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Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder.
Segura-Puimedon M, Sahún I, Velot E, Dubus P, Borralleras C, Rodrigues AJ, Valero MC, Valverde O, Sousa N, Herault Y, Dierssen M, Pérez-Jurado LA, Campuzano V. Segura-Puimedon M, et al. Among authors: sousa n. Hum Mol Genet. 2014 Dec 15;23(24):6481-94. doi: 10.1093/hmg/ddu368. Epub 2014 Jul 15. Hum Mol Genet. 2014. PMID: 25027326
Essential role of the N-terminal region of TFII-I in viability and behavior.
Lucena J, Pezzi S, Aso E, Valero MC, Carreiro C, Dubus P, Sampaio A, Segura M, Barthelemy I, Zindel MY, Sousa N, Barbero JL, Maldonado R, Pérez-Jurado LA, Campuzano V. Lucena J, et al. Among authors: sousa n. BMC Med Genet. 2010 Apr 19;11:61. doi: 10.1186/1471-2350-11-61. BMC Med Genet. 2010. PMID: 20403157 Free PMC article.
Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome.
Santos M, Summavielle T, Teixeira-Castro A, Silva-Fernandes A, Duarte-Silva S, Marques F, Martins L, Dierssen M, Oliveira P, Sousa N, Maciel P. Santos M, et al. Among authors: sousa n. Neuroscience. 2010 Oct 13;170(2):453-67. doi: 10.1016/j.neuroscience.2010.07.010. Epub 2010 Jul 13. Neuroscience. 2010. PMID: 20633611
Glucocorticoid programing of the mesopontine cholinergic system.
Borges S, Coimbra B, Soares-Cunha C, Ventura-Silva AP, Pinto L, Carvalho MM, Pêgo JM, Rodrigues AJ, Sousa N. Borges S, et al. Among authors: sousa n. Front Endocrinol (Lausanne). 2013 Dec 13;4:190. doi: 10.3389/fendo.2013.00190. eCollection 2013. Front Endocrinol (Lausanne). 2013. PMID: 24379803 Free PMC article.
961 results