSCLE BIOLOGY SYMPOSIUM: Ecological and dietary impactors of foodborne pathogens and methods to reduce fecal shedding in cattle1,2

Callaway, T. R., Edrington, T. S., & Nisbet, D. J. (2014) · Journal of Animal Science · doi:10.2527/jas.2013-7308 · Cited by 18

Context‐dependent effects of glucocorticoids on the lizard gut microbiome

MacLeod, K. J., Kohl, K. D., Trevelline, B. K., & Langkilde, T. L. (2021) · Molecular Ecology · doi:10.1111/mec.16229 · Cited by 16

Supplementation of Diets With Bovine Colostrum Influences Immune and Gut Function in Kittens

Gore, A. M., Satyaraj, E., Labuda, J., Engler, R., Sun, P., Kerr, W. W., & Conboy-Schmidt, L. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.675712 · Cited by 19

Microbial Endocrinology

Sharaff, F., & Freestone, P. P. E. (2011) · Open Life Sciences · doi:10.2478/s11535-011-0067-z · Cited by 17

The role of gut microbiota in the treatment of irritable bowel syndrome

Leylabadlo, H. E., Heravi, F. S., Soltani, E., Abbasi, A., Kafil, H. S., Parsaei, M., Sanaie, S., Ahmadian, Z., & Ghotaslou, R. (2021) · Reviews in Medical Microbiology · doi:10.1097/mrm.0000000000000284 · Cited by 16

Social Isolation and Breast Cancer

Hilakivi-Clarke, L. A., & Andrade, F. D. O. (2023) · Endocrinology · doi:10.1210/endocr/bqad126 · Cited by 22

Homeostasis alteration within small intestinal mucosa after acute enteral refeeding in total parenteral nutrition mouse model

Feng, Y., Barrett, M., Hou, Y., Yoon, H. K., Ochi, T., & Teitelbaum, D. H. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00335.2015 · Cited by 15

What goes around comes around: novel pharmacological targets in the gut–brain axis

González‐Arancibia, C., Escobar-Luna, J., Barrera-Bugueño, C., Díaz-Zepeda, C., González-Toro, M. P., Olavarría‐Ramírez, L., Zanelli-Massai, F., Gotteland, M., Bravo, J. A., & Julio‐Pieper, M. (2016) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x16630718 · Cited by 17

The Gut Microbiome and Metabolome of Two Riparian Communities in the Amazon

Pires, E. S., Hardoim, C. C. P., Miranda, K. R., Secco, D., Lobo, L. A., de Carvalho, D. P., Han, J., Borchers, C. H., Ferreira, R. B. R., Salles, J. F., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02003 · Cited by 17

Effects of Stress on the Mucus-microbial Interactions in the Gut

He, J., Guo, H., Zheng, W., & Yao, W. (2018) · Current Protein and Peptide Science · doi:10.2174/1389203719666180514152406 · Cited by 17

Potential improvements of the cognition of piglets through a synbiotic supplementation from 1 to 28 days via the gut microbiota

Parois, S. P., Eicher, S. D., Lindemann, S. R., & Marchant, J. N. (2021) · Scientific Reports · doi:10.1038/s41598-021-03565-5 · Cited by 17

Norepinephrine induces growth of Desulfovibrio vulgaris in an iron dependent manner

Coffman, C. N., Varga, M. G., Alcock, J., Carroll‐Portillo, A., Singh, S., Xue, X., & Lin, H. C. (2022) · Anaerobe · doi:10.1016/j.anaerobe.2022.102582 · Cited by 15

Implication of microbiota gut-brain axis in the manifestation of obsessive-compulsive disorder: Preclinical and clinical evidence

Kamble, S. R., & Dandekar, M. P. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.176014 · Cited by 16

Cecal microbiota contribute to the development of woody breast myopathy

Zhang, X., Zhang, L., Li, X., White, S., Campbell, Y. L., Abdallah-Ruiz, A., To, K. V., Zhai, W., & Schilling, M. W. (2021) · Poultry Science · doi:10.1016/j.psj.2021.101124 · Cited by 14

Severe Sepsis Facilitates Intestinal Colonization by Extended-Spectrum-β-Lactamase-Producing Klebsiella pneumoniae and Transfer of the SHV-18 Resistance Gene to Escherichia coli during Antimicrobial Treatment

Guan, J., Liu, S., Lin, Z., Li, W., Liu, X., & Chen, D. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01632-13 · Cited by 13

The Role of the Microbiome in the Relationship of Asthma and Affective Disorders

Trueba, A. F., Ritz, T., & Trueba, G. A. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-20215-0_13 · Cited by 13

Data Analysis Methodology

Edalat, F. D., & Abdi, M. R. (2017) · International series in management science/operations research/International series in operations research & management science · doi:10.1007/978-3-319-64143-0_7 · Cited by 13

Characterization of Gut Microbiota in Prenatal Cold Stress Offspring Rats by 16S rRNA Sequencing

Zheng, J., Zhu, T., Wang, L., Wang, J., & Lian, S. (2020) · Animals · doi:10.3390/ani10091619 · Cited by 13

Breathomics profiling of metabolic pathways affected by major depression: Possibilities and limitations

Gbaoui, L., Fachet, M., Lüno, M., Meyer-Lotz, G., Frodl, T., & Hoeschen, C. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.1061326 · Cited by 12

The Irritable Bowel Syndrome: How Stress Can Affect the Amygdala Activity and the Brain-Gut Axis

Bonaz, B. L., Sonia Pellissier, A., Sinniger, V., Clarençon, D., Peinnequin, A., & Canini, F. (2012) · InTech eBooks · doi:10.5772/52066 · Cited by 12

Novel methods for pathogen control in livestock pre-harvest: an update * *Mandatory Disclaimer: Proprietary or brand names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard of the product, and the use of the name by the USDA implies no approval of the product, or exclusion of others that may be suitable.

Callaway, T. R., Anderson, R. C., Edrington, T. S., Genovese, K. J., Harvey, R. B., Poole, T. L., & Nisbet, D. J. (2013) · Elsevier eBooks · doi:10.1533/9780857098740.4.275 · Cited by 12

Discrete patterns of microbiome variability across timescales in a wild rodent population

Fenn, J., Taylor, C. H., Goertz, S., Wanelik, K. M., Paterson, S., Begon, M., Jackson, J., & Bradley, J. (2023) · BMC Microbiology · doi:10.1186/s12866-023-02824-x · Cited by 11

Stressor-Induced Increases in Circulating, but Not Colonic, Cytokines Are Related to Anxiety-like Behavior and Hippocampal Inflammation in a Murine Colitis Model

Maltz, R. M., Marte-Ortiz, P., Rajasekera, T. A., Loman, B. R., Gur, T., & Bailey, M. T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042000 · Cited by 10

Stressor-Induced Reduction in Cognitive Behavior is Associated with Impaired Colonic Mucus Layer Integrity and is Dependent Upon the LPS-Binding Protein Receptor CD14

Jaggers, R. M., DiSabato, D. J., Loman, B. R., Kontic, D., Spencer, K. D., Allen, J. M., Godbout, J. P., Quan, N., Gur, T. L., & Bailey, M. T. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s332793 · Cited by 11

Diet and the Gut Microbiota – How the Gut

Tuohy, K. M., Venuti, P., Cuva, S., Furlanello, C., Gasperotti, M., Mancini, A., Ceppa, F., Cavalieri, D., Filippo, C. D., Vrhovšek, U., et al. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-407825-3.00015-0 · Cited by 10

Pediatric surgery and the human microbiome

Carlisle, E. M., & Morowitz, M. J. (2011) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2010.12.018 · Cited by 10

Bacterial communities on food court tables and cleaning equipment in a shopping mall

Dingsdag, S. A., & Coleman, N. V. (2012) · Epidemiology and Infection · doi:10.1017/s0950268812002142 · Cited by 10

Attenuated Streptococcus agalactiae WC1535 ∆Sia perturbs the gut microbiota of Oreochromis niloticus, massively colonizes the intestine, and induces intestinal mucosal immunity after intraperitoneal inoculation

Hao, J., Wang, S., Yang, J., Zhang, Q., Wu, Z., Zhang, D., & Li, A. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1036432 · Cited by 9

Anxiety-like Behavior in Female Sprague Dawley Rats Associated with Cecal Clostridiales

Bear, T., Roy, N. C., Dalziel, J. E., Butts, C. A., Coad, J., Young, W., Parkar, S. G., HEDDERLEY, D. I., Dinnan, H., Martell, S., et al. (2023) · Microorganisms · doi:10.3390/microorganisms11071773 · Cited by 9

Handling stress-induced rumianal microbiota changes reduce grass hay degradability in sheep

Yoshihara, Y., & Ogawa, Y. (2021) · Journal of Animal and Feed Sciences · doi:10.22358/jafs/135543/2021 · Cited by 9

Effects of Dietary Alfalfa Inclusion on Salmonella Typhimurium Populations in Growing Layer Chicks

Escarcha, J. F., Callaway, T. R., Byrd, J. A., Miller, D. N., Edrington, T. S., Anderson, R. C., & Nisbet, D. J. (2012) · Foodborne Pathogens and Disease · doi:10.1089/fpd.2012.1251 · Cited by 9

Validation of Fecal Glucocorticoid Metabolites as Non-Invasive Markers for Monitoring Stress in Common Buzzards (Buteo buteo)

Grundei, L.-L., Wolf, T. E., Brandes, F., Schütte, K., Freise, F., Siebert, U., Touma, C., & Pees, M. (2024) · Animals · doi:10.3390/ani14081234 · Cited by 8

Magnesium Oxide Reduces Anxiety-like Behavior in Mice by Inhibiting Sulfate-Reducing Bacteria

Coffman, C. N., Carroll‐Portillo, A., Alcock, J., Singh, S., Rumsey, K., Braun, C. A., Xue, B., & Lin, H. C. (2024) · Microorganisms · doi:10.3390/microorganisms12071429 · Cited by 9

Ornamentation and body condition, but not glucocorticoids, predict wild songbird cloacal microbiome community and diversity

Slevin, M. C., Houtz, J. L., Vitousek, M. N., Baldassarre, D. T., & Anderson, R. C. (2024) · Oikos · doi:10.1111/oik.10905 · Cited by 7

Restraint Stress Disrupted Intestinal Homeostasis via 5-HT/HTR7/Wnt/β-Catenin/NF-kB Signaling

Yu, J., Wang, Z., Chen, Y., & Dong, Y. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094021 · Cited by 8

Glutathione S-transferase (GST) and cortisol levels vs. microbiology of the digestive system of sheep during lambing

Szeligowska, N., Cholewińska, P., Smoliński, J., Wojnarowski, K., Pokorny, P., Czyż, K., & Pogoda-Sewerniak, K. (2022) · BMC Veterinary Research · doi:10.1186/s12917-022-03201-y · Cited by 8

Enteric glial cells contribute to chronic stress-induced alterations in the intestinal microbiota and barrier in rats

Lu, T., Huang, C., Weng, R., Wang, Z., Sun, H., & Ma, X. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24899 · Cited by 9

An Enterobacteriaceae Bloom in Aging Animals is Restrained by the Gut Microbiome

Shapira, M., Choi, R., Bodkhe, R., Pees, B., Kim, D., Berg, M., Monnin, D., Cho, J., Narayan, V., Deller, E., et al. (2024) · doi:10.59368/agingbio.20240024 · Cited by 8

A Possible Role of Bacterial Biofilm in the Pathogenesis of Atherosclerosis

Wolcott, R. D., Wolcott, J. J., & Palacio, C. (2012) · Journal of Bacteriology & Parasitology · doi:10.4172/2155-9597.1000127 · Cited by 8

Interaction between a Broad-spectrum Antibiotic and Silver Nanoparticles in a Human Gut Ecosystem

Das, P., Saulnier, E., Carlucci, C., Allen Vercoe, E., Shah, V., & Vk, W. (2016) · Journal of Nanomedicine & Nanotechnology · doi:10.4172/2157-7439.1000408 · Cited by 8

Effects of indoor and outdoor rearing system on geese biochemical parameters and cecal microbial composition

Lin, Y., Chang, P.-E., Shen, S.-Y., & Wang, S.-D. (2023) · Poultry Science · doi:10.1016/j.psj.2023.102731 · Cited by 10

Soil intake modifies the gut microbiota and alleviates Th2-type immune response in an ovalbumin-induced asthma mouse model

Li, M., Li, N., Dong, Y., Zhang, H., Bai, Z., Zhang, R., Fei, Z., Zhu, W., Xiao, P., Sun, X. S., et al. (2024) · World Allergy Organization Journal · doi:10.1016/j.waojou.2024.100897 · Cited by 8

The Commensal Microbiota

Patterson, J. A. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1311-0_1 · Cited by 8

Citrobacter rodentium infection at the gut–brain axis interface

Martins, F. H., & Cuesta, S. (2021) · Current Opinion in Microbiology · doi:10.1016/j.mib.2021.06.003 · Cited by 9

Genomics of Probiotic–Host Interactions

Ajithdoss, D. K., Dowd, S. E., & Suchodolski, J. S. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1311-0_4 · Cited by 7

Impaired responses to gliadin and gut microbes of immune cells from mice with altered stress-related behavior and premature immune senescence

Palma, G. D., Vida, C., Santacruz, A., Castro, N. M. D., la Fuente, M. D., & Sanz, Y. (2014) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2014.08.007 · Cited by 7

Influence of Stress Connected with Moving to a New Farm on Potentially MAP-Infected Mouflons

Dziedzinská, R., Slaná, I., Lamka, J., & Pavlík, I. (2014) · ISRN Microbiology · doi:10.1155/2014/450130 · Cited by 7

High Doses of Halotolerant Gut-Indigenous Lactobacillus plantarum Reduce Cultivable Lactobacilli in Newborn Calves without Increasing Its Species Abundance

Rodriguez‐Palacios, A., Staempfli, H. R., & Weese, J. S. (2017) · International Journal of Microbiology · doi:10.1155/2017/2439025 · Cited by 7

Mice Deficient in Epithelial or Myeloid Cell Iκκβ Have Distinct Colonic Microbiomes and Increased Resistance to Citrobacter rodentium Infection

Mackos, A. R., Allen, J. M., Kim, E., Ladaika, C., Gharaibeh, R. Z., Moore, C. C., Parry, N. M., Boyaka, P. N., & Bailey, M. T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02062 · Cited by 6

Role of intestinal microbiota in regulation of immune reactions of gut-associated lymphoid tissue under stress and following the modulation of its composition by antibiotics and probiotics administration

Topol, I. A., Polyakova, I. S., & Elykova, A. V. (2023) · Journal of microbiology epidemiology immunobiology · doi:10.36233/0372-9311-270 · Cited by 7

The gut microbiome modulates the susceptibility to traumatic stress in a sex‐dependent manner

Shen, D., Chang, L., Su, F., Huang, S., Xu, H., Si, Y., Wang, F., & Xue, Y.-X. (2024) · Journal of Neuroscience Research · doi:10.1002/jnr.25315 · Cited by 6

Assessing Fecal Microbial Diversity and Hormone Levels as Indicators of Gastrointestinal Health in Reintroduced Przewalski’s Horses (Equus ferus przewalskii)

Li, Z., Luo, Z., & Hu, D. (2024) · Animals · doi:10.3390/ani14172616 · Cited by 6

Spatial and temporal changes in gut microbiota composition of farmed Asian seabass ( Lates calcarifer ) in different aquaculture settings

Soh, M., Er, S., Low, A., Jaafar, Z., de Boucher, R., & Seedorf, H. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.01989-24 · Cited by 6

Glucocorticoids and the Intestinal Environment

Ünsal, H., & Balkay, M. (2012) · InTech eBooks · doi:10.5772/51977 · Cited by 6

Removal of roosters alters the domestic phenotype and microbial and genetic profile of hens

Xiang, H., Chen, S., Zhang, H., Zhu, X., Wang, D., Liu, H., Wang, J., Yin, T., Liu, L., Kong, M., et al. (2021) · Science China Life Sciences · doi:10.1007/s11427-020-1770-1 · Cited by 6

The Gut–Brain Axis and Peroxisome Proliferator-Activated Receptors in the Regulation of Epileptogenesis

Zubareva, O. E., & Melik-Kasumov, T. B. (2021) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093021040013 · Cited by 6

Dietary purple potatoes shape gut microbiota and ameliorate colitis in IL-10-deficient mice

Zhu, M. J., Bibi, S., Sun, Q., He, Y. Q., Xue, Y., Su, Y., Navarre, D. A., & Du, ‬. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106321 · Cited by 6

Chronic dexamethasone exposure retards growth without altering the digestive tract microbiota composition in goats

Hua, C., Geng, Y., Qu, C., Niu, L., Cai, L., Tao, S., Ni, Y., & Zhao, R. (2018) · BMC Microbiology · doi:10.1186/s12866-018-1253-1 · Cited by 6

Effects of husbandry systems and Chinese indigenous chicken strain on cecum microbial diversity

Dong, X., Hu, B., Wan, W., Gong, Y., & Feng, Y. (2019) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.19.0157 · Cited by 6

Research Note: Integrated gut microbiome and short-chain fatty acids responds to dominance hierarchy in roosters

Chen, S., Yan, C., Liu, W., Chen, K., Xing, L., Li, H., & Zhao, X. (2021) · Poultry Science · doi:10.1016/j.psj.2021.101670 · Cited by 6

Stress and the Gastrointestinal System

Bonaz, B. L. (2016) · Springer eBooks · doi:10.1007/978-3-319-28609-9_7 · Cited by 6

Probiotics as a possible novel therapeutic option to mitigate perioperative neurocognitive disorders: A review exploring the latest research findings

Horill, S., Zhou, X., & Jin, W. (2025) · Journal of Clinical Anesthesia · doi:10.1016/j.jclinane.2025.111801 · Cited by 7

The intricate relationship between stress and animal welfare: from historical perspective to new avenues

Wu, F., Tilbrook, A. J., Maloney, S. K., & Blache, D. (2025) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.70057 · Cited by 5

Microbial regulation of stress-associated signaling molecules and its role in health and disease

Sie, C., & Tropini, C. (2026) · npj Biofilms and Microbiomes · doi:10.1038/s41522-026-00932-w · Cited by 7

Effects of floor- and net-rearing systems on intestinal growth and microbial diversity in the ceca of ducks

Chen, X., Huang, L., Cheng, L., Hu, B., Liu, H., Hu, J., Hu, S., Han, C., He, H., Kang, B., et al. (2022) · BMC Microbiology · doi:10.1186/s12866-022-02478-1 · Cited by 5

Out of the stable: Social disruption and concurrent shifts in the feral mare (Equus caballus) fecal microbiota

Vaziri, G. J., Jones, M. M., Carr, H. A., & Nuñez, C. M. V. (2023) · Ecology and Evolution · doi:10.1002/ece3.10079 · Cited by 5

Radiation enteropathy‐related depression: A neglectable course of disease by gut bacterial dysbiosis

Liu, X. W., Li, Y., Gu, M., Xu, T., Wang, C., & Chang, P. (2024) · Cancer Medicine · doi:10.1002/cam4.6865 · Cited by 4

Intra‐nucleus‐accumbens SKF38393 improved the impaired acquisition of morphine‐conditioned place preference in depression‐like rats

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Mode of Action of Dietary Dexamethasone May Not Be Dependent Upon Microbial Mechanisms in Broilers

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