Associated Papers
Structure of human phagocyte NADPH oxidase in the activated state.
Liu X et al.
Nature, 2024
Structure of the core human NADPH oxidase NOX2.
Noreng S et al.
Nature Communications, 2022
36241643 (PubMed )
Supplement: 41467_2022_33711_MOESM1_ESM.pdf
Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants - identification of 11 novel mutations in CYBB.
Mollin M et al.
Clinical and Experimental Immunology, 2021
Chronic granulomatous disease of childhood: an unusual cause of recurrent uncommon infections in a 61-year-old man.
Isman-Nelkenbaum G et al.
Clinical and Experimental Dermatology, 2011
Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase properties.
Wolach B et al.
Journal of Clinical Immunology, 2011
[The X+ chronic granulomatous disease as a fabulous model to study the NADPH oxidase complex activation].
Stasia MJ
Medecine Sciences : M/s, 2007
Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells.
Bionda C et al.
Human Genetics, 2004
[Chronic granulomatous disease (CGD)].
Takikawa K et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine, 1977
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