Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes (2008)
- Authors:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Immunology
- Volume/Número/Paginação/Ano: v. 127, suppl. 1, 2008
- Conference titles: Annual Meeting of Federation of Clinical Immunology Societies - FOCIS
-
ABNT
LUENGO, Marcos et al. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. Orlando: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 11 mar. 2026. , 2008 -
APA
Luengo, M., Prado, C., Bustamante, J., Pereira, P. V., Aragão-filho, W., Padden, C., et al. (2008). Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. Orlando: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Luengo M, Prado C, Bustamante J, Pereira PV, Aragão-filho W, Padden C, Casanova J-L, Newburger P, Condino Neto A. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. 2008 ; 127[citado 2026 mar. 11 ] -
Vancouver
Luengo M, Prado C, Bustamante J, Pereira PV, Aragão-filho W, Padden C, Casanova J-L, Newburger P, Condino Neto A. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. 2008 ; 127[citado 2026 mar. 11 ] - Infecção por Blastomicose em pacientes com Hiper IgM ligada ao X (HIGM1)
- Papel essencial do nf-kappab na expressão dos genes ncf1 e ncf2 do sistema nadph oxidase em leucócitos saudáveis e de pacientes com displasia ectodérmica anidrótica (eda-id), doença granulomatosa crônica (cgd) ou com defeitos no eixo il-12/23-ifngamma.
- Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation
- IFN-β, IFN-γ, and TNF-α decrease erythrophagocytosis by human monocytes independent of SIRP-α or SHP-1 expression
- Do HLA class II genes protect against pulmonary tuberculosis? A systematic review and meta-analysis
- Toll-like receptors’ pathway disturbances are associated with increased susceptibility to infections in humans
- ICON: the early diagnosis of congenital immunodeficiencies
- Regulation of CYBB gene expression in human phagocytes by a distant upstream NF-κB binding site
- The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS)
- Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
