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Fatty-acid-based antimiR-23b delivery in the DMSXL model: A potential therapeutic strategy for brain dysfunction in myotonic dystrophy type 1.

Overview

Authors: Diego Piqueras-Losilla1, Andrea Garcia-Rey1, Aline Huguet-Lachon2, Argimiro Mayoral-Olmos1, Isabel Campillo1, Melanie Nufer1, Mouli Chakraborty1, Ana Díaz-Maqueda1, Nuria Barquero1, Anchel Gonzalez-Barriga2, José Martinez-Hernandez3,4, María Gracia de Garnica García5, Geneviève Gourdon2, Ruben Artero6,7,8, Beatriz Llamusí1, Estefanía Cerro-Herreros1
  1. ARTHEx Biotech. Parque Científico de la Universidad de Valencia, Calle del Catedrático Agustín Escardino Benlloch, 9, 46980 Paterna, Valencia, Spain
  2. Sorbonne Université, Inserm, Centre de Recherche en Myologie, Paris, France
  3. Fonds de Dotation Clinatec, Grenoble, France
  4. Grenoble Institute Neurosciences, Inserm, University Grenoble Alpes, Grenoble, France
  5. Micros Veterinaria S.L., León, Spain
  6. Human Translational Genomics. University Research Institute for Biotechnology and Biomedicine (BIOTECMED), Universidad de Valencia, Av. Dr. Moliner 50, 46100 Valencia, Spain
  7. INCLIVA Biomedical Research Institute, Av. Menéndez Pelayo 4 acc, 46010 Valencia, Spain
  8. CIBERER ISCIII, Av. Monforte de Lemos 3-5, 28029 Madrid, Spain
Journal: Cell reports. Medicine, volume 7, issue 8, article 102929
Dates: received 7 November 2025; accepted 24 June 2026; published online 22 July 2026; in print August 2026
Type: Research article · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1016/j.xcrm.2026.102929 · PMID 42486096 · PMCID PMC13522761 · OpenAlex W7170083443
Open access: gold, a free copy (OpenAlex)
Status: code on request
Categories: human (organism), mouse (organism), cellular / molecular (subfield)
Methods: Statistics, Physiology & signal measures
Keywords: myotonic dystrophy, antisense oligonucleotides, miR-23b, MBNL, alternative splicing, brain delivery, blood-brain barrier, CNS alterations, behavior correction, rare disease
MeSH: Brain*, MicroRNAs*, Myotonic Dystrophy*, Animals, Blood-Brain Barrier, Disease Models, Animal, DNA-Binding Proteins, Humans, Male, Mice, Mice, Transgenic, Myotonin-Protein Kinase, RNA-Binding Proteins (* major topic)
Topic: Genetic Neurodegenerative Diseases (Cellular and Molecular Neuroscience, Neuroscience), according to OpenAlex
Citations: not cited yet (Europe PMC); 90 references in the paper
Research resources: HRP-conjugated anti-GAPDH antibody RRID:AB_10847862, anti-MBNL1 antibody: for QDB assay RRID:AB_2140186, anti-NeuN antibody RRID:AB_2298772, RRID:AB_2340363, anti-MBNL1 monoclonal antibody RRID:AB_2618248, Anti-MBNL2 monoclonal antibody RRID:AB_2618250, RRID:AB_2633277, RRID:AB_2860576

Abstract

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Code

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Data

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Code and data availability statement

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Read it in the paper: doi.org/10.1016/j.xcrm.2026.102929.

Versions

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Version 2, 28 September 2026

  • Authors: added Diego Piqueras-Losilla (0009-0003-2667-234X); removed Diego Piqueras-Losilla
  • Funding: added “la Caixa” Foundation; Ministerio de Ciencia, Innovación y Universidades; Centro para el Desarrollo Tecnológico Industrial; Generalitat Valenciana; Instituto de Salud Carlos III; Agència Valenciana de la Innovació

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 16 authors, 10 keywords, 13 MeSH terms, 89 references, 8 RRIDs.

Cite

This paper

Piqueras-Losilla, D., Garcia-Rey, A., Huguet-Lachon, A., Mayoral-Olmos, A., Campillo, I., Nufer, M., Chakraborty, M., Díaz-Maqueda, A., Barquero, N., Gonzalez-Barriga, A., Martinez-Hernandez, J., de Garnica García, M. G., Gourdon, G., Artero, R., Llamusí, B., & Cerro-Herreros, E. (2026). Fatty-acid-based antimiR-23b delivery in the DMSXL model: A potential therapeutic strategy for brain dysfunction in myotonic dystrophy type 1. Cell reports. Medicine, 7(8), 102929. https://doi.org/10.1016/j.xcrm.2026.102929

BibTeX

@article{piqueraslosilla2026fatty,
author = {Piqueras-Losilla, Diego and Garcia-Rey, Andrea and Huguet-Lachon, Aline and Mayoral-Olmos, Argimiro and Campillo, Isabel and Nufer, Melanie and Chakraborty, Mouli and Díaz-Maqueda, Ana and Barquero, Nuria and Gonzalez-Barriga, Anchel and Martinez-Hernandez, José and de Garnica García, María Gracia and Gourdon, Geneviève and Artero, Ruben and Llamusí, Beatriz and Cerro-Herreros, Estefanía},
title = {{Fatty-acid-based antimiR-23b delivery in the DMSXL model: A potential therapeutic strategy for brain dysfunction in myotonic dystrophy type 1}},
journal = {Cell reports. Medicine},
year = {2026},
month = jul,
volume = {7},
number = {8},
pages = {102929},
publisher = {Elsevier},
issn = {2666-3791},
doi = {10.1016/j.xcrm.2026.102929},
url = {https://doi.org/10.1016/j.xcrm.2026.102929},
pmid = {42486096},
pmcid = {PMC13522761}
}

RIS

TY - JOUR
AU - Piqueras-Losilla, Diego
AU - Garcia-Rey, Andrea
AU - Huguet-Lachon, Aline
AU - Mayoral-Olmos, Argimiro
AU - Campillo, Isabel
AU - Nufer, Melanie
AU - Chakraborty, Mouli
AU - Díaz-Maqueda, Ana
AU - Barquero, Nuria
AU - Gonzalez-Barriga, Anchel
AU - Martinez-Hernandez, José
AU - de Garnica García, María Gracia
AU - Gourdon, Geneviève
AU - Artero, Ruben
AU - Llamusí, Beatriz
AU - Cerro-Herreros, Estefanía
TI - Fatty-acid-based antimiR-23b delivery in the DMSXL model: A potential therapeutic strategy for brain dysfunction in myotonic dystrophy type 1
T2 - Cell reports. Medicine
J2 - Cell Rep Med
PY - 2026
DA - 2026/07/22
VL - 7
IS - 8
SP - 102929
SN - 2666-3791
PB - Elsevier
DO - 10.1016/j.xcrm.2026.102929
UR - https://doi.org/10.1016/j.xcrm.2026.102929
LA - en
ER -

CSL-JSON

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