Evidence map›Paper›PMID 30816177›Full record

ArticleScientific reports2019

Targeting NAD

Chi Fung Lee, Arianne Caudal, Lauren Abell, G A Nagana Gowda, Rong Tian

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

84 citing papers in PubMed, 120 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Ndufs4GeroScience · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Therapies for Mitochondrial Disease: Past, Present, and Future.Journal of inherited metabolic disease · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. NAD metabolism and heart failure: Mechanisms and therapeutic potentials.Journal of molecular and cellular cardiology · 2024
    Review

24 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Chi Fung LeeMitochondria and Metabolism Center, University of Washington, Seattle, WA, 98109, USA.
Arianne CaudalMitochondria and Metabolism Center, University of Washington, Seattle, WA, 98109, USA.
Lauren AbellMitochondria and Metabolism Center, University of Washington, Seattle, WA, 98109, USA.
G A Nagana GowdaMitochondria and Metabolism Center, University of Washington, Seattle, WA, 98109, USA.ORCID 0000-0002-0544-7464
Rong TianMitochondria and Metabolism Center, University of Washington, Seattle, WA, 98109, USA. rongtian@u.washington.edu.
University of Washington · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1986 to 2026
$41.4M
NAD+/NADH ratio, protein acetylation and mitochondrial functionR01HL110349 · NHLBI · UNIVERSITY OF WASHINGTON · PI TIAN, RONG · 2011 to 2020
$5.7M
Bioengineering Cardiovascular Training GrantT32EB001650 · NIBIB · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2004 to 2019
$3.6M
Emergent properties of signaling network degradation that mediate homeostatic failure during agingR01AG056359 · NIA · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT, VILLEN, JUDIT · 2017 to 2021
$2.9M
Mechanisms of mitochondrial disease suppression in Ndufs4 knockout miceR01NS098329 · NINDS · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT, VILLEN, JUDIT · 2017 to 2021
$2.4M
Mitochondrial function and glycolytic switch in pathological cardiac hypertrophyR01HL142628 · NHLBI · UNIVERSITY OF WASHINGTON · PI TIAN, RONG · 2018 to 2021
$2.4M
American Heart Association-American Stroke Association 13POST16200007NHLBI NIH HHS R01 HL110349NHLBI NIH HHS R01 HL142628NIA NIH HHS R01 AG056359NIBIB NIH HHS T32 EB001650NIDDK NIH HHS P30 DK017047NINDS NIH HHS R01 NS098329
6 · The paper itself

Abstract

Leigh syndrome is a mitochondrial disease characterized by neurological disorders, metabolic abnormality and premature death. There is no cure for Leigh syndrome; therefore, new therapeutic targets are urgently needed. In Ndufs4-KO mice, a mouse model of Leigh syndrome, we found that Complex I deficiency led to declines in NAD

Indexed as

AnimalsBrainDisease Models, AnimalElectron Transport Complex IFemaleLeigh DiseaseLongevityMaleMiceMice, KnockoutMitochondriaMolecular Targeted TherapyNADNicotinamide MononucleotideElectron Transport Complex INADNdufs4 protein, mouseNicotinamide Mononucleotide

Identifiers

PMID30816177
PMCPMC6395802
OpenAlexW2916497674

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.