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PreviewIssue DateTitleAuthor(s)AdvisorType
1996Prognostic significance of BCR-ABL rearrangement in chronic myeloid leukemiaColleoni, GWB; Costa, FF; Grignolli, CRE; Silva, RS; Chauffaille, MLLF; Kerbauy, J; Saad, STO-Artigo de periódico
1998Mild clinical expression of S-beta thalassemia in a Brazilian patient with the beta(+) IVS-I-6 (T -> C) mutationSonati, MD; Kaeda, J; Kimura, EM; Costa, FF; Luzzatto, L-Artigo de periódico
2002beta-Spectrin Sao Paulo(II), a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNABasseres, DS; Tavares, AC; Costa, FF; Saad, STO-Artigo de periódico
1998The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaVigorito, AC; Lorand-Metze, I; Chauffaile, MD; Costa, FF; Saad, STO-Artigo de periódico
2012Prevalence of alpha-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, BrazilAlcoforado, GHD; Bezerra, CM; Lemos, TMAM; de Oliveira, DM; Kimura, EM; Costa, FF; Sonati, MD; de Medeiros, TMD-Artigo de periódico
2002Presence of the RHD pseudogene and the hybrid RHD-CE-D-s gene in Brazilians with the D-negative phenotypeRodrigues, A; Rios, M; Pellegrino, J; Costa, FF; Castilho, L-Artigo de periódico
2011Functional characterization and target discovery of glycoside hydrolases from the digestome of the lower termite Coptotermes gestroiCairo, JPLF; Leonardo, FC; Alvarez, TM; Ribeiro, DA; Buchli, F; Costa-Leonardo, AM; Carazzolle, MF; Costa, FF; Leme, AFP; Pereira, GAG; Squina, FM-Artigo de periódico
2010Death switch for gene therapy: application to erythropoietin transgene expressionSouza, DS; Spencer, DM; Salles, TSI; Salomao, MA; Payen, E; Beuzard, Y; Carvalho, HF; Costa, FF; Saad, STO-Artigo de periódico
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