Different organs are affected by pathology intwo mouse strains chronically infected by a Trypanosoma cruzi clone: a model for immunogenetic studies in Chaga's disease (2004)
- Authors:
- USP affiliated authors: MOSIG, JOSE MARIA ALVAREZ - ICB ; LIMA, MARIA REGINA D IMPERIO - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical and Investigative Medicine
- Volume/Número/Paginação/Ano: v.27, p. 126B, T45.118, 2004
- Conference titles: International Congress of Immunology
-
ABNT
MARINHO, Claudio Romero Farias et al. Different organs are affected by pathology intwo mouse strains chronically infected by a Trypanosoma cruzi clone: a model for immunogenetic studies in Chaga's disease. Clinical and Investigative Medicine. Montreal: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2004 -
APA
Marinho, C. R. F., Bucci, D., Dagli, M. L. Z., Bastos, K. R. B., Grisotto, M. G., Sardinha, L. R., et al. (2004). Different organs are affected by pathology intwo mouse strains chronically infected by a Trypanosoma cruzi clone: a model for immunogenetic studies in Chaga's disease. Clinical and Investigative Medicine. Montreal: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Marinho CRF, Bucci D, Dagli MLZ, Bastos KRB, Grisotto MG, Sardinha LR, Baptista CRGM, Gonçalves CP, Lima MRD'I, Alvarez JM. Different organs are affected by pathology intwo mouse strains chronically infected by a Trypanosoma cruzi clone: a model for immunogenetic studies in Chaga's disease. Clinical and Investigative Medicine. 2004 ;27 126B.[citado 2024 out. 09 ] -
Vancouver
Marinho CRF, Bucci D, Dagli MLZ, Bastos KRB, Grisotto MG, Sardinha LR, Baptista CRGM, Gonçalves CP, Lima MRD'I, Alvarez JM. Different organs are affected by pathology intwo mouse strains chronically infected by a Trypanosoma cruzi clone: a model for immunogenetic studies in Chaga's disease. Clinical and Investigative Medicine. 2004 ;27 126B.[citado 2024 out. 09 ] - IFN-γ priming effects on the maintenance of effector memory CD4(+) T cells and on phagocyte function: evidences from infectious diseases
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- Comparative analysis of activation phenotype, proliferation and ifn-γ production by spleen nk1.1+ and nk1.1- t-cells during plasmodium chabaudi as malaria.
- Long-lasting protection against secondary challenge with Plasmodium chabaudi AS in the absence of classical memory T and B cell responses
- Sustained challenge with homologous parasites exacerbates TH1 and TH2 immune response, but does not alter cardiac pathology in mice chronically infected by Sylvio-X10/4Trypanosoma cruzi parasites
- Expression of b7-1 and b7-2 costimulatory molecules on b lymphocytes during primary and secondary responses to plasmodium chabaudi chabaudi
- Cytokone production by cd8 low tcr alfa beta low cells in T. cruzi chronic infected mice
- Role of IgG-isotypes in the protection against erythocytic stages of Plasmodium chabaudi chabaudi
- IFN-'gama' production by 'CD45RB POT. HIGH' and ÇD45RB POT. LOW' 'CD4 POT. +' T cell subsets along the acute and chronic phases of experimental Chagas disease
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