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The Value of Mouse Models of Rare Diseases: A Spanish Experience.
Murillo-Cuesta S, Artuch R, Asensio F, de la Villa P, Dierssen M, Enríquez JA, Fillat C, Fourcade S, Ibáñez B, Montoliu L, Oliver E, Pujol A, Salido E, Vallejo M, Varela-Nieto I. Murillo-Cuesta S, et al. Among authors: de la villa p. Front Genet. 2020 Oct 14;11:583932. doi: 10.3389/fgene.2020.583932. eCollection 2020. Front Genet. 2020. PMID: 33173540 Free PMC article.
RasGRF1 disruption causes retinal photoreception defects and associated transcriptomic alterations.
Fernández-Medarde A, Barhoum R, Riquelme R, Porteros A, Núñez A, de Luis A, de Las Rivas J, de la Villa P, Varela-Nieto I, Santos E. Fernández-Medarde A, et al. Among authors: de las rivas j, de luis a, de la villa p. J Neurochem. 2009 Jul;110(2):641-52. doi: 10.1111/j.1471-4159.2009.06162.x. Epub 2009 May 11. J Neurochem. 2009. PMID: 19457086 Free article.
Megalencephalic leukoencephalopathy with subcortical cysts protein 1 regulates glial surface localization of GLIALCAM from fish to humans.
Sirisi S, Folgueira M, López-Hernández T, Minieri L, Pérez-Rius C, Gaitán-Peñas H, Zang J, Martínez A, Capdevila-Nortes X, De La Villa P, Roy U, Alia A, Neuhauss S, Ferroni S, Nunes V, Estévez R, Barrallo-Gimeno A. Sirisi S, et al. Among authors: de la villa p. Hum Mol Genet. 2014 Oct 1;23(19):5069-86. doi: 10.1093/hmg/ddu231. Epub 2014 May 12. Hum Mol Genet. 2014. PMID: 24824219 Free article.
108 results