Characterization and genetic analysis of human complement Factor I deficiency (2007)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Imunologia
- Publisher place: Rio de Janeiro
- Date published: 2007
- Source:
- Título: Abstracts
- Conference titles: International Congress of Immunology
-
ABNT
DELCOLLI, M. I. M. V. et al. Characterization and genetic analysis of human complement Factor I deficiency. 2007, Anais.. Rio de Janeiro: Sociedade Brasileira de Imunologia, 2007. . Acesso em: 10 jan. 2026. -
APA
Delcolli, M. I. M. V., Rodrigues, V. H., Reis, E. S., Florido, M. P. C., Nudelmann, V., Goldenberg, J., & Isaac, L. (2007). Characterization and genetic analysis of human complement Factor I deficiency. In Abstracts. Rio de Janeiro: Sociedade Brasileira de Imunologia. -
NLM
Delcolli MIMV, Rodrigues VH, Reis ES, Florido MPC, Nudelmann V, Goldenberg J, Isaac L. Characterization and genetic analysis of human complement Factor I deficiency. Abstracts. 2007 ;[citado 2026 jan. 10 ] -
Vancouver
Delcolli MIMV, Rodrigues VH, Reis ES, Florido MPC, Nudelmann V, Goldenberg J, Isaac L. Characterization and genetic analysis of human complement Factor I deficiency. Abstracts. 2007 ;[citado 2026 jan. 10 ] - Ligação de leptospira interrogans serovar pomona às diferentes variantes de fator H (TYR402 and HIS402)
- Intravitreal levels of human complement factor F (CFH) in patients with exudative age-related macular degeneration (AMD)
- Associação entre polimorfismo de fator H (Y402H) e degeneração da mácula relacionada à idade
- Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians
- ARG 127 his substitution in SCR-2 of the regulatory complement protein factor H is found in a factor H deficient patient with concomitant lack of complement component C9
- Immunological and genetic characterization of deficiency of the component C5 of the human complement system
- Human complement factor H (Y402H) polymorphism and age-related macular degeneration (AMD) in brazilian patients
- A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9
- Leptospira Immunoglobulin-like proteins bind human complement regulator Factor H
- The contribution of the component C5 in fatty liver disease: a murine model
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
