An Aicardi-Goutières Syndrome–Causative Point Mutation in Adar1 Gene Invokes Multiorgan Inflammation and Late-Onset Encephalopathy in Mice-Reference-Cited by-同舟云学术

An Aicardi-Goutières Syndrome–Causative Point Mutation in Adar1 Gene Invokes Multiorgan Inflammation and Late-Onset Encephalopathy in Mice

Published:2021-11-12 Issue:12 Volume:207 Page:3016-3027
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J.I.

Author:

Inoue Maal^ORCID,Nakahama Taisuke^ORCID,Yamasaki Ryuichiro,Shibuya Toshiharu^ORCID,Kim Jung In^ORCID,Todo Hiroyuki^ORCID,Xing Yanfang,Kato Yuki^ORCID,Morii Eiichi,Kawahara Yukio^ORCID

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference59 articles.

1. Characterization of human disease phenotypes associated with mutations inTREX1,RNASEH2A,RNASEH2B,RNASEH2C,SAMHD1,ADAR, andIFIH1

2. Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

3. Systemic inflammation and chronic kidney disease in a patient due to the RNASEH2B defect.;He;Pediatr. Rheumatol. Online J.,2021

4. Bilateral striatal necrosis in two subjects with Aicardi-Goutières syndrome due to mutations inADAR1(AGS6)

5. Type I interferonopathies in children: an overview.;d’Angelo;Front Pediatr.,2021

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