Evidence map›Paper›PMID 37639584›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

AMPK-FOXO-IP3R signaling pathway mediates neurological and developmental defects caused by mitochondrial DNA mutations.

Hu Zhang, Yunan Zhu, Yuji Suehiro, Shohei Mitani, Ding Xue

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Review
  5. HAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  6. Forkhead box O proteins in chondrocyte aging and diseases.Journal of orthopaedic translation · 2025
    Review
  7. Article
  8. Article
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  11. Review
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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 2 countries.

Hu Zhang *Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309.ORCID 0009-0001-1772-2355
Yunan Zhu *Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309.ORCID 0009-0001-5933-7551
Yuji SuehiroDepartment of Physiology, Tokyo Women's Medical University, School of Medicine, Tokyo 162-8666, Japan.ORCID 0000-0002-4977-2816
Shohei MitaniDepartment of Physiology, Tokyo Women's Medical University, School of Medicine, Tokyo 162-8666, Japan.ORCID 0000-0002-5710-2425
Ding XueDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309.ORCID 0000-0002-8429-8136
University of Colorado Boulder · USTokyo Women's Medical University · JP

Funding

Fundamental mechanisms of paternal mitochondrial eliminationand radiation-induced bystander effectsR35GM118188 · NIGMS · UNIVERSITY OF COLORADO · PI DING XUE · 2016 to 2026
$6.8M
NIGMS NIH HHS R35 GM118188
6 · The paper itself

Abstract

Pathological mutations in human mitochondrial genomes (mtDNA) can cause a series of neurological, behavioral, and developmental defects, but the underlying molecular mechanisms are poorly understood. We show here that the energy-sensing adenosine monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway plays a key role in mediating similar defects caused by different mtDNA mutations in

Indexed as

AMP-Activated Protein KinasesCaenorhabditis elegansAdenosine TriphosphateAnimalsDNA, MitochondrialEmbryo LossFemaleHumansMutationPregnancySignal TransductionAdenosine TriphosphateAMP-Activated Protein KinasesDNA, MitochondrialAMP-activated protein kinaseCaenorhabditis eleganscalcium homeostasismitochondrial genome mutationsneurological and developmental defects

Identifiers

PMID37639584
PMCPMC10483642
OpenAlexW4386212776

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.