Associated Papers
Monogenic forms of inflammatory bowel disease: Genetic mechanisms, models, and clinical implications.
Ghorbanpour A et al.
Molecular Medicine (cambridge, Mass.), 2026
A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and literature review.
Motallebi F et al.
Molecular Biology Reports, 2024
Pathogenic Interleukin-10 Receptor Alpha Variants in Humans - Balancing Natural Selection and Clinical Implications.
Aschenbrenner D et al.
Journal of Clinical Immunology, 2023
36370291 (PubMed )
Supplement: 10875_2022_1366_MOESM9_ESM.xlsx › Table_S3
Phenotypic and genotypic characterization of inflammatory bowel disease in children under six years of age in China.
Fang YH et al.
World Journal of Gastroenterology, 2018
Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.
Xiao Y et al.
World Journal of Gastroenterology, 2016
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
Glocker EO et al.
The New England Journal of Medicine, 2009
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