Evidence map›Paper›PMID 31566762›Full record

ArticleThe EMBO journal2019

E2F transcription regulation: an orphan cyclin enters the stage.

Heike Ilona Rösner, Claus Storgaard Sørensen

Abstract readComment
In one paragraph

Article in The EMBO journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Heike Ilona RösnerBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen N, Denmark.ORCID 0000-0002-6201-3195
Claus Storgaard SørensenBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen N, Denmark.ORCID 0000-0001-6022-9710

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Marked cyclin protein oscillations over the cell cycle ensure tight regulation of all cell cycle transitions. Despite expression patterns closely mirroring those of cyclin A, cyclin F has long been regarded as an odd outlier within the cyclin family. Constituting part of an E3 ubiquitin ligase, its main role was seen as highly restricted to timely degradation of very few key substrates to ensure termination of one error-free round of replication. Now, a recent series of studies suggests that cyclin F has very similar roles as its closest relatives, merely mediated through a very different mechanism.

Indexed as

Cell Cycle ProteinsCyclinsCell CycleE2F Transcription FactorsProteolysisSynthetic Lethal MutationsTranscription FactorsCell Cycle ProteinsCyclinsE2F Transcription FactorsTranscription Factors

Identifiers

PMID31566762
PMCPMC6792015

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.