Evidence map›Paper›PMID 40129245›Full record

ReviewChannels (Austin, Tex.)2025

Exploring the potential for gene therapy in Cav1.4-related retinal channelopathies.

Matthias Ganglberger, Alexandra Koschak

Abstract readReview
In one paragraph

Review in Channels (Austin, Tex.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Matthias GanglbergerPharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-6852-9523
Alexandra KoschakPharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-5758-1166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The visual process begins with photon detection in photoreceptor outer segments within the retina, which processes light signals before transmission to the thalamus and visual cortex. Cav1.4 L-type calcium channels play a crucial role in this process, and dysfunction of these channels due to pathogenic variants in corresponding genes leads to specific manifestations in visual impairments. This review explores the journey from basic research on Cav1.4 L-type calcium channel complexes in retinal physiology and pathophysiology to their potential as gene therapy targets. Moreover, we provide a concise overview of key findings from studies using different animal models to investigate retinal diseases. It will critically examine the constraints these models present when attempting to elucidate retinal channelopathies. Additionally, the paper will explore potential strategies for addressing Cav1.4 channel dysfunction and discuss the current challenges facing gene therapy approaches in this area of research.

Indexed as

Calcium Channels, L-TypeChannelopathiesGenetic TherapyRetinaRetinal DiseasesAnimalsHumansCalcium Channels, L-Typegene therapyL-type calcium channelphotoreceptorribbon synapseVoltage-gated ion channel

Identifiers

PMID40129245
PMCPMC11938310

What OpenQuestion holds

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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.