Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria.

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Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@en

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@nl

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Item

label

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@en

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@nl

prefLabel

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@en

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@nl

P1476

Eight Novel Mutations of the A ...... atosis Symmetrica Hereditaria.

@en

P2093

Chen Tu

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Cheng-Wen Ma

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Sheng-Xiang Xiao

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Shuang Wang

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Tian Wang

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Xiao-Peng Wang

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Yan Liu

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Zhuang-Li Tang

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P2860

Expression and regulation by interferon of a double-stranded-RNA-specific adenosine deaminase from human cells: evidence for two forms of the deaminase

The role of binding domains for dsRNA and Z-DNA in the in vivo editing of minimal substrates by ADAR1

Functions of the RNA Editing Enzyme ADAR1 and Their Relevance to Human Diseases

Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

Genomic organization and chromosomal location of the human dsRNA adenosine deaminase gene: the enzyme for glutamate-activated ion channel RNA editing

Requirement of the RNA editing deaminase ADAR1 gene for embryonic erythropoiesis

Dynamic association of RNA-editing enzymes with the nucleolus

Stress-induced apoptosis associated with null mutation of ADAR1 RNA editing deaminase gene

Primer3--new capabilities and interfaces

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.

P304

104-108

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P31

scholarly article

P356

10.1089/GTMB.2017.0207

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P433

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P478

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P577

2017-11-29T00:00:00Z

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P698

29185800

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P921

dyschromatosis symmetrica hereditaria

P932

5806071

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