Polyamines and Gut Microbiota

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

Host-gut microbiota metabolic interactions

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

Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease

Pickard, J. M., Zeng, M. Y., Caruso, R., & Núñez, G. (2017) · Immunological Reviews · doi:10.1111/imr.12567 · Cited by 1,699

Microbial culturomics: paradigm shift in the human gut microbiome study

Lagier, J., Armougom, F., Million, M., Hugon, P., Pagnier, I., Robert, C., Bittar, F., Fournous, G., Gimenez, G., Maraninchi, M., et al. (2012) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12023 · Cited by 1,200

Next-generation probiotics: the spectrum from probiotics to live biotherapeutics

O’Toole, P. W., Marchesi, J. R., & Hill, C. (2017) · Nature Microbiology · doi:10.1038/nmicrobiol.2017.57 · Cited by 971 · cited 1×

A perspective of polyamine metabolism

WALLACE, H. M., Fraser, A. V., & Hughes, A. D. (2003) · Biochemical Journal · doi:10.1042/bj20031327 · Cited by 933

Modulation of cellular function by polyamines

Igarashi, K., & Kashiwagi, K. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.07.009 · Cited by 852

The Gastrointestinal Microbiome: A Review

Barko, P. C., McMichael, M. A., Swanson, K. S., & Williams, D. A. (2018) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.14875 · Cited by 750

Remaining mysteries of molecular biology: the role of polyamines in the cell

Miller-Fleming, L., Olin-Sandoval, V., Campbell, K., & Ralser, M. (2015) · Journal of Molecular Biology · doi:10.1016/j.jmb.2015.06.020 · Cited by 658

Microbial Ecology along the Gastrointestinal Tract

Hillman, E. T., Lu, H., Yao, T., & Nakatsu, C. H. (2017) · Microbes and Environments · doi:10.1264/jsme2.me17017 · Cited by 614

The Salmon Microbial Genome Atlas enables novel insights into bacteria-host interactions via functional mappingPreprint

de León, A. V., Hoetzinger, M., Hensen, T., Gupta, S., Weston, B. R., Johnsen, S. M., Rasmussen, J. A., Clausen, C. G., Pless, L., Verissimo, A. R., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.10.570985 · Cited by 3

Interspecies interactions drive bacterial proteome reorganisation and emergent metabolismPreprint

Kamrad, S., Mozzachiodi, S., Blasche, S., Aulakh, S. K., Scheidweiler, D., Basile, A., Guan, R., Bradley, R., van den Berg, N. I., Mülleder, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.14.653412 · Cited by 3

Gut microbiome: new diagnostic and treatment options

Mayev, I. V., & Lyamina, S. (2024) · Clinical Medicine (Russian Journal) · doi:10.30629/0023-2149-2024-102-4-297-308 · Cited by 2

Site-Specific Gut Microbial Signatures in Non-Celiac Gluten Sensitivity

Dixit, K. K., Ahmed, A., Singh, A., Inamdar, M., Chavan, S., Bodkhe, R., Mehtab, W., Chauhan, A. K., Saroj, S. D., Ahuja, V., et al. (2024) · Gut Microbes Reports · doi:10.1080/29933935.2024.2438621 · Cited by 2

A fluorescence-based assay for measuring aminopropyltransferase activity

Singh, P., Choi, J., & Mamoun, C. B. (2025) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2025.01.067 · Cited by 2

ZuoJin Pill intervention in HCT116 tumor-bearing mice: Modulation of tumor growth, intestinal barrier integrity and microbial composition

Chen, J., Wang, Y., Liu, X., Chen, M. Y., Zang, L., & Wang, G. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156847 · Cited by 2

Spatial metabolic and phenotypic characterization of the germ‐free mouse model

Adams, L., Hulme, H., Dritsa, C., Lynch, C. P., Taylor, V., Raşid, O., Burchmore, R., Goodwin, R. J. A., & Wall, D. M. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.70002 · Cited by 2

Innovative Approaches to Medical Rehabilitation: Regeneration, Immune Training, Homeostasis, and Microbiome Synergy

Garaci, E., Russo, M. A., Pariano, M., Puccetti, M., Fabi, C., Balucchi, S., Bellet, M. M., Ricci, M., Fini, M., & Romani, L. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178687 · Cited by 2

Dysbiosis modulates CD8+ tissue-resident memory cells through a mechanism requiring polyamine metabolism during HIV infection

Jayaraman, S., Mahalingam, S. S., Lederman, M. M., Faddoul, F., da Silva, A. P., Asaad, R. J., Shriver, L. P., Bhaskaran, N., Schneider, E., Heine, G., et al. (2025) · iScience · doi:10.1016/j.isci.2025.113679 · Cited by 2

Integrating gut microbiome and host transcriptomics for the personalized management of IBD

Barry, D., Thachuk, C., & Trink, J. (2025) · Epigenomics · doi:10.1080/17501911.2025.2591594 · Cited by 3

Prebiotic and Probiotic Foods in MASLD: Microbiome-Mediated Therapeutic Strategies

Cui, B., Liu, Y., Joyce, H., Jieying, C., Jia-hang, X., Jian-Peng, T., & Chun, L. H. (2025) · Synthetic biology and engineering · doi:10.70322/sbe.2025.10018 · Cited by 3

Yeast protein modulates metabolites derived from the human gut microbiota of older male adults ex vivo to strengthen gut barrier function and reduce inflammation

den Abbeele, P. V., Vu, L. D., Poppe, J., van Hengel, I. A. J., Baudot, A., Zhang, Y., Chen, Z., & Yan, J. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1697734 · Cited by 2

Biosynthesis of polyamine-polyphosphate granules for colitis alleviation

Fan, Z., Zhang, X., Ge, X., Zhu, L., Zhu, M., & Yang, L. (2026) · iScience · doi:10.1016/j.isci.2026.114679 · Cited by 2

Socioeconomic position and the gut microbiota: a narrative synthesis of the association and recommendations

Ratcliff, J. S., Meena Kumari, B., Varga‐Weisz, P., & O’Gorman, R. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2623356 · Cited by 3

Advanced Real-Time, Non-Destructive Spectral Fingerprinting for Early microbial Spoilage Detection: AI-Integrated Raman Biosensing Platform for Scalable Food Safety and Quality

Bhowmik, D., Rickard, J. J. S., & Oppenheimer, P. G. (2026) · Food Research International · doi:10.1016/j.foodres.2026.118745 · Cited by 2

Probiotic and microbial modulation of polyamine production: an emerging avenue for neuroprotection in neurodegenerative disorders

Adhikari, T., & Saha, P. (2026) · Amino Acids · doi:10.1007/s00726-026-03505-5 · Cited by 2

Influence of postbiotics on the microbiota-gut-brain axis in cognitive impairment and dementia

Kang, T.-B., Lee, J. Y., & Cheon, S. Y. (2026) · Journal of Functional Foods · doi:10.1016/j.jff.2026.107279 · Cited by 2

Gut microbiome dysbiosis in uveitis – mechanistic insights and emerging therapeutic strategies

Suresh, G., Nath, M., Tiwari, A., Halder, N., Chawla, R., & Velpandian, T. (2026) · Experimental Eye Research · doi:10.1016/j.exer.2026.111073 · Cited by 2

Microbiome-orchestrated cross-organ immunity in autoimmunity: from metabolites to therapeutic targets

Rao, X., Zou, L., Cai, X., Yao, Y., & Zhong, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1761834 · Cited by 2

Gut microbiome metabolites meet immunometabolism in inflammatory bowel disease

Li, Q., Formiga, R. D. O., & Sokol, H. (2026) · Trends in Immunology · doi:10.1016/j.it.2026.06.001 · Cited by 2

Paradigm Shift of Microbiota-gut-brain Axis During Aging: Potential Role of Probiotics to Improve Cognitive Decline

Dutta, S., Dutta, T. K., Nanda, P. K., Dhar, P., Das, A. K., & Bhunia, A. K. (2026) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-026-11136-1 · Cited by 2

Gut Microbes and Drosophila Behavior

Kadoguchi, H., Hori, A., & Kuraishi, T. (2022) · Neuromethods · doi:10.1007/978-1-0716-2321-3_5 · Cited by 2

Microbiome therapeutics for the cancer management

Punetha, A., & Punetha, A. K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99336-4.00012-4 · Cited by 2

Commensal Microbes and Their Metabolites: Influence on Host Pathways in Health and Cancer

Méndez, R., Banerjee, S., & Banerjee, S. (2021) · Physiology in health and disease · doi:10.1007/978-3-030-67951-4_10 · Cited by 1

The microbiome and cardiovascular disease: Implications in Precision Medicine

Wang, Z., & Osborn, L. J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-824010-6.00022-8 · Cited by 2

Functional maturation of the gut microbiota at weaning is influenced by maternal environment in pigletsPreprint

Beaumont, M., Cauquil, L., Bertide, A., Ahn, I., Barilly, C., Gil, L., Canlet, C., Zemb, O., Pascal, G., Samson, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.02.022913 · Cited by 2

Biogenic Amines

Suzzi, G., Perpetuini, G., & Tofalo, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818766-1.00243-9 · Cited by 2

Diversity and prevalence of amino acid decarboxylase enzymes in the human gut microbiome – a bioinformatics investigationPreprint

Sandoval, M., & Shah, D. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.06.627230 · Cited by 2

Plasma polyamines during pregnancy and their relationships with maternal allergies and the immune response of the neonates

Gázquez, A., García‐Serna, A. M., Hernández‐Caselles, T., Martín‐Orozco, E., Cantero‐Cano, E., Prieto‐Sánchez, M. T., Molina‐Ruano, M. D., Castillo‐Lacalle, R., Vioqué, J., Morales, E., et al. (2024) · Pediatric Allergy and Immunology · doi:10.1111/pai.14167 · Cited by 1

Microbiome-derived metabolites in cancer-associated anemia: An underexplored mechanistic link

Wang, Z., & Wang, F. (2025) · World Journal of Gastrointestinal Pharmacology and Therapeutics · doi:10.4292/wjgpt.v16.i3.110305 · Cited by 1

Role of gut microbiota in gastrointestinal diseases via microbiota–gut–liver–brain axis and microbiota-centered therapies

Srivastava, A. K., Singh, A., Yadav, D. P., Nath, G., & Ganju, L. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-34039-0.00009-3 · Cited by 1

Enteric microbiome and obesity: a multidimensional narrative review

Barat, B., Ghosh, K., Kulkarni, B. P., Banerjee, P., & Ghosh, K. (2025) · Microbial Genomics · doi:10.1099/mgen.0.001562 · Cited by 1

Bioactive metabolites in neonates of mothers supplemented with Bifidobacterium animalis are linked to microbiota-related compounds in milk and maternal plasma in mice

Rodrigues, P. B., Valentin, C., Woenande, E., Delbauve, S., Vermijlen, D., Köhler, A., Flamand, V., & Everard, A. (2026) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2026.110301 · Cited by 3

The gut-tumor metabolic axis: A comprehensive exploration of bidirectional crosstalk in cancer immunotherapy

Kawuribi, V., Awere‐Duodu, A., Adjei, F. A., Osman, A.-H., Bomansaan, H., Madadi, M. M., Tampuri, J. U., & Adu‐Amankwaah, J. (2026) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2026.105280 · Cited by 2

Panflemmotic triggers to metastatic pathways: Complex signatures of tumorigenesis in the colonic microenvironment

Reyed, R. M., & Prabhakar, P. K. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-36500-3.00008-8 · Cited by 1

Roles of acidic residues in SpeG acetyltransferases—insights into importance for kinetic activity and polyamine binding in allosteric and acceptor sites

Martel, H. N. L., Le, V. T. B., Filippova, E. V., Fenton, A. W., Law, M., Marquez-Ramirez, M., & Kuhn, M. L. (2026) · Biochemical Journal · doi:10.1042/bcj20260162 · Cited by 1

Gut Microbiota in Colorectal Cancer: Mechanistic Insights, Clinical Strategies, and a Regional Perspective with a Focus on Sichuan, China

Liu, Z., Ang, M. Y., & Kue, C. S. (2026) · Cancers · doi:10.3390/cancers18111693 · Cited by 1

Microbiota–Gut–Brain Axis: An Integrative Overview of Communication Pathways

Martínez‐Porchas, M., Medina‐Félix, D., Olivas-Bernal, C. A., Guirado-Flores, J. S. O., Vargas‐Albores, F., Porchas‐Quijada, M., & Garibay-Valdéz, E. (2026) · Advanced Gut & Microbiome Research · doi:10.1155/agm3/8142006 · Cited by 1

Signaling Metabolites in the Gut Microbiota–Organ Axes

Beyoğlu, D., & Idle, J. R. (2026) · Cells · doi:10.3390/cells15171558 · Cited by 1

Gut microbiome-mediated primary and acquired resistance to immune checkpoint inhibitors in MSI-H/dMMR colorectal cancer: mechanisms, biomarkers, and therapeutic implications-a narrative review

Marjanovic, M., Maletin, N., Kukic, B. P., Nikolić, I., Petrović, N., Radić, J., Đurić, A., Knezevic, M., Dejanović, B., & Calic, V. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1907957 · Cited by 1

CD8+ tissue-resident memory cells- do they modulate peripheral nervous system and neuroinflammation?

Pandiyan, P. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1933495 · Cited by 1

Changes of L-Arginine Metabolism in Rat`S Colon Mucosa Under the Conditions of COX/LOX Inhibition and Acute Stress Action

Denysenko, N. V., & Sklyarov, A. (2021) · Biosciences Biotechnology Research Asia · doi:10.13005/bbra/2918 · Cited by 1

Bacterial polyamines: a key mediator to combat stress tolerance in plants

Sadiqa, A., Shahzadi, B., & Faisal, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91632-5.00009-4 · Cited by 1

Probiotics-based Anticancer Immunity in Breast Cancer

Masood, N., & Malik, S. S. (2023) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815124781123030009 · Cited by 1

Gut Microbiome Metabolites and the Intestinal Homeostasis

Metwally, H., & Kishimoto, T. (2024) · Journal of Clinical Research and Reports · doi:10.31579/2690-1919/371 · Cited by 2

Polyamine Content of Enteral Nutrition Formulas: Effect of Daily Intake on the Feeding Tolerance of Patients During the First Week in the Intensive Care Unit

Sánchez, M., Rodríguez-Hernández, E., Suárez, L., Cantabrana, B., & García, M. G. (2025) · Applied Sciences · doi:10.3390/app15020659 · Cited by 1

Probiotics in Colon Cancer: A Therapeutic Approach

Nair, A., Anto, E. M., & Jayamurthy, P. (2021) · Springer eBooks · doi:10.1007/978-3-030-64668-4_18 · Cited by 1

Excessive Oral Intake of Vitamin B12 Alters Microbe-host Interactions That Stimulate Citrobacter Rodentium Growth and Virulence in Mice.Preprint

Forgie, A. J., Pepin, D. M., Ju, T., Tollenaar, S. L., Sergi, C. M., Gruenheid, S., & Willing, B. P. (2022) · Research Square · doi:10.21203/rs.3.rs-1236545/v1 · Cited by 1

Microbial lipid shifts in a multi-stage simulated gutPreprint

Tamanna, I., Salonen, K., Mannochio-Russo, H., Kråkström, M., Gomes, P. W. P., Charron‐Lamoureux, V., Mohanty, I., Forssten, S. D., Ouwehand, A. C., Hyötyläinen, T., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.25.678496 · Cited by 1

The Microbiome and Urologic Cancers

Krishnamoorthy, M., Vareki, S. M., & Burton, J. P. (2021) · Physiology in health and disease · doi:10.1007/978-3-030-67951-4_8

Bioactive Components in Fermented Foods and Food By-Products

Verardo, V., Gómez‐Caravaca, A. M., & Tabanelli, G. (2020) · MDPI eBooks · doi:10.3390/books978-3-03928-852-6

Intestines—Inflammatory and digestive system

da Silva, E. M., Alves, R. W., Doretto-Silva, L., & Andrade‐Oliveira, V. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821385-8.00007-x

Integrated de novo gene prediction and peptide assembly of metagenomic sequencing data

Thippabhotla, S., Liu, B., Podgorny, A., Yooseph, S., Yang, Y., Zhang, J., & Zhong, C. (2023) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqad023

Gut Microbiome and Its Metabolites in Ageing

Dutta, S., & Duttaroy, A. K. (2023) · Springer eBooks · doi:10.1007/978-981-99-0534-8_10

Exploring the microbiota to better understand pancreatic cancer physiologyPreprint

Chen, A., Zhao, F., Wu, X., Deng, X., Yang, J., & Xue, J. (2023) · Research Square · doi:10.21203/rs.3.rs-3526694/v1

Intestinal epithelial Atg16l1 influences pregnancy-induced fecal microbiota shifts in micePreprint

López-Agudelo, V. A., Falk‐Paulsen, M., Rehman, A., Bharti, R., Sommer, F., Wacker, E. M., Ellinghaus, D., Luzius, A., Sievers, L. K., Kaser, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.10.570427

Introduction to gut microbiome and epigenetics

Oshinjo, A. M., Michael, O. S., Adedayo, L. D., Adetunji, C. O., Bamidele, O., Adetunji, J. B., Morakinyo, A., Akinwale, E. O., Ajayi, O. O., Awobajo, F. O., et al. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-91190-0.00009-6

The Epigenetic Impact of the Human Microbiota on Host Cells

Stein, R. A., Cui, R., Faussete, K. C., & Riber, L. (2024) · Springer eBooks · doi:10.1007/978-981-97-3790-1_5

Discovery of a Widespread Polyamine–Low-Molecular-Weight Thiol Hybrid Pathway in Clostridioides difficile

Hunt, R. L., Oh, J., Jain, A., Kuo, T.-H., Berardi, D., Jian, W., Song, D., Wu, Q., Goodman, A. L., Palm, N. W., et al. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5c00286

Homéostasie de la Barrière Intestinale : rôle des métabolites bactériens

Liquard, R., Oukacha, K., Seksik, P., Sauvonnet, N., Thenet, S., & Carrière, V. (2025) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2025.11.002

Additional file 5 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565909

Additional file 1 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565897

Additional file 2 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986603

Additional file 6 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651610

Additional file 7 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651613

Additional file 7 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986618

Additional file 3 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986606

Additional file 3 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651601

Additional file 13 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986597

Additional file 3 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565903

Additional file 1 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651595

Additional file 4 of A meta-analysis study of the robustness and universality of gut microbiome-metabolome associations

Muller, E., Algavi, Y. M., & Borenstein, E. (2021) · Figshare · doi:10.6084/m9.figshare.16800610

Additional file 14 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986600

Additional file 5 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651607

Additional file 5 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986612

Additional file 6 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986615

Additional file 6 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565912

Additional file 4 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651604

Additional file 4 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565906

Additional file 2 of Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment

Ma, B., Gavzy, S. J., France, M., Song, Y., Lwin, H. W., Kensiski, A., Saxena, V., Piao, W., Lakhan, R., Iyyathurai, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26651598

Additional file 1 of Heterogeneous changes in gut and tumor microbiota in patients with pancreatic cancer: insights from clinical evidence

Zhao, F., Chen, A., Wu, X., Deng, X., Yang, J., & Xue, J. (2024) · Figshare · doi:10.6084/m9.figshare.26707047

Additional file 10 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986588

Additional file 11 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986591

Additional file 9 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986624

Additional file 2 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565900

Additional file 7 of Effects of aging on the skin and gill microbiota of farmed seabass and seabream

Rosado, D., Pérez-Losada, M., Pereira, A., Severino, R., & Xavier, R. (2021) · Figshare · doi:10.6084/m9.figshare.13565915

Additional file 3 of A meta-analysis study of the robustness and universality of gut microbiome-metabolome associations

Muller, E., Algavi, Y. M., & Borenstein, E. (2021) · Figshare · doi:10.6084/m9.figshare.16800607

Additional file 12 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986594

Additional file 8 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986621

Additional file 4 of Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J.-F., Cheng, Y., Dai, M.-Y., Zhu, W.-F., Yang, X.-W., Gonzalez, F. J., & Li, F. (2021) · Figshare · doi:10.6084/m9.figshare.16986609

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