Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules (2001)
- Authors:
- USP affiliated authors: LIMA, MARIA REGINA D'IMPERIO - ICB ; ABRAHAMSOHN, ISES DE ALMEIDA - ICB ; MOSIG, JOSE MARIA ALVAREZ - ICB
- Unidade: ICB
- Subjects: IMUNOLOGIA; MICROBIOLOGIA
- Language: Inglês
- Imprenta:
- Source:
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ABNT
GRISOTTO, Marcos Grigolin et al. Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules. Scandinavian Journal of Immunology, 2001Tradução . . Acesso em: 10 mar. 2026. -
APA
Grisotto, M. G., Lima, M. R. D. 'I., Marinho, C. R. F., Tadokoro, C. E., Abrahansohn, I. de A., & Alvarez, J. M. (2001). Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules. Scandinavian Journal of Immunology. -
NLM
Grisotto MG, Lima MRD'I, Marinho CRF, Tadokoro CE, Abrahansohn I de A, Alvarez JM. Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules. Scandinavian Journal of Immunology. 2001 ;[citado 2026 mar. 10 ] -
Vancouver
Grisotto MG, Lima MRD'I, Marinho CRF, Tadokoro CE, Abrahansohn I de A, Alvarez JM. Most parasite-specific CD+ cells in Trypanosoma cruzi infected chronic mice are down-regulated for TCRsalpha-beta and CDB molecules. Scandinavian Journal of Immunology. 2001 ;[citado 2026 mar. 10 ] - 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
- Most parasite specific CD8+ cells in Trypanosoma cruzi-infected chronic mice are down regulated for TCR<alfa><Beta> and CD8 Molecules
- Most parasite-specific CD8 + cells in Trypanossoma cruzi infected chronic mice are down-regulated for T-cell receptor alpha, beta and CD8 molecules
- 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-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
- Anti-IL-2 treatment impairs the expansion of Treg cell population during acute malaria and enhances the Th1 cell response at the chronic disease
- TCR'a''b'/CD8 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
- IL-2 and 'T IND.REG' cells in polyclonal lymphocyte activation (PLA) induced by Plasmodium chabaudi infection
- Role of CD1d- and I-Ab-restricted T cells during the polyclonal lymphocyte activation induced by blood-stage Plasmodium chabaudi AS malaria
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