Rare hereditary autoinflammatory disorders: Towards an understanding of critical in vivo inflammatory pathways
Journal of Dermatological Science, 06/12/2012
Kanazawa N – Finally, proteasome disability syndromes with PSMB8 mutations include Nakajo–Nishimura syndrome and related disorders distributed globally. Analyses of these diseases have unexpectedly shown a critical role of the ubiquitin–proteasome system in the regulation or homeostasis of inflammation/metabolism.



