The paracoccidioidomycotic granuloma (2009)
- Authors:
- Autor USP: BURGER, EVA - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Congress of the International Society for Human and Animal Mycology - ISHAM
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ABNT
BURGER, Eva e MOLINA, Raphael F. e NISHIKAKU, Angela S. The paracoccidioidomycotic granuloma. 2009, Anais.. Tokyo: Instituto de Ciências Biomédicas, Universidade de São Paulo, 2009. . Acesso em: 03 mar. 2026. -
APA
Burger, E., Molina, R. F., & Nishikaku, A. S. (2009). The paracoccidioidomycotic granuloma. In Abstracts. Tokyo: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Burger E, Molina RF, Nishikaku AS. The paracoccidioidomycotic granuloma. Abstracts. 2009 ;[citado 2026 mar. 03 ] -
Vancouver
Burger E, Molina RF, Nishikaku AS. The paracoccidioidomycotic granuloma. Abstracts. 2009 ;[citado 2026 mar. 03 ] - Granulomatous lesions in experimental Paracoccidioides brasiliensis infection
- Fibrosis treatment in experimental Paracoccidioides brasiliensis infection
- Enhanced expression of inflammatory or regulatory cytokines respectively in granulomas of resistant or susceptible mice infected with a virulent P. brasiliensis isolate
- Effects of drugs on the extracellular matrix in Paracoccidoiodomycotic granulomas
- Evaluation of paracoccidioidomycosis treatment with sulfamethoxazol-trimethoprin using immunological parameters in a murine model
- Concentration of IFN-'gama', IL-10, GM-CSF, KC, LTB-4, TNF-'alfa' and TGF-'beta' in air pouch of susceptible & resistant mice to "P. brasiliensis"
- Matrix metalloproteinases in murine experimental paracoccidioidomycosis: possible participation in the pattern of granulomatous lesions
- Differential cytokines expression pattern in granulomas of susceptible and resistant mice infected with a low virulent P. brasiliensis isolate
- Immune pattern reversion in acute murine paracoccidioidomycosis elicited by liposomal amphotericin B administration
- Alterations of granuloma architecture, cellularity and severity of the early infection in murine paracoccidioidomycosis by IFN-'alfa', celecoxib or lumiracoxib treatment
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