Browsing by Author Basseres, DS

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Showing results 1 to 13 of 13
PreviewIssue DateTitleAuthor(s)AdvisorType
1999Mutation analysis of the HFE gene in Brazilian populationsAgostinho, MF; Arruda, VR; Basseres, DS; Bordin, S; Soares, MCP; Menezes, RC; Costa, FF; Saad, STO-Artigo de periódico
2005Characterisation of a new splice variant of MASK-BP3(ARF) and MASK human genes, and their expression patterns during haematopoietic cell differentiationDuarte, ADS; Traina, F; Favaro, PMB; Basseres, DS; de Carvalho, IC; Medina, SD; Costa, FF; Saad, STO-Artigo de periódico
1998Expression of spectrin alpha I/50 hereditary elliptocytosis and its association with the alpha(LELY) alleleBasseres, DS; Pranke, PHL; Vicentim, D; Costa, FF; Saad, STO-Artigo de periódico
1996Expression of spectrin alpha I/65 hereditary elliptocytosis in patients from BrazilPranke, PHL; Basseres, DS; Costa, FF; Saad, STO-Artigo de periódico
2002DNAase I hypersensitive site 3 ' to the beta-globin gene cluster contains a TAA Insertion specific for beta(s)-Benin haplotypeBordin, S; Crespi, VG; Duarte, ASS; Basseres, DS; Melo, MB; Vieira, APZ; Saad, STO; Costa, FF-Artigo de periódico
2001Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expressionGallagher, PG; Sabatino, DE; Basseres, DS; Nilson, DM; Wong, C; Cline, AP; Garrett, LJ; Bodine, DM-Artigo de periódico
2003Human leukocyte formin: a novel protein expressed in lymphoid malignancies and associated with AktFavaro, PMB; Medina, SD; Traina, F; Basseres, DS; Costa, FF; Saad, STO-Artigo de periódico
1998Presence of allele alpha(LELY) in an Amazonian Indian populationBasseres, DS; Salles, TSI; Costa, FF; Saad, STO-Artigo de periódico
2002ARHGAP10, a novel human gene coding for a potentially cytoskeletal Rho-GTPase activating proteinBasseres, DS; Tizzei, EV; Duarte, AAS; Costa, FF; Saad, STO-Artigo de periódico
2000Association of the alpha-spectrin R28H mutation with allele alpha(LELY) and with alpha I/alpha II domain haplotypes in three Brazilian familiesBasseres, DS; Bordin, S; Costa, FF; Saad, STO-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
2001beta-Spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicismBasseres, DS; Duarte, ASS; Hassoun, H; Costa, FF; Saad, STO-Artigo de periódico
1997beta-Spectrin Campinas: A novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosisBasseres, DS; Pranke, PHL; Sales, TSI; Costa, FF; Saad, STO-Artigo de periódico