Evidence map›Paper›PMID 33742057›Full record

ArticleCommunications biology2021

A non-canonical function for Centromere-associated protein-E controls centrosome integrity and orientation of cell division.

Mikito Owa, Brian Dynlacht

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 15 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

2 authors at 1 institution in 1 country.

Mikito OwaDepartment of Pathology, New York University Cancer Institute, New York University School of Medicine, New York, NY, USA. Mikito.Owa@nyumc.org.ORCID 0000-0002-4578-1352
Brian DynlachtDepartment of Pathology, New York University Cancer Institute, New York University School of Medicine, New York, NY, USA. Brian.Dynlacht@nyumc.org.ORCID 0000-0001-9485-512X
New York University · US

Funding

Elucidating the regulators of ciliogenesis - Revision - Equipment SupplementR01GM120776 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Brian D Dynlacht · 2016 to 2026
$4.6M
NIGMS NIH HHS R01 GM120776
6 · The paper itself

Abstract

Centromere-associated protein-E (CENP-E) is a kinesin motor localizing at kinetochores. Although its mitotic functions have been well studied, it has been challenging to investigate direct consequences of CENP-E removal using conventional methods because CENP-E depletion resulted in mitotic arrest. In this study, we harnessed an auxin-inducible degron system to achieve acute degradation of CENP-E. We revealed a kinetochore-independent role for CENP-E that removes pericentriolar material 1 (PCM1) from centrosomes in late S/early G

Indexed as

MitosisAntigensAutoantigensCase-Control StudiesCell Cycle ProteinsCell LineCentromereChromosomal Proteins, Non-HistoneHumansMicrocephalyMutationPhosphorylationPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsRetinal Pigment EpitheliumAntigensAutoantigensCell Cycle Proteinscentromere protein EChromosomal Proteins, Non-HistonePCM1 protein, humanpericentrinPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID33742057
PMCPMC7979751
OpenAlexW3137553209

What OpenQuestion holds

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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.