Evidence map›Paper›PMID 41478871›Full record

ReviewNature reviews. Neuroscience2026

Long-range axon branching: contributions to brain network plasticity and repair.

Linda J Richards, Cheng Huang, Adam Q Bauer, Jin-Moo Lee

Abstract readReview
In one paragraph

Review in Nature reviews. Neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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.

Linda J RichardsDepartment of Neuroscience, Washington University in St. Louis Medical School, St. Louis, MO, USA. linda.richards@wustl.edu.ORCID http://orcid.org/0000-0002-7590-7390
Cheng HuangDepartment of Neuroscience, Washington University in St. Louis Medical School, St. Louis, MO, USA.ORCID http://orcid.org/0000-0001-9936-4813
Adam Q BauerDepartment of Radiology, Washington University in St. Louis Medical School, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-8364-3209
Jin-Moo LeeDepartment of Neurology, Washington University in St. Louis Medical School, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-3979-0906

Funding

Washington University University of Texas Southwestern VCID Consortium SiteUF1NS125512 · NINDS · WASHINGTON UNIVERSITY · PI Hongyu An, Andria Lee Ford · 2021 to 2026
$6.3M
Emergence of activity patterns in the cerebral cortex and their influence on brain circuit development and functionDP1NS127279 · NINDS · WASHINGTON UNIVERSITY · PI RICHARDS, LINDA J · 2021 to 2025
$5.5M
VCID Center Without Walls for Understanding and Leveraging Small Vessel Cerebrovascular Disease Mechanisms in ADRDRF1NS139970 · NINDS · WASHINGTON UNIVERSITY · PI CRUCHAGA, CARLOS, GOYAL, MANU S · 2024 to 2024
$4.4M
Plasticizing the Cortex to Enhance Stroke RecoveryR37NS110699 · NINDS · WASHINGTON UNIVERSITY · PI LEE, JIN-MOO · 2019 to 2025
$3.5M
Integrating TPM and PAM to examine the metabolic underpinning of neurovascular repair after strokeR01NS120481 · NINDS · WASHINGTON UNIVERSITY · PI HU, SONG, LEE, JIN-MOO · 2021 to 2025
$3.1M
Imaging and Reversibility of Cellular and Network Metabolic Dysfunction in Alzheimer's DiseaseRF1AG079503 · NIA · WASHINGTON UNIVERSITY · PI BAUER, ADAM Q, GOYAL, MANU S · 2022 to 2022
$2.2M
OPTOGENETIC MAPPING OF CELL SPECIFIC CONNECTIONS IN THE MOUSE BRAIN AFTER STROKER01NS102870 · NINDS · WASHINGTON UNIVERSITY · PI BAUER, ADAM Q · 2018 to 2022
$2.1M
Determining the efficacy of therapeutic interventions after stroke from cell specific functional connectomesR01NS126326 · NINDS · WASHINGTON UNIVERSITY · PI ADAM Q BAUER · 2023 to 2026
$1.8M
Imaging and Reversibility of Cellular and Network Metabolic Dysfunction in Alzheimer's DiseaseR01AG079503 · NIA · WASHINGTON UNIVERSITY · PI ADAM Q BAUER, Manu S Goyal · 2025 to 2026
$1.4M
NIA NIH HHS R01 AG079503NIA NIH HHS RF1 AG079503NINDS NIH HHS DP1 NS127279NINDS NIH HHS R01 NS102870NINDS NIH HHS R01 NS120481NINDS NIH HHS R01 NS126326NINDS NIH HHS R37 NS110699NINDS NIH HHS RF1 NS139970NINDS NIH HHS UF1 NS125512
6 · The paper itself

Abstract

Brain function requires exquisitely adapted plasticity at multiple scales, from synapses to whole-brain networks. Evidence for large-scale plasticity in functional brain networks comes from neuroimaging data across a variety of species, particularly during development and following injury. However, how large-scale network remodelling is achieved at the microscopic level is unknown as the growth of entirely new long-distance axons is unlikely to occur. Recent insights from electron microscopic connectome studies and single-cell projectomes of neurons in the brains of multiple model organisms have provided new evidence for the incredible structural complexity of axons and their branches that traverse the brain. This evidence shows highly arborized axonal projections, differentially myelinated branches of the same axon, and axonal regions devoid of synaptic contacts but with the potential to form synaptic connections in new or additional areas. Recent electron microscopic data suggest that these axonal features may be evolutionarily conserved. Here we consider whether these features could enable long-range and large-scale neuroplastic changes at a functional level, particularly following focal brain injury. These insights contribute to our emerging understanding of how the brain undergoes large-scale reorganization to adapt to changing circumstances.

Indexed as

AxonsBrainBrain InjuriesNerve NetNeuronal PlasticityAnimalsHumans

Identifiers

PMID41478871
PMCPMC12904670

What OpenQuestion holds

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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.