Changes in intestinal microbiota composition and metabolism coincide with increased intestinal permeability in young adults under prolonged physiological stress

QIIME allows analysis of high-throughput community sequencing data

Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887

Search and clustering orders of magnitude faster than BLAST

Edgar, R. C. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq461 · Cited by 21,056

Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy

Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00062-07 · Cited by 20,145

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

Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences

Langille, M. G. I., Zaneveld, J., Caporaso, J. G., McDonald, D., Knights, D., Reyes, J. A., Clemente, J. C., Burkepile, D. E., Vega Thurber, R. L., Knight, R., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2676 · Cited by 9,116

Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies.

Klindworth, A., Pruesse, E., Schweer, T., Peplies, J., Quast, C., Horn, M., & Glöckner, F. O. (2013) · Nucleic Acids Research · doi:10.1093/nar/gks808 · Cited by 8,850

Aviat space environ med

(1992) · Applied Ergonomics · doi:10.1016/0003-6870(92)90338-v · Cited by 7,153

An improved Greengenes taxonomy with explicit ranks for ecological and evolutionary analyses of bacteria and archaea

McDonald, D. T., Price, M. N., Goodrich, J. K., Nawrocki, E. P., DeSantis, T. Z., Probst, A. J., Andersen, G. L., Knight, R. D., & Hugenholtz, P. (2011) · The ISME Journal · doi:10.1038/ismej.2011.139 · Cited by 5,133

Host-gut microbiota metabolic interactions

Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662

Neuropsychiatric Ramifications of COVID‐19: Short‐Chain Fatty Acid Deficiency and Disturbance of Microbiota‐Gut‐Brain Axis Signaling

Sajdel, E. M. (2021) · BioMed Research International · doi:10.1155/2021/7880448 · Cited by 49

Potential role of gut microbiota in prostate cancer: immunity, metabolites, pathways of action?

Zha, C., Peng, Z., Huang, K., Tang, K., Wang, Q., Zhu, L. J., Che, B., Li, W., Xu, S., Huang, T., et al. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1196217 · Cited by 49

Increased Plasma Levels of Gut-Derived Phenolics Linked to Walking and Running Following Two Weeks of Flavonoid Supplementation

Nieman, D. C., Kay, C. D., Rathore, A., Grace, M. H., Strauch, R. C., Stephan, E. H., Sakaguchi, C. A., & Lila, M. A. (2018) · Nutrients · doi:10.3390/nu10111718 · Cited by 46

Intestinal Barrier Dysfunction and Gut Microbiota in Non-Alcoholic Fatty Liver Disease: Assessment, Mechanisms, and Therapeutic Considerations

Long, C., Zhou, X., Xia, F., & Zhou, B. (2024) · Biology · doi:10.3390/biology13040243 · Cited by 50

Attributes of Physical Activity and Gut Microbiome in Adults: A Systematic Review

Tzemah-Shahar, R., Koren, O., Greenfeld, S. M., Shochat, T., Magzal, F., & Agmon, M. (2020) · International Journal of Sports Medicine · doi:10.1055/a-1157-9257 · Cited by 43

Review article: bugs, inflammation and mood—a microbiota‐based approach to psychiatric symptoms in inflammatory bowel diseases

Thomann, A., Mak, J. W. Y., Zhang, J., Wüstenberg, T., Ebert, M. P., Sung, J. J. �., Bernstein, C. N., Reindl, W., & Ng, S. C. (2020) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15787 · Cited by 44

Nutritional Requirements for Sustaining Health and Performance During Exposure to Extreme Environments

Pasiakos, S. M. (2020) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-011720-122637 · Cited by 47

Microbiome and substances of abuse

Salavrakos, M., Leclercq, S., de Timary, P., & Dom, G. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110113 · Cited by 45

Probiotics as a therapeutic strategy in obesity and overweight: a systematic review

Tomé-Castro, X. M., Rodríguez-Arrastia, M. J., Cardona, D., Rueda‐Ruzafa, L., Molina‐Torres, G., & Román, P. (2021) · Beneficial Microbes · doi:10.3920/bm2020.0111 · Cited by 43

Microbiome Modulation as a Novel Strategy to Treat and Prevent Respiratory Infections

Mindt, B. C., & DiGiandomenico, A. (2022) · Antibiotics · doi:10.3390/antibiotics11040474 · Cited by 47

Gut Microbial Stability is Associated with Greater Endurance Performance in Athletes Undertaking Dietary Periodization

Furber, M., Young, G. R., Holt, G. S., Pyle, S., Davison, G., Roberts, M. G., Roberts, J., Howatson, G., & Smith, D. (2022) · mSystems · doi:10.1128/msystems.00129-22 · Cited by 43

Bidirectional crosstalk between the gut microbiota and cellular compartments of brain: Implications for neurodevelopmental and neuropsychiatric disorders

Shiadeh, S. M. J., Chan, W. K., Rasmusson, S., Hassan, N., Joca, S. R. L., Westberg, L., Elfvin, A., Mallard, C. E., & Ardalan, M. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03504-2 · Cited by 52

The effects of sustained fitness improvement on the gut microbiome: A longitudinal, repeated measures case‐study approach

Barton, W., Cronin, O., García‐Pérez, I., Whiston, R., Holmes, E. C., Woods, T., Molloy, C. B., Molloy, M. G., Shanahan, F., Cotter, P. D., et al. (2020) · Translational Sports Medicine · doi:10.1002/tsm2.215 · Cited by 40

The relationship between gut microbiome and human diseases: mechanisms, predisposing factors and potential intervention

Shabani, M., Ghoshehy, A., Mottaghi, A. M., Chegini, Z., Kerami, A., Shariati, A., & Moghadam, M. T. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1516010 · Cited by 48

Gut microbiota: an overlooked factor that plays a significant role in osteoporosis

Hao, M.-L., Wang, G., Zuo, X.-Q., Qu, C.-J., Yao, B.-C., & Wang, D. (2019) · Journal of International Medical Research · doi:10.1177/0300060519860027 · Cited by 39

Association between increased intestinal permeability and disease: A systematic review

Leech, B., Schloss, J. M., & Steel, A. (2019) · Advances in Integrative Medicine · doi:10.1016/j.aimed.2018.08.003 · Cited by 32

What is the leaky gut? Clinical considerations in humans

Camilleri, M. (2021) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000778 · Cited by 36

Gut-muscle-brain axis: Molecular mechanisms in neurodegenerative disorders and potential therapeutic efficacy of probiotic supplementation coupled with exercise

Morella, I., Negro, M., Dossena, M., Brambilla, R., & D’Antona, G. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109718 · Cited by 36

Mechanisms underlying alterations of the gut microbiota by exercise and their role in shaping ecological resilience

Mohr, A. E., Mach, N., Pugh, J. N., Grosicki, G. J., Allen, J. M., Karl, J. P., & Whisner, C. M. (2025) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf037 · Cited by 37

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

Effects of different doses of omega-3 polyunsaturated fatty acids on gut microbiota and immunity

Zhu, X., Bi, Z., Yang, C., Guo, Y., Yuan, J., Li, L., & Guo, Y. (2021) · Food & Nutrition Research · doi:10.29219/fnr.v65.6263 · Cited by 34

Examining the Influence of the Human Gut Microbiota on Cognition and Stress: A Systematic Review of the Literature

Cooke, M. B., Catchlove, S. J., & Tooley, K. L. (2022) · Nutrients · doi:10.3390/nu14214623 · Cited by 40

How strong is the evidence that gut microbiota composition can be influenced by lifestyle interventions in a cardio-protective way?

Gerdes, V. E. A., Gueimonde, M., Pajunen, L., Nieuwdorp, M., & Laitinen, K. (2020) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2020.08.028 · Cited by 34

The influence of exercise training volume alterations on the gut microbiome in highly‐trained middle‐distance runners

Craven, J., Cox, A. J., Bellinger, P., Desbrow, B., Irwin, C. G., Buchan, J., McCartney, D., & Sabapathy, S. (2021) · European Journal of Sport Science · doi:10.1080/17461391.2021.1933199 · Cited by 33

Psychological intervention to treat distress: An emerging frontier in cancer prevention and therapy

Yang, M., Zhang, Z., Nice, E. C., Wang, C., Zhang, W., & Huang, C. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188665 · Cited by 35

Positive effects of physical activity in autism spectrum disorder: how influences behavior, metabolic disorder and gut microbiota

Ranieri, A., Mennitti, C., Falcone, N., La Monica, I., Di Iorio, M. R., Tripodi, L., Gentile, A., Vitale, M., Pero, R., Pastore, L., et al. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1238797 · Cited by 32

Mining the equine gut metagenome: poorly-characterized taxa associated with cardiovascular fitness in endurance athletes

Mach, N., Midoux, C., Leclercq, S., Pennarun, S., Moyec, L. L., Rué, O., Robert, C., Sallé, G., & Barrey, É. (2022) · Communications Biology · doi:10.1038/s42003-022-03977-7 · Cited by 38

Severe, short-term sleep restriction reduces gut microbiota community richness but does not alter intestinal permeability in healthy young men

Karl, J. P., Whitney, C. C., Wilson, M. A., Fagnant, H. S., Radcliffe, P. N., Chakraborty, N., Campbell, R., Hoke, A. V., Gautam, A., Hammamieh, R., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-27463-0 · Cited by 34

Sex differences in body composition and serum metabolome responses to sustained, physical training suggest enhanced fat oxidation in women compared with men

Beckner, M. E., Thompson, L., Radcliffe, P. N., Cherian, R. V., Wilson, M. A., Barringer, N., Margolis, L. M., & Karl, J. P. (2023) · Physiological Genomics · doi:10.1152/physiolgenomics.00180.2022 · Cited by 33

Effects of medical plants on alleviating the effects of heat stress on chickens

Mahasneh, Z. M. H., Abuajamieh, M., Abedal-Majed, M. A., Al‐Qaisi, M., Abdelqader, A., & Al-Fataftah, A.-R. A. (2024) · Poultry Science · doi:10.1016/j.psj.2023.103391 · Cited by 32

Roles of Microbiota in Cancer: From Tumor Development to Treatment

Bagheri, Z., Moeinzadeh, L., & Razmkhah, M. (2022) · Journal of Oncology · doi:10.1155/2022/3845104 · Cited by 32

Intensity-specific considerations for exercise for patients with inflammatory bowel disease

Ordille, A. J., & Phadtare, S. (2022) · Gastroenterology report · doi:10.1093/gastro/goad004 · Cited by 33

Emerging mycotoxins and preventive strategies related to gut microbiota changes: probiotics, prebiotics, and postbiotics – a systematic review

Lázaro, Á., Donat, P. V., & Manyes, L. (2024) · Food & Function · doi:10.1039/d4fo01705f · Cited by 48

Intestinal barrier functions in hematologic and oncologic diseases

Haroun, E., Kumar, P. A., Saba, L., Kassab, J. T., Ghimire, K. B., Dutta, D., & Lim, S. H. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04091-w · Cited by 36

Gut‐Brain Axis Impact on Canine Anxiety Disorders: New Challenges for Behavioral Veterinary Medicine

Sacoor, C., Marugg, J. D., Lima, N. R., Empadinhas, N., & Montezinho, L. (2024) · Veterinary Medicine International · doi:10.1155/2024/2856759 · Cited by 33

Dietary Strategies to Improve Exercise Performance by Modulating the Gut Microbiota

Zhang, L., Li, H., Song, Z., Liu, Y., & Zhang, X. (2024) · Foods · doi:10.3390/foods13111680 · Cited by 34

A diet of U.S. military food rations alters gut microbiota composition and does not increase intestinal permeability

Karl, J. P., Armstrong, N. J., McClung, H. L., Player, R. A., Rood, J. C., Racicot, K., Soares, J. W., & Montain, S. J. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.108217 · Cited by 32

Immune status, well-being and gut microbiota in military supplemented with synbiotic ice cream and submitted to field training: a randomised clinical trial

Valle, M. C. P., Vieira, I. A., Fino, L. D. C., Gallina, D. A., Esteves, A. M., da Cunha, D. T., Cabral, L., Benatti, F. B., Maróstica, M. R., Batista, Â. G., et al. (2021) · British Journal Of Nutrition · doi:10.1017/s0007114521000568 · Cited by 34

Gut Microbiota, Microbial Metabolites and Human Physical Performance

Lensu, S., & Pekkala, S. (2021) · Metabolites · doi:10.3390/metabo11110716 · Cited by 32

The diet-microbiota axis: a key regulator of intestinal permeability in human health and disease

Tamang, R. L., Juritsch, A. F., Ahmad, R., Salomon, J., Dhawan, P., Ramer‐Tait, A. E., & Singh, A. B. (2022) · Tissue Barriers · doi:10.1080/21688370.2022.2077069 · Cited by 29

What happens to gut microorganisms and potential repair mechanisms when meet heavy metal(loid)s

Liu, X., Zhang, J., Si, J., Li, P., Gao, H., Li, W., & Chen, Y. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2022.120780 · Cited by 32

Physical activity‐induced alterations of the gut microbiota are BMI dependent

Shah, S., Mu, C., Moossavi, S., Shen‐Tu, G., Schlicht, K., Rohmann, N., Geisler, C., Laudes, M., Franke, A., Züllig, T., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202201571r · Cited by 34

Oral Sub-Chronic Ochratoxin a Exposure Induces Gut Microbiota Alterations in Mice

Izco, M., Vettorazzi, A., de Toro, M., Sáenz, Y., & Alvarez‐Erviti, L. (2021) · Toxins · doi:10.3390/toxins13020106 · Cited by 29

The stress concept in gastroenterology: from Selye to today

Elsenbruch, S., & Enck, P. (2017) · F1000Research · doi:10.12688/f1000research.12435.1 · Cited by 31

The Role of Gut Microbiota in Different Types of Physical Activity and Their Intensity: Systematic Review and Meta-Analysis

Ghaffar, T., Ubaldi, F., Volpini, V., Valeriani, F., & Spica, V. R. (2024) · Sports · doi:10.3390/sports12080221 · Cited by 31

Microbiota and Alcohol Use Disorder: Are Psychobiotics a Novel Therapeutic Strategy?

Rodríguez‐González, A., & Orío, L. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200122153541 · Cited by 29

Non-invasive Assessment of Fecal Stress Biomarkers in Hunting Dogs During Exercise and at Rest

Zannoni, A., Pietra, M., Gaspardo, A., Accorsi, P. A., Barone, M., Turroni, S., Laghi, L., Zhu, C., Brigidi, P., & Forni, M. (2020) · Frontiers in Veterinary Science · doi:10.3389/fvets.2020.00126 · Cited by 28

The Relationship among Physical Activity, Intestinal Flora, and Cardiovascular Disease

Yan, Q., Zhai, W., Yang, C., Li, Z., Mao, L., Zhao, M., & Wu, X. (2021) · Cardiovascular Therapeutics · doi:10.1155/2021/3364418 · Cited by 28

“Sentinel or accomplice”: gut microbiota and microglia crosstalk in disorders of gut–brain interaction

Zheng, H., Zhang, C., Zhang, J., & Duan, L. (2023) · Protein & Cell · doi:10.1093/procel/pwad020 · Cited by 29

The current state and future direction of DoD gut microbiome research: a summary of the first DoD gut microbiome informational meeting

Arcidiacono, S. M., Soares, J. W., Karl, J. P., Chrisey, L. A., Dancy, C. P. T. B. C. R., Goodson, M. S., Gregory, F., Hammamieh, R., Kelley‐Loughnane, N., Kokoska, R. J., et al. (2018) · Standards in Genomic Sciences · doi:10.1186/s40793-018-0308-0 · Cited by 29

From dysbiosis to longevity: a narrative review into the gut microbiome’s impact on aging

Tseng, C., & Wu, C. (2025) · Journal of Biomedical Science · doi:10.1186/s12929-025-01179-x · Cited by 31

Gut Microbiota and Fecal Metabolome Perturbation in Children with Autism Spectrum Disorder

Mohamadkhani, A. (2018) · Middle East Journal of Digestive Diseases · doi:10.15171/mejdd.2018.112 · Cited by 28

Bi-Directionality of the Microbiota-Gut-Brain Axis in Patients With Functional Dyspepsia: Relevance of Psychotherapy and Probiotics

Rupp, S. K., & Stengel, A. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.844564 · Cited by 29

Effects of active, inactive, and derivatives of Akkermansia muciniphila on the expression of the endocannabinoid system and PPARs genes

Ghaderi, F., Sotoodehnejadnematalahi, F., Hajebrahimi, Z., Fateh, A., & Siadat, S. D. (2022) · Scientific Reports · doi:10.1038/s41598-022-13840-8 · Cited by 29

Innovative mechanisms of micro- and nanoplastic-induced brain injury: Emphasis on the microbiota-gut-brain axis

Shi, L., Feng, Y., Wang, J., Xiao, R., Wang, L., Tian, P., Jin, X., Zhao, J., & Wang, G. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123107 · Cited by 28

Gut feelings on short-chain fatty acids to regulate respiratory health

Rowland, S. N., Green, C. G., Halliwill, J. R., Singanayagam, A., & Heaney, L. M. (2025) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2024.12.007 · Cited by 30

Evaluation of Probiotics for Warfighter Health and Performance

Agans, R., Giles, G. E., Goodson, M. S., Karl, J. P., Leyh, S. M., Mumy, K. L., Racicot, K., & Soares, J. W. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.00070 · Cited by 26

Gut check: Unveiling the influence of acute exercise on the gut microbiota

Grosicki, G. J., Langan, S. P., Bagley, J. R., Galpin, A. J., Garner, D., Hampton‐Marcell, J., Allen, J. M., & Robinson, A. T. (2023) · Experimental Physiology · doi:10.1113/ep091446 · Cited by 27

A systematic review: Role of dietary supplements on markers of exercise-associated gut damage and permeability

Chantler, S., Griffiths, A., Matu, J., Davison, G., Holliday, A., & Jones, B. L. (2022) · PLoS ONE · doi:10.1371/journal.pone.0266379 · Cited by 31

Associations Between Brain Morphology, Inflammatory Markers, and Symptoms of Fatigue, Depression, or Anxiety in Active and Remitted Crohn’s Disease

Thomann, A., Schmitgen, M. M., Stephan, J. C., Ebert, M. P., Thomann, P. A., Szabo, K., Reindl, W., & Wolf, R. C. (2024) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjae078 · Cited by 25

Could environmental exposure and climate change Be a key factor in the rising incidence of early onset colorectal cancer?

Alzaabi, A. A., Younus, H. A., Al-Reasi, H. A., & Al-Hajri, R. S. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e35935 · Cited by 27

Exercise protects intestinal epithelial barrier from high fat diet- induced permeabilization through SESN2/AMPKα1/HIF-1α signaling

Yu, C., Liu, S., Niu, Y., & Fu, L. (2022) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.109059 · Cited by 23

The impact of diet on disease activity in spondyloarthritis: A systematic literature review

Ortolan, A., Felicetti, M., Lorenzin, M., Cozzi, G., Ometto, F., Striani, G., Favero, M., Doria, A., & Ramonda, R. (2022) · Joint Bone Spine · doi:10.1016/j.jbspin.2022.105476 · Cited by 25

A review on Impact of dietary interventions, drugs, and traditional herbal supplements on the gut microbiome

Karim, M. R., Iqbal, S., Mohammad, S., Lee, J. H., Jung, D.-H., Mathiyalagan, R., Yang, D., Yang, D. U., & Yang, D. U. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127346 · Cited by 27

Gut microbiota alternation with training periodization and physical fitness in Japanese elite athletes

Akazawa, N., Nakamura, M., Eda, N., Murakami, H., Nakagata, T., Nanri, H., Park, J., Hosomi, K., Mizuguchi, K., Kunisawa, J., et al. (2023) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2023.1219345 · Cited by 24

Optimizing the Gut Microbiota for Individualized Performance Development in Elite Athletes

Nolte, S., Krüger, K., Lenz, C., & Zentgraf, K. (2023) · Biology · doi:10.3390/biology12121491 · Cited by 28

Effect of the Intake of a Traditional Mexican Beverage Fermented with Lactic Acid Bacteria on Academic Stress in Medical Students

Márquez-Morales, L., El-Kassis, E. G., Cavazos‐Arroyo, J., Rocha–Rocha, V. M., Martínez‐Gutiérrez, F., & Pérez‐Armendáriz, B. (2021) · Nutrients · doi:10.3390/nu13051551 · Cited by 29

Gut—brain barrier dysfunction bridge autistic‐like behavior in mouse model of maternal separation stress: A behavioral, histopathological, and molecular study

Rowshan, N., Anjomshoa, M., Farahzad, A., Bijad, E., & Amini-Khoei, H. (2024) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10329 · Cited by 22

Neurobiological Processes Induced by Aerobic Exercise through the Endocannabinoidome

Forteza, F., Giorgini, G., & Raymond, F. (2021) · Cells · doi:10.3390/cells10040938 · Cited by 23

Effect of dark environment on intestinal flora and expression of genes related to liver metabolism in zebrafish (Danio rerio)

Feng, C. T., Sarigaiqiqige, Liu, W., Chen, H., Dong, W., & Yang, J. (2021) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2021.109100 · Cited by 23

Association of lung-intestinal microecology and lung cancer therapy

Kong, L., Chen, X.-Y., Lu, X., Caiyin, Q., & Yang, D. (2023) · Chinese Medicine · doi:10.1186/s13020-023-00742-8 · Cited by 22

Exploring the Impact of the Gut Microbiome on Obesity and Weight Loss: A Review Article

Noor, J., Chaudhry, A., Batool, S. A., Noor, R., & Fatima, G. (2023) · Cureus · doi:10.7759/cureus.40948 · Cited by 28

Gut flora in multiple sclerosis: implications for pathogenesis and treatment

Zhang, W., Wang, Y., Zhu, M., Liu, K., & Zhang, H. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.387974 · Cited by 24

Integrating metagenomics and metabolomics to study the gut microbiome and host relationships in sports across different energy systems

Aya, V., Pardo-Rodriguez, D., Vega, L. C., Cala, M. P., & Ramírez, J. D. (2025) · Scientific Reports · doi:10.1038/s41598-025-98973-2 · Cited by 30

Modulatory Impacts of Multi-Strain Probiotics on Rabbits’ Growth, Nutrient Transporters, Tight Junctions and Immune System to Fight against Listeria monocytogenes Infection

El-Hamid, M. I. A., Ibrahim, D., Hamed, R. I., Nossieur, H. H., Elbana, M. H., Baz, H., Abd-Allah, E. M., Oksh, A. S. A. E., Ibrahim, G. A., Khalifa, E., et al. (2022) · Animals · doi:10.3390/ani12162082 · Cited by 22

Immune Function, Nutrition, and Exercise

Aoi, W., & Naito, Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813922-6.00007-2 · Cited by 20

Probiotics for pancreatic β-cell function: from possible mechanism of action to assessment of effectiveness

Kobyliak, N. M., Khomenko, M., Falalyeyeva, T. M., Fedchenko, O., Savchuk, О., Tseyslyer, Y. V., & Остапченко, Л. І. (2023) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2023.2257776 · Cited by 21

Biomarkers for warfighter safety and performance in hot and cold environments

LEE, J. K. W., Tan, B., Kingma, B., Haman, F., & Epstein, Y. (2022) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2022.12.006 · Cited by 19

Combined probiotics with vitamin D3 supplementation improved aerobic performance and gut microbiome composition in mixed martial arts athletes

Przewłócka, K., Folwarski, M., Kaczmarczyk, M., Skonieczna‐Żydecka, K., Palma, J., Bytowska, Z. K., Kujach, S., & Kaczor, J. J. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1256226 · Cited by 20

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Zheng, J., Wang, Z., Pu, D., Li, P., Wei, X., Li, M., Li, D., Gao, L., & Zhai, X. (2023) · Fishes · doi:10.3390/fishes8110555 · Cited by 15

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