Evidence map›Paper›PMID 36061596›Full record

ArticleFrontiers in neuroscience2022

Ascl1 phospho-site mutations enhance neuronal conversion of adult cortical astrocytes

Hussein Ghazale, EunJee Park, Lakshmy Vasan, James Mester, Fermisk Saleh, Andrea Trevisiol, Dawn Zinyk, Vorapin Chinchalongporn, Mingzhe Liu, Taylor Fleming and 7 more

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
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  8. Review
  9. Article
  10. Article
  11. Article
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  15. Article
  16. Review
  17. Insights and applications of direct neuronal reprogramming.Current opinion in genetics & development · 2023
    Review
  18. Article
  19. Review
  20. Neuroplasticity and regeneration after spinal cord injury.North American Spine Society journal · 2023
    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

17 authors.

Hussein GhazaleSunnybrook Research Institute, Toronto, ON, Canada.
EunJee ParkSunnybrook Research Institute, Toronto, ON, Canada.
Lakshmy VasanSunnybrook Research Institute, Toronto, ON, Canada.
James MesterSunnybrook Research Institute, Toronto, ON, Canada.
Fermisk SalehSunnybrook Research Institute, Toronto, ON, Canada.
Andrea TrevisiolSunnybrook Research Institute, Toronto, ON, Canada.
Dawn ZinykSunnybrook Research Institute, Toronto, ON, Canada.
Vorapin ChinchalongpornSunnybrook Research Institute, Toronto, ON, Canada.
Mingzhe LiuSunnybrook Research Institute, Toronto, ON, Canada.
Taylor FlemingSunnybrook Research Institute, Toronto, ON, Canada.
Oleksandr ProkopchukSunnybrook Research Institute, Toronto, ON, Canada.
Natalia KleninDepartment of Medical Genetics, Cumming School of Medicine, Hotchkiss Brain Institute, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.
Deborah KurraschDepartment of Medical Genetics, Cumming School of Medicine, Hotchkiss Brain Institute, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.
Maryam FaizDepartment of Surgery, University of Toronto, Toronto, ON, Canada.
Bojana StefanovicSunnybrook Research Institute, Toronto, ON, Canada.
JoAnne McLaurinSunnybrook Research Institute, Toronto, ON, Canada.
Carol SchuurmansSunnybrook Research Institute, Toronto, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Direct neuronal reprogramming, the process whereby a terminally differentiated cell is converted into an induced neuron without traversing a pluripotent state, has tremendous therapeutic potential for a host of neurodegenerative diseases. While there is strong evidence for astrocyte-to-neuron conversion

Indexed as

adeno-associated virusastrocytescerebral cortexglial fibrillary acidic proteininduced neuronneuronal reprogrammingphospho-site mutationsproneural bHLH transcription factors

Identifiers

PMID36061596
PMCPMC9434350

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.