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DataTítuloAutor(es)TipoAcesso
16-Jun-2023Learning the biochemical basis of axonal guidance: using Caenorhabditis elegans as a modelCastro, Andreia Cristiana Teixeira; Sousa, João Carlos; Vieira, Cármen Maria Leal, et al.ArtigoAcesso aberto
21-Out-2015Limited effect of chronic valproic acid treatment in a mouse model of Machado-Joseph diseaseEsteves, Sofia; Silva, Sara Carina Duarte; Naia, Luana, et al.ArtigoAcesso aberto
Out-2006Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in EuropeansSantos, Monica; Maciel, P.; The GAMES Collaborative GroupArtigoAcesso restrito UMinho
2014Lithium chloride therapy fails to improve motor function in a transgenic mouse model of Machado-Joseph diseaseSilva, Sara Duarte; Carvalho, Andreia Neves; Cunha, Carina Soares, et al.ArtigoAcesso aberto
Jun-2007MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patientsCoutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, et al.ArtigoAcesso restrito UMinho
25-Jun-2022Microglial depletion has no impact on disease progression in a mouse model of machado–joseph diseaseCampos, Ana Bela; Silva, Sara Carina Duarte; Fernandes, Bruno, et al.ArtigoAcesso aberto
Nov-2003Molecular diagnosis of Huntington disease in Portugal : implications for genetic counselling and clinical practiceCosta, Maria do Carmo; Magalhães, Paula; Ferreirinha, Fátima, et al.ArtigoAcesso aberto
Jan-2012Molecular genetics of intellectual disabilityBessa, C.; Lopes, Fátima; Maciel, P.Capítulo de livroAcesso aberto
13-Out-2010Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndromeSantos, M.; Summavielle, T.; Teixeira-Castro, A., et al.ArtigoAcesso restrito UMinho
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