Pascual Sanz
Affiliations: | Instituto de Biomedicina de Valencia, València, Comunidad Valenciana, Spain |
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Parents
Sign in to add mentor| Enrique Herrero Perpiñán | grad student | University of Valencia, Spain | |
| Rafael Sentandreu Ramón | grad student | University of Valencia, Spain | |
| Marian Carlson | post-doc | (Microtree) | |
| David Meyer | post-doc |
Children
Sign in to add trainee| Teresa Rubio | grad student | IDIBELL | |
| Carla Rubio-Villena | grad student | European University of Madrid | |
| Carmen Munoz-Ballester | grad student | 2012-2017 | Instituto de Biomedicina de Valencia |
| Carlos Romá Mateo | post-doc | University of Valencia, Spain | |
| Eva Pérez-Jiménez | post-doc | Instituto de Biomedicina de Valencia | |
| Santiago Vernia | post-doc | MRC Clinical Sciences Center, Imperial College | |
| Rosa Viana | post-doc | Instituto de Biomedicina de Valencia | |
| Maria Adelaida García-Gimeno | research scientist | Universidad Politécnica de Valencia |
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Publications
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| Rubio T, Campos-Rodríguez Á, Sanz P. (2023) Beneficial Effect of Fingolimod in a Lafora Disease Mouse Model by Preventing Reactive Astrogliosis-Derived Neuroinflammation and Brain Infiltration of T-lymphocytes. Molecular Neurobiology |
| Moreno-Estellés M, Campos-Rodríguez Á, Rubio-Villena C, et al. (2023) Deciphering the Polyglucosan Accumulation Present in Lafora Disease Using an Astrocytic Cellular Model. International Journal of Molecular Sciences. 24 |
| Rubio T, Viana R, Moreno-Estellés M, et al. (2022) TNF and IL6/Jak2 signaling pathways are the main contributors of the glia-derived neuroinflammation present in Lafora disease, a fatal form of progressive myoclonus epilepsy. Neurobiology of Disease. 176: 105964 |
| Vela M, García-Gimeno MA, Sanchis A, et al. (2021) Neuroprotective Effect of IND1316, an Indole-Based AMPK Activator, in Animal Models of Huntington Disease. Acs Chemical Neuroscience |
| Brewer MK, Machio-Castello M, Viana R, et al. (2021) An empirical pipeline for personalized diagnosis of Lafora disease mutations. Iscience. 24: 103276 |
| Kumarasinghe L, Xiong L, Garcia-Gimeno MA, et al. (2021) TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases. Cells. 10 |
| Perez-Jimenez E, Viana R, Muñoz-Ballester C, et al. (2020) Endocytosis of the glutamate transporter 1 is regulated by laforin and malin: Implications in Lafora disease. Glia |
| Sanz P, Garcia-Gimeno MA. (2020) Reactive Glia Inflammatory Signaling Pathways and Epilepsy. International Journal of Molecular Sciences. 21 |
| Espinós C, Galindo MI, García-Gimeno MA, et al. (2020) Oxidative Stress, a Crossroad Between Rare Diseases and Neurodegeneration. Antioxidants (Basel, Switzerland). 9 |
| Sanchez-Martin P, Lahuerta M, Viana R, et al. (2019) Regulation of the autophagic PI3KC3 complex by laforin/malin E3-ubiquitin ligase, two proteins involved in Lafora disease. Biochimica Et Biophysica Acta. Molecular Cell Research. 1867: 118613 |