Browsing by Author Basseres D.S.

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Showing results 1 to 14 of 14
PreviewIssue DateTitleAuthor(s)AdvisorType
1996Expression Of Spectrin α(i/65) Hereditary Elliptocytosis In Patients From BrazilPranke P.H.L.; Basseres D.S.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2001β-spectrin Sta Bárbara: A Novel Frameshift Mutation In Hereditary Spherocytosis Associated With Detectable Levels Of Mrna And A Germ Cell Line MosaicismBasseres D.S.; Duarte A.S.S.; Hassoun H.; Costa F.F.; Saad S.T.O.-Artigo de periódico
1994Ca2+-dependent Permeabilization Of The Inner Mitochondrial Membrane By 4,4′-diisothiocyanatostilbene-2,2′-disulfonic Acid (dids)Bernardes C.F.; Meyer-Fernandes JosR.; Basseres D.S.; Castilho R.F.; Vercesi A.E.-Artigo de periódico
1998Expression Of Spectrin αi/50 Hereditary Elliptocytosis And Its Association With The α(lely) AlleleBasseres D.S.; Pranke P.H.L.; Vicentim D.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2005Characterisation Of A New Splice Variant Of Mask-bp3arf And Mask Human Genes, And Their Expression Patterns During Haematopoietic Cell DifferentiationDuarte A.D.S.S.; Traina F.; Favaro P.M.B.; Basseres D.S.; De Carvalho I.C.; Medina S.D.S.; Costa F.F.; Saad S.T.O.-Artigo de periódico
1997β-spectrin Campinas: A Novel Shortened β-chain Variant Associated With Skipping Of Exon 30 And Hereditary ElliptocytosisBasseres D.S.; Pranke P.H.L.; Sales T.S.I.; Costa F.F.; Saad S.T.O.-Artigo de periódico
1998Presence Of Allele α(lely) In An Amazonian Indian PopulationBasseres D.S.; Salles T.S.I.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2002β-spectrin São Pauloii, A Novel Frameshift Mutation Of The β-spectrin Gene Associated With Hereditary Spherocytes And Instability Of The Mutant MrnaBasseres D.S.; Tavares A.C.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2002Dnaase I Hypersensitive Site 3′ To The β-globin Gene Cluster Contains A Taa Insertion Specific For βs-benin HaplotypeBordin S.; Crespi V.G.; Duarte A.S.S.; Basseres D.S.; Melo M.B.; Zilli Vieira A.P.; Saad S.T.O.; Costa F.F.-Artigo de periódico
1998β-spectrin Promissao: A Translation Initiation Codon Mutation Of The β-spectrin Gene (atg → Gtg) Associated With Hereditary Spherocytosis And Spectrin Deficiency In A Brazilian Family [8]Basseres D.S.; Vicentim D.L.; Costa F.F.; Saad S.T.O.; Hassoun H.-Carta
2000Low Frequency Of Ankyrin Mutations In Hereditary Spherocytosis: Identification Of Three Novel Mutations.Leite R.C.; Basseres D.S.; Ferreira J.S.; Alberto F.L.; Costa F.F.; Saad S.T.-Artigo de periódico
2000Human T-celllymphotropic Virus Type L Transac1tvator Tax And Transcription Factor Sp1 Interact On The Gata3 PromoterGilli S.C.O.; Basseres D.S.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2000Association Of The α-spectrin R28h Mutation With Allele α(lely) And With αi/αii Domain Haplotypes In Three Brazilian FamiliesBasseres D.S.; Bordin S.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2000Novel Mutation In The Myoc Gene In Primary Open Angle Glaucoma PatientsVasconcellos J.P.C.; Melo M.B.; Costa V.P.; Tsukumo D.M.L.; Basseres D.S.; Bordin S.; Saad S.T.O.; Costa F.F.-Carta