Viviana Pérez Fernández

Sepulveda, M., Traub, F. M., Ojeda, P., Perez, V., Ojeda, J., Mella, J., … & Hetz, C. (2025). Expression of protein disulfide isomerase A3Q481K variant associated with amyotrophic lateral sclerosis triggers disease features in mice. Neurobiology of disease, 212. Doi: 10.1016/j.nbd.2025.106947

 

Rozas, P., Pinto, C., Traub, F. M., Díaz, R., Pérez, V., Becerra, D., … & Medinas, D. B. (2021). Protein disulfide isomerase ERp57 protects early muscle denervation in experimental ALS. Acta neuropathologica communications, 9(1), 21. Doi: 10.1186/s40478-020-01116-z

 

Pinto, C., Pérez, V., Mella, J., Albistur, M., Caprile, T., Bronfman, F. C., & Henríquez, J. P. (2021). Transport and Secretion of the Wnt3 Ligand by Motor Neuron-like Cells and Developing Motor Neurons. Biomolecules, 11(12), 1898. Doi: 10.3390/biom11121898

 

Ojeda, J., Bermedo-García, F., Pérez, V., Mella, J., Hanna, P., Herzberg, D., … & Henríquez, J. P. (2020). The Mouse Levator Auris Longus Muscle: An Amenable Model System to Study the Role of Postsynaptic Proteins to the Maintenance and Regeneration of the Neuromuscular Synapse. Frontiers in Cellular Neuroscience, 14, 225. Doi: 10.3389/fncel.2020.00225

 

Mella, J., Pérez, V., Zelada, D., Moreno, N., Ionescu, A., Perlson, E., & Henríquez, J. P. (2019). Efficient gene transfer into primary muscle cells to analyse nerve-independent postsynaptic organization in vitro. Neuromuscular Disorders, 29(7), 533-545. doi: 10.1016/j.nmd.2019.05.005

 

Pérez, V., Bermedo-Garcia, F., Zelada, D., Pérez, M. Á., Fuenzalida, M., Ábrigo, J., … & Hetz, C. (2019). The p75 NTR neurotrophin receptor is required to organize the mature neuromuscular synapse by regulating synaptic vesicle availability. Acta neuropathologica communications, 7(1), 147. doi: 10.1186/s40478-019-0802-7

Toledo, L., Racine, L., Pérez, V., Henríquez, J. P., Auzely-Velty, R., & Urbano, B. F. (2018). Physical nanocomposite hydrogels filled with low concentrations of TiO2 nanoparticles: Swelling, networks parameters and cell retention studies. Materials Science and Engineering: C, 92, 769-778. doi: 10.1016/j.msec.2018.07.024

 

Woehlbier, U., Colombo, A., Saaranen, M. J., Pérez, V., Ojeda, J., Bustos, F. J., . . . Hetz, C. (2016). ALS-linked protein disulfide isomerase variants cause motor dysfunction. The EMBO Journal, 35(8), 845-865. doi:10.15252/embj.201592224