Associated Papers
Transcriptional reprogramming by mutated IRF4 in lymphoma.
Schleussner N et al.
Nature Communications, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.
Thouenon R et al.
The Journal of Experimental Medicine, 2023
IRF4 haploinsufficiency in a family with Whipple's disease.
Guérin A et al.
Elife, 2018
IRF-4 suppresses BCR/ABL transformation of myeloid cells in a DNA binding-independent manner.
Jo SH et al.
The Journal of Biological Chemistry, 2012
Select a paper to view details