Evidence map›Paper›PMID 33083017›Full record

ArticleCell death discovery2020

A defined N6-methyladenosine (m

Brandon J Gheller, Jamie E Blum, Ern Hwei Hannah Fong, Olga V Malysheva, Benjamin D Cosgrove, Anna E Thalacker-Mercer

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 74 citations in OpenAlex.

  1. The role of mNaunyn-Schmiedeberg's archives of pharmacology · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. YTHDC1-Mediated mJournal of agricultural and food chemistry · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Effect of mAnimals : an open access journal from MDPI · 2025
    Article
  13. IncreasedInternational journal of molecular sciences · 2025
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Epigenetics of Skeletal Muscle Atrophy.International journal of molecular sciences · 2024
    Review
  19. Epigenetic control of skeletal muscle atrophy.Cellular & molecular biology letters · 2024
    Review
  20. Article
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

6 authors at 2 institutions in 1 country.

Brandon J GhellerDivision of Nutritional Sciences, Cornell University, Ithaca, NY USA.
Jamie E BlumDivision of Nutritional Sciences, Cornell University, Ithaca, NY USA.
Ern Hwei Hannah FongMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY USA.
Olga V MalyshevaDivision of Nutritional Sciences, Cornell University, Ithaca, NY USA.
Benjamin D CosgroveMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY USA.
Anna E Thalacker-MercerDivision of Nutritional Sciences, Cornell University, Ithaca, NY USA.
Cornell University · USUniversity of Alabama at Birmingham · US

Funding

Revealing muscle stem cell heterogeneity in mice and humans through deep single-cell analysisR01AG058630 · NIA · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2018 to 2022
$2.9M
In Vivo Optical and MicroCT Imaging Instruments for the Cornell BRC Imaging FacilityS10OD025049 · OD · CORNELL UNIVERSITY · PI WILLIAMS, REBECCA M · 2018 to 2018
$750k
Combinatorial biomimetic systems to enable high-throughput evaluation and expansion of genome-edited dystrophic muscle stem cellsR21AR072265 · NIAMS · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2018 to 2019
$397k
NIAMS NIH HHS R21 AR072265NIA NIH HHS R01 AG058630NIH HHS S10 OD025049
6 · The paper itself

Abstract

Muscle-specific adult stem cells (MuSCs) are required for skeletal muscle regeneration. To ensure efficient skeletal muscle regeneration after injury, MuSCs must undergo state transitions as they are activated from quiescence, give rise to a population of proliferating myoblasts, and continue either to terminal differentiation, to repair or replace damaged myofibers, or self-renewal to repopulate the quiescent population. Changes in MuSC/myoblast state are accompanied by dramatic shifts in their transcriptional profile. Previous reports in other adult stem cell systems have identified alterations in the most abundant internal mRNA modification, N6-methyladenosine (m

Indexed as

Muscle stem cellsStem-cell differentiationTranscriptomics

Identifiers

PMID33083017
PMCPMC7524727
OpenAlexW3089770012

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.