Evidence map›Paper›PMID 33107823›Full record

ArticleeLife2020

SARM1 depletion rescues NMNAT1-dependent photoreceptor cell death and retinal degeneration.

Yo Sasaki, Hiroki Kakita, Shunsuke Kubota, Abdoulaye Sene, Tae Jun Lee, Norimitsu Ban, Zhenyu Dong, Joseph B Lin, Sanford L Boye, Aaron DiAntonio and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. A Role for SARM1 in Photoreceptor Cell Death.Advances in experimental medicine and biology · 2025
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Expression of NMNAT1 in the photoreceptors is sufficient to preventMolecular therapy. Methods & clinical development · 2023
    Article
  17. SARM1 detection in myelinating glia:Frontiers in cellular neuroscience · 2023
    Article
  18. A duplex structure of SARM1 octamers stabilized by a new inhibitor.Cellular and molecular life sciences : CMLS · 2022
    Article
  19. Article
  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

13 authors at 2 institutions in 2 countries.

Yo SasakiDepartment of Genetics, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0003-0024-0031
Hiroki KakitaDepartment of Genetics, Washington University School of Medicine, St. Louis, United States.
Shunsuke KubotaDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.
Abdoulaye SeneDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.
Tae Jun LeeDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0003-2699-2573
Norimitsu BanDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.
Zhenyu DongDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.
Joseph B LinDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0001-6667-9018
Sanford L BoyeDepartment of Pediatrics, Powell Gene Therapy Center, Gainesville, United States.ORCID 0000-0002-8803-9369
Aaron DiAntonioDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0002-7262-0968
Shannon E BoyeDepartment of Pediatrics, Division of Cellular and Molecular Therapy, Gainesville, United States.ORCID 0000-0002-7312-3197
Rajendra S ApteDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0003-2281-2336
Jeffrey MilbrandtDepartment of Genetics, Washington University School of Medicine, St. Louis, United States.
Washington University in St. Louis · USAichi Medical University · JP

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
PHYSIOLOGY AND GENETICS OF THE GDNF HOMOLOG NEURTURINR01AG013730 · NIA · WASHINGTON UNIVERSITY · PI JEFFREY D MILBRANDT · 1996 to 2026
$10.6M
Engineering AAV for safe and efficient gene delivery to the human retinaR01EY024280 · NEI · UNIVERSITY OF FLORIDA · PI Shannon Elizabeth Boye · 2014 to 2026
$7.5M
DISSECTION OF SARM1-INDUCED AXON DEGENERATION AND CELL DEATHR01NS087632 · NINDS · WASHINGTON UNIVERSITY · PI Aaron Diantonio, JEFFREY D MILBRANDT · 2014 to 2026
$6.4M
THE IMPORTANCE OF MACROPHAGE SENESCENCE IN REGULATING ANGIOGENESIS IN THE EYER01EY019287 · NEI · WASHINGTON UNIVERSITY · PI APTE, RAJENDRA S · 2010 to 2021
$3.9M
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
Compromised LDH activity causes motor deficits and hastens ALS progressionR56AG013730 · NIA · WASHINGTON UNIVERSITY · PI MILBRANDT, JEFFREY D · 2022 to 2022
$503k
NCI NIH HHS CA219866NCI NIH HHS R01 CA219866NEI NIH HHS EY019287-06NEI NIH HHS R01 EY019287NEI NIH HHS R01 EY024280NIA NIH HHS AG013730NIA NIH HHS R01 AG013730NIA NIH HHS R56 AG013730NIA NIH HHS RF1 AG013730NIDDK NIH HHS P30 DK020579NIGMS NIH HHS T32 GM007200NINDS NIH HHS NS087632NINDS NIH HHS R01 NS087632
6 · The paper itself

Abstract

Leber congenital amaurosis type nine is an autosomal recessive retinopathy caused by mutations of the NAD

Indexed as

Cell DeathAnimalsArmadillo Domain ProteinsCytoskeletal ProteinsDisease Models, AnimalFemaleHumansLeber Congenital AmaurosisMaleMiceNicotinamide-Nucleotide AdenylyltransferasePhotoreceptor Cells, VertebrateRetinal DegenerationArmadillo Domain ProteinsCytoskeletal ProteinsNicotinamide-Nucleotide AdenylyltransferaseNmnat1 protein, mouseSARM1 protein, mouseaxonal degenerationLCA9mouseNAD+neuroscienceNMNAT1retinal degenerationsSARM1

Identifiers

PMID33107823
PMCPMC7591247
OpenAlexW3093492129

What OpenQuestion holds

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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.