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Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 2009 | Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta 122 (GH5) Phe -> Ser], a probable case of germ line mutation, and Hb Olinda [beta 22 (B4)-25 (B7)], a deletion of a 12 base-pair sequence | Bezerra, MAC; Albuquerque, DM; Santos, MNN; Kimura, EM; Jorge, SEDC; Oliveira, DM; Domingues, BLTB; Peres, JC; Araujo, AS; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2004 | A transcript finishing initiative for closing gaps in the human transcriptome | Sogayar, MC; Camargo, AA; Bettoni, F; Carraro, DM; Pires, LC; Parmigiani, MB; Ferreira, EN; Moreira, ES; Latorre, MRDO; Simpson, AJG; Cruz, LO; Degaki, TL; Festa, F; Massirer, KB; Camargo, F; Camargo, LP; Cunha, MAV; De Souza, SJ; Faria, M; Giuliatti, S; Kopp; Oliviera, PSL; Paiva, PB; Pereira, AA; Pinheiro, DG; Puga, RD; Souza, JES; Albuquerque, DM; Andrade, LEC; Baia, GS; Briones, MRS; Cavaleiro-Luna, AMS; Cerutti, JM; Costa, FF; Constanzi-Strauss, E; Espreafico, EM; Ferrasi, AC; Ferro, ES; Fortes, MAHZ; Furchi, JRF; Gianella-Neto, D; Goldman, GH; Goldman, MHS; Gruber, A; Guimaraes, GS; Hackel, C; Henrique-Silva, F; Kimura, ET; Leoni, SG; Macedo, C; Malnic, B; Manzini, CV; Marie, SKN; Martinez-Rossi, NM; Menossi, M; Miracca, EC; Nagai, MA; Nobrega, FG; Nobrega, MP; Oba-Shinjo, SM; Oliviera, MK; Orabona, GM; Otsuke, AY; Paco-Larson, ML; Paixao, BMC; Pandolfi, JRC; Pardini, MIMC; Passos-Bueno, MR; Passos, GAS; Pesquero, JB; Pessoa, JG; Rahal, P; Rainho, CA; Reis, CP; Ricca, TI; Rodriguez, V; Rogatto, SR; Romano, CM; Romeiro, JG; Rossi, A; Sa, RG; Sales, MM; SantAnna, SC; Santarosa, PL; Segato, F; Silva, WA; Silva, IDCG; Silva, NP; Soares-Costa, A; Sonati, MF; Strauss, BE; Tajara, EH; Valentini, SR; Villanova, FE; Ward, LS; Zanette, DL | - | Artigo de periódico |
| 2002 | A novel beta-globin variant: Hb Pocos de Caldas [beta 61(E5)Lys -> Gln] | Kimura, EM; Jorge, SB; Ogo, SH; Cesquini, M; Albuquerque, DM; Fattori, A; Saad, STO; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2013 | A new beta(0)-thalassemia frameshift mutation [beta 48 (-T)] in a Uruguayan family | Da Luz, J; Lopez, P; Kimura, EM; Albuquerque, DM; Costa, FF; Sans, M; Sonati, MF | - | Artigo de periódico |
| 2008 | Regulation of human alpha-globin gene expression and alpha-thalassemia | Ribeiro, DM; Sonati, MF | - | Artigo de periódico |
| 2012 | Expression profiles of phosphatidylinositol phosphate kinase genes during normal human in vitro erythropoiesis | Zaccariotto, TR; Lanaro, C; Albuquerque, DM; Santos, MNN; Bezerra, MAC; Cunha, FGP; Lorand-Metze, I; Araujo, AS; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2009 | Influence of the polymorphisms of the alpha-major regulatory element HS-40 on in vitro gene expression | Ribeiro, DM; Zaccariotto, TR; Santos, MNN; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 1996 | Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil | Figueiredo, MS; Kerbauy, J; Goncalves, MS; Arruda, VR; Saad, STO; Sonati, MF; Stoming, T; Costa, FF | - | Artigo de periódico |
| 2007 | Hb Indianapolis [beta 112 (G14) Cys -> Arg] as the probable cause of moderate hemolytic anemia and renal damage in a Brazilian patient | Fattori, A; Kimura, EM; Albuquerque, DM; Oliveira, DM; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 1999 | Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] and alpha-thalassemia-2 (-alpha(3.7)) | Grignoli, CRE; Wenning, MRSC; Sonati, MF; Kimura, EM; Arruda, VR; Saad, STO; Costa, FF | - | Artigo de periódico |
| 2006 | Hb Florida: A novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype | Weinstein, BI; Erramouspe, B; Albuquerque, DM; Oliveira, DM; Kimura, EM; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2000 | Hb Campinas [alpha 26(B7)Ala -> Val]: a novel, electrophoretically silent, variant | Wenning, MRSC; Silva, NM; Jorge, SB; Kimura, EM; Costa, FF; Torsoni, MA; Ogo, SH; Sonati, MF | - | Artigo de periódico |
| 2003 | Haplotypes of alpha-globin gene regulatory element in two Brazilian native populations | Ribeiro, DM; Figueiredo, MS; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 1997 | G6PD sumare: A novel mutation in the G6PD gene (1292 T->G) associated with chronic nonspherocytic anemia | Saad, ST; Salles, TSI; Arruda, VR; Sonati, MF; Costa, FE | - | Artigo de periódico |
| 1996 | Hereditary hemoglobinopathies in a population from southeast Brazil | Sonati, MF; Kimura, EM; Grotto, HZW; Gervasio, SA; Costa, FF | - | Artigo de periódico |
| 1997 | Hematological phenotype and the type of beta thalassemia mutation in Brazil | Bertuzzo, CS; Sonati, MF; Costa, FF | - | Artigo de periódico |
| 2002 | Hemoglobin H disease resulting from the association of the - alpha(3.7) rightward deletion and the (alpha alpha)(MM) deletion in a Brazilian patient | Wenning, MRSC; Harteveld, CL; Giordano, PC; Kimura, EM; Saad, STO; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2006 | Reticulocyte evaluation in alpha(+)-thalassemia | Krugner, F; Zaccariotto, TR; Rosim, ET; Costa, FF; Grotto, HZW; Sonati, MF | - | Artigo de periódico |
| 2002 | alpha-thalassemia does not significantly contribute to the low MCV level of Hb C trait | Silva, NM; Soledade, CS; Costa, FF; Sonati, MF | - | Artigo de periódico |
| 2003 | Thalassemia intermedia as a result of heterozygosis for beta(0)-thalassemia and alpha alpha alpha(anti-3.7)/alpha alpha genotype in a Brazilian patient | Kimura, EM; Grignoli, CRE; Pinheiro, VRP; Costa, FF; Sonati, MF | - | Artigo de periódico |