Evidence map›Paper›PMID 19892785›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2010

Developmental expression of the oligodendrocyte myelin glycoprotein in the mouse telencephalon.

Vanessa Gil, Zoe Bichler, Jae K Lee, Oscar Seira, Franc Llorens, Ana Bribian, Ricardo Morales, Enric Claverol-Tinture, Eduardo Soriano, Lauro Sumoy and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  11. Agenesis of the corpus callosum in Nogo receptor deficient mice.The Journal of comparative neurology · 2017
    Article
  12. Article
  13. Age-dependent decline of nogo-a protein in the mouse cerebrum.Cellular and molecular neurobiology · 2014
    Article
  14. Review
  15. Review
  16. Article
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  20. Review
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 6 institutions in 2 countries.

Vanessa GilMolecular and Cellular Neurobiotechnology laboratory, Institute for Bioengineering of Catalonia (IBEC), Barcelona E-08028, Spain.
Zoe Bichler
Jae K Lee
Oscar Seira
Franc Llorens
Ana Bribian
Ricardo Morales
Enric Claverol-Tinture
Eduardo Soriano
Lauro Sumoy
Binhai Zheng
Jose A Del Río
Institute for Bioengineering of Catalonia · ESUniversitat de Barcelona · ESUniversity of California, San Diego · USBiomedical Research Networking Center on Neurodegenerative Diseases · ESInstitute for Research in Biomedicine · ESInstitute of Predictive and Personalized Medicine of Cancer · ES

Funding

Genetic analysis of myelin inhibitors and PTEN in injury-inducedCNS axon growthR01NS054734 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHENG, BINHAI · 2007 to 2015
$3.2M
NINDS NIH HHS R01 NS054734PHS HHS R0INS054734
6 · The paper itself

Abstract

The oligodendrocyte myelin glycoprotein is a glycosylphosphatidylinositol-anchored protein expressed by neurons and oligodendrocytes in the central nervous system. Attempts have been made to identify the functions of the myelin-associated inhibitory proteins (MAIPs) after axonal lesion or in neurodegeneration. However, the developmental roles of some of these proteins and their receptors remain elusive. Recent studies indicate that NgR1 and the recently discovered receptor PirB restrict cortical synaptic plasticity. However, the putative factors that trigger these effects are unknown. Because Nogo-A is mostly associated with the endoplasmic reticulum and myelin associated glycoprotein appears late during development, the putative participation of OMgp should be considered. Here, we examine the pattern of development of OMgp immunoreactive elements during mouse telencephalic development. OMgp immunoreactivity in the developing cortex follows the establishment of the thalamo-cortical barrel field. At the cellular level, we located OMgp neuronal membranes in dendrites and axons as well as in brain synaptosome fractions and axon varicosities. Lastly, the analysis of the barrel field in OMgp-deficient mice revealed that although thalamo-cortical connections were formed, their targeting in layer IV was altered, and numerous axons ectopically invaded layers II-III. Our data support the idea that early expressed MAIPs play an active role during development and point to OMgp participating in thalamo-cortical connections.

Indexed as

AnimalsBrain MappingCell DifferentiationCerebral CortexGene Expression Regulation, DevelopmentalGPI-Linked ProteinsGrowth ConesHEK293 CellsHumansMiceMice, KnockoutMyelin-Associated GlycoproteinMyelin-Oligodendrocyte GlycoproteinMyelin ProteinsNerve Fibers, MyelinatedNeural PathwaysGPI-Linked ProteinsMOG protein, humanMog protein, mouseMog protein, ratMyelin-Associated GlycoproteinMyelin-Oligodendrocyte GlycoproteinMyelin ProteinsOMG protein, humanOmg protein, mouse

Identifiers

PMID19892785
PMCPMC2901018
OpenAlexW2143728953

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.