Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders

Author:

Kadowaki Tomonori,Ohnishi Hidenori,Kawamoto Norio,Hori Tomohiro,Nishimura Kenichi,Kobayashi Chie,Shigemura Tomonari,Ogata Shohei,Inoue YuzaburoORCID,Kawai Tomoki,Hiejima Eitaro,Takagi Masatoshi,Imai KohsukeORCID,Nishikomori Ryuta,Ito Shuichi,Heike Toshio,Ohara Osamu,Morio Tomohiro,Fukao Toshiyuki,Kanegane Hirokazu

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference16 articles.

1. A20: linking a complex regulator of ubiquitylation to immunity and human disease;Ma;Nat Rev Immunol,2012

2. NF-kappaB pathway in autoinflammatory diseases: dysregulation of protein modifications by ubiquitin defines a new category of autoinflammatory diseases;Aksentijevich;Front Immunol,2017

3. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20);Duncan;Ann Rheum Dis,2017

4. Criteria for diagnosis of Behcet's disease. International Study Group for Behcet's Disease;Lancet,1990

5. Behcet disease: evolution of clinical manifestations;Ideguchi;Medicine (Baltimore),2011

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