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Journal of Autoimmunity|November 19, 2022
NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunityNigel Sharfe, Ilan Dalal, Zahra Naghdi, et al.The Journal of Allergy and Clinical Immunology|August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)Harjit Dadi, Tyler A Jones, Daniele Merico, et al.Clinical Genetics|September 5, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiencyMaian Roifman, Kirsten M Niles, Lauren MacNeil, et al.The Journal of Allergy and Clinical Immunology|June 12, 2017
Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutationsJennifer W Leiding, Satoshi Okada, David Hagin, et al.Pageof 2