(Dis)Trust your gut: the gut microbiome in age-related inflammation, health, and disease

Protective and Damaging Effects of Stress Mediators

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Role of the microbiota in immunity and inflammation.

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Metagenomic Analysis of the Human Distal Gut Microbiome

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Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis

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Gut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson's disease

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Ecological and Evolutionary Forces Shaping Microbial Diversity in the Human Intestine

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Gut microbiota composition correlates with diet and health in the elderly

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Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43

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Longitudinal Changes in Fecal Microbiota During Hospitalization in Horses With Different Types of Colic

Loublier, C., Costa, M., Taminiau, B., Lecoq, L., Daube, G., Amory, H., & Cesarini, C. (2025) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.70039 · Cited by 4

Novel approaches to optimize nutrition in the elderly patients

Martyushev-Poklad, A. V., Yankevich, D. S., Petrova, M. V., & Savitskaya, N. G. (2022) · Clinical nutrition and metabolism · doi:10.17816/clinutr108594 · Cited by 4

What Is the Microbiota and What Is Its Role in Colic?

Arnold, C. E., & Pilla, R. (2023) · Veterinary Clinics of North America Equine Practice · doi:10.1016/j.cveq.2023.03.004 · Cited by 5

Fecal bacteria-free filtrate transplantation is proved as an effective way for the recovery of radiation-induced individuals in mice

Zhang, H., Dong, M., Zheng, J., Yang, Y., He, J., Liu, T., & Wei, H. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1343752 · Cited by 4

Dietary nitrate maintains intestinal epithelia homeostasis in aged mice

Wang, X., Liu, H., Yue, M., Wang, J., Zhang, C., Qin, L., Wang, S., & Hu, L. (2024) · Biogerontology · doi:10.1007/s10522-024-10127-5 · Cited by 5

Retrospective, propensity score--matched study examining the relationship between frailty and Clostridioides difficile infection in a national cohort of US veterans

Reveles, K. R., Strey, K. A., Albuquerque, E. L., Jacota, D., Jones, X., & Carreno, J. J. (2024) · American Journal of Infection Control · doi:10.1016/j.ajic.2024.08.020 · Cited by 4

Ketogenic Diet‐Associated Worsening of Osteoarthritis Histologic Secerity, Increased Pain Sensitivity and Gut Microbiome Dysbiosis in Mice

Dyson, G., Barrett, M. R., Schlupp, L., Prinz, E., Hanebutt, N., Szymczak, A., Brawner, C. M., & Jeffries, M. A. (2025) · ACR Open Rheumatology · doi:10.1002/acr2.11794 · Cited by 4

Human Microbiome: Implication of Age and External Factors

Bashir, H., Bawa, A., & Kumar, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-7672-7_1 · Cited by 4

Comparison of the Fecal Bacteriome of HIV-Positive and HIV-Negative Older Adults

Sánchez‐Conde, M., Alba, C., Castro, I., Dronda, F., Ramírez, M., Arroyo, R., Moreno, S., Rodríguez, J. M., & Brañas, F. (2023) · Biomedicines · doi:10.3390/biomedicines11082305 · Cited by 4

MNEMONIC: MetageNomic Experiment Mining to create an OTU Network of Inhabitant Correlations

Perz, A., Giles, C. B., Brown, C. A., Porter, H. L., Roopnarinesingh, X., & Wren, J. D. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-2623-x · Cited by 5

A Review of the Relationship Between Gut Microbiota and Memory

Benmelouka, A. Y., Sherif, A., & Ebada, M. A. (2019) · Springer eBooks · doi:10.1007/978-981-13-9636-6_8 · Cited by 4

Variation in the Gut Microbiota of Common Marmosets: Differences with Colony of Origin and IntegrationPreprint

Cooper, R., Mangus, L. M., Lynch, J., Schonvisky, K., Wright, J., McLimans, C. J., Wong, H. T., See, J. R. C., Lamendella, R., & Mankowski, J. L. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.31.276733 · Cited by 4

Human-like associations between gut microbiome composition and inattention, hyperactivity, and impulsivity in dogs

Salamon, A., Szabó, A., Felföldi, T., Rhali, S. B., Andics, A., Miklósi, Á., Kubinyi, E., & Gácsi, M. (2025) · BMC Biology · doi:10.1186/s12915-025-02410-9 · Cited by 3

Gut Microbiome–Sphingolipid Metabolism–Brain Axis Interactions: Neuroprotective Effects of Amitriptyline as Functional Inhibitor of Acid Sphingomyelinase in a Mouse Model of Tauopathy

Ibrahim, M., Khalil, A. M., Attia, H., Alseekh, S., Mohamed, A. F., & El-Yamany, M. F. (2026) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-025-10270-x · Cited by 3

Taxonomic and functional remodeling of the gut microbiota during aging and implications for microbiota-derived biomarkers

Tekin, B., & Gurbanov, R. (2026) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-026-05017-6 · Cited by 4

Lycium ruthenicum Murray anthocyanins alleviate neuroinflammation in MPTP-induced Parkinson's disease by modulating gut microbiota and tryptophan metabolism

Guo, H., Qin, X., Tang, Y., Wang, C., Luo, Q., Gao, H., & Gao, Q. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117051 · Cited by 3

Gut Microbiota and Ageing: Mechanisms, Age-Related Diseases, and Therapeutic Perspectives

Ferreira, J. M. A., Тукаєв, С., & Giannouli, V. (2026) · Healthcare · doi:10.3390/healthcare14142117 · Cited by 4

Mechanistic insights of the anti-ageing dietary plant secondary metabolites vis-à-vis the modern hallmarks of ageing: Implications for developing novel anti-ageing foods

Sharma, R., & Sharma, A. (2024) · Translational Medicine of Aging · doi:10.1016/j.tma.2024.09.001 · Cited by 3

The Effect of Probiotic Lactic Acid Bacteria on the Symptoms of Mental Disorders

Novikova, V. A., Bondarenko, K. D., Сазонов, А. Э., & Розанов, А. С. (2024) · Nanobiotechnology Reports · doi:10.1134/s2635167624602092 · Cited by 3

A Retrospective Analysis of Pain Etiology in Middle-Aged Patients with Peripheral Neuropathy

Szewczyk, A. K., Jamróz-Wiśniewska, A., & Rejdak, K. (2021) · Medicina · doi:10.3390/medicina57080787 · Cited by 4

Maternal Gut Microbiome Decelerates Fetal Endochondral Bone Formation by Inducing Inflammatory Reaction

Uchida‐Fukuhara, Y., Hattori, T., Fu, S., Kondo, S., Kuwahara, M., Fukuhara, D., Islam, M. M., Kataoka, K., Ekuni, D., Kubota, S., et al. (2022) · Microorganisms · doi:10.3390/microorganisms10051000 · Cited by 3

Metformin, Microbiota and Health

Paz, G. S., & Fernandes, J. (2022) · Journal of Exploratory Research in Pharmacology · doi:10.14218/jerp.2022.00032 · Cited by 3

The Role of the Gut Microbiome in Youth with Polycystic Ovary Syndrome: A Systematic Review

Tsinopoulou, V. R., Kotanidou, E. P., Athanasiadis, N., Sapountzi, E., Bacopoulou, F., Ntzani, E., Galli‐Τsinopoulou, A., & Christoforidis, A. (2023) · Children · doi:10.3390/children10121872 · Cited by 5

Gut Microbiota: A Future Clinical Magic Bullet to Manifest Pathogenic Disease in the Current Future

Mina, P. R. (2023) · Journal of Pure and Applied Microbiology · doi:10.22207/jpam.17.1.43 · Cited by 3

The Molecular Architecture of Variable Lifespan in Diversity Outbred MicePreprint

Hackett, S. R., Magzoub, M. M., Maile, T. M., Vu, N., Wright, K. M., Melamud, E., Haas, W., McAllister, F. E., Churchill, G. A., & Bennett, B. D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.26.564069 · Cited by 3

On the Gut Microbiome as a Central Player in Aging: Mechanisms and Health Outcomes

Melnitskaia, A. A., Matchekhina, L. V., Константиновна, И. А., & Strazhesko, I. D. (2024) · Advances in Gerontology · doi:10.1134/s207905702560003x · Cited by 2

Comparative Analysis of Compound Probiotics, Seasonal Variation, and Age on Gut Microbial Composition and Function in Endangered Forest Musk Deer

Jiang, F., Song, P., Cai, Z., Wu, G., He, S., Gu, H., Gao, H., & Zhang, T. (2025) · Microorganisms · doi:10.3390/microorganisms13091991 · Cited by 2

Biochemical and structural improvements in ileum and colon with concurrent gut microbiota enhancement through intermittent fasting plasma infusions

Tan, M., Ceylani, T., Gurbanov, R., Keskin, S., Açıkgöz, E., Sağır, E., & Teker, H. T. (2025) · Scientific Reports · doi:10.1038/s41598-025-21183-3 · Cited by 2

Tetrandrine enhances cognition in SAH rats via gut microbiota CYP51 and TLR4 signaling

Liu, H., Zou, Q., Xiang, T., Zhu, R., Chen, Z., & Chen, R. (2025) · Scientific Reports · doi:10.1038/s41598-025-22980-6 · Cited by 2

Fecal microbiota transplantation from gestational diabetes mellitus patients induces glucose intolerance and subclinical inflammation in mice

Huang, J., Yin, X., Zhang, Y., Zheng, W., & Li, G. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1723816 · Cited by 2

Age-Related Neurovascular Dysfunction in the Retina and Potential Pathogenic Mechanisms

Wu, Y., Cao, Q., & Liu, Q. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.4.16 · Cited by 2

Microbiome changes in aging

Reveles, K. R., Young, E. H., Zeidan, A. R., & Dong, Q. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-815962-0.00017-2 · Cited by 2

Gut Dysbiosis in Insomnia and Diurnal Cycle

Kumar, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-6760-2_8 · Cited by 2

Rsearch progress on the relationship between aging and microbiota in sarcopenia

Cheng, J., Chen, X. '., & Chen, J. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1549733 · Cited by 4

Acute Exposure to the Food-Borne Pathogen Listeria monocytogenes Does Not Induce α-Synuclein Pathology in the Colonic ENS of Nonhuman Primates

Mancinelli, A. M., Vichich, J. M., Zinnen, A. D., Hugon, A. M., Bondarenko, V., Metzger, J. M., Simmons, H. A., Golos, T. G., & Emborg, M. E. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s337549 · Cited by 2

The Interplay Between the Microbiome and Cardiovascular Risk

Minnifield, B. A., & Aslibekyan, S. W. (2018) · Current Genetic Medicine Reports · doi:10.1007/s40142-018-0142-0 · Cited by 2

Gut Microbiota Pattern of Centenarians

Wu, L. H., Zinellu, A., Milanesi, L., Rubino, S., Kelvin, D. J., & Carru, C. (2019) · Springer eBooks · doi:10.1007/978-3-030-20762-5_9 · Cited by 2

Risk of subsequent ischemic stroke in patients with nontyphoidal salmonellosis: A nationwide population-based cohort study

Chang, R., Wei, J. C., Lin, M., Hung, Y., & Hung, C. (2020) · Journal of Infection · doi:10.1016/j.jinf.2020.06.026 · Cited by 2

Longitudinal profiling of the gut microbiome in patients with psoriatic arthritis and ankylosing spondylitis: a multicentre, prospective, observational study

Blanco, J. M., Borghese, F., McHugh, N. J., Kelleher, P., Sengupta, R., Marchesi, J. R., & Abraham, S. (2020) · BMC Rheumatology · doi:10.1186/s41927-020-00155-2 · Cited by 2

Contribution of the Microbiota to Healthy Aging

Forssten, S. D., & Ouwehand, A. C. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00059-0 · Cited by 2

Gut–Brain Axis: Role of Gut Microbiota in Neurodegenerative Disease

Narang, A., & Sandhir, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-6760-2_1 · Cited by 1

Obesity, inflammation, and aging

Chu, J. J., & Mehrzad, R. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90960-0.00001-1 · Cited by 1

The gut microbiome as a central player in aging: mechanisms and health outcomes

Melnitskaia, A. A., Matchekhina, L. V., Константиновна, И. А., & Strazhesko, I. D. (2024) · Problems of Geroscience · doi:10.37586/2949-4745-3-2024-154-160 · Cited by 2

Pathogenic SIV infection is associated with acceleration of epigenetic age in rhesus macaques

Jasinska, A. J., Sivanandham, R., Sivanandham, S., Xu, C., Gordevičius, J., Milčiūtė, M., Brooke, R. T., Sette, P., He, T., Brocca‐Cofano, E., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci189574 · Cited by 1

Oral olsalazine/ellagic acid/ZnCl2‐modified in situ-forming hydrogels alleviates anxiety/depression-like symptoms and brain neural activity in colitis mice

Li, T., Li, N., Sheng, H., Zhang, L., Luo, Q., Liu, S., Zhao, Y., Chen, W., Liu, D., & Wang, Z. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.102058 · Cited by 1

An Olsalazine-Loaded Hollow Mesoporous Prussian Blue/Polydopamine Nanozyme Alleviates Anxiety/Depression-like Behavior and Enhances Brain Neural Activity in Colitis Mice

Luo, Q., Liu, D., Yang, J., Li, T., Sheng, H., Liu, S., Zhou, X., Zhou, C., Wang, H., Wang, Z., et al. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c13154 · Cited by 1

Association between pro-inflammatory dietary patterns and chronic pain in community-dwelling older adults: A cross-sectional study

Nishimoto, J., Deguchi, N., Hatanaka, S., Shida, T., Ohta, T., Kojima, N., Shirobe, M., Motokawa, K., Hirano, H., Okamura, T., et al. (2025) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2025.106035 · Cited by 1

Multistage oral astaxanthin targeted delivery system: Increasing serotonin levels with a dual therapeutic effect for alleviating inflammatory bowel disease and psychiatric disorders

Sun, M., Xu, L., Chen, Q., Lu, Z., Rao, H., Zhao, X., Chen, O., & Wang, Y. (2025) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2025.115177 · Cited by 1

Mechanistic Insights into a Smart Nanomotor‐Laden Inulin Hydrogel Reprogramming Gut‐Brain Axis for Combinatorial Inflammatory Bowel Disease‐Depression Therapy

Luo, Z., Liu, Z., Chen, H., Chen, G., Lu, G., Zhu, Z., Fang, X., & Luo, J. F. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202519453 · Cited by 1

Identification of fecal microbiome signatures associated with longevity through 16S rRNA sequencing in different age groups in China

Wang, Y., LIU, J., Wang, W., Xu, G., Lin, Y., Song, P., Zhou, X., & Zheng, K. (2026) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-026-13752-x · Cited by 1

Ulcerative colitis-driven gut dysbiosis exacerbates periodontal bone loss through the gut–oral axis /Th17/Treg imbalance

Huang, Y., Hu, Y., Zhao, Y., Li, Y., Liu, Y., Wang, M., Wang, Q., & Hu, H. (2026) · npj Biofilms and Microbiomes · doi:10.1038/s41522-026-01015-6 · Cited by 1

An implementation of infants' gut microbiome maturation analyses by 16s rRNA from stool samples in extraction solution of room temperature

Liang, B., Fan, W., Han, J. G., Chen, N., & Zhao, N. (2017) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm.2017.8217778 · Cited by 1

The Relationship Between Telomeres, Cognition, Mood, and Physical Function: A Systematic Review

Sheikh-Wu, S. F., Liang, Z., & Downs, C. A. (2022) · Biological Research For Nursing · doi:10.1177/10998004221132287 · Cited by 1

Clostridium difficile Infection: Risk and Poor Prognostic Factors at a Tertiary Hospital in the Eastern Region of Saudi Arabia

Miqdad, M. A., Kosaraju, K., Mohamad, A. S., Hulwi, H., Rais, U., Taleb, M., & Aloreibi, T. (2023) · Cureus · doi:10.7759/cureus.39193 · Cited by 1

A Revitalising Approach towards Aging: Unveiling the Potential Use of Probiotics for Wellness in Elderly Populations

Desai, S. P., Kurian, C., Das, S., Rebello, S. J., Acharyya, S., & Paari, K. A. (2023) · Journal of Health Science and Medical Research · doi:10.31584/jhsmr.20231015 · Cited by 1

Immune mRNA Expression and Fecal Microbiome Composition Change Induced by Djulis (Chenopodium formosanum Koidz.) Supplementation in Aged Mice: A Pilot Study

Villanueva, B. H. A., Huang, H.-Y., Tyan, Y., Lin, P.-J., Li, C., Minh, H., Tayo, L. L., & Chuang, K. (2024) · Medicina · doi:10.3390/medicina60091545 · Cited by 1

Diet, Microbiome, Inflammation, and Cancer

Zhang, X., & Daniel, C. R. (2021) · Physiology in health and disease · doi:10.1007/978-3-030-67951-4_11 · Cited by 1

Microbiota Changes Throughout Life - An Overview

Bačić, A., & Rajilić-Stojanović, M. D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00107-8 · Cited by 1

Microorganisms in Pathogenesis and Management of Systemic Lupus Erythematosus (SLE)

Yi, P., Zhao, M., & Lu, Q. (2022) · Springer eBooks · doi:10.1007/978-981-19-1946-6_20 · Cited by 1

Sarcopenia and its Impact on the Immune System

(2023) · Immunology Research and Immunotherapy · doi:10.59462/irit.1.1.101 · Cited by 1

Prospective evaluation of the fecal microbiome in dogs with large-cell lymphoma receiving chop chemotherapy

Couto, J. I. (2021) · doi:10.32469/10355/88084 · Cited by 1

The prebiotic effects of amadumbe (Colocasia Esculenta) and okra (Abelmoschus esculentus) mucilage

Gajadhar, S. (2023) · DUT Open Scholar (Durban University of Technology) · doi:10.51415/10321/4803 · Cited by 1

The Mutual Interactions of Silymarin and Colon Microbiota from Healthy Young and Healthy Elder SubjectsPreprint

Tomisova, K., Jarošová, V., Maršík, P., Mascellani, A., Cinek, O., Hlinakova, L., Klouček, P., Janoušek, V., Valentová, K., & Havlík, J. (2024) · ChemRxiv · doi:10.26434/chemrxiv-2024-4drz1 · Cited by 1

Defining microbiota-derived metabolite butyrate as a senomorphic: therapeutic potential in the age-related T cell senescencePreprint

Duggal, N. A., Rees, N. P., Conway, J., Dugan, B., Parker, A., & Carding, S. R. (2025) · Research Square · doi:10.21203/rs.3.rs-6419928/v1 · Cited by 1

Structural Variations in Circulating Lipopolysaccharide may Increase Severity of Exercise-Induced Heat Illness

Wright, S. S. (2018) · OpenCommons - UConn (University of Connecticut)

The Aging Gut Microbiota

Keebaugh, E. S., Williams, L. D., & Ja, W. W. (2019) · Springer eBooks · doi:10.1007/978-3-030-28737-5_12

Current and future trends in diagnostics and treatment

Orlando, L. A., Shirts, B. H., & Henrich, V. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816015-2.00009-2

Reply to Marcialis et al

Gu, S., Chen, Y., Lv, L., & Li, L. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciaa966

Towards A New Understanding of Larval Disease in the Honey Bee (Apis mellifera)

Floyd, A. S. (2019) · UA Campus Repository (The University of Arizona)

Diet and Microbiota in the Elderly

Alvarado-Jasso, G. M., Arboleya, S., González, S., Reyes‐Gavilán, C. G. D. L., Salazar, N., & Gueimonde, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00088-7

Breaking down the barriers : The effects of aging, gut microbiota and bile acids on intestinal health

van der Lugt, B. (2021) · doi:10.18174/549523

Preserving Health and Achieving Longevity Through Caloric Restriction and Symbiotic Equilibrium with Gut Microbiome

Nikhra, V. (2019) · Current Trends in Biomedical Engineering & Biosciences · doi:10.19080/ctbeb.2019.19.556003

Ageing Mucosal Immunity and Its Consequences for Infectious Diseases in the Aged; A First Glance

van der Heiden, M., & van Baarle, D. (2021) · Healthy ageing and longevity · doi:10.1007/978-3-030-87532-9_6

Digestion and inflammatory responses

Maji, H. S., & Ray, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821232-5.00016-1

Nasopharyngeal Microbiome

Yadav, M., & Bhambi, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00078-4

An integrative analysis of the biological clock hypothesis in human gut microbiomePreprint

Moss, A. D., Sun, S., Blakley, I., & Fodor, A. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.22.485238

Faculty Opinions recommendation of Heterochronic faecal transplantation boosts gut germinal centres in aged mice.

Valenzano, D. R. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735897629.793564141

Metataxonomic Analysis of Feces from Older Adults with and without HIV Title 2: Aging, HIV, and Gut DysbiosisPreprint

Sánchez‐Conde, M., Alba, C., Castro, I., Dronda, F., Ramírez, M., Arroyo, R., Moreno, S., Rodríguez, J. M., & Brañas, F. (2022) · Research Square · doi:10.21203/rs.3.rs-2054510/v1

Effect of various types of gut microbiota in patients on the diminished ovarian reservePreprint

Li, G., Jiao, J., Xiang, S., Dong, S., Fu, L., Zuo, N., Guan, W., Li, W.-S., Miao, L., Yao, W., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2063027/v1

A Preliminary Mini-Review on the Relations Between Lipofuscin, Aging and the Oxidative Stress Status - the Possible Implications of Gut Functionality

ALI, M. A. M., & Ciobica, A. S. (2020) · Annals of the Academy of Romanian Scientists Series on Biological Sciences · doi:10.56082/annalsarscibio.2020.1.45

Gut Microbiota Peculiarities in Aged HIV-Infected Individuals: Molecular Understanding and Therapeutic Perspectives

Vignesh, R., Ganesh, P. S., Sankar, S., Chattopadhyay, I., Yong, Y. K., Larsson, M., & Shankar, E. M. (2023) · Healthy ageing and longevity · doi:10.1007/978-3-031-14023-5_20

Moxibustion ameliorated age-related alterations in neurological behavior and gut microbiota in mice.

Lin, Y., Xing, M., Liu, N., Ouyang, X., He, R., Huang, C., Yao, Q., Liu, Y.-J., Huang, Y., Xue, Y., et al. (2023) · PubMed Central

Additional file 2 of Spatial heterogeneity of bacterial colonization across different gut segments following inter-species microbiota transplantation

Li, N., Zuo, B., Huang, S., Zeng, B., Han, D., Li, T., Liu, T., Wu, Z., Wei, H., Zhao, J., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13257810

Causal Relationship Between Gut Microbiota and Acquired Immune Deficiency Syndrome: A Two-Sample Mendelian Randomization StudyPreprint

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Additional file 3 of Fecal microbiota transplantation protects rotenone-induced Parkinson’s disease mice via suppressing inflammation mediated by the lipopolysaccharide-TLR4 signaling pathway through the microbiota-gut-brain axis

Zhao, Z., Ning, J., 鲍秀琦, Shang, M., Ma, J., Li, G., & Zhang, D. (2021) · Figshare · doi:10.6084/m9.figshare.17030702

Additional file 2 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662759

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Additional file 5 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662774

Additional file 4 of Fecal microbiota transplantation protects rotenone-induced Parkinson’s disease mice via suppressing inflammation mediated by the lipopolysaccharide-TLR4 signaling pathway through the microbiota-gut-brain axis

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Additional file 3 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662762

Additional file 4 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662768

Additional file 1 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662756

Additional file 6 of The pleiotropic effects of prebiotic galacto-oligosaccharides on the aging gut

Arnold, J. W., Roach, J., Fabela, S., Moorfield, E., Ding, S., Blue, E., Dagher, S. F., Magness, S. T., Tamayo, R., Bruno-Bárcena, J. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13662783

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