Phenotypic Variation in Aicardi–Goutières Syndrome Explained by Cell-Specific IFN-Stimulated Gene Response and Cytokine Release-Reference-Cited by-同舟云学术

Phenotypic Variation in Aicardi–Goutières Syndrome Explained by Cell-Specific IFN-Stimulated Gene Response and Cytokine Release

Published:2015-03-13 Issue:8 Volume:194 Page:3623-3633
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J.I.

Author:

Cuadrado Eloy,Michailidou Iliana,van Bodegraven Emma J.,Jansen Machiel H.,Sluijs Jacqueline A.,Geerts Dirk,Couraud Pierre-Olivier,De Filippis Lidia,Vescovi Angelo L.,Kuijpers Taco W.,Hol Elly M.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference49 articles.

1. A Progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

2. Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

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

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

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

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