Evidence map›Paper›PMID 22517369›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2012

Hepatitis C virus: a new class of virus associated with particles derived from very low-density lipoproteins.

Jin Ye

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Chaperones in hepatitis C virus infection.World journal of hepatology · 2016
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
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

1 author.

Jin YeDepartment of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390-9046, USA. jin.ye@utsouthwestern.edu

Funding

TRANSCRIPTIONAL REGULATION OF LDL RECEPTOR PROMOTERP01HL020948 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI RUSSELL, DAVID W. · 1985 to 2021
$103.1M
Regulated Intramembrane Proteolysis of CREB3L1 in Innate Antiviral ResponseR01AI090119 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI YE, JIN · 2010 to 2014
$1.9M
NHLBI NIH HHS HL-20948NHLBI NIH HHS P01 HL020948NIAID NIH HHS AI090119NIAID NIH HHS R01 AI090119
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infects 3% of the world population and is the leading cause of liver failure in the United States. A unique feature of HCV is that the viral particles are integral to very low-density lipoprotein (VLDL)-derived lipoprotein particles. The virus is assembled into VLDL in hepatocytes and released out of the cells together with VLDL. The virus then infects more hepatocytes by entering the cells through the low-density lipoprotein receptor, which mediates uptake of majorities of VLDL-derived lipoprotein particles. These observations suggest that HCV may belong to a novel class of viruses that is associated with VLDL. Understanding the relationship between HCV and VLDL metabolism may reveal new strategies to treat HCV infection.

Indexed as

AnimalsDNA VirusesHepacivirusHepatitis CHepatocytesHumansLipoproteins, VLDLVirionLipoproteins, VLDL

Identifiers

PMID22517369
PMCPMC3331997

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.