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DataTítuloAutor(es)TipoAcesso
2010Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strainFernandes, Anabela Silva; Sousa, Nuno; Oliveira, Pedro, et al.ArtigoAcesso aberto
Out-2010Motor uncoordination and neuropathology in a transgenic mouse model of Machado-Joseph disease lacking intranuclear inclusions and ataxin-3 cleavage productsFernandes, Anabela Silva; Costa, Maria do Carmo; Silva, Sara Carina Duarte, et al.ArtigoAcesso aberto
30-Jul-2008Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation typeTemudo, Teresa; Ramos, Elisabete; Dias, Karin, et al.ArtigoAcesso restrito UMinho
Out-2010Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesisPinho, Teresa; Silva-Fernandes, Anabela; Bousbaa, Hassan, et al.ArtigoAcesso aberto
Jan-2009Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patientsSantos, Mónica; Temudo, Teresa; Kay, Teresa, et al.ArtigoAcesso aberto
Nov-2007NEDD8: a new ataxin-3 interactorFerro, Anabela; Carvalho, Ana Luísa; Castro, Andreia Cristiana Teixeira, et al.ArtigoAcesso aberto
22-Jun-2007Neurodevelopment milestone abnormalities in rats exposed to stress in early lifeMesquita, Ana Raquel Marcelino; Pêgo, José M.; Summavielle, Teresa, et al.ArtigoAcesso restrito UMinho
Ago-2005Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvementMaciel, P.; Cruz, V. T.; Constante, M., et al.ArtigoAcesso aberto
1-Ago-2011Neuron-specific proteotoxicity of mutant ataxin-3 in C. elegans: rescue by the DAF-16 and HSF-1 pathwaysCastro, Andreia Cristiana Teixeira de; Ailion, Michael; Jalles, Ana, et al.ArtigoAcesso aberto
Mai-2018Neuroprotective effects of creatine in the CMVMJD135 mouse model of Spinocerebellar Ataxia type 3Silva, Sara Carina Duarte; Carvalho, Andreia Alexandra Neves; Cunha, Carina Isabel Soares, et al.ArtigoAcesso aberto
2021Neurotherapeutic effect of Hyptis spp. leaf extracts in Caenorhabditis elegans models of tauopathy and polyglutamine disease: role of the glutathione redox cycleVilasboas-Campos, Daniela; Costa, Marta Daniela Araújo; Castro, Andreia Cristiana Teixeira, et al.ArtigoAcesso restrito UMinho
2019Neurotoxic effects of MPTP on mouse cerebral cortex: Modulation of neuroinflammation as a neuroprotective strategyMendes, Mariana Oliveira; Rosa, Alexandra Isabel; Carvalho, Andreia Neves, et al.ArtigoAcesso aberto
2005Nonsense mutation in TITF1 in a Portuguese family with benign hereditary choreaCosta, Maria do Carmo; Costa, Cristina; Silva, Ana Paula, et al.ArtigoAcesso aberto
2015Novel candidate blood-based transcriptional biomarkers of Machado-Joseph diseaseRaposo, Mafalda; Bettencourt, Conceição; Maciel, P., et al.ArtigoAcesso aberto
21-Set-2017A novel microduplication of ARID1B: Clinical, genetic, and proteomic findingsSeabra, Catarina M.; Szoko, Nicholas; Erdin, Serkan, et al.ArtigoAcesso aberto
Jun-2009Nucleocytoplasmic shuttling activity of ataxin-3Maciel, P.; Ribeiro, Sandra Macedo; Cortes, Luísa, et al.ArtigoAcesso aberto
2013Patterns of mitochondrial DNA damage in blood and brain tissues of a transgenic mouse model of Machado-Joseph diseaseKazachkova, Nadiya; Raposo, Mafalda; Montiel, Rafael, et al.ArtigoAcesso aberto
2018Pharmacological therapies for Machado-Joseph diseaseSilva, Sara Carina Duarte; Maciel, P.Capítulo de livroAcesso aberto
2013Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2Lopes, Fátima; Bessa, C.; Maciel, P.ArtigoAcesso aberto
2005Population genetics of wild-type CAG repeats in the Machado-Joseph disease gene in PortugalLima, M.; Costa, Maria do Carmo; Montiel, R., et al.ArtigoAcesso aberto
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