Immunological and genetic characterization of deficiency of the component C5 of the human complement system (2007)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Immunology
- Volume/Número/Paginação/Ano: v. 44, n. 16, 2007
- Conference titles: European Meeting on Complement in Human Disease
-
ABNT
AGUILAR-RAMIREZ, P. et al. Immunological and genetic characterization of deficiency of the component C5 of the human complement system. Molecular Immunology. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 23 abr. 2024. , 2007 -
APA
Aguilar-Ramirez, P., Florido, M. P. C., Reis, E. S., Kierstman, D., Costa-Carvalho, B. T., & Isaac, L. (2007). Immunological and genetic characterization of deficiency of the component C5 of the human complement system. Molecular Immunology. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Aguilar-Ramirez P, Florido MPC, Reis ES, Kierstman D, Costa-Carvalho BT, Isaac L. Immunological and genetic characterization of deficiency of the component C5 of the human complement system. Molecular Immunology. 2007 ; 44( 16):[citado 2024 abr. 23 ] -
Vancouver
Aguilar-Ramirez P, Florido MPC, Reis ES, Kierstman D, Costa-Carvalho BT, Isaac L. Immunological and genetic characterization of deficiency of the component C5 of the human complement system. Molecular Immunology. 2007 ; 44( 16):[citado 2024 abr. 23 ] - 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
