Rosa Viana
Affiliations: | Instituto de Biomedicina de Valencia, València, Comunidad Valenciana, Spain |
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| 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 |
| Brewer MK, Machio-Castello M, Viana R, et al. (2021) An empirical pipeline for personalized diagnosis of Lafora disease mutations. Iscience. 24: 103276 |
| 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 |
| 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 |
| Muñoz-Ballester C, Santana N, Perez-Jimenez E, et al. (2019) In vivo glutamate clearance defects in a mouse model of Lafora disease. Experimental Neurology. 112959 |
| Garcia-Gimeno MA, Rodilla-Ramirez PN, Viana R, et al. (2018) A novel EPM2A mutation yields a slow progression form of Lafora disease. Epilepsy Research. 145: 169-177 |
| Sanz P, Viana R, Garcia-Gimeno MA. (2018) AMPK Protein Interaction Analyses by Yeast Two-Hybrid. Methods in Molecular Biology (Clifton, N.J.). 1732: 143-157 |
| Rubio-Villena C, Viana R, Bonet J, et al. (2018) Astrocytes: new players in progressive myoclonus epilepsy of Lafora type. Human Molecular Genetics |
| López-González I, Viana R, Sanz P, et al. (2017) Inflammation in Lafora Disease: Evolution with Disease Progression in Laforin and Malin Knock-out Mouse Models. Molecular Neurobiology. 54: 3119-3130 |
| Sanz P, Viana R, Garcia-Gimeno MA. (2016) AMPK in Yeast: The SNF1 (Sucrose Non-fermenting 1) Protein Kinase Complex. Experientia Supplementum (2012). 107: 353-374 |