Chitooligosaccharides improves intestinal mucosal immunity and intestinal microbiota in blue foxes

Fusobacterium nucleatum — symbiont, opportunist and oncobacterium

Brennan, C. A., & Garrett, W. S. (2019) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0129-6 · Cited by 1,205 · see citing works

Bifidobacteria and Their Role as Members of the Human Gut Microbiota

O’Callaghan, A. A., & van Sinderen, D. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00925 · Cited by 1,108 · see citing works

The role of goblet cells and mucus in intestinal homeostasis

Gustafsson, J. K., & Johansson, M. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-022-00675-x · Cited by 721 · see citing works

Tight junction proteins occludin and ZO‐1 as regulators of epithelial proliferation and survival

Kuo, W., Odenwald, M. A., Turner, J. R., & Zuo, L. (2022) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14798 · Cited by 633 · see citing works

Production of Chitooligosaccharides and Their Potential Applications in Medicine

Aam, B. B., Heggset, E. B., Norberg, A. L., Sørlie, M., Vårum, K. M., & Eijsink, V. G. H. (2010) · Marine Drugs · doi:10.3390/md8051482 · Cited by 603 · see citing works

Chitosan oligosaccharide (COS): An overview

Naveed, M., Phil, L., Sohail, M., Hasnat, M., Baig, M. M. F. A., Ihsan, A. U., Shumzaid, M., Kakar, M. U., Khan, T. M., Akabar, M., et al. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.01.192 · Cited by 518 · see citing works

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision

Häberle, J., Burlina, A., Chakrapani, A., Dixon, M., Karall, D., Lindner, M. S., Mandel, H., Martinelli, D., Pintos‐Morell, G., Santer, R., et al. (2019) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12100 · Cited by 510 · see citing works

Weaning stress and intestinal health of piglets: A review

Tang, X., Xiong, K., Fang, R., & Li, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1042778 · Cited by 415 · see citing works

Antimicrobial peptides and gut microbiota in homeostasis and pathology

Ostaff, M. J., Stange, E. F., & Wehkamp, J. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201201773 · Cited by 348 · see citing works

Rethinking mucosal antibody responses: IgM, IgG and IgD join IgA

Chen, K., Magri, G., Grasset, E. K., & Cerutti, A. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-019-0261-1 · Cited by 339 · see citing works

Verrucomicrobia use hundreds of enzymes to digest the algal polysaccharide fucoidan

Sichert, A., Corzett, C. H., Schechter, M. S., Unfried, F., Markert, S., Becher, D., Fernàndez-Guerra, A., Liebeke, M., Schweder, T., Polz, M. F., et al. (2020) · Nature Microbiology · doi:10.1038/s41564-020-0720-2 · Cited by 329 · see citing works

Inhibition of Dectin-1 Signaling Ameliorates Colitis by Inducing Lactobacillus-Mediated Regulatory T Cell Expansion in the Intestine

Tang, C., Kamiya, T., Liu, Y., Kadoki, M., Kakuta, S., Oshima, K., Hattori, M., Takeshita, K., Kanai, T., Saijo, S., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.07.003 · Cited by 285 · see citing works

Inflammatory lipid mediators in adipocyte function and obesity

Iyer, A., Fairlie, D. P., Prins, J. B., Hammock, B. D., & Brown, L. (2010) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2009.264 · Cited by 284 · see citing works

Bifidobacterium dentium Fortifies the Intestinal Mucus Layer via Autophagy and Calcium Signaling Pathways

Engevik, M. A., Luk, B., Chang‐Graham, A. L., Hall, A., Herrmann, B. I., Ruan, W. H., Endres, B. T., Shi, Z., Garey, K. W., Hyser, J. M., et al. (2019) · mBio · doi:10.1128/mbio.01087-19 · Cited by 276 · see citing works

Predominant gut Lactobacillus murinus strain mediates anti-inflammaging effects in calorie-restricted mice

Pan, F., Zhang, L., Li, M., Hu, Y., Zeng, B., Yuan, H., Zhao, L., & Zhang, C. (2018) · Microbiome · doi:10.1186/s40168-018-0440-5 · Cited by 237 · see citing works

Effects of chito-oligosaccharide supplementation on the growth performance, nutrient digestibility, intestinal morphology, and fecal shedding of Escherichia coli and Lactobacillus in weaning pigs1

Liu, P., Piao, X., Kim, S. W., Wang, L., Shen, Y. B., Lee, H. S., & Li, S. Y. (2008) · Journal of Animal Science · doi:10.2527/jas.2007-0668 · Cited by 201 · see citing works

Integrated meta-omics reveals new ruminal microbial features associated with feed efficiency in dairy cattle

Xue, M., Xie, Y., Zhong, Y., Ma, X., Sun, H., & Liu, J. (2022) · Microbiome · doi:10.1186/s40168-022-01228-9 · Cited by 192 · see citing works

A review on the preparation of chitosan oligosaccharides and application to human health, animal husbandry and agricultural production

Yuan, X., Zheng, J., Jiao, S., Cheng, G., Feng, C., Du, Y., & Liu, H. (2019) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2019.05.050 · Cited by 186 · see citing works

A Simple and Novel Fecal Biomarker for Colorectal Cancer: Ratio of Fusobacterium Nucleatum to Probiotics Populations, Based on Their Antagonistic Effect

Guo, S., Li, L., Xu, B., Mang-hui, L., Zeng, Q., Han, X., Ying, X., Wu, Y., Wang, Y., Liu, W., et al. (2018) · Clinical Chemistry · doi:10.1373/clinchem.2018.289728 · Cited by 171 · see citing works

Spirulina platensis polysaccharides attenuate lipid and carbohydrate metabolism disorder in high-sucrose and high-fat diet-fed rats in association with intestinal microbiota

Li, T., Huang, Z., Jia, R., Lv, X., Zhao, C., & Liu, B. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110530 · Cited by 122 · see citing works

Plasma postheparin diamine oxidase. Sensitive provocative test for quantitating length of acute intestinal mucosal injury in the rat.

Luk, G. D., Bayless, T. M., & Baylin, S. B. (1983) · Journal of Clinical Investigation · doi:10.1172/jci110881 · Cited by 113 · see citing works

Effect of chito-oligosaccharide on growth performance, intestinal barrier function, intestinal morphology and cecal microflora in weaned pigs1

Yang, C., Ferket, P. R., Hong, Q., Zhou, J., Cao, G., Zhou, L., & Chen, A. G. (2012) · Journal of Animal Science · doi:10.2527/jas.2011-4699 · Cited by 109 · see citing works

Effect of low dosage of chito-oligosaccharide supplementation on intestinal morphology, immune response, antioxidant capacity, and barrier function in weaned piglets

Xiong, X., Yang, H., Wang, X. C., Hu, Q., Liu, C. X., Wu, X., Deng, D., Hou, Y., Nyachoti, C. M., Xiao, D., et al. (2015) · Journal of Animal Science · doi:10.2527/jas.2014-7851 · Cited by 108 · see citing works

Alopex lagopus

Audet, A. M., Robbins, C. B., & Larivière, S. (2002) · Mammalian Species · doi:10.1644/1545-1410(2002)713 · Cited by 105 · see citing works

Sialylation as an Important Regulator of Antibody Function

Vattepu, R., Sneed, S. L., & Anthony, R. M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.818736 · Cited by 98 · see citing works

Specific antibody activity, glycan heterogeneity and polyreactivity contribute to the protective activity of S-IgA at mucosal surfaces

Mestecky, J. F., & Russell, M. W. (2009) · Immunology Letters · doi:10.1016/j.imlet.2009.03.013 · Cited by 92 · see citing works

Novel mechanism by which extracellular vesicles derived from Lactobacillus murinus alleviates deoxynivalenol-induced intestinal barrier disruption

Fan, J., Zhang, Y., Zuo, M., Ding, S., Li, J., Feng, S., Xiao, Y., & Tao, S. (2024) · Environment International · doi:10.1016/j.envint.2024.108525 · Cited by 87 · see citing works

Pretreatment with chitosan oligosaccharides attenuate experimental severe acute pancreatitis via inhibiting oxidative stress and modulating intestinal homeostasis

Mei, Q., Hu, J.-H., Huang, Z., Fan, J., Huang, C., Lu, Y., Wang, X., & Zeng, Y. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-00581-5 · Cited by 85 · see citing works

Autophagy and Intestinal Homeostasis

Patel, K., & Stappenbeck, T. S. (2012) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183658 · Cited by 84 · see citing works

Revealing proteome-level functional redundancy in the human gut microbiome using ultra-deep metaproteomics

Li, L., Wang, T., Ning, Z., Zhang, X., Butcher, J., Serrana, J. M., Simopoulos, C. M. A., Mayne, J., Stintzi, A. P., Mack, D. R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39149-2 · Cited by 82 · see citing works

Megasphaera elsdenii: Its Role in Ruminant Nutrition and Its Potential Industrial Application for Organic Acid Biosynthesis

Cabral, L. D. S., & Weimer, P. J. (2024) · Microorganisms · doi:10.3390/microorganisms12010219 · Cited by 74 · see citing works

Exploring Effects of Chitosan Oligosaccharides on Mice Gut Microbiota in in vitro Fermentation and Animal Model

Zhang, C., Jiao, S., Wang, Z. A., & Du, Y. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02388 · Cited by 68 · see citing works

Effects of dietary administering chitosan on growth performance, jejunal morphology, jejunal mucosal sIgA, occluding, claudin-1 and TLR4 expression in weaned piglets challenged by enterotoxigenic Escherichia coli

Xiao, D., Tang, Z., Yin, Y., Zhang, B., Hu, X., Feng, Z., & Wang, J. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.07.023 · Cited by 67 · see citing works

Short-Chain Cello-oligosaccharides: Intensification and Scale-up of Their Enzymatic Production and Selective Growth Promotion among Probiotic Bacteria

Zhong, C., Ukowitz, C., Domig, K. J., & Nidetzky, B. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c02660 · Cited by 66 · see citing works

Immune response, hematological traits, biochemical blood parameters, and histological status of laying hens influenced by dietary chitosan-oligosaccharides

Youssef, I. M., Khalil, H. A., Shakoori, A. M., Bagadood, R. M., Alyahyawi, A. Y., Alhazzaa, R. A., Fakiha, K. G., Nasr, S., Abo-Samra, M. A. E.-F., HASSAN, M. S. H., et al. (2023) · Poultry Science · doi:10.1016/j.psj.2023.102834 · Cited by 66 · see citing works

Molecular Weight-Dependent Immunostimulative Activity of Low Molecular Weight Chitosan via Regulating NF-κB and AP-1 Signaling Pathways in RAW264.7 Macrophages

Zheng, B., Wen, Z., Huang, Y.-J., Xia, M., Xiang, X., & Qu, Y. (2016) · Marine Drugs · doi:10.3390/md14090169 · Cited by 64 · see citing works

Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes

Conte, M. L., Cosorich, I., Ferrarese, R., Cencicchio, M. A., Nobili, A., Palmieri, V., Massimino, L., Lamparelli, L. A., Liang, W., Riba, M., et al. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2023.104567 · Cited by 62 · see citing works

A novel chitosan oligosaccharide derivative: Synthesis, antioxidant and antibacterial properties

Xia, W., Wei, X., Xie, Y., & Zhou, T. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119608 · Cited by 61 · see citing works

Advances in extraction, utilization, and development of chitin/chitosan and its derivatives from shrimp shell waste

Gao, M., Tang, H.-Q., & HongGuang, Z. (2024) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.70008 · Cited by 61 · see citing works

Role of non-covalent enzyme‒substrate interactions in the reaction catalysed by cellobiose phosphorylase from Cellulomonas uda

Nidetzky, B., Christian, E. I. S., & Albert, M. (2000) · Biochemical Journal · doi:10.1042/0264-6021:3510649 · Cited by 60 · see citing works

d-lactate as a marker of venous-induced intestinal ischemia: An experimental study in pigs

Nielsen, C., Lindholt, J. S., Erlandsen, E. J., & Mortensen, F. V. (2011) · International Journal of Surgery · doi:10.1016/j.ijsu.2011.04.004 · Cited by 55 · see citing works

FISH analysis of Lactobacillus biofilms in the gastrointestinal tract of different hosts

Lebeer, S., Verhoeven, T. L. A., Claes, I. J. J., Hertogh, G., Vermeire, S., Buyse, J., Immerseel, F. V., Vanderleyden, J., & Keersmaecker, S. C. J. D. (2010) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2010.02994.x · Cited by 49 · see citing works

The Protect Effects of Chitosan Oligosaccharides on Intestinal Integrity by Regulating Oxidative Status and Inflammation under Oxidative Stress

Lan, R., Chang, Q., Wei, L., & Zhao, Z. (2021) · Marine Drugs · doi:10.3390/md19020057 · Cited by 45 · see citing works

Applications and prospects of functional oligosaccharides in pig nutrition: A review

Liu, N., Shen, H., Zhang, F., Liu, X., Xiao, Q., Jiang, Q., Tan, B., & Ma, X. (2023) · Animal nutrition · doi:10.1016/j.aninu.2023.02.002 · Cited by 43 · see citing works

Chitosan Oligosaccharide Attenuates Lipopolysaccharide-Induced Intestinal Barrier Dysfunction through Suppressing the Inflammatory Response and Oxidative Stress in Mice

Tao, W., Wang, G., Pei, X., Sun, W., & Wang, M. (2022) · Antioxidants · doi:10.3390/antiox11071384 · Cited by 42 · see citing works

Effects and Mechanisms of Chitosan and ChitosanOligosaccharide on Hepatic Lipogenesis and Lipid Peroxidation, Adipose Lipolysis, and Intestinal Lipid Absorption in Rats with High-Fat Diet-Induced Obesity

Liu, S., Chen, R.-Y., & Chiang, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031139 · Cited by 41 · see citing works

Clostridium butyricum and Chitooligosaccharides in Synbiotic Combination Ameliorate Symptoms in a DSS-Induced Ulcerative Colitis Mouse Model by Modulating Gut Microbiota and Enhancing Intestinal Barrier Function

Huang, X., Hu, J., Zhang, H., Li, J., Zhu, X., Liu, Y., Liang, Y., & Mei, Y. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.04370-22 · Cited by 41 · see citing works

Effects of chitosan oligosaccharides (COS) and FMT from COS-dosed mice on intestinal barrier function and cell apoptosis

Na, K., Wei, J., Zhang, L., Fang, Y. Z., Li, X., Lu, S., & Guo, X. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.120043 · Cited by 40 · see citing works

Evaluation of Megasphaera elsdenii supplementation on rumen fermentation, production performance, carcass traits and health of ruminants: a meta-analysis

Susanto, I., Wiryawan, K. G., Suharti, S., Retnani, Y., Zahera, R., & Jayanegara, A. (2023) · Animal Bioscience · doi:10.5713/ab.22.0258 · Cited by 32 · see citing works

Gut Microbial Diversity Analysis of Different Native Chickens and Screening of Chicken-Derived Probiotics

Chen, L., Bai, X., Wang, T., Liu, J., Miao, X., Zeng, B., & Li, D. (2023) · Animals · doi:10.3390/ani13233672 · Cited by 32 · see citing works

Polyguluronate alleviates ulcerative colitis by targeting the gut commensal Lactobacillus murinus and its anti-inflammatory metabolites.

Pan, L., Ma, M., Wang, Y., Dai, W., Fu, T., Wang, L., Shang, Q., & Yu, G.-L. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.128592 · Cited by 29 · see citing works

Chitosan oligosaccharide improves intestinal function by promoting intestinal development, alleviating intestinal inflammatory response, and enhancing antioxidant capacity in broilers aged d 1 to 14

Lan, R., Wu, F. H., Wang, Y., Lin, Z., Wang, H., Zhang, J., & Zhao, Z. (2023) · Poultry Science · doi:10.1016/j.psj.2023.103381 · Cited by 29 · see citing works

Oat-based postbiotics ameliorate high-sucrose induced liver injury and colitis susceptibility by modulating fatty acids metabolism and gut microbiota

Wei, S., Wen, R., Liu, T., Zhou, L., Wang, G., Dai, X., & Shi, L. S. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109553 · Cited by 28 · see citing works

Genetic parameters for fur quality graded on live animals and dried pelts of American mink (Neovison vison)

Thirstrup, J. P., Jensen, J., & Lund, M. S. (2017) · Journal of Animal Breeding and Genetics · doi:10.1111/jbg.12258 · Cited by 24 · see citing works

Effects of chitosan oligosaccharides on intestinal oxidative stress and inflammation response in heat stressed rats

Wei, L., Li, Y., Chang, Q., Guo, G., & Lan, R. (2020) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.20-0085 · Cited by 22 · see citing works

Chitosan oligosaccharide improves the mucosal immunity of small intestine through activating SIgA production in mice: Proteomic analysis

Wen, J., Niu, X., Chen, S., Chen, Z., Wu, S., Wang, X., Yong, Y., Liu, X., Yu, Z., Ma, X., et al. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108826 · Cited by 21 · see citing works

Immunity and reproduction protective effects of Chitosan Oligosaccharides in Cyclophosphamide/Busulfan-induced premature ovarian failure model mice

Li, X., Ye, H., Su, T., Hu, C., Huang, Y.-Q., Fu, X., Zhong, Z., Du, X., & Zheng, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1185921 · Cited by 21 · see citing works

The gastrointestinal tract of farmed mink (Neovison vison) maintains a diverse mucosa‐associated microbiota following a 3‐day fasting period

Bahl, M. I., Hammer, A. S., Clausen, T. N., Jakobsen, A., Skov, S., & Andresen, L. O. (2017) · MicrobiologyOpen · doi:10.1002/mbo3.434 · Cited by 20 · see citing works

Protective Effect of Low Molecular Weight Seleno-Aminopolysaccharide on the Intestinal Mucosal Oxidative Damage

Wen, Z., Tang, Z., Ma, L., Zhu, T.-L., Wang, Y., Xiang, X., & Zheng, B. (2019) · Marine Drugs · doi:10.3390/md17010064 · Cited by 20 · see citing works

Fur colour in the Arctic fox: genetic architecture and consequences for fitness

Tietgen, L., Hagen, I., Kleven, O., Bernardi, C. D., Kvalnes, T., Norén, K., Hasselgren, M., Wallén, J., Angerbjörn, A., Landa, A., et al. (2021) · Proceedings of the Royal Society B · doi:10.1098/rspb.2021.1452 · Cited by 20 · see citing works

Dietary variation in Icelandic arctic fox (Vulpes lagopus) over a period of 30 years assessed through stable isotopes

Ellgutter, J. A. C., Ehrich, D., Killengreen, S. T., Ims, R. A., & Unnsteinsdóttir, E. R. (2019) · Oecologia · doi:10.1007/s00442-019-04580-0 · Cited by 20 · see citing works

Distribution of digestive enzyme activities along intestine in blue fox, mink, ferret and rat

Олейник, В. М. (1995) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(95)00090-t · Cited by 19 · see citing works

Imbalances in TCA, Short Fatty Acids and One-Carbon Metabolisms as Important Features of Homeostatic Disruption Evidenced by a Multi-Omics Integrative Approach of LPS-Induced Chronic Inflammation in Male Wistar Rats

Hernández-Baixauli, J., Abasolo-Zabalo, N., Palacios-Jordan, H., Foguet‐Romero, E., Suñol, D., Galofré, M., Caimari, A., Baselga‐Escudero, L., Bas-Prior, J. M. D., & Mulero, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052563 · Cited by 19 · see citing works

Maternal chitosan oligosaccharide intervention optimizes the production performance and health status of gilts and their offspring

Ho, T., Jahan, M., Haque, Z., Kracht, S., WYNN, P. C., Du, Y., Gunn, A. J., & Wang, B. (2020) · Animal nutrition · doi:10.1016/j.aninu.2020.02.001 · Cited by 19 · see citing works

Effects of Chitosan Oligosaccharide on Production Performance, Egg Quality and Ovarian Function in Laying Hens with Fatty Liver Syndrome

Tao, W., Jin, F., Fan, Q., Zhao, N., Wang, G., Du, E., Chen, F., Guo, W., Huang, S., Chen, M., et al. (2022) · Animals · doi:10.3390/ani12182465 · Cited by 18 · see citing works

Nutrient Requirements of Mink and Foxes

National Research Council (1968) · National Academies Press eBooks · doi:10.17226/20678 · Cited by 18 · see citing works

Epithelial and Mesenchymal Contribution to the Niche: A Safeguard for Intestinal Stem Cell Homeostasis

Smith, N. R., Davies, P. S., Silk, A. D., & Wong, M. H. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.10.024 · Cited by 15 · see citing works

Ketogenic Diet Exacerbates L-Arginine-Induced Acute Pancreatitis and Reveals the Therapeutic Potential of Butyrate

Xia, H., Guo, J., Shen, J. F., Jiang, S., Han, S., & Li, L. (2023) · Nutrients · doi:10.3390/nu15204427 · Cited by 15 · see citing works

Obese dogs exhibit different fecal microbiome and specific microbial networks compared with normal weight dogs

Kim, H., Seo, J., Park, T., Seo, K., Cho, H.-W., Chun, J. L., & Kim, K. H. (2023) · Scientific Reports · doi:10.1038/s41598-023-27846-3 · Cited by 14 · see citing works

Dietary Chito-oligosaccharide attenuates LPS-challenged intestinal inflammation via regulating mitochondrial apoptotic and MAPK signaling pathway

Meng, T., Liu, C., Chen, Y., Yu, M., He, J., Tan, B., Fu, X., He, J., & Xiao, D. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111153 · Cited by 11 · see citing works

Adhesion mechanisms of Bifidobacterium animalis subsp. lactis JCM 10602 to dietary fiber

TANIGUCHI, M., NAMBU, M., Katakura, Y., & Yamasaki-Yashiki, S. (2020) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2020-003 · Cited by 10 · see citing works

Requirements and Metabolism for Calcium, Phosphorus and Vitamin D3 in the Growing–Furring Blue Foxes

Li, T., Du, Z., Xu, Y., Bai, X., & Li, G. (2022) · Animals · doi:10.3390/ani12202776 · Cited by 6 · see citing works

Corrigendum: Hydrolytic Capabilities as a Key to Environmental Success: Chitinolytic and Cellulolytic Acidobacteria From Acidic Sub-arctic Soils and Boreal Peatlands

Belova, S. E., Ravin, N. V., Панкратов, Т. А., Rakitin, A. L., Ivanova, A. A., Beletsky, A. V., Mardanov, A. V., Damsté, J. S. S., & Dedysh, S. N. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.856396 · Cited by 6 · see citing works

Effects of Glycine Supplementation in Drinking Water on the Growth Performance, Intestinal Development, and Genes Expression in the Jejunum of Chicks

Zheng, X., Xie, Y., Chen, Z., He, J., & Chen, J. (2023) · Animals · doi:10.3390/ani13193109 · Cited by 4 · see citing works

Impact of Astragalus polysaccharide, chitosan and xylo-oligosaccharide on intestinal physicochemical properties and gut microbiota disorder of Pelteobagrus fulvidraco caused by transport stress

Bai, C., Huang, G., Qi, X., Wang, J., Qiu, L., Wang, L., & Liao, T. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.146169 · Cited by 9 · see citing works

Effects of chitosan oligosaccharide on the growth performance, antioxidant capacity, immune function, intestinal digestive capacity and morphological structure in growing female minks

Liu, H., Li, W., Fan, G., Chen, Q. Y., Zhang, S., & Zhang, B. (2025) · PLoS ONE · doi:10.1371/journal.pone.0332818

Effects of chitosan oligosaccharides (COS) and FMT from COS-dosed mice on intestinal barrier function and cell apoptosis

Na, K., Wei, J., Zhang, L., Fang, Y. Z., Li, X., Lu, S., & Guo, X. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.120043 · Cited by 40 · see citing works

Dietary Chitooligosaccharide Inclusion as an Alternative to Antibiotics Improves Intestinal Morphology, Barrier Function, Antioxidant Capacity, and Immunity of Broilers at Early Age

Li, J., Cheng, Y., Chen, Y., Qu, H., Zhao, Y., Wen, C., & Zhou, Y. (2019) · Animals · doi:10.3390/ani9080493 · Cited by 70 · see citing works

Chitooligosaccharides Prevents the Development of Colitis-Associated Colorectal Cancer by Modulating the Intestinal Microbiota and Mycobiota

Wu, M., Li, J., An, Y., Li, P., Xiong, W., Li, J., Yan, D., Wang, M., & Zhong, G. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02101 · Cited by 84 · see citing works

Orally Administered Chitooligosaccharides Modulate Colon Microbiota in Normal and Colitis Mice

Long, T., Zhi-jun, Y., Wang, J., Liu, J., & He, B. (2018) · International Journal of Pharmacology · doi:10.3923/ijp.2018.291.300 · Cited by 19 · see citing works

Dietary chitooligosaccharide supplementation alleviates intestinal barrier damage, and oxidative and immunological stress in lipopolysaccharide-challenged laying hens

Gu, Y., Chen, Y., Jin, R., Wang, C., Wen, C., & Zhou, Y. (2022) · Poultry Science · doi:10.1016/j.psj.2022.101701 · Cited by 41 · see citing works