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Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis

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Apoptosis and NET formation in the pathogenesis of SLE

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Autophagy

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Measurement and meaning of markers of reactive species of oxygen, nitrogen and sulfur in healthy human subjects and patients with inflammatory joint disease

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Differential oxidative modification of proteins in MRL+/+ and MRL/lpr mice: Increased formation of lipid peroxidation-derived aldehyde-protein adducts may contribute to accelerated onset of autoimmune response

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Oxidative stress as a potential biomarker for determining disease activity in patients with Rheumatoid Arthritis

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Neutrophil Extracellular Traps That Are Not Degraded in Systemic Lupus Erythematosus Activate Complement Exacerbating the Disease

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The Impact of Various Reactive Oxygen Species on the Formation of Neutrophil Extracellular Traps

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P67-phox (NCF2) Lacking Exons 11 and 12 Is Functionally Active and Leads to an Extremely Late Diagnosis of Chronic Granulomatous Disease (CGD)

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Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease: Figure 1

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Practical and Theoretical Considerations in Study Design for Detecting Gene-Gene Interactions Using MDR and GMDR Approaches

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Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase

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Neutrophils Activate Plasmacytoid Dendritic Cells by Releasing Self-DNA-Peptide Complexes in Systemic Lupus Erythematosus

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The Human NADPH Oxidase: Primary and Secondary Defects Impairing the Respiratory Burst Function and the Microbicidal Ability of Phagocytes

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Six differentCYBAmutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease

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Serious infections in British patients with systemic lupus erythematosus: hospitalisations and mortality

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A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

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Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies

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Chronic Granulomatous Disease: The European Experience

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p47phox Deficiency Induces Macrophage Dysfunction Resulting in Progressive Crystalline Macrophage Pneumonia

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Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease

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(2008) Eric M. Lewis et al.   CLINICAL IMMUNOLOGY

Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort

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Biological Roles for the NOX Family NADPH Oxidases

(2008) William M. Nauseef   JOURNAL OF BIOLOGICAL CHEMISTRY