An Approach for a Synthetic CTL Vaccine Design against Zika Flavivirus Using Class I and Class II Epitopes Identified by Computer Modeling (2017)
- Authors:
- Autor USP: CUNHA NETO, EDECIO - FM
- Unidade: FM
- DOI: 10.3389/fimmu.2017.00640
- Subjects: VACINAS VIRAIS; ZIKA VÍRUS; FLAVIVIRUS; HIV; EPITOPOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Frontiers in Immunology
- ISSN: 1664-3224
- Volume/Número/Paginação/Ano: v. 8, art. 640,p. 1-12, 2017
- Status:
- Artigo publicado em periódico de acesso aberto (Gold Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
CUNHA-NETO, Edecio et al. An Approach for a Synthetic CTL Vaccine Design against Zika Flavivirus Using Class I and Class II Epitopes Identified by Computer Modeling. Frontiers in Immunology, v. 8, p. 1-12, 2017Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2017.00640. Acesso em: 17 mar. 2026. -
APA
Cunha-Neto, E., Rosa, D. S., Harris, P. E., Olson, T., Morrow, A., Ciotlos, S., et al. (2017). An Approach for a Synthetic CTL Vaccine Design against Zika Flavivirus Using Class I and Class II Epitopes Identified by Computer Modeling. Frontiers in Immunology, 8, 1-12. doi:10.3389/fimmu.2017.00640 -
NLM
Cunha-Neto E, Rosa DS, Harris PE, Olson T, Morrow A, Ciotlos S, Herst CV, Rubsamen RM. An Approach for a Synthetic CTL Vaccine Design against Zika Flavivirus Using Class I and Class II Epitopes Identified by Computer Modeling [Internet]. Frontiers in Immunology. 2017 ; 8 1-12.[citado 2026 mar. 17 ] Available from: https://doi.org/10.3389/fimmu.2017.00640 -
Vancouver
Cunha-Neto E, Rosa DS, Harris PE, Olson T, Morrow A, Ciotlos S, Herst CV, Rubsamen RM. An Approach for a Synthetic CTL Vaccine Design against Zika Flavivirus Using Class I and Class II Epitopes Identified by Computer Modeling [Internet]. Frontiers in Immunology. 2017 ; 8 1-12.[citado 2026 mar. 17 ] Available from: https://doi.org/10.3389/fimmu.2017.00640 - Increased expression of circulating microRNA 101-3p in type 1 diabetes patients: new insights into miRNA-regulated pathophysiological pathways for type 1 diabetes
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- Linfócitos T
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