Effects of amino acid-derived luminal metabolites on the colonic epithelium and physiopathological consequences

Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly

Beckman, J. S., & Koppenol, W. H. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.5.c1424 · Cited by 5,513

Environmental and Heritable Factors in the Causation of Cancer — Analyses of Cohorts of Twins from Sweden, Denmark, and Finland

Lichtenstein, P., Holm, N. V., Verkasalo, P. K., Iliadou, A., Kaprio, J., Koskenvuo, M., Pukkala, E., Skytthe, A., & Hemminki, K. (2000) · New England Journal of Medicine · doi:10.1056/nejm200007133430201 · Cited by 4,114

Polyamine metabolism and function

Pegg, A. E., & McCann, P. P. (1982) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1982.243.5.c212 · Cited by 1,661

Utilization of Nutrients by Isolated Epithelial Cells of the Rat Colon

Roediger, W. E. W. (1982) · Gastroenterology · doi:10.1016/s0016-5085(82)80339-9 · Cited by 1,187

Toxicology Of Hydrogen Sulfide

Reiffenstein, R. J., Hulbert, W. C., & Roth, S. (1992) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.32.040192.000545 · Cited by 971

Balancing Life-Style and Genomics Research for Disease Prevention

Willett, W. C. (2002) · Science · doi:10.1126/science.1071055 · Cited by 888

Polyamines in cell growth and cell death: molecular mechanisms and therapeutic applications

Thomas, T., & Thomas, T. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000852 · Cited by 862

The uncoupling protein homologues: UCP1, UCP2, UCP3, StUCP and AtUCP

Ricquier, D., & Bouillaud, F. (2000) · Biochemical Journal · doi:10.1042/bj3450161 · Cited by 811

Effects of short chain fatty acids on gut morphology and function

Scheppach, W. (1994) · Gut · doi:10.1136/gut.35.1_suppl.s35 · Cited by 756

THE COLONIC EPITHELIUM IN ULCERATIVE COLITIS: AN ENERGY-DEFICIENCY DISEASE?

Roediger, W. E. W. (1980) · The Lancet · doi:10.1016/s0140-6736(80)91934-0 · Cited by 728

The Sick Adipose Tissue: New Insights Into Defective Signaling and Crosstalk With the Myocardium

Bermúdez, V., Durán, P., Rojas, E., Diaz, M. P., Rivas, J., Nava, M., Chacín, M., de Bravo, M. C., Carrasquero, R., Ponce, C. C., et al. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.735070 · Cited by 31

Modulation of gut microbiota: The effects of a fruits and vegetables supplement

Lakshmanan, A. P., Mingione, A., Pivari, F., Dogliotti, E., Brasacchio, C., Murugesan, S., Cusi, D., Lazzaroni, M., Soldati, L., & Terranegra, A. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.930883 · Cited by 30

Co-dependence of genotype and dietary protein intake to affect expression on amino acid/peptide transporters in porcine skeletal muscle

Liu, Y., Kong, X., Li, F., Tan, B., Li, Y., Duan, Y., Yin, Y., He, J., Hu, C., Blachier, F., et al. (2015) · Amino Acids · doi:10.1007/s00726-015-2066-2 · Cited by 29

Intestinal gene expression in pigs: effects of reduced feed intake during weaning and potential impact of dietary components

Bauer, E., Metzler-Zebeli, B., Verstegen, M., & Mosenthin, R. (2011) · Nutrition research reviews · doi:10.1017/s0954422411000047 · Cited by 26

Knockout of the non-essential gene SUGCT creates diet-linked, age-related microbiome disbalance with a diabetes-like metabolic syndrome phenotype

Niska-Blakie, J., Gopinathan, L., Low, K. N., Kien, Y. L., Goh, C. M. F., Caldez, M. J., Pfeiffenberger, E., Jones, O. S., Ong, C. B., Kurochkin, I. V., et al. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03359-z · Cited by 28

Effect of antibiotic-free, low-protein diets with specific amino acid compositions on growth and intestinal flora in weaned pigs

Zhou, J., Wang, Y., Zeng, X., Zhang, T., Li, P., Yao, B., Wang, L., Qiao, S., & Zeng, X. (2019) · Food & Function · doi:10.1039/c9fo02724f · Cited by 28

Meta-analysis to evaluate the impact of the reduction of dietary crude protein on the gut health of post-weaning pigs

Luise, D., Chalvon‐Demersay, T., Lambert, W., Bosi, P., & Trevisi, P. (2021) · Italian Journal of Animal Science · doi:10.1080/1828051x.2021.1952911 · Cited by 29

Interactions between gut microbiota and Parkinson's disease: The role of microbiota-derived amino acid metabolism

Wang, W., Jiang, S., Xu, C., Tang, L., Liang, Y., Zhao, Y., & Zhu, G. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.976316 · Cited by 29

Proteomics, human gut microbiota and probiotics

Aires, J., & Butel, M. (2011) · Expert Review of Proteomics · doi:10.1586/epr.11.5 · Cited by 28

Immunomodulatory and Antioxidant Properties of a Novel Potential Probiotic Bacillus clausii CSI08

Khokhlova, E. V., Colom, J., Simon, A., Mazhar, S., García‐Laínez, G., Llopis, S., González, N., Enrique-López, M., Álvarez, B., Martorell, P., et al. (2023) · Microorganisms · doi:10.3390/microorganisms11020240 · Cited by 35

Methionine Deficiency Affects Liver and Kidney Health, Oxidative Stress, and Ileum Mucosal Immunity in Broilers

Song, B., Fu, M., He, F., Zhao, H., Wang, Y., Nie, Q., & Wu, B. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.722567 · Cited by 26

Early-life food nutrition, microbiota maturation and immune development shape life-long health

Zhou, X., Du, L., Shi, R., Chen, Z., Zhou, Y., & Li, Z. (2018) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1485628 · Cited by 27

Soybean Okara modulates gut microbiota in rats fed a high-fat diet

Pérez-López, E., Veses, A. M., Redondo, N., Tenorio-Sanz, M.-D., Villanueva, M. J., Redondo, A., Marcos, A., Nova, E., Mateos‐Aparicio, I., & Rupérez, P. (2018) · Bioactive Carbohydrates and Dietary Fibre · doi:10.1016/j.bcdf.2018.09.002 · Cited by 27

Effects of Brewer’s spent grain and carrot pomace on digestibility, fecal microbiota, and fecal and urinary metabolites in dogs fed low- or high-protein diets1

Eisenhauer, L., Vahjen, W., Dadi, T. H., Kohn, B., & Zentek, J. (2019) · Journal of Animal Science · doi:10.1093/jas/skz264 · Cited by 25

Canine gastrointestinal physiology: Breeds variations that can influence drug absorption

Oswald, H., Sharkey, M., Pade, D., & Martinez, M. N. (2015) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2015.09.009 · Cited by 25

Modification of selected bacteria and markers of protein fermentation in the distal gastrointestinal tract of pigs upon consumption of chitosan is accompanied by heightened manure odor emissions1

O’Shea, C. J., Sweeney, T., Lynch, M. B., Callan, J. J., & O’Doherty, J. V. (2011) · Journal of Animal Science · doi:10.2527/jas.2010-2922 · Cited by 24

The risks of self-made diets: the case of an amateur bodybuilder

Guardia, L. D., Cavallaro, M., & Cena, H. (2015) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-015-0077-8 · Cited by 29

Prebiotic peptides, their formation, fermentation in the gut, and health implications

Ashaolu, T. J., & Ashaolu, J. O. (2021) · Biotechnology Progress · doi:10.1002/btpr.3142 · Cited by 24

The impact of metallic nanoparticles on gut fermentation processes: An integrated metabolomics and metagenomics approach following an in vitro digestion and fecal fermentation model.

Vaccari, F., Zhang, L.-L., Giuberti, G., Grasso, A., Bandini, F., García-Pérez, P., Copat, C., Lucini, L., Dall'Asta, M., Ferrante, M., et al. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.131331 · Cited by 17

Effect of diet and individual dietary guidance on gastrointestinal endocrine cells in patients with irritable bowel syndrome (Review)

Mazzawi, T. R. E., & El‐Salhy, M. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3096 · Cited by 23

Tenebrio molitor Larvae Meal Affects the Cecal Microbiota of Growing Pigs

Meyer, S., Geßner, D. K., Maheshwari, G., Röhrig, J., Friedhoff, T., Most, E., Zorn, H., Ringseis, R., & Eder, K. (2020) · Animals · doi:10.3390/ani10071151 · Cited by 24

Supplementing Synbiotic in Sows' Diets Modifies Beneficially Blood Parameters and Colonic Microbiota Composition and Metabolic Activity in Suckling Piglets

Ma, C., Gao, Q., Zhang, W., Zhu, Q., Tang, W., Blachier, F., Ding, H., & Kong, X. (2020) · Frontiers in Veterinary Science · doi:10.3389/fvets.2020.575685 · Cited by 22

Intestinal microbiota profiles in a genetic model of colon tumorigenesis correlates with colon cancer biomarkers

Vitali, F., Tortora, K., Paola, M. D., Bartolucci, G., Menicatti, M., Filippo, C. D., & Caderni, G. (2022) · Scientific Reports · doi:10.1038/s41598-022-05249-0 · Cited by 22

Evidence for validity of ileal digestibility coefficients in monogastrics

Columbus, D. A., & de Lange, C. F. M. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512002334 · Cited by 24

Ileal, colonic and total tract nutrient digestibility in dogs (Canis familiaris) compared with total tract digestibility in mink (Neovison vison)

Tjernsbekk, M. T., Tauson, A., & Ahlstrøm, Ø. (2014) · Archives of Animal Nutrition · doi:10.1080/1745039x.2014.915137 · Cited by 22

Unveiling the Biogeography and Potential Functions of the Intestinal Digesta- and Mucosa-Associated Microbiome of Donkeys

Zhang, R., Zhang, J., Dang, W., Irwin, D. M., Wang, Z., & Zhang, S. Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.596882 · Cited by 22

Microbiome and metabolome profiles of high screen time in a cohort of healthy college students

Jasbi, P., Mohr, A. E., Shi, X., Mahmood, T. N., Zhu, Q., Bruening, M. M., Gu, H., & Whisner, C. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-07381-3 · Cited by 21

Fermented Soy and Fish Protein Dietary Sources Shape Ileal and Colonic Microbiota, Improving Nutrient Digestibility and Host Health in a Piglet Model

Li, Y., Han, Y., Zhao, Q., Tang, C., Zhang, J., & Qin, Y. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.911500 · Cited by 22

Global urinary metabolic profiling of the osteonecrosis of the femoral head based on UPLC–QTOF/MS

Yang, G., Zhao, G., Zhang, J., Gao, S., Chen, T., Ding, S., & Zhu, Y. (2019) · Metabolomics · doi:10.1007/s11306-019-1491-8 · Cited by 20

Treatment with mixed probiotics induced, enhanced and diversified modulation of the gut microbiome of healthy rats

He, Q., Huang, J., Zheng, T., Lin, D. Y., Zhang, H., Li, J., & Sun, Z. (2021) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiab151 · Cited by 21

Digestibility and Palatability of the Diet and Intestinal Functionality of Dogs Fed a Blend of Yeast Cell Wall and Oregano Essential Oil

Soares, N. M. M., Bastos, T. S., Kaelle, G. C. B., de Souza, R. B. M. D. S., de Oliveira, S. G., & Félix, A. P. (2023) · Animals · doi:10.3390/ani13152527 · Cited by 19

Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase

Lan, A., Blais, A., Coelho, D., Capron, J., Maarouf, M., Benamouzig, R., Lancha, A. H., Walker, F., Tomé, D., & Blachier, F. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00433.2015 · Cited by 20

Proanthocyanidin-containing polyphenol extracts from fruits prevent the inhibitory effect of hydrogen sulfide on human colonocyte oxygen consumption

Andriamihaja, M., Lan, A., Beaumont, M., Grauso, M., Gotteland, M., Pastene, E., Cires, M. J., Carrasco‐Pozo, C., Tomé, D., & Blachier, F. (2018) · Amino Acids · doi:10.1007/s00726-018-2558-y · Cited by 20

Interaction of genotype and diet on small intestine microbiota of Japanese quail fed a cholesterol enriched diet

Liu, S., Tun, H. M., Leung, F. C.-C., Bennett, D. C., Zhang, H., & Cheng, K. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-20508-9 · Cited by 20

Organic matter disappearance and production of short- and branched-chain fatty acids from selected fiber sources used in pet foods by a canine in vitro fermentation model1

Donadelli, R. A., Titgemeyer, E. C., & Aldrich, C. G. (2019) · Journal of Animal Science · doi:10.1093/jas/skz302 · Cited by 20

Short‐chain fatty acids and bile acids in human faeces are associated with the intestinal cholesterol conversion status

Matysik, S., Krautbauer, S., Liebisch, G., Schött, H.-F., Kjølbæk, L., Astrup, A. V., Blachier, F., Beaumont, M., Nieuwdorp, M., Hartstra, A. V., et al. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15440 · Cited by 20

Dietary fat and low fiber in purified diets differently impact the gut-liver axis to promote obesity-linked metabolic impairments

Daniel, N., Perazza, L. R., Varin, T. V., Trottier, J., Marcotte, B., St‐Pierre, P., Barbier, O., Chassaing, B., & Marette, A. (2021) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00028.2021 · Cited by 19

Maternal Supplementation With Different Probiotic Mixture From Late Pregnancy to Day 21 Postpartum: Consequences for Litter Size, Plasma and Colostrum Parameters, and Fecal Microbiota and Metabolites in Sows

Han, L., Azad, M. A. K., Huang, P., Wang, W., Zhang, W., Blachier, F., & Kong, X. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.726276 · Cited by 22

Host–diet–microbiota interplay in intestinal nutrition and health

Ignatiou, A., & Pitsouli, C. (2024) · FEBS Letters · doi:10.1002/1873-3468.14966 · Cited by 21

Lipo‐Protein Emulsion Structure in the Diet Affects Protein Digestion Kinetics, Intestinal Mucosa Parameters and Microbiota Composition

Oberli, M., Douard, V., Beaumont, M., Jaoui, D., Devime, F., Laurent, S., Chaumontet, C., Mat, D. J. L., Feunteun, S. L., Michon, C., et al. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700570 · Cited by 19

Colon epithelial cells luminal environment and physiopathological consequences: impact of nutrition and exercise

Blachier, F., Resende, A. D. S., Leite, G. D. S. F., da Costa, A. V., & Lancha, A. H. (2018) · Nutrire · doi:10.1186/s41110-018-0061-6 · Cited by 22

Nonprotein Nitrogen Is Absorbed from the Large Intestine and Increases Nitrogen Balance in Growing Pigs Fed a Valine-Limiting Diet

Columbus, D. A., Lapierre, H., Htoo, J. K. K., & de Lange, C. F. M. (2014) · Journal of Nutrition · doi:10.3945/jn.113.187070 · Cited by 19

Physico-chemical properties of pea fibre and pea protein blends and the implications for in vitro batch fermentation using human inoculum

Karlsson, J., López-Sánchez, P., Marques, T. M., Hyötyläinen, T., Castro‐Alves, V., Krona, A., & Ström, A. (2024) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2024.109732 · Cited by 18

Low Crude Protein Diet Affects the Intestinal Microbiome and Metabolome Differently in Barrows and Gilts

Tao, X., Deng, B., Yuan, Q., Men, X., Wu, J., & Xu, Z. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.717727 · Cited by 18

Poultry nutrition

Barszcz, M., Tuśnio, A., & Taciak, M. (2022) · Physical Sciences Reviews · doi:10.1515/psr-2021-0122 · Cited by 18

Amino Acids Regulate Glycolipid Metabolism and Alter Intestinal Microbial Composition

Xie, F., Liu, Z., Liu, M., Chen, L., Ding, W., & Zhang, H. (2020) · Current Protein and Peptide Science · doi:10.2174/1389203721666200219100216 · Cited by 18

Squid meal and shrimp hydrolysate as novel protein sources for dog food

Guilherme-Fernandes, J., Aires, T., Fonseca, A. J. M., Yergaliyev, T., Camarinha‐Silva, A., Lima, S. A. C., Maia, M. R. G., & Cabrita, A. R. J. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1360939 · Cited by 21

Effects of Increasing Levels of Purified Beta-1,3/1,6-Glucans on the Fecal Microbiome, Digestibility, and Immunity Variables of Healthy Adult Dogs

Marchi, P. H., Vendramini, T. H. A., Zafalon, R. V. A., Príncipe, L. D. A., Cesar, C. G. L., Perini, M. P., Putarov, T. C., Massoco, C. D. O., Balieiro, J. C. D. C., & Brunetto, M. A. (2024) · Microorganisms · doi:10.3390/microorganisms12010113 · Cited by 16

The dynamic crosslinking between gut microbiota and inflammation during aging: reviewing the nutritional and hormetic approaches against dysbiosis and inflammaging

Chaudhary, S., Kaur, P., Singh, T. A., Bano, K. S., Vyas, A., Mishra, A. K., Singh, P., & Mehdi, M. M. (2024) · Biogerontology · doi:10.1007/s10522-024-10146-2 · Cited by 17

Multi‐Omics Analysis of the Effects of Egg Ovotransferrin on the Gut Environment in Mice: Mucosal Gene Expression, Microbiota Composition, and Intestinal Structural Homeostasis

Zhang, Q., Tan, W., Yang, L., Lu, M. P., Dong, S., Liu, X., & Duan, X. L. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201901024 · Cited by 17

Breath response following a nutritional challenge monitored by secondary electrospray ionization high-resolution mass spectrometry

Wüthrich, C., de Figueiredo, M., Burton-Pimentel, K. J., Vergères, G., Wahl, F., Zenobi, R., & Giannoukos, S. (2022) · Journal of Breath Research · doi:10.1088/1752-7163/ac894e · Cited by 16

Effects of therapeutic hypothermia on the gut microbiota and metabolome of infants suffering hypoxic-ischemic encephalopathy at birth

Watkins, C., Murphy, K., Yen, S., Carafa, I., Dempsey, E. M., O'Shea, C., Allen‐Vercoe, E., Ross, R. P., Stanton, C., & Ryan, C. A. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.08.017 · Cited by 17

Grain free diets for utility dogs during training work: Evaluation of the nutrient digestibility and faecal characteristics

Chiofalo, B., Vita, G. D., Presti, V. L., Cucinotta, S., Gaglio, G., Leone, F., & Rosa, A. R. D. (2019) · Animal nutrition · doi:10.1016/j.aninu.2019.05.001 · Cited by 21

Machine learning liquid chromatography retention time prediction model augments the dansylation strategy for metabolite analysis of urine samples

Choi, E., Yoo, W. J., Jang, H.-Y., Kim, T., Lee, S. K., & Oh, H. B. (2023) · Journal of Chromatography A · doi:10.1016/j.chroma.2023.464167 · Cited by 15

Precision Dietary Intervention: Gut Microbiome and Meta-metabolome as Functional Readouts

Luo, J., & Wang, Y. (2025) · Phenomics · doi:10.1007/s43657-024-00193-7 · Cited by 18

Structure of protein emulsion in food impacts intestinal microbiota, caecal luminal content composition and distal intestine characteristics in rats

Beaumont, M., Jaoui, D., Douard, V., Mat, D. J. L., Koeth, F., Goustard, B., Mayeur, C., Mondot, S., Hovaghimian, A., Feunteun, S. L., et al. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700078 · Cited by 15

Effects of different protein sources on fermentation metabolites and nutrient digestibility of brachycephalic dogs

Urrego, M. I. G., Matheus, L. F. D. O., Santos, K. D. M., Ernandes, M. C., Monti, M., de Souza, D. F., Balieiro, J. C. D. C., Araújo, L. F., Pontieri, C. F. F., & Brunetto, M. A. (2017) · Journal of Nutritional Science · doi:10.1017/jns.2017.46 · Cited by 15

In Vitro Fermentation of Pleurotus eryngii Mushrooms by Human Fecal Microbiota: Metataxonomic Analysis and Metabolomic Profiling of Fermentation Products

Christodoulou, P., Vlassopoulou, M., Zervoú, M., Xanthakos, E., Moulos, P., Koutrotsios, G., Zervakis, G. I., Kerezoudi, E. N., Mitsou, E. K., Saxami, G., et al. (2023) · Journal of Fungi · doi:10.3390/jof9010128 · Cited by 16

The role of fiber in modulating plant protein-induced metabolic responses

Partanen, M., Luhio, P., Gómez-Gallego, C., & Kolehmainen, M. (2024) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2024.2392149 · Cited by 16

Mitochondria-Microbiota Interaction in Neurodegeneration

Krämer, P. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.776936 · Cited by 14

Prebiotics and type 2 diabetes: targeting the gut microbiota for improved glycaemic control?

Robertson, M. D. (2020) · Practical Diabetes · doi:10.1002/pdi.2285 · Cited by 15

Effect of a novel animal milk oligosaccharide biosimilar on the gut microbial communities and metabolites of in vitro incubations using feline and canine fecal inocula

Oba, P. M., Vidal, S., Wyss, R., Miao, Y., Adesokan, Y., & Swanson, K. S. (2020) · Journal of Animal Science · doi:10.1093/jas/skaa273 · Cited by 14

Fueling the fire: colonocyte metabolism and its effect on the colonic epithelia

Martínez-Ruiz, M., Robeson, M. S., & Piccolo, B. D. (2025) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2025.2507701 · Cited by 15

In Vitro Evaluation of the Effects of Tylosin on the Composition and Metabolism of Canine Fecal Microbiota

Pinna, C., Vecchiato, C. G., Grandi, M., Mammi, L. M. E., Stefanelli, C., & Biagi, G. (2020) · Animals · doi:10.3390/ani10010098 · Cited by 13

Fermentation and Metabolism of Dietary Protein by Intestinal Microorganisms

Zhang, K., Wang, N., Lü, L., & Ma, X. (2020) · Current Protein and Peptide Science · doi:10.2174/1389203721666200212095902 · Cited by 13

Influence of different inclusion levels and chain length of inulin on microbial ecology and the state of mucosal protective barrier in the large intestine of young pigs

Barszcz, M., Taciak, M., & Skomiał, J. (2017) · Animal Production Science · doi:10.1071/an16014 · Cited by 13

The role of the gut microbiota in the pathophysiology of mental and neurological disorders

Pusceddu, M. M., & Bas-Prior, J. M. D. (2020) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000255 · Cited by 15

Transcriptome Analysis and Postprandial Expression of Amino Acid Transporter Genes in the Fast Muscles and Gut of Chinese Perch (Siniperca chuatsi)

Wu, P., Li, Y., Cheng, J. R., Chen, L., Zeng, M., Wu, Y., Wang, J., Zhang, J., & Chu, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159533 · Cited by 13

Metabolic activity of gut microbial enrichment cultures from different marine species and their transformation abilities to plastic additives

Zhang, S., Hou, R., Sun, C., Huang, Q.-Y., Lin, L., Li, H., Liu, S., Cheng, Y., & Xu, X. (2024) · Environment International · doi:10.1016/j.envint.2024.108882 · Cited by 12

Gut Microbiota and Metabolism

İlhan, N. (2018) · International journal of medical biochemistry/International journal of medical biochemistry : · doi:10.14744/ijmb.2018.92400 · Cited by 13

Functional metabolic capacity of pig colonocytes is differentially modulated by fermentable fibre and poorly digestible protein

Bekebrede, A. F., Noorman, L., Keijer, J., de Boer, V. C. J., & Gerrits, W. J. J. (2022) · animal · doi:10.1016/j.animal.2022.100625 · Cited by 11

The effect of organic and inorganic zinc source, used with lignocellulose or potato fiber, on microbiota composition, fermentation, and activity of enzymes involved in dietary fiber breakdown in the large intestine of pigs

Barszcz, M., Taciak, M., Tuśnio, A., Święch, E., Skomiał, J., Čobanová, K., & Grešáková, Ľ. (2021) · Livestock Science · doi:10.1016/j.livsci.2021.104429 · Cited by 11

Expression of proposed methionine transporters along the gastrointestinal tract of pigs and their regulation by dietary methionine sources

Romanet, S., Aschenbach, J. R., Pieper, R., Zentek, J., Htoo, J. K. K., Whelan, R., & Mastrototaro, L. (2021) · Genes & Nutrition · doi:10.1186/s12263-021-00694-4 · Cited by 11

Histological and biochemical evaluation of supplementing broiler diet with β-hydroxy-methyl butyrate calcium (β-HMB-Ca).

Ahmed, S. K., Al-Shamire, J. S., & Dhyaa, A. A. (2018) · Europe PMC (PubMed Central) · Cited by 11

In vitro evaluation of the effects of Yucca schidigera and inulin on the fermentation potential of the faecal microbiota of dogs fed diets with low or high protein concentrations

Vierbaum, L., Eisenhauer, L., Vahjen, W., & Zentek, J. (2019) · Archives of Animal Nutrition · doi:10.1080/1745039x.2019.1616498 · Cited by 11

A Pilot Study on the 1H-NMR Serum Metabolic Profile of Takotsubo Patients Reveals Systemic Response to Oxidative Stress

Vanni, D., Viceconte, N., Petrella, G., Biccirè, F. G., Pelliccia, F., Tanzilli, G., & Cicero, D. O. (2021) · Antioxidants · doi:10.3390/antiox10121982 · Cited by 11

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