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Identification of NOX2 regions for normal biosynthesis of cytochrome b<sub>558</sub> in phagocytes highlighting essential residues for p<sub>22phox</sub> binding.
- Published in:
- Biochemical Journal, 2014, v. 464, n. 3, p. 425, doi. 10.1042/BJ20140555
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- Article
Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease - Identification of Eight Novel Mutations in CYBB and NCF2 Genes.
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- Journal of Clinical Immunology, 2012, v. 32, n. 5, p. 942, doi. 10.1007/s10875-012-9698-8
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- Article
Erratum to: Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease-Identification of Eight Novel Mutations in CYBB and NCF2 Genes.
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- 2012
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- Correction notice
CRISPR-gene-engineered CYBB knock-out PLB-985 cells, a useful model to study functional impact of X-linked chronic granulomatous disease mutations: application to the G412E X91<sup>+</sup>-CGD mutation.
- Published in:
- Clinical & Experimental Immunology, 2023, v. 212, n. 2, p. 156, doi. 10.1093/cei/uxad028
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- Article
MC1R expression in HaCaT keratinocytes inhibits UVA-induced ROS production via NADPH Oxidase- and cAMP-dependent mechanisms.
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- Journal of Cellular Physiology, 2012, v. 227, n. 6, p. 2578, doi. 10.1002/jcp.22996
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- Article
Second Report of Chronic Granulomatous Disease in Jordan: Clinical and Genetic Description of 31 Patients From 21 Different Families, Including Families From Lybia and Iraq.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.639226
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- Article