Evidence map›Paper›PMID 11145205›Full record

ReviewBrain pathology (Zurich, Switzerland)2001

The pathobiology of myelin mutants reveal novel biological functions of the MBP and PLP genes.

A T Campagnoni, R P Skoff

Open access · bronzeAbstract readReview
In one paragraph

Review in Brain pathology (Zurich, Switzerland), 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
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  3. Review
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  15. Neurogenetics of Pelizaeus-Merzbacher disease.Handbook of clinical neurology · 2018
    Review
  16. Article
  17. Article
  18. Review
  19. Neonatal hyperoxia exposure disrupts axon-oligodendrocyte integrity in the subcortical white matter.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  20. Autophagy promotes oligodendrocyte survival and function following dysmyelination in a long-lived myelin mutant.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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

2 authors at 2 institutions in 1 country.

A T CampagnoniNeuropsychiatric Institute, UCLA School of Medicine, 90024, USA. acampagnoni@mednet.ucla.edu
R P Skoff
Upsala College · USWayne State University · US

Funding

PROCESSING AND DEGRADATION OF PROTEOLIPID PROTEINR01NS038236 · NINDS · WAYNE STATE UNIVERSITY · PI SKOFF, ROBERT P · 1999 to 2016
$4.2M
SYNTHESIS AND ASSEMBLY OF BASIC PROTEINS INTO MYELINR01NS023022 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CAMPAGNONI, ANTHONY T · 1985 to 2009
$2.9M
GENETIC ELEMENTS REGULATIONG MYELIN GENE EXPRESSIONR01NS033091 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CAMPAGNONI, ANTHONY T · 1994 to 2001
$522k
NINDS NIH HHS NS23022NINDS NIH HHS NS33091NINDS NIH HHS NS38236
6 · The paper itself

Abstract

Substantial biological data indicate that the myelin basic protein (MBP) and myelin proteolipid protein (PLP/DM20) genes produce products with functions beyond that of serving as myelin structural proteins. Much of this evidence comes from studies on naturally-occurring and man-made mutations of these genes in mice and other species. This review focuses upon recent evidence showing the existence of other products of these genes that may account for some of these other functions, and recent studies providing evidence for alternative biological functions of PLP/DM20. The MBP and PLP/DM20 genes each encode the classic MBP and PLP isoforms, as well as a second family of proteins that are not involved in myelin structure. The biological roles of these other products of the genes are becoming clarified. The non-classic MBP gene products appear to be components of transcriptional complexes in the nucleus, and they also may be involved in signaling pathways in T-cells and in neural cells. The non-classic PLP/DM20 gene products appear to be components of intracellular transport vesicles in oligodendrocytes. There is evidence for other functions of the classic PLP/DM20 proteins, including a role in neural cell death mechanisms, autocrine and paracrine regulation of oligodendrocytes and neurons, intracellular transport and oligodendrocyte migration.

Indexed as

Amino Acid SequenceAnimalsCell CommunicationGene ExpressionHumansMutationMyelin Basic ProteinMyelin Proteolipid ProteinMyelin SheathOligodendrogliaProtein ConformationMyelin Basic ProteinMyelin Proteolipid Protein

Identifiers

PMID11145205
PMCPMC8098301
OpenAlexW2032598875

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.