Browsing by Author "Matute, Carlos"

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  • Gomis González, Maria; Busquets Garcia, Arnau, 1985-; Matute, Carlos; Maldonado, Rafael, 1961-; Mato, Susana; Ozaita Mintegui, Andrés, 1969- (MDPI, 2016)
    Fragile X syndrome (FXS) is the most common monogenetic cause of intellectual disability. The cognitive deficits in the mouse model for this disorder, the Fragile X Mental Retardation 1 (Fmr1) knockout (KO) mouse, have ...
  • Borralleras Fumaña, Cristina, 1988-; Mato, Susana; Amédée, Thierry; Matute, Carlos; Mulle, Christophe; Pérez Jurado, Luis Alberto; Campuzano Uceda, María Victoria (BioMed Central, 2016)
    Mice heterozygous for a complete deletion (CD) equivalent to the most common deletion found in individuals with Williams-Beuren syndrome (WBS) recapitulate relevant features of the neurocognitive phenotype, such as ...
  • Busquets Garcia, Arnau, 1985-; Gomis González, Maria; Guegan, Thomas, 1983-; Agustín Pavón, Carmen; Pastor, Antonio; Mato, Susana; Pérez Samartín, A.; Matute, Carlos; Torre Fornell, Rafael de la; Dierssen, Mara; Maldonado, Rafael, 1961-; Ozaita Mintegui, Andrés, 1969- (Nature Publishing Group, 2013)
    Fragile X syndrome (FXS), the most common monogenic cause of inherited intellectual disability and autism, is caused by the silencing of the FMR1 gene, leading to the loss of fragile X mental retardation protein (FMRP), a ...