publicaciones seleccionadas artículo académico Expression of protein disulfide isomerase A3Q481K variant associated with amyotrophic lateral sclerosis triggers disease features in mice. NEUROBIOLOGY OF DISEASE. 212. 2025 Protein disulfide isomerase ERp57 protects early muscle denervation in experimental ALS. ACTA NEUROPATHOLOGICA COMMUNICATIONS. 9(1). 2021 Transport and Secretion of the Wnt3 Ligand by Motor Neuron-like Cells and Developing Motor Neurons. BIOMOLECULES. 11(12). 2021 The Mouse Levator Auris Longus Muscle: An Amenable Model System to Study the Role of Postsynaptic Proteins to the Maintenance and Regeneration on the Neuromuscular Synapse. FRONTIERS IN CELLULAR NEUROSCIENCE. 14. 2020 Efficient gene transfer into primary muscle cells to analyze nerve-independent postsynaptic organization in vitro. NEUROMUSCULAR DISORDERS. 29(7):533-545. 2019 The p75(NTR) neurotrophin receptor is required to organize the mature neuromuscular synapse by regulating synaptic vesicle availability. ACTA NEUROPATHOLOGICA COMMUNICATIONS. 7(1):1-18. 2019 Physical nanocomposite hydrogels filled with low concentrations of TiO2 nanoparticles: Swelling, networks parameters and cell retention studies. MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS. 92:769-778. 2018 ALS-linked protein disulfide isomerase variants cause motor dysfunction. EMBO JOURNAL. 35(8):845-865. 2016