Microbial regulation of organismal energy homeostasis

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444

A human gut microbial gene catalogue established by metagenomic sequencing

MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624

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 gut microbiota as an environmental factor that regulates fat storage

Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245

Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease

Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597

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

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

The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism

den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048

Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice

Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819

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

Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity

Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511

Effects of probiotic/synbiotic supplementation on body weight in patients with diabetes: a systematic review and meta-analyses of randomized-controlled trials

Soltani, S., Ashoori, M., Dehghani, F., Meshkini, F., Clayton, Z. S., & Abdollahi, S. (2023) · BMC Endocrine Disorders · doi:10.1186/s12902-023-01338-x · Cited by 28

Environmental cadmium exposure alters the internal microbiota and metabolome of Sprague–Dawley rats

Liu, S., Deng, X., Li, Z., Zhou, W., Wang, G., Zhan, J., & Hu, B. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2023.1219729 · Cited by 27

Dose-Dependent Effects of Histamine on Growth, Immunity and Intestinal Health in Juvenile Grouper (Epinephelus coioides)

Liu, Z., Yang, H., Hu, L.-H., Yang, W., Ai, C., & Sun, Y. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.685720 · Cited by 26

Effect of microbiota metabolites on the progression of chronic hepatitis B virus infection

Sun, X. L., Pan, C. Q., & Xing, H. (2021) · Hepatology International · doi:10.1007/s12072-021-10230-6 · Cited by 26

Gut microbiome: Linking together obesity, bariatric surgery and associated clinical outcomes under a single focus

Georgiou, K. E., Belev, N. A., Koutouratsas, T., Katifelis, H., & Gazouli, M. (2022) · World Journal of Gastrointestinal Pathophysiology · doi:10.4291/wjgp.v13.i3.59 · Cited by 27

Effects of a wholegrain-rich diet on markers of colonic fermentation and bowel function and their associations with the gut microbiome: a randomised controlled cross-over trial

Procházková, N., Venlet, N. V., Hansen, M. L., Lieberoth, C. B., Dragsted, L. O., Bahl, M. I., Licht, T. R., Kleerebezem, M., Lauritzen, L., & Roager, H. M. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1187165 · Cited by 26

Gut Microbiota and Adipose Tissue Microenvironment Interactions in Obesity

Wang, C., Yi, Z., Ye, J., Shen, Z., Yang, F., & Zhu, S. (2023) · Metabolites · doi:10.3390/metabo13070821 · Cited by 23

n-3 polyunsaturated fatty acids in the regulation of adipose tissue browning and thermogenesis in obesity: Potential relationship with gut microbiota

Zapata, J. L., Gallardo, A., Romero, C., Valenzuela, R., Garcia-Diaz, D., Duarte-Silva, L., Bustamante, A., Gasaly, N., Gotteland, M., & Echeverría, F. (2021) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2021.102388 · Cited by 26

Mediating effects of gut microbiota in the associations of air pollutants exposure with adverse pregnancy outcomes

Gan, Q., Ye, W., Zhao, X., Teng, Y., Mei, S., Long, Y., Ma, J., Rehemutula, R., Zhang, X., Zeng, F., et al. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113371 · Cited by 25

Contribution of skeletal muscle to cancer immunotherapy: A focus on muscle function, inflammation, and microbiota

Deng, Y., Zhao, L., Huang, X., Zeng, Y., Xiong, Z., & Zuo, M. (2022) · Nutrition · doi:10.1016/j.nut.2022.111829 · Cited by 27

Multi-omics insights into the mechanisms of muscle damage induced by molybdenum exposure in goats

Zhou, X., & Shen, X. (2025) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2025.118373 · Cited by 24

Dietary Energy Level Impacts the Performance of Donkeys by Manipulating the Gut Microbiome and Metabolome

Zhang, C., Zhang, C., Wang, Y., Du, M., Zhang, G., & Lee, Y. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.694357 · Cited by 24

Gut Microbes and Eye Disease

Donabedian, P. L., Dawson, E. A., Li, Q., & Chen, J. (2021) · Ophthalmic Research · doi:10.1159/000519457 · Cited by 24

Microbiome mediation of animal life histories via metabolites and insulin‐like signalling

Warne, R. W., & Dallas, J. W. (2022) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12833 · Cited by 24

Food Reward Alterations during Obesity Are Associated with Inflammation in the Striatum in Mice: Beneficial Effects of Akkermansia muciniphila

Huwart, S. J. P., d’Oplinter, A. D. W., Rastelli, M., Hul, M. V., de Vos, W. M., Luquet, S. H., Cani, P. D., & Everard, A. (2022) · Cells · doi:10.3390/cells11162534 · Cited by 24

Bacillus licheniformis FA6 Affects Zebrafish Lipid Metabolism through Promoting Acetyl-CoA Synthesis and Inhibiting β-Oxidation

Chen, S., Ye, W., Clements, K. D., Zan, Z., Zhao, W., Zou, H., Wang, G., & Wu, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010673 · Cited by 24

Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward

d’Oplinter, A. D. W., Verce, M., Huwart, S. J. P., Lessard‐Lord, J., Depommier, C., Hul, M. V., Desjardins, Y., Cani, P. D., & Everard, A. (2023) · Microbiome · doi:10.1186/s40168-023-01526-w · Cited by 25

Autonomously Assembled Living Capsules by Microbial Coculture for Enhanced Bacteriotherapy of Inflammatory Bowel Disease

Qiao, J., Zeng, R., Chen, Q., Zheng, D., Hao, P.-L., Liu, X., Zhao, F., & Zhang, X. (2023) · Nano Letters · doi:10.1021/acs.nanolett.3c00657 · Cited by 24

Improvements in estrogen deficiency-induced hypercholesterolemia by Hypericum perforatum L. extract are associated with gut microbiota and related metabolites in ovariectomized (OVX) rats

Chen, L., Liu, Y., Tang, Z., Shi, X., Song, Z., Cao, F., Wei, P., Li, M., Li, X., Jiang, D., et al. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111131 · Cited by 24

Regulatory effect of volatile compounds in fermented alcoholic beverages on gut microbiota and serum metabolism in a mouse model

Ji, M., Fang, C., Jia, W. P., Du, H., & Xu, Y. (2021) · Food & Function · doi:10.1039/d0fo03028g · Cited by 24

Personal diet–microbiota interactions and weight loss

Roager, H. M., & Christensen, L. H. (2022) · Proceedings of The Nutrition Society · doi:10.1017/s0029665122000805 · Cited by 23

An overview of traditional Chinese medicine affecting gut microbiota in obesity

Li, D., Tang, W., Wang, Y., Gao, Q., Zhang, H., Zhang, Y., Wang, Y., Yang, Y., Zhou, Y., Zhang, Y., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1149751 · Cited by 23

Progress on network modeling and analysis of gut microecology: a review

Luo, M., Zhu, J., Jia, J., Zhang, H., & Zhao, J. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.00092-24 · Cited by 24

Propionic Acid Impact on Multiple Sclerosis: Evidence and Challenges

Lorefice, L., & Żołędziewska, M. (2024) · Nutrients · doi:10.3390/nu16223887 · Cited by 23

Antimicrobial therapy during cancer treatment: Beyond antibacterial effects

Ghanem, S., Kim, C. J., Dutta, D., Salifu, M. O., & Lim, S. H. (2020) · Journal of Internal Medicine · doi:10.1111/joim.13238 · Cited by 23

The role of gut microbiota in insulin resistance: recent progress

Ji, H., Su, S., Chen, M., Liu, S., Liu, S., & Guo, J. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1633029 · Cited by 22

Characteristics and Clinical Significance of Intestinal Microbiota in Patients with Chronic Hepatitis B Cirrhosis and Type 2 Diabetes Mellitus

Sun, X. L., Chi, X., Zhao, Y., Liu, S., & Xing, H. (2022) · Journal of Diabetes Research · doi:10.1155/2022/1826181 · Cited by 22

Metagenomic and metabolomic analysis showing the adverse risk–benefit trade-off of the ketogenic diet

Qiu, H., Kan, C., Han, F., Luo, Y., Qu, N., Zhang, K., Ma, Y., Hou, N., Wu, D., Sun, X., et al. (2024) · Lipids in Health and Disease · doi:10.1186/s12944-024-02198-7 · Cited by 22

MicroRNAs and extracellular vesicles in the gut: new host modulators of the microbiome?

Du, X., Ley, R. E., & Buck, A. H. (2021) · microLife · doi:10.1093/femsml/uqab010 · Cited by 20

Microbial composition differs between production systems and is associated with growth performance and carcass quality in pigs

Maltecca, C., Dunn, R. R., He, Y., McNulty, N. P., Schillebeeckx, C., Schwab, C. R., Shull, C. M., Fix, J., & Tiezzi, F. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00118-z · Cited by 20

Environmental Perturbations during the Rehabilitation of Wild Migratory Birds Induce Gut Microbiome Alteration and Antibiotic Resistance Acquisition

Song, H., Yi, S., Kim, W.-H., Guk, J.-H., Ha, M., Kwak, I., Han, J., Yeon, S., & Cho, S. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01163-22 · Cited by 20

Big Data for a Small World: A Review on Databases and Resources for Studying Microbiomes

Sengupta, P., Sivabalan, S. K. M., Mahesh, A., Palanikumar, I., Baskaran, D. K. K., & Raman, K. (2023) · Journal of the Indian Institute of Science · doi:10.1007/s41745-023-00370-z · Cited by 20

Does the gut microbiota contribute to the antiobesity effect of exercise? A systematic review and meta‐analysis

Zheng, C., Chen, X., Tian, X. Y., Chun‐Hang, A., & Wong, S. H. (2022) · Obesity · doi:10.1002/oby.23345 · Cited by 20

The Role of Gut Microbiota in Host Lipid Metabolism: An Eye on Causation and Connection

Wang, K., Liang, X., Pang, Y., & Jiang, C. (2019) · Small Methods · doi:10.1002/smtd.201900604 · Cited by 19

Integrated Analyses of Microbiomics and Metabolomics Explore the Effect of Gut Microbiota Transplantation on Diabetes-Associated Cognitive Decline in Zucker Diabetic Fatty Rats

Bi, T., Zhang, L., Zhan, L., Feng, R., Zhao, T., Ren, W., Hang, T., Zhou, W., & Lu, X. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.913002 · Cited by 19

Whole-Grain Highland Barley Attenuates Atherosclerosis Associated with NLRP3 Inflammasome Pathway and Gut Microbiota in ApoE−/− Mice

Wu, T., Yu, Q., Luo, Y., Dai, Z., Zhang, Y., Wang, C., Shen, Q., & Xue, Y. (2023) · Nutrients · doi:10.3390/nu15194186 · Cited by 19

In vitro human gut microbiota fermentation of litchi pulp polysaccharides as affected by Lactobacillus pre-treatment

Xia, C., Zhang, R., Jia, X., Dong, L., Ma, Q., Zhao, D. H., Lee, Y. K., Sun, Z., Huang, F., & Zhang, M. (2024) · Food Chemistry · doi:10.1016/j.foodchem.2024.138734 · Cited by 19

Exploring the Benefit of 2-Methylbutyric Acid in Patients Undergoing Hemodialysis Using a Cardiovascular Proteomics Approach

Wu, P., Chiu, Y., Zou, H.-B., Hsu, C., Lee, S., Lin, Y., Tsai, Y., Kuo, M., & Hwang, S. (2019) · Nutrients · doi:10.3390/nu11123033 · Cited by 19

Characterization of Purified Mulberry Leaf Glycoprotein and Its Immunoregulatory Effect on Cyclophosphamide-Treated Mice

Shan, Y., Sun, C., Li, J., Shao, X., Wu, J., Zhang, M., Yao, H. L., & Wu, X. (2022) · Foods · doi:10.3390/foods11142034 · Cited by 19

Fecal microbiota transplantation from methionine-restricted diet mouse donors reduces fat deposition in obese mice by remodeling the gut microbiota

Yang, Y., Cui, G., Qian, J., Xu, Y., Li, B., Shi, Y., Le, G., & Xie, Y. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.104255 · Cited by 18

The Impact of Lifestyle on Reproductive Health: Microbial Complexity, Hormonal Dysfunction, and Pregnancy Outcomes

Barraza-Ortega, E., Gómez‐Gil, B., García-Gasca, T., Lizárraga, D., Díaz, N., & García-Gasca, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178574 · Cited by 18

Gut microbiome dysbiosis in patients with hepatitis B virus-related hepatocellular carcinoma after extended hepatectomy liver failure

Peng, Y., Xu, J., Zeng, C.-F., Zhao, X., Li, L., & Qi, L. (2022) · Annals of Translational Medicine · doi:10.21037/atm-22-1958 · Cited by 18

Pea albumin extracted from pea (Pisum sativum L.) seed protects mice from high fat diet-induced obesity by modulating lipid metabolism and gut microbiota

Liu, N., Song, Z., Jin, W., Yang, Y., Sun, S., Zhang, Y., Zhang, S., Liu, S., Ren, F., & Wang, P. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105234 · Cited by 18

Decreased Paneth cell α-defensins promote fibrosis in a choline-deficient L-amino acid-defined high-fat diet-induced mouse model of nonalcoholic steatohepatitis via disrupting intestinal microbiota

Nakamura, S., Nakamura, K., Yokoi, Y., Shimizu, Y., Ohira, S., Hagiwara, M., Song, Z., Gan, L. H., Aizawa, T., Hashimoto, D., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-30997-y · Cited by 18

Comparing measured dietary variation within and between tropical hunter-gatherer groups to the Paleo Diet

Lieberman, D. E., Worthington, S., Schell, L. D., Parkent, C. M., Devinsky, O., & Carmody, R. N. (2023) · American Journal of Clinical Nutrition · doi:10.1016/j.ajcnut.2023.06.013 · Cited by 18

The keystone gut species Christensenella minuta boosts gut microbial biomass and voluntary physical activity in mice

Akbuğa-Schön, T., Suzuki, T. A., Jakob, D., Vu, D. L., Waters, J. L., & Ley, R. E. (2023) · mBio · doi:10.1128/mbio.02836-23 · Cited by 18

Kansuiphorin C and Kansuinin A ameliorate malignant ascites by modulating gut microbiota and related metabolic functions

Zhang, Y., Lou, J.-W., An, K., Zhang, Q., Zhou, S.-K., Bao, B., Cao, Y., Yao, W., Tang, Y., & Zhang, L. (2019) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2019.112423 · Cited by 18

Imbalance in the force: the dark side of the microbiota on stroke risk and progression

Kumar, K. P., & Wong, C. H. Y. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.10.002 · Cited by 18

Gut Microbial Dysbiosis Associated with Type 2 Diabetes Aggravates Acute Ischemic Stroke

Chen, X., Wu, Q., Gao, X., Wang, H., Zhu, J., Xia, G., He, Y., Song, W., & Xu, K. (2021) · mSystems · doi:10.1128/msystems.01304-21 · Cited by 18

Gut microbiota of homing pigeons shows summer–winter variation under constant diet indicating a substantial effect of temperature

Dietz, M. W., Matson, K. D., Versteegh, M. A., van der Velde, M., Parmentier, H. K., Arts, J. A. J., Salles, J. F., & Tieleman, B. I. (2022) · Animal Microbiome · doi:10.1186/s42523-022-00216-6 · Cited by 17

Multi-omics analysis revealed the differences in lipid metabolism of the gut between adult and juvenile yellowfin tuna (Thunnus albacares)

Zou, Y., Zhang, Y., Wu, D., Lu, Z., Xiao, J., Huang, H., Fu, Q., & Guo, Z. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1326247 · Cited by 18

The Interplay of Microbiome Dysbiosis and Cardiovascular Disease

Zaher, A., ElSaygh, J., Peterson, S. J., Weisberg, I. S., Parikh, M. A., & Frishman, W. H. (2024) · Cardiology in Review · doi:10.1097/crd.0000000000000701 · Cited by 17

Metabolic heterogeneity in tumor microenvironment – A novel landmark for immunotherapy

Chen, C., Han, P., & Qing, Y. (2024) · Autoimmunity Reviews · doi:10.1016/j.autrev.2024.103579 · Cited by 17

Chronological dynamics of the gut microbiome in response to the pasture grazing system in geese

Ali, Q., Ma, S., Farooq, U., Liu, B., Wang, Z., Sun, H., Cui, Y., Li, D., & Shi, Y. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04188-23 · Cited by 17

Modulation of inflammatory markers in type 2 diabetes mellitus through gut microbiome-targeted interventions: An umbrella review on meta-analyses

Habibi, A., Letafatkar, N., Sattari, N., Nobakht, S., Rafat, Z., Moghadam, S. S., Mirdamadi, A., Javid, M., Jamilian, P., Hassanipour, S., et al. (2024) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2024.11.011 · Cited by 17

The novel intervention effect of cold green tea beverage on high-fat diet induced obesity in mice

Ma, H., Zhang, B., Hu, Y., Li, X., Wang, J., Yang, F., Ji, X., & Wang, S. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104279 · Cited by 17

Impact of High-Pressure Processed Onion on Colonic Metabolism Using a Dynamic Gastrointestinal Digestion Simulator

Fernández-Jalao, I., Balderas, C., Calvo, M. V., Fontecha, J., Sánchez‐Moreno, C., & de Ancos, B. (2021) · Metabolites · doi:10.3390/metabo11050262 · Cited by 17

Multi-omics reveals the regulatory mechanisms of zinc exposure on the intestine-liver axis of golden pompano Trachinotus ovatus

Ma, S., Shu, X., & Wang, W. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.151497 · Cited by 17

Microbes, oxytocin and stress: Converging players regulating eating behavior

Cuesta‐Marti, C., Uhlig, F., Muguerza, B., Hyland, N. P., Clarke, G. A., & Schellekens, H. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13243 · Cited by 17

The Connection and Disconnection Between Microbiome and Metabolome: A Critical Appraisal in Clinical Research

Misra, B. B. (2020) · Biological Research For Nursing · doi:10.1177/1099800420903083 · Cited by 17

Current knowledge of the Southern Hemisphere marine microbiome in eukaryotic hosts and the Strait of Magellan surface microbiome project

Ochoa‐Sánchez, M., Gómez, E. P. A., Ramírez-Fernández, L., Eguiarte, L. E., & Souza, V. (2023) · PeerJ · doi:10.7717/peerj.15978 · Cited by 16

Phenolic compounds in dietary target the regulation of gut microbiota: Role in health and disease

Zhang, Q., Xu, Y., Bukvički, D., Peng, Y., Li, F., Zhang, Q., Yan, J., Lin, S., Liu, S., & Qin, W. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105107 · Cited by 16

Rehmannia glutinosa polysaccharides enhance intestinal immunity of mice through regulating the microbiota

Yu, L., Lin, F., Yu, Y., Deng, X., Shi, X., Lu, X., Lu, Y., & Wang, D. Y. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137878 · Cited by 16

Tryptophan-producing bacteria to mitigate osteoporosis and intestinal dysfunction

Tian, B., Wang, H., Zhang, Y., Lv, J., Li, D., Zhou, C., Xu, J., Ni, Y., Wu, B., Zhang, M., et al. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.05.013 · Cited by 16

Микробиом кишечника: от эталона нормы к патологии

Юрьевич, П. М., Михайловна, М. Ю., Efimochkina, N. R., Борисовна, К. И., & Анатольевна, Ш. С. (2020) · PubMed · doi:10.24411/0042-8833-2020-10040 · Cited by 16

The Emerging Role of Metabolism in Brain-Heart Axis: New Challenge for the Therapy and Prevention of Alzheimer Disease. May Thioredoxin Interacting Protein (TXNIP) Play a Role?

Perrone, L., & Valente, M. (2021) · Biomolecules · doi:10.3390/biom11111652 · Cited by 16

Integrated omics analysis: the relationship between significantly increased Klebsiella post-hepatectomy and decreased hub-metabolite 3-methyl-2-oxobutanoic acid is associated with induced liver failure

Peng, Y., Zhao, X.-H., Zeng, C.-F., Xu, J., Qi, L., & Li, L. (2022) · Journal of Gastrointestinal Oncology · doi:10.21037/jgo-21-906 · Cited by 16

The Effects of Oral Probiotic Supplementation in Postmenopausal Women with Overweight and Obesity: A Systematic Review and Meta-analysis of Randomized Controlled Trials

Li, Z., Li, Y., Pan, B., Wang, X., Wu, Y. F., Guo, K., Yang, M., Ma, M., Qiao, C., & Yang, K. (2022) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-022-10037-3 · Cited by 16

Heptadecanoic acid and pentadecanoic acid crosstalk with fecal-derived gut microbiota are potential non-invasive biomarkers for chronic atrophic gastritis

Xiao, G., Qian, P., Benqiong, G., Zheng, Y., Fu, Z., Yang, D.-C., Zhu, C., Cao, Y., Niu, J., Ling, J., et al. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1064737 · Cited by 16

An overview of basic pathophysiological interactions between gut bacteria and their host

Simonson, M., Simonson, T., & Nobécourt, E. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1565609 · Cited by 14

Betulinic acid from Inonotus obliquus ameliorates T2DM by modulating short-chain fatty acids producing bacteria and amino acids metabolism in db/db mice

Lin, B., Bai, G., Zhang, Y., Wang, Y., & Chen, S. (2025) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2025.119417 · Cited by 15

Obesity Reshapes the Microbial Population Structure along the Gut-Liver-Lung Axis in Mice

Galaris, A., Fanidis, D., Stylianaki, E.-A., Harokopos, V., Kalantzi, A.-S., Moulos, P., Dimas, A. S., Hatzis, P., & Aidinis, V. (2022) · Biomedicines · doi:10.3390/biomedicines10020494 · Cited by 15

Influence of Aging, Macronutrient Composition and Time-Restricted Feeding on the Fischer344 x Brown Norway Rat Gut Microbiota

Hernandez, A. R., Kemp, K. M., Burke, S. N., Buford, T. W., & Carter, C. S. (2022) · Nutrients · doi:10.3390/nu14091758 · Cited by 15

Intestinal Bacteroides sp. Imbalance Associated With the Occurrence of Childhood Undernutrition in China

Li, D., Li, Y., Dai, W., Wang, H. H., Qiu, C., Feng, S., Zhou, Q., Wang, W., Feng, X., Yao, K., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02635 · Cited by 15

The Combined Effects of High-Intensity Interval Exercise Training and Dietary Supplementation on Reduction of Body Fat in Adults with Overweight and Obesity: A Systematic Review

Gaweł, E., Hall, B., Siatkowski, S., Grabowska, A., & Zwierzchowska, A. (2024) · Nutrients · doi:10.3390/nu16030355 · Cited by 14

The gut–eye axis: from brain neurodegenerative diseases to age-related macular degeneration

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Harnessing microfluidic technology for bacterial single-cell analysis in mammals

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Effects of BBIBP-CorV vaccine on gut microbiota and short-chain fatty acids in mice exposed to bis (2-ethylhexyl) phthalate and dioctyl terephthalate

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Lactobacillus crispatus-Mediated Gut–Reproductive Tract Axis-Alleviated Microbial Dysbiosis and Oviductal Inflammation in a Laying Hen Model

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