Evidence map›Paper›PMID 20424320›Full record

ArticleThe Journal of clinical investigation2010

Caveat mTOR: aberrant signaling disrupts corticogenesis.

Lucy R Osborne

Open access · bronzeAbstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 82% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Lucy R OsborneDepartment of Medicine and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada. lucy.osborne@utoronto.ca
University of Toronto · CA

Funding

Canadian Institutes of Health Research MOP-77720Canadian Institutes of Health Research MOP-86457
6 · The paper itself

Abstract

The mammalian target of rapamycin (mTOR) signaling pathway is activated in several disorders associated with benign tumors and malformations of the cerebral cortex. In this issue of the JCI, Orlova et al. have now definitively added another disorder to this group by demonstrating that activation of mTOR signaling is associated with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE), which is characterized by severe intractable epilepsy and megalencephaly. PMSE is caused by lack of the pseudokinase STE20-related kinase adaptor alpha (STRADalpha), and Orlova et al. show that reduction of STRADalpha levels during corticogenesis in the mouse results in a cellular phenotype and neuronal migration defects similar to those observed in patients with PMSE, clearly demonstrating a pivotal role for STRADalpha in cell polarity and growth. This study helps pave the way for possible therapeutic intervention with rapamycin to control the epilepsy and learning disabilities associated with this disorder.

Indexed as

Gene Expression RegulationSignal TransductionAdaptor Proteins, Vesicular TransportAnimalsBrainCell MovementEpilepsyHumansIntracellular Signaling Peptides and ProteinsLearning DisabilitiesMiceMice, KnockoutModels, BiologicalNeuronsPhenotypeProtein KinasesAdaptor Proteins, Vesicular TransportIntracellular Signaling Peptides and ProteinsMTOR protein, humanmTOR protein, mouseProtein KinasesProtein Serine-Threonine Kinasessterile 20-like protein kinase nerve injury-associated kinaseSTRAD protein, mouseTOR Serine-Threonine Kinases

Identifiers

PMID20424320
PMCPMC2860937
OpenAlexW2107749499

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.