Literature DB >> 20430589

Four novel and two recurrent mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria.

Xiao-peng Wang, Wan-juan Wang, Jun-min Wang, Yan Liu, Sheng-xiang Xiao.   

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Year:  2010        PMID： 20430589     DOI： 10.1016/j.jdermsci.2010.03.021

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN： 0923-1811            Impact factor:   4.563


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  3 in total

1.  Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.

Authors:  Qi Liu; Zhen Wang; Yuhong Wu; Lihua Cao; Qingzhu Tang; Xuesha Xing; Hongwei Ma; Shifa Zhang; Yang Luo
Journal:  BMC Med Genet       Date:  2014-06-20       Impact factor: 2.103

2.  A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation.

Authors:  Ding'an Zhou; Zhiyun Wei; Zhongshu Kuang; Huangchao Luo; Jiangshu Ma; Xing Zeng; Ke Wang; Beizhong Liu; Fang Gong; Jing Wang; Shanchuan Lei; Dongsheng Wang; Jiawei Zeng; Teng Wang; Yong He; Yongqiang Yuan; Hongying Dai; Lin He; Qinghe Xing
Journal:  J Cell Mol Med       Date:  2016-11-25       Impact factor: 5.310

3.  Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria.

Authors:  Tomoko Kobayashi; Michihiro Kono; Mutsumi Suganuma; Hirotaka Akita; Ayaka Takai; Kiyohiro Tsutsui; Yu Inasaka; Takuya Takeichi; Yoshinao Muro; Masashi Akiyama
Journal:  Nagoya J Med Sci       Date:  2018-05       Impact factor: 1.131
  3 in total

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