Evidence map›Paper›PMID 25013353›Full record

ArticleCurrent topics in membranes2010

Claudin Proteins And Neuronal Function.

Jérôme Devaux, Bozena Fykkolodziej, Alexander Gow

Abstract read
In one paragraph

Article in Current topics in membranes, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact, top 88% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Stochastic left-right neuronal asymmetry in Caenorhabditis elegans.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  9. Article
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

3 authors at 2 institutions in 2 countries.

Jérôme DevauxDépartement Signalisation Neuronale, CRN2M, UMR 6231, CNRS, Université de la Méditerranée-Université Paul Cézanne, IFR Jean Roche, Marseille, France.
Bozena FykkolodziejCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Alexander GowCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, 48201, USA. ; Carman and Ann Adams Dept of Pediatrics, Wayne State University School of Medicine, Detroit, MI, 48201, USA. ; Dept of Neurology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Wayne State University · USCentre National de la Recherche Scientifique · FR

Funding

Molecular Mechanisms of NeurodegenerationR01NS043783 · NINDS · WAYNE STATE UNIVERSITY · PI GOW, ALEXANDER · 2002 to 2010
$2.6M
Hearing loss in claudin 11-null miceR01DC006262 · NIDCD · WAYNE STATE UNIVERSITY · PI GOW, ALEXANDER · 2003 to 2007
$1.2M
NIDCD NIH HHS R01 DC006262NINDS NIH HHS R01 NS043783
6 · The paper itself

Abstract

The identification and characterization of the claudin family of tight junction (TJ) proteins in the late 1990s ushered in a new era for research into the molecular and cellular biology of intercellular junctions. Since that time, TJs have been studied in the contexts of many diseases including deafness, male infertility, cancer, bacterial invasion and liver and kidney disorders. In this review, we consider the role of claudins in the nervous system focusing on the mechanisms by which TJs in glial cells are involved in neuronal function. Electrophysiological evidence suggests that claudins may operate in the central nervous system (CNS) in a manner similar to polarized epithelia. We also evaluate hypotheses that TJs are the gatekeepers of an immune-privileged myelin compartment and that TJs emerged during evolution to form major adhesive forces within the myelin sheath. Finally, we consider the implications of CNS myelin TJs in the contexts of behavioral disorders (schizophrenia) and demyelinating/hypomyelinating diseases (multiple sclerosis and the leukodystrophies), and explore evidence of a possible mechanism governing affective disorder symptoms in patients with white matter abnormalities.

Indexed as

axoglialexperimental allergic encephalomyelitisoligodendrocyte specific proteinproteolipid proteinradial componentsaltatory conductiontransverse bands

Identifiers

PMID25013353
PMCPMC4086801
OpenAlexW1541427282

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.