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23. Aicardi-Goutières syndrome: a model disease for systemic autoimmunity. Lee-Kirsch MA; Wolf C; Günther C Clin Exp Immunol; 2014 Jan; 175(1):17-24. PubMed ID: 23786362 [TBL] [Abstract][Full Text] [Related]
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25. Inhibition of the de-myelinating properties of Aicardi-Goutières syndrome lymphocytes by cathepsin D silencing. Pulliero A; Marengo B; Longobardi M; Fazzi E; Orcesi S; Olivieri I; Cereda C; Domenicotti C; Balottin U; Izzotti A Biochem Biophys Res Commun; 2013 Jan; 430(3):957-62. PubMed ID: 23261460 [TBL] [Abstract][Full Text] [Related]
26. Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus. Abe J; Izawa K; Nishikomori R; Awaya T; Kawai T; Yasumi T; Hiragi N; Hiragi T; Ohshima Y; Heike T Rheumatology (Oxford); 2013 Feb; 52(2):406-8. PubMed ID: 22829693 [No Abstract] [Full Text] [Related]
27. Aicardi-Goutières syndrome-associated mutation at ADAR1 gene locus activates innate immune response in mouse brain. Guo X; Wiley CA; Steinman RA; Sheng Y; Ji B; Wang J; Zhang L; Wang T; Zenatai M; Billiar TR; Wang Q J Neuroinflammation; 2021 Jul; 18(1):169. PubMed ID: 34332594 [TBL] [Abstract][Full Text] [Related]
28. A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study. Abe J; Nakamura K; Nishikomori R; Kato M; Mitsuiki N; Izawa K; Awaya T; Kawai T; Yasumi T; Toyoshima I; Hasegawa K; Ohshima Y; Hiragi T; Sasahara Y; Suzuki Y; Kikuchi M; Osaka H; Ohya T; Ninomiya S; Fujikawa S; Akasaka M; Iwata N; Kawakita A; Funatsuka M; Shintaku H; Ohara O; Ichinose H; Heike T Rheumatology (Oxford); 2014 Mar; 53(3):448-58. PubMed ID: 24300241 [TBL] [Abstract][Full Text] [Related]
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