His primary areas of investigation include Trypanosoma cruzi, Biochemistry, Cell biology, Microbiology and Proinflammatory cytokine. The Trypanosoma cruzi study combines topics in areas such as Tumor necrosis factor alpha, Cytokine, Immunology, Chagas disease and Glycoprotein. Igor C. Almeida has researched Chagas disease in several fields, including Benznidazole, Internal medicine, Randomized controlled trial and Antigen.
His Mucin, Intracellular and ATP synthase study in the realm of Biochemistry interacts with subjects such as Midgut. His Cell biology study integrates concerns from other disciplines, such as Vesicle, Innate immune system, Amastigote and Virulence. His Microbiology research includes elements of Micrococcus luteus, Antibody, Antibacterial agent and Serine.
Trypanosoma cruzi, Biochemistry, Chagas disease, Microbiology and Cell biology are his primary areas of study. His studies deal with areas such as Serology, Virology, Glycoprotein, Antigen and Mucin as well as Trypanosoma cruzi. His work in Biochemistry covers topics such as Molecular biology which are related to areas like Histone H1.
The study incorporates disciplines such as Benznidazole and Intracellular in addition to Chagas disease. He focuses mostly in the field of Microbiology, narrowing it down to topics relating to Macrophage and, in certain cases, Proinflammatory cytokine. In Cell biology, Igor C. Almeida works on issues like Vesicle, which are connected to Secretion.
His main research concerns Trypanosoma cruzi, Chagas disease, Cell biology, Virology and Antibody. His study in Trypanosoma cruzi is interdisciplinary in nature, drawing from both Immunology, Antigen, Interaction with host, Mucin and Macrophage. Igor C. Almeida works mostly in the field of Chagas disease, limiting it down to concerns involving Benznidazole and, occasionally, Internal medicine and Serology.
He combines subjects such as Innate immune system, Immune system and Trypanosoma brucei with his study of Cell biology. His studies in Virology integrate themes in fields like Epitope and Leishmania major. The concepts of his Antibody study are interwoven with issues in Parasite hosting, Tick and Glycan.
Igor C. Almeida focuses on Internal medicine, Epitope, Virology, Antibody and Immune system. His study in Immune system is interdisciplinary in nature, drawing from both Microvesicles, Intracellular, Cell biology and Antigen. Igor C. Almeida has included themes like Interaction with host, Trypanosoma cruzi and Chagas disease in his Microvesicles study.
The Trypanosoma cruzi study combines topics in areas such as Secretory protein, Cruzipain, Glycoprotein and Microbiology. The Cell biology study which covers Virulence factor that intersects with Infectivity. Glycan is the subject of his research, which falls under Biochemistry.
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Activation of Toll-like receptor-2 by glycosylphosphatidylinositol anchors from a protozoan parasite.
Marco A. S. Campos;Igor C. Almeida;Osamu Takeuchi;Shizuo Akira.
Journal of Immunology (2001)
Randomised trial of efficacy of benznidazole in treatment of early Trypanosoma cruzi infection
Ana Lúcia Sampaio Sgambatti de Andrade;Fabio Zicker;Renato Mauricio de Oliveira;Simone Almeida e Silva.
The Lancet (1996)
Extracellular Vesicles Produced by Cryptococcus neoformans Contain Protein Components Associated with Virulence
Marcio L. Rodrigues;Ernesto S. Nakayasu;Debora L. Oliveira;Leonardo Nimrichter.
Eukaryotic Cell (2008)
Vesicular transport in Histoplasma capsulatum: an effective mechanism for trans-cell wall transfer of proteins and lipids in ascomycetes
Priscila Costa Albuquerque;Ernesto S. Nakayasu;Marcio L. Rodrigues;Susana Frases.
Cellular Microbiology (2008)
Highly purified glycosylphosphatidylinositols from Trypanosoma cruzi are potent proinflammatory agents.
Igor C. Almeida;Igor C. Almeida;Maristela M. Camargo;Daniela O. Procópio;Luiz S. Silva.
The EMBO Journal (2000)
Kinetics of cytokine gene expression in experimental chagasic cardiomyopathy: tissue parasitism and endogenous IFN-γ as important determinants of chemokine mRNA expression during infection with Trypanosoma cruzi.
André Talvani;André Talvani;Cristiana S Ribeiro;Júlio C.S Aliberti;Vladimir Michailowsky.
Microbes and Infection (2000)
Glycosylphosphatidylinositol-anchored mucin-like glycoproteins isolated from Trypanosoma cruzi trypomastigotes initiate the synthesis of proinflammatory cytokines by macrophages.
Maristela M. Camargo;Igor C. Almeida;Maria E S Pereira;Michael A J Ferguson.
Journal of Immunology (1997)
The mucin-like glycoprotein super-family of Trypanosoma cruzi: structure and biological roles.
Alvaro Acosta-Serrano;Igor C. Almeida;Lucio H. Freitas-Junior;Nobuko Yoshida.
Molecular and Biochemical Parasitology (2001)
Proteomic Analysis of Trypanosoma cruzi Secretome: Characterization of Two Populations of Extracellular Vesicles and Soluble Proteins
Ethel Bayer-Santos;Clemente Aguilar-Bonavides;Silas Pessini Rodrigues;Esteban Maurício Cordero.
Journal of Proteome Research (2013)
Characterization of yeast extracellular vesicles: evidence for the participation of different pathways of cellular traffic in vesicle biogenesis.
Débora L. Oliveira;Ernesto S. Nakayasu;Ernesto S. Nakayasu;Luna S. Joffe;Allan J. Guimarães.
PLOS ONE (2010)
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