Gut Microbiota Interacts with Markers of Adipose Tissue Browning, Insulin Action and Plasma Acetate in Morbid Obesity

Fast gapped-read alignment with Bowtie 2

Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400 · see citing works

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 · see citing works

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 · see citing works

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762 · see citing works

Quality control and preprocessing of metagenomic datasets

Schmieder, R., & Edwards, R. A. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr026 · Cited by 4,989 · see citing works

Gut metagenome in European women with normal, impaired and diabetic glucose control

Karlsson, F. H., Tremaroli, V., Nookaew, I., Bergström, G., Behre, C. J., Fagerberg, B., Nielsen, J., & Bäckhed, F. (2013) · Nature · doi:10.1038/nature12198 · Cited by 3,115 · see citing works

Short-chain fatty acids in control of body weight and insulin sensitivity

Canfora, E. E., Jocken, J. W., & Blaak, E. E. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.128 · Cited by 2,298 · see citing works

Energy-balance studies reveal associations between gut microbes, caloric load, and nutrient absorption in humans

Jumpertz, R., Le, D. S., Turnbaugh, P. J., Trinidad, C., Bogardus, C., Gordon, J. I., & Krakoff, J. (2011) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.110.010132 · Cited by 1,232 · see citing works

Microbial community profiling for human microbiome projects: Tools, techniques, and challengesPreprint

Hamady, M., & Knight, R. D. (2009) · Genome Research · doi:10.1101/gr.085464.108 · Cited by 998 · see citing works

Ablation of PRDM16 and Beige Adipose Causes Metabolic Dysfunction and a Subcutaneous to Visceral Fat Switch

Cohen, P., Levy, J. D., Zhang, Y., Frontini, A., Kolodin, D., Svensson, K. J., Lo, J. C., Zeng, X., Ye, L., Khandekar, M. J., et al. (2014) · Cell · doi:10.1016/j.cell.2013.12.021 · Cited by 878 · see citing works

Meta‐analyses of human gut microbes associated with obesity and IBD

Walters, W. A., Xu, Z., & Knight, R. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.09.039 · Cited by 836 · see citing works

Gut Microbiota Orchestrates Energy Homeostasis during Cold

Chevalier, C., Stojanović, O., Colin, D. J., Suarez-Zamorano, N., Tarallo, V., Veyrat-Durebex, C., Rigo, D., Fabbiano, S., Stevanović, A., Hagemann, S., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.004 · Cited by 829 · see citing works

Brown and beige fat in humans: thermogenic adipocytes that control energy and glucose homeostasis

Sidossis, L. S., & Kajimura, S. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78362 · Cited by 689 · see citing works

Intermittent Fasting Promotes White Adipose Browning and Decreases Obesity by Shaping the Gut Microbiota

Li, G., Xie, C., Lu, S., Nichols, R. G., Tian, Y., Li, L., Patel, D., Ma, Y., Brocker, C. N., Yan, T., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.08.019 · Cited by 667 · see citing works

Exercise Modifies the Gut Microbiota with Positive Health Effects

Monda, V., Villano, I., Messina, A., Valenzano, A., Esposito, T., Moscatelli, F., Viggiano, A., Cibelli, G., Chieffi, S., Monda, M., et al. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3831972 · Cited by 654 · see citing works

Short chain fatty acids prevent high-fat-diet-induced obesity in mice by regulating g protein-coupled receptors and gut microbiota

Lu, Y., Fan, C., Li, P., Lu, Y., Chang, X., & Qi, K. (2016) · Scientific Reports · doi:10.1038/srep37589 · Cited by 638 · see citing works

Metabolic adaptation to a high-fat diet is associated with a change in the gut microbiota

Sérino, M., Luche, É., Grès, S., Baylac, A., Bergé, M., Cénac, C., Waget, A., Klopp, P., Iacovoni, J. S., Klopp, C., et al. (2011) · Gut · doi:10.1136/gutjnl-2011-301012 · Cited by 621 · see citing works

The gut microbiota in human energy homeostasis and obesity

Rosenbaum, M., Knight, R., & Leibel, R. L. (2015) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2015.07.002 · Cited by 450 · see citing works

Growth dynamics of gut microbiota in health and disease inferred from single metagenomic samples

Korem, T., Zeevi, D., Suez, J., Weinberger, A., Avnit-Sagi, T., Lotan‐Pompan, M., Matot, E., Jona, G., Harmelin, A., Cohen, N., et al. (2015) · Science · doi:10.1126/science.aac4812 · Cited by 437 · see citing works

Responses of gut microbiota to diet composition and weight loss in lean and obese mice

Ravussin, Y., Koren, O., Spor, A., LeDuc, C., Gutman, R., Stombaugh, J., Knight, R., Ley, R. E., & Leibel, R. L. (2012) · Obesity · doi:10.1038/oby.2011.111 · Cited by 406 · see citing works

The Gut Microbiota Modulates Energy Metabolism in the Hibernating Brown Bear Ursus arctos

Sommer, F., Ståhlman, M., Ilkayeva, O., Arnemo, J. M., Kindberg, J., Josefsson, J., Newgard, C. B., Fröbert, O., & Bäckhed, F. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.01.026 · Cited by 370 · see citing works

The Intestinal Metabolome: An Intersection Between Microbiota and Host

Ursell, L. K., Haiser, H. J., Treuren, W. V., Garg, N., Reddivari, L., Vanamala, J., Dorrestein, P. C., Turnbaugh, P. J., & Knight, R. D. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.03.001 · Cited by 357 · see citing works

Exercise Effects on White Adipose Tissue: Beiging and Metabolic Adaptations

Stanford, K. I., Middelbeek, R. J. W., & Goodyear, L. J. (2015) · Diabetes · doi:10.2337/db15-0227 · Cited by 342 · see citing works

Colonic infusions of short-chain fatty acid mixtures promote energy metabolism in overweight/obese men: a randomized crossover trial

Canfora, E. E., van der Beek, C. M., Jocken, J. W. E., Goossens, G. H., Holst, J. J., Olde Damink, S. W. M., Lenaerts, K., Dejong, C. H. C., & Blaak, E. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-02546-x · Cited by 331 · see citing works

Modulation of gut microbiota by antibiotics improves insulin signalling in high-fat fed mice

Carvalho, B. M., Guadagnini, D., Tsukumo, D. M. L., Schenka, A. A., Latuf-Filho, P., Vassallo, J., Dias, J. C., Kubota, L. T., Carvalheira, J. B. C., & Saad, M. J. A. (2012) · Diabetologia · doi:10.1007/s00125-012-2648-4 · Cited by 314 · see citing works

Roux-en-Y gastric bypass surgery of morbidly obese patients induces swift and persistent changes of the individual gut microbiota

Pallejá, A., Kashani, A., Allin, K. H., Nielsen, T., Zhang, C., Li, Y., Brach, T., Liang, S., Feng, Q., Jørgensen, N. B., et al. (2016) · Genome Medicine · doi:10.1186/s13073-016-0312-1 · Cited by 312 · see citing works

Two Healthy Diets Modulate Gut Microbial Community Improving Insulin Sensitivity in a Human Obese Population

Haro, C., Montes-Borrego, M., Rangel-Zúñiga, O. A., Alcala-Diaz, J. F., Gómez-Delgado, F., Pérez‐Martínez, P., Delgado‐Lista, J., Quintana‐Navarro, G. M., Tinahones, F. J., Landa, B. B., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-3351 · Cited by 302 · see citing works

Gut microorganisms as promising targets for the management of type 2 diabetes

Delzenne, N. M., Cani, P. D., Everard, A., Neyrinck, A. M., & Bindels, L. B. (2015) · Diabetologia · doi:10.1007/s00125-015-3712-7 · Cited by 264 · see citing works

Reprogramming of hepatic fat accumulation and 'browning' of adipose tissue by the short-chain fatty acid acetate

Sahuri-Arisoylu, M., Brody, L., Parkinson, J. R. C., Parkes, H. G., Navaratnam, N., Miller, A. D., Thomas, E. L., Frost, G. S., & Bell, J. D. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.23 · Cited by 255 · see citing works

Distal, not proximal, colonic acetate infusions promote fat oxidation and improve metabolic markers in overweight/obese men

van der Beek, C. M., Canfora, E. E., Lenaerts, K., Troost, F. J., Olde Damink, S. W. M., Holst, J. J., Masclee, A. A. M., Dejong, C. H. C., & Blaak, E. E. (2016) · Clinical Science · doi:10.1042/cs20160263 · Cited by 230 · see citing works

IRF3 promotes adipose inflammation and insulin resistance and represses browning

Kumari, M., Wang, X., Lantier, L., Lyubetskaya, A., Eguchi, J., Kang, S., Tenen, D. E., Roh, H. C., Kong, X., Kazak, L., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci86080 · Cited by 178 · see citing works

Role of Gut Microbiota and Short Chain Fatty Acids in Modulating Energy Harvest and Fat Partitioning in Youth

Goffredo, M., Maas, K. R., Parks, E. J., Wagner, D. A., McClure, E. A., Graf, J., Savoye, M., Pierpont, B. M., Cline, G. W., & Santoro, N. (2016) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2016-1797 · Cited by 178 · see citing works

Effects of Acetate on Lipid Metabolism in Muscles and Adipose Tissues of Type 2 Diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) Rats

YAMASHITA, H., MARUTA, H., JOZUKA, M., KIMURA, R., IWABUCHI, H., YAMATO, M., SAITO, T., FUJISAWA, K., TAKAHASHI, Y., KIMOTO, M., et al. (2009) · Bioscience, Biotechnology, and Biochemistry · doi:10.1271/bbb.80634 · Cited by 146 · see citing works

Short-Chain Fatty Acid Acetate Stimulates Adipogenesis and Mitochondrial Biogenesis via GPR43 in Brown Adipocytes

Hu, J., Kyrou, I., Tan, B. K., Dimitriadis, G. K., Ramanjaneya, M., Tripathi, G., Patel, V. C., James, S. G., Kawan, M., Chen, J., et al. (2016) · Endocrinology · doi:10.1210/en.2015-1944 · Cited by 138 · see citing works

The stool microbiota of insulin resistant women with recent gestational diabetes, a high risk group for type 2 diabetes

Fugmann, M., Breier, M., Rottenkolber, M., Banning, F., Ferrari, U., Sacco, V., Grallert, H., Parhofer, K. G., Seissler, J., Clavel, T., et al. (2015) · Scientific Reports · doi:10.1038/srep13212 · Cited by 131 · see citing works

Association of Intestinal Microbiota with Metabolic Markers and Dietary Habits in Patients with Type 2 Diabetes

Yamaguchi, Y., Adachi, K., Sugiyama, T., Shimozato, A., Ebi, M., Ogasawara, N., Funaki, Y., Goto, C., Sasaki, M., & Kasugai, K. (2016) · Digestion · doi:10.1159/000447690 · Cited by 119 · see citing works

The role of gut microbiota in human obesity: Recent findings and future perspectives

Tagliabue, A., & Elli, M. (2013) · Nutrition, Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2012.09.002 · Cited by 118 · see citing works

Insulin Resistance Modulates Iron-Related Proteins in Adipose Tissue

Moreno‐Navarrete, J. M., Novelle, M. G., Catalán, V., Ortega, F. J., Moreno, M., Gómez‐Ambrosi, J., Xifra, G., Serrano, M., Guerra, E., Ricart, W., et al. (2014) · Diabetes Care · doi:10.2337/dc13-1602 · Cited by 82 · see citing works

Hydrogenotrophic culture enrichment reveals rumenLachnospiraceaeandRuminococcaceaeacetogens and hydrogen-responsiveBacteroidetesfrom pasture-fed cattle

Gagen, E. J., Padmanabha, J., Denman, S. E., & McSweeney, C. S. (2015) · FEMS Microbiology Letters · doi:10.1093/femsle/fnv104 · Cited by 80 · see citing works

Acetate alters expression of genes involved in beige adipogenesis in 3T3-L1 cells and obese KK-Ay mice

Hanatani, S., Motoshima, H., Takaki, Y., Kawasaki, S., Igata, M., Matsumura, T., Kondo, T., Senokuchi, T., Ishii, N., Kawashima, J., et al. (2016) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.16-23 · Cited by 73 · see citing works

ProbioticLactobacillus gasseriSBT2055 improves glucose tolerance and reduces body weight gain in rats by stimulating energy expenditure

Shirouchi, B., Nagao, K., Umegatani, M., Shiraishi, A., Morita, Y., Kai, S., Yanagita, T., Ogawa, A., Kadooka, Y., & Satô, M. (2016) · British Journal Of Nutrition · doi:10.1017/s0007114516002245 · Cited by 61 · see citing works

Lipopolysaccharide-binding protein is a negative regulator of adipose tissue browning in mice and humans

Gavaldà‐Navarro, A., Moreno‐Navarrete, J. M., Quesada‐López, T., Cairó, M., Giralt, M., Fernández‐Real, J. M., & Villarroya, F. (2016) · Diabetologia · doi:10.1007/s00125-016-4028-y · Cited by 57 · see citing works

Transfer of dysbiotic gut microbiota has beneficial effects on host liver metabolism

Nicolas, S., Blasco‐Baqué, V., Fournel, A., Gilleron, J., Klopp, P., Waget, A., Ceppo, F., Marlin, A., Padmanabhan, R., Iacovoni, J. S., et al. (2017) · Molecular Systems Biology · doi:10.15252/msb.20167356 · Cited by 54 · see citing works

PRDM16 sustains white fat gene expression profile in human adipocytes in direct relation with insulin action

Moreno‐Navarrete, J. M., Ortega, F. J., Moreno, M., Xifra, G., Ricart, W., & Fernández‐Real, J. M. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.01.042 · Cited by 14 · see citing works

Mr. A. R. Wallace's “Australasia”

EVERETT, A. H. (1880) · Nature · doi:10.1038/021535a0 · Cited by 1 · see citing works

The Short-Chain Fatty Acid Acetate in Body Weight Control and Insulin Sensitivity

Hernández, M. A. G., Canfora, E. E., Jocken, J. W. E., & Blaak, E. E. (2019) · Nutrients · doi:10.3390/nu11081943 · Cited by 632 · see citing works

Gut microbiota in obesity

Liu, B., Liu, X., Liang, Z., & Wang, J. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i25.3837 · Cited by 625 · see citing works

Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases

Demine, S., Renard, P., & Arnould, T. (2019) · Cells · doi:10.3390/cells8080795 · Cited by 476 · see citing works

Metabolically healthy versus metabolically unhealthy obesity

Iacobini, C., Pugliese, G., Blasetti Fantauzzi, C., Federici, M., & Menini, S. (2019) · Metabolism · doi:10.1016/j.metabol.2018.11.009 · Cited by 453 · see citing works

Metabolism and Metabolic Disorders and the Microbiome: The Intestinal Microbiota Associated With Obesity, Lipid Metabolism, and Metabolic Health—Pathophysiology and Therapeutic Strategies

Aron-Wisnewsky, J., Warmbrunn, M. V., Nieuwdorp, M., & Clément, K. (2021) · Gastroenterology · doi:10.1053/j.gastro.2020.10.057 · Cited by 452 · see citing works

Circulating but not faecal short-chain fatty acids are related to insulin sensitivity, lipolysis and GLP-1 concentrations in humans

Müller, M., Hernández, M. A. G., Goossens, G. H., Reijnders, D., Holst, J. J., Jocken, J. W. E., van Eijk, H. M. H., Canfora, E. E., & Blaak, E. E. (2019) · Scientific Reports · doi:10.1038/s41598-019-48775-0 · Cited by 333 · see citing works

Probiotics, Prebiotics, Synbiotics, Postbiotics, and Obesity: Current Evidence, Controversies, and Perspectives

Vallianou, N. G., Stratigou, T., Christodoulatos, G. S., Tsigalou, C., & Dalamaga, Μ. (2020) · Current Obesity Reports · doi:10.1007/s13679-020-00379-w · Cited by 251 · see citing works

Impact of Gut Microbiota on Host Glycemic Control

Gérard, C., & Vidal, H. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00029 · Cited by 209 · see citing works

Mechanisms and implications of the gut microbial modulation of intestinal metabolic processes

Jyoti, & Dey, P. (2025) · npj Metabolic Health and Disease · doi:10.1038/s44324-025-00066-1 · Cited by 217 · see citing works

The human gut microbiota and glucose metabolism: a scoping review of key bacteria and the potential role of SCFAs

Palmnäs, M. S. A., Costabile, G., Vetrani, C., Åberg, S., Hjalmarsson, Y., Dicksved, J., Riccardi, G., & Landberg, R. (2022) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqac217 · Cited by 192 · see citing works

Panax notoginseng saponins modulate the gut microbiota to promote thermogenesis and beige adipocyte reconstruction via leptin-mediated AMPKα/STAT3 signaling in diet-induced obesity

Xu, Y., Wang, N., Tan, H., Li, S., Zhang, C., Zhang, Z., & Feng, Y. (2020) · Theranostics · doi:10.7150/thno.47746 · Cited by 173 · see citing works

Type 2 Diabetes Mellitus Associated with Obesity (Diabesity). The Central Role of Gut Microbiota and Its Translational Applications

Ortega, M. A., Fraile‐Μartinez, O., Naya, I., García‐Honduvilla, N., Álvarez‐Mon, M., Buján, J., Asúnsolo, Á., & de la Torre, B. (2020) · Nutrients · doi:10.3390/nu12092749 · Cited by 117 · see citing works

The gut microbiota modulates both browning of white adipose tissue and the activity of brown adipose tissue

Moreno‐Navarrete, J. M., & Fernández‐Real, J. M. (2019) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-019-09523-x · Cited by 106 · see citing works

Modulation of Adipocyte Metabolism by Microbial Short-Chain Fatty Acids

May, K. S., & den Hartigh, L. J. (2021) · Nutrients · doi:10.3390/nu13103666 · Cited by 97 · see citing works

Regulation of Adaptive Thermogenesis and Browning by Prebiotics and Postbiotics

Reynés, B., Palou, M., Rodríguez, A. M., & Palou, A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2018.01908 · Cited by 82 · see citing works

Microbiota populations and short-chain fatty acids production in cecum of immunosuppressed broilers consuming diets containing γ-irradiated Astragalus polysaccharides

Liu, Y. S., Li, S., Wang, X., Xing, T., Li, J. L., Zhu, X. D., Zhang, L., & Gao, F. (2020) · Poultry Science · doi:10.1016/j.psj.2020.09.089 · Cited by 83 · see citing works

Detection of Early Disease Risk Factors Associated with Metabolic Syndrome: A New Era with the NMR Metabolomics Assessment

Hernández-Baixauli, J., Quesada‐Vázquez, S., Mariné-Casadó, R., Cardoso, K. G., Caimari, A., Bas-Prior, J. M. D., Escoté, X., & Baselga‐Escudero, L. (2020) · Nutrients · doi:10.3390/nu12030806 · Cited by 73 · see citing works

A multi-omics machine learning framework in predicting the survival of colorectal cancer patients

Yang, M., Yang, H., Ji, L., Hu, X., Tian, G., Wang, B., & Yang, J. (2022) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2022.105516 · Cited by 71 · see citing works

Brown and Brite: The Fat Soldiers in the Anti-obesity Fight

Srivastava, S., & Veech, R. L. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00038 · Cited by 70 · see citing works

Phocea, Pseudoflavonifractor and Lactobacillus intestinalis: Three Potential Biomarkers of Gut Microbiota That Affect Progression and Complications of Obesity-Induced Type 2 Diabetes Mellitus

Wang, Y., Ouyang, M., Gao, X., Wang, S., Fu, C., Zeng, J., & He, X. (2020) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s240728 · Cited by 66 · see citing works

Deciphering the Anti-obesity Benefits of Resveratrol: The “Gut Microbiota-Adipose Tissue” Axis

Zhou, L., Xiao, X., Zhang, Q., Zheng, J., & Deng, M. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00413 · Cited by 66 · see citing works

From white to beige adipocytes: therapeutic potential of dietary molecules against obesity and their molecular mechanisms

Wang, S., Pan, M., Hung, W., Tung, Y., & Ho, C. (2019) · Food & Function · doi:10.1039/c8fo02154f · Cited by 61 · see citing works

Cross-Talk Between Gut Microbiota and Adipose Tissues in Obesity and Related Metabolic Diseases

Wu, D., Wang, H., Xie, L., & Hu, F. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.908868 · Cited by 61 · see citing works

Adipokines and Adipose Tissue-Related Metabolites, Nuts and Cardiovascular Disease

Weschenfelder, C., de Quadros, A. S., dos Santos, J. L., Garofallo, S. B., & Marcadenti, A. (2020) · Metabolites · doi:10.3390/metabo10010032 · Cited by 58 · see citing works

The intestinal 3M (microbiota, metabolism, metabolome) zeitgeist – from fundamentals to future challenges

Dey, P., Chaudhuri, S. R., Efferth, T., & Pal, S. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.09.026 · Cited by 55 · see citing works

Gut microbiota associations with metabolic syndrome and relevance of its study in pediatric subjects

Carrizales-Sánchez, A. K., García‐Cayuela, T., Hernández‐Brenes, C., & Senés‐Guerrero, C. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1960135 · Cited by 53 · see citing works

Diet-Related Changes of Short-Chain Fatty Acids in Blood and Feces in Obesity and Metabolic Syndrome

Ilyés, T., Silaghi, C. N., & Craciun, A. M. (2022) · Biology · doi:10.3390/biology11111556 · Cited by 52 · see citing works

Gut microbiome and microbial metabolites: a new system affecting metabolic disorders

Federici, M. (2019) · Journal of Endocrinological Investigation · doi:10.1007/s40618-019-01022-9 · Cited by 50 · see citing works

Effects of cyanidin-3-O-glucoside on 3-chloro-1,2-propanediol induced intestinal microbiota dysbiosis in rats

Chen, G., Wang, G., Zhu, C., Jiang, X., Sun, J., Tian, L., & Bai, W. (2019) · Food and Chemical Toxicology · doi:10.1016/j.fct.2019.110767 · Cited by 48 · see citing works

Mitochondrial Energy Metabolism in the Regulation of Thermogenic Brown Fats and Human Metabolic Diseases

Takeda, Y., Harada, Y., Yoshikawa, T., & Dai, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021352 · Cited by 47 · see citing works

Dietary polyphenols turn fat “brown”: A narrative review of the possible mechanisms

Hu, J., Wang, Z., Tan, B. K., & Christian, M. (2020) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2020.01.013 · Cited by 46 · see citing works

Endocannabinoid Receptor-1 and Sympathetic Nervous System Mediate the Beneficial Metabolic Effects of Gastric Bypass

Ye, Y., Haija, M. A. E., Morgan, D. A., Guo, D., Song, Y., Frank, A. P., Tian, L., Riedl, R. A., Burnett, C. M.-L., Gao, Z., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108270 · Cited by 42 · see citing works

Dietary Composition and Cardiovascular Risk: A Mediator or a Bystander?

Korakas, E., Dimitriadis, G., Raptis, A. E., & Lambadiari, V. (2018) · Nutrients · doi:10.3390/nu10121912 · Cited by 42 · see citing works

The Crosstalk between Gut Microbiota and White Adipose Tissue Mitochondria in Obesity

Colangeli, L., Marcillo, D. I. E., Simonelli, V., Iorio, E., Rinaldi, T. G., Sbraccia, P., Fortini, P., & Guglielmi, V. (2023) · Nutrients · doi:10.3390/nu15071723 · Cited by 39 · see citing works

Nicotine' actions on energy balance: Friend or foe?

Seoane-Collazo, P., Diéguez, C., Nogueiras, R., Rahmouni, K., Fernández-Real, J., & López, M. (2020) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2020.107693 · Cited by 38 · see citing works

Beige Adipocyte as the Flame of White Adipose Tissue: Regulation of Browning and Impact of Obesity

Altınova, A. E. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab921 · Cited by 39 · see citing works

Anthocyanin-Rich Butterfly Pea Flower Extract Ameliorating Low-Grade Inflammation in a High-Fat-Diet and Lipopolysaccharide-Induced Mouse Model

Yu, Q., Yu, F. S., Li, Q., Zhang, J., Peng, Y., Wang, X., Li, T., Yin, N., Sun, G., Ouyang, H., et al. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c02696 · Cited by 37 · see citing works

Keys to the switch of fat burning: stimuli that trigger the uncoupling protein 1 (UCP1) activation in adipose tissue

Gong, D., Lei, J., He, X., Hao, J., Zhang, F., Huang, X., Gu, W., Yang, X., & Yu, J. (2024) · Lipids in Health and Disease · doi:10.1186/s12944-024-02300-z · Cited by 36 · see citing works

The concept of probiotics, prebiotics, postbiotics, synbiotics, nutribiotics, and pharmabiotics

Chaudhari, A., & Dwivedi, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823733-5.00013-1 · Cited by 35 · see citing works

Intermittent Fasting Regulates Metabolic Homeostasis and Improves Cardiovascular Health

Diab, R., Dimachkie, L., Zein, O., Dakroub, A. H., & Eid, A. H. (2024) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-024-01314-9 · Cited by 38 · see citing works

Effects of protocatechuic acid on ameliorating lipid profiles and cardio-protection against coronary artery disease in high fat and fructose diet fed in rats

Li, L., Shuo, L. I. U., Tang, H., Song, S.-Q., Lu, L., Zhang, P., & Li, X. (2020) · Journal of Veterinary Medical Science · doi:10.1292/jvms.20-0245 · Cited by 34 · see citing works

Metabolomic Connections between Schizophrenia, Antipsychotic Drugs and Metabolic Syndrome: A Variety of Players

Molina, J. D. D., Avila, S., Rubio, G., & Lopez-Munoz, F. J. (2021) · Current Pharmaceutical Design · doi:10.2174/1381612827666210804110139 · Cited by 34 · see citing works

Zeaxanthin ameliorates obesity by activating the β3-adrenergic receptor to stimulate inguinal fat thermogenesis and modulating the gut microbiota

Xie, J., Liu, M., Liu, H., Jin, Z., Guan, F., Ge, S., Yan, J., Zheng, M., Cai, D., & Liu, J. (2021) · Food & Function · doi:10.1039/d1fo02863d · Cited by 34 · see citing works

DNA Methylation in Babies Born to Nonsmoking Mothers Exposed to Secondhand Smoke during Pregnancy: An Epigenome-Wide Association Study

Fuemmeler, B. F., Dozmorov, M. G., Do, E. K., Zhang, J. J., Grenier, C., Huang, Z., Maguire, R. L., Kollins, S. H., Hoyo, C., & Murphy, S. K. (2021) · Environmental Health Perspectives · doi:10.1289/ehp8099 · Cited by 30 · see citing works

The Impact of a Very-Low-Calorie Ketogenic Diet in the Gut Microbiota Composition in Obesity

Zambrano, A. K., Cadena-Ullauri, S., Guevara‐Ramírez, P., Frías-Toral, E., Ruiz‐Pozo, V. A., Paz‐Cruz, E., Tamayo‐Trujillo, R., Chapela, S. P., Montalván, M., Sarno, G., et al. (2023) · Nutrients · doi:10.3390/nu15122728 · Cited by 30 · see citing works

Sick Individuals and Sick (Microbial) Populations: Challenges in Epidemiology and the Microbiome

Renson, A., Herd, P., & Dowd, J. B. (2019) · Annual Review of Public Health · doi:10.1146/annurev-publhealth-040119-094423 · Cited by 28 · see citing works

Modulation of adipose tissue metabolism by microbial-derived metabolites

Liu, W., Ge, Y., Liu, P., Jiang, X. M., & Xin, Y. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1031498 · Cited by 30 · see citing works

Role of the Gut Microbiome in Beta Cell and Adipose Tissue Crosstalk: A Review

Martínez‐Montoro, J. I., Damas-Fuentes, M., Fernández‐García, J. C., & Tinahones, F. J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.869951 · Cited by 28 · see citing works

Exercise-Induced Adipose Tissue Thermogenesis and Browning: How to Explain the Conflicting Findings?

Zhu, Y., Qi, Z., & Ding, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113142 · Cited by 26 · see citing works

Gamma-Aminobutyric Acid Promotes Beige Adipocyte Reconstruction by Modulating the Gut Microbiota in Obese Mice

Ma, X., Yan, H., Hong, S., Yu, S., Gong, Y., Wu, D., Li, Y., & Xiao, H. (2023) · Nutrients · doi:10.3390/nu15020456 · Cited by 23 · see citing works

Control of Adipose Cell Browning and Its Therapeutic Potential

Lizcano, F., & Arroyave, F. (2020) · Metabolites · doi:10.3390/metabo10110471 · Cited by 23 · see citing works

Food phenolics stimulate adipocyte browning via regulating gut microecology

Wang, Z., Zeng, M., Wang, Z., Qin, F., Wang, Y., Chen, J., Christian, M., & He, Z. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1997905 · Cited by 22 · see citing works

Fu brick tea protects against high-fat diet-induced obesity phenotypes via promoting adipose browning and thermogenesis in association with gut microbiota

Du, H., Shi, L. S., Yan, T., Wang, Q., Wang, Y., Zhao, Y., & Yang, X. (2022) · Food & Function · doi:10.1039/d2fo02063g · Cited by 20 · see citing works

Aqueous extracts of Aconite promote thermogenesis in rats with hypothermia via regulating gut microbiota and bile acid metabolism

Liu, J., Tan, Y., Ao, H., Feng, W., & Peng, C. Y. (2021) · Chinese Medicine · doi:10.1186/s13020-021-00437-y · Cited by 20 · see citing works

Weight Loss Supplements

Dini, I., & Mancusi, A. (2023) · Molecules · doi:10.3390/molecules28145357 · Cited by 19 · see citing works

Brown Adipose Tissue: New Challenges for Prevention of Childhood Obesity. A Narrative Review

Verduci, E., Calcaterra, V., Profio, E. D., Fiore, G., Rey, F., Magenes, V. C., Todisco, C. F., Carelli, S., & Zuccotti, G. (2021) · Nutrients · doi:10.3390/nu13051450 · Cited by 20 · see citing works

Anthropometric and DXA-derived measures of body composition in relation to pre-diabetes among adults

Mohammad, A., Ziyab, A. H., & Mohammad, T. (2023) · BMJ Open Diabetes Research & Care · doi:10.1136/bmjdrc-2023-003412 · Cited by 18 · see citing works

Modulation of Gut Microbiota and Metabolites by Berberine in Treating Mice With Disturbances in Glucose and Lipid Metabolism

Fang, X., Wu, H., Wang, X., Lian, F., Li, M., Miao, R., Wei, J., & Tian, J. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.870407 · Cited by 18 · see citing works

In-situ biogenic FeS boosted acetate accumulation through CO2 capture and valorization using microbial electrosynthesis (MES)

Wu, H., Ding, L., Wang, H., Man, S., Kim, J., Qiu, L., & Yan, Q. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.152563 · Cited by 14 · see citing works

The Role of Leptin Levels in Adaptation to Cold Climates

Никанорова, А. А., Алексеевич, Б. Н., Сергеевич, Н. С., Пшенникова, В. Г., Solovyev, A. V., Romanov, G. P., Семеновна, К. С., Sazonov, N. N., Бурцева, Т. Е., Odland, J. Ø., et al. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17061854 · Cited by 14 · see citing works

Soybean oil-based HFD induces gut dysbiosis that leads to steatosis, hepatic inflammation and insulin resistance in mice

JACOB, T. K., Sindhu, S. T. A. K., Hasan, A., Malik, M. Z., Arefanian, H., Al‐Rashed, F., Nizam, R., Kochumon, S., Thomas, R., Bahman, F., et al. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1407258 · Cited by 14 · see citing works

Common traits between the beige fat-inducing stimuli

Stojanović, O., Kieser, S., & Trajkovski, M. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.05.011 · Cited by 13 · see citing works

Mucosa-associated microbiota in the jejunum of patients with morbid obesity: alterations in states of insulin resistance and metformin treatment

Gutiérrez‐Repiso, C., Moreno‐Indias, I., Martín‐Núñez, G. M., Ho‐Plagaro, A., Rodríguez‐Cañete, A., Gonzalo, M., García‐Fuentes, E., & Tinahones, F. J. (2020) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2020.04.008 · Cited by 14 · see citing works

The Relationship between Circulating Acetate and Human Insulin Resistance before and after Weight Loss in the DiOGenes Study

Hernández, M. A. G., Canfora, E. E., Pasmans, K., Astrup, A. V., Saris, W. H. M., & Blaak, E. E. (2020) · Nutrients · doi:10.3390/nu12020339 · Cited by 13 · see citing works

Antibiotic Treatment Reduces the Health Benefits of Soy Protein

Sánchez‐Tapia, M., Moreno-Vicencio, D., Ordáz‐Nava, G., Guevara‐Cruz, M., Granados‐Portillo, O., Vargas‐Castillo, A., Torres, N., & Tovar, A. R. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000532 · Cited by 13 · see citing works

Urinary Microbiota and Serum Metabolite Analysis in Patients with Diabetic Kidney Disease

Yang, Y. H., Ma, C., Li, S., Cai, W., Dai, W., Zhang, X., Yin, L., Tang, D., Liu, F., & Dai, Y. (2022) · Heliyon · doi:10.1016/j.heliyon.2023.e17040 · Cited by 12 · see citing works

New Mediators in the Crosstalk between Different Adipose Tissues

Gómez‐Hernández, A., Heras, N. D. L., Gálvez, B. G., Fernández‐Marcelo, T., Fernández‐Millán, E., & Escribano, Ó. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094659 · Cited by 12 · see citing works

Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia

Никанорова, А. А., Алексеевич, Б. Н., Геннадиевна, П. В., Gotovtsev, N. N., Romanov, G. P., Solovyev, A. V., Семеновна, К. С., Sazonov, N. N., & Федорова, С. А. (2022) · Genes · doi:10.3390/genes13091612 · Cited by 11 · see citing works

Relationships between rumen microbes, short-chain fatty acids, and markers of white adipose tissue browning during the cold season in grazing Mongolian sheep (Ovis aries)

Zhang, Y., Zhao, Y., Li, C., Wang, L., Tian, F., Erdene, K., Ao, C., & Hai, J. (2022) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2022.103386 · Cited by 12 · see citing works

Polyphenols Influence the Development of Endometrial Cancer by Modulating the Gut Microbiota

Baranowska‐Wójcik, E., Winiarska‐Mieczan, A., Olcha, P., Kwiecień, M., Jachimowicz-Rogowska, K., Nowakowski, Ł., Miturski, A., & Gałczyński, K. (2024) · Nutrients · doi:10.3390/nu16050681 · Cited by 12 · see citing works

Fecal microbiota composition is related to brown adipose tissue 18F-fluorodeoxyglucose uptake in young adults

Ortiz-Alvarez, L., Acosta, F. M., Xu, H., Sánchez‐Delgado, G., Vilchez‐Vargas, R., Link, A., Plaza‐Díaz, J., Elvira, J. M. L., Gil, Á., Labayen, I., et al. (2022) · Journal of Endocrinological Investigation · doi:10.1007/s40618-022-01936-x · Cited by 12 · see citing works

Distinct Gut Microbiome Induced by Different Feeding Regimes in Weaned Piglets

Zhang, J., Long, X., Liao, Q., Chai, J., Zhang, T., Chen, L., He, H., Yuan, Y., Wan, K., Wang, J., et al. (2022) · Genes · doi:10.3390/genes14010049 · Cited by 9 · see citing works

The effect of chronic intermittent hypobaric hypoxia improving liver damage in metabolic syndrome rats through ferritinophagy

Cui, F., Mi, H., Wang, R., Du, Y., Li, F., Chang, S., Su, Y., Liu, A., & Shi, M. (2023) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-023-02860-6 · Cited by 7 · see citing works

Understanding the Roles of Selenium on Thyroid Hormone-Induced Thermogenesis in Adipose Tissue

Ruswandi, Y. A. R., Lesmana, R., Rosdianto, A. M., Gunadi, J. W., Goenawan, H., & Zulhendri, F. (2023) · Biological Trace Element Research · doi:10.1007/s12011-023-03854-2 · Cited by 7 · see citing works

Effects of Time-Restricted Eating (Early and Late) Combined with Energy Restriction vs. Energy Restriction Alone on the Gut Microbiome in Adults with Obesity

Habe, B., Črešnovar, T., Hladnik, M., Pražnikar, J., Kenig, S., Bandelj, D., Mohorko, N., Petelin, A., & Pražnikar, Z. J. (2025) · Nutrients · doi:10.3390/nu17142284 · Cited by 6 · see citing works

Short-chain fatty acids

Dagbasi, A., Cai, M., Hirdaramani, A., Hanyaloglu, A. C., Morrison, D. J., & Frost, G. S. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01579-9 · Cited by 6 · see citing works

Diacylglycerol Acetyltransferase Gene Isolated from Euonymus europaeus L. Altered Lipid Metabolism in Transgenic Plant towards the Production of Acetylated Triacylglycerols

Mihálik, D., Lančaričová, A., Mrkvová, M., Kaňuková, Š., Moravčí­ková, J., Glasa, M., Šubr, Z., Predajňa, L., Hančinský, R., Grešíková, S., et al. (2020) · Life · doi:10.3390/life10090205 · Cited by 6 · see citing works

Role of Protocatechuic Acid in Obesity-Related Pathologies: An Update

D’Archivio, M., Scazzocchio, B., Silenzi, A., Giovannini, C., & Masella, R. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813006-3.00014-3 · Cited by 6 · see citing works

Multiomics strategy-based obesity biomarkers discovery for precision medicine

Ye, Z.-W., Yang, Q.-Y., Xu, W., Li, F., Luo, P., Qin, S., & Wang, F. (2025) · International Journal of Obesity · doi:10.1038/s41366-025-01906-2 · Cited by 5 · see citing works

Mitigative effect of natural resistant starch from kudzu on intestinal-hepatic injury in mice exposed to high-fat diet and dextran sulfate sodium

Dong, H., Zhu, F., Yang, M., Zhang, L., Liu, X., Zhang, H., Huang, Y., Zhu, W., & Xie, L. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.151338 · Cited by 5 · see citing works

Dietary Supplementation With Yeast Cell Wall Modulates Gut Microbiota and SCFAs Production to Improve Intestinal Health in Adult Cats

Liu, X., Wang, H., Lu, Y., Jin, G., Fu, L., Mao, H., Wu, Y., & Liu, P. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.71007 · Cited by 4 · see citing works

МІКРОБІОМ ТА ОЖИРІННЯ

Мельник, Т., & Pivtorak, K. V. (2024) · ГРААЛЬ НАУКИ · doi:10.36074/grail-of-science.12.04.2024.065 · Cited by 3 · see citing works

Gut microbiota composition combined with reduced intestinal fatty acid uptake prevents hepatic steatosis in obesity-resistant mice fed a high-fat diet

Vratarić, M., Teofilović, A., Milutinović, D. V., Veličković, N. A., Đmura, G., & Djordjevic, A. D. (2025) · Scientific Reports · doi:10.1038/s41598-025-20768-2 · Cited by 2 · see citing works

Role of terpenes and terpenoids in cross-talk between adipocyte browning and gut microbiome in obesity

Pillay, D., Kuppusamy, U. R., & Arumugam, B. (2026) · Fitoterapia · doi:10.1016/j.fitote.2026.107113 · Cited by 2 · see citing works

Zongyangia acetica sp. nov. and Blautia acetica sp. nov., two acetate-producing bacteria isolated from human fecal in the order Eubacteriales

Chen, H.-Y., Sun, X., Huang, H., Huang, W.-Q., Liu, C., & Liu, S. (2026) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2026.126696 · Cited by 2 · see citing works

A sympathetic gut connection drives the metabolic benefits of Roux-en-Y gastric bypass

Hankir, M. K. (2020) · Cell Stress · doi:10.15698/cst2020.12.236 · Cited by 2 · see citing works

The Emerging Role of Gut Microbiota in Metabolic Diseases

Safi, S. Z. (2024) · Premier journal of science. · doi:10.70389/pjs.100020 · Cited by 1 · see citing works

Gut Microbiota Dynamics in Obesity and Metabolic Regulation

Farhood, A. H., & Shalal, S. H. (2025) · Academia Open · doi:10.21070/acopen.10.2025.12579 · Cited by 1 · see citing works

Exploring the gut microbiome in type 2 diabetes across different insulin resistance levels: a machine learning approach

He, Y., Liu, L., Liu, Y., Jia, J., Chen, Y., Zhang, X., & Liu, Y. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1747767 · Cited by 1 · see citing works

Hierarchical analysis of metabolic phenotype reveals distinct microbiota and circulatory transcriptome in metabolic dysfunction–associated steatotic liver disease

Tung, C.-Y., Lin, Y., Chang, Y.-Y., Ruan, J., Chen, P.-C., Chen, C., Yeh, H., Shen, H., Tsai, H., Li, T.-H., et al. (2026) · Gene · doi:10.1016/j.gene.2026.150292 · Cited by 1 · see citing works

Сучасні підходи до терапії синдрому подразненого кишечника через призму осі «кишечник — мозок»

Sirchak, Y. S. (2018) · GASTROENTEROLOGY · doi:10.22141/2308-2097.52.3.2018.141845 · Cited by 1 · see citing works

Implications of microbiota in the pathogenesis of diabetes mellitus and cardiovascular disease

Tănase, D. M., Leustean, A. M., & Gosav, E. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821039-0.00005-8

Diet-Induced Adipocyte Browning

Wiśniewski, O. W., Rajczewski, A., Szumigała, A., & Gibas-Dorna, M. (2021) · Polish Journal of Food and Nutrition Sciences · doi:10.31883/pjfns/143164

Changes of serum and urine microbiota and metabolite spectrum in patients with diabetic kidney diseasePreprint

Yang, Y. H., Li, S., Ma, C., Cai, W., Dai, W., Zhang, X., Yin, L., Tang, D., Liu, F., & Dai, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-1543293/v1

Impact of gut-derived metabollites on substrate metabolism and metabolic health

Gonzalez Hernandez Manuel, A. (2020) · doi:10.26481/dis.20201027mgh

Microbiota intestinal y modulación del tejido adiposo en la patogénesis de la obesidad

Leonario-Rodriguez, M., & Saavedra, N. (2022) · Archivos Latinoamericanos de Nutrición · doi:10.37527/2022.72.2.004

Gut Microbiome and Brown Adipose Tissue

Moreno‐Navarrete, J. M. (2023) · Endocrinology · doi:10.1007/978-3-031-08115-6_6-1

Gut Microbiome and Brown Adipose Tissue

Moreno‐Navarrete, J. M. (2024) · Endocrinology · doi:10.1007/978-3-031-35064-1_6

Weight management: functional foods for a balanced body

Emam‐Djomeh, Z., Samieitousi, S., Gashtasbi, S., Behmadi, H., Azarpazhooh, E., & Ramaswamy, H. S. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-28862-3.00006-6

Puerarin Regulates Gut Homeostasis in T2DM Rats Involving Structural and Functional Alterations of Gut Microbiota and Paneth Cell Function

Wu, Y.-Z., Wang, L., Sun, Y.-X., Yang, W., Wei, X., Tao, Q., Liang, Q., Min, H.-Y., & Gao, Q. (2025) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-025-3831-z

Characterization of gut microbiota and adipose tissues in the regulation of obesity-induced insulin resistance

황인재 (2018)

Temporal relationship among adiposity, gut microbiota, and insulin resistance in a longitudinal human cohort

Deng, K., Shuai, M., Zhang, Z., Jiang, Z., Fu, Y., Shen, L., Zheng, J., & Chen, Y. (2022) · BMC Medicine · doi:10.1186/s12916-022-02376-3 · Cited by 54 · see citing works

Modulation of the gut microbiome-adipose tissue axis by maqui supplementation improved insulin resistance and lipid metabolism in mice under a high-fat diet

Tume, R., Cruz, M. B., Sandoval, V., Iglesias-Vejar, L., Sanz‐Lamora, H., Pérez‐Martí, A., Torres‐Oteros, D., Cubedo, M., Carmona-Pontaque, F., Martínez‐Huélamo, M., et al. (2026) · Food Chemistry Molecular Sciences · doi:10.1016/j.fochms.2026.100383

Multiomics of the intestine-liver-adipose axis in multiple studies unveils a consistent link of the gut microbiota and the antiviral response with systemic glucose metabolism

Castells‐Nobau, A., Moreno‐Navarrete, J. M., de la Vega-Correa, L., Puig, I., Federici, M., Sun, J., Burcelin, R., Guzylack‐Piriou, L., Gourdy, P., Cazals, L., et al. (2024) · Gut · doi:10.1136/gutjnl-2024-332602 · Cited by 25 · see citing works

Negative association of acetate with visceral adipose tissue and insulin levels

Layden, B. T., Yalamanchi, S. K., Wolever, T. M. S., Dunaif, A., & Lowe Jr, W. L. (2012) · DOAJ (DOAJ: Directory of Open Access Journals)