João Santana da Silva spends much of his time researching Immunology, Chemokine, Cytokine, Trypanosoma cruzi and Immune system. His Immunology research is multidisciplinary, incorporating perspectives in Periodontitis, Nitric oxide and Microbiology. His Chemokine research is multidisciplinary, relying on both Proinflammatory cytokine and CCL5.
João Santana da Silva has included themes like Interferon, Matrix metalloproteinase and Leukocyte migration in his Cytokine study. His Trypanosoma cruzi research is multidisciplinary, incorporating elements of In vitro, Macrophage, Chagas disease, Virology and In vivo. His research in Immune system intersects with topics in Interleukin 12, Rhipicephalus sanguineus and Saliva.
Immunology, Immune system, Trypanosoma cruzi, Chemokine and Cytokine are his primary areas of study. His study ties his expertise on Microbiology together with the subject of Immunology. The concepts of his Immune system study are interwoven with issues in Proinflammatory cytokine and Saliva.
As a part of the same scientific family, João Santana da Silva mostly works in the field of Trypanosoma cruzi, focusing on Chagas disease and, on occasion, Myocarditis. His study with Chemokine involves better knowledge in Receptor. His study in Interleukin 10 and Interferon gamma falls under the purview of Cytokine.
João Santana da Silva mainly investigates Immunology, Immune system, Internal medicine, Inflammasome and Gut flora. His studies deal with areas such as Cell migration and Asymptomatic as well as Immunology. His Immune system research focuses on Inflammation and how it connects with Spleen.
As part of the same scientific family, he usually focuses on Internal medicine, concentrating on Endocrinology and intersecting with Mesenteric lymph nodes. His Inflammasome research also works with subjects such as
João Santana da Silva focuses on Immunology, Internal medicine, Immune system, Inflammasome and Endocrinology. His Immunology research includes elements of Trypanosoma cruzi and STAT protein. João Santana da Silva has researched Trypanosoma cruzi in several fields, including Cardiomyopathy, Downregulation and upregulation, Signal transduction, Protozoan infection and Heart disease.
His study in Immune system is interdisciplinary in nature, drawing from both Inflammation, Proinflammatory cytokine, Kidney and Macrophage. He interconnects NLRC5, NLRP1, Immunopathology and Cutaneous leishmaniasis in the investigation of issues within Inflammasome. João Santana da Silva combines subjects such as Acute kidney injury and Macrophage polarization with his study of Endocrinology.
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A cascade of cytokines mediates mechanical inflammatory hypernociception in mice
T. M. Cunha;W. A. Verri;J. S. Silva;S. Poole.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Nitric oxide is involved in control of Trypanosoma cruzi-induced parasitemia and directly kills the parasite in vitro.
G N R Vespa;Fernando de Queiroz Cunha;João Santana da Silva.
Infection and Immunity (1994)
Interleukin 10 and interferon gamma regulation of experimental Trypanosoma cruzi infection.
J S Silva;P J Morrissey;K H Grabstein;K M Mohler.
Journal of Experimental Medicine (1992)
Regulation of Trypanosoma cruzi infections in vitro and in vivo by transforming growth factor beta (TGF-beta).
J S Silva;D R Twardzik;S G Reed.
Journal of Experimental Medicine (1991)
Chemokines in Oral Inflammatory Diseases: Apical Periodontitis and Periodontal Disease
T.A. Silva;G.P. Garlet;S.Y. Fukada;J.S. Silva.
Journal of Dental Research (2007)
Tumor necrosis factor alpha mediates resistance to Trypanosoma cruzi infection in mice by inducing nitric oxide production in infected gamma interferon-activated macrophages.
J. S. Silva;G. N. R. Vespa;M. A. G. Cardoso;J. C. S. Aliberti.
Infection and Immunity (1995)
Interleukin-12 mediates resistance to Trypanosoma cruzi in mice and is produced by murine macrophages in response to live trypomastigotes.
J C Aliberti;M A Cardoso;G A Martins;R T Gazzinelli.
Infection and Immunity (1996)
Patterns of chemokines and chemokine receptors expression in different forms of human periodontal disease.
Gustavo P. Garlet;Walter Martins;Beatriz R. Ferreira;Cristiane M. Milanezi.
Journal of Periodontal Research (2003)
Cytokine expression pattern in compression and tension sides of the periodontal ligament during orthodontic tooth movement in humans
Thiago P. Garlet;Ulisses Coelho;João S. Silva;Gustavo P. Garlet.
European Journal of Oral Sciences (2007)
Evidence of the presence of T helper type 17 cells in chronic lesions of human periodontal disease.
C. R. Cardoso;G. P. Garlet;G. E. Crippa;A. L. Rosa.
Oral Microbiology and Immunology (2009)
Profile was last updated on December 6th, 2021.
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