Evidence map›Paper›PMID 38266764›Full record

ArticleExperimental neurology2024

Dietary NMN supplementation enhances motor and NMJ function in ALS.

Samuel Lundt, Nannan Zhang, Luis Polo-Parada, Xinglong Wang, Shinghua Ding

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Redox Molecules in Aging and Neurodegenerative Disorders.International journal of molecular sciences · 2026
    Review
  2. Article
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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

5 authors at 2 institutions in 1 country.

Samuel LundtInterdisciplinary Neuroscience Program, University of Missouri, Columbia, MO 65211, United States of America; Dalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, United States of America.
Nannan ZhangDalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, United States of America.
Luis Polo-ParadaDalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, United States of America; Department of Medical, Physiology and Pharmacology, University of Missouri, Columbia, MO 65211, United States of America.
Xinglong WangDepartment of Pharmacology & Toxicology, University of Arizona, Tucson, AZ 85721, United States of America.
Shinghua DingInterdisciplinary Neuroscience Program, University of Missouri, Columbia, MO 65211, United States of America; Dalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, United States of America; Department of Chemical and Biomedical Engineering, University of Missouri, Columbia, MO 65211, United States of America. Electronic address: dings@missouri.edu.
University of Missouri · USUniversity of Arizona · US

Funding

The Role of Gliotransmission in Cerebral IschemiaR01NS069726 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI DING, SHINGHUA · 2010 to 2022
$3.3M
Pathogenesis and motor neuron degeneration of a novel disease associated with a P158A mutation in NAMPTR01NS123023 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI Shinghua Ding · 2022 to 2026
$2.3M
THE ROLE AND MECHANISMS OF PBEF IN ACUTE BRAIN INJURY AND LONG-TERM STROKE OUTCOMES AFTER FOCAL ISCHEMIC STROKER01NS094539 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI DING, SHINGHUA · 2015 to 2019
$1.6M
A novel therapeutic approach for Alzheimer Disease (AD)R21AG080715 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI DING, SHINGHUA · 2023 to 2023
$392k
NIA NIH HHS R21 AG080715NINDS NIH HHS R01 NS069726NINDS NIH HHS R01 NS094539NINDS NIH HHS R01 NS123023
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease that causes the degeneration of motor neurons in the motor cortex and spinal cord. Patients with ALS experience muscle weakness and atrophy in the limbs which eventually leads to paralysis and death. NAD

Indexed as

Amyotrophic Lateral SclerosisNeurodegenerative DiseasesAnimalsDietary SupplementsDisease Models, AnimalHumansMiceMice, TransgenicNADNeuromuscular JunctionSuperoxide Dismutase-1NADSuperoxide Dismutase-1ALSEPPNAD+Neuromuscular junctionNMN

Identifiers

PMID38266764
PMCPMC12696721
OpenAlexW4391112828

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.