Evidence map›Paper›PMID 34707482›Full record

ArticleFrontiers in cellular neuroscience2021

Neuronal NMNAT2 Overexpression Does Not Achieve Significant Neuroprotection in Experimental Autoimmune Encephalomyelitis/Optic Neuritis.

Pingting Liu, Haoliang Huang, Fang Fang, Liang Liu, Liang Li, Xue Feng, Wei Chen, Roopa Dalal, Yang Sun, Yang Hu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2021. 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
0.6field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Mitochondrial behavior when things go wrong in the axon.Frontiers in cellular neuroscience · 2022
    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

10 authors at 2 institutions in 2 countries.

Pingting LiuDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Haoliang HuangDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Fang FangDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Liang LiuDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Liang LiDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Xue FengDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Wei ChenDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Roopa DalalDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Yang SunDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Yang HuDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA, United States.
Stanford University · USSecond Xiangya Hospital of Central South University · CN

Funding

Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Jeffrey L Goldberg · 2017 to 2026
$8.0M
Elucidating Neuron-Intrinsic Molecular Mechanisms of Optic Nerve RegenerationR01EY024932 · NEI · TEMPLE UNIV OF THE COMMONWEALTH · PI Yang Hu · 2015 to 2026
$4.8M
Neuroprotection by Modulating ER Stress in GlaucomaR01EY023295 · NEI · TEMPLE UNIV OF THE COMMONWEALTH · PI HU, YANG · 2013 to 2022
$3.8M
Developing Novel Neuroprotective Strategies for EAE/Optic NeuritisR01EY028106 · NEI · STANFORD UNIVERSITY · PI HU, YANG · 2018 to 2021
$1.9M
Development and Characterization of Silicone Oil-Induced Reversible Ocular Hypertension Glaucoma Model R21EY031063 · NEI · STANFORD UNIVERSITY · PI HU, YANG · 2019 to 2019
$324k
NEI NIH HHS P30 EY026877NEI NIH HHS R01 EY023295NEI NIH HHS R01 EY024932NEI NIH HHS R01 EY028106NEI NIH HHS R21 EY031063
6 · The paper itself

Abstract

Optic neuritis, inflammation, and demyelination of the optic nerve (ON), is one of the most common clinical manifestations of multiple sclerosis; affected patients suffer persistent visual symptoms due to ON degeneration and secondary retinal ganglion cell (RGC) death. The mouse experimental autoimmune encephalomyelitis (EAE) model replicates optic neuritis and significant RGC soma and axon loss. Nicotinamide mononucleotide adenylyltransferases (NMNATs) are NAD

Indexed as

multiple sclerosisneurodegenerationneuroprotectionNMNAT2optic neuritis

Identifiers

PMID34707482
PMCPMC8542903
OpenAlexW3206971680

What OpenQuestion holds

Textmetadata
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.