Evidence map›Paper›PMID 38737544›Full record

ArticleDystonia (Lausanne, Switzerland)2023

Transcriptional regulatory network for neuron-glia interactions and its implication for DYT6 dystonia.

Dhananjay Yellajoshyula

Abstract read
In one paragraph

Article in Dystonia (Lausanne, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

1 author.

Dhananjay YellajoshyulaDepartment of Neurosciences, Case Western Reserve University, Cleveland, OH, United States.

Funding

Role of DYT6 Dystonia Protein THAP1 in Oligodendroglial Mediated ECM Homeostasis During CNS DevelopmentR01NS122990 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI WILLIAM T. DAUER, Dhananjay Yellajoshyula · 2022 to 2026
$2.3M
NINDS NIH HHS R01 NS122990
6 · The paper itself

Abstract

Advances in sequencing technologies have identified novel genes associated with inherited forms of dystonia, providing valuable insights into its genetic basis and revealing diverse genetic pathways and mechanisms involved in its pathophysiology. Since identifying genetic variation in the transcription factor coding

Indexed as

dystoniamyelinationTHAP1transcriptionwhite matterYY1

Identifiers

PMID38737544
PMCPMC11087070

What OpenQuestion holds

Textmetadata
LicenceTDM
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.