Publicaciones en colaboración con investigadores/as de Pierre and Marie Curie University (5)

2022

  1. Deciphering the Complex Molecular Pathogenesis of Myotonic Dystrophy Type 1 through Omics Studies

    International Journal of Molecular Sciences, Vol. 23, Núm. 3

  2. Moxifloxacin rescues SMA phenotypes in patient-derived cells and animal model

    Cellular and Molecular Life Sciences, Vol. 79, Núm. 8

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2020

  1. miR-7 Restores Phenotypes in Myotonic Dystrophy Muscle Cells by Repressing Hyperactivated Autophagy

    Molecular Therapy - Nucleic Acids, Vol. 19, pp. 278-292

2018

  1. RbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences

    Nature Communications, Vol. 9, Núm. 1