Evidence map›Paper›PMID 28808228›Full record

ArticleScientific reports2017

Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors.

Susitha Premarathne, Mariyam Murtaza, Nicholas Matigian, Lachlan A Jolly, Stephen A Wood

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  9. Advances in the Development Ubiquitin-Specific Peptidase (USP) Inhibitors.International journal of molecular sciences · 2021
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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

5 authors at 2 institutions in 1 country.

Susitha PremarathneEskitis Institute for Drug Discovery, Griffith University, Nathan Brisbane 4111, Queensland, Australia.
Mariyam MurtazaEskitis Institute for Drug Discovery, Griffith University, Nathan Brisbane 4111, Queensland, Australia.
Nicholas MatigianEskitis Institute for Drug Discovery, Griffith University, Nathan Brisbane 4111, Queensland, Australia.
Lachlan A JollyRobinson Institute, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide 5005, South Australia, Australia.
Stephen A WoodEskitis Institute for Drug Discovery, Griffith University, Nathan Brisbane 4111, Queensland, Australia. s.wood@griffith.edu.au.ORCID 0000-0002-2576-7457
Griffith University · AUThe University of Adelaide · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of neural progenitors depends upon the coordination of appropriate intrinsic responses to extrinsic signalling pathways. Here we show the deubiquitylating enzyme, Usp9x regulates components of both intrinsic and extrinsic fate determinants. Nestin-cre mediated ablation of Usp9x from embryonic neural progenitors in vivo resulted in a transient disruption of cell adhesion and apical-basal polarity and, an increased number and ectopic localisation of intermediate neural progenitors. In contrast to other adhesion and polarity proteins, levels of β-catenin protein, especially S33/S37/T41 phospho-β-catenin, were markedly increased in Usp9x

Indexed as

Animalsbeta CateninCell AdhesionCell LineFemaleHEK293 CellsHumansMaleMiceNervous SystemReceptors, NotchSignal TransductionUbiquitin ThiolesteraseWnt Signaling Pathwaybeta CateninReceptors, NotchUbiquitin ThiolesteraseUSP9X protein, human

Identifiers

PMID28808228
PMCPMC5556043
OpenAlexW2745221419

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.