Evidence map›Paper›PMID 31997102›Full record

ReviewNeurochemical research2020

Extrinsic Factors Driving Oligodendrocyte Lineage Cell Progression in CNS Development and Injury.

Maryna Baydyuk, Vivianne E Morrison, Phillip S Gross, Jeffrey K Huang

Open access · hybridAbstract readReview
In one paragraph

Review in Neurochemical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  17. Transcriptional and bioinformatic analysis of GABAFrontiers in molecular neuroscience · 2023
    Article
  18. Lysophosphatidic acid signaling via LPAJournal of neurochemistry · 2022
    Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Maryna BaydyukDepartment of Biology and Center for Cell Reprogramming, Georgetown University, Washington, DC, 20057, USA.
Vivianne E MorrisonDepartment of Biology and Center for Cell Reprogramming, Georgetown University, Washington, DC, 20057, USA.
Phillip S GrossDepartment of Biology and Center for Cell Reprogramming, Georgetown University, Washington, DC, 20057, USA.
Jeffrey K HuangDepartment of Biology and Center for Cell Reprogramming, Georgetown University, Washington, DC, 20057, USA. jh1659@georgetown.edu.ORCID http://orcid.org/0000-0003-0996-9451
Georgetown University · US

Funding

Predoctoral Training in Intergrative NeuroscienceT32NS041231 · NINDS · GEORGETOWN UNIVERSITY · PI Ludise Malkova, Ashley S VanMeter · 2001 to 2026
$6.8M
Training in Neural Injury &PlasticityT32NS041218 · NINDS · GEORGETOWN UNIVERSITY · PI MARK P BURNS, Kathleen Anne Maguire-Zeiss · 2001 to 2026
$3.5M
Immunoregulation in CNS remyelinationR01NS107523 · NINDS · GEORGETOWN UNIVERSITY · PI HUANG, JEFFREY K · 2018 to 2022
$1.7M
Congressionally Directed Medical Research Programs W81XWH-17-1-0268National Multiple Sclerosis Society JF-1806-31381National Science Foundation DGE-0903443National Science Foundation Internal grant number: RX2700 403NINDS NIH HHS 1R01NS107523-01NINDS NIH HHS R01 NS107523NINDS NIH HHS T32 NS041218NINDS NIH HHS T32 NS041231
6 · The paper itself

Abstract

Oligodendrocytes (OLs) generate myelin membranes for the rapid propagation of electrical signals along axons in the central nervous system (CNS) and provide metabolites to support axonal integrity and function. Differentiation of OLs from oligodendrocyte progenitor cells (OPCs) is orchestrated by a multitude of intrinsic and extrinsic factors in the CNS. Disruption of this process, or OL loss in the developing or adult brain, as observed in various neurological conditions including hypoxia/ischemia, stroke, and demyelination, results in axonal dystrophy, neuronal dysfunction, and severe neurological impairments. While much is known regarding the intrinsic regulatory signals required for OL lineage cell progression in development, studies from pathological conditions highlight the importance of the CNS environment and external signals in regulating OL genesis and maturation. Here, we review the recent findings in OL biology in the context of the CNS physiological and pathological conditions, focusing on extrinsic factors that facilitate OL development and regeneration.

Indexed as

AnimalsCell DifferentiationCell LineageCentral Nervous SystemCentral Nervous System DiseasesDisease ProgressionHumansMyelin SheathOligodendrogliaStem CellsDemyelinationDiffuse white matter injuryMultiple sclerosisMyelinOligodendrocyte precursor cells (OPCs)OligodendrocytesRemyelination

Identifiers

PMID31997102
PMCPMC7058689
OpenAlexW3004170930

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.