Systemic lupus erythematosus and deficiencies of early components of the complement classical pathway (2016)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- DOI: 10.3389/fimmu.2016.00055
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Frontiers in Immunology
- ISSN: 1664-3224
- Volume/Número/Paginação/Ano: v. 7, art. 55, p. 1-7, 2016
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
MACEDO, Ana Catarina e ISAAC, Lourdes. Systemic lupus erythematosus and deficiencies of early components of the complement classical pathway. Frontiers in Immunology, v. 7, p. 1-7, 2016Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2016.00055. Acesso em: 23 abr. 2024. -
APA
Macedo, A. C., & Isaac, L. (2016). Systemic lupus erythematosus and deficiencies of early components of the complement classical pathway. Frontiers in Immunology, 7, 1-7. doi:10.3389/fimmu.2016.00055 -
NLM
Macedo AC, Isaac L. Systemic lupus erythematosus and deficiencies of early components of the complement classical pathway [Internet]. Frontiers in Immunology. 2016 ; 7 1-7.[citado 2024 abr. 23 ] Available from: https://doi.org/10.3389/fimmu.2016.00055 -
Vancouver
Macedo AC, Isaac L. Systemic lupus erythematosus and deficiencies of early components of the complement classical pathway [Internet]. Frontiers in Immunology. 2016 ; 7 1-7.[citado 2024 abr. 23 ] Available from: https://doi.org/10.3389/fimmu.2016.00055 - Ultrastructural aspects of alpha - 2 - macroglobulin activited mouse macrophages
- Thioester bond plays a role in the human complement component c4 alpha chain cleavage by activated c1s
- A hereditary human complement C3 deficiency due reduced C3 mRNA
- Molecular caracterization of factor I deficency in two brazilian sisters
- Deficiency of factor I is present in two sisters from a family with low levels of factor H
- Parcial analysis of factor I gene in two deficient sisters of this protein
- Um novo caso de deficiência de C3 do sistema complemento humano
- Immunological characterization of a human C3 deficiency
- Inherited complete factor I deficiency associated with systemic lupus enythematosus, higher susceptibility to infection and low levels of factor H
- Concentrations of regulatory complement proteins in Brazilian Nealthy children and adults
Informações sobre o DOI: 10.3389/fimmu.2016.00055 (Fonte: oaDOI API)
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