Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules (2001)
- Authors:
- USP affiliated authors: LIMA, MARIA REGINA D'IMPERIO - ICB ; ABRAHAMSOHN, ISES DE ALMEIDA - ICB ; MOSIG, JOSE MARIA ALVAREZ - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: International Congress of Immunology
-
ABNT
GRISOTTO, M et al. Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules. Scandinavian Journal of Immunology. Stockholm: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 2001 -
APA
Grisotto, M., Lima, M. R. D. 'I., Marinho, C., Tadokoro, M., Abrahamson, I., & Alvarez, J. M. (2001). Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules. Scandinavian Journal of Immunology. Stockholm: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Grisotto M, Lima MRD'I, Marinho C, Tadokoro M, Abrahamson I, Alvarez JM. Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules. Scandinavian Journal of Immunology. 2001 ;[citado 2024 nov. 12 ] -
Vancouver
Grisotto M, Lima MRD'I, Marinho C, Tadokoro M, Abrahamson I, Alvarez JM. Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules. Scandinavian Journal of Immunology. 2001 ;[citado 2024 nov. 12 ] - Most parasite-specific CD8+ cells in trypanosoma cruzi-infected chronic mice are down-rgulated for T-cell receptor-'alfa''Beta' and CD8 molecules
- IL-2 and 'T POT. REG' cells in polyclonal lymphocyte activation (PLA) induced by Plasmodium chabaudi infection
- TCRalpha-beta/CDB down-regulated CD8+ cells in the spleen of Trypanosoma cruzi-infected chronic mice are responsive to in vitro and in vivo stimulation with the parasite
- Role of IL-2 in the early CD4+ T cell response to blood-stage Plasmodium chabaudi malaria
- Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules
- Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules
- Most parasite-specific CD8 + cells in Trypanossoma cruzi infected chronic mice are down-regulated for T-cell receptor alpha, beta and CD8 molecules
- Anti-IL-2 treatment impairs the expansion of Treg cell population during acute malaria and enhances the Th1 cell response at the chronic disease
- IL-2 and 'T IND.REG' cells in polyclonal lymphocyte activation (PLA) induced by Plasmodium chabaudi infection
- 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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