Unraveling molecular effects of ADAR1 overexpression in HEK293T cells by label-free quantitative proteomics-Reference-Cited by-同舟云学术

Unraveling molecular effects of ADAR1 overexpression in HEK293T cells by label-free quantitative proteomics

Published:2016-05-26 Issue:12 Volume:15 Page:1591-1601
ISSN:1538-4101
Container-title:Cell Cycle
language:en
Short-container-title:Cell Cycle

Author:

Guo Jisheng¹,Wang Xiaoyue¹,Lü Xin¹,Jing Ruirui¹,Li Junqiang¹,Li CuiLing¹,Wang Daoguang¹,Bi Baibin¹,Chen Xinjun¹,Wang Fengqin¹,Sun Shengnan¹,Gong Jing¹,Azadzoi Kazem M.²,Yang Jing-Hua¹²

Affiliation:

1. Cancer Research Center, Shandong University School of Medicine, Jinan, China

2. Departments of Surgery and Urology, VA Boston Healthcare System, Boston University School of Medicine, Boston, MA, USA

Publisher

Informa UK Limited

Subject

Cell Biology,Developmental Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15384101.2016.1176657

Reference39 articles.

1. The RNA-editing Enzyme ADAR1 Is Localized to the Nascent Ribonucleoprotein Matrix on Xenopus Lampbrush Chromosomes but Specifically Associates with an Atypical Loop

2. Mechanism of Interferon Action: Double-Stranded RNA-Specific Adenosine Deaminase from Human Cells Is Inducible by Alpha and Gamma Interferons

3. The Interferon-Inducible, Double-Stranded RNA-Specific Adenosine Deaminase Gene (DSRAD) Maps to Human Chromosome 1q21.1–21.2

4. Subcellular Distribution of ADAR1 Isoforms Is Synergistically Determined by Three Nuclear Discrimination Signals and a Regulatory Motif

5. ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling

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