Evidence map›Paper›PMID 39100309›Full record

ArticleACS omega2024

Bioluminescent Assay for the Quantification of Cellular Glycogen Levels.

Donna Leippe, Rebeca Choy, Gediminas Vidugiris, Hanne Merritt, Kevin T Mellem, David T Beattie, Julie C Ullman, Jolanta Vidugiriene

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review of in vitro approaches for assessing the toxicity of chemical stressors across diverse physiological systems.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    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

8 authors.

Donna LeippeResearch and Development, Promega Corporation, Madison, Wisconsin 53711, United States.ORCID https://orcid.org/0009-0008-3234-914X
Rebeca ChoyMaze Therapeutics, South San Francisco, California 94080, United States.
Gediminas VidugirisResearch and Development, Promega Corporation, Madison, Wisconsin 53711, United States.
Hanne MerrittMaze Therapeutics, South San Francisco, California 94080, United States.
Kevin T MellemMaze Therapeutics, South San Francisco, California 94080, United States.
David T BeattieMaze Therapeutics, South San Francisco, California 94080, United States.
Julie C UllmanMaze Therapeutics, South San Francisco, California 94080, United States.ORCID https://orcid.org/0000-0003-1325-0650
Jolanta VidugirieneResearch and Development, Promega Corporation, Madison, Wisconsin 53711, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycogen is a large polymer of glucose that functions as an important means of storing energy and maintaining glucose homeostasis. Glycogen synthesis and degradation pathways are highly regulated and their dysregulation can contribute to disease. Glycogen storage diseases are a set of disorders that arise from improper glycogen metabolism. Glycogen storage disease II, known as Pompe disease, is caused by a genetic mutation that leads to increased glycogen storage in cells and tissues, resulting in progressive muscle atrophy and respiratory decline for patients. One approach for treating Pompe disease is to reduce glycogen levels by interfering with the glycogen synthesis pathway through glycogen synthase inhibitors. To facilitate the study of glycogen synthase inhibitors in biological samples, such as cultured cells, a high-throughput approach for measuring cellular glycogen was developed. A bioluminescent glycogen detection assay was automated and used to measure the glycogen content in cells grown in 384-well plates. The assay successfully quantified reduced glycogen stores in cells treated with a series of glycogen synthase 1 inhibitors, validating the utility of the assay for drug screening efforts and demonstrating its value for therapy development and glycogen metabolism research.

Identifiers

PMID39100309
PMCPMC11292620

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.