Evidence map›Paper›PMID 22745803›Full record

ArticlePloS one2012

Fluorescence-based phenotypic selection allows forward genetic screens in haploid human cells.

Lidia M Duncan, Richard T Timms, Eszter Zavodszky, Florencia Cano, Gordon Dougan, Felix Randow, Paul J Lehner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Hunting Viral Receptors Using Haploid Cells.Annual review of virology · 2015
    Review
  11. Article
  12. The binding of TAPBPR and Tapasin to MHC class I is mutually exclusive.Journal of immunology (Baltimore, Md. : 1950) · 2013
    Article
  13. Tapasin-related protein TAPBPR is an additional component of the MHC class I presentation pathway.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  14. Article
  15. Article
  16. Review
  17. Review
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

7 authors at 3 institutions in 1 country.

Lidia M DuncanCambridge Institute for Medical Research, Addenbrooke's Hospital, Cambridge, United Kingdom.
Richard T Timms
Eszter Zavodszky
Florencia Cano
Gordon Dougan
Felix Randow
Paul J Lehner
Addenbrooke's Hospital · GBMRC Laboratory of Molecular Biology · GBWellcome Sanger Institute · GB

Funding

Medical Research Council G9800943Medical Research Council MC_U105170648Wellcome Trust
6 · The paper itself

Abstract

The isolation of haploid cell lines has recently allowed the power of forward genetic screens to be applied to mammalian cells. The interest in applying this powerful genetic approach to a mammalian system is only tempered by the limited utility of these screens, if confined to lethal phenotypes. Here we expand the scope of these approaches beyond live/dead screens and show that selection for a cell surface phenotype via fluorescence-activated cell sorting can identify the key molecules in an intracellular pathway, in this case MHC class I antigen presentation. Non-lethal haploid genetic screens are widely applicable to identify genes involved in essentially any cellular pathway.

Indexed as

HaploidyFlow CytometryFluorescenceGenetic TestingHumans

Identifiers

PMID22745803
PMCPMC3382162
OpenAlexW2070127159

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.