Evidence map›Paper›PMID 35511030›Full record

ArticleeLife2022

Katelyn J Hoff, Jayne E Aiken, Mark A Gutierrez, Santos J Franco, Jeffrey K Moore

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Missense variants in TUBA4A cause myo-tubulinopathies.Brain : a journal of neurology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Mechanisms of microtubule dynamics from single-molecule measurements.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Culturing Primary Cortical Neurons for Live-Imaging.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  10. Article
  11. Case report: Structural brain abnormalities inFrontiers in pediatrics · 2023
    Article
  12. MAPping tubulin mutations.Frontiers in cell and developmental biology · 2023
    Review
  13. Article
  14. Article
  15. Review
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.

Katelyn J HoffDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, United States.ORCID 0000-0002-2678-1859
Jayne E AikenDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, United States.
Mark A GutierrezDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, United States.
Santos J FrancoDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, United States.
Jeffrey K MooreDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, United States.ORCID 0000-0003-3262-3248
University of Colorado Anschutz Medical Campus · US

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Predoctoral Training Program in Molecular and Cellular Biology (Supplement: Mentoring in the Research Environment)T32GM136444 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI MICHAEL A MCMURRAY, Rytis Prekeris · 2020 to 2026
$3.7M
Beyond the tubulin code: Understanding how subunit diversity regulates the formation and function of microtubulesR35GM136253 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI MOORE, JEFFREY KYLE · 2020 to 2024
$2.1M
NCATS NIH HHS UL1 TR002535NIGMS NIH HHS R35 GM136253NIGMS NIH HHS T32 GM136444
6 · The paper itself

Abstract

Heterozygous, missense mutations in α- or β-tubulin genes are associated with a wide range of human brain malformations, known as tubulinopathies. We seek to understand whether a mutation's impact at the molecular and cellular levels scale with the severity of brain malformation. Here, we focus on two mutations at the valine 409 residue of TUBA1A, V409I, and V409A, identified in patients with pachygyria or lissencephaly, respectively. We find that ectopic expression of

Indexed as

LissencephalyTubulinAnimalsHumansMiceMicrotubule-Associated ProteinsMicrotubulesNeurogenesisNeuronsRatsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsMicrotubule-Associated ProteinsSaccharomyces cerevisiae ProteinsSTU2 protein, S cerevisiaeTUBA1A protein, humanTuba1a protein, mouseTubulinbrain developmentcell biologydevelopmental biologymicrotubulemouseratS. cerevisiaetubulintubulinopathy

Identifiers

PMID35511030
PMCPMC9236607
OpenAlexW4229018862

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.