Interleukin-10 (IL-10) inhibits the induction of nitric oxide synthase by interferon-γ in murine macrophages

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor

Palmer, R. M. J., Ferrige, A. G., & Moncada, S. (1987) · Nature · doi:10.1038/327524a0 · Cited by 10,704

Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production.

Ding, A. H., Nathan, C., & Stuehr, D. J. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.141.7.2407 · Cited by 2,840

Two types of mouse T helper cell. IV. Th2 clones secrete a factor that inhibits cytokine production by Th1 clones.

Fiorentino, D. F., Bond, M. W., & Mosmann, T. R. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.170.6.2081 · Cited by 2,733

Interleukin 10 (IL-10) and viral IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression.

Malefyt, R. D. W., Haanen, J. B. A. G., Spits, H., Roncarolo, M., Velde, A. A. T., Figdor, C. G., Johnson, K., KASTELEIN, R. A., Yssel, H., & de Vries, J. E. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.174.4.915 · Cited by 1,930

IL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells

Fiorentino, D. F., Zlotnik, A., Vieira, P., Mosmann, T. R., Howard, M., Moore, K. W., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.146.10.3444 · Cited by 1,866

Reciprocal expression of interferon gamma or interleukin 4 during the resolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets.

Heinzel, F. P., Sadick, M. D., Holaday, B. J., Coffman, R. L., & Locksley, R. M. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.1.59 · Cited by 1,454

Homology of Cytokine Synthesis Inhibitory Factor (IL-10) to the Epstein-Barr Virus Gene BCRFI

Moore, K. W., Vieira, P., Fiorentino, D. F., Trounstine, M. L., Khan, T. A., & Mosmann, T. R. (1990) · Science · doi:10.1126/science.2161559 · Cited by 1,143

Correlation between nitric oxide formation during degradation of organic nitrates and activation of guanylate cyclase

Feelisch, M., & Noack, E. (1987) · European Journal of Pharmacology · doi:10.1016/0014-2999(87)90493-6 · Cited by 887

Immunoregulation of cutaneous leishmaniasis. T cell lines that transfer protective immunity or exacerbation belong to different T helper subsets and respond to distinct parasite antigens.

Scott, P., Natovitz, P., Coffman, R. L., Pearce, E. J., & Sher, A. (1988) · The Journal of Experimental Medicine · doi:10.1084/jem.168.5.1675 · Cited by 705

Macrophage deactivating factor and transforming growth factors- beta 1 - beta 2 and - beta 3 inhibit induction of macrophage nitrogen oxide synthesis by IFN-gamma.

Ding, A. H., Nathan, C., Graycar, J. L., Derynck, R., Stuehr, D. J., & Srimal, S. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.3.940 · Cited by 500

There is no Regulatory Role for Induced Nitric Oxide in the Regulation of the in vitro Proliferative Response of Bovine Mononuclear Cells to Mitogens, Alloantigens or Superantigens

Schuberth, H., Hendricks, A., & Leibold, W. (1998) · Immunobiology · doi:10.1016/s0171-2985(98)80051-x · Cited by 13

Interleukin-10 (IL-10)

Benjamin, D. (1995) · Cancer treatment and research · doi:10.1007/978-1-4613-1241-3_12 · Cited by 13

Concanavalin-A displays leishmanicidal activity by inducing ROS production in human peripheral blood mononuclear cells

Thomazelli, A. P. F. D. S., Tomiotto‐Pellissier, F., Miranda-Sapla, M. M., da Silva, S. S., Alvarenga, D. S., Panis, C., Cataneo, A. H. D., Bordignon, J., Silveira, G. F., Yamauchi, L. M., et al. (2018) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2018.1510960 · Cited by 12

Porcine hepatic response to sepsis and its amplification by an adrenergic receptor α1 agonist and a β2 antagonist

Tighe, D., Moss, R. F., & Bennett, D. (1998) · Clinical Science · doi:10.1042/cs0950467 · Cited by 12

Human T helper cells reactive with somatic bacterial antigens belong to the Th1 subset

Schlaak, J., Nieder, P., B�schenfelde, K.-H. M. Z., & Fleischer, B. (1994) · Medical Microbiology and Immunology · doi:10.1007/bf00196051 · Cited by 12

Nitric Oxide in Influenza

Akaike, T., & Maeda, H. (2002) · Springer eBooks · doi:10.1007/0-306-46816-6_19 · Cited by 11

IL-10 Inhibits Nitric Oxide Synthesis in Murine Uterus

Ogando, D. G., Cella, M., Ribeiro, M. L., Weissmann, C., Aisemberg, J., & Franchi, A. M. (2004) · NeuroImmunoModulation · doi:10.1159/000075322 · Cited by 10

Immunization with heat-killed Toxoplasma gondii stimulates an early IFN-γ response and induces protection against virulent murine malaria

Haque, A., Graille, M., Kasper, L. H., & Haque, S. (1999) · Vaccine · doi:10.1016/s0264-410x(99)00050-x · Cited by 10

Enhanced nitric oxide production associated with airway hyporesponsiveness in the absence of IL-10

Ameredes, B. T., Sethi, J. M., He-liang, L., Choi, A. M. K., & Calhoun, W. J. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00207.2004 · Cited by 10

The truncated Rv2820c of Mycobacterium tuberculosis Beijing family augments intracellular survival of M. smegmatis by altering cytokine profile and inhibiting NO generation

Zhai, X., Luò, T., Peng, X., Ma, P., Wang, C., Zhang, C., Suo, J., & Bao, L. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.01.027 · Cited by 9

Vaccinia virus-induced inhibition of nitric oxide production

Bellows, C. F., Garry, R. F., & Jaffe, B. M. (2003) · Journal of Surgical Research · doi:10.1016/s0022-4804(03)00079-9 · Cited by 9

Characterization of clonally derived, spontaneously transformed bone marrow macrophage cell lines from lipopolysaccharide hyporesponsive LPS(d) and normal LPS(n) mice

Monner, D. A., & Denker, B. (1997) · Journal of Leukocyte Biology · doi:10.1002/jlb.61.4.469 · Cited by 8

Cytokine Regulation of Nitric Oxide Production

Mühl, H., & Dinarello, C. A. (2002) · Springer eBooks · doi:10.1007/0-306-46816-6_5 · Cited by 8

A Study on the Inhibitory Effect and Mechanism of Lonicera Japonica on Type I Interferon

Kang, Y.-G., Ryu, I.-H., Kim, S.-B., Choi, C., Seo, Y.-J., & Cho, H.-B. (2013) · The Journal of Korean Obstetrics and Gynecology · doi:10.15204/jkobgy.2013.26.2.017 · Cited by 7

Le rétrocontrôle négatif de l'inflammation: rôle des cytokines antiinflammatoires

Marie, C., & Cavaillon, J. (1997) · Bulletin de l Institut Pasteur · doi:10.1016/s0020-2452(97)82541-9 · Cited by 7

Interleukin 10 and its role in the regulation of the cell-mediated immune response in syphilis.

Łusiak, M., & Podwińska, J. (2001) · PubMed · Cited by 7

A Breath of Fresh Air for Lung Transplant Recipients

Wilkes, D. S. (2009) · Science Translational Medicine · doi:10.1126/scitranslmed.3000380 · Cited by 6

Opposite effects of interleukin‐4 and interleukin‐10 on nitric oxide production in murine macrophages

Maru, A., & Jackson, S. K. (1996) · Mediators of Inflammation · doi:10.1155/s096293519600018x · Cited by 6

Nitric Oxide in Malaria

Anstey, N. M., Weinberg, J. B., & Granger, D. L. (2002) · Springer eBooks · doi:10.1007/0-306-46816-6_15 · Cited by 6

Inhibition of Nitric Oxide Synthase Activity in Circulatory Shock: Friend or Foe?

Thiemermann, C. (1995) · Update in intensive care and emergency medicine · doi:10.1007/978-3-642-79920-4_13 · Cited by 6

Cytokine pattern in patients with infections after liver transplantation

Mueller, A. R., Platz, K. P., Wiehe, I., Monticelli, F. C., Lierath, J., Keitel, M., Streich, R., Bechstein, W. O., & Neuhaus, P. (1996) · Springer eBooks · doi:10.1007/978-3-662-00818-8_32 · Cited by 6

Blocking IL-10 signaling with soluble IL-10 receptor restores in vitro specific lymphoproliferative response in dogs with leishmaniasis caused by Leishmania infantum

Santos, C. D. O., Costa, S. F., Souza, F. S., Mendes, J. M. F., de Pinheiro, C. G. M., Moreira, D. R. M., Silva, L. K., de Lima, V. M. F., & Oliveira, G. G. D. S. (2021) · PLoS ONE · doi:10.1371/journal.pone.0239171 · Cited by 5

Enhancement of nitric oxide synthase induction in alveolar macrophages by in vivo administration of docetaxel

Saito, F., Matsusaka, S., Takahashi, Y., & Wakabayashi, I. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.006 · Cited by 5

Macrophage activation by lipopolysaccharide, interferon‐γ and interleukin‐4: effect of fatty acid metabolism

Darmani, H., Harwood, J. L., Parton, J., & Jackson, S. K. (1995) · Mediators of Inflammation · doi:10.1155/s0962935195000056 · Cited by 5

Blockade of Nitric Oxide Formation Enhances Thermal and Behavioral Responses in Rats during Turpentine Abscess

Soszyński, D. (2000) · NeuroImmunoModulation · doi:10.1159/000054279 · Cited by 5

Indirect Stimulatory Effects of Murine Interleukin-12 on In Vitro Production of Nitric Oxide by Mouse Peritoneal Cells

Zı́dek, Z., Lotzová, E., Franková, D., & Savary, C. A. (1996) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.1996.16.389 · Cited by 5

Effect of exposure to nitrogen dioxide on alveolar macrophage-mediated immunosuppressive activity in rats

Koike, E., Kobayashi, T., & Utsunomiya, R. (2001) · Toxicology Letters · doi:10.1016/s0378-4274(01)00331-9 · Cited by 4

CHARACTERISTICS OF NITRIC OXIDE-INDUCED APOPTOSIS AND ITS TARGET CELLS IN MITOGEN-STIMULATED PERIPHERAL BLOOD MONONUCLEAR CELLS FROM HIV+ SUBJECTS

García, M., Llano, A., Cruz-Colón, E., Saavedra, S., Lavergne, J. A., & Lavergne, J. A. (2001) · Immunological Investigations · doi:10.1081/imm-100108163 · Cited by 4

Development of sandwich ELISA for IL-10 quantification in olive flounder (Paralichthys olivaceus) and its application to protein-level analysis during viral hemorrhagic septicemia virus (VHSV) infection

Kim, J.-Y., Castro, F., Shin, S.-M., Kwon, S. R., & Jung, S. (2026) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2026.111270 · Cited by 3

Interactions of Leukocytes and Coagulation Factors with the Vessel Wall

Visovatti, S., Ohtsuka, T., & Pinsky, D. J. (2010) · Springer eBooks · doi:10.1007/978-0-387-87429-6_26 · Cited by 3

Inhibitory effects of interleukin(IL)-10 and viral IL-10 (vIL-10) on the functions of monocytes/macrophages.

Nemoto, Y., Otsuka, T., Niiro, H., Kuga, S., Tanaka, Y., Nakashima, H., & Niho, Y. (1995) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.18.152 · Cited by 3

Interleukin-10 Production during Septic Shock

Goldman, M., & Marchant, A. (1996) · Yearbook of intensive care and emergency medicine · doi:10.1007/978-3-642-80053-5_10 · Cited by 3

Immuno-Mechanical Signaling Network Integration in Temporomandibular Joint Pathology: A TMID Conceptual Framework

Kim, H.-J., Kim, J., & Yun, J.-I. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083363 · Cited by 2

Shock

Takhar, S., & Rosenthal, M. H. (2001) · Springer eBooks · doi:10.1007/978-1-4757-6645-5_5 · Cited by 2

Splenic autotransplantation reverses interferon‐gamma and nitric oxide production and resistance to Listeria monocytogenes in splenectomized mice

Perobelli, S. M., Alves, C. C. D. S., Rezende, A. B., Farias, R. E., Nunes, S., & Teixeira, H. C. (2010) · Transplant Infectious Disease · doi:10.1111/j.1399-3062.2010.00562.x · Cited by 2

Assessment of leukocyte activity in mice devoid of the glucocorticoid receptor in the noradrenergic system (GRDBHCre)

Roman, A., Kuśmierczyk, J., Kreiner, G., & Nalepa, I. (2017) · Immunobiology · doi:10.1016/j.imbio.2017.10.022 · Cited by 2

Nitric Oxide in Schistosomiasis

Oswald, I. P. (2002) · Springer eBooks · doi:10.1007/0-306-46816-6_16 · Cited by 2

Interleukin‐10 Inhibited the Expression of Tumor Antigens and Major Histocompatibility Complex Antigen on EJ‐ras Oncogene Transformants

Tsuruma, T., Yagihashi, A., Torigoe, T., Okada, Y., Sato, N., Kikuchi, K., & Hirata, K. (1996) · Artificial Organs · doi:10.1111/j.1525-1594.1996.tb04565.x · Cited by 2

Aminoguanidine administered during the induction of oral tolerance alters the systemic response of the tolerised rats

Franco, L. G., Feledi, C. A., Massouh, E. J., & Benencia, F. (2009) · Cellular Immunology · doi:10.1016/j.cellimm.2009.10.010 · Cited by 2

Leishmania amazonensis and macrophage interactions: immune factors necessary to kill the parasite

Mukbel, R. (2005) · doi:10.31274/rtd-180813-12322 · Cited by 2

Biology of Nitric Oxide in Neuroimmunoregulation

Liew, F. Y. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb23083.x · Cited by 2

Nitric oxide and bone destruction

Macpherson, H. K., & Ralston, S. H. (2000) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8482-2_12 · Cited by 2

Nitric Oxide in Pulmonary Processes: Role in Physiology and Pathophysiology of Lung Disease

(2000) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8474-7 · Cited by 2

Sphingosine-1-phosphate receptor signaling regulates an ERK1/2–p65 molecular switch in macrophages during Leishmania donovani infection

Arish, M., & Naz, F. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1769137 · Cited by 1

Assessment and management of the care of children with nocturnal enuresis: guidelines for primary care.

Stark, M. (1994) · PubMed · Cited by 1

Nitric Oxide in Listeriosis

Boockvar, K. S., Maybodi, M., Poston, R. M., Kurlander, R. L., & Granger, D. L. (2002) · Springer eBooks · doi:10.1007/0-306-46816-6_22 · Cited by 1

The role of microglia phenotypes in modulating CD4 + T cell responses

Ebner, F. (2014) · doi:10.18452/16882 · Cited by 1

Characterization and immunogenicity of the heat shock protein, hsp60 of Brucella abortus

Gor, D. O. (1994) · doi:10.31274/rtd-180813-10325 · Cited by 1

NO and Glomerulonephritis

Cattell, V., & Cook, H. T. (1997) · Springer eBooks · doi:10.1007/978-1-4615-6039-5_15 · Cited by 1

Hyporesponsiveness in leukocytes in sepsis: in vitro models reveal paradoxical effects of IL-10

Cavaillon, J., Adib‐Conquy, M., Marie, C., & Fitting, C. (1999) · Journal of Endotoxin Research · doi:10.1177/09680519990050010701 · Cited by 1

Oh no, not nitric oxide!

Bhagat, K. (1999) · PubMed · Cited by 1

The Putative Role of HIV-1 Envelope Proteins in the Neuroimmunology and Neuropathology of CNS Aids

Koka, P. S., & Merrill, J. E. (1996) · Springer eBooks · doi:10.1007/978-1-4899-0191-0_21 · Cited by 1

Interleukin-10

Deng, J. C., & Standiford, T. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-08-102723-3.00053-6 · Cited by 1

Duct-to-duct biliary reconstruction following liver transplantation for primary sclerosing cholangitis

Distante, V., Farouk, M., Kurzawinski, T. R., Monticelli, S. W., Burroughs, A. K., Davidson, B. R., & Rolles, K. (1996) · Transplant International · doi:10.1111/j.1432-2277.1996.tb01588.x · Cited by 1

Recent Insights into the Molecular Pathophysiology of Viral Myocarditis

Tran, T. T., Rossen, R. D., & Mann, D. L. (2007) · Humana Press eBooks · doi:10.1007/978-1-59259-878-6_9

Nitric Oxide in Airway Inflammation

Lee, Y. C., Kim, S. R., Jo, E., Pae, H., & Chung, H. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-373866-0.00025-3

Defining CCL20's Role in Carcinogenesis

Schafer, M. (2012) · doi:10.15760/honors.5

Efeitos de derivados nitro heterocíclicos sintéticos sobre formas promastigotas e amastigotas intracelular de Leishmania (Leishmania) infantum

Petri, S. C. S. (2015) · doi:10.11606/d.5.2015.tde-26102015-145221

Transcriptional Regulation of the Macrophage NOS2 Gene

Goldring, C. E., Reveneau, S., & Jeannin, J. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5081-5_17

Estudo dos tipos e subtipos celulares predominantes e da expressão da enzima óxido nítrico sintase induzível (iNOS) na Paracoccidioidomicose Bucal

Batista, A. C. (2004) · doi:10.11606/t.25.2004.tde-10102007-162134

The Mechanistic Involvement of Vanin-1 in Protection against Acetaminophen Hepatotoxicity

Ferreira, D. W. (2013) · OpenCommons - UConn (University of Connecticut)

Caracterização dos mecanismos imunológicos associados com os efeitos protetores e deletérios do óxido nitrico na Paracoccidioidomicose pulmonar.

Bernardino, S. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2009.tde-01122009-101538

Estudo da interação de Sporothrix shenckii com macrófagos murinos

Franco, D. D. L. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.9.2009.tde-25092009-152023

Gene expression changes in macrophages infected with pathogenic M. tuberculosis and non-pathogenic M. smegmatis and M. bovis BCG

Mpongoshe, V. (2014) · SUNScholar (Stellenbosch University)

IL-10 in Human Newborns : Ontogeny of IL-10 secretion and relation to the secretion of IFN-g, immunoglobulin M, G, and A, and mononuclear cell composition in newborns

Kotiranta-Ainamo, A. (2006) · Työväentutkimus Vuosikirja

A FUNÇÃO DA IL-10 NA PARACOCCIDIOIDOMISE

Murina, P. (2010)

Susceptibility to ozone-induced pulmonary inflammation: Investigating the role of the innate immune response

Hazzard, B., & Swift, G. L. (2006)

Modulation of dendritic cell function through delivery of effector proteins by genetically modified lactococcus lactis

Loos, M. (2007) · Ghent University Academic Bibliography (Ghent University)

Apoptose de linfócitos na imunossupressão da leishmaniose visceral em hamsteres infectados com Leishmania (Leishmania) chagasi

Paulo, S. (2010)

Tnf(alpha)-dependent and Tnf(alpha)-independent Activation of Macrophage Effector Function

Clemons-Miller, A. R. (1998) · Digital Commons - East Tennessee State University (East Tennessee State University)

Interleukin-10-Induced Immune Suppression in Cancer

Yang, A. S., & Lattime, E. C. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-743-7_9

IL-10) NA DOR INFLAMATÓRIA EXPERIMENTAL: Papel de células residentes e citocinas

Farmacologia, F. E., & Pós, C. D. (2000)

INFLUENCE OF THERAPY UPON LPS-INDUCED CYTOKINE SECRETION BY THE BLOOD-DERIVED INNATE IMMUNITY CELLS OF THE BRONCHIAL ASTHMA PATIENTS

Serov, D. A., Kabanov, D. S., Ивановна, К. Н., & Прохоренко, И. Р. (2019) · Medical Immunology (Russia) · doi:10.15789/1563-0625-2019-4-789-796

Genesis and Characterization of Human eNOS-Based Platelet Subpopulations. Implications for Haemostasis and Thrombosis

Lesyk, G. M. (2019) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-pk4m-h082

Ocular Blast Trauma: Mechanisms of Degeneration and a Potential Therapeutic Strategy

Bricker-Anthony, C. (2016)

Dendritic cells activated by CpG motifs are potent inducers of a Th1 immune response that protects mice against leishmaniasis

Ramírez, P., & Robinson, J. (2003)

Interleukin-10

Enk, A. (1997) · Growth factors and cytokines in health and disease · doi:10.1016/s1874-5687(97)80029-8

Mucosal immunity in mycobacterial infections.

Tjärnlund, A. (2007) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Caractérisation des bases moléculaires et cellulaires de la reprogrammation fonctionnelle radio-induite des macrophages dans le cadre du traitement du cancer

Nathan, A. D. (2023) · theses.fr (ABES) · doi:10.70675/16998154z3c40z4b59z9eddz3735ec9df3f3

Pathogenic T-bet + memory B cells worsen multiple sclerosis through myeloid cell activationPreprint

Jain, R. W., Goiko, M., Mendes, A., Xue, S., Zein, S., Gorter, R. P., Mørch, M. T., Prat, A., Li, R., & Yong, V. W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.01.748682

Role of Nitric Oxide in Airway Inflammation

Haddad, E. (2000) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8474-7_8

Cytokine Control of Nitric Oxide Production: Therapeutic Possibilities

Evans, T. J. (1999) · Springer eBooks · doi:10.1007/978-3-642-58630-9_9

Induction of macrophage nitric oxide production by interferon‐γ and tumor necrosis factor‐α is enhanced by interleukin‐10

Corradin, S. B., Fasel, N. J., Buchmüller-Rouiller, Y., Ransijn, A., Smith, J., & Mauël, J. (1993) · European Journal of Immunology · doi:10.1002/eji.1830230851 · Cited by 83

Opposite effects of interleukin‐4 and interleukin‐10 on nitric oxide production in murine macrophages

Maru, A., & Jackson, S. K. (1996) · Mediators of Inflammation · doi:10.1155/s096293519600018x · Cited by 6

Interleukin-10 in combination with interferon-gamma and tumor necrosis factor-alpha enhances in vitro production of nitric oxide by murine resident paritoneal macrophage.

Zı́dek, Z., & Franková, D. (1999) · PubMed · Cited by 7

Influence of maternal antibodies on vaccine responses: inhibition of antibody but not T cell responses allows successful early prime-boost strategies in mice

Siegrist, C., Barrios, C. S., Martínez, X., Brandt, C., Berney, M., Córdova, M., Kovařík, J., & Lambert, P. (1998) · European Journal of Immunology · doi:10.1002/(sici)1521-4141(199812)28:12 · Cited by 184

Mediators of Inflammation 5, 110-112 (1996)

Maru, A., & Jackson, S. K. (2013)