Evidence map›Paper›PMID 33548217›Full record

ArticleExperimental neurology2021

SARM1 is required in human derived sensory neurons for injury-induced and neurotoxic axon degeneration.

Yi-Hsien Chen, Yo Sasaki, Aaron DiAntonio, Jeffrey Milbrandt

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  4. Article
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  8. Article
  9. Surveying the landscape of emerging and understudied cell death mechanisms.Biochimica et biophysica acta. Molecular cell research · 2023
    Review
  10. Abnormal Intraepidermal Nerve Fiber Density in Disease: A Scoping Review.medRxiv : the preprint server for health sciences · 2023
    Article
  11. Article
  12. NADOxidative medicine and cellular longevity · 2023
    Review
  13. SARM1 detection in myelinating glia:Frontiers in cellular neuroscience · 2023
    Article
  14. Peripheral mechanisms of peripheral neuropathic pain.Frontiers in molecular neuroscience · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. SARM1 can be a potential therapeutic target for spinal cord injury.Cellular and molecular life sciences : CMLS · 2022
    Review
  20. 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

4 authors at 1 institution in 1 country.

Yi-Hsien ChenNeedleman Center for Neurometabolism and Axonal Therapeutics, Washington University School of Medicine, St. Louis, MO 63110, USA; Genome Engineering and iPSC Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
Yo SasakiDepartment of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: sasaki@wustl.edu.
Aaron DiAntonioDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Needleman Center for Neurometabolism and Axonal Therapeutics, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: diantonio@wustl.edu.
Jeffrey MilbrandtDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Needleman Center for Neurometabolism and Axonal Therapeutics, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: jmilbrandt@wustl.edu.
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
PHYSIOLOGY AND GENETICS OF THE GDNF HOMOLOG NEURTURINR01AG013730 · NIA · WASHINGTON UNIVERSITY · PI JEFFREY D MILBRANDT · 1996 to 2026
$10.6M
DISSECTION OF SARM1-INDUCED AXON DEGENERATION AND CELL DEATHR01NS087632 · NINDS · WASHINGTON UNIVERSITY · PI Aaron Diantonio, JEFFREY D MILBRANDT · 2014 to 2026
$6.4M
Regulating NAD Metabolism to Inhibit Axon Degeneration in Neurodegenerative DiseasesRF1AG013730 · NIA · WASHINGTON UNIVERSITY · PI MILBRANDT, JEFFREY D · 2017 to 2017
$2.8M
(PQ#9) Promoting Axon Stability to Prevent Therapy-induced Peripheral NeuropathyR01CA219866 · NCI · WASHINGTON UNIVERSITY · PI DIANTONIO, AARON, MILBRANDT, JEFFREY D · 2017 to 2021
$2.3M
NCI NIH HHS P30 CA091842NCI NIH HHS R01 CA219866NIA NIH HHS R01 AG013730NIA NIH HHS RF1 AG013730NINDS NIH HHS R01 NS087632
6 · The paper itself

Abstract

Axonal degeneration contributes to the pathogenesis of many neurodegenerative disorders, motivating efforts to dissect the mechanism of pathological axon loss in order to develop therapies for axonal preservation. SARM1 is a particularly attractive therapeutic target, as it is an inducible NAD

Indexed as

Armadillo Domain ProteinsAxonsBase SequenceCell LineCytoskeletal ProteinsGene Knockout TechniquesHumansInduced Pluripotent Stem CellsNerve DegenerationSensory Receptor CellsArmadillo Domain ProteinsCytoskeletal ProteinsSARM1 protein, humanAxon degenerationNADaseNeurodegenerationSarmoptosisTIR domain

Identifiers

PMID33548217
PMCPMC8171232
OpenAlexW3127895150

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.