Evidence map›Paper›PMID 26256788›Full record

ReviewNature reviews. Microbiology2015

The yin and yang of hepatitis C: synthesis and decay of hepatitis C virus RNA.

You Li, Daisuke Yamane, Takahiro Masaki, Stanley M Lemon

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 37 citations in OpenAlex.

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  13. RNA triphosphatase DUSP11 enables exonuclease XRN-mediated restriction of hepatitis C virus.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 2 countries.

You Li1] Lineberger Comprehensive Cancer Center, Division of Infectious Diseases, Department of Medicine and Department of Microbiology &Immunology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27517-7292, USA. [2].
Daisuke Yamane1] Lineberger Comprehensive Cancer Center, Division of Infectious Diseases, Department of Medicine and Department of Microbiology &Immunology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27517-7292, USA. [2].
Takahiro Masaki1] Lineberger Comprehensive Cancer Center, Division of Infectious Diseases, Department of Medicine and Department of Microbiology &Immunology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27517-7292, USA. [2] Department of Virology II, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Stanley M Lemon1] Lineberger Comprehensive Cancer Center, Division of Infectious Diseases, Department of Medicine and Department of Microbiology &Immunology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27517-7292, USA. [2] The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7292, USA.
University of North Carolina at Chapel Hill · US

Funding

Micro-RNA 122 and Chronic Hepatitis CR01AI095690 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEMON, STANLEY M. · 2011 to 2020
$3.7M
Murine Model of HCV-Associated Human Liver CancerR01CA164029 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEMON, STANLEY M., SU, LISHAN · 2012 to 2016
$2.3M
NCI NIH HHS R01 CA164029NCI NIH HHS R01-CA164029NIAID NIH HHS R01 AI095690NIAID NIH HHS R01-AI095690
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is an unusual RNA virus that has a striking capacity to persist for the remaining life of the host in the majority of infected individuals. In order to persist, HCV must balance viral RNA synthesis and decay in infected cells. In this Review, we focus on interactions between the positive-sense RNA genome of HCV and the host RNA-binding proteins and microRNAs, and describe how these interactions influence the competing processes of viral RNA synthesis and decay to achieve stable, long-term persistence of the viral genome. Furthermore, we discuss how these processes affect hepatitis C pathogenesis and therapeutic strategies against HCV.

Indexed as

Antiviral AgentsGene Expression Regulation, ViralHepacivirusHepatitis CHumansRNA, ViralAntiviral AgentsRNA, Viral

Identifiers

PMID26256788
PMCPMC4756644
OpenAlexW1155762006

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.