Evidence map›Paper›PMID 29030390›Full record

ArticleG3 (Bethesda, Md.)2017

APC/C

Jeffrey C Medley, Lauren E DeMeyer, Megan M Kabara, Mi Hye Song

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Distinct D-box Motifs in SPD-2 Mediate APC/CbioRxiv : the preprint server for biology · 2025
    Article
  3. The E3 ligase Poe promotes Pericentrin degradation.Molecular biology of the cell · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. Mitotic Cell Division inGenetics · 2019
    Review
  8. Article
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 at 1 institution in 1 country.

Jeffrey C MedleyDepartment of Biological Sciences, Oakland University, Rochester, Michigan 48309.ORCID 0000-0002-0965-4233
Lauren E DeMeyerDepartment of Biological Sciences, Oakland University, Rochester, Michigan 48309.ORCID 0000-0003-1277-6503
Megan M KabaraDepartment of Biological Sciences, Oakland University, Rochester, Michigan 48309.ORCID 0000-0002-7942-8039
Mi Hye SongDepartment of Biological Sciences, Oakland University, Rochester, Michigan 48309 msong2@oakland.edu.ORCID 0000-0001-8326-6602
Oakland University · US

Funding

WormBase: a core data resource for C. elegans and other nematodesU41HG002223 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI KERSEY, PAUL, SCHEDL, TIM · 2013 to 2017
$20.5M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Regulation of Centrosome Assembly by PhosphorylationR15GM101633 · NIGMS · OAKLAND UNIVERSITY · PI SONG, MI HYE · 2012 to 2012
$336k
Biotechnology and Biological Sciences Research CouncilMedical Research CouncilNHGRI NIH HHS U41 HG002223NIH HHS P40 OD010440
6 · The paper itself

Abstract

As the primary microtubule-organizing center, centrosomes play a key role in establishing mitotic bipolar spindles that secure correct transmission of genomic content. For the fidelity of cell division, centrosome number must be strictly controlled by duplicating only once per cell cycle. Proper levels of centrosome proteins are shown to be critical for normal centrosome number and function. Overexpressing core centrosome factors leads to extra centrosomes, while depleting these factors results in centrosome duplication failure. In this regard, protein turnover by the ubiquitin-proteasome system provides a vital mechanism for the regulation of centrosome protein levels. Here, we report that FZR-1, the

Indexed as

CentrosomeAnaphase-Promoting Complex-CyclosomeAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsGene DuplicationMicrotubule-Organizing CenterMitosisProtein KinasesUbiquitin-Protein LigasesAnaphase-Promoting Complex-CyclosomeCaenorhabditis elegans ProteinsCell Cycle Proteinsfzr-1 protein, C elegansProtein KinasesSAS-5 protein, C elegansUbiquitin-Protein Ligaseszyg-1 protein, C elegansC. elegansCentrosomeE3 ubiquitin ligaseFZR-1SAS-5

Identifiers

PMID29030390
PMCPMC5714490
OpenAlexW2949687214

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.