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

Agostini, L., Martinon, F., Burns, K., McDermott, M. F., Hawkins, P. N., & Tschopp, J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00046-9 · Cited by 1,768

Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2

Inohara, N., Ogura, Y., Fontalba, A., Gutierrez, O., Pons, F., Crespo, J., Fukase, K., Inamura, S., Kusumoto, S., Hashimoto, M., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200673200 · Cited by 1,694

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

Kuida, K., Lippke, J. A., Ku, G., Harding, M. W., Livingston, D. J., Su, M. S. S., & Flavell, R. A. (1995) · Science · doi:10.1126/science.7535475 · Cited by 1,631

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

Li, P., Allen, H., Banerjee, S., Franklin, S., Herzog, L., Johnston, C. G., McDowell, J., Paskind, M. P., Rodman, L., Salfeld, J. G., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90490-5 · Cited by 1,408

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

Metabolic re‐programming of keratinocytes in response to contact allergens

Menzel, M., Mraz, V., Vaher, H., Geisler, C., & Bonefeld, C. M. (2023) · Contact Dermatitis · doi:10.1111/cod.14462 · Cited by 5

Gasdermin D and Gasdermin E Are Dispensable for Silica-Mediated IL-1β Secretion from Mouse Macrophages

Leung, J., Chang, M., Moore, R. E., Dagvadorj, J., Sutterwala, F. S., & Cassel, S. L. (2024) · ImmunoHorizons · doi:10.4049/immunohorizons.2400019 · Cited by 5

The pyroptosis and fibrotic diseases: a bibliometric analysis from 2010 to 2024

Zhu, L., Ou, L., Liu, B., Yang, Y., Su, C., Liu, O., & Feng, H. (2024) · Systematic Reviews · doi:10.1186/s13643-024-02703-0 · Cited by 4

Regulation of immune response genes in the skin of allergic and clinically tolerant individuals exposed to p‐phenylenediamine

Meisser, S. S., Mitamura, Y., Altunbulakli, C., Bandier, J., Opstrup, M. S., Gadsbøll, A.-S. Ø., Li, M., Tan, G., Akdiş, M., Akdiş, C. A., et al. (2024) · Allergy · doi:10.1111/all.16031 · Cited by 4

Retention of ES cell-derived 129S genome drives NLRP1 hypersensitivity and transcriptional deregulation in Nlrp3tm1Flv mice

Weiss, F. D., Alvarez, Y., Shakeri, F., Sahu, A., Leka, P., Dernst, A., Rollheiser, J., Vasconcelos, M. B., Geraci, A., Duthie, F., et al. (2024) · Cell Death and Differentiation · doi:10.1038/s41418-024-01379-2 · Cited by 4

Assessment of Inflammasome Activation by Cytokine and Danger Signal Detection.

Riteau, N., Gombault, A., & Couillin, I. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3566-6_3 · Cited by 3

Autoinflammatory diseases and kidney involvement

Mukhin, N. A., Bogdanova, M. V., Рамеев, В. В., & Kozlovskaya, L. V. (2017) · Terapevticheskii arkhiv · doi:10.17116/terarkh20178964-20 · Cited by 4

Neutrophilic Pleuritis Is a Severe Complication of Klebsiella pneumoniae Pneumonia in Old Mice

Hollwedel, F., Maus, R., Stolper, J., Jonigk, D. D., Hildebrand, C. B., Welte, T., Brandenberger, C., & Maus, U. A. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2200413 · Cited by 4

PF-04620110, a Potent Antidiabetic Agent, Suppresses Fatty Acid-Induced NLRP3 Inflammasome Activation in Macrophages

Jo, S. I., Bae, J. H., Kim, S. J., Lee, J. M., Jeong, J. H., & Moon, J. (2019) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2019.0112 · Cited by 4

Self-oligomerization of ASC PYD Domain Prevents the Assembly of Inflammasome In Vitro

Narayanan, K. B., Jang, T.-H., & Park, H. H. (2014) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-014-0819-0 · Cited by 4

NOD ‐Like Receptors

Arnold, C. M., Kienes, I., Sowa, A. S., & Kufer, T. A. (2018) · Wiley eBooks · doi:10.1002/9780470015902.a0026236 · Cited by 4

The activation of NLRP3 inflammasome and its function in anti-infection immunity of largemouth bass (Micropterus salmoides)

Jiang, H., Wu, M., Liu, Y., Chen, X., Yang, G., & Li, H. (2025) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2025.110607 · Cited by 3

Multifunctional hollow manganese silicate nanoparticles for the treatment of acute lung injury and Pseudomonas aeruginosa pulmonary infection

Ma, J., Du, L., Shen, X., Wang, J., Qian, H., Wu, C., & Xu, J. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123944 · Cited by 3

ASC- and caspase-1-deficient C57BL/6 mice do not develop demyelinating disease after infection with Theiler’s murine encephalomyelitis virus

Li, D., Bühler, M., Runft, S., Gerold, G., Marek, K., Baumgärtner, W., Strowig, T., & Gerhauser, I. (2023) · Scientific Reports · doi:10.1038/s41598-023-38152-3 · Cited by 3

Investigation of the anti-apoptotic activity of ozone therapy in rainbow trout macrophages infected with Yersinia ruckeri

Küçükgül, A., Küçükgül, A., Gönenci, R., Özsoy, Ş. Y., Kutlu, B., & İşgör, M. M. (2019) · Aquaculture International · doi:10.1007/s10499-019-00364-8 · Cited by 3

Inflammasomes in Myeloid Cells: Warriors Within

Jha, S., Brickey, W. J., & Ting, J. P.-Y. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch17 · Cited by 3

Human amnionic progenitor cell secretome mitigates the consequence of traumatic optic neuropathy in a mouse model

McCartan, R., Gratkowski, A., Browning, M., Hahn-Townsend, C., Ferguson, S., Morin, A., Bachmeier, C. J., Pearson, A., Brown, L. R., MULLAN, M. J., et al. (2023) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2023.04.002 · Cited by 3

Analgesic C20-diterpenoid alkaloids from the lateral roots of Aconitum carmichaelii Debeaux: Natural inhibitors of NLRP3 activation

Yin, W., Wang, M., Zhang, F., Pan, X.-G., Ding, K., Zhu, H., Wang, D.-G., Li, L.-Z., Xia, C., Zhang, W., et al. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.108321 · Cited by 3

Discovery of a novel Thiazole amide inhibitor of Inflammasome and Pyroptosis pathways

Dai, Z., Wang, K., Bai, C., Li, Y., Yu, Q., Chen, Z., Liao, J., Ding, J., & Wang, D. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.108477 · Cited by 3

NLRP3 in the dorsal raphe nucleus manipulates the depressive-like behaviors

Cai, J., Zhao, J., Peng, R., Yu, H., He, Y., Zhou, Q., Wang, Y., & Xie, P. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111405 · Cited by 3

Assembling the Inflammasome, Piece by Piece

Humphries, F., & Fitzgerald, K. A. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900764 · Cited by 3

Pleiotropic effects of inflammasome modulation in chronic gout and associated comorbidities: potential therapeutic implications

Cuchacovich, R., García-Valladares, I., & Espinoza, L. R. (2011) · International Journal of Clinical Rheumatology · doi:10.2217/ijr.11.58 · Cited by 3

Nigella sativa Linn. seed extract modulates the activity of ASC complex of NLRP3 inflammasome in rats subjected to experimental pancreatitis

Suguna, P., Geetha, A., Aruna, R., & Siva, G. V. (2014) · Biomedicine & Preventive Nutrition · doi:10.1016/j.bionut.2013.12.008 · Cited by 3

Cullin1 represses systematic inflammasome activation by binding and catalyzing NLRP3 ubiquitinationPreprint

Wan, P., Zhang, Q., Liu, W., Jia, Y., Wang, T., Wang, W., Pan, P., Yang, G., Xiang, Q., Huang, S., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/289637 · Cited by 3

From Diet to Inflammasome: Ultra-Processed Foods as Upstream Drivers of NLRP3-Mediated Intestinal Inflammation in Inflammatory Bowel Disease

Rutgrink, J. M. I., & Velde, A. A. T. (2026) · Immuno · doi:10.3390/immuno6020024 · Cited by 2

Innate immune sensors of inflammasomes and PANoptosomes: structural–mechanistic insights and therapeutic implications

Upadhyay, S., Nagampalli, R., Resende, S., & Kanneganti, T. (2026) · Cell Research · doi:10.1038/s41422-026-01287-9 · Cited by 2

Novel insights into molecular and cellular aspects of delayed drug hypersensitivity reactions

Elzagallaai, A. A., & Rieder, M. J. (2023) · Expert Review of Clinical Pharmacology · doi:10.1080/17512433.2023.2289543 · Cited by 2

Cardio-Rheumatic Diseases: Inflammasomes Behaving Badly

Issa, F., Abdulla, M., Retnowati, F. D., Al‐Khawaga, H., AlHiraky, H. N., Al-Harbi, K. M., Al-Haidose, A., Maayah, Z. H., & Abdallah, A. M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083520 · Cited by 2

Mechanisms of Irritant and Allergic Contact Dermatitis

Martin, S. F., & Bonefeld, C. M. (2019) · Springer eBooks · doi:10.1007/978-3-319-72451-5_59-1 · Cited by 2

Immunologic mechanisms in allergic and irritant contact dermatitis

Ale, I. S., & Maibach, H. I. (2012) · Informa Healthcare eBooks · doi:10.3109/9781841848570.011 · Cited by 2

Hereditary recurrent fevers

Kim, P. W., Aksentijevich, I. A., Colburn, N. T., & Kastner, D. L. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-06551-1.00163-9 · Cited by 2

Classic Autoinflammatory Diseases

de Jesus, A. A., Ferguson, P. J., & Goldbach‐Mansky, R. T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00024-8 · Cited by 2

COPD and Other Inflammatory Diseases of the Lung: Focus on AhR Signaling

Beamer, C. A., Seaver, B. P., & Shepherd, D. M. (2012) · Molecular and integrative toxicology · doi:10.1007/978-1-61779-812-2_13 · Cited by 2

The Innate Response to Biomaterials

Lalor, P. A., & Jones, L. C. (2011) · Elsevier eBooks · doi:10.1016/b978-0-08-055294-1.00003-9 · Cited by 2

Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals

Nishikawa, M., Iwaki, M., Tashiro, K., & Kurose, K. (2020) · Xenobiotica · doi:10.1080/00498254.2020.1767320 · Cited by 2

Familial Autoinflammatory Syndromes

Simon, A., van der Meer, J. W. M., & Drenth, J. P. H. (2009) · Elsevier eBooks · doi:10.1016/b978-1-4160-3285-4.10113-5 · Cited by 2

Intestinal edema induced by LPS-induced endotoxemia is associated with an inflammasome adaptor ASC

Yamamoto, T., Kurata, M., Kaneko, N., & Masumoto, J. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281746 · Cited by 3

DNA Damage Responses in Atherosclerosis

Shimada, K., Crother, T. R., & Arditi, M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-404732-7.00010-1 · Cited by 2

Familial Autoinflammatory Syndromes

Simon, A., van der Meer, J. W. M., & Drenth, J. P. H. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4377-1738-9.00097-9 · Cited by 2

Genetic targeting of Card19 is linked to disrupted Ninj1 expression , impaired cell lysis, and increased susceptibility to Yersinia infectionPreprint

Bjånes, E., Sillas, R. G., Matsuda, R., Demarco, B., Fettrelet, T., DeLaney, A. A., Kornfeld, O. S., Lee, B. L., Rodriguez-Lopez, E., Grubaugh, D., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.19.436207 · Cited by 2

Defective endosome-TGN retrograde transport promotes NLRP3 inflammasome activationPreprint

Zhang, Z., Li, R., Venditti, R., Liu, Z., Schürmann, A., Bonifacino, J. S., Matteis, M. A. D., & Ricci, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.14.460331 · Cited by 2

Development of Anti-inflammatory Drugs with Novel Mechanisms of Action Targeting Pyroptosis

Takemura, N. (2023) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.23-00135 · Cited by 1

Research progress on NLRP3 inflammasomes in male reproductive immunity

Zhang, X., Dong, X., Kang, Y., Liu, X., Zhang, C., Zhang, J. H., Chen, S., & Huang, D. (2024) · Exploration of Immunology · doi:10.37349/ei.2024.00154 · Cited by 2

Development of RT h-CLAT, a Rapid Assessment Method for Skin Sensitizers Using THP-1 Cells as a Biosensor

Koyama, H., Maeda, A., Zhai, P., Koiwai, K., & Kurose, K. (2024) · Biosensors · doi:10.3390/bios14120632 · Cited by 1

Discovery of novel Bis-amide analogue ST12 for the treatment of inflammatory bowel diseases (IBD) by inhibiting NLRP3 inflammasome activation

Sun, Z., Zang, Q., Xu, C., Zhang, X., Kang, Z., Yang, Y., Li, L., & Chen, J. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.108402 · Cited by 1

Lactoferrin protects against radiation-induced intestinal injury by regulating pyroptosis and mitophagy

Shan, W., Wei, W., Zhang, Y., Zhang, L.-L., Zhao, Y., Gu, J. L., Zhao, L., Hidayat, K., Liu, Y., Chong, Y., et al. (2026) · Food & Function · doi:10.1039/d5fo04989j · Cited by 1

HCA2 Receptors in Lymphocytes and Keratinocytes Affect Murine Contact Allergic Inflammation

Polkownik, S., Meens, J., Lange, H., Weil, J., Kruse, B., Buzzai, A. C., Wulff, K., Braun, A. D., Bonfiatius, S., Tüting, T., et al. (2026) · Experimental Dermatology · doi:10.1111/exd.70254 · Cited by 1

Cardiolipin Induces CXCL9/CXCL10 Expression in Tumor-Infiltrating Lymphocytes

Lérias, J. R., de Sousa, E., Gorgulho, C. M., Kamiki, J., António, P. A., Eduardo., R., Sedas, M., Figueiredo, N., Han, J., Jeong, S., et al. (2026) · Cells · doi:10.3390/cells15090798 · Cited by 1

Oral epithelial barrier: Gatekeeper of mucosal immunity and driver of disease

Wang, Q., Li, X., Xue, F., Zhao, P., & Mu, Y. (2026) · Microbiological Research · doi:10.1016/j.micres.2026.128568 · Cited by 2

Lactate acts as a metabolic brake on inflammation by repressing NLRP3 transcription via NF-κB inhibition

Lin, H.-A., Lin, H.-C., Chiou, C.-Y., Peng, H., Chen, Y.-J., Bao, B.-Y., Tsai, K.-J., Lin, C., Shih, C., Hu, S.-I., et al. (2026) · Inflammation Research · doi:10.1007/s00011-026-02290-x · Cited by 1

Role of NLRP3 Inflammasome Inhibitors in Endothelial Dysfunction and Vascular Repair

Samyuktha, T., Sridharan, Y., Ganesan, K., & Ramkumar, K. M. (2026) · Antioxidants · doi:10.3390/antiox15070784 · Cited by 1

Modulators of the Acute Inflammatory Response: A Dissertation

Karmarkar, D. (2013) · eScholarship@UMassChan · doi:10.13028/m2kc7v · Cited by 1

Defining the Function of Pyrin, the Familial Mediterranean Fever-associated Protein, in Inflammation

Hesker, P. R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/z8zz-6k39 · Cited by 1

Dendritic cell-mediated modulation of the immune system by endogenous danger signals

Andréoni, C. (2009) · Cited by 1

4.3 The Innate Response to Biomaterials ☆

Lalor, P. A., & Jones, L. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803581-8.10237-1 · Cited by 2

Systemic Disease and the Skin

Patterson, J. W., Kwock, J. M., Flowers, R. H., Guffey, D. J., Pruitt, L., Stowman, A. M., & David, B. A. M. (2020) · Springer eBooks · doi:10.1007/978-3-319-45134-3_48-1 · Cited by 1

In vitro complex formation of human PYRIN domain-only protein 3 prevented by self-oligomerization of ASC PYD domain

Bhat, E. A., Sajjad, N., Tantray, J. A., Hor, Y.-Y., & Rather, I. A. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2020.12.049 · Cited by 1

Dendritic cells as vaccine targets

Iseghohi, F., Aondona, P. Y., Rowaiye, A. B., & Oli, A. N. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91146-7.00010-x · Cited by 1

Epicutaneous immunization with TNP-Ig antigen induces CD11c+IL-10+ dendritic cells that promote suppression of Th1-mediated contact hypersensitivity in humanized HLA-DR4 transgenic mice

Majewska‐Szczepanik, M., Strzępa, A., Marcińska, K., & Szczepanik, M. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110281 · Cited by 1

The Effects and Treatment of Inflammation on Diabetes Mellitus and Cardiovascular Disease

Hattar, L., Mumtaz, T., Mouhayyar, C. E., Matevossian, A., & Johnstone, M. T. (2023) · Contemporary cardiology · doi:10.1007/978-3-031-13177-6_10 · Cited by 1

Innate Immune Signaling and Negative Regulators in Cancer

Wang, H. Y., & Wang, R. (2011) · Springer eBooks · doi:10.1007/978-1-4419-9914-6_6 · Cited by 1

Inflammasomes in viral infection

Ichinohe, T., & Iwasaki, A. (2009) · Uirusu · doi:10.2222/jsv.59.13 · Cited by 1

Autoinflammatory diseases - a new entity of inflammation

Heike, T., Saito, M. K., Nishikomori, R., Yasumi, T., & Nakahata, T. (2011) · Inflammation and Regeneration · doi:10.2492/inflammregen.31.125 · Cited by 1

Auto-inflammation and the Skin

Lichtenberger, R., Contassot, E., French, L. E., & Navarini, A. A. (2018) · Springer eBooks · doi:10.1007/978-3-319-72649-6_24 · Cited by 1

Autoinflammatory Diseases

Lee, S. (2014) · Journal of Rheumatic Diseases · doi:10.4078/jrd.2014.21.5.228 · Cited by 1

Mechanisms for activation and inhibition of inflammasomes

Janczy, J. R. (2014) · doi:10.17077/etd.gqld9sco · Cited by 1

Breakdown of the Molecular Processes Driving the Adverse Outcome Pathways (AOPs) of Skin and Respiratory Sensitization Induction in Humans Exposed to Xenobiotics and Proteins

Roggen, E. (2014) · Wiley eBooks · doi:10.1002/9783527676965.ch4 · Cited by 1

Microbe-Induced Activation of Inflammatory Cytokine Response in Human Cells

Veckman, V. (2007) · STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · Cited by 1

Mechanism of linezolid-induced NLRP3 inflammasome activation

He, Q. (2012) · doi:10.17077/etd.s5eoktcw · Cited by 1

The impact of cytokine modulation in acquired and inherited inflammatory disease and AA amyloidosis

Lane, T. (2016) · UCL Discovery (University College London) · Cited by 1

Nod1 and Nod2 in innate immune responses, adaptive immunity and bacterial infection.

Bourhis, L. L. (2010) · TSpace (University of Toronto) · Cited by 1

Biochemical and Functional Characterization of the Mitochondrial Immune Signaling Protein Complex

Lei, Y. L. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/sr3j-8s02 · Cited by 1

Role of NLRP3 in colitis and colitis associated colorectal cancer

Perera, A. P. (2019) · UTAS Research Repository · doi:10.25959/100.00034330 · Cited by 1

Evasion of LPS-TLR4 Signaling as a Virulence Determinate for Yersinia pestis

Paquette, S. W. M. (2009) · University of Massachusetts (UMass) Chan Medical School · doi:10.13028/cz1q-z918 · Cited by 1

Apoptosis and TH17 Cell Differentiation

Blander, J. M. (2011) · Springer eBooks · doi:10.1007/978-1-4419-9371-7_5

Persistent enteric mycobacterial infection sensitizes mice to intestinal epithelial injury

Johnson, C. S. (2010) · Iowa State University Digital Repository (Iowa State University) · doi:10.31274/etd-180810-2147

Papel dos inflamassomas na ativação de células dendríticas e na modulação da resposta imune adaptativa.

da Costa, T. B. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2014.tde-27112014-084955

Avaliação dos mecanismos moleculares envolvidos na expressão de iNOS mediada pelo eixo NAIP5/NLRC4-Caspase-1.

Carina Cristina Oliveira de, L. I. M. A. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2014.tde-11072014-093448

Implication de l’immunité innée au-delà de la réponse à l’infection — Immunité innée et insuffisance rénale aiguë

Lerolle, N., Duveau, A., & Carlier, L. (2010) · Réanimation · doi:10.1007/s13546-010-0114-1

Dendritic cell responses to apoptotic cells : Is there life after death?

Johansson, U. (2010) · Figshare

Activation of NLRP3 inflammasomes during complement-mediated phagocytosis by macrophages

Suresh, R. (2015) · University Libraries (University of Maryland) · doi:10.13016/m2c939

Rapid Vascular Responses to Anthrax Lethal Toxin in Mice Containing a Segment of Chromosome 11 from the CAST/Ei Strain on a C57BL/6 Genetic Background

Weigel, K. J., Rues, L., Doyle, E. J., Buchheit, C. L., Wood, J. G., Gallagher, R. J., Kelly, L. E., Radel, J. D., Bradley, K. A., & LeVine, S. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040126

CASP1 (caspase 1, apoptosis-related cysteine peptidase (interleukin 1, beta, convertase))

Kumar, Y., Radha, V., & Swarup, G. (2011) · Atlas of Genetics and Cytogenetics in Oncology and Haematology · doi:10.4267/2042/38540

INNATE IMMUNE SENSING OF A BACTERIAL PORE-FORMING TOXIN: THE ROLE OF THE NLRP3 INFLAMMASOME

Chu, J. (2010) · D-Scholarship@Pitt (University of Pittsburgh)

Interleukin-1 as a therapeutic target in systemic-onset juvenile idiopathic arthritis

Allantaz, F., Stichweh, D., & Pascual, V. (2007) · Future Rheumatology · doi:10.2217/17460816.2.3.305

Mvin mediates Francisella Tularensis virulence through evasion of AIM2 inflammasome activation

Ulland, T. K. (2010) · doi:10.17077/etd.c04zmq85

Hormonal regulation of immune modulators in human breast tissue

Morad, V. (2015) · Linköping University medical dissertations · doi:10.3384/diss.diva-117983

L'inflammasome, les maladies auto-inflammatoires et la goutte

Pétrilli, V., & Martinon, F. (2007) · Revue du Rhumatisme · doi:10.1016/j.rhum.2007.04.005

Inflammasomes in Inflammatory Bowel Disease

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Genetic variations in the NALP3 inflammasome

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