HDAC6, A Novel Cargo for Autophagic Clearance of Stress Granules, Mediates the Repression of the Type I Interferon Response During Coxsackievirus A16 Infection
出版年份 2020 全文链接
标题
HDAC6, A Novel Cargo for Autophagic Clearance of Stress Granules, Mediates the Repression of the Type I Interferon Response During Coxsackievirus A16 Infection
作者
关键词
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出版物
Frontiers in Microbiology
Volume 11, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2020-01-31
DOI
10.3389/fmicb.2020.00078
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Stress Granule Assembly Disrupts Nucleocytoplasmic Transport
- (2018) Ke Zhang et al. CELL
- Cargo recognition and degradation by selective autophagy
- (2018) Damián Gatica et al. NATURE CELL BIOLOGY
- Autophagy during viral infection — a double-edged sword
- (2018) Younho Choi et al. NATURE REVIEWS MICROBIOLOGY
- Differences between acute and chronic stress granules, and how these differences may impact function in human disease
- (2018) Lucas C. Reineke et al. BIOCHEMICAL PHARMACOLOGY
- Enterovirus 71 induces anti-viral stress granule-like structures in RD cells
- (2016) Yuanmei Zhu et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- ATPase-Modulated Stress Granules Contain a Diverse Proteome and Substructure
- (2016) Saumya Jain et al. CELL
- Zika Virus NS4A and NS4B Proteins Deregulate Akt-mTOR Signaling in Human Fetal Neural Stem Cells to Inhibit Neurogenesis and Induce Autophagy
- (2016) Qiming Liang et al. Cell Stem Cell
- Regulation of antiviral innate immune signaling by stress-induced RNA granules
- (2016) Mitsutoshi Yoneyama et al. JOURNAL OF BIOCHEMISTRY
- Principles and Properties of Stress Granules
- (2016) David S.W. Protter et al. TRENDS IN CELL BIOLOGY
- Enterovirus Control of Translation and RNA Granule Stress Responses
- (2016) Richard Lloyd Viruses-Basel
- The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
- (2016) Yingying Shi et al. VIROLOGICA SINICA
- Interferon-stimulated Gene 15 (ISG15) and ISG15-linked Proteins Can Associate with Members of the Selective Autophagic Process, Histone Deacetylase 6 (HDAC6) and SQSTM1/p62
- (2014) Hiroshi Nakashima et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Interactions between Autophagy Receptors and Ubiquitin-like Proteins Form the Molecular Basis for Selective Autophagy
- (2014) Vladimir Rogov et al. MOLECULAR CELL
- AUF1 is recruited to the stress granules induced by coxsackievirus B3
- (2014) Shuo Wu et al. VIRUS RESEARCH
- Coxsackievirus A16 infection triggers apoptosis in RD cells by inducing ER stress
- (2013) Guoguo Zhu et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Eukaryotic Stress Granules Are Cleared by Autophagy and Cdc48/VCP Function
- (2013) J. Ross Buchan et al. CELL
- SQSTM1/p62 Interacts with HDAC6 and Regulates Deacetylase Activity
- (2013) Jin Yan et al. PLoS One
- Poliovirus infection induces the co-localization of cellular protein SRp20 with TIA-1, a cytoplasmic stress granule protein
- (2013) Kerry D. Fitzgerald et al. VIRUS RESEARCH
- p62/SQSTM1/A170: Physiology and pathology
- (2012) Masaaki Komatsu et al. PHARMACOLOGICAL RESEARCH
- Induction of GADD34 Is Necessary for dsRNA-Dependent Interferon-β Production and Participates in the Control of Chikungunya Virus Infection
- (2012) Giovanna Clavarino et al. PLoS Pathogens
- Poliovirus Unlinks TIA1 Aggregation and mRNA Stress Granule Formation
- (2011) J. P. White et al. JOURNAL OF VIROLOGY
- Dengue Virus-Induced Autophagy Regulates Lipid Metabolism
- (2010) Nicholas S. Heaton et al. Cell Host & Microbe
- RNA granules: post-transcriptional and epigenetic modulators of gene expression
- (2009) Paul Anderson et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
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