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Granulomatous Disease, Chronic

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  • A missense mutation in the neutrophil cytochrome-b heavy-chain in cytochrome-positive x-linked chronic granulomatous-disease  Academic Article
  • A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease  Academic Article
  • Effects of granulocytes on human neuro-blastoma cells measured by chemi-luminescence and chromium-51 release assay  Academic Article
  • Genomic structure of the human p47-phox (ncf1) gene  Academic Article
  • Lysis of neuro-blastoma cells by the adcc-reaction - granulocytes of patients with chronic granulomatous-disease are more effective than those of healthy donors  Academic Article
  • Neutrophil nicotinamide adenine-dinucleotide phosphate oxidase assembly - translocation of p47-phox and p67-phox requires interaction between p47-phox and cytochrome-b558  Academic Article
  • Phosphorylation of the oxidase-related k-48 phosphoprotein family in the unusual autosomal cytochrome-negative and x-linked cytochrome-positive types of chronic granulomatous-disease  Academic Article
  • Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA  Academic Article

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