Evidence map›Paper›PMID 39068495›Full record

ArticleNeural development2024

A zebrafish gephyrinb mutant distinguishes synaptic and enzymatic functions of Gephyrin.

Emma J Brennan, Kelly R Monk, Jiaxing Li

Abstract read
In one paragraph

Article in Neural development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

3 authors.

Emma J BrennanVollum Institute, Oregon Health & Science University, Portland, OR, USA.
Kelly R MonkVollum Institute, Oregon Health & Science University, Portland, OR, USA.
Jiaxing LiVollum Institute, Oregon Health & Science University, Portland, OR, USA. jiaxingli2024@gmail.com.

Funding

Mechanisms of neuron-oligodendrocyte precursor cell interactionsR21NS120650 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MONK, KELLY R · 2021 to 2022
$424k
NINDS NIH HHS 1R21NS120650NINDS NIH HHS R21 NS120650
6 · The paper itself

Abstract

Gephyrin is thought to play a critical role in clustering glycine receptors at synapses within the central nervous system (CNS). The main in vivo evidence for this comes from Gephyrin (Gphn)-null mice, where glycine receptors are depleted from synaptic regions. However, these mice die at birth, possibly due to impaired molybdenum cofactor (MoCo) synthesis, an essential role Gephyrin assumes throughout an animal. This complicates the interpretation of synaptic phenotypes in Gphn-null mice and raises the question whether the synaptic and enzymatic functions of Gephyrin can be investigated separately. Here, we generated a gephyrinb zebrafish mutant, vo84, that almost entirely lacks Gephyrin staining in the spinal cord. gephyrinb

Indexed as

Carrier ProteinsMembrane ProteinsMutationSpinal CordSynapsesZebrafishAnimalsAnimals, Genetically ModifiedMolybdenum CofactorsMotor ActivityMyelin SheathNeuronsPteridinesReceptors, GlycineZebrafish ProteinsCarrier ProteinsgephyrinMembrane ProteinsMolybdenum CofactorsmolybdopterinPteridinesReceptors, GlycineZebrafish ProteinsGephyrinGlycine receptorMolybdenum cofactor (MoCo)RheotaxisSynapseZebrafish

Identifiers

PMID39068495
PMCPMC11282723

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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.