The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Inflammasome-derived IL-1β production induces nitric oxide–mediated resistance to Leishmania
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nitric oxide: physiology, pathophysiology, and pharmacology.
Moncada, S., Palmer, R. M., & Higgs, E. A. (1991) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06663-3 · Cited by 15,525
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
Nitric oxide as a secretory product of mammalian cells
Nathan, C. (1992) · The FASEB Journal · doi:10.1096/fasebj.6.12.1381691 · Cited by 4,350
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
Hornung, V., Bauernfeind, F., Halle, A., Samstad, E. O., Kono, H., Rock, K. L., Fitzgerald, K. A., & Latz, E. (2008) · Nature Immunology · doi:10.1038/ni.1631 · Cited by 3,065
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658
The Inflammasomes: Guardians of the Body
Martinon, F., Mayor, A., & Tschopp, J. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132715 · Cited by 2,436
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., & Dixit, V. M. (2004) · Nature · doi:10.1038/nature02664 · Cited by 1,839
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 1,616
Self-citationVisceral leishmaniasis: what are the needs for diagnosis, treatment and control?
Chappuis, F., Sundar, S., Hailu, A., Ghalib, H., Rijal, S., Peeling, R. W., Alvar, J., & Boelaert, M. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1748 · Cited by 1,490
Activation of the NALP3 inflammasome is triggered by low intracellular potassium concentration
Pétrilli, V, Papin, S., Dostert, C., Mayor, A., Martinon, F., & Tschopp, J. (2007) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4402195 · Cited by 1,445
Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major
Darrah, P. A., Patel, D. T., De Luca, P. M., Lindsay, R. W. B., Davey, D. F., Flynn, B. J., Hoff, S. T., Andersen, P., Reed, S. G., Morris, S. L., et al. (2007) · Nature Medicine · doi:10.1038/nm1592 · Cited by 1,378
Reithinger, R., Dujardin, J.-C., Louzir, H., Pirmez, C., Alexander, B., & Brooker, S. (2007) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(07)70209-8 · Cited by 1,334
The immunology of susceptibility and resistance to Leishmania major in mice
Sacks, D., & Noben-Trauth, N. (2002) · Nature Reviews Immunology · doi:10.1038/nri933 · Cited by 1,208
Glyburide inhibits the Cryopyrin/Nalp3 inflammasome
Lamkanfi, M., Mueller, J. L., Vitari, A. C., Misaghi, S., Fedorova, A., Deshayes, K., Lee, W. P., Hoffman, H. M., & Dixit, V. M. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200903124 · Cited by 820
NOD-Like Receptors: Role in Innate Immunity and Inflammatory Disease
Chen, G., Shaw, M. H., Kim, Y.-G., & Nuñez, G. (2009) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev.pathol.4.110807.092239 · Cited by 772
The pCL vector system: rapid production of helper-free, high-titer, recombinant retroviruses
Naviaux, R. K., Costanzi, E., Haas, M., & Verma, I. M. (1996) · Journal of Virology · doi:10.1128/jvi.70.8.5701-5705.1996 · Cited by 732
Green, S. J., Meltzer, M. S., Hibbs, J. B., & Nacy, C. A. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.144.1.278 · Cited by 675
Interleukin-1β as a potent hyperalgesic agent antagonized by a tripeptide analogue
Ferreira, S. H., Lorenzetti, B. B., Bristow, A. F., & Poole, S. (1988) · Nature · doi:10.1038/334698a0 · Cited by 624
Nitrate Synthesis in the Germfree and Conventional Rat
Green, L. C., Tannenbaum, S. R., & Goldman, P. (1981) · Science · doi:10.1126/science.6451927 · Cited by 557
Suzuki, T., Franchi, L., Toma, C., Ashida, H., Ogawa, M., Yoshikawa, Y., Mimuro, H., Inohara, N., Sasakawa, C., & Nuñez, G. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030111 · Cited by 535
Zamboni, D. S., Kobayashi, K. S., Kohlsdorf, T., Ogura, Y., Long, E. M., Vance, R. E., Kuida, K., Mariathasan, S., Dixit, V. M., Flavell, R. A., et al. (2006) · Nature Immunology · doi:10.1038/ni1305 · Cited by 515
Self-citationImmune recognition of Pseudomonas aeruginosa mediated by the IPAF/NLRC4 inflammasome
Sutterwala, F. S., Mijares, L. A., Li, L., Ogura, Y., Kazmierczak, B. I., & Flavell, R. A. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20071239 · Cited by 513
Self-citationA role for the NLRP3 inflammasome in metabolic diseases—did Warburg miss inflammation?
Wen, H., Ting, J. P.-Y., & O'Neill, L. A. J. (2012) · Nature Immunology · doi:10.1038/ni.2228 · Cited by 457
Green, S. J., Crawford, R. M., Hockmeyer, J. T., Meltzer, M. S., & Nacy, C. A. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.12.4290 · Cited by 456
Späth, G. F., & Beverley, S. M. (2001) · Experimental Parasitology · doi:10.1006/expr.2001.4656 · Cited by 376
Liu, D., & Uzonna, J. E. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00083 · Cited by 364
Belkaid, Y., Mendez, S., Lira, R., Kadambi, N., Milon, G., & Sacks, D. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.2.969 · Cited by 363
Franchi, L., Kanneganti, T.-D., Dubyak, G. R., & Núñez, G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610762200 · Cited by 356
Role of the caspase-1 inflammasome in Salmonella typhimurium pathogenesis
Lara-Tejero, M., Sutterwala, F. S., Ogura, Y., Grant, E. P., Bertin, J., Coyle, A. J., Flavell, R. A., & Galán, J. E. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060206 · Cited by 354
Self-citationMarim, F. M., Silveira, T. N., Lima, D. S., & Zamboni, D. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015263 · Cited by 351
Self-citationStenger, S., Thüring, H., Röllinghoff, M., & Bogdan, C. (1994) · The Journal of experimental medicine · doi:10.1084/jem.180.3.783 · Cited by 302
Tetrahydrobiopterin-dependent formation of nitrite and nitrate in murine fibroblasts.
Werner-Felmayer, G., Werner, E. R., Fuchs, D., Hausen, A., Reibnegger, G., & Wachter, H. (1990) · The Journal of experimental medicine · doi:10.1084/jem.172.6.1599 · Cited by 287
Immune responses associated with susceptibility of C57BL/10 mice to Leishmania amazonensis
Afonso, L. C., & Scott, P. (1993) · Infection and Immunity · doi:10.1128/iai.61.7.2952-2959.1993 · Cited by 277
Liew, F. Y., Li, Y., Moss, D., Parkinson, C., Rogers, M. V., & Moncada, S. (1991) · European Journal of Immunology · doi:10.1002/eji.1830211216 · Cited by 199
Muraille, E., De Trez, C., Brait, M., De Baetselier, P., Leo, O., & Carlier, Y. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.8.4237 · Cited by 193
Montaser, M., Lalmanach, G., & Mach, L. (2002) · Biological Chemistry · doi:10.1515/bc.2002.147 · Cited by 167
MACROPHAGE KILLING OF LEISHMANIA AMAZONENSIS AMASTIGOTES REQUIRES BOTH NITRIC OXIDE AND SUPEROXIDE
Mukbel, R., PATTEN, C., GIBSON, K., Ghosh, M., Petersen, C. A., & Jones, D. E. (2007) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.2007.76.669 · Cited by 137
Subversion of host cell signalling by the protozoan parasiteLeishmania
Gregory, D. J., & Olivier, M. (2005) · Parasitology · doi:10.1017/s0031182005008139 · Cited by 110
Host Cell Signalling andLeishmaniaMechanisms of Evasion
Shio, M. T., Hassani, K., Isnard, A., Ralph, B., Contreras, I., Gómez, M. A., Abu‐Dayyeh, I., & Olivier, M. (2011) · Journal of Tropical Medicine · doi:10.1155/2012/819512 · Cited by 107
Hamon, M. A., & Cossart, P. (2011) · Infection and Immunity · doi:10.1128/iai.01243-10 · Cited by 105
Modulation of Dendritic Cell Function by Leishmania Parasites
Soong, L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.7.4355 · Cited by 94
Immunopathology of experimental cutaneous leishmaniasis.
Andrade, Z. A., Reed, S. G., Roters, S. B., et al. (1984) · PubMed · Cited by 87
Down-regulation of dendritic cell signaling pathways by Leishmania amazonensis amastigotes
Xin, L., Li, K., & Soong, L. (2008) · Molecular Immunology · doi:10.1016/j.molimm.2008.04.018 · Cited by 80
Disease Severity in Patients Infected with Leishmania mexicana Relates to IL-1β
Fernández-Figueroa, E. A., Rangel‐Escareño, C., Espinosa-Mateos, V., Carrillo‐Sánchez, K., Salaiza‐Suazo, N., Carrada-Figueroa, G., March-Mifsut, S., & Becker, I. (2012) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0001533 · Cited by 73
Bosque, Saravia, Valderrama, V., & Milon (2000) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.2000.00724.x · Cited by 61
Debus, A., Gläsner, J., Röllinghoff, M., & Gessner, A. (2003) · Infection and Immunity · doi:10.1128/iai.71.12.7215-7218.2003 · Cited by 61
Kostka, S. L., Knop, J., Konur, A., Udey, M. C., & von Stebut, E. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700309 · Cited by 49
IL-1 signalling is dispensable for protective immunity in Leishmania-resistant mice
Kautz‐Neu, K., Kostka, S. L., Dinges, S., Iwakura, Y., Udey, M. C., & von Stebut, E. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01172.x · Cited by 35
Moravej, A., Rasouli, M., Kalani, M., Asaei, S., Kiany, S., Najafipour, S., Kouhpayeh, S. A., & Abdollahi, A. (2012) · Molecular Biology Reports · doi:10.1007/s11033-012-1517-z · Cited by 30
The TNF receptor family member CD27 signals to Jun N-terminal kinase via Traf-2
Eugster (1998) · Pure Amsterdam UMC · doi:10.1002/(sici)1521-4141(199807)28:07 · Cited by 2
Cited by
Nitric oxide synthase in innate and adaptive immunity: an update
Bogdan, C. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.01.003 · Cited by 862
The adaptor ASC has extracellular and 'prionoid' activities that propagate inflammation
Franklin, B. S., Bossaller, L., De Nardo, D., Ratter, J. M., Stutz, A., Engels, G., Brenker, C., Nordhoff, M., Mirandola, S. R., Al-Amoudi, A., et al. (2014) · Nature Immunology · doi:10.1038/ni.2913 · Cited by 773
Cutaneous leishmaniasis: Immune responses in protection and pathogenesis
Scott, P., & Novais, F. O. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.72 · Cited by 591
Caspase-11 activation requires lysis of pathogen-containing vacuoles by IFN-induced GTPases
Meunier, E., Dick, M. S., Dreier, R. F., Schürmann, N., Broz, D. K., Warming, S., Roose-Girma, M., Bumann, D., Kayagaki, N., Takeda, K., et al. (2014) · Nature · doi:10.1038/nature13157 · Cited by 485
Organization of the skin immune system and compartmentalized immune responses in infectious diseases
Quaresma, J. A. S. (2019) · Clinical Microbiology Reviews · doi:10.1128/cmr.00034-18 · Cited by 149
Metadata
- Authors
- Lima-Junior, D. S., Costa, D. L., Carregaro, V., Cunha, L. D., Silva, A. L. N., Mineo, T. W. P., Gutierrez, F. R. S., Bellio, M., Bortoluci, K. R., Flavell, R. A., Bozza, M. T., Silva, J. S., & Zamboni, D. S.
- Venue
- Nature Medicine
- Published
- 2013-06-09
- Volume
- 19
- Issue
- 7
- Pages
- 909-915
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W2020930525
- Cited by
- 360
- References
- 51
- FWCI
- 11.30
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.