Evidence map›Paper›PMID 22247330›Full record

ReviewFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

Host gene targets for novel influenza therapies elucidated by high-throughput RNA interference screens.

Victoria A Meliopoulos, Lauren E Andersen, Katherine F Birrer, Kaylene J Simpson, John W Lowenthal, Andrew G D Bean, John Stambas, Cameron R Stewart, S Mark Tompkins, Victor W van Beusechem and 9 more

Abstract readReview
In one paragraph

Review in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 58 citations in OpenAlex.

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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

19 authors at 11 institutions in 6 countries.

Victoria A MeliopoulosDepartment of Infectious Diseases, University of Georgia, 111 Carlton St., Athens, GA 30602, USA.
Lauren E Andersen
Katherine F Birrer
Kaylene J Simpson
John W Lowenthal
Andrew G D Bean
John Stambas
Cameron R Stewart
S Mark Tompkins
Victor W van Beusechem
Iain Fraser
Musa Mhlanga
Samantha Barichievy
Queta Smith
Devin Leake
Jon Karpilow
Amy Buck
Ghil Jona
Ralph A Tripp
University of Georgia · USThermo Fisher Scientific (United States) · USCommonwealth Scientific and Industrial Research Organisation · AUCouncil for Scientific and Industrial Research · ZADeakin University · AUAmsterdam UMC Location VUmc · NLAustralian Centre for Disease Preparedness · AUCentre for Immunity, Infection and Evolution · GBNational Institute of Allergy and Infectious Diseases · USUniversity of Melbourne · AUWeizmann Institute of Science · IL

Funding

RNAi Screening in Hematopoietic CellsZIAAI001106 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FRASER, IAIN · 2009 to 2025
$12.4M
Analysis of Innate Immune Signaling NetworksZIAAI001107 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FRASER, IAIN · 2009 to 2025
$11.9M
Biotechnology and Biological Sciences Research Council BB/G01552X/1Intramural NIH HHS ZIA AI001106Intramural NIH HHS ZIA AI001107
6 · The paper itself

Abstract

Influenza virus encodes only 11 viral proteins but replicates in a broad range of avian and mammalian species by exploiting host cell functions. Genome-wide RNA interference (RNAi) has proven to be a powerful tool for identifying the host molecules that participate in each step of virus replication. Meta-analysis of findings from genome-wide RNAi screens has shown influenza virus to be dependent on functional nodes in host cell pathways, requiring a wide variety of molecules and cellular proteins for replication. Because rapid evolution of the influenza A viruses persistently complicates the effectiveness of vaccines and therapeutics, a further understanding of the complex host cell pathways coopted by influenza virus for replication may provide new targets and strategies for antiviral therapy. RNAi genome screening technologies together with bioinformatics can provide the ability to rapidly identify specific host factors involved in resistance and susceptibility to influenza virus, allowing for novel disease intervention strategies.

Indexed as

RNA InterferenceAnimalsHigh-Throughput Screening AssaysHumansInfluenza A virusInfluenza, HumanMeta-Analysis as TopicMicroRNAsNF-kappa BProtein Kinase CRNA, Small InterferingSignal TransductionViral ProteinsMicroRNAsNF-kappa BProtein Kinase CRNA, Small InterferingViral Proteins

Identifiers

PMID22247330
PMCPMC3316894
OpenAlexW2110555084

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.