Associated Papers
Monogenic disorders of the IRF transcription factors.
Stojcic MP et al.
The Journal of Experimental Medicine, 2026
IRF4 haploinsufficiency in a multiplex family with Whipple's disease.
Ünal S et al.
Journal of Human Immunity, 2026
Allogeneic hematopoietic stem cell transplantation in a patient with combined immunodeficiency caused by IRF4 mutation.
Wang P et al.
Clinical Immunology (orlando, Fla.), 2025
Transcriptional reprogramming by mutated IRF4 in lymphoma.
Schleussner N et al.
Nature Communications, 2023
Molecular basis for the functional roles of the multimorphic T95R mutation of IRF4 causing human autosomal dominant combined immunodeficiency.
Wang G et al.
Structure (london, England : 1993), 2023
Inborn errors of human B cell development, differentiation, and function.
Tangye SG et al.
The Journal of Experimental Medicine, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency.
Fornes O et al.
Science Immunology, 2023
Human inborn errors of immunity associated with IRF4.
Thouenon R et al.
Frontiers in Immunology, 2023
The molecular basis for the development of adult T-cell leukemia/lymphoma in patients with an IRF4K59R mutation.
Sundararaj S et al.
Protein Science : a Publication of the Protein Society, 2022
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