Evidence map›Paper›PMID 7732663›Full record

ArticleVirus genes1995

Complete sequence of the RNA genome of human rhinovirus 16, a clinically useful common cold virus belonging to the ICAM-1 receptor group.

W M Lee, W Wang, R R Rueckert

Abstract read
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In one paragraph

Article in Virus genes, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

40 citing papers in PubMed, 65 citations in OpenAlex.

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  10. Reverse genetics system for studying human rhinovirus infections.Methods in molecular biology (Clifton, N.J.) · 2015
    Article
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  13. Effects of rhinovirus species on viral replication and cytokine production.The Journal of allergy and clinical immunology · 2014
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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

3 authors at 1 institution in 1 country.

W M LeeInstitute for Molecular Virology, University of Wisconsin, Madison 53706, USA.
W Wang
R R Rueckert
University of Wisconsin–Madison · US

Funding

PATHWAYS OF RESISTANCE TO ANTIPICORNAVIRAL DRUGSR01AI031960 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI RUECKERT, ROLAND R · 1992 to 1996
–
NIAID NIH HHS AI 31960-02
6 · The paper itself

Abstract

We report here the complete nucleotide sequence and predicted polyprotein sequence of HeLa cell-adapted human rhinovirus 16 (HRV16). This virus is more suitable than human rhinovirus 14 (HRV14) for clinical studies, and its growth and physical properties are favorable for biochemical and crystallographic analysis. The complete message-sense RNA genome of HRV16 is composed of 7124 bases, not including the poly(A) tail. An open reading frame, extending from base 626 to 7084 predicts a polyprotein containing 2152 amino acid residues. Comparison with other rhinovirus sequences shows HRV16 is much more representative of human rhinoviruses than HRV14. No apparent relationship was found between receptor group and amino acid sequence in VP1, the capsid protein bearing the binding site for the intercellular adhesion molecule-1 (ICAM-1) in both HRV14 and HRV16.

Indexed as

Base SequenceHeLa CellsHumansIntercellular Adhesion Molecule-1Molecular Sequence DataReceptors, VirusRhinovirusRNA, MessengerRNA, ViralSequence Homology, Amino AcidViral ProteinsIntercellular Adhesion Molecule-1Receptors, VirusRNA, MessengerRNA, ViralViral Proteins

Identifiers

PMID7732663
OpenAlexW2014537550

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.