Critical Role for NALP3/CIAS1/Cryopyrin in Innate and Adaptive Immunity through Its Regulation of Caspase-1

The Inflammasome

Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066

IL-33, an Interleukin-1-like Cytokine that Signals via the IL-1 Receptor-Related Protein ST2 and Induces T Helper Type 2-Associated Cytokines

Schmitz, J., Owyang, A. M., Oldham, E. R., Song, Y., Murphy, E., McClanahan, T. K., Zurawski, G., Moshrefi, M., Qin, J., Li, X., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.09.015 · Cited by 3,773

Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection

Girardin, S. E., Boneca, I. G., Viala, J., Chamaillard, M., Labigne-Roussel, A., Thomas, G. D., Philpott, D. J., & Sansonetti, P. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200651200 · Cited by 2,397

Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf

Mariathasan, S., Newton, K., Monack, D. M., Vucic, D., French, D. M., Lee, W. P., Roose-Girma, M., Erickson, S. L., & Dixit, V. M. (2004) · Nature · doi:10.1038/nature02664 · Cited by 1,864

NALP3 Forms an IL-1β-Processing Inflammasome with Increased Activity in Muckle-Wells Autoinflammatory Disorder

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Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2

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Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndrome

Hoffman, H. M., Mueller, J. L., Broide, D. H., Wanderer, A. A., & Kolodner, R. D. (2001) · Nature Genetics · doi:10.1038/ng756 · Cited by 1,679

Altered Cytokine Export and Apoptosis in Mice Deficient in Interleukin-1β Converting Enzyme

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Mice deficient in IL-1β-converting enzyme are defective in production of mature IL-1β and resistant to endotoxic shock

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NOD-LRR PROTEINS: Role in Host-Microbial Interactions and Inflammatory Disease

Inohara, N., Chamaillard, M., McDonald, C., & Núñez, G. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133347 · Cited by 1,019

Acidosis Potentiates the Host Proinflammatory Interleukin-1β Response to Pseudomonas aeruginosa Infection

Torres, I. M., Patankar, Y. R., Shabaneh, T. B., Dolben, E. F., Hogan, D. A., Leib, D. A., & Berwin, B. L. (2014) · Infection and Immunity · doi:10.1128/iai.02024-14 · Cited by 18

Synthesis, activity and mechanism of alkoxy-, carbamato-, sulfonamido-, thioureido-, and ureido-derivatives of 2,4,5-trimethylpyridin-3-ol against inflammatory bowel disease

Chaudhary, C. L., Gurung, P., Jang, S., Banskota, S., Nam, T., Kim, J., & Jeong, B. (2019) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2019.1677637 · Cited by 18

Macrophage cell death upon intracellular bacterial infection

Lai, X., Xu, Y., Chen, X.-M., & Ren, Y. (2015) · Macrophage · doi:10.14800/macrophage.779 · Cited by 18

Lipoxin A4 inhibits proliferation and inflammatory cytokine/chemokine production of human epidermal keratinocytes associated with the ERK1/2 and NF-κB pathways

Hu, F., Liu, X., Wang, X., Alashkar, M., Zhang, S., Xu, J., Zhong, X.-L., He, M. L., Feng, A.-P., & Chen, H. (2015) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2015.03.009 · Cited by 18

Engineered Pigs Carrying a Gain-of-Function NLRP3 Homozygous Mutation Can Survive to Adulthood and Accurately Recapitulate Human Systemic Spontaneous Inflammatory Responses

Li, W., Shi, L., Zhuang, Z., Wu, H., Lian, M., Chen, Y., Li, L., Ge, W., Jin, Q., Zhang, Q., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901468 · Cited by 18

Knockout of Sirt2 alleviates traumatic brain injury in mice

Wang, W., Gong, Q.-Y., Cai, L., Yao, J., Yang, D.-X., Yuan, F., Chen, H., & Tian, H.-L. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.346457 · Cited by 18

Pathophysiology of drug hypersensitivity

Elzagallaai, A. A., & Rieder, M. J. (2022) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.15645 · Cited by 18

Electrical stimulation facilitates NADPH production in pentose phosphate pathway and exerts an anti-inflammatory effect in macrophages

Uemura, M., Maeshige, N., Yamaguchi, A., Ma, X., Matsuda, M., Nishimura, Y., Hasunuma, T., Inoue, T., Yan, J., Wang, J., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-44886-x · Cited by 17

Nano‑selenium alleviates the pyroptosis of cardiovascular endothelial cells in chicken induced by decabromodiphenyl ether through ERS-TXNIP-NLRP3 pathway

Jiang, Y., Dong, B., Xing, J., Shan, J., Fang, C., Zhang, K., Li, D., Xu, C., & Zhang, Z. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.170129 · Cited by 17

Novel in vitro evidence on the beneficial effect of quercetin treatment in vascular calcification

Ceccherini, E., Gisone, I., Persiani, E., Ippolito, C., Falleni, A., Cecchettini, A., & Vozzi, F. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1330374 · Cited by 18

Purification and Analysis of the Interactions of Caspase-1 and ASC for Assembly of the Inflammasome

Narayanan, K. B., & Park, H. H. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-014-1471-4 · Cited by 16

IL-10 immunodepletion from meningococcal sepsis plasma induces extensive changes in gene expression and cytokine release in stimulated human monocytes

Gopinathan, U., Brusletto, B. S., Olstad, O. K., Kierulf, P., Berg, J. P., Brandtzaeg, P., & Øvstebø, R. (2014) · Innate Immunity · doi:10.1177/1753425914547743 · Cited by 17

Glyburide inhibits the bone resorption induced by traumatic occlusion in rats

Arita, Y., Yoshinaga, Y., Kaneko, T., Kawahara, Y., Nakamura, K., Ohgi, K., Arita, S., Ryu, T., Takase, M., & Sakagami, R. (2020) · Journal of Periodontal Research · doi:10.1111/jre.12731 · Cited by 17

Demethyleneberberine blocked the maturation of IL-1β in inflammation by inhibiting TLR4-mitochondria signaling

Zhao, Y., Liu, P., Zhang, Y., Jiang, H., Luan, H., Ying-mei, X., Zhang, Y., & Li, R. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109319 · Cited by 17

Therapeutic Administration of a Monoclonal Anti-Il-1β Antibody Protects Against Experimental Melioidosis

Weehuizen, T. A. F., Lankelma, J. M., de Jong, H. K., de Boer, O. J., Roelofs, J. J. T. H., Day, N., Gram, H., de Vos, A. F., & Wiersinga, W. J. (2016) · Shock · doi:10.1097/shk.0000000000000625 · Cited by 17

Innate immunity against Legionella pneumophila during pulmonary infections in mice

Park, B., Park, G., Kim, J., Lim, S. A., & Lee, K. (2017) · Archives of Pharmacal Research · doi:10.1007/s12272-016-0859-9 · Cited by 17

Inhibitory effects of dietary soy isoflavone and gut microbiota on contact hypersensitivity in mice

Nagano, T., Katase, M., & Tsumura, K. (2018) · Food Chemistry · doi:10.1016/j.foodchem.2018.08.043 · Cited by 17

The Role of Peroxiredoxins in the Regulation of Sepsis

Aki, T., Unuma, K., & Uemura, K. (2022) · Antioxidants · doi:10.3390/antiox11010126 · Cited by 16

Microglial- neuronal crosstalk in chronic viral infection through mTOR, SPP1/OPN and inflammasome pathway signaling

Lopez, C. A., & Brown, A. M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1368465 · Cited by 16

Shared Inflammatory Pathology of Stroke and COVID-19

Sánchez, K. E., & Rosenberg, G. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23095150 · Cited by 16

Neurological Manifestations of Primary Immunodeficiencies.

Chavoshzadeh, Z., Hashemitari, A., & Darougar, S. (2018) · Iranian journal of child neurology. · doi:10.22037/ijcn.v12i3.21586 · Cited by 16

The Endogenous Danger Signal Uric Acid Augments Contact Hypersensitivity Responses in Mice

Liu, L., Inoue, H., Nakayama, H., Kanno, R., & Kanno, M. (2007) · Pathobiology · doi:10.1159/000103377 · Cited by 16

New insights into the nature of autoinflammatory diseases from mice with Nlrp3 mutations

Meng, G., & Strober, W. (2010) · European Journal of Immunology · doi:10.1002/eji.200940191 · Cited by 17

GSNOR negatively regulates the NLRP3 inflammasome via S-nitrosation of MAPK14

Liu, Q., Jiao, L., Ye, M.-S., Ma, Z., Yu, J., Su, L., Zou, W.-Y., Yang, L.-X., Chen, C., & Yao, Y. (2024) · Cellular and Molecular Immunology · doi:10.1038/s41423-024-01155-9 · Cited by 15

The DNA sensor AIM2 mediates psoriasiform inflammation by inducing type 3 immunity

Martins, T. V., de Melo, B. M. S., Toller-Kawahisa, J. E., da Silva, G. V. L., Silva, C. E. A., Paiva, I. M., Públio, G. A., Rosa, M. H., Souza, C. D. S., Zamboni, D. S., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.171894 · Cited by 15

The inflammasome and alum-mediated adjuvanticity

Kang, S., & Locksley, R. M. (2009) · F1000 Biology Reports · doi:10.3410/b1-15 · Cited by 16

Immune Complexes Indirectly Suppress the Generation of Th17 Responses In Vivo

Çıracı, C., Janczy, J. R., Jain, N., Haasken, S., Silva, C. P. E., Benjamim, C. F., Sadler, J. J., Olivier, A. K., Iwakura, Y., Shayakhmetov, D. M., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151252 · Cited by 15

Epidemiology of major burns at the Lebanese Burn Center in Geitawi, Lebanon.

Ghanime, G., Rizkallah, N., & Said, J.-M. (2013) · Europe PMC (PubMed Central) · Cited by 15

Damage control: Management of cellular stress by the NLRP 3 inflammasome

Haasken, S., & Sutterwala, F. S. (2013) · European Journal of Immunology · doi:10.1002/eji.201343848 · Cited by 15

Small molecule inhibitors of NLRP3 inflammasome and GSK-3β in the management of traumatic brain injury: A review

Ghouse, S. M., Joshi, S. V., Akunuri, R., Rana, P., Rahman, Z., Polomoni, A., Yaddanapudi, V. M., Dandekar, M. P., & Nanduri, S. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115718 · Cited by 15

Orchestration of inflammation in contact allergy by innate immune and cellular stress responses

Martin, S. F., Rühl‐Muth, A., & Esser, P. R. (2023) · Allergo Journal International · doi:10.1007/s40629-023-00275-4 · Cited by 15

Francisella tularensis Live Vaccine Strain Folate Metabolism and Pseudouridine Synthase Gene Mutants Modulate Macrophage Caspase-1 Activation

Ulland, T. K., Janowski, A. M., Buchan, B. W., Faron, M. L., Cassel, S. L., Jones, B. D., & Sutterwala, F. S. (2012) · Infection and Immunity · doi:10.1128/iai.00991-12 · Cited by 14

Collagen Type II and a Thermo-Responsive Polymer of N-Isopropylacrylamide Induce Arthritis Independent of Toll-Like Receptors

Shakya, A. K., Kumar, A., Klaczkowska, D., Hultqvist, M. H., Hagenow, K., Holmdahl, R., & Nandakumar, K. S. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.07.034 · Cited by 14

Effect of Tripterygium wilfordii Polycoride on the NOXs-ROS-NLRP3 Inflammasome Signaling Pathway in Mice with Ulcerative Colitis

Ma, F., Ke, Y., Jihong, Z., Yan, S., & Liu, Y. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/9306283 · Cited by 14

Audiometric characteristics of a Dutch family with Muckle-Wells syndrome

Weegerink, N. J. D., Schraders, M., Leijendeckers, J. M., Slieker, K., Huygen, P. L. M., Hoefsloot, L. H., Oostrik, J., Pennings, R. J. E., Simon, A., Snik, A. M., et al. (2011) · Hearing Research · doi:10.1016/j.heares.2011.07.006 · Cited by 14

Cecal Ligation and Puncture-Induced Impairment of Innate Immune Function Does Not Occur in the Absence of Caspase-1

Murphey, E. D. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002102 · Cited by 14

Regulation of inflammation and immunity in sepsis by E3 ligases

Shao, S., Zhou, D., Feng, J., Liu, Y., Baturuhu, Yin, H., & Zhan, D. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1124334 · Cited by 13

Octyl gallate has potent anti‐inflammasome activity by directly binding to NLRP3 LRR domain

Park, H., Ko, R., Seo, J., Ahn, G. Y., Choi, S., Kwon, M., & Lee, S. Y. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31196 · Cited by 13

Prediction of Skin Sensitizers using Alternative Methods to Animal Experimentation

Johansson, H., & Lindstedt, M. (2014) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.12199 · Cited by 13

Langerhans Cells Suppress CD49a+ NK Cell–Mediated Skin Inflammation

Scholz, F., Naik, S., Sutterwala, F. S., & Kaplan, D. H. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500935 · Cited by 13

Overexpression of Macrophage-Inducible C-Type Lectin Mincle Aggravates Proinflammatory Responses to Streptococcus pneumoniae with Fatal Outcome in Mice

Hollwedel, F., Maus, R., Stolper, J., Khan, A., Stocker, B. L., Timmer, M. S. M., Lu, X., Pich, A., Welte, T., Yamasaki, S., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000509 · Cited by 13

Ipriflavone suppresses NLRP3 inflammasome activation in host response to biomaterials and promotes early bone healing

Chen, Y., Li, J., Shi, J., Ning, D., Feng, J., Lin, W., He, F., & Xie, Z. (2022) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.13647 · Cited by 13

Identification and Validation of PKR as a Direct Target for the Novel Sulfonamide-Substituted Tetrahydroquinoline Nonselective Inhibitor of the NLRP3 Inflammasome

Yang, F., Dai, Z., Xue, M.-Y., Chen, X.-Y., Liu, J., Li, W., Xu, L., & Di, B. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c00343 · Cited by 12

Heat shock transcription factor 2 reduces the secretion of IL-1β by inhibiting NLRP3 inflammasome activation in ulcerative colitis

Zhang, F., Zhao, W., Zhou, J., Wang, W., Luo, J., Feng, Y., Wu, J., Li, M., Wang, K., Niu, J., et al. (2020) · Gene · doi:10.1016/j.gene.2020.145299 · Cited by 13

Auditory Phenotype and Histopathologic Findings of a Mutant Nlrp3 Expression Mouse Model

Kim, Y., Lee, S.-Y., Kim, M. Y., Park, K., Han, J. H., Kim, J. H., Kim, B. J., & Choi, B. Y. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.890256 · Cited by 12

The Mechanism of Adjuvanticity of Aluminium-Containing Formulas

Fierens, K., & Kool, M. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212800166004 · Cited by 13

Clinical Evaluation of Humira® Biosimilar ONS-3010 in Healthy Volunteers: Focus on Pharmacokinetics and Pharmacodynamics

Dillingh, M. R., Reijers, J. A. A., Malone, K. E., Burggraaf, J., Bahrt, K., Yamashita, L., Rehrig, C. D., & Moerland, M. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00508 · Cited by 12

Review: Progress of the NLRP3 inflammasome in tumours and perspectives for cholangiocarcinoma

Zhuo, Z., Xie, Y., Zou, H., Tan, B., Dong, Q., Dong, B., & Zhu, C. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02416-4 · Cited by 11

Inhibitors of NLRP3 Inflammasome Formation: A Cardioprotective Role for the Gasotransmitters Carbon Monoxide, Nitric Oxide, and Hydrogen Sulphide in Acute Myocardial Infarction

Payne, F. M., Dabb, A. R., Harrison, J. C., & Sammut, I. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179247 · Cited by 13

NEDD4 E3 ligase-catalyzed NAMPT ubiquitination and autophagy activation are essential for pyroptosis-independent NAMPT secretion in human monocytes

Rodriguez, M., Xu, H., Hernandez, A., Ingraham, J., Canizales, J., Arce, F. T., Camp, S. M., Briggs, S., Ooi, A., Burke, J. M., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02164-5 · Cited by 13

Molecular determinants for a cardiovascular collapse in anthrax

Goldman, D. L. (2014) · Frontiers in Bioscience-Elite · doi:10.2741/e697 · Cited by 11

Research progress of P2X7 receptor in inflammatory bowel disease

Liu, Y., & Liu, X. (2019) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2019.1609077 · Cited by 11

Current Knowledge on Procaspase-1 Variants with Reduced or Abrogated Enzymatic Activity in Autoinflammatory Disease

Luksch, H., Winkler, S., Heymann, M. C., Schulze, F., Hofmann, S. R., Roesler, J., & Rösen‐Wolff, A. (2015) · Current Rheumatology Reports · doi:10.1007/s11926-015-0520-5 · Cited by 11

Lactic acid drives NLRP3 inflammasome activation and caspase-1–like cytokine cleavage via intracellular acidification

Lin, H., Lin, H., Tsai, M.-H., Chen, Y.-J., Bao, B., Tsai, K.-J., Shih, C., Yu, J., Chien, K., Huang, K., et al. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08708-y · Cited by 10

Innate Immune Mechanisms in Contact Dermatitis

Martin, S. F., & Esser, P. R. (2021) · Handbook of experimental pharmacology · doi:10.1007/164_2021_482 · Cited by 10

Dermal exposure to cobalt studiedin vitroin keratinocytes – effects of cobalt exposure on inflammasome activated cytokines, and mRNA response

Klasson, M., Lindberg, M., Westberg, H., Bryngelsson, I.-L., Tuerxun, K., Persson, A., & Särndahl, E. (2021) · Biomarkers · doi:10.1080/1354750x.2021.1975823 · Cited by 11

Cigarette smoke depletes alveolar macrophages and delays clearance of Legionella pneumophila

Fleischmann, M., Jarnicki, A., Brown, A. S., Yang, C., Anderson, G. P., Garbi, N., Hartland, E. L., van Driel, I. R., & Ng, G. Z. (2023) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00268.2022 · Cited by 9

Ultraviolet B induces high mobility group box 1 release from mouse peritoneal macrophages in vitro via caspase-1 mediated secretion pathway

Chakraborty, R., Bhatt, K. H., & Sodhi, A. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.02.006 · Cited by 10

Hereditary Hearing Impairment with Cutaneous Abnormalities

Lee, T.-L., Lin, P., Chen, P., Hong, J., & Wu, C. (2020) · Genes · doi:10.3390/genes12010043 · Cited by 9

Hepatitis B vaccine induces apoptotic death in Hepa1–6 cells

Hamza, H., Cao, J., Li, X., Li, C., Zhu, M., & Zhao, S. (2012) · APOPTOSIS · doi:10.1007/s10495-011-0690-1 · Cited by 10

An additional piece in the puzzle of neutrophil‐derived IL‐1β: The NLRP3 inflammasome

Tamassia, N., Zimmermann, M., & Cassatella, M. A. (2012) · European Journal of Immunology · doi:10.1002/eji.201242399 · Cited by 10

A Shope Fibroma virus PYRIN-only protein modulates the host immune response

Dorfleutner, A., Talbott, S. J., Bryan, N. B., Funya, K. N., Rellick, S. L., Reed, J. C., Shi, X., Rojanasakul, Y., Flynn, D. C., & Stehlik, C. (2006) · Virus Genes · doi:10.1007/s11262-006-0065-9 · Cited by 10

The involvement of the primo vascular system in local enteritis and its modification by electroacupuncture

Nan, S., Wan, J., Lei, Q., Wang, X., Ma, N., Yin, R., Zhu, J., Ding, M., & Ding, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1072996 · Cited by 9

Genetic disruption of the inflammasome adaptor ASC has minimal impact on the pathogenesis of Duchenne muscular dystrophy in mdx Mice

Lau, Y.-S., Zhao, L., Zhang, C., Li, H., & Han, R.-Z. (2020) · Life Science · doi:10.1016/j.lfs.2020.118069 · Cited by 9

State of the art paper Does aspirin-induced oxidative stress cause asthma exacerbation?

Kacprzak, D., & Pawliczak, R. (2015) · Archives of Medical Science · doi:10.5114/aoms.2014.41960 · Cited by 9

Inflammasome Activation by Danger Signals

Pelegrı́n, P. (2011) · Springer eBooks · doi:10.1007/978-3-0348-0148-5_7 · Cited by 9

Metabolic Stress Boosts Humoral Responses In Vivo Independently of Inflammasome and Inflammatory Reaction

Andris, F., Denanglaire, S., Baus, E., Rongvaux, A., Steuve, J., Flavell, R. A., & Léo, O. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002333 · Cited by 10

Heme oxygenase (HO-1) is involved in the negative regulation of contact sensitivity reaction.

Majewska, M., Zajac, K., Dulak, J., & Szczepanik, M. (2008) · PubMed · Cited by 9

Lipoxin A4 inhibits lipopolysaccharide-induced production of inflammatory cytokines in keratinocytes by up-regulating SOCS2 and down-regulating TRAF6

Hu, F., Feng, A.-P., Liu, X., Zhang, S., Xu, J., Wang, X., Zhong, X.-L., He, M. L., & Chen, H. (2015) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-015-1448-8 · Cited by 9

Physiopathogénie de l'inflammation microcristalline

Lioté, F., & Ea, H. (2007) · Revue du Rhumatisme · doi:10.1016/j.rhum.2006.12.006 · Cited by 9

Combination therapies and other therapeutic approaches targeting the NLRP3 inflammasome and neuroinflammatory pathways: a promising approach for traumatic brain injury

Montazeri-Khosh, Z., Ebrahimpour, A., Keshavarz, M., Sheybani‐Arani, M., & Samiei, A. (2025) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2024.2444956 · Cited by 8

The crosstalk of neutrophil extracellular trap-inflammasome and their roles in disease progression

Xiong, J., Xue, J., Zhou, H., Qi, W., & Zhu, H. (2025) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2025.101419 · Cited by 9

Minyak ikan Lemuru (Sardinella longicep) menurunkan apoptosis osteoblas pada tulang alveolaris tikus wistar (Fish oil of Lemuru (Sardinella longicep) reduced the osteoblast apoptosis in wistar rat alveolar bone)

Indahyani, D. E. (2013) · Dental Journal (Majalah Kedokteran Gigi) · doi:10.20473/j.djmkg.v46.i4.p185-189 · Cited by 8

MCC950 inhibits the inflammatory response and excessive proliferation of canine corneal stromal cells induced by Staphylococcus pseudintermedius

Guo, L., Wang, Z., Zhu, C., Li, J., Cui, L., Dong, J., Meng, X., Zhu, G., Li, J., & Wang, H. (2022) · Molecular Immunology · doi:10.1016/j.molimm.2022.11.001 · Cited by 8

Feeding of a fat‐enriched diet causes the loss of resistance to contact hypersensitivity

Rühl‐Muth, A., Maler, M. D., Esser, P. R., & Martin, S. F. (2021) · Contact Dermatitis · doi:10.1111/cod.13927 · Cited by 9

Crosstalk between contact hypersensitivity reaction and antidepressant drugs

Curzytek, K., Kubera, M., Szczepanik, M., Basta‐Kaim, A., Leśkiewicz, M., Budziszewska, B., Lasoń, W., & Maes, M. H. J. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)71529-9 · Cited by 8

Association between celiac sprue and cryopyrin associated autoinflammatory disorders: a case report

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Poly-D,L-Lactic Acid Filler Attenuates Ultraviolet B-Induced Skin Pigmentation by Reducing Destruction of the Basement Membrane

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