X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.
about
Identification of NOX2 regions for normal biosynthesis of cytochrome b558 in phagocytes highlighting essential residues for p22phox bindingHematologically important mutations: X-linked chronic granulomatous disease (third update)Residual NADPH oxidase and survival in chronic granulomatous diseaseCancer resistance of SR/CR mice in the genetic knockout backgrounds of leukocyte effector mechanisms: determinations for functional requirements.Molecular analysis of X-linked chronic granulomatous disease in five unrelated Korean patients.Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution melting.Evolution of the ferric reductase domain (FRD) superfamily: modularity, functional diversification, and signature motifsChronic granulomatous disease presenting as aseptic ascites in a 2-year-old child.NOX2β: A novel splice variant of NOX2 that regulates NADPH oxidase activity in macrophagesOxidative stress, redox signalling and endothelial dysfunction in ageing-related neurodegenerative diseases: a role of NADPH oxidase 2.Long polymerase chain reaction-based fluorescence in situ hybridization analysis of female carriers of X-linked chronic granulomatous disease deletions.A Dual Reporter Splicing Assay Using HaloTag-containing Proteins.Residual NADPH oxidase activity and isolated lung involvement in x-linked chronic granulomatous disease.Essential role of nuclear factor-kappaB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes.Functional Restoration of gp91phox-Oxidase Activity by BAC Transgenesis and Gene Targeting in X-linked Chronic Granulomatous Disease iPSCs.Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease.The human NADPH oxidase: primary and secondary defects impairing the respiratory burst function and the microbicidal ability of phagocytes.Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece.ICON: the early diagnosis of congenital immunodeficiencies.Monocyte/macrophage-specific NADPH oxidase contributes to antimicrobial host defense in X-CGD.Induction of antimicrobial pathways during early-phase immune response to Salmonella spp. in murine macrophages: gamma interferon (IFN-gamma) and upregulation of IFN-gamma receptor alpha expression are required for NADPH phagocytic oxidase gp91-stimNeutrophils to the ROScue: Mechanisms of NADPH Oxidase Activation and Bacterial Resistance.Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry.Immunological mechanisms underlying the genetic predisposition to severe Staphylococcus aureus infection in the mouse model.Inhibition of NADPH oxidase activation by peptides mapping within the dehydrogenase region of Nox2-A "peptide walking" study.Stimulation of gp91 phagocytic oxidase and reactive oxygen species in neutrophils by an avirulent Salmonella enterica serovar infantis strain protects gnotobiotic piglets from lethal challenge with serovar Typhimurium strain F98 without inducing intHigh-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost-effective method for screening molecular defects: four novel mutations found in X-linked chronic granulomatous disease.Transplantation of a fetus with paternal Thy-1(+)CD34(+)cells for chronic granulomatous disease.Heme-ligating histidines in flavocytochrome b(558): identification of specific histidines in gp91(phox).Crucial role of two potential cytosolic regions of Nox2, 191TSSTKTIRRS200 and 484DESQANHFAVHHDEEKD500, on NADPH oxidase activation.Unusual polyclonal anti-gp91 peptide antibody interactions with X-linked chronic granulomatous disease-derived human neutrophils are not from compensatory expression of Nox proteins 1, 3, or 4.Crystal structures and atomic model of NADPH oxidase.Genetical analysis of all Danish patients diagnosed with chronic granulomatous disease.Identification of two novel mutations in patients with X-linked primary immunodeficiencies.Considerations in the Diagnosis of Chronic Granulomatous Disease.
P2860
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P2860
X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
X-Linked chronic granulomatous ...... t of respiratory-burst oxidase
@nl
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@ast
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@en
type
label
X-Linked chronic granulomatous ...... t of respiratory-burst oxidase
@nl
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@ast
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@en
prefLabel
X-Linked chronic granulomatous ...... t of respiratory-burst oxidase
@nl
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@ast
X-Linked chronic granulomatous ...... of respiratory-burst oxidase.
@en
P2093
P2860
P356
P1476
X-Linked chronic granulomatous ...... t of respiratory-burst oxidase
@en
P2093
P2860
P304
P356
10.1086/301874
P407
P577
1998-06-01T00:00:00Z