Exopolysaccharides of Lactobacillus reuteri: Their Influence on Adherence of E. Coli to Epithelial Cells and Inflammatory Response

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works

Colorimetric Method for Determination of Sugars and Related Substances

DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956) · Analytical Chemistry · doi:10.1021/ac60111a017 · Cited by 52,269 · see citing works

A simple and rapid method for the permethylation of carbohydrates

Ciucanu, I., & Kerek, F. (1984) · Carbohydrate Research · doi:10.1016/0008-6215(84)85242-8 · Cited by 3,581 · see citing works

Simplified method for the measurement of total non-starch polysaccharides by gas-liquid chromatography of constituent sugars as alditol acetates

Englyst, H. N., & Cummings, J. H. (1984) · The Analyst · doi:10.1039/an9840900937 · Cited by 1,096 · see citing works

Production of interleukin 22 but not interleukin 17 by a subset of human skin-homing memory T cells

Duhen, T., Geiger, R., Jarrossay, D., Lanzavecchia, A., & Sallusto, F. (2009) · Nature Immunology · doi:10.1038/ni.1767 · Cited by 1,079 · see citing works

Tumor necrosis factor and interleukin-1 lead to phosphorylation and loss of I kappa B alpha: a mechanism for NF-kappa B activation.

Beg, A. A., Finco, T. S., Nantermet, P. V., & Baldwin, A. S. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.6.3301 · Cited by 1,027 · see citing works

PCR detection and quantitation of predominant anaerobic bacteria in human and animal fecal samples

Wang, R. F., Cao, W. W., & Cerniglia, C. E. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.4.1242-1247.1996 · Cited by 502 · see citing works

New Perspectives for Lactobacilli Exopolysaccharides

Badel, S., Bernardi, T., & Michaud, P. (2011) · Biotechnology Advances · doi:10.1016/j.biotechadv.2010.08.011 · Cited by 497 · see citing works

Detection of Mycoplasma in cell cultures

Young, L., Sung, J., Stacey, G., & Masters, J. R. (2010) · Nature Protocols · doi:10.1038/nprot.2010.43 · Cited by 437 · see citing works

Impaired expression of peroxisome proliferator-activated receptor γ in ulcerative colitis

Dubuquoy, L., Jansson, E. Å., Deeb, S. S., Rakotobé, S., Karoui, M., Colombel, J., Auwerx, J. H., Pettersson, S., & Desreumaux, P. (2003) · Gastroenterology · doi:10.1016/s0016-5085(03)00271-3 · Cited by 425 · see citing works

Cell Wall Structure and Function in Lactic Acid Bacteria

Chapot-Chartier, M.-P., & Kulakauskas, S. (2014) · Microbial Cell Factories · doi:10.1186/1475-2859-13-s1-s9 · Cited by 410 · see citing works

A PRACTICAL GUIDE TO THE METHYLATION ANALYSIS OF CARBOHYDRATES.

Jansson, P., Kenne, L., Liedgren, H., Lindberg, B., & Lōnngren, J. (1976) · Cited by 295 · see citing works

Exopolysaccharides Produced by Probiotic Strains Modify the Adhesion of Probiotics and Enteropathogens to Human Intestinal Mucus

Ruas‐Madiedo, P., Gueimonde, M., Margollés, A., Reyes‐Gavilán, C. G. D. L., & Salminen, S. (2006) · Journal of Food Protection · doi:10.4315/0362-028x-69.8.2011 · Cited by 241 · see citing works

Immunomodulatory and antioxidant potential of <i>Lactobacillus</i> exopolysaccharides

Liu, C., Tseng, K., Chiang, S., Lee, B., Hsu, W., & Pan, T. (2011) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.4456 · Cited by 230 · see citing works

Capsule Shields the Function of Short Bacterial Adhesins

Schembri, M. A., Dalsgaard, D., & Klemm, P. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.5.1249-1257.2004 · Cited by 217 · see citing works

Production of Exopolysaccharide by <i>Lactobacillus rhamnosus</i> R and Analysis of Its Enzymatic Degradation during Prolonged Fermentation

Pham, P. L., Dupont, I., Roy, D., Lapointe, G., & Cerning, J. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.6.2302-2310.2000 · Cited by 212 · see citing works

Antioxidant Activity of an Exopolysaccharide Purified from Lactococcus lactis subsp. lactis 12

Pan, D., & Mei, X. (2010) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2010.01.005 · Cited by 211 · see citing works

Antiviral and immunoregulatory effect of a novel exopolysaccharide from a marine thermotolerant Bacillus licheniformis

Arena, A., Maugeri, T. L., Pavone, B., Iannello, D., Gugliandolo, C., & Bisignano, G. (2005) · International Immunopharmacology · doi:10.1016/j.intimp.2005.07.004 · Cited by 207 · see citing works

Biosorption of heavy metals by the exopolysaccharide produced by Paenibacillus jamilae

Morillo, J. A., Ribera, R. G., Quesada, T., Aguilera, J., Alberto Ramos-cormenzana, A., & Monteoliva‐Sánchez, M. (2008) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-008-9800-9 · Cited by 200 · see citing works

Production of a Novel Extracellular Polysaccharide by Lactobacillus sake 0-1 and Characterization of the Polysaccharide

van den Berg, D. J. C., Robijn, G. W., Janssen, A., Giuseppin, M. L. F., Vreeker, R., Kamerling, J. P., Vliegenthart, J. F. G., Ledeboer, A. M., & Verrips, C. T. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.8.2840-2844.1995 · Cited by 173 · see citing works

Cholesterol Lowering Activity of Ropy Fermented Milk

NAKAJIMA, H., SUZUKI, Y., & HIROTA, T. (1992) · Journal of Food Science · doi:10.1111/j.1365-2621.1992.tb06848.x · Cited by 170 · see citing works

The Novel Porcine Lactobacillus sobrius Strain Protects Intestinal Cells from Enterotoxigenic Escherichia coli K88 Infection and Prevents Membrane Barrier Damage ,

Roselli, M., Finamore, A., Britti, M. S., Konstantinov, S. R., Smidt, H., de Vos, W. M., & Mengheri, E. (2007) · Journal of Nutrition · doi:10.1093/jn/137.12.2709 · Cited by 169 · see citing works

Extract of Reishi Polysaccharides Induces Cytokine Expression via TLR4-Modulated Protein Kinase Signaling Pathways

Hsu, H., Hua, K., Lin, C., Lin, C., Hsu, J., & Wong, C. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.10.5989 · Cited by 161 · see citing works

Microbial Exopolysaccharides - their Role in Microbial Adhesion in Aqueous Systems

Sutherland, I. W. (1982) · CRC Critical Reviews in Microbiology · doi:10.3109/10408418209113562 · Cited by 157 · see citing works

Exopolysaccharides from lactic acid bacteria: Structural analysis, molecular weight effect on immunomodulation

Surayot, U., Wang, J., Seesuriyachan, P., Kuntiya, A., Tabarsa, M., Lee, Y., Kim, J., Park, W., & You, S. (2014) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2014.05.005 · Cited by 141 · see citing works

Toll-like receptor 4 and cytokine expression involved in functional immune response in an originally established porcine intestinal epitheliocyte cell line

Moue, M., Tohno, M., Shimazu, T., Kido, T., Aso, H., Saito, T., & Kitazawa, H. (2007) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2007.11.006 · Cited by 134 · see citing works

Structure and functions of exopolysaccharide produced by gut commensal Lactobacillus reuteri 100-23

Sims, I. M., Frese, S. A., Walter, J., Loach, D. M., Wilson, M., Appleyard, K., Eason, J. R., Livingston, M. K., Baird, M. A., Cook, G. M., et al. (2011) · The ISME Journal · doi:10.1038/ismej.2010.201 · Cited by 123 · see citing works

Structural analysis of the α-d-glucan (EPS180) produced by the Lactobacillus reuteri strain 180 glucansucrase GTF180 enzyme

van Leeuwen, S. S., Kralj, S., van Geel-Schutten, I. H., Gerwig, G. J., Dijkhuizen, L., & Kamerling, J. P. (2008) · Carbohydrate Research · doi:10.1016/j.carres.2008.01.042 · Cited by 121 · see citing works

Isolation and Characterization of Lactococcal Bacteriophages from Cultured Buttermilk Plants in the United States

Moineau, S., Borkaev, M., Holler, B. J., Walker, S. A., Kondo, J. K., Vedamuthu, E. R., & Vandenbergh, P. A. (1996) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(96)76584-0 · Cited by 118 · see citing works

Exopolysaccharide-producing Bifidobacterium strains elicit different in vitro responses upon interaction with human cells

López, P., Monteserín, D. C., Gueimonde, M., Reyes‐Gavilán, C. G. D. L., Margollés, A., Suárez, A., & Ruas‐Madiedo, P. (2011) · Food Research International · doi:10.1016/j.foodres.2011.11.020 · Cited by 113 · see citing works

Intermediate chains of exopolysaccharides fromLactobacillus rhamnosusRW-9595M increase IL-10 production by macrophages

Bleau, C., Monges, A., Rashidan, K. K., Laverdure, J., Lacroix, M., Calsteren, M. V., Millette, M., Savard, R., & Lamontagne, L. (2009) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2009.04450.x · Cited by 108 · see citing works

Real-time PCR quantification of bacterial adhesion to Caco-2 cells: Competition between bifidobacteria and enteropathogens

Candela, M., Seibold, G. M., Vitali, B., Lachenmaier, S., Eikmanns, B. J., & Brigidi, P. (2005) · Research in Microbiology · doi:10.1016/j.resmic.2005.04.006 · Cited by 84 · see citing works

Anti-adhesive activity of sulphated exopolysaccharides of microalgae on attachment of red sore disease-associated bacteria and Helicobacter pylori to tissue culture cells

Guzmán-Murillo, M. A., & Ascencio, F. (2000) · Letters in Applied Microbiology · doi:10.1046/j.1472-765x.2000.00751.x · Cited by 75 · see citing works

Structural analysis of the α-d-glucan (EPS35-5) produced by the Lactobacillus reuteri strain 35-5 glucansucrase GTFA enzyme

van Leeuwen, S. S., Kralj, S., van Geel-Schutten, I. H., Gerwig, G. J., Dijkhuizen, L., & Kamerling, J. P. (2008) · Carbohydrate Research · doi:10.1016/j.carres.2008.01.044 · Cited by 69 · see citing works

New method for exopolysaccharide determination in culture broth using stirred ultrafiltration cells

Bergmaier, D., Lacroix, C., Macedo, M. G., & Champagne, C. P. (2001) · Applied Microbiology and Biotechnology · doi:10.1007/s002530100764 · Cited by 53 · see citing works

Functional Alteration of Macrophages by a Slime-Forming Lactococcus lactis ssp. cremoris

Kitazawa, H., Nomura, M., Itoh, T., & Yamaguchi, T. (1991) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(91)78380-x · Cited by 27 · see citing works

Cytokine mRNA expression in porcine cell lines stimulated by enterotoxigenic Escherichia coli

Pavlová, B., Volf, J., Alexa, P., Rychlı́k, I., Matiašovic, J., & Faldyna, M. (2008) · Veterinary Microbiology · doi:10.1016/j.vetmic.2008.04.024 · Cited by 25 · see citing works

Flax-seed oil and Lactobacillus plantarum supplementation modulate TLR and NF-κB gene expression in enterotoxigenic Escherichia coli challenged gnotobiotic pigs

Chytilová, M., Nemcová, R., Gancarčíková, S., Mudroňová, D., & Tkáčiková, Ľ. (2014) · Acta Veterinaria Hungarica · doi:10.1556/avet.2014.024 · Cited by 12 · see citing works

Role of Lactobacillus reuteri in Human Health and Diseases

Mu, Q., Tavella, V. J., & Luo, X. M. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00757 · Cited by 744 · see citing works

Exopolysaccharides of lactic acid bacteria: Structure, bioactivity and associations: A review

Zhou, Y., Cui, Y., & Qu, X. (2018) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2018.11.093 · Cited by 414 · see citing works

Exopolysaccharides Produced by Lactic Acid Bacteria: From Biosynthesis to Health-Promoting Properties

Jurášková, D., Ribeiro, S. C., & Silva, C. C. G. (2022) · Foods · doi:10.3390/foods11020156 · Cited by 342 · see citing works

Lactic Acid Bacteria Exopolysaccharides Producers: A Sustainable Tool for Functional Foods

Prete, R., Alam, M. K., Perpetuini, G., Perla, C., Pittia, P., & Corsetti, A. (2021) · Foods · doi:10.3390/foods10071653 · Cited by 194 · see citing works

Exopolysaccharides production by Lactobacillus acidophilus LA5 and Bifidobacterium animalis subsp. lactis BB12: Optimization of fermentation variables and characterization of structure and bioactivities

Amiri, S., Mokarram, R. R., Khiabani, M. S., Bari, M. R., & Alizadeh, M. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.11.084 · Cited by 160 · see citing works

The Beneficial Role of Probiotic Lactobacillus in Respiratory Diseases

Du, T., Lei, A., Zhang, N., & Zhu, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.908010 · Cited by 147 · see citing works

Characterization and sulfated modification of an exopolysaccharide from Lactobacillus plantarum ZDY2013 and its biological activities

Zhang, Z., Liu, Z., Tao, X., & Wei, H. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2016.07.084 · Cited by 142 · see citing works

Biomarkers and Utility of the Antioxidant Potential of Probiotic Lactobacilli and Bifidobacteria as Representatives of the Human Gut Microbiota

Averina, O., Poluektova, E., Marsova, M., & Danilenko, V. (2021) · Biomedicines · doi:10.3390/biomedicines9101340 · Cited by 126 · see citing works

Lactic acid bacteria-derived exopolysaccharide: Formation, immunomodulatory ability, health effects, and structure-function relationship

Zhang, J., Xiao, Y., Wang, H., Zhang, H., Chen, W., & Lu, W. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127432 · Cited by 140 · see citing works

Polysaccharide from Gracilaria Lemaneiformis prevents colitis in Balb/c mice via enhancing intestinal barrier function and attenuating intestinal inflammation

Han, R., Wang, L., Zhao, Z., You, L., Pedišić, S., Kulikouskaya, V. I., & Lin, Z. (2020) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2020.106048 · Cited by 112 · see citing works

Bifidobacteria cell wall-derived exo-polysaccharides, lipoteichoic acids, peptidoglycans, polar lipids and proteins – their chemical structure and biological attributes

Pyclik, M. J., Šrůtková, D., Schwarzer, M., & Górska, S. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.12.227 · Cited by 92 · see citing works

Exopolysaccharides produced byLactobacillussp.: Biosynthesis and applications

Oleksy, M., & Klewicka, E. (2016) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2016.1187112 · Cited by 93 · see citing works

Probiotic Species in the Management of Periodontal Diseases: An Overview

Zhang, Y., Ding, Y., & Guo, Q. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.806463 · Cited by 80 · see citing works

Lactobacillus reuteri in digestive system diseases: focus on clinical trials and mechanisms

Peng, Y., Ma, Y., Luo, Z., Jiang, Y.-F., Xu, Z., & Yu, R. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1254198 · Cited by 77 · see citing works

Bifidobacterium brevereduces apoptotic epithelial cell shedding in an exopolysaccharide and MyD88-dependent manner

Hughes, K. R., Harnisch, L. C., Alcon-Giner, C., Mitra, S., Wright, C. J., Ketskemety, J., van Sinderen, D., Watson, A. J. M., & Hall, L. J. (2017) · Open Biology · doi:10.1098/rsob.160155 · Cited by 72 · see citing works

Disease managing capacities and mechanisms of host effects of lactic acid bacteria

Ren, C., Faas, M. M., & de Vos, P. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1758625 · Cited by 71 · see citing works

Exopolysaccharides from lactic acid bacteria, as an alternative to antibiotics, on regulation of intestinal health and the immune system

Yang, S., Xu, X., Peng, Q., Ma, L., Qiao, Y., & Shi, B. (2023) · Animal nutrition · doi:10.1016/j.aninu.2023.02.004 · Cited by 65 · see citing works

Lactobacillus Reuteri Vesicles Regulate Mitochondrial Function of Macrophages to Promote Mucosal and Cutaneous Wound Healing

Chen, Y., Huang, X., Liu, A., Fan, S., Liu, S., Li, Z., Yang, X., Guo, H., Wu, M., Liu, M., et al. (2024) · Advanced Science · doi:10.1002/advs.202309725 · Cited by 63 · see citing works

Antioxidant, antimicrobial and emulsification properties of exopolysaccharides from lactic acid bacteria of bovine milk: Insights from biochemical and genomic analysis

Tarannum, N., Hossain, T. J., Ali, F., Das, T., Dhar, K., & Nafiz, I. H. (2023) · LWT · doi:10.1016/j.lwt.2023.115263 · Cited by 69 · see citing works

The multiple benefits of bioactive polysaccharides: From the gut to overall health

Huang, R., Zhang, J., Xu, X., Sun, M., Xu, L., Kuang, H., Xu, C., & Guo, L. (2024) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2024.104677 · Cited by 58 · see citing works

Extracellular membrane vesicles from Limosilactobacillus reuteri strengthen the intestinal epithelial integrity, modulate cytokine responses and antagonize activation of TRPV1

Pang, Y., Lundberg, L. E., Forsberg, M. M., Ahl, D., Bysell, H., Pallin, A., Sverremark‐Ekström, E., Karlsson, R., Jonsson, H., & Roos, S. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1032202 · Cited by 56 · see citing works

Characterization of novel exopolysaccharide of Enterococcus faecium WEFA23 from infant and demonstration of its in vitro biological properties

Jia, K., Tao, X., Liu, Z., Zhan, H., He, W., Zhang, Z., Zeng, Z., & Wei, H. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.12.245 · Cited by 56 · see citing works

Lactobacillus reuteri Surface Mucus Adhesins Upregulate Inflammatory Responses Through Interactions With Innate C-Type Lectin Receptors

Bene, K., Kavanaugh, D. W., Leclaire, C., Gunning, A. P., MacKenzie, D. A., Wittmann, A., Young, I. D., Kawasaki, N., Rajnavölgyi, É., & Juge, N. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00321 · Cited by 55 · see citing works

’Ropy’ Phenotype, Exopolysaccharides and Metabolism: Study on Food Isolated Potential Probiotics LAB

Cirrincione, S., Breuer, Y., Mangiapane, E., Mazzoli, R., & Pessione, E. (2018) · Microbiological Research · doi:10.1016/j.micres.2018.07.004 · Cited by 53 · see citing works

Potential of lactic acid bacteria derived polysaccharides for the delivery and controlled release of oral probiotics

Liao, N., Pang, B., Han, J., Xu, X., Yan, L., Li, H., Shao, D., & Shi, J. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.04.022 · Cited by 48 · see citing works

Exopolysaccharides isolated from fermented milk-associated lactic acid bacteria and applied to produce functional value-added probiotic yogurt

Nemati, V., & Mozafarpour, R. (2024) · LWT · doi:10.1016/j.lwt.2024.116116 · Cited by 45 · see citing works

Improvement of inflammatory bowel disease by lactic acid bacteria-derived metabolites: a review

Guo, W.-L., Mao, B.-Y., Tang, X., Zhang, Q.-X., Zhao, J.-X., Zhang, H., Chen, W., & Cui, S.-M. (2023) · Critical reviews in food science and nutrition · doi:10.1080/10408398.2023.2291188 · Cited by 37 · see citing works

New Levan-Type Exopolysaccharide from Bacillus amyloliquefaciens as an Antiadhesive Agent against Enterotoxigenic Escherichia coli

Cai, G., Liu, Y., Li, X., & Lu, J. Z. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b03234 · Cited by 42 · see citing works

A metabolic reconstruction of Lactobacillus reuteri JCM 1112 and analysis of its potential as a cell factory

Kristjansdottir, T., Bosma, E. F., dos Santos, F. B., Özdemir, E., Herrgård, M. J., França, L., Ferreira, B. S., Nielsen, A. T., & Guðmundsson, S. (2019) · Microbial Cell Factories · doi:10.1186/s12934-019-1229-3 · Cited by 40 · see citing works

Studying on the structure-activity relationship of Flammulina velutipes polysaccharides via ultrasonic degradation: Insights into molecular weight, chain conformation, and anti-inflammatory activity

Zhang, J., Chen, X., Zhan, Q., Wang, Y., Meng, K., Hu, Q., & Zhao, L. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.140480 · Cited by 39 · see citing works

Alleviative Effects of Exopolysaccharide Produced by Lactobacillus helveticus KLDS1.8701 on Dextran Sulfate Sodium-Induced Colitis in Mice

Liu, Y., Zheng, S., Cui, J., Guo, T., Zhang, J., & Li, B. (2021) · Microorganisms · doi:10.3390/microorganisms9102086 · Cited by 38 · see citing works

Health promoting benefits of postbiotics produced by lactic acid bacteria: Exopolysaccharide

Gezginç, Y., Erdem, T. K., Tatar, H. D., Ayman, S., Ganiyusufoğlu, E., & Dayısoylu, K. S. (2022) · Biotech Studies · doi:10.38042/biotechstudies.1159166 · Cited by 38 · see citing works

Lyophilized alginate-based microspheres containing Lactobacillus fermentum D12, an exopolysaccharides producer, contribute to the strain’s functionality in vitro

Butorac, K., Novak, J., Bellich, B., Terán, L. C., Banić, M., Pavunc, A. L., Zjalić, S., Cescutti, P., Šušković, J., & Kos, B. (2021) · Microbial Cell Factories · doi:10.1186/s12934-021-01575-6 · Cited by 37 · see citing works

Limosilactobacillus reuteri Regulating Intestinal Function: A Review

Jiang, J., Li, K., Xiao, Y., Zhong, A., Tang, J., Duan, Y., & Li, Z. (2022) · Fermentation · doi:10.3390/fermentation9010019 · Cited by 36 · see citing works

Gene Replacement and Fluorescent Labeling to Study the Functional Role of Exopolysaccharides in Bifidobacterium animalis subsp. lactis

Castro-Bravo, N., Hidalgo-Cantabrana, C., Rodríguez-Carvajal, M. Á., Ruas‐Madiedo, P., & Margollés, A. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01405 · Cited by 35 · see citing works

Characterization and comparison of yeasts from different sources for some probiotic properties and exopolysaccharide production

YILDIRAN, H., Kılıç, G. B., & Karahan, A. G. (2019) · Food Science and Technology · doi:10.1590/fst.29818 · Cited by 35 · see citing works

Recent advances in the concept of paraprobiotics: Nutraceutical/functional properties for promoting children health

Kumar, H., Schütz, F., Bhardwaj, K., Sharma, R., Nepovimová, E., Dhanjal, D. S., Verma, R., Kumar, D., Kuča, K., & Martins, N. A. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1996327 · Cited by 36 · see citing works

Extrusion of Dissolved Oxygen by Exopolysaccharide From Leuconostoc mesenteroides and Its Implications in Relief of the Oxygen Stress

Yan, M., Wang, B., Xu, X., der Meister, T. J., Tabγač, H.-T., Hwang, F.-F., & Liu, Z. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02467 · Cited by 31 · see citing works

Lactobacilli-Derived Microbe-Associated Molecular Patterns (MAMPs) in Host Immune Modulation

Furnari, S., Ciantia, R., Garozzo, A., Furneri, P. M., & Fuochi, V. (2025) · Biomolecules · doi:10.3390/biom15111609 · Cited by 33 · see citing works

Production, purification, and functional characterization of glucan exopolysaccharide produced by Enterococcus hirae strain OL616073 of fermented food origin

Kavitake, D., Tiwari, S., Devi, P. B., Shah, I. A., Reddy, G. B., & Shetty, P. H. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.129105 · Cited by 29 · see citing works

Microbiota and Probiotics: The Role of Limosilactobacillus Reuteri in Diverticulitis

Piccioni, A., Franza, L., Vaccaro, V., Saviano, A., Zanza, C., Candelli, M., Covino, M., Franceschi, F., & Ojetti, V. (2021) · Medicina · doi:10.3390/medicina57080802 · Cited by 28 · see citing works

Anti-Helicobacter pylori Activity of a Lactobacillus sp. PW-7 Exopolysaccharide

Hu, J., Tian, X., Wei, T., Wu, H., Lü, J., Lyu, M., & Wang, S. (2021) · Foods · doi:10.3390/foods10102453 · Cited by 27 · see citing works

Immunomodulatory Effect of Lactobacillus reuteri (Limosilactobacillus reuteri) and Its Exopolysaccharides Investigated on Epithelial Cell Line IPEC-J2 Challenged with Salmonella Typhimurium

Kiššová, Z., Tkáčiková, Ľ., Mudroňová, D., & Bhide, M. R. (2022) · Life · doi:10.3390/life12121955 · Cited by 27 · see citing works

Limosilactobacillus reuteri Strains as Adjuvants in the Management of Helicobacter pylori Infection

Dargenio, C., Dargenio, V. N., Bizzoco, F., Indrio, F., Francavilla, R., & Cristofori, F. (2021) · Medicina · doi:10.3390/medicina57070733 · Cited by 26 · see citing works

Macrophage activation by exopolysaccharides from Streptococcus thermophilus fermented milk through TLRs-mediated NF-κB and MAPK pathways

Xu, W., Cao, F., Zhao, M., Fu, X., Yin, S., Sun, Y., Valencak, T. G., & Ren, D. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108875 · Cited by 26 · see citing works

Isolation and characterization of a high molecular mass β-glucan from Lactobacillus fermentum Lf2 and evaluation of its immunomodulatory activity

Vitlić, A., Sadiq, S., Ahmed, H. I., Ale, E. C., Binetti, A. G., Collett, A., Humpreys, P. N., & Laws, A. P. (2019) · Carbohydrate Research · doi:10.1016/j.carres.2019.03.003 · Cited by 24 · see citing works

Lactic Acid Bacteria—From Nature Through Food to Health

Teneva‐Angelova, T., Hristova, I., Pavlov, A. I., & Бешкова, Д. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811443-8.00004-9 · Cited by 24 · see citing works

LsrR-like protein responds to stress tolerance by regulating polysaccharide biosynthesis in Lactiplantibacillus plantarum

Meng, F., Lyu, Y., Zhao, H., Lyu, F., Bie, X., Lu, Y., Zhao, M., Chen, Y., & Lu, Z. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.11.180 · Cited by 20 · see citing works

Lung-Gut Microbiota and Tryptophan Metabolites Changes in Neonatal Acute Respiratory Distress Syndrome

Yang, J.-L., He, Y., Ai, Q., Liu, C., Ruan, Q.-Q., & Shi, Y. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s459496 · Cited by 15 · see citing works

Influence of Lactobacillus reuteri L26 Biocenol™ on immune response against porcine circovirus type 2 infection in germ-free mice

Karaffová, V., Csank, T., Mudroňová, D., Király, J., Révajová, V., Gancarčíková, S., Nemcová, R., Pistl, J., Vilček, Š., & Levkut, M. (2017) · Beneficial Microbes · doi:10.3920/bm2016.0114 · Cited by 18 · see citing works

Understanding Exopolysaccharides from Lactic Acid Bacteria: Synthesis, Functions, and Applications

Li, H., Jin, Y. J., Li, H., Zhao, J., Stanton, C., Ross, R. P., Chen, W., & Yang, B. K. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c04613 · Cited by 18 · see citing works

Influence of the Probiotic L. reuteri on Periodontal Clinical Parameters after Nonsurgical Treatment: A Systematic Review

Ochôa, C., de Castro, F. C., Frias‐Bulhosa, J., Manso, M. C., Fernandes, J. C. H., & Fernandes, G. V. O. (2023) · Microorganisms · doi:10.3390/microorganisms11061449 · Cited by 21 · see citing works

Role of Bacteria-Derived Exopolysaccharides in Inflammatory Bowel Disease with a Special Focus on Cyanobacterial Exopolysaccharides

Manoharan, D., Sivakumar, N., Billamboz, M., & Jawhara, S. (2024) · Applied Microbiology · doi:10.3390/applmicrobiol4010017 · Cited by 17 · see citing works

Polyphenols and Lactobacillus reuteri in oral health

Naureen, Z., Medori, M. C., Dhuli, K., Donato, K., Connelly, S., Bellinato, F., Gisondi, P., & Bertelli, M. (2022) · Journal of preventive medicine and hygiene · doi:10.15167/2421-4248/jpmh2022.63.2s3.2767 · Cited by 18 · see citing works

Exopolysaccharide from Lactobacillus casei NA-2 attenuates Escherichia coli O157:H7 surface adhesion via modulation of membrane surface properties and adhesion-related gene expression

Ma, L., Xu, X., Peng, Q., Yang, S., Zhang, Y., Tian, D., Shi, L., Qiao, Y., & Shi, B. (2022) · Microbial Pathogenesis · doi:10.1016/j.micpath.2022.105863 · Cited by 15 · see citing works

Protective effects of Lactobacillus reuteri SJ-47 strain exopolysaccharides on human skin fibroblasts damaged by UVA radiation

Zhao, J., Fu, H., Zhang, Y., Li, M., Wang, D., Zhao, D., Zhang, J., & Wang, C. (2022) · Bioresources and Bioprocessing · doi:10.1186/s40643-022-00617-0 · Cited by 15 · see citing works

Use of Limosilactobacillus reuteri DSM 17938 in paediatric gastrointestinal disorders: an updated review

Dargenio, V. N., Cristofori, F., Dargenio, C., Giordano, P., Indrio, F., Celano, G., & Francavilla, R. (2022) · Beneficial Microbes · doi:10.3920/bm2021.0151 · Cited by 15 · see citing works

Capsular Polysaccharides of Lactobacillus spp.: Theoretical and Practical Aspects of Simple Visualization Methods

Oleksy, M., & Klewicka, E. (2017) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-017-9295-5 · Cited by 13 · see citing works

Comprehensive mapping of the cell response to E. coli infection in porcine intestinal epithelial cells pretreated with exopolysaccharide derived from Lactobacillus reuteri

Tkáčiková, Ľ., Mochnáčová, E., Tyagi, P., Kiššová, Z., & Bhide, M. R. (2020) · Veterinary Research · doi:10.1186/s13567-020-00773-1 · Cited by 13 · see citing works

α-Glucan-type exopolysaccharides with varied linkage patterns: Mitigating post-prandial glucose spike and prolonging the glycemic response

Lim, H.-E., Song, Y.-B., Choi, H., & Lee, B.-H. (2024) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2024.121898 · Cited by 12 · see citing works

Structural characteristics of Lacticaseibacillus rhamnosus ACS5 exopolysaccharide in association with its antioxidant and antidiabetic activity in vitro

İnanan, T., Darilmaz, D. Ö., YEŞİLDAL, T. K., Yüksekdağ, Z., & Yavuz, S. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136148 · Cited by 12 · see citing works

Immunomodulatory effect of low molecular-weight seleno-aminopolysaccharides in intestinal epithelial cells

Gu, L.-X., Wen, Z., Xiang, X., Ma, L., Wang, X.-B., Jian-yin, M., & Qu, Y. (2017) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2017.03.008 · Cited by 12 · see citing works

The Protective Effects of Lactobacillus reuteri Combined With Clostridium butyricum Miyairi 588 on Intestinal Barrier Function, Water Transport, and Oxidative Stress in a Rat Model of 5FU ‐Induced Diarrhea

Tang, S., Chuang, W., Liao, J., Tsai, Y., Chen, L., Liao, J., Ko, J., & Ou, C. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70318 · Cited by 11 · see citing works

The impact of Limosilactobacillus reuteri in combination with non-surgical periodontal therapy on periodontal clinical parameters and salivary and subgingival microbiota composition in individuals with stage III–IV periodontitis: a randomized controlled trial

Huo, P., Deng, L., Lu, J., Kan, P., Jing, R., & Luo, L.-J. (2025) · BMC Oral Health · doi:10.1186/s12903-025-06084-1 · Cited by 9 · see citing works

Anti-Colitic Effect of an Exopolysaccharide Fraction from Pediococcus pentosaceus KFT-18 on Dextran Sulfate Sodium-Induced Colitis through Suppression of Inflammatory Mediators

Lee, J., Chung, K., Shin, J., Jung, S.-H., Lee, S., Lee, M.-K., Hong, H., Rhee, Y. K., & Lee, K. (2022) · Polymers · doi:10.3390/polym14173594 · Cited by 9 · see citing works

Potential of lactic acid bacteria as starter cultures for food fermentation and as producers of biochemicals for value addition

Padhi, S., Sharma, S., Sahoo, D., Montēt, D., & Rai, A. K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89875-1.00009-2 · Cited by 9 · see citing works

Hierarchical arming of probiotics for improved viability to synergistically alleviate ulcerative colitis

Liu, Z., Feng, L., Huang, Q., Liu, H., Liu, H., & Wan, H. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123791 · Cited by 9 · see citing works

Progress of research on the alleviation of intestinal inflammation by regulating intestinal mucosal function with postbiotics

Li, A., Yang, S., Han, X., Liu, C., Zheng, J., Ma, Y., Cheng, S., Zhao, J., Zhou, W., & Du, P. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.103437 · Cited by 8 · see citing works

Exopolysaccharide secreted by Lactiplantibacillus plantarum Y12 showed inhibitory effect on the pathogenicity of Shigella flexneri in vitro and in vivo

Song, Y., Sun, M., Mu, G., & Tuo, Y. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.129478 · Cited by 8 · see citing works

Characterization of Some Microorganisms from Human Stool Samples and Determination of Their Effects on CT26 Colorectal Carcinoma Cell Line

Kahraman, M. S., Karahan, A. G., & Terzioğlu, M. E. (2022) · Current Microbiology · doi:10.1007/s00284-022-02915-4 · Cited by 8 · see citing works

Lactobacillus reuteri for chronic periodontitis: focus on underlying mechanisms and future perspectives

Zhou, K., Xie, J., Su, Y., & Fang, J. (2023) · Biotechnology and Genetic Engineering Reviews · doi:10.1080/02648725.2023.2183617 · Cited by 8 · see citing works

Exopolysaccharides from camel milk-derived Limosilactobacillus reuteri C66: Structural characterization, bioactive and rheological properties for food applications

Kober, A. K. M. H., Abdin, M., Subhash, A. J., Liu, S., Dertli, E., Abu‐Jdayil, B., Show, P. L., & Ayyash, M. M. (2025) · Food Chemistry X · doi:10.1016/j.fochx.2025.102164 · Cited by 7 · see citing works

Harnessing the Potential of Lactobacillus Species for Therapeutic Delivery at the lumenal-mucosal Interface

Spangler, J. R., Caruana, J. C., Medintz, I. L., & Walper, S. A. (2021) · Future Science OA · doi:10.2144/fsoa-2020-0153 · Cited by 7 · see citing works

Exopolysaccharides from Lactic Acid Bacteria: A Review on Functions, Biosynthesis and Applications in Food Industry

Erdem, T. K., Tatar, H. D., Ayman, S., & Gezginç, Y. (2023) · Turkish Journal of Agriculture - Food Science and Technology · doi:10.24925/turjaf.v11i2.414-423.5213 · Cited by 7 · see citing works

Immunomodulatory effect of probiotic exopolysaccharides in a porcine in vitro co-culture model mimicking the intestinal environment on ETEC infection

Kiššová, Z., Mudroňová, D., Link, R., & Tkáčiková, Ľ. (2023) · Veterinary Research Communications · doi:10.1007/s11259-023-10237-4 · Cited by 7 · see citing works

Systemic immune response of gnotobiotic mice infected with porcine circovirus type 2 after administration of Lactobacillus reuteri L26 Biocenol™

Mudroňová, D., Karaffová, V., Csank, T., Király, J., Révajová, V., Gancarčíková, S., Nemcová, R., Pistl, J., Vilček, Š., & Levkut, M. (2018) · Beneficial Microbes · doi:10.3920/bm2017.0147 · Cited by 7 · see citing works

Preparation and structural characterization of selenium nanoparticles from Lactobacillus reuteri and their protective effects on DSS-induced ulcerative colitis in mice

Sun, L., Liu, S., Ding, Y., Yang, R., & Zeng, H. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105293 · Cited by 6 · see citing works

Treatment and prevention of pigeon diarrhea through the application of Lactobacillus SNK-6

Fan, W., Zhu, Y., Hou, H., Yao, J., Zhu, L., Liu, H., & Yan, H. (2024) · Poultry Science · doi:10.1016/j.psj.2024.103476 · Cited by 6 · see citing works

Limosilactobacillus reuteri metabolites modulate immune pathways and intestinal barrier repair after 5 fluorouracil exposure

Lasaviciute, G., Plana, M. L., Örtegren, S. S., Telli, S., Kourmoulakis, S., Lundberg, L. E., Lidberg, K., Peiris, O., Sinha, I., Jonsson, A., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-45524-y · Cited by 5 · see citing works

Newly Isolated Limosilactobacillus reuteri B1/1 Modulates the Expression of Cytokines and Antimicrobial Proteins in a Porcine ex Vivo Model

Kiššová, Z., Štofilová, J., Mudroňová, D., & Karaffová, V. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2905180 · Cited by 5 · see citing works

Exopolysaccharides from Limosilactobacillus reuteri: their influence on in vitro activation of porcine monocyte-derived dendritic cells - brief report

Kiššová, Z., Schusterová, P., Mudroňová, D., Novotny, J. F., & Tkáčiková, Ľ. (2024) · Veterinary Research Communications · doi:10.1007/s11259-024-10445-6 · Cited by 5 · see citing works

Postbiotics: Production to consumption as natural enhancers and preservatives in the food industry

Akhavan, F., Bari, M. R., Noori, S. M. A., & Amiri, S. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108865 · Cited by 4 · see citing works

Limosilactobacillus reuteri DSM 17938 Produce Bioactive Components during Formulation in Sucrose

Lundberg, L. E., Forsberg, M. M., Lemanczyk, J., Sverremark‐Ekström, E., Sandström, C., Roos, S., & Håkansson, S. (2024) · Microorganisms · doi:10.3390/microorganisms12102058 · Cited by 4 · see citing works

Chemical Analysis and Health Benefits of a Novel Polysaccharide Produced by Paenibacillus mucilaginosus

Ali, S. K., Abdelgawad, M. A., Selim, S., Keshek, D. E.-G., Mohamed, H. S., & Hamed, E. A. (2025) · Current Microbiology · doi:10.1007/s00284-025-04300-3 · Cited by 4 · see citing works

Gut-Protective and Multifunctional Exopolysaccharide from Enterococcus faecium HDRsEf1: Structural Characterization and Protective Effects Against Enteropathogenic E. coli-Induced Intestinal Inflammation

Dong, Z., Li, X., Wu, Y., Wang, Z., Cui, W., Hu, S., Shi, D., Huang, Q., Xiao, Y., Zhou, H., et al. (2025) · Nutrients · doi:10.3390/nu17233667 · Cited by 4 · see citing works

Sourdough bread enriched with exopolysaccharides and gazpacho by-products modulates in vitro the microbiota dysbiosis

Nieto, J. A., Rosés, C., Viadel, B., Gallego, E., Romo‐Hualde, A., Milagro, F. I., Barceló, A., Virto, R., Saldaña, G., & Luengo, E. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.132906 · Cited by 4 · see citing works

Probiotic applications of bifidobacteria in poultry: administration methods and microencapsulation techniques

Argañaraz-Martínez, E., Apella, M. C., Chaia, A. P., & Babot, J. D. (2024) · Microbiome Research Reports · doi:10.20517/mrr.2025.64 · Cited by 3 · see citing works

Structural characteristics and immunomodulatory activity of an exopolysaccharide from Antarctic Pseudoalteromonas sp. LP6-12-2

Wang, D., Li, H., Zhao, Y. X., Cong, B., & Zhang, P. (2025) · Extremophiles · doi:10.1007/s00792-025-01394-2 · Cited by 3 · see citing works

Exopolysaccharides May Increase Gastrointestinal Stress Tolerance of Lactobacillus reuteri

Fedorová, M., Nemcová, R., Mudroňová, D., Styková, E., Brudňáková, M., & Reiffová, K. (2018) · Folia veterinaria · doi:10.2478/fv-2018-0034 · Cited by 3 · see citing works

The probiotic characteristics of Lactobacillus reuteri ZJ617 and its resistance to Escherichia coli O157:H7 challenge in HFD-fed mice

Ma, Y., Mao, Y., Deng, Z., Wang, S., Liu, J., & Wang, H. (2025) · Animal Nutriomics · doi:10.1017/anr.2025.3 · Cited by 2 · see citing works

Exploring the Therapeutic Potential of Diverse Bacterial Strains for Management of Periodontal Diseases

Amani, A., Koroupi, K., Langarizadeh, M. A., Aghilinasab, A., Tavakoli, M. R., Afshari, A., & Forootanfar, H. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10786-x · Cited by 2 · see citing works

PROBIOTIC PROPERTIES OF LACTOBACILLUS REUTERI (L. REUTERI) STRAINS

Novikova, V. P., & Магомедова, Д. М. (2023) · Children s medicine of the North-West · doi:10.56871/cmn-w.2023.75.34.002 · Cited by 3 · see citing works

Acetolactate Decarboxylase as an Important Regulator of Intracellular Acidification, Morphological Features, and Antagonism Properties in the Probiotic Lactobacillus reuteri

Wang, X., Chen, P., Wang, J., Wang, Y., Yu, M., Wang, X., Li, Q., Zhang, X., & Duan, J. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300337 · Cited by 2 · see citing works

The MATH test. A three-phase assay?

Salas-Tovar, J. A., Escobedo‐García, S., Olivas, G. I., Acosta‐Muñiz, C. H., Harte, F., & Sepulveda, D. R. (2024) · FEMS Microbiology Letters · doi:10.1093/femsle/fnae045 · Cited by 2 · see citing works

Atık Sulardan İzole Edilen Pseudomonas Spp.’ lerin Ekzopolisakkarit Üretimine Bazı Ağır Metallerin Etkisi

Yalçın, S., Öztürk, Ş., & Keloğlu, B. (2018) · Nevşehir Bilim ve Teknoloji Dergisi · doi:10.17100/nevbiltek.402196 · Cited by 1 · see citing works

Limosilactobacillus reuteri L26 BiocenolTM and its exopolysaccharide: Their influence on rotavirus-induced immune molecules in enterocyte-like cells

Schusterová, P., Mudroňová, D., Peňazziová, K., Hajdučková, V., & Csank, T. (2024) · Veterinární Medicína · doi:10.17221/106/2023-vetmed · Cited by 1 · see citing works

Extracellular Polysaccharides: An Innovative Prebiotic with Potential Health Benefits Targeting Gut Flora

Ray, M., Ashwini, M., Bhargava, N., & Mondal, K. C. (2025) · Springer eBooks · doi:10.1007/978-3-031-94472-7_14 · Cited by 1 · see citing works

Limosilactobacillus reuteri DSM 17648 as an adjuvant in the fight against Helicobacter pylori infection: Mechanisms of action, clinical efficacy, and prospects

Sitkin, S. I. (2026) · Almanac of Clinical Medicine · doi:10.18786/2072-0505-2026-54-001 · Cited by 1 · see citing works

Probiyotik Mayalar ve Özellikleri

YILDIRAN, H., Kılıç, G. B., & Karahan, A. G. (2017) · Turkish Journal of Agriculture - Food Science and Technology · doi:10.24925/turjaf.v5i10.1148-1155.1239 · Cited by 1 · see citing works

BEYAZ PEYNİRDEN İZOLE EDİLEN CRYPTOCOCCUS HUMICOLA SUŞLARININ STARTER AKTİVİTELERİNİN ARAŞTIRILMASI

UZUNDAĞ, D. (2020) · GIDA / THE JOURNAL OF FOOD · doi:10.15237/gida.gd20076 · Cited by 1 · see citing works

Comprehensive mapping of the cell response to E. coli infection in porcine intestinal epithelial cells pretreated with exopolysaccharide derived from Lactobacillus reuteri

Tkáčiková, Ľ., Mochnáčová, E., Tyagi, P., Kiššová, Z., & Bhide, M. R. (2020) · Veterinary Research · doi:10.1186/s13567-020-00773-1 · Cited by 13 · see citing works

Exopolysaccharide Synthesized byLactobacillus reuteriDecreases the Ability of EnterotoxigenicEscherichia coliTo Bind to Porcine Erythrocytes

Wang, Y., Gänzle, M. G., & Schwab, C. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.03137-09 · Cited by 77 · see citing works

Structure and Function Relationships of Exopolysaccharides Produced by Lactic Acid Bacteria

Chen, X. (2017) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3445hq7c · Cited by 1 · see citing works

Immunomodulatory effect of probiotic exopolysaccharides in a porcine in vitro co-culture model mimicking the intestinal environment on ETEC infection

Kiššová, Z., Mudroňová, D., Link, R., & Tkáčiková, Ľ. (2023) · Veterinary Research Communications · doi:10.1007/s11259-023-10237-4 · Cited by 7 · see citing works

Strain specific immunostimulatory potential of lactobacilli-derived exopolysaccharides

Ciszek‐Lenda, M., Strus, M., Górska, S., Targosz‐Korecka, M., Heczko, P. B., Gamian, A., & Marcinkiewicz, J. (2011) · Jagiellonian University Repository (Jagiellonian University) · Cited by 17 · see citing works