NALP Inflammasomes: a central role in innate immunity

The plant immune system

Jones, J. D. G., & Dangl, J. L. (2006) · Nature · doi:10.1038/nature05286 · Cited by 13,177

The Inflammasome

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

Gout-associated uric acid crystals activate the NALP3 inflammasome

Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326

The Danger Model: A Renewed Sense of Self

Matzinger, P. (2002) · Science · doi:10.1126/science.1071059 · Cited by 4,205

The Consensus Coding Sequences of Human Breast and Colorectal Cancers

Sjöblom, T., Jones, S., Wood, L. D., Parsons, D. W., Lin, J., Barber, T. D., Mandelker, D. L., Leary, R. J., Ptak, J., Silliman, N., et al. (2006) · Science · doi:10.1126/science.1133427 · Cited by 3,161

Cryopyrin activates the inflammasome in response to toxins and ATP

Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080

A novel heterodimeric cysteine protease is required for interleukin-1βprocessing in monocytes

Thornberry, N. A., Bull, H. G., Calaycay, J. R., Chapman, K. T., Howard, A. D., Kostura, M. J., Miller, D. K., Molineaux, S. M., Weidner, J. R., Aunins, J. G., et al. (1992) · Nature · doi:10.1038/356768a0 · Cited by 2,613

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 1,822

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

The leucine-rich repeat as a protein recognition motif

Kobe, B. (2001) · Current Opinion in Structural Biology · doi:10.1016/s0959-440x(01)00266-4 · Cited by 1,720

Pattern recognition receptors of innate immunity and their application to tumor immunotherapy

Seya, T., Shime, H., Ebihara, T., Oshiumi, H., & Matsumoto, M. (2009) · Cancer Science · doi:10.1111/j.1349-7006.2009.01442.x · Cited by 37

Autoinflammatory disease in the lung

Scambler, T., Holbrook, J. A., Savic, S., McDermott, M., & Peckham, D. G. (2018) · Immunology · doi:10.1111/imm.12937 · Cited by 37

Gut–Liver Axis and Inflammasome Activation in Cholangiocyte Pathophysiology

Maroni, L., Ninfole, E., Pinto, C., Benedetti, A., & Marzioni, M. (2020) · Cells · doi:10.3390/cells9030736 · Cited by 37

Polymorphisms inNLRP1gene and susceptibility to autoimmune thyroid disease

Alkhateeb, A. M., Jarun, Y., & Tashtoush, R. (2013) · Autoimmunity · doi:10.3109/08916934.2013.768617 · Cited by 37

Microarray-based identification of novel biomarkers in IL-1-mediated diseases

Allantaz, F., Chaussabel, D., Banchereau, J., & Pascual, V. (2007) · Current Opinion in Immunology · doi:10.1016/j.coi.2007.10.003 · Cited by 37

1,25-Dihydroxyvitamin D3 attenuates IL-1β secretion by suppressing NLRP1 inflammasome activation by upregulating the NRF2-HO-1 pathway in epidermal keratinocytes

Nakajo, T., Katayoshi, T., Kitajima, N., & Tsuji, K. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102203 · Cited by 37

Construction of a large scale integrated map of macrophage pathogen recognition and effector systems

Raza, S., McDerment, N. A., Lacaze, P. A., Robertson, K. A., Watterson, S., Chen, Y., Chisholm, M., Eleftheriadis, G., Monk, S. L., O'Sullivan, M., et al. (2010) · BMC Systems Biology · doi:10.1186/1752-0509-4-63 · Cited by 36

To protect or adversely affect? The dichotomous role of the NLRP1 inflammasome in human disease

Tupik, J. D., Nagai-Singer, M. A., & Allen, I. C. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100858 · Cited by 35

Structure and regulation of cytoplasmic adapter proteins involved in innate immune signaling

Monie, T., Moncrieffe, M. C., & Gay, N. J. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00735.x · Cited by 36

Sebum, inflammasomes and the skin: current concepts and future perspective

Oyewole, A. O., & Birch‐Machin, M. A. (2015) · Experimental Dermatology · doi:10.1111/exd.12774 · Cited by 33

The NLRP3 Inflammasome as a Pathogenic Player Showing Therapeutic Potential in Rheumatoid Arthritis and Its Comorbidities: A Narrative Review

Chen, P., Tang, K., & Chen, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25010626 · Cited by 33

Human parvovirus B19 nonstructural protein NS1 activates NLRP3 inflammasome signaling in adult‑onset Still's disease

Chen, D., Chen, Y., Chen, H., Hsieh, C., Gung, N., Hung, W., Tzang, B., & Hsu, T. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.8275 · Cited by 31

NLRP9 in innate immunity and inflammation

Mullins, B., & Chen, J. (2020) · Immunology · doi:10.1111/imm.13290 · Cited by 33

Expression of NALPs in adipose and the fibrotic progression of non-alcoholic fatty liver disease in obese subjects

Mehta, R., Neupane, A. S., Wang, L., Goodman, Z. D., Baranova, A. V., & Younossi, Z. M. (2014) · BMC Gastroenterology · doi:10.1186/s12876-014-0208-8 · Cited by 28

Necroptosis inhibitors as therapeutic targets in inflammation mediated disorders - a review of the current literature and patents

Kopalli, S. R., Kang, T., & Koppula, S. (2016) · Expert Opinion on Therapeutic Patents · doi:10.1080/13543776.2016.1230201 · Cited by 28

Induction and maintenance of protective CD8+ T cells against malaria liver stages: implications for vaccine development

Tse, S., Radtke, A. J., & Zavala, F. P. (2011) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762011000900022 · Cited by 26

Ketogenic Diet and Cancer—a Perspective

Smyl, C. (2016) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-319-42118-6_11 · Cited by 24

Dietary interactions with the bacterial sensing machinery in the intestine: the plant polyphenol case

Nasef, N. A., Mehta, S. Y., & Ferguson, L. R. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00064 · Cited by 25

Opportunities for future therapeutic interventions for hyperoxaluria: targeting oxidative stress

Joshi, S. N., & Khan, S. R. (2019) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2019.1599359 · Cited by 24

Analysis of Pelagia noctiluca proteome Reveals a Red Fluorescent Protein, a Zinc Metalloproteinase and a Peroxiredoxin

Frazão, B., Campos, A. M. O., Osório, H., Thomas, B., Leandro, S. M., Teixeira, A., Vasconcelos, V. M., & Antunes, A. (2017) · The Protein Journal · doi:10.1007/s10930-017-9695-0 · Cited by 24

The pivotal roles of the NOD-like receptors with a PYD domain, NLRPs, in oocytes and early embryo development†

Amoushahi, M., Sunde, L., & Lykke‐Hartmann, K. (2019) · Biology of Reproduction · doi:10.1093/biolre/ioz098 · Cited by 23

Induction of Early Growth Response-1 Mediates Microglia Activation In Vitro But is Dispensable In Vivo

Langmann, T., Ebert, S., Walczak, Y., Weigelt, K., Ehrengruber, M. U., Stiewe, T., & Weber, B. H. F. (2009) · NeuroMolecular Medicine · doi:10.1007/s12017-009-8061-6 · Cited by 22

Association of NALP2 polymorphism with arsenic induced skin lesions and other health effects

Bhattacharjee, P., Das, N., Chatterjee, D., Banerjee, A. M., Das, J. K., Basu, S., Banerjee, S., Majumder, P., Goswami, P., & Giri, A. K. (2013) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2013.04.010 · Cited by 22

NLRC3 promotes host resistance against Pseudomonas aeruginosa-induced keratitis by promoting the degradation of IRAK1

Guo, L., Kong, Q., Dong, Z., Dong, W., Fu, X., Su, L., & Tan, X. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3077 · Cited by 21

Crystal structure of the human NLRP9 pyrin domain reveals a bent N‐terminal loop that may regulate inflammasome assembly

Ha, H. J., & Park, H. H. (2020) · FEBS Letters · doi:10.1002/1873-3468.13866 · Cited by 21

Mitochondria as Regulators of Nonapoptotic Cell Death in Cancer

Malla, S., Neupane, R., Sood, S., Hussein, N. A., Abou-Dahech, M. S., Terrero, D., Ashby, C. R., Babu, R. J., & Tiwari, A. K. (2025) · MedComm · doi:10.1002/mco2.70244 · Cited by 20

Developmental expression and possible functional roles of mouse Nlrp4e in preimplantation embryos

Chang, B., Liu, X., Liu, J., Quan, F., Guo, Z., & Zhang, Y. (2013) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-013-9638-9 · Cited by 19

Screening for NLRP7 Mutations in Familial and Sporadic Recurrent Hydatidiform Moles

Landolsi, H., Rittore, C., Philibert, L., Missaoui, N., Hmissa, S., Touitou, I., Gribaa, M., & Yacoubi, M. T. (2011) · International Journal of Gynecological Pathology · doi:10.1097/pgp.0b013e31820dc3b0 · Cited by 18

TLR4 sensing of IsdB of Staphylococcus aureus induces a proinflammatory cytokine response via the NLRP3-caspase-1 inflammasome cascade

González, J. J. I., Hossain, M. F., Neef, J., Zwack, E. E., Tsai, C., Raafat, D., Fechtner, K., Herzog, L., Kohler, T. P., Schlüter, R., et al. (2023) · mBio · doi:10.1128/mbio.00225-23 · Cited by 16

Rotavirus activates MLKL‐mediated host cellular necroptosis concomitantly with apoptosis to facilitate dissemination of viral progeny

Mukhopadhyay, U., Patra, U., Chandra, P., Saha, P., Gope, A., Dutta, M., & Chawla‐Sarkar, M. (2021) · Molecular Microbiology · doi:10.1111/mmi.14874 · Cited by 17

Celastrol Regulates the Hsp90-NLRP3 Interaction to Alleviate Rheumatoid Arthritis

Yang, J., He, B., Dang, L., Liu, J., Liu, G., Zhao, Y., Yu, P., Wang, Q., Wang, L., & Xin, W. (2024) · Inflammation · doi:10.1007/s10753-024-02060-z · Cited by 19

Chronic immune stimulation as a contributing cause of chronic disease in opiate addiction including multi-system ageing

Reece, A. S. (2010) · Medical Hypotheses · doi:10.1016/j.mehy.2010.07.047 · Cited by 17

NLRP7 Mutation Analysis in Sporadic Hydatidiform Moles in Tunisian Patients: NLRP7 and Sporadic Mole

Landolsi, H., Rittore, C., Philibert, L., Hmissa, S., Gribaa, M., Touitou, I., & Yacoubi, M. T. (2012) · Archives of Pathology & Laboratory Medicine · doi:10.5858/arpa.2011-0399-oa · Cited by 16

The microbiota-inflammasome-brain axis as a pathogenic mediator of neurodegenerative disorders

Sarkar, S. K., Gubert, C., & Hannan, A. J. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106276 · Cited by 15

Could ER Stress Be A Major Link Between Oxidative Stress And Autoimmunity In Vitiligo?

Mansuri, M. S., & Singh, M. (2014) · Journal of Pigmentary Disorders · doi:10.4172/2376-0427.1000123 · Cited by 14

Apoptosis inhibition or inflammation: the role of NAIP protein expression in Hodgkin and non-Hodgkin lymphomas compared to non-neoplastic lymph node

Mazrouei, S., Ziaei, A., Tanhaei, A. P., Keyhanian, K., Esmaeili, M., Baradaran, A., & Salehi, M. (2012) · Journal of Inflammation · doi:10.1186/1476-9255-9-4 · Cited by 14

Natural History of Innate Host Defense Peptides

Linde, A., Wachter, B., Höner, O. P., Dib, L. H., Ross, C., Tamayo, A., Blecha, F., & Melgarejo, T. (2009) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-009-9031-x · Cited by 13

Design, synthesis and biological evaluation of phenyl vinyl sulfone based NLRP3 inflammasome inhibitors

Zhang, X., Xu, A., Ran, Y., Wei, C., Xie, F., & Wu, J. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.106010 · Cited by 12

Periodische Fiebersyndrome/autoinflammatorische Syndrome

Kötter, I., Schedel, J., & Kümmerle-Deschner, J. B. (2009) · Zeitschrift für Rheumatologie · doi:10.1007/s00393-009-0449-z · Cited by 12

The therapeutic potential of colchicine in the complications of COVID19. Could the immunometabolic properties of an old and cheap drug help?

Ribeiro, S. A. G., Lopes, C., Amaral, R., & do Amaral, A. R. (2020) · Metabolism Open · doi:10.1016/j.metop.2020.100045 · Cited by 11

Autoinflammatorische Syndrome/Fiebersyndrome

Schedel, J., Bach, B., Kümmerle-Deschner, J. B., & Kötter, I. (2011) · Der Hautarzt · doi:10.1007/s00105-010-2124-3 · Cited by 11

Reducing Lung ATP Levels and Alleviating Asthmatic Airway Inflammation through Adeno-Associated Viral Vector-Mediated CD39 Expression

Huang, Y.-A., Chen, J., Wu, C., Hsu, C., Ko, A. M., Chen, L., & Kuo, M. (2021) · Biomedicines · doi:10.3390/biomedicines9060656 · Cited by 10

The structure of NLRP9 reveals a unique C‐terminal region with putative regulatory function

Kamitsukasa, Y., Nakano, K., Murakami, K., Hirata, K., Yamamoto, M., Shimizu, T., & Ohto, U. (2022) · FEBS Letters · doi:10.1002/1873-3468.14302 · Cited by 10

Interleukin-18: a biomarker with therapeutic potential in adult-onset Still’s disease

Chen, P., Wey, S.-J., & Chen, D. (2022) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2022.2096592 · Cited by 10

Expression of NALP3 in the spleen of mice with portal hypertension

Xia, Z., Wang, G., Wan, C., Liu, T., Wang, S., Wang, B., & Cheng, R. (2010) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-010-0207-0 · Cited by 9

Inflammasome Inhibition Suppresses Alveolar Cell Permeability Through Retention of Neuregulin-1 (NRG-1)

Rajanbabu, V., Galam, L., Cox, R., Fukumoto, J., Cho, Y. S., Parthasarathy, P. T., Lockey, R. F., & Kolliputi, N. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000430169 · Cited by 9

In vitro inflammatory/anti-inflammatory effects of nitrate esters of purines

Maugé, L., Fotopoulou, T., Delemasure, S., Dutartre, P., Koufaki, M., & Connat, J. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.02.022 · Cited by 9

Emergency and therapeutic vaccination – Is stimulating innate immunity an option?

Foster, N. M., Berndt, A., Lalmanach, A.-C., Methner, U., Pasquali, P., Rychlı́k, I., Velge, P., Zhou, X., & Barrow, P. (2011) · Research in Veterinary Science · doi:10.1016/j.rvsc.2011.05.018 · Cited by 9

NLRX1: friend or foe?

Meylan, E., & Tschopp, J. (2008) · EMBO Reports · doi:10.1038/embor.2008.23 · Cited by 9

Atherosclerosis: an Athero-Thrombo-Inflammatory Disease

Manolis, A. S., Manolis, T. A., & Melita, H. (2012) · Hospital chronicles/Hospital Chronicles · doi:10.2015/hc.v7i4.528 · Cited by 8

Activación y regulación del inflamasoma NLRP3 en las enfermedades infecciosas

López, J. C. H., & Inchima, S. U. (2012) · IATREIA · doi:10.17533/udea.iatreia.13134 · Cited by 8

Autoinflammatory Diseases in the Neonate: Mimickers of Neonatal Infections

Lionetti, G., Lapidus, S., Goldbach‐Mansky, R. T., & Frankovich, J. (2010) · NeoReviews · doi:10.1542/neo.11-10-e566 · Cited by 7

Hypothalamic Pathophysiology in the Neuroimmune,Dysmetabolic and Longevity Complications of Chronic Opiate Dependency

Hulse, A. S. R. G. K. (2014) · Journal of Forensic Toxicology and Pharmacology · doi:10.4172/2325-9841.1000126 · Cited by 7

Autoimmunity versus Autoinflammation - Friend or Foe?

Kanazawa, N., Tchernev, G., & Wollina, U. (2014) · Wiener Medizinische Wochenschrift · doi:10.1007/s10354-014-0290-0 · Cited by 7

Monoclonal antibodies for equine IL-1β enable the quantification of mature IL-1β in horses

Babasyan, S., Rollins, A., & Wagner, B. (2024) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2024.110805 · Cited by 5

NLRs: Nucleotide-Binding Domain and Leucine-Rich-Repeat-Containing Proteins

Carneiro, L. A. M., Fritz, J. H., Kufer, T. A., Travassos, L. H., Benkő, S., & Philpott, D. J. (2009) · EcoSal Plus · doi:10.1128/ecosalplus.8.8.3 · Cited by 5

Bacillus anthracis genomic DNA enhances lethal toxin–induced cytotoxicity through TNF-α production

Jeon, J. H., Kim, Y. H., Choi, M. K., Kim, K.-A., Lee, H., Jang, J., Kim, Y.-R., Chun, J., Eo, S. K., Kim, T. S., et al. (2014) · BMC Microbiology · doi:10.1186/s12866-014-0300-9 · Cited by 4

Molecular mechanism and immunological function of pyroptosis

Dong, N., & Shao, F. (2019) · Scientia Sinica Vitae · doi:10.1360/ssv-2019-0242 · Cited by 4

Mucosal Bacterial Recognition and Signaling Systems in the Intestine

Fukata, M., & Abreu, M. T. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382026-6.00041-5 · Cited by 4

Innate Defense against Aspergillus: the Phagocyte

Chignard, M. (2014) · ASM Press eBooks · doi:10.1128/9781555815523.ch18 · Cited by 4

Macrophage Function Disorders

Bowdish, D. M. E., & Gordon, S. (2009) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0002174.pub2 · Cited by 4

The inflammasome sensor NLRP3 interacts with REV7 to maintain genome integrity through homologous recombination

Burlet, D., Khan, M. M., Hacot, S., Buthmann, H., Bardoulet, L., Huber, A., Gorry, J., Föhr, B., López, B. S., Couté, Y., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf554 · Cited by 3

[Inhibitory effect of Biejiajian pills against diethylnitrosamine-induced hepatocarcinogenesis in rats].

Feng, M., He, S., Huang, S., Lin, J., Yang, H., Wang, J., & Pang, J. (2020) · PubMed Central · doi:10.12122/j.issn.1673-4254.2020.08.12 · Cited by 3

Impact of Spinal Cord Injury

Brackett, N., Ibrahim, E., & Lynne, C. (2020) · Male Infertility · doi:10.1007/978-1-4614-3335-4_32 · Cited by 7

Calcium Pyrophosphate Dihydrate Crystals Increase the Granulocyte/Monocyte Progenitor (GMP) and Enhance Granulocyte and Monocyte Differentiation In Vivo

Onai, N., & Ogasawara, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010262 · Cited by 3

Systematic analysis of genetic variants in cancer-testis genes identified two novel lung cancer susceptibility loci in Chinese population

Li, Z., Tang, J., Wen, W. X., Wu, W., Wang, J., Xu, J., Yu, Y., He, Z., Pan, X., Wei, H., et al. (2020) · Journal of Cancer · doi:10.7150/jca.40002 · Cited by 3

The N-end rule E3 ligase UBR2 activates Nlrp1b inflammasomesPreprint

Xu, H., Shi, J., Yang, Z., Shao, F., & Dong, N. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/429225 · Cited by 3

HSP90 inhibitors beyond oncology: optimization and mechanism insights in non-oncological diseases

Yin, X., Shu, H., Wang, D., You, Q., Zhang, Q., & Wang, L. (2025) · Drug Discovery Today · doi:10.1016/j.drudis.2025.104514 · Cited by 2

miR-22-3p relieves the osteoarthritis by targeting to inflammasome in vivo and in vitro

Bai, L., Xia, W. L., Bo, L. Q., Zhang, L., & Fen, F. Z. (2022) · Turkish Journal of Biochemistry · doi:10.1515/tjb-2021-0223 · Cited by 2

Replicating Dynamic Immune Responses at Single‐Cell Resolution within a Microfluidic Human Skin Equivalent

Hindle, S. A., Brook, H. B., Chrysanthou, A., Chambers, E. S., Caley, M. P., & Connelly, J. T. (2025) · Advanced Science · doi:10.1002/advs.202415717 · Cited by 3

Current Understanding of the Etiology of Vitiligo

Koshoffer, A., & Boissy, R. E. (2014) · Current Dermatology Reports · doi:10.1007/s13671-014-0067-0 · Cited by 2

Autoimmune Addison’s Disease: Genetic Aetiology and Pathophysiology

Pazderska, A., Pearce, S. H. S., & Mitchell, A. L. (2017) · Contemporary Endocrinology · doi:10.1007/978-3-319-62470-9_4 · Cited by 2

Retinal Pigment Epithelium in Age-Related Macular Degeneration

Kaarniranta, K., Salminen, A., & Kauppinen, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-28384-1_9 · Cited by 2

Mechanism of Adjuvanticity of Aluminum-Containing Formulas

Kool, M., & Lambrecht, B. N. (2013) · Springer eBooks · doi:10.1007/978-3-319-00978-0_14 · 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

BRAIN'S IMMUNE SYSTEM AND TRAUMATIC BRAIN INJURY: THE MEANS FOR ITS CORRECTION

Dmitrienko, E. V., Akimoto, N., Naoe, S., Noda, M., Георгиевна, Р. Е., & Korneva, E. A. (2013) · Medical academic journal · doi:10.17816/maj1347-18 · Cited by 1

ASSOCIATION STUDY OF NEURONAL APOPTOSIS INHIBITORY PROTEIN GENE IN OVERWEIGHT AND OBESITY

Apostol, P., Danut, C., Spandole-Dinu, S., Toma, M., Stavarachi, M., Radu, I., Serafinceanu, C., Crăciun, A. M., BERCA, L.-M., Adriana, I. D., et al. (2013) · Cited by 1

Targeting the Metabolic Syndrome and Type 2 Diabetes by Preventing Inflammation

Ardestani, A. D., Shu, L., & Maedler, K. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-385083-6.00019-x · Cited by 1

Involvement of inflammation in autoinflammation and autoimmune disease

Furuichi, K., Wada, T., & Kaneko, S. (2011) · Inflammation and Regeneration · doi:10.2492/inflammregen.31.81 · Cited by 1

New insights in caspase-11 functions in noncanonical inflammasome signalling

Bodnar‐Wachtel, M., & Pétrilli, V. (2014) · Inflammasome · doi:10.2478/infl-2014-0001 · Cited by 1

Inflamasoma, piroptosis y su posible relación con la fisiopatología de la COVID-19

Pedreáñez, A. B., Mosquera, J., & Muñóz, N. (2020) · Investigación Clínica · doi:10.22209/ic.v61n3a07 · Cited by 1

CNS Cytokines

Kasten‐Jolly, J., & Lawrence, D. A. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7104-3_12 · Cited by 1

Molecular Mechanism of AGC Kinases in Human Malignant

Shu, S. (2010) · Digital Commons - University of South Florida (University of South Florida) · Cited by 1

Apoptosome and Caspase Activation

Declercq, W., & Vandenabeele, P. (2008) · Wiley eBooks · doi:10.1002/9780470048672.wecb019 · Cited by 1

Characterization of Anti-Fungal Inflammasome Responses and the Role of Caspase-8 in Innate Immune Signaling: A Dissertation

Ganesan, S. (2014) · eScholarship@UMassChan · doi:10.13028/m28c8f · Cited by 1

Monocyte Regulation By Soluble Uric Acid

McLaughlin, R. J. (2014) · doi:10.26686/wgtn.17006731.v1 · Cited by 1

Examining mechanisms of virulence gene regulation and the early host interactions in Francisella tularenisis

Faron, M. L. (2014) · doi:10.17077/etd.ov6i9woa

Efeitos do tratamento crônico com fluoxetina na reatividade da artéria mesentérica de resistência e no leito arterial mesentérico isolado de ratos

Pereira, C. A. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2014.tde-07072014-110258

Roles in innate immune receptors: Host : pathogen interactions and strengthening vaccines

Nyström, S. (2013) · Figshare

Influência do reconhecimento da flagelina extra e intracelular no processo de piroptose em macrófagos.

Lage, S. L. (2011) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2011.tde-03112011-111330

CASPASE-3 PROMOTES CELL PROLIFERATION AND INHIBITS DNA-DAMAGE INDUCED NECROSIS IN COLORECTAL CANCER

Brown, M. F. (2013) · D-Scholarship@Pitt (University of Pittsburgh)

DNA damage-induced cell death : The role of caspase-2

Vakifahmetoglu, H. (2009) · Figshare

Genetic variations in the NALP3 inflammasome

Verma, D. (2009)

XXIV CICLO DEL DOTTORATO DI RICERCA IN MEDICINA MATERNO INFANTILE, PEDIATRIA DELLO SVILUPPO E DELL'EDUCAZIONE, PERINATOLOGIA

Ventura, A. (2011)

Elucidation of the functional consequences of «NLRP7» mutations

Bukhari, E. (2009) · eScholarship@McGill (McGill) · doi:10.82308/26380

Revisitando a cavidade peritoneal de camundongos: identificação de novos subtipos funcionais de linfócitos B-1 e macrófagos

Ghosn, E. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.9.2016.tde-27102016-185248

COPs and POPs: Modulators of Inflammasome Activity 1

Stehlik, C., & Dorfleutner, A. (2007)

Necrobiology of Liver Cancer: Autophagy and Cellular Senescence

Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26587-2_179-1

Papel de inflamassomas e vias lisossomais na morte celular e resposta imune induzidas pela flagelina.

Lage, S. L. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2016.tde-25022016-095353

Choque séptico: integrando imunologia e biologia de sistemas

da Silva, F. P. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2016.tde-14062016-105916

ASC Apoptosis-associated speck-like protein con-

Martinon, F., Gaide, O., Pétrilli, V., Mayor, A., & Domain, C. C. R. (2007)

Inflammasomes: guardians of cytosolic sanctity

Lamkanfi, M., & Dixit, V. M. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00730.x · Cited by 372

NALPs: a novel protein family involved in inflammation

Tschopp, J., Martinon, F., & Burns, K. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1019 · Cited by 739

Pyrin Domain (PYD)-containing Inflammasome in Innate Immunity

Hong, S., Park, S., & Yu, J. (2011) · Journal of Bacteriology and Virology · doi:10.4167/jbv.2011.41.3.133 · Cited by 25

The inflammasome: a danger sensing complex triggering innate immunity

Pétrilli, V., Dostert, C., Muruve, D. A., & Tschopp, J. (2007) · Current Opinion in Immunology · doi:10.1016/j.coi.2007.09.002 · Cited by 700