Core components of DNA lagging strand synthesis machinery are essential for hepatitis B virus cccDNA formation
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Title
Core components of DNA lagging strand synthesis machinery are essential for hepatitis B virus cccDNA formation
Authors
Keywords
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Journal
Nature Microbiology
Volume 5, Issue 5, Pages 715-726
Publisher
Springer Science and Business Media LLC
Online
2020-03-10
DOI
10.1038/s41564-020-0678-0
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Note: Only part of the references are listed.- DNA Polymerase alpha is essential for intracellular amplification of hepatitis B virus covalently closed circular DNA
- (2019) Liudi Tang et al. PLoS Pathogens
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- (2018) Kouichi Kitamura et al. PLoS Pathogens
- T5 exonuclease hydrolysis of Hepatitis B Virus replicative intermediates allows reliable quantification and fast drug efficacy testing of covalently closed circular DNA by PCR
- (2018) Bingqian Qu et al. JOURNAL OF VIROLOGY
- HBVcircle: A novel tool to investigate hepatitis B virus covalently closed circular DNA
- (2017) Zhipeng Yan et al. JOURNAL OF HEPATOLOGY
- Identification of an Intermediate in Hepatitis B Virus Covalently Closed Circular (CCC) DNA Formation and Sensitive and Selective CCC DNA Detection
- (2017) Jun Luo et al. JOURNAL OF VIROLOGY
- Detection of HBV Covalently Closed Circular DNA
- (2017) Xiaoling Li et al. Viruses-Basel
- Long-term hepatitis B infection in a scalable hepatic co-culture system
- (2017) Benjamin Y. Winer et al. Nature Communications
- The role of host DNA ligases in hepadnavirus covalently closed circular DNA formation
- (2017) Quanxin Long et al. PLoS Pathogens
- Attacking hepatitis B virus cccDNA – The holy grail to hepatitis B cure
- (2016) Julie Lucifora et al. JOURNAL OF HEPATOLOGY
- The ORFeome Collaboration: a genome-scale human ORF-clone resource
- (2016) NATURE METHODS
- DNA Polymerase κ Is a Key Cellular Factor for the Formation of Covalently Closed Circular DNA of Hepatitis B Virus
- (2016) Yonghe Qi et al. PLoS Pathogens
- HBV cccDNA: viral persistence reservoir and key obstacle for a cure of chronic hepatitis B
- (2015) Michael Nassal GUT
- Hepadnavirus Genome Replication and Persistence
- (2015) Jianming Hu et al. Cold Spring Harbor Perspectives in Medicine
- Determinants of hepatitis B and delta virus host tropism
- (2015) Benjamin Y Winer et al. Current Opinion in Virology
- Does Tyrosyl DNA Phosphodiesterase-2 Play a Role in Hepatitis B Virus Genome Repair?
- (2015) Xiuji Cui et al. PLoS One
- Involvement of the host DNA-repair enzyme TDP2 in formation of the covalently closed circular DNA persistence reservoir of hepatitis B viruses
- (2014) Christian Königer et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Sodium taurocholate cotransporting polypeptide is a functional receptor for human hepatitis B and D virus
- (2012) Huan Yan et al. eLife
- A robust system for production of minicircle DNA vectors
- (2010) Mark A Kay et al. NATURE BIOTECHNOLOGY
- A possible mechanism for exonuclease 1-independent eukaryotic mismatch repair
- (2009) F. A. Kadyrov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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