Human gut bacteria as potent class I histone deacetylase inhibitors in vitro through production of butyric acid and valeric acid

Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy

Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951

Gut microbiota, metabolites and host immunity

Rooks, M. G., & Garrett, W. S. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.42 · Cited by 3,409

Formation of propionate and butyrate by the human colonic microbiota

Louis, P., & Flint, H. J. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13589 · Cited by 3,028

Epigenetic modifications and human disease

Portela, A., & Esteller, M. (2010) · Nature Biotechnology · doi:10.1038/nbt.1685 · Cited by 2,938

The gut microbiota influences blood-brain barrier permeability in mice

Braniste, V., Al-Asmakh, M., Kowal, C., Anuar, F., Abbaspour, A., Tóth, M., Korecka, A., Bakocevic, N., Ng, L. G., Kundu, P., et al. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3009759 · Cited by 2,530

Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota

MetaHIT consortium, Forslund, K., Hildebrand, F., Nielsen, T., Falony, G., Le Chatelier, E., Sunagawa, S., Prifti, E., Vieira-Silva, S., Gudmundsdottir, V., et al. (2015) · Nature · doi:10.1038/nature15766 · Cited by 2,116

New and emerging HDAC inhibitors for cancer treatment

West, A. C., & Johnstone, R. W. (2014) · Journal of Clinical Investigation · doi:10.1172/jci69738 · Cited by 1,404

New evidences on the altered gut microbiota in autism spectrum disorders

Strati, F., Cavalieri, D., Albanese, D., De Felice, C., Donati, C., Hayek, J., Jousson, O., Leoncini, S., Renzi, D., Calabrò, A., et al. (2017) · Microbiome · doi:10.1186/s40168-017-0242-1 · Cited by 1,040

Gut microbes and the brain: paradigm shift in neuroscience

Mayer, E. A., Knight, R., Mazmanian, S. K., Cryan, J. F., & Tillisch, K. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3299-14.2014 · Cited by 1,033

Exogenous Stimuli Maintain Intraepithelial Lymphocytes via Aryl Hydrocarbon Receptor Activation

Li, Y., Innocentin, S., Withers, D. R., Roberts, N. A., Gallagher, A., Grigorieva, E. F., Wilhelm, C., & Veldhoen, M. (2011) · Cell · doi:10.1016/j.cell.2011.09.025 · Cited by 837

Night-Restricted Feeding Improves Gut Health by Synchronizing Microbe-Driven Serotonin Rhythm and Eating Activity-Driven Body Temperature Oscillations in Growing Rabbits

Wang, Q., Guo, Y., Zhang, K., Zhang, L., Geng, S., Shan, C., Liu, P., Zhu, M., Jin, Q.-Y., Zhong-ying, L., et al. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.771088 · Cited by 26

Sodium Butyrate Inhibits Neovascularization Partially via TNXIP/VEGFR2 Pathway

Xiao, X., Chen, M., Xu, Y., Huang, S., Liang, J., Cao, Y., & Chen, H. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/6415671 · Cited by 24

Nicotinamide Ameliorates Dextran Sulfate Sodium-Induced Chronic Colitis in Mice through Its Anti-Inflammatory Properties and Modulates the Gut Microbiota

Kang, K., Sun, Y., Pan, D., Chang, B., & Sang, L.-X. (2021) · Journal of Immunology Research · doi:10.1155/2021/5084713 · Cited by 24

Clinical Management of the Microbiome in Irritable Bowel Syndrome

Andrews, C. N., Sidani, S., & Marshall, J. K. (2019) · Journal of the Canadian Association of Gastroenterology · doi:10.1093/jcag/gwz037 · Cited by 25

Pinto beans modulate the gut microbiome, augment MHC II protein, and antimicrobial peptide gene expression in mice fed a normal or western-style diet

Ojo, B. A., Lu, P., Alake, S. E., Keirns, B. H., Anderson, K. L., Gallucci, G., Hart, M. D., El-Rassi, G. D., Ritchey, J. W., Chowanadisai, W., et al. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108543 · Cited by 22

Microbial community networks across body sites are associated with susceptibility to respiratory infections in infants

Reyman, M., Clerc, M., van Houten, M. A., Arp, K., Chu, M. L. J. N., Hasrat, R., Sanders, E. A. M., & Bogaert, D. (2021) · Communications Biology · doi:10.1038/s42003-021-02755-1 · Cited by 24

A Screening of Native (Poly)phenols and Gut‐Related Metabolites on 3D HCT116 Spheroids Reveals Gut Health Benefits of a Flavan‐3‐ol Metabolite

Rubert, J., Gatto, P., Pancher, M., Sidarovich, V., Curti, C., Mena, P. R., Rio, D. D., Quattrone, A., & Mattivi, F. (2022) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202101043 · Cited by 23

Association Between the Gut Microbiota and Alzheimer’s Disease: An Update on Signaling Pathways and Translational Therapeutics

Kulkarni, R., Kumari, S., Dhapola, R., Sharma, P., Singh, S. K., Medhi, B., & HariKrishnaReddy, D. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04545-2 · Cited by 26

The differential crosstalk of the skin–gut microbiome axis as a new emerging actor in systemic sclerosis

Russo, E., Bellando-Randone, S., Carboni, D., Fioretto, B. S., Romano, E., Baldi, S., Aoufy, K. E., Ramazzotti, M., Rosa, I., Lepri, G., et al. (2023) · Rheumatology · doi:10.1093/rheumatology/kead208 · Cited by 22

GC-MS-based fecal metabolomics reveals gender-attributed fecal signatures in ankylosing spondylitis

He, Z., Wang, M., Li, H., & Wen, C. (2019) · Scientific Reports · doi:10.1038/s41598-019-40351-w · Cited by 22

Gut–Adipose Tissue Axis and Metabolic Health

Borozan, S., Fernandez, C. J., Samee, A., & Pappachan, J. M. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47060424 · Cited by 21

Dietary phytochemicals that influence gut microbiota: Roles and actions as anti-Alzheimer agents

Wang, Y., Lim, Y. Y., He, Z., Wong, W., & Lai, W. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1882381 · Cited by 23

The Role of the Gut Microbiota and Microbial Metabolites in the Pathogenesis of Alzheimer’s Disease

Wang, Y. (2022) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527321666220417005115 · Cited by 21

Role of Gut Microbiota, Immune Imbalance, and Allostatic Load in the Occurrence and Development of Diabetic Kidney Disease

Han, Y. Z., Zheng, H., Du, B. X., Zhang, Y., Zhu, X. Y., Li, J., Wang, Y., & Liu, W. J. (2023) · Journal of Diabetes Research · doi:10.1155/2023/8871677 · Cited by 21

The potential influence of microplastics on the microbiome and disease susceptibility in sea turtles

Iurk, V. B., Ingles, M., Correa, G. S., Silva, C. R., Staichak, G., Pileggi, S. A. V., Christo, S. W., Domit, C., & Pileggi, M. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.174298 · Cited by 21

Determination of prebiotic activity and probiotic encapsulation ability of inulin type fructans obtained from Inula helenium roots

Dikmen, H., Özcan, F. Ş., Özcan, N. A., Bozkurt, F., & Sağdıç, O. (2024) · Journal of Food Science · doi:10.1111/1750-3841.17261 · Cited by 23

The Role of Histone Acetylation and the Microbiome in Phytochemical Efficacy for Cardiovascular Diseases

Evans, L. W., Athukorala, M., Martinez, K., & Ferguson, B. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114006 · Cited by 22

Interaction between gut microbiota and T cell immunity in colorectal cancer

Jing, Z., Wu, Y., Chu, J., Zhanbo, Q., Wu, X., & Han, S. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103807 · Cited by 20

Metabolic Analysis of Regionally Distinct Gut Microbial Communities Using an In Vitro Platform

Firrman, J., Liu, L., Tanes, C., Friedman, E. S., Bittinger, K. L., Daniel, S. G., den Abbeele, P. V., & Evans, B. S. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b05202 · Cited by 19

Characteristics of Intestinal Microbiota in Japanese Patients with Mild Cognitive Impairment and a Risk-Estimating Method for the Disorder

Hatayama, K., Ebara, A., Okuma, K., Tokuno, H., Hasuko, K., Masuyama, H., Ashikari, I., & Shirasawa, T. (2023) · Biomedicines · doi:10.3390/biomedicines11071789 · Cited by 21

Chemical interplay between gut microbiota and epigenetics: Implications in circadian biology

Sharma, S. A., Oladejo, S. O., & Kuang, Z. (2024) · Cell chemical biology · doi:10.1016/j.chembiol.2024.04.016 · Cited by 19

Short-chain fatty and carboxylic acid changes associated with fecal microbiota transplant communally influence microglial inflammation

Churchward, M. A., Michaud, E. R., Mullish, B. H., Blanco, J. M., Perez, I. G., Marchesi, J. R., Xu, H., Kao, D. H., & Todd, K. G. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e16908 · Cited by 20

Assessment of in vitro digestion of reduced sugar biscuits with extruded brewers’ spent grain

Gutiérrez-Barrutia, M. B., Cozzano, S., Arcia, P., & del Castillo, M. D. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113160 · Cited by 18

Metabolic Interaction Between Host and the Gut Microbiota During High-Fat Diet-Induced Colorectal Cancer

Lee, C., Lee, S., & Yoo, W. (2024) · The Journal of Microbiology · doi:10.1007/s12275-024-00123-2 · Cited by 20

Potential antitumor effects of short-chain fatty acids in breast cancer models

Muradás, T. C., Freitas, R. D. S., Gonçalves, J. I. B., Xavier, F. A. C., & Marinowic, D. R. (2024) · American Journal of Cancer Research · doi:10.62347/etuq6763 · Cited by 21

Megasphaera contributes to lactate-driven valerate production in the human gut

Huertas‐Díaz, L., Elvan, M., Marietou, A., Hosek, J., Thams, L., Dalgaard, L. B., Hansen, M., & Schwab, C. (2025) · Microbiome · doi:10.1186/s40168-025-02207-6 · Cited by 17

Microbial natural compounds and secondary metabolites as Immunomodulators: A review

Mahmoudi, F., Jalayeri, M. H. T., Montaseri, A., Khosroshahi, L. M., & Baradaran, B. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.134778 · Cited by 20

Therapeutic innovation in Parkinson’s disease: a 2020 update on disease-modifying approaches

Colombo, D., Pnevmatikou, P., Melloni, E., & Keywood, C. (2020) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2020.1800454 · Cited by 18

Host and microbial-derived metabolites for Clostridioides difficile infection: Contributions, mechanisms and potential applications

Gao, Y., Ma, L., & Su, J. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127113 · Cited by 17

Therapeutics Targeting the Gut Microbiome: Rigorous Pipelines for Drug Development

Markey, K. A., van den Brink, M. R. M., & Peled, J. U. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.01.022 · Cited by 16

Up-regulation of neprilysin mediates the protection of fructo-oligosaccharides against Alzheimer's disease

Wu, S., Zhang, J., Jiang, C., Wang, S., Que, R., & An, L. (2020) · Food & Function · doi:10.1039/d0fo00161a · Cited by 16

Social Isolation and Breast Cancer

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

Recent advances in antiviral effects of probiotics: potential mechanism study in prevention and treatment of SARS-CoV-2

Montazeri‐Najafabady, N., Kazemi, K., & Gholami, A. (2022) · Biologia · doi:10.1007/s11756-022-01147-y · Cited by 16

The correlation between gut and intra-tumor microbiota and PDAC: Etiology, diagnostics and therapeutics

Qian, J., Zhang, X., Wei, B., Tang, Z., & Zhang, B. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.188943 · Cited by 16

Dietary butyrate and valerate glycerides impact diarrhea severity and immune response of weaned piglets under ETEC F4-ETEC F18 coinfection conditions

Kovanda, L. L., Park, J., Park, S., Kim, K., Li, X., & Liu, Y. (2023) · Journal of Animal Science · doi:10.1093/jas/skad401 · Cited by 17

Genetic and epigenetic perspective of microbiota

Celiker, C., & Kalkan, R. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10849-9 · Cited by 15

Dietary fiber derived short-chain fatty acids as a critical driver of the gut–bone axis in animal bone health: A review

Zulfiqar, Z., Huang, S., & Shi, Y. (2025) · Animal nutrition · doi:10.1016/j.aninu.2025.05.002 · Cited by 17

The gut microbiota composition is linked to subsequent occurrence of ventilator-associated pneumonia in critically ill patients

Orieux, A., Enaud, R., Imbert, S., Boyer, P., Begot, E., Camino, A., Boyer, A., Berger, P., Gruson, D., Delhaès, L., et al. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.00641-23 · Cited by 14

Self-assembling butyric acid prodrug acts as a sensitizer for cancer radiotherapy

Shashni, B., & Nagasaki, Y. (2023) · Nano Today · doi:10.1016/j.nantod.2023.102103 · Cited by 14

Dietary patterns interfere with gut microbiota to combat obesity

Lou, X., Li, P., Luo, X., Lei, Z., Liu, X., Liu, Y., Gao, L., Xu, W., & Liu, X. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1387394 · Cited by 20

Non-invasive VOCs detection to monitor the gut microbiota metabolism in-vitro

Dell’Olio, A., Rubert, J., Capozzi, V., Tonezzer, M., Betta, E., Fogliano, V., & Franco Biasioli, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-66303-7 · Cited by 14

Predicting Inchinkoto efficacy, in patients with obstructive jaundice associated with malignant tumors, through pharmacomicrobiomics

Yamashita, H., Nishiyama, M., Ohbuchi, K., Kanno, H., Tsuchiya, K., Yamaguchi, J., Mizuno, T., Ebata, T., Nagino, M., & Yokoyama, Y. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105981 · Cited by 13

Specific Gut Microbiome Signatures in Children with Cow’s Milk Allergy

Moriki, D., León, E. D., García-Gamero, G., Jiménez‐Hernández, N., Artacho, A., Pons, X., Koumpagioti, D., Dinopoulos, A., Papaevangelou, V., Priftis, K. Ν., et al. (2024) · Nutrients · doi:10.3390/nu16162752 · Cited by 13

Urinary fatty acid biomarkers for prostate cancer detection

Landa, E. N., Quaye, G. E., Su, X., Badmos, S., Holbrook, K. L., Polascik, T. J., Adams, E. S., DEIVASIGAMANI, S. R., Gao, Q., Annabi, M. H., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0297615 · Cited by 12

Gut Microbiota and Epigenetics in Colorectal Cancer: Implications for Carcinogenesis and Therapeutic Intervention

Pandey, M., & Bhattacharyya, J. (2024) · Epigenomics · doi:10.2217/epi-2023-0382 · Cited by 13

Mechanisms of Male Reproductive Sterility Triggered by Dysbiosis of Intestinal Microorganisms

Wei, M., Liu, H., Wang, Y., Sun, M., & Shang, P. (2024) · Life · doi:10.3390/life14060694 · Cited by 15

New findings in the metabolism of the saffron apocarotenoids, crocins and crocetin, by the human gut microbiota

García, C. J., Beltrán, D., Frutos-Lisón, M. D., García‐Conesa, M., Tomás-Barberán, F. A., & Garcı́a-Villalba, R. (2024) · Food & Function · doi:10.1039/d4fo02233e · Cited by 12

Metabolites in the Dance: Deciphering Gut-Microbiota-Mediated Metabolic Reprogramming of the Breast Tumor Microenvironment

Altrawy, A., Khalifa, M. M., Abdelmaksoud, A., khaled, Y., Saleh, Z. M., Sobhy, H., Abdel-Ghany, S. E., Alqosaibi, A. I., Almuhanna, A., Almulhim, J., et al. (2024) · Cancers · doi:10.3390/cancers16244132 · Cited by 13

Mexican Traditional Plant-Foods: Polyphenols Bioavailability, Gut Microbiota Metabolism and Impact Human Health

Mercado‐Mercado, G., Blancas‐Benítez, F. J., Zamora-Gasga, V. M., & Sáyago‐Ayerdi, S. G. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666191011093753 · Cited by 15

Effects of fecal microbiota transplantation from yaks on weaning diarrhea, fecal microbiota composition, microbial network structure and functional pathways in Chinese Holstein calves

Li, Y., Li, X. V., Wu, Y., & Zhang, W. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.898505 · Cited by 12

Molecular and genetic aspects of health risks and their association with adverse environmental conditions and diets (systemic review)

Mazhaeva, T. V., Dubenko, S. E., Chernova, J. S., & Nosova, I. A. (2022) · Health Risk Analysis · doi:10.21668/health.risk/2022.4.18 · Cited by 11

Exercise reshapes gut microbiota to ameliorate core symptoms in PCOS: molecular mechanisms and therapeutic implications

Li, Q., Chen, L., & Wang, R. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1652731 · Cited by 14

A specific structure and high richness characterize intestinal microbiota of HIV-exposed seronegative individuals

Lopera, T. J., Luján, J., Zurek, E. E., Zapata, W., Hernández, J. C., Toro-Londoño, M., Álzate, J. F., Taborda, N. A., Rugeles, M. T., & Aguilar-Jiménez, W. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260729 · Cited by 11

Retinoic Acid Signaling Is Compromised in DSS-Induced Dysbiosis

Li, Y., Sheng, L., Jena, P. K., Gilbert, M. C., Wan, Y. Y., & Mao, H. (2022) · Nutrients · doi:10.3390/nu14142788 · Cited by 12

Lung microbiota and potential treatment of respiratory diseases

Zhou, Y., Liu, M., Liu, K., Wu, G., & Tan, Y. (2023) · Microbial Pathogenesis · doi:10.1016/j.micpath.2023.106197 · Cited by 13

Research on preventive effect of Akkermansia muciniphila AKK PROBIO on acute gouty arthritis in mice

Ma, X., Zhu, N., Yu, X., Wang, W., & Wu, W. (2024) · Food Science & Nutrition · doi:10.1002/fsn3.4367 · Cited by 12

Prebiotics in vitro digestion by gut microbes, products’ chemistry, and clinical relevance

Ashaolu, T. J., & Ashaolu, J. O. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-11021-z · Cited by 11

Modulation of gut flore by dietary fibers from Pyrus bretschneideri Rehd.: Evaluation of fermentation characteristics using a colonic in vitro fermentation model

Liang, X., Liu, H., Wei, Z., Ye, G., Xu, L., Ye, Y., & Qin, J. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105466 · Cited by 10

Effects of a Sorghum Beverage with Lacticaseibacillus paracasei on Body Composition, Lipid Profiles, and Intestinal Health in Overweight and Obese Adults: A Randomized Single-Blind Pilot Study

da Silva, L. A., José, V. P. B. D. S., Rodrigues, L. A., do Prado, P. V. C., Toledo, R. C. L., de Barros, F. A. R., de Souza, A. M., Antoniassi, R., de Carvalho, C. W. P., Queiróz, V. A. V., et al. (2024) · Foods · doi:10.3390/foods13193128 · Cited by 10

The nexus of gut microbiota, diet, and health

Bhattarai, S., & Janaswamy, S. (2022) · Functional Food Science · doi:10.31989/ffs.v2i2.885 · Cited by 12

Komagataeibacter hansenii CGMCC 3917 alleviates alcohol-induced liver injury by regulating fatty acid metabolism and intestinal microbiota diversity in mice

Lin, D., Jiang, X., Zhao, Y., Zhai, X., & Yang, X. (2020) · Food & Function · doi:10.1039/c9fo02040c · Cited by 10

Characterization of the “gut microbiota-immunity axis” and microbial lipid metabolites in atrophic and potential celiac disease

Ricci, F., Russo, E., Renzi, D., Baldi, S., Nannini, G., Lami, G., Menicatti, M., Pallecchi, M., Bartolucci, G., Niccolai, E., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.886008 · Cited by 11

Antitumor properties of traditional lactic acid bacteria: Short-chain fatty acid production and interleukin 12 induction

Mobasherpour, P., Yavarmanesh, M., & Dovom, M. R. E. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e36183 · Cited by 9

Sodium butyrate attenuates liver fibrogenesis via promoting H4K8 crotonylation

Tang, R., Zha, H., Liu, R., Lv, J., Cao, D., & Li­, ­. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05274-3 · Cited by 9

Dietary Alaska Pollock Protein Attenuates the Experimental Colitis Induced by Dextran Sulfate Sodium via Regulation of Gut Microbiota and Its Metabolites in Mice

Tanaka, G., Hagihara, N., Hosomi, R., Shimono, T., Kanda, S., Nishiyama, T., Yoshida, M., & Fukunaga, K. (2022) · Metabolites · doi:10.3390/metabo12010044 · Cited by 9

Multispecies probiotic affects fecal short-chain fatty acids in postmenopausal women with obesity: A post hoc analysis of a randomized, double-blind, placebo-controlled study

Łoniewski, I., Szulińska, M., Kaczmarczyk, M., Podsiadło, K., Styburski, D., Skonieczna‐Żydecka, K., & Bogdański, P. (2023) · Nutrition · doi:10.1016/j.nut.2023.112109 · Cited by 10

The role of the gut microbiome and microbial metabolism in mediating opioid-induced changes in the epigenome

Kolli, U., & Roy, S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1233194 · Cited by 9

Antibiotics and probiotics-induced effects on the total fatty acid composition of feces in a rat model

Marosvölgyi, T., Mintál, K., Farkas, N., Sipos, Z., Makszin, L., Szabó, É., Tóth, A., Kocsis, B., Kovács, K., Hormay, E., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-57046-6 · Cited by 9

Aromatics from fossil fuels and breast cancer

Hilakivi-Clarke, L. A., Jolejole, T. K. B., da Silva, J. L., Andrade, F. D. O., Dennison, G., & Mueller, S. (2025) · iScience · doi:10.1016/j.isci.2025.112204 · Cited by 9

Performance Evaluation of a Novel Combination of Four- and Five-Carbon [Butyric and Valeric] Short-Chain Fatty Acid Glyceride Esters in Broilers

Gracia, M. I., Vazquez, P., Ibáñez-Pernía, Y., Pos, J., & Tawde, S. (2024) · Animals · doi:10.3390/ani14040617 · Cited by 8

Decoding host cell interaction– and fluconazole-induced metabolic alterations and drug resistance in Candida auris

Ismail, S. H. H., Hamdy, R., Altaie, A. M., Fayed, B. E., Dakalbab, S., El‐Awady, R., & Soliman, S. S. M. (2024) · Mycologia · doi:10.1080/00275514.2024.2363730 · Cited by 8

Up-flow anaerobic sludge blanket bioreactor for the production of carboxylates: effect of inocula on process performance and microbial communities

Lago, A., Greses, S., Moreno, I., & González‐Fernández, C. (2025) · Bioresources and Bioprocessing · doi:10.1186/s40643-025-00839-y · Cited by 7

Examining the Role of Microbiota-Centered Interventions in Cancer Therapeutics: Applications for Urothelial Carcinoma

Drobner, J. C., Lichtbroun, B. J., Singer, E. A., & Ghodoussipour, S. B. (2023) · Technology in Cancer Research & Treatment · doi:10.1177/15330338231164196 · Cited by 7

A novel hepatocyte ketone production assay to help the selection of nutrients for the ketogenic diet treatment of epilepsy

Meeusen, H., Romagnolo, A., Holsink, S. A. C., van den Broek, T. J. M., van Helvoort, A., Gorter, J. A., van Vliet, E. A., Verkuyl, J. M., Silva, J., & Aronica, E. (2024) · Scientific Reports · doi:10.1038/s41598-024-62723-7 · Cited by 7

Effect of Butyric Acid in the Proliferation and Migration of Junctional Epithelium in the Progression of Periodontitis: An In Vitro Study

Ishikawa, T., Sasaki, D., Aizawa, R., Shimoyama, Y., Yamamoto, M., Irié, T., & Sasaki, M. (2021) · Dentistry Journal · doi:10.3390/dj9040044 · Cited by 7

Foods may modify responsiveness to cancer immune checkpoint blockers by altering both the gut microbiota and activation of estrogen receptors in immune cells

Hilakivi-Clarke, L. A., Verma, V., McDermott, M., Koak, P., & Andrade, F. D. O. (2022) · Frontiers in Microbiomes · doi:10.3389/frmbi.2022.1049688 · Cited by 7

Role of the Intestinal Microbiota in the Genesis of Major Depression and the Response to Antidepressant Drug Therapy: A Narrative Review

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Vildagliptin modulates the microbiota and induces an immunometabolic profile compatible with neuroprotection in type 2 diabetes

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