C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene (2007)
- Authors:
- USP affiliated authors: ISAAC, LOURDES - ICB ; FARAH, SHAKER CHUCK - IQ
- Unidades: ICB; IQ
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinics
- Volume/Número/Paginação/Ano: v. 62, suppl. 2, 2007
- Conference titles: LAGID Meeting of the Autoimmunity in Primary Immunodeficiencies
-
ABNT
AMANO, M. T. et al. C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene. Clinics. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 27 jan. 2026. , 2007 -
APA
Amano, M. T., Ferriani, V. P. L., Florido, M. P. C., Reis, E. S., Farah, C. S., Delcolli, M. I. M. V., et al. (2007). C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene. Clinics. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Amano MT, Ferriani VPL, Florido MPC, Reis ES, Farah CS, Delcolli MIMV, Azzolini AECS, Assis-Pandochi AI, Sjohölm AG, Jensenius JC, Isaac L. C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene. Clinics. 2007 ; 62[citado 2026 jan. 27 ] -
Vancouver
Amano MT, Ferriani VPL, Florido MPC, Reis ES, Farah CS, Delcolli MIMV, Azzolini AECS, Assis-Pandochi AI, Sjohölm AG, Jensenius JC, Isaac L. C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene. Clinics. 2007 ; 62[citado 2026 jan. 27 ] - C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of anormal C1s gene
- Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability
- Native conformations of human complement components C3 and C4 show different dependencies on thioester formation
- Homozygous hereditary C3 deficiency due to a premature stop codon
- Combined PCR/gapped-duplex method for site-directed mutagenesis
- Um novo modelo de camundongos geneticamente selecionados que apresentam alta resposta inflamatória aguda e o gene NAMP-1 de resistência, na ausência de C5
- Human complement factor H (Y402H) polymorphism and age-related macular degeneration (AMD) in brazilian patients
- Immunological and genetic characterization of deficiency of the component C5 of the human complement system
- 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
