Evidence map›Paper›PMID 39829751›Full record

ArticlebioRxiv : the preprint server for biology2025

Developmental axon diameter growth of central nervous system axons does not depend on ensheathment or myelination by oligodendrocytes.

Jenea M Bin, Katie Emberley, Tobias J Buscham, Maria A Eichel-Vogel, Ryan A Doan, Anna M Steyer, Matthew F Nolan, Wiebke Möbius, Kelly R Monk, Hauke B Werner and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

12 authors.

Jenea M BinCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.ORCID 0000-0002-0450-5300
Katie EmberleyJungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.ORCID 0000-0003-2333-2289
Tobias J BuschamDepartment of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.ORCID 0000-0002-6916-3102
Maria A Eichel-VogelCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.ORCID 0000-0002-9925-7249
Ryan A DoanJungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.ORCID 0000-0002-6944-3921
Anna M SteyerDepartment of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.ORCID 0000-0002-4814-7517
Matthew F NolanCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.ORCID 0000-0003-1062-6501
Wiebke MöbiusDepartment of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.ORCID 0000-0002-2902-7165
Kelly R MonkJungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.ORCID 0000-0003-1803-3495
Hauke B WernerDepartment of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.ORCID 0000-0002-7710-5738
Ben EmeryJungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.ORCID 0000-0002-9132-3045
David A LyonsCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.ORCID 0000-0003-1166-4454

Funding

Neuroscience of Aging, Neurodegeneration and Alzheimer’s DiseaseT32AG055378 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOB RABER, HENRYK F URBANSKI · 2018 to 2026
$4.3M
Neuronal responses to chronic demyelinationR01NS120981 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI EMERY, BEN · 2021 to 2025
$2.1M
Mechanisms of Axon-Schwann cell interactionsR01NS120651 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MONK, KELLY R · 2021 to 2025
$1.9M
NIA NIH HHS T32 AG055378NINDS NIH HHS R01 NS120651NINDS NIH HHS R01 NS120981Wellcome Trust
6 · The paper itself

Abstract

Myelination facilitates the rapid conduction of action potentials along axons. In the central nervous system (CNS), myelinated axons vary over 100-fold in diameter, with conduction speed scaling linearly with increasing diameter. Axon diameter and myelination are closely interlinked, with axon diameter exerting a strong influence on myelination. Conversely, myelinating Schwann cells in the peripheral nervous system can both positively and negatively affect axon diameter. However, whether axon diameter is regulated by CNS oligodendrocytes is less clear. Here, we investigated CNS axon diameter growth in the absence of myelin using mouse (

Identifiers

PMID39829751
PMCPMC11741303

What OpenQuestion holds

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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.