Percorrer por assunto Mutation

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DataTítuloAutor(es)TipoAcesso
2019Lack of KBTBD4 mutations in molecularly classified Brazilian medulloblastomasLeal, Letícia Ferro; Cavagna, Rodrigo de Oliveira; Campanella, Nathalia Cristina, et al.ArtigoAcesso restrito autor
2012Mesenchymal transition and PDGFRA amplification/mutation are key distinct oncogenic events in pediatric diffuse intrinsic pontine gliomasPuget, Stephanie; Philippe, Cathy; Bax, Dorine A, et al.ArtigoAcesso aberto
2009A method for the generation of ectromelia virus (ECTV) recombinants: in vivo analysis of ECTV vCD30 deletion mutantsAlejo, Ali; Saraiva, Margarida; Ruiz-Argüello, Maria Begoña, et al.ArtigoAcesso aberto
2017Mild Left Ventricular Hypertrophy Unravels a Novel Nonsense Mutation of the GLA Gene Associated with the Classical Phenotype of Fabry DiseaseAzevedo, Olga; Gago, Miguel; Miltenberger-Miltenyi, Gabriel, et al.ArtigoAcesso restrito autor
Nov-2008Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutantAlonso, Isabel; Marques, Joana M.; Sousa, Nuno, 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
Set-2011Mutation-based artificial fish swarm algorithm for bound constrained global optimizationRocha, Ana Maria A. C.; Fernandes, Edite Manuela da G. P.Artigo em ata de conferênciaAcesso aberto
Nov-2019Mutational profile of driver genes in Brazilian melanomasVicente, Anna Luiza S. A.; Crovador, Camila S.; Macedo, Graziela, et al.ArtigoAcesso aberto
Abr-2017Mutational profile of TP53 in esophageal squamous cell carcinoma associated with chagasic megaesophagusLacerda, C. F.; Cruvinel-Carloni, A.; Oliveira, A. T. Torres de, 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
Jul-2007Nitric oxide signaling is disrupted in the yeast model for Batten diseaseOsório, Nuno S.; Carvalho, Agostinho; Almeida, Agostinho J., et al.ArtigoAcesso aberto
2017Origin and spread of human mitochondrial DNA haplogroup U7Sahakyan, Hovhannes; Hooshiar Kashani, Baharak; Tamang, Rakesh, et al.ArtigoAcesso aberto
2010Overeating yeast display fatty acid-induced necrotic cell deathLudovico, PaulaEditorial em revistaAcesso aberto
2018Pharmacological therapies for Machado-Joseph diseaseSilva, Sara Carina Duarte; Maciel, P.Capítulo de livroAcesso aberto
2018PIK3CA mutations are frequent in esophageal squamous cell carcinoma associated with chagasic megaesophagus and are associated with a worse patient outcomeMunari, Fernanda Franco; Cruvinel-Carloni, Adriana; Lacerda, Croider Franco, et al.ArtigoAcesso aberto
31-Out-2009Proliferation and survival molecules implicated in the inhibition of BRAF pathway in thyroid cancer cells harbouring different genetic mutationsPreto, Ana; Gonçalves, Joana; Rebocho, Ana P, et al.ArtigoAcesso aberto
2014Role of the DHH1 gene in the regulation of monocarboxylic acids transporters expression in Saccharomyces cerevisiaeMota, Sandra; Vieira, Neide; Barbosa, Sónia, et al.ArtigoAcesso aberto
2014Self mutagens affect detrimentally PCR analysis of food fungi by creating potential mutantsPaterson, R. R. M.; Lima, NelsonArtigoAcesso aberto
14-Mar-2014Serrated pathway in colorectal carcinogenesisYamane, Letícia; Scapulatempo-Neto, Cristovam; Reis, R. M., et al.ArtigoAcesso restrito UMinho
Abr-2007Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutationsTemudo, T.; Oliveira, P.; Santos, M., et al.ArtigoAcesso restrito UMinho
Mostrar 20-39 de um total de 41 resultados. < anterior   próximo >