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Issue DateTitleAuthor(s)Type
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
2013A substantial prehistoric European ancestry amongst Ashkenazi maternal lineagesCosta, MD; Pereira, JB; Pala, M; Fernandes, V; Olivieri, A; Achilli, A; Perego, UA; Rychkov, S; Naumova, O; Hatina, J; Woodward, SR; Eng, KK; Macaulay, V; Carr, M; Soares, P; Pereira, L; Richards, MBArtigo em Revista Científica Internacional
2002Bantu and European Y-lineages in Sub-Saharan AfricaPereira, L; Gusmão, L; Alves, C; Amorim, A; Prata, MJArtigo em Revista Científica Internacional
2017Caveolin-1-mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotypePortugal, CC; Socodato, R; Canedo, T; Silva, CM; Martins, T; Coreixas, VS; Loiola, EC; Gess, B; Röhr, D; Santiago, AR; Young, P; Minshall, RD; Paes-de-Carvalho, R; Ambrósio, AF; Relvas, JBArtigo em Revista Científica Internacional
2007Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markersNavarro-Costa, P; Pereira, L; Alves, C; Gusmão, L; Proença, C; Marques-Vidal, P; Rocha, T; Correia, SC; Jorge, S; Neves, A; Soares, AP; Nunes, J; Calhaz-Jorge, C; Amorim, A; Plancha, CE; Gonçalves, JArtigo 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
2011Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversityPereira, L; Soares, P; Radivojac, P; Li, B; Samuels, DCArtigo em Revista Científica Internacional
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
2000Diversity of mtDNA lineages in Portugal: not a genetic edge of European variationPereira, L; Prata, MJ; Amorim, AArtigo em Revista Científica Internacional
2015Early Holocenic and historic mtDNA African signatures in the Iberian Peninsula: the Andalusian region as a paradigmHernández, CL; Soares, P; Dugoujon, JM; Novelletto, A; Rodríguez, JN; Rito, T; Oliveira, M; Melhaoui, M; Baali, A; Pereira, L; Calderón, RArtigo em Revista Científica Internacional
2016Fibrinogen scaffolds with immunomodulatory properties promote in vivo bone regenerationVasconcelos, DM; Gonçalves, RM; Almeida, CR; Pereira, IO; Oliveira, MI; Neves, N; Silva, AM; Ribeiro, AC; Cunha, C; Almeida, AR; Ribeiro, CC; Gil, AM; Seebach, E; Kynast, KL; Richter, W; Lamghari, M; Santos, SG; Barbosa, MAArtigo 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
2014Intracellular trafficking of AIP56, an NF-κB-cleaving toxin from Photobacterium damselae subsp. PiscicidaPereira, LM; Pinto, RD; Silva, DS; Moreira, AR; Beitzinger, C; Oliveira, P; Sampaio, P; Benz, R; Azevedo, JE; Santos, NM; Vale, AArtigo em Revista Científica Internacional
2006Islands inside an island: reproductive isolates on Jerba IslandLoueslati, BY; Cherni, L; Enaafaa, H; Khodjet el Khil, H; Pereira, L; Amorim, A; Ben Ayed, F; El Gaaied, AArtigo em Revista Científica Internacional
2015Machado-Joseph disease in a Nigerian family: mutational origin and review of the literatureOgun, SA; Martins, S; Adebayo, PB; Dawodu, CO; Sequeiros, J; Finkel, MFArtigo em Revista Científica Internacional
2005Mitochondrial DNA haplotyping revealed the presence of mixed up benign and neoplastic tissue sections from two individuals on the same prostatic biopsy slideAlonso, A; Alves, C; Suárez-Mier, MP; Albarrán, C; Pereira, L; Fernandez de Simón, LF; Martín, P; Garcia, O; Gusmão, L; Sancho, M; Amorim, AArtigo em Revista Científica Internacional
2003Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlersBrehm, A; Pereira, L; Kivisild, T; Amorim, AArtigo 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
2008Mutation ‘C11994T’ in the mitochondrial ND4 gene is not a cause of low sperm motility in PortugalPereira, L; Gonçalves, J; Bandelt, H-JArtigo em Revista Científica Internacional