Evidence map›Paper›PMID 30618605›Full record

ReviewFrontiers in molecular neuroscience2018

Yeast Models of Prion-Like Proteins That Cause Amyotrophic Lateral Sclerosis Reveal Pathogenic Mechanisms.

Zachary T Monahan, Shannon N Rhoads, Debra S Yee, Frank P Shewmaker

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Invertebrate genetic models of amyotrophic lateral sclerosis.Frontiers in molecular neuroscience · 2024
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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

4 authors at 1 institution in 1 country.

Zachary T MonahanDepartment of Pharmacology and Molecular Therapeutics, Uniformed Services University, Bethesda, MD, United States.
Shannon N RhoadsDepartment of Pharmacology and Molecular Therapeutics, Uniformed Services University, Bethesda, MD, United States.
Debra S YeeDepartment of Pharmacology and Molecular Therapeutics, Uniformed Services University, Bethesda, MD, United States.
Frank P ShewmakerDepartment of Pharmacology and Molecular Therapeutics, Uniformed Services University, Bethesda, MD, United States.
Uniformed Services University of the Health Sciences · US

Funding

Turning off the molecular switch for pathological self-assembly of FUSR01GM118530 · NIGMS · BROWN UNIVERSITY · PI FAWZI, NICOLAS LUX · 2016 to 2020
$1.6M
Using naturally-occurring fungal prions as models of neurodegenerative protein misfoldingR35GM119790 · NIGMS · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI FENG, YUANYI · 2016 to 2020
$1.4M
NIGMS NIH HHS R01 GM118530NIGMS NIH HHS R35 GM119790
6 · The paper itself

Abstract

Many proteins involved in the pathogenic mechanisms of amyotrophic lateral sclerosis (ALS) are remarkably similar to proteins that form prions in the yeast

Indexed as

ALSamyloidEWSR1FUSHNRNPA2B1prionTAF15TDP-43

Identifiers

PMID30618605
PMCPMC6297178
OpenAlexW2904732035

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.