Associated Papers
Monogenic forms of inflammatory bowel disease: Genetic mechanisms, models, and clinical implications.
Ghorbanpour A et al.
Molecular Medicine (cambridge, Mass.), 2026
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2.
Lipinski S et al.
Cold Spring Harbor Molecular Case Studies, 2019
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
Schwerd T et al.
Mucosal Immunology, 2018
Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel Disease.
Hayes P et al.
Cellular and Molecular Gastroenterology and Hepatology, 2015
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