Browsing by Author Costa, FF

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PreviewIssue DateTitleAuthor(s)AdvisorType
2003Thalassemia intermedia as a result of heterozygosis for beta(0)-thalassemia and alpha alpha alpha(anti-3.7)/alpha alpha genotype in a Brazilian patientKimura, EM; Grignoli, CRE; Pinheiro, VRP; Costa, FF; Sonati, MF-Artigo de periódico
2001The (A)gamma-195 (C -> G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitroSchreiber, R; Goncalves, MS; Junqueira, ML; Saad, STO; Krieger, JE; Costa, FF-Artigo de periódico
2006High levels of neopterin and interleukin-3 in sickle cell disease patientsRodrigues, L; Costa, FF; Saad, STO; Grotto, HZW-Artigo de periódico
2010Both Interleukin-3 and Interleukin-6 Are Necessary for Better Ex Vivo Expansion of CD133+Cells From Umbilical Cord BloodBordeaux-Rego, P; Luzo, A; Costa, FF; Saad, STO; Crosara-Alberto, DP-Artigo de periódico
1997The mutation Ala677->Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosisArruda, VR; vonZuben, PM; Chiaparini, LC; AnnichinoBizzacchi, JM; Costa, FF-Artigo de periódico
1996Hereditary hemoglobinopathies in a population from southeast BrazilSonati, MF; Kimura, EM; Grotto, HZW; Gervasio, SA; Costa, FF-Artigo de periódico
2002Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter Polymorphisms among distinct ethnic groups from BrazilFertrin, KY; Goncalves, MS; Saad, STO; Costa, FF-Artigo de periódico
2013POLYMORPHISM IN THE HMOX1 GENE IS ASSOCIATED WITH HIGH LEVELS OF FETAL HEMOGLOBIN IN BRAZILIAN PATIENTS WITH SICKLE CELL ANEMIAGil, GP; Ananina, G; Oliveira, MB; Costa, FF; Silva, MJ; Santos, MNN; Bezerra, MAC; Hatzlhofer, BLD; Araujo, AS; Melo, MB-Artigo de periódico
2008Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma riskLima, CSP; Ortega, MA; Ozelo, MC; Araujo, RC; De Souza, CA; Lorand-Metze, I; Annichino-Bizzacchi, JA; Costa, FF-Artigo de periódico
2007Polymorphisms in methylenetetrahydrofolate reductase gene (MTHFR) and the age of onset of sporadic colorectal adenocarcinomaLima, CSP; Nascimento, H; Bonadia, LC; Teori, MT; Coy, CSR; Goes, JRN; Costa, FF; Bertuzzo, CS-Artigo de periódico
2003Polymorphisms of glutathione S-transferase Mu1 (GSTM1)and Theta1 (GSTT1) genes in multiple myelomaOrtega, MM; Nascimento, H; Melo, MB; Teori, MT; Costa, FF; Lima, CSP-Artigo de periódico
2004Polymorphism of the human platelet antigen-5 system is a risk factor for occlusive vascular complications in patients with sickle cell anemiaCastro, V; Alberto, FL; Costa, RNP; Lepikson-Neto, J; Gualandro, SFM; Figueiredo, MS; Annichino-Bizzacchi, JM; Saad, STO; Costa, FF-Artigo de periódico
2010Global gene expression reveals a set of new genes involved in the modification of cells during erythroid differentiationda Cunha, AF; Brugnerotto, AF; Duarte, AS; Lanaro, C; Costa, GGL; Saad, STO; Costa, FF-Artigo de periódico
2008Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and functiondos Santos, CO; Zhou, S; Secolin, R; Wang, X; Cunha, AF; Higgs, DR; Kwiatkowski, JL; Thein, SL; Gallagher, PG; Costa, FF; Weiss, MJ-Artigo de periódico
2002alpha-thalassemia does not significantly contribute to the low MCV level of Hb C traitSilva, NM; Soledade, CS; Costa, FF; Sonati, MF-Artigo de periódico
2011Alterations in cell maturity and serum survival factors may modulate neutrophil numbers in sickle cell diseaseAlmeida, CB; Favero, ME; Pereira-Cunha, FG; Lorand-Metze, I; Saad, STO; Costa, FF; Conran, N-Artigo de periódico
2013Viability of umbilical cord blood mononuclear cell subsets until 96 hours after collectionPereira-Cunha, FG; Duarte, ASS; Costa, FF; Saad, STO; Lorand-Metze, I; Luzo, ACM-Artigo de periódico
2004Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen)Rodrigues, A; Rios, M; Costa, FF; Saad, STO; Pellegrino, J; Castilho, L-Artigo de periódico
1998Prevalence of the mutation C677 -> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in BrazilArruda, VR; Siqueira, LH; Goncalves, MS; von Zuben, PM; Soares, MCP; Menezes, R; Annichino-Bizzacchi, JM; Costa, FF-Artigo de periódico
1997Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial diseaseArruda, VR; AnnichinoBizzacchi, JM; Goncalves, MS; Costa, FF-Artigo de periódico