Evidence map›Paper›PMID 33616084›Full record

ReviewJCI insight2021

CNS critical periods: implications for dystonia and other neurodevelopmental disorders.

Jay Li, Sumin Kim, Samuel S Pappas, William T Dauer

Abstract readReview
In one paragraph

Review in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. More Than a Small Brain: The Importance of Studying Neural Function during Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. THAP1 modulates oligodendrocyte maturation by regulating ECM degradation in lysosomes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. 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

4 authors.

Jay LiMedical Scientist Training Program, University of Michigan, Ann Arbor, Michigan, USA.
Sumin KimCellular and Molecular Biology Graduate Program, University of Michigan, Ann Arbor, Michigan, USA.
Samuel S PappasPeter O'Donnell Jr. Brain Institute.
William T DauerPeter O'Donnell Jr. Brain Institute.

Funding

MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Development of an Animal Model of Task Specific DystoniaR01NS109227 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI DAUER, WILLIAM T. · 2020 to 2023
$1.7M
Development of an Animal Model of Task Specific DystoniaR56NS109227 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI DAUER, WILLIAM T. · 2019 to 2019
$509k
Striatal Cholinergic Interneuron Dysfunction in Dystonia PathophysiologyF31NS113433 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, JAY · 2020 to 2020
$21k
NIGMS NIH HHS T32 GM007315NIGMS NIH HHS T32 GM007863NINDS NIH HHS F31 NS113433NINDS NIH HHS R01 NS109227NINDS NIH HHS R56 NS109227
6 · The paper itself

Abstract

Critical periods are discrete developmental stages when the nervous system is especially sensitive to stimuli that facilitate circuit maturation. The distinctive landscapes assumed by the developing CNS create analogous periods of susceptibility to pathogenic insults and responsiveness to therapy. Here, we review critical periods in nervous system development and disease, with an emphasis on the neurodevelopmental disorder DYT1 dystonia. We highlight clinical and laboratory observations supporting the existence of a critical period during which the DYT1 mutation is uniquely harmful, and the implications for future therapeutic development.

Indexed as

AnimalsDisease Models, AnimalDystoniaHumansMolecular ChaperonesMutationNeurodevelopmental DisordersMolecular ChaperonesTOR1A protein, human

Identifiers

PMID33616084
PMCPMC7934928

What OpenQuestion holds

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Registered trials

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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.