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Issue DateTitleAuthor(s)Type
2017Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?Maia, N; Loureiro, JR; Oliveira, B; Marques, I; Santos, R; Jorge, P; Martins, SArtigo em Revista Científica Internacional
2015To Be or Not to Be a Pseudogene: A Molecular Epidemiological Approach to the mclx Genes and Its Impact in TuberculosisSantos, CL; Nebenzahl-Guimaraes, H; Mendes, MV; Soolingen, D; Correia-Neves, MArtigo em Revista Científica Internacional
2015Clonal evolution of CD8+ T cell responses against latent viruses: relationship among phenotype, localization, and functionRemmerswaal, EB; Klarenbeek, PL; Alves, NL; Doorenspleet, ME; Schaik, BD; Esveldt, RE; Idu, MM; Leeuwen, EM; der, Bom-Baylon, N; Kampen, AH; Koch, SD; Pircher, H; Bemelman, FJ; Ten, Brinke, A; Baas, F; Ten, Berge, IJ; Lier, RA; de, Vries, NArtigo em Revista Científica Internacional
2014Dysregulation of T cell receptor N-glycosylation: A molecular mechanism involved in ulcerative colitisDias, A; Dourado, J; Lago, P; Cabral, J; Marcos-Pinto, R; Salgueiro, P; Almeida, CR; Carvalho, S; Fonseca, S; Lima, M; Vilanova, M; Dinis-Ribeiro, M; Reis, CA; Pinho, SSArtigo em Revista Científica Internacional
2013Somatic mutations and deletions of the E-cadherin gene predict poor survival of patients with gastric cancer.Corso, G; Carvalho, J; Marrelli, D; Vindigni, C; Carvalho, B; Seruca, R; Roviello, F; Oliveira, CArtigo em Revista Científica Internacional
2013Frequency of TERT promoter mutations in human cancersVinagre, J; Almeida, A; Pópulo, H; Batista, R; Lyra, J; Pinto, V; Coelho, R; Celestino, R; Prazeres, H; Lima, L; Melo, M; Rocha, AG da; Preto, A; Castro, P; Castro, L; Pardal, F; Lopes, JM; Santos, LL; Reis, RM; Cameselle-Teijeiro, JM; Sobrinho-Simões, M; Lima, J; Máximo, V; Soares, PArtigo em Revista Científica Internacional
2005MtDNA single macrodeletions associated with myopathies: absence of haplogroup-related increased riskGoios, A; Nogueira, C; Pereira, C; Vilarinho, L; Amorim, A; Pereira, LArtigo em Revista Científica Internacional
2017TERT, BRAF and NRAS in primary thyroid cancer and metastatic diseaseMelo, M; Gaspar da Rocha, A; Batista, R; Vinagre, J; Martins, MJ; Costa, G; Ribeiro, C; Carilho, F; Leite, V; Lobo, C; Cameselle-Teijeiro, JM; Cavadas, B; Pereira, L; Sobrinho-Simões, M; Soares, PArtigo em Revista Científica Internacional
2013A founder SDHB mutation in Portuguese paraganglioma patientsMartins, RG; Nunes, JB; Máximo, V; Soares, P; Peixoto, J; Catarino, T; Rito, T; Soares, P; Pereira, L; Sobrinho-Simões, M; Santos, AP; Couto, J; Henrique, R; Matos-Loureiro, J; Dias, P; Torres, I; Lima, JArtigo em Revista Científica Internacional
2017A pentanucleotide ATTTC repeat insertion in the non-coding region of DAB1, mapping to SCA37, causes spinocerebellar ataxia.Seixas, AI; Loureiro, JR; Costa, C; Ordóñez-Ugalde, A; Marcelino, H; Oliveira, CL; Loureiro, JL; Dhingra, A; Brandão, E; Cruz, VT; Timóteo, A; Quintáns, B; Rouleau, GA; Rizzu, P; Carracedo, A; Bessa, J; Heutink, P; Sequeiros, J; Sobrido, MJ; Coutinho, P; Silveira, IArtigo em Revista Científica Internacional