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Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

Universidade Estadual Paulista (Unesp) (2011-11-16)

Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has reduced expression in adults, ranging from 0 to 1% of total hemoglobin. Increased levels of Hb F are due to mutations in ...

Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

Universidade Estadual Paulista (Unesp) (2011-11-16)

Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

Carrocini, G. C S; Bonini-Domingos, C. R. (2014)

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 (Assoc Bras Divulg CientificaSao PauloBrasil, 2003)

Determination of neutral polymorphisms (frameworks) of the human beta globin gene in beta thalassaemias by PCR/DGGE

Universidade Estadual Paulista (Unesp); Universidade Estadual de Campinas (UNICAMP) (1997-02-01)

Purpose: Considering the importance of type beta thalassaemias as hereditary syndromes of high significance in different populations of Mediterranean origin and, by extension, in the Brazilian population, the objective of ...

Determination of neutral polymorphisms (frameworks) of the human beta globin gene in beta thalassaemias by PCR/DGGE

Universidade Estadual Paulista (Unesp); Universidade Estadual de Campinas (UNICAMP) (1997-02-01)

Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster

de Andrade, TG; Peterson, KR; Cunha, AF; Moreira, LS; Fattori, A; Saad, STO; Costa, FF (Academic Press Inc Elsevier ScienceSan DiegoEUA, 2006)

Haplotype analysis and (A)gamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin

Bordin, S; Martins, JT; Goncalves, MS; Melo, MB; Saad, STO; Costa, FF (Wiley-lissNew YorkEUA, 1998)

DNAase I hypersensitive site 3 ' to the beta-globin gene cluster contains a TAA Insertion specific for beta(s)-Benin haplotype

Bordin, S; Crespi, VG; Duarte, ASS; Basseres, DS; Melo, MB; Vieira, APZ; Saad, STO; Costa, FF (Ferrata Storti FoundationPaviaItália, 2002)

DNAase I hypersensitive site 3 ' to the beta-globin gene cluster containing two Taa insertions and a G -> A polymorphism is predominantly associated with the beta(+)-thalassemia ivs-1-6 (T -> C) mutation

Martins, JTN; Bordin, S; de Albuquerque, DM; Saad, STO; Costa, FF (Marcel Dekker IncNew YorkEUA, 2005)

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Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population

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

Determination of neutral polymorphisms (frameworks) of the human beta globin gene in beta thalassaemias by PCR/DGGE

Determination of neutral polymorphisms (frameworks) of the human beta globin gene in beta thalassaemias by PCR/DGGE

Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster

Haplotype analysis and (A)gamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin

DNAase I hypersensitive site 3 ' to the beta-globin gene cluster contains a TAA Insertion specific for beta(s)-Benin haplotype

DNAase I hypersensitive site 3 ' to the beta-globin gene cluster containing two Taa insertions and a G -> A polymorphism is predominantly associated with the beta(+)-thalassemia ivs-1-6 (T -> C) mutation