Associated Papers
In search of a function for human type III interferons: insights from inherited and acquired deficits.
Zhang Q et al.
Current Opinion in Immunology, 2024
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
Fulminant Viral Hepatitis in Two Siblings with Inherited IL-10RB Deficiency.
Korol CB et al.
Journal of Clinical Immunology, 2023
36308662 (PubMed )
Supplement: 10875_2022_1376_MOESM1_ESM.docx
Clinical Phenotypes and Outcomes in Monogenic Versus Non-monogenic Very Early Onset Inflammatory Bowel Disease.
Collen LV et al.
Journal of Crohn's & Colitis, 2022
Alterations in T and B Cell Receptor Repertoires Patterns in Patients With IL10 Signaling Defects and History of Infantile-Onset IBD.
Werner L et al.
Frontiers in Immunology, 2020
Enhanced TH17 Responses in Patients with IL10 Receptor Deficiency and Infantile-onset IBD.
Shouval DS et al.
Inflammatory Bowel Diseases, 2017
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