Evidence map›Paper›PMID 24142862›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2015

Cdk5 phosphorylation of ErbB4 is required for tangential migration of cortical interneurons.

Sonja Rakić, Shigeaki Kanatani, David Hunt, Clare Faux, Anna Cariboni, Francesca Chiara, Shabana Khan, Olivia Wansbury, Beatrice Howard, Kazunori Nakajima and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

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  17. Molecular mechanisms controlling the migration of striatal interneurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
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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

12 authors at 5 institutions in 2 countries.

Sonja RakićDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Shigeaki KanataniDepartment of Anatomy, Keio University School of Medicine, Tokyo 160-8582, Japan.
David HuntDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Clare FauxDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Anna CariboniDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Francesca ChiaraDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Shabana KhanDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
Olivia WansburyBreakthrough Breast Cancer Research Centre, Institute of Cancer Research, London SW3 6JB, UK.
Beatrice HowardBreakthrough Breast Cancer Research Centre, Institute of Cancer Research, London SW3 6JB, UK.
Kazunori NakajimaDepartment of Anatomy, Keio University School of Medicine, Tokyo 160-8582, Japan.
Margareta NikolićDepartment of Cellular and Molecular Neuroscience, Imperial College School of Medicine, London W12 0NN, UK.
John G ParnavelasDepartment of Cell and Developmental Biology, University College London, London WC1 6BT, UK.
University College London · GBKeio University · JPBreast Cancer Now · GBImperial College London · GBInstitute of Cancer Research · GB

Funding

Breast Cancer Now BREAST CANCER NOW RESEARCH CENTREWellcome Trust 074549Wellcome Trust 089775
6 · The paper itself

Abstract

Interneuron dysfunction in humans is often associated with neurological and psychiatric disorders, such as epilepsy, schizophrenia, and autism. Some of these disorders are believed to emerge during brain formation, at the time of interneuron specification, migration, and synapse formation. Here, using a mouse model and a host of histological and molecular biological techniques, we report that the signaling molecule cyclin-dependent kinase 5 (Cdk5), and its activator p35, control the tangential migration of interneurons toward and within the cerebral cortex by modulating the critical neurodevelopmental signaling pathway, ErbB4/phosphatidylinositol 3-kinase, that has been repeatedly linked to schizophrenia. This finding identifies Cdk5 as a crucial signaling factor in cortical interneuron development in mammals.

Indexed as

AnimalsCell MovementCerebral CortexCOS CellsCyclin-Dependent Kinase 5GABAergic NeuronsGlutamate DecarboxylaseInterneuronsKeratinsMice, TransgenicPhosphatidylinositol 3-KinasePhosphorylationPhosphotransferasesReceptor, ErbB-4Signal TransductionCdk5 protein, mouseCdk5r1 protein, mouseCyclin-Dependent Kinase 5Erbb4 protein, mouseGlutamate Decarboxylaseglutamate decarboxylase 1KeratinsPhosphatidylinositol 3-KinasePhosphotransferasesReceptor, ErbB-4cerebral cortexinterneuronsmigrationmousephosphorylation

Identifiers

PMID24142862
PMCPMC4380000
OpenAlexW2131717457

What OpenQuestion holds

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LicenceCC BY
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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.