Rosa Viana

Instituto de Biomedicina de Valencia, València, Comunidad Valenciana, Spain 
"Rosa Viana"
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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
Muñoz-Ballester C, Berthier A, Viana R, et al. (2016) Homeostasis of the astrocytic glutamate transporter GLT-1 is altered in mouse models of Lafora disease. Biochimica Et Biophysica Acta. 1862: 1074-83
Sánchez-Martín P, Romá-Mateo C, Viana R, et al. (2015) Ubiquitin conjugating enzyme E2-N and sequestosome-1 (p62) are components of the ubiquitination process mediated by the malin-laforin E3-ubiquitin ligase complex. The International Journal of Biochemistry & Cell Biology. 69: 204-14
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