Evidence map›Paper›PMID 33724077›Full record

ArticleSLAS discovery : advancing life sciences R & D2021

High-Throughput Phenotypic Assay for Compounds That Influence Mitochondrial Health Using iPSC-Derived Human Neurons.

Courtney MacMullen, Ronald L Davis

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Courtney MacMullenDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL, USA.
Ronald L DavisDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL, USA.
Scripps Research Institute · US

Funding

Suite of high content assays for mitochondrial dynamics in neuronsR01MH109957 · NIMH · SCRIPPS FLORIDA · PI DAVIS, RONALD L · 2016 to 2019
$2.9M
NIMH NIH HHS R01 MH109957
6 · The paper itself

Abstract

There is a critical need to develop high-throughput assays to identify compounds that offer therapy for individuals suffering from neurodegenerative diseases. Most brain disorders, including neurodegenerative diseases, share the common neuropathology of mitochondria dysfunction, which can lead to apoptosis of neurons, overproduction of reactive oxygen species (ROS), and other cellular neuropathologies characteristic of these diseases. Human induced pluripotent stem cells (iPSCs) with a stable genomic insertion of the

Indexed as

Biological AssayCell DifferentiationCells, CulturedGenes, MitochondrialGene TargetingHigh-Throughput Screening AssaysHumansInduced Pluripotent Stem CellsMitochondriaMitochondrial DiseasesMitochondrial DynamicsNeurodegenerative DiseasesNeuronsPhenotypehigh-throughput assayhuman neuroniPSCmitochondria

Identifiers

PMID33724077
PMCPMC8525616
OpenAlexW3139313316

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.