Evidence map›Paper›PMID 41948612›Full record

ArticleFrontiers in neurology

Seizures, increased interhemispheric synchrony, altered brain transcriptomics and a leaky blood-brain barrier result from loss of

Sulagna Banerjee, Cabriana W Earl, Samuel C Robson, Paul Szyszka, Caroline W Beck

Abstract read
In one paragraph

Article in Frontiers in neurology. 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. 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

5 authors.

Sulagna BanerjeeDepartment of Zoology, University of Otago, Dunedin, New Zealand.
Cabriana W EarlDepartment of Zoology, University of Otago, Dunedin, New Zealand.
Samuel C RobsonInstitute of Life Sciences and Healthcare, School of Medicine, Pharmacy and Biomedical Sciences, University of Portsmouth, Portsmouth, United Kingdom.
Paul SzyszkaDepartment of Zoology, University of Otago, Dunedin, New Zealand.
Caroline W BeckDepartment of Zoology, University of Otago, Dunedin, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Loss-of-function variants in AP3B2, a neuronal adaptor protein required for synaptic vesicle formation, cause a severe early-onset neurodevelopmental epilepsy known as Developmental and Epileptic Encephalopathy 48 (DEE48). Methods: To investigate how AP3B2 loss alters brain development, leading to increased seizure susceptibility, we generated a Results: Conclusion: Our results suggest that traditional anti-seizure medications designed to alter ion transport and GABA metabolism could be augmented with drugs targeting neuroinflammation, as adjunct seizure control options in infants with DEE48.

Indexed as

AP3B2CRISPRdevelopmental and epileptic encephalopathyGABA pathwayGCaMP6smodel organismseizureXenopus laevis

Identifiers

PMID41948612
PMCPMC13050717

What Socratic holds

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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 Socratic graph.