Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations-Reference-Cited by-同舟云学术

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations

Published:2016-04 Issue:4 Volume:136 Page:875-878
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Kono Michihiro,Matsumoto Fumihiro,Suzuki Yasuhiro,Suganuma Mutsumi,Saitsu Hirotomo,Ito Yasutomo,Fujiwara Sakuhei,Moriwaki Shinichi,Matsumoto Kazuhiko,Matsumoto Naomichi,Tomita Yasushi,Sugiura Kazumitsu,Akiyama Masashi

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference8 articles.

1. Induction of protein translation by ADAR1 within living cell nuclei is not dependent on RNA editing;Herbert;Mol Cell,2002

2. Dyschromatosis symmetrica hereditaria associated with neurological disorders;Kondo;J Dermatol,2008

3. Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?;Kono;Int J Dermatol,2013

4. The RNA-editing enzyme ADAR1 controls innate immune responses to RNA;Mannion;Cell Rep,2014

5. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003

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