Evidence map›Paper›PMID 24623518›Full record

ReviewGenesis (New York, N.Y. : 2000)2014

The role of targeted protein degradation in early neural development.

Banu Saritas-Yildirim, Elena M Silva

Abstract readReview
In one paragraph

Review in Genesis (New York, N.Y. : 2000), 2014. 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
0.9field-weighted citation impact, top 28% 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, 12 citations in OpenAlex.

  1. Article
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  4. Review
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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.

Banu Saritas-YildirimDepartment of Biology, Georgetown University, Washington, DC.
Elena M Silva
Georgetown University · US

Funding

Regulation of neural development by F-box mediated ubiquitinationR03HD060698 · NICHD · GEORGETOWN UNIVERSITY · PI SILVA, ELENA M · 2010 to 2011
$150k
NICHD NIH HHS HD060698NICHD NIH HHS R03 HD060698
6 · The paper itself

Abstract

As neural stem cells differentiate into neurons during neurogenesis, the proteome of the cells is restructured by de novo expression and selective removal of regulatory proteins. The control of neurogenesis at the level of gene regulation is well documented and the regulation of protein abundance through protein degradation via the Ubiquitin/26S proteasome pathway is a rapidly developing field. This review describes our current understanding of the role of the proteasome pathway in neurogenesis. Collectively, the studies show that targeted protein degradation is an important regulatory mechanism in the generation of new neurons.

Indexed as

ProteolysisAnimalsGene Expression Regulation, DevelopmentalHumansNervous SystemNeurogenesisProteasome Endopeptidase ComplexSignal TransductionUbiquitinated ProteinsUbiquitinationUbiquitin-Protein LigasesProteasome Endopeptidase ComplexUbiquitinated ProteinsUbiquitin-Protein LigasesF-box proteinsneural inductionneurogenesisubiquitin ligase

Identifiers

PMID24623518
PMCPMC4059693
OpenAlexW1744654424

What OpenQuestion holds

Textmetadata
LicenceTDM
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.