Associated Papers
A Novel Mutation of the ADAR1 Gene in a Chinese Family with Dyschromatosis Symmetrica Hereditaria and Literature Review.
Ge H et al.
Clinical, Cosmetic and Investigational Dermatology, 2024
The role of RNA editing enzyme ADAR1 in human disease.
Song B et al.
Wiley Interdisciplinary Reviews. Rna, 2022
ADAR1 interaction with Z-RNA promotes editing of endogenous double-stranded RNA and prevents MDA5-dependent immune activation.
de Reuver R et al.
Cell Reports, 2021
Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features.
Piccoli C et al.
Pediatric Neurology, 2021
Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.
Wang P et al.
Molecular Genetics & Genomic Medicine, 2019
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.
Rice GI et al.
Neuropediatrics, 2017
Double-stranded RNA-specific adenosine deaminase (DSRAD) gene mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).
Dong Y et al.
International Journal of Dermatology, 2011
A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation.
Hayashi M et al.
Archives of Dermatological Research, 2010
Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria.
Li M et al.
Archives of Dermatological Research, 2010
Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria.
Hou Y et al.
Acta Dermato-venereologica, 2007
Select a paper to view details