Evidence map›Paper›PMID 40227275›Full record

ReviewBiotech (Basel (Switzerland))2025

STXBP1 Syndrome: Biotechnological Advances, Challenges, and Perspectives in Gene Therapy, Experimental Models, and Translational Research.

Silvestre Ruano-Rodríguez, Mar Navarro-Alonso, Benito Domínguez-Velasco, Manuel Álvarez-Dolado, Francisco J Esteban

Abstract readReview
In one paragraph

Review in Biotech (Basel (Switzerland)), 2025. 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.

  1. Article
  2. Review
  3. Cognitive and Motor Dysfunction in STXBP1 R406H Mice.Journal of molecular neuroscience : MN · 2026
    Article
  4. 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.

Silvestre Ruano-RodríguezAndalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), CSIC-US-JA-UPO, Américo Vespuccio Avenue 24, Cartuja Scientific and Technological Park, 41092 Seville, Spain.
Mar Navarro-AlonsoAndalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), CSIC-US-JA-UPO, Américo Vespuccio Avenue 24, Cartuja Scientific and Technological Park, 41092 Seville, Spain.ORCID 0000-0002-2559-9131
Benito Domínguez-VelascoAndalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), CSIC-US-JA-UPO, Américo Vespuccio Avenue 24, Cartuja Scientific and Technological Park, 41092 Seville, Spain.ORCID 0009-0002-0621-650X
Manuel Álvarez-DoladoAndalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), CSIC-US-JA-UPO, Américo Vespuccio Avenue 24, Cartuja Scientific and Technological Park, 41092 Seville, Spain.ORCID 0000-0002-0655-8289
Francisco J EstebanSystems Biology Unit, Department of Experimental Biology, University of Jaén, Campus Las Lagunillas s/n, 23071 Jaén, Spain.ORCID 0000-0002-7135-2973

Funding

Agencia Estatal de Investigación PID2021-127044OB-I00Junta de Andalucía BIO-302Ministerio de Ciencia, Innovación y Universidades RTI2018-099768-B-100Universidad de Jaén PAIUJA-EI_CTS02_2023
6 · The paper itself

Abstract

STXBP1 syndrome is a severe early-onset epileptic encephalopathy characterized by developmental delay and intellectual disability. This review addresses key challenges in STXBP1 syndrome research, focusing on advanced therapeutic approaches and experimental models. We explore gene therapy strategies, including CRISPR-Cas9, adeno-associated viral (AAV) vectors, and RNA therapies such as antisense oligonucleotides (ASOs), aimed at correcting STXBP1 genetic dysfunctions. This review presents in vivo and in vitro models, highlighting their contributions to understanding disease mechanisms. Additionally, we provide a proposal for a detailed bioinformatic analysis of a Spanish cohort of 41 individuals with STXBP1-related disorders, offering insights into specific mutations and their biological implications. Clinical and translational perspectives are discussed, emphasizing the potential of personalized medicine approaches. Future research directions and key challenges are outlined, including the identification of STXBP1 interactors, unexplored molecular pathways, and the need for clinically useful biomarkers. This comprehensive review underscores the complexity of STXBP1-related infantile epileptic encephalopathy and opens new avenues for advancing the understanding and treatment of this heterogeneous disease.

Indexed as

antisense oligonucleotidesbioinformaticsepilepsygene and cell therapygenomicshaploinsufficiencyinduced pluripotent stem cellsinfantile epileptic encephalopathymurine modelspersonalized medicineSTXBP1

Identifiers

PMID40227275
PMCPMC11939967

What OpenQuestion 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 OpenQuestion graph.