Evidence map›Paper›PMID 21739613›Full record

ReviewDevelopmental neurobiology2011

Extracellular matrix functions during neuronal migration and lamination in the mammalian central nervous system.

Santos J Franco, Ulrich Müller

Open access · bronzeAbstract readReview
In one paragraph

Review in Developmental neurobiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 117 citations in OpenAlex.

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  18. Modeling the Human Brain WithFrontiers in neuroscience · 2022
    Article
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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.

Santos J FrancoDepartment of Cell Biology, Dorris Neuroscience Center, The Scripps Research Institute, La Jolla, California 92037, USA. franco@scripps.edu
Ulrich Müller
Scripps Research Institute · US

Funding

C57BI/6 Mouse Lines Expressing CRE-Recombinase in the Nervous SystemU01MH078833 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI MUELLER, ULRICH · 2006 to 2010
$7.7M
Cell Adhesion Molecules in CNS DevelopmentR01NS046456 · NINDS · SCRIPPS RESEARCH INSTITUTE, THE · PI MUELLER, ULRICH · 2004 to 2013
$4.4M
Mechanisms of Reelin Action on neuronal Migration During Neocortical LaminationF32NS060355 · NINDS · SCRIPPS RESEARCH INSTITUTE, THE · PI FRANCO, SANTOS JOE · 2009 to 2011
$174k
NIMH NIH HHS MH078833NIMH NIH HHS U01 MH078833NINDS NIH HHS F32 NS060355NINDS NIH HHS NS046456NINDS NIH HHS NS060355NINDS NIH HHS R01 NS046456
6 · The paper itself

Abstract

Extracellular matrix (ECM) glycoproteins are expressed in the central nervous system (CNS) in complex and developmentally regulated patterns. The ECM provides a number of critical functions in the CNS, contributing both to the overall structural organization of the CNS and to control of individual cells. At the cellular level, the ECM affects its functions by a wide range of mechanisms, including providing structural support to cells, regulating the activity of second messenger systems, and controlling the distribution and local concentration of growth and differentiation factors. Perhaps the most well known role of the ECM is as a substrate on which motile cells can migrate. Genetic, cell biological, and biochemical studies provide strong evidence that ECM glycoproteins such as laminins, tenascins, and proteoglycans control neuronal migration and positioning in several regions of the developing and adult brain. Recent findings have also shed important new insights into the cellular and molecular mechanisms by which reelin regulates migration. Here we will summarize these findings, emphasizing the emerging concept that ECM glycoproteins promote different modes of neuronal migration such as radial, tangential, and chain migration. We also discuss several studies demonstrating that mutations in ECM glycoproteins can alter neuronal positioning by cell nonautonomous mechanisms that secondarily affect migrating neurons.

Indexed as

AnimalsCell MovementCentral Nervous SystemExtracellular MatrixExtracellular Matrix ProteinsHumansLamininMammalsNeuronsProteoglycansReelin ProteinTenascinExtracellular Matrix ProteinsLamininProteoglycansReelin ProteinRELN protein, humanTenascin

Identifiers

PMID21739613
PMCPMC3490208
OpenAlexW1981881062

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.