Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations-Reference-Cited by-同舟云学术

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations

Published:2014-11-17 Issue:12 Volume:124 Page:5516-5520
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Jeremiah Nadia,Neven Bénédicte,Gentili Matteo,Callebaut Isabelle,Maschalidi Sophia,Stolzenberg Marie-Claude,Goudin Nicolas,Frémond Marie-Louis,Nitschke Patrick,Molina Thierry J.,Blanche Stéphane,Picard Capucine,Rice Gillian I.,Crow Yanick J.,Manel Nicolas,Fischer Alain,Bader-Meunier Brigitte,Rieux-Laucat Frédéric

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference21 articles.

1. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

2. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

3. Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

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

5. Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

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