Evidence map›Paper›PMID 28902568›Full record

ReviewCell cycle (Georgetown, Tex.)2017

Interlinked bistable mechanisms generate robust mitotic transitions.

Lukas H Hutter, Scott Rata, Helfrid Hochegger, Béla Novák

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2017. 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
–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

17 citing papers in PubMed.

  1. Article
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  5. On the assembly of the mitotic spindle, bistability and hysteresis.Cellular and molecular life sciences : CMLS · 2023
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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

4 authors.

Lukas H Huttera Department of Biochemistry , University of Oxford , Oxford , UK.ORCID http://orcid.org/0000-0002-3888-8231
Scott Rataa Department of Biochemistry , University of Oxford , Oxford , UK.
Helfrid Hocheggerc Genome Damage and Stability Centre, School of Life Sciences , University of Sussex , Falmer, Brighton , UK.ORCID http://orcid.org/0000-0001-8366-6198
Béla Nováka Department of Biochemistry , University of Oxford , Oxford , UK.ORCID http://orcid.org/0000-0002-6961-1366

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transitions between phases of the cell cycle have evolved to be robust and switch-like, which ensures temporal separation of DNA replication, sister chromatid separation, and cell division. Mathematical models describing the biochemical interaction networks of cell cycle regulators attribute these properties to underlying bistable switches, which inherently generate robust, switch-like, and irreversible transitions between states. We have recently presented new mathematical models for two control systems that regulate crucial transitions in the cell cycle: mitotic entry and exit,

Indexed as

MitosisAnimalsCDC2 Protein KinaseCyclin BHumansModels, BiologicalM Phase Cell Cycle CheckpointsCDC2 Protein KinaseCyclin BAurora Bbiochemical switchescancer cellsCDK1checkpoint controlcyclinserror correctionGreatwallmitosisPP2A:B55spindle assembly checkpoint

Identifiers

PMID28902568
PMCPMC5638388

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.