Publications dans lesquelles il/elle collabore avec JUAN MANUEL FERNANDEZ COSTA (17)

2024

  1. Taurine activates the AKT-mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy

    Disease models & mechanisms, Vol. 17, Núm. 4

2023

  1. BlockmiR AONs as Site-Specific Therapeutic MBNL Modulation in Myotonic Dystrophy 2D and 3D Muscle Cells and HSALR Mice

    Pharmaceutics, Vol. 15, Núm. 4

2021

  1. Bioengineered in vitro 3D model of myotonic dystrophy type 1 human skeletal muscle

    Biofabrication, Vol. 13, Núm. 3

  2. Inhibition of autophagy rescues muscle atrophy in a LGMDD2 Drosophila model

    FASEB Journal, Vol. 35, Núm. 10

  3. Preclinical characterization of antagomiR-218 as a potential treatment for myotonic dystrophy

    Molecular Therapy - Nucleic Acids, Vol. 26, pp. 174-191

2020

  1. Rabphilin involvement in filtration and molecular uptake in Drosophila nephrocytes suggests a similar role in human podocytes

    DMM Disease Models and Mechanisms, Vol. 13, Núm. 9

2018

  1. MiR-23b and miR-218 silencing increase Muscleblind-like expression and alleviate myotonic dystrophy phenotypes in mammalian models

    Nature Communications, Vol. 9, Núm. 1

2017

  1. Myotonic dystrophy: candidate small molecule therapeutics

    Drug Discovery Today, Vol. 22, Núm. 11, pp. 1740-1748

2016

  1. Derepressing muscleblind expression by miRNA sponges ameliorates myotonic dystrophy-like phenotypes in Drosophila

    Scientific Reports, Vol. 6

  2. Six serum miRNAs fail to validate as myotonic dystrophy type 1 biomarkers

    PLoS ONE, Vol. 11, Núm. 2

2015

  1. Increased autophagy and apoptosis contribute to muscle atrophy in a myotonic dystrophy type 1 Drosophila model

    DMM Disease Models and Mechanisms, Vol. 8, Núm. 7, pp. 679-690

2013

  1. Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients

    Human Molecular Genetics, Vol. 22, Núm. 4, pp. 704-716

  2. Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model

    DMM Disease Models and Mechanisms, Vol. 6, Núm. 1, pp. 184-196

2011

  1. Alternative splicing regulation by Muscleblind proteins: From development to disease

    Biological Reviews, Vol. 86, Núm. 4, pp. 947-958

2010

  1. A GFP-tagged muscleblind C protein isoform reporter construct

    Fly, Vol. 4, Núm. 4

  2. A conserved motif controls nuclear localization of Drosophila Muscleblind

    Molecules and Cells, Vol. 30, Núm. 1, pp. 65-70

2008

  1. Drosophila muscleblind is involved in troponin T alternative splicing and apoptosis

    PLoS ONE, Vol. 3, Núm. 2