Microbial recognition by Toll-like receptors

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631

A Toll-like receptor recognizes bacterial DNA

Hemmi, H., Takeuchi, O., Kawai, T., Kaisho, T., Sato, S., Sanjo, H., Matsumoto, M., Hoshino, K., Wagner, H., Takeda, K., et al. (2000) · Nature · doi:10.1038/35047123 · Cited by 6,491 · cited 1×

Toll-Like Receptors

Takeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141126 · Cited by 6,143

A human homologue of the Drosophila Toll protein signals activation of adaptive immunity

Medzhitov, R., Preston-Hurlburt, P., & Janeway, C. A. J. (1997) · Nature · doi:10.1038/41131 · Cited by 6,137

Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3

Alexopoulou, L., Holt, A. C., Medzhitov, R., & Flavell, R. A. (2001) · Nature · doi:10.1038/35099560 · Cited by 6,129

Toll-like receptors: critical proteins linking innate and acquired immunity

Akira, S., Takeda, K., & Kaisho, T. (2001) · Nature Immunology · doi:10.1038/90609 · Cited by 4,777

The Dorsoventral Regulatory Gene Cassette spätzle/Toll/cactus Controls the Potent Antifungal Response in Drosophila Adults

Lemaître, B., Nicolas, E., Michaut, L., Reichhart, J., & Hoffmann, J. A. (1996) · Cell · doi:10.1016/s0092-8674(00)80172-5 · Cited by 4,224

Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components.

Takeuchi, O., Hoshino, K., Kawai, T., Sanjo, H., Takada, H., Ogawa, T., Takeda, K., & Akira, S. (1999) · Immunity · doi:10.1016/s1074-7613(00)80119-3 · Cited by 3,680

The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5

Hayashi, F., Smith, K. D., Ozinsky, A., Hawn, T. R., Yi, E. C., Goodlett, D. R., Eng, J. K., Akira, S., Underhill, D. M., & Aderem, A. A. (2001) · Nature · doi:10.1038/35074106 · Cited by 3,605

Cutting Edge: Toll-Like Receptor 4 (TLR4)-Deficient Mice Are Hyporesponsive to Lipopolysaccharide: Evidence for TLR4 as the Lps Gene Product

Hoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Takeda, K., & Akira, S. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.3749 · Cited by 3,374

Overview and Outlook of Toll-like Receptor ligand–antigen Conjugate Vaccines

Fujita, Y., & Taguchi, H. (2012) · Therapeutic Delivery · doi:10.4155/tde.12.52 · Cited by 45

Toll-like receptor 2 and Toll-like receptor 4 polymorphisms in invasive pneumococcal disease

Moens, L., Verhaegen, J., Pierik, M. J., Vermeire, S., Boeck, K. D., Peetermans, W. E., & Bossuyt, X. (2006) · Microbes and Infection · doi:10.1016/j.micinf.2006.10.002 · Cited by 44

Efficient Chemokine-dependent Migration and Primary and Secondary IL-12 Secretion by Human Dendritic Cells Stimulated Through Toll-like Receptors

Lehner, M., Morhart, P., Stilper, A., Petermann, D., Weller, P., Stachel, D., & Holter, W. (2007) · Journal of Immunotherapy · doi:10.1097/01.cji.0000211345.11707.46 · Cited by 43

Lactobacillus rhamnosus GG triggers intestinal epithelium injury in zebrafish revealing host dependent beneficial effects

Zhang, Z., Zhang, H., Yang, D., Hao, Q., Yang, H., Meng, D., de Vos, W. M., Guan, L. L., Liu, S., Teame, T., et al. (2024) · iMeta · doi:10.1002/imt2.181 · Cited by 44

Experimental Meningococcal Sepsis in Congenic Transgenic Mice Expressing Human Transferrin

Szatanik, M., Hong, E., Ruckly, C., Ledroit, M., Giorgini, D., Jopek, K., Nicola, M., Deghmane, A., & Taha, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022210 · Cited by 41

Should We Inhibit Type I Interferons in Sepsis?

Mahieu, T., & Libert, C. (2006) · Infection and Immunity · doi:10.1128/iai.00829-06 · Cited by 42

Dendritic Cell Subsets and Toll-Like Receptors

Hochrein, H., & O’Keeffe, M. A. (2007) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-72167-3_8 · Cited by 42

Suppression of homodimerization of toll-like receptor 4 by isoliquiritigenin

Park, S., & Youn, H. (2010) · Phytochemistry · doi:10.1016/j.phytochem.2010.07.008 · Cited by 42

Fusobacterium nucleatum Enters Normal Human Oral Fibroblasts In Vitro

Dabija‐Wolter, G., Cimpan, M. R., Costea, D. E., Johannessen, A. C., Sørnes, S., Neppelberg, E., Al‐Haroni, M., Skaug, N., & Bakken, V. (2009) · Journal of Periodontology · doi:10.1902/jop.2009.090051 · Cited by 41

TLR2 agonists and their structure–activity relationships

Lu, B. L., Williams, G. M., & Brimble, M. A. (2020) · Organic & Biomolecular Chemistry · doi:10.1039/d0ob00942c · Cited by 41

MYD88 L265P and CD79B double mutations type (MCD type) of diffuse large B-cell lymphoma: mechanism, clinical characteristics, and targeted therapy

Chen, R., Zhou, D., Wang, L., Zhu, L., & Ye, X. (2022) · Therapeutic Advances in Hematology · doi:10.1177/20406207211072839 · Cited by 42

Functional expression of TLR9 in esophageal cancer

Zhang, Y., WANG, Q., Ma, A., Li, Y., Li, R., & Wang, Y. (2014) · Oncology Reports · doi:10.3892/or.2014.3095 · Cited by 40

Antibacterial responses of retinal Müller glia: production of antimicrobial peptides, oxidative burst and phagocytosis

Singh, P. K., Shiha, M. J., & Kumar, A. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-33 · Cited by 41

Immune Response in Thyroid Cancer: Widening the Boundaries

Ward, L. S. (2014) · Scientifica · doi:10.1155/2014/125450 · Cited by 40

Toll-Like Receptor 4 Modulates Myocardial Ischaemia–Reperfusion Injury: Role of Matrix Metalloproteinases

Stapel, H., Kim, S.-C., Osterkamp, S., Knuefermann, P., Hoeft, A., Meyer, R., Grohé, C., & Baumgarten, G. (2006) · European Journal of Heart Failure · doi:10.1016/j.ejheart.2006.03.005 · Cited by 38

High-throughput living cell-based optical biosensor for detection of bacterial lipopolysaccharide (LPS) using a red fluorescent protein reporter system

Jiang, H., Jiang, D., Shao, J., Sun, X., & Wang, J.-S. (2016) · Scientific Reports · doi:10.1038/srep36987 · Cited by 38

My D 88 is essential for alveolar bone loss induced by A ggregatibacter actinomycetemcomitans lipopolysaccharide in mice

Madeira, M. F. M., Queiroz‐Junior, C. M., Cisalpino, D., Werneck, S. M. C., Kikuchi, H., Fujise, O., Ryffel, B., Silva, T. A., Teixeira, M. M., & Souza, D. G. (2013) · Molecular Oral Microbiology · doi:10.1111/omi.12034 · Cited by 37

TLR-4 and -6 agonists reverse apoptosis and promote maturation of simian virus 5-infected human dendritic cells through NFkB-dependent pathways

Arimilli, S., Johnson, J. B., Alexander‐Miller, M. A., & Parks, G. D. (2007) · Virology · doi:10.1016/j.virol.2007.02.035 · Cited by 38

Molecular cloning and expression analysis of chicken MyD88 and TRIF genes

Wheaton, S., Wheaton, S., Lambourne, M. D., Wheaton, S., Lambourne, M. D., Sarson, A. J., Brisbin, J. T., Mayameei, A., & Sharif, S. (2007) · DNA sequence · doi:10.1080/10425170701295856 · Cited by 36

Stimulation of mast cells via FcɛR1 and TLR2: The type of ligand determines the outcome

Fehrenbach, K., Port, F., Grochowy, G., Kalis, C., Bessler, W. G., Galanos, C., Krystal, G., Freudenberg, M. A., & Huber, M. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.09.011 · Cited by 36

Ontogeny of bivalve immunity: assessing the potential of next‐generation sequencing techniques

Bassim, S., Génard, B., Gauthier-Clerc, S., Moraga, D., & Tremblay, R. (2014) · Reviews in Aquaculture · doi:10.1111/raq.12064 · Cited by 35

Correlation of TLR1-10 expression in peripheral blood mononuclear cells with chronic hepatitis B and chronic hepatitis B-related liver failure

Wang, K., Liu, H., He, Y., Chen, T., Yang, Y., Niu, Y., Chen, H., Chen, Y., Liu, J., Ye, F., et al. (2010) · Human Immunology · doi:10.1016/j.humimm.2010.07.013 · Cited by 35

Toll‐like receptors as novel therapeutic targets for herpes simplex virus infection

Jahanban‐Esfahlan, R., Seidi, K., Majidinia, M., Karimian, A., Yousefi, B., Nabavi, S. M., Astani, A., Berindan‐Neagoe, I., Gulei, D., Fallarino, F., et al. (2019) · Reviews in Medical Virology · doi:10.1002/rmv.2048 · Cited by 34

Pellino-1 derived cationic antimicrobial prawn peptide: Bactericidal activity, toxicity and mode of action

Ravichandran, G., Kumaresan, V., Arasu, M. V., Al-Dhabi, N. A., Munuswamy‐Ramanujam, G., Mahesh, A., Dhayalan, A., Pasupuleti, M., & Arockiaraj, J. (2016) · Molecular Immunology · doi:10.1016/j.molimm.2016.09.015 · Cited by 33

Innate immune adaptor MyD88 deficiency prevents skin inflammation in SHARPIN-deficient mice

Sharma, B. R., Karki, R., Lee, E., Zhu, Q., Gurung, P., & Kanneganti, T. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0159-7 · Cited by 33

Contribution of the microbiome for better phenotyping of people living with obesity

Ciaula, A. D., Bonfrate, L., Khalil, M., Garruti, G., & Portincasa, P. (2023) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-023-09798-1 · Cited by 40

TLRs antiviral effect on hepatitis B virus in HepG2 cells

Xia, C., Lu, M., Zhang, Z., Meng, Z., Zhang, Z., & Shi, C. (2008) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2008.03896.x · Cited by 33

Bacterial Infections and Ceramide

Grassmé, H., & Becker, K. A. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-7091-1511-4_15 · Cited by 32

Wolbachia- andOnchocerca volvulus-Induced Keratitis (River Blindness) Is Dependent on Myeloid Differentiation Factor 88

Gillette‐Ferguson, I., Hise, A. G., Sun, Y., Diaconu, E., McGarry, H. F., Taylor, M. J., & Pearlman, E. M. (2006) · Infection and Immunity · doi:10.1128/iai.74.4.2442-2445.2006 · Cited by 32

Altered Levels ofSalmonellaDNA Adenine Methylase Are Associated with Defects in Gene Expression, Motility, Flagellar Synthesis, and Bile Resistance in the Pathogenic Strain 14028 but Not in the Laboratory Strain LT2

Badie, G., Heithoff, D. M., Sinsheimer, R. L., & Mahan, M. J. (2006) · Journal of Bacteriology · doi:10.1128/jb.01580-06 · Cited by 31

Toll‐Like Receptors and Tissue Remodeling: The Pro/Cons Recent Findings

Micera, A., Balzamino, B. O., Zazzo, A. D., Biamonte, F., Sica, G., & Bonini, S. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25124 · Cited by 29

The Vertebrate TLR Supergene Family Evolved Dynamically by Gene Gain/Loss and Positive Selection Revealing a Host–Pathogen Arms Race in Birds

Khan, I., Maldonado, E., Silva, L., Almeida, D., Johnson, W. E., O’Brien, S. J., Zhang, G., Jarvis, E. D., Gilbert, M. T. P., & Antunes, A. (2019) · Diversity · doi:10.3390/d11080131 · Cited by 29

Hostile Communication of Measles Virus with Host Innate Immunity and Dendritic Cells

Hahm, B. (2008) · Current topics in microbiology and immunology · doi:10.1007/978-3-540-70617-5_13 · Cited by 29

Plasticity of dendritic cell function in response to prostaglandin E2 (PGE2) and interferon-γ (IFN-γ)

Lehner, M., Stilper, A., Morhart, P., & Holter, W. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0307153 · Cited by 29

Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells duringStaphylococcus aureusInternalization

Medina-Estrada, I., López-Meza, J. E., & Ochoa‐Zarzosa, A. (2016) · Mediators of Inflammation · doi:10.1155/2016/6120509 · Cited by 29

Aging in the absence of TLR2 is associated with reduced IFN-γ responses in the large intestine and increased severity of induced colitis

Albert, E. J., & Marshall, J. S. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0807557 · Cited by 29

Tumor necrosis factor‐α and interleukin‐1β expression pathway induced by Streptococcus mutans in macrophage cell line RAW 264.7

Kim, J. S., Kim, K. D., Na, H. S., Jeong, S., Park, H. R., Kim, S., & Chung, J. (2012) · Molecular Oral Microbiology · doi:10.1111/j.2041-1014.2012.00639.x · Cited by 28

Mouse Macrophages Are Permissive to MotileLegionellaSpecies That Fail To Trigger Pyroptosis

Whitfield, N. N., Byrne, B. G., & Swanson, M. S. (2009) · Infection and Immunity · doi:10.1128/iai.00070-09 · Cited by 28

Brucella infection and Toll-like receptors

Yu, H. L., Gu, X., Wang, D., & Wang, Z. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1342684 · Cited by 27

Recognition of Candida albicans by gingival fibroblasts: The role of TLR2, TLR4/CD14, and MyD88

Pinheiro, C. R., Coelho, A. L., de Oliveira, C. E., Gasparoto, T. H., Garlet, G. P., Silva, J. S., Santos, C. F., Cavassani, K. A., Hogaboam, C. M., & Campanelli, A. P. (2017) · Cytokine · doi:10.1016/j.cyto.2017.10.013 · Cited by 27

Mannan binding lectin attenuates double‐stranded RNA‐mediated TLR3 activation and innate immunity

Liu, H., Zhou, J., Ma, D., Lu, X., Ming, S., Shan, G., Zhang, X., Hou, J., Chen, Z., & Zuo, D. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.01.064 · Cited by 27

Expression of Toll-like receptors and downstream genes in lipopolysaccharide-induced porcine alveolar macrophages

Islam, M. A., Çınar, M. U., Uddin, M. J., Tholen, E., Tesfaye, D., Looft, C., & Schellander, K. (2012) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2012.02.001 · Cited by 26

Network Pharmacology Analysis of the Mechanisms of Compound Herba Sarcandrae (Fufang Zhongjiefeng) Aerosol in Chronic Pharyngitis Treatment

Zhang, Y., Yuan, T., Li, Y., Wu, N., & Dai, X. (2021) · Drug Design Development and Therapy · doi:10.2147/dddt.s304708 · Cited by 26

Strategies used by Yersinia enterocolitica to evade killing by the host: thinking beyond Yops

Dhar, M. S., & Virdi, J. S. (2013) · Microbes and Infection · doi:10.1016/j.micinf.2013.11.002 · Cited by 25

Human monocytoid cells as a model to study Toll-like receptor-mediated activation

Remer, K. A., Brcic, M., Sauter, K., & Jungi, T. W. (2006) · Journal of Immunological Methods · doi:10.1016/j.jim.2005.07.026 · Cited by 25

PRE- AND POSTOPERATIVE CYTOKINE RELEASE AFTER IN VITRO WHOLE BLOOD LIPOPOLYSACCHARIDE STIMULATION AND FREQUENT TOLL-LIKE RECEPTOR 4 POLYMORPHISMS

Kumpf, O., Hamann, L., Schlag, P. M., & Schumann, R. R. (2006) · Shock · doi:10.1097/01.shk.0000190823.44030.e6 · Cited by 25

Oleanolic Acid Acetate Exerts Anti-Inflammatory Activity via IKKα/β Suppression in TLR3-Mediated NF-κB Activation

Lim, H. J., Jang, H., Kim, M. H., Lee, S., Lee, S., Lee, S. W., & Rho, M. (2019) · Molecules · doi:10.3390/molecules24214002 · Cited by 24

N-Palmitoyl-D-Glucosamine Inhibits TLR-4/NLRP3 and Improves DNBS-Induced Colon Inflammation through a PPAR-α-Dependent Mechanism

Palenca, I., Seguella, L., Re, A., Franzin, S. B., Corpetti, C., Pesce, M., Rurgo, S., Steardo, L., Sarnelli, G., & Esposito, G. (2022) · Biomolecules · doi:10.3390/biom12081163 · Cited by 23

Baicalin suppresses expression of TLR2/4 and NF-κB in chlamydia trachomatis–infected mice

Huang, H., Gufu, H., Lei, F., Dang, L., & Zhongliang, Y. (2011) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2011.580756 · Cited by 23

TLR Ligand-Induced Type I IFNs Affect Thymopoiesis

Baron, M., Gauchat, D., Motte-Mohs, R. N. L., Kettaf, N., Abdallah, A., Michiels, T., Zúñiga‐Pflücker, J. C., & Sékaly, R. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.11.7134 · Cited by 24

3LPS-binding protein and its interactions with P. gingivalis LPS modulate pro-inflammatory response and Toll-like receptor signaling in human oral keratinocytes

Ding, P., Darveau, R. P., Wang, C., & Jin, L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173223 · Cited by 23

Development and function of chicken XCR1+ conventional dendritic cells

Wu, Z., Shih, B. B.-J., Macdonald, J., Meunier, D., Hogan, K., Chintoan‐Uta, C., Gilhooley, H. J., Hu, T., Beltrán, M., Henderson, N. C., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1273661 · Cited by 22

Interleukin‐18 Increases TLR4 and Mannose Receptor Expression and Modulates Cytokine Production in Human Monocytes

Dias‐Melicio, L. A., Fernandes, R. K., Rodrigues, D. R., Golim, M. D. A., & Soares, Â. M. V. D. C. (2015) · Mediators of Inflammation · doi:10.1155/2015/236839 · Cited by 24

Activation of cell membrane-localized Toll-like receptor 3 by siRNA

Pirher, N., Pohar, J., Manček‐Keber, M., Benčina, M., & Jerala, R. (2017) · Immunology Letters · doi:10.1016/j.imlet.2017.03.019 · Cited by 23

Toll like receptor 4 and membrane-bound CD14 expressions in gingivitis, periodontitis and CsA-induced gingival overgrowth

Becerik, S., Özsan, N., Gürkan, A., Öztürk, V. Ö., Atilla, G., & Emingil, G. (2010) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2010.11.008 · Cited by 22

Release of Interleukins 6 and 8 Induced by Zymosan and Mediated by MAP Kinase and NF-κB Signaling Pathways in Human Corneal Fibroblasts

Nomi, N., Kimura, K., & Nishida, T. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4823 · Cited by 22

Toll-like receptors (TLRs) respond to tributyltin chloride (TBT-Cl) exposure in the river pufferfish (Takifugu obscurus): Evidences for its toxic injury function

Zhao, C.-S., Fang, D., & Xu, D. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.02.050 · Cited by 20

A Novel Function of TLR2 and MyD88 in the Regulation of Leukocyte Cell Migration Behavior During Wounding in Zebrafish Larvae

Hu, W., van Steijn, L., Li, C., Verbeek, F. J., Cao, L., Merks, R. M. H., & Spaink, H. P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.624571 · Cited by 21

Nuclear PTEN enhances the maturation of a microRNA regulon to limit MyD88-dependent susceptibility to sepsis

Sisti, F., Wang, S., Brandt, S. L., Glosson, N. L., Mayo, L. D., Son, Y. M., Sturgeon, S. M., Filgueiras, L. R., Jancar, S., Wong, H. R., et al. (2018) · Science Signaling · doi:10.1126/scisignal.aai9085 · Cited by 19

TLR9 agonists: Immune mechanisms and therapeutic potential in domestic animals

Mutwiri, G. (2011) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2011.05.032 · Cited by 18

Correlation of Circulating TLR2/4 Expression with CD3 + /4 + /8 + T Cells and Treg cells in HBV-Related Liver Cirrhosis

Lian, J., Wang, X., Zhang, Y., Huang, C., & Bai, X. (2009) · Viral Immunology · doi:10.1089/vim.2009.0039 · Cited by 19

Toll-like receptors in hepatocellular carcinoma: potential novel targets for pharmacological intervention

Zou, H., Wang, W.-K., Liu, Y., Braddock, M., Zheng, M., & Huang, D. (2016) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2016.1168809 · Cited by 18

RNA interference-mediated silencing of genes involved in the immune responses of the soybean pod borer Leguminivora glycinivorella (Lepidoptera: Olethreutidae)

Ran, R., Li, T., Liu, X., Ni, H., Li, W., & Meng, F. (2018) · PeerJ · doi:10.7717/peerj.4931 · Cited by 18

Wild-typeLeishmania donovanipromastigotes block maturation, increase integrin expression and inhibit detachment of human monocyte-derived dendritic cells – the influence of phosphoglycans

Tejle, K., Lindroth, M., Magnusson, K., & Rasmusson, B. J. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.01013.x · Cited by 18

Mechanical Ventilation Augments Poly(I:C)-Induced Lung Injury via a WISP1-Integrin β3-Dependent Pathway in Mice

Jin, S., Chen, Z., Ding, X., Zhao, X., Jiang, X., Tong, Y., Billiar, T. R., & Li, Q. (2016) · Molecular Medicine · doi:10.2119/molmed.2015.00233 · Cited by 17

Effect of Low-Fat Diet in Obese Mice Lacking Toll-like Receptors

Rau, C., Wu, S., Lu, T., Wu, Y.-C., Wu, C., Chien, P., Kuo, P., Lin, C.-W., Tsai, C.-W., & Hsieh, C. (2018) · Nutrients · doi:10.3390/nu10101464 · Cited by 17

An in vitro investigation of immunomodulatory properties of Lactobacillus plantarum and L. delbrueckii cells and their extracellular polysaccharides

Kishimoto, M., Nomoto, R., Mizuno, M., & Osawa, R. (2017) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.17-001 · Cited by 17

Lactobacillus plantarum RS-09 Induces M1-Type Macrophage Immunity Against Salmonella Typhimurium Challenge via the TLR2/NF-κB Signalling Pathway

Zhao, C., Chen, H., Liang, H., Zhao, X., Tang, W., Wei, M., Li, Y., Zhang, J., Yu, X., Chen, G., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.832245 · Cited by 16

Evolution of Resistance Genes in Plants

Xiao, S., Wang, W., & Yang, X. (2007) · Nucleic acids and molecular biology · doi:10.1007/978-3-540-73930-2_1 · Cited by 16

miR-146a modulates TLR1/2 and 4 induced inflammation and links it with proliferation and lipid production via the indirect regulation of GNG7 in human SZ95 sebocytes

Dull, K., Fazekas, F., Deák, D., Kovács, D., Póliska, S., Szegedi, A., Zouboulis, C. C., & Törőcsik, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-00907-1 · Cited by 17

Toll-Like Receptor Ligands Reverse Suppression of Contact Hypersensitivity Reactions Induced by Epicutaneous Immunization with Protein Antigen

Ptak, W., Bryniarski, K., Ptak, M., Majewska, M., Gamian, A., Lobo, F. M., & Szczepanik, M. (2006) · International Archives of Allergy and Immunology · doi:10.1159/000091164 · Cited by 15

Goose toll-like receptor 3 (TLR3) mediated IFN-γ and IL-6 in anti-H5N1 avian influenza virus response

Yong, Y., Liu, S.-F., Hua, G., Jia, R., Gooneratne, R., Zhao, Y., Liao, M., & Ju, X. (2018) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2018.01.010 · Cited by 15

Mental Disorders Linked to Crosstalk between The Gut Microbiome and The Brain

Choi, T.-Y., Choi, Y. P., & Koo, J. W. (2020) · Experimental Neurobiology · doi:10.5607/en20047 · Cited by 18

Differential expression of Toll-like receptors and inflammatory cytokines in ovine interdigital dermatitis and footrot

Davenport, R., Heawood, C., Sessford, K., Baker, M., Baiker, K., Blacklaws, B., Kaler, J., Green, L. E., & Tötemeyer, S. S. (2014) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2014.07.007 · Cited by 15

Simulated spatial radiation impacts learning and memory ability with alterations of neuromorphology and gut microbiota in mice

Song, C., Gao, X., Song, W., Zeng, D., Shan, S., Yin, Y., Li, Y., Baranenko, D., & Lu, W. (2020) · RSC Advances · doi:10.1039/d0ra01017k · Cited by 14

Specific loss of Toll-like receptor 2 on bone marrow derived cells decreases atherosclerosis in LDL receptor null mice*The senior author, Stewart C. Whitman, passed away on 19 February 2010. The manuscript has been communicated by Ross W. Milne (e-mail: rmilne@ottawaheart.ca) and Yves L. Marcel (e-mail: ylmarcel@ottawaheart.ca), University of Ottawa Heart Institute, 40 Ruskin Street, Ottawa, ON K1Y 4W7, Canada.

Hasu, M., Thabet, M., Tam, N. W. N., & Whitman, S. C. (2011) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y11-071 · Cited by 14

Cytokine Reporter Mouse System for Screening Novel IL12/23 p40-inducing Compounds

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