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1
Identification of intronic RNA expression in CD34+ cells of patients with myelodysplatic syndrome by RNA microarray analysis
Identification of intronic RNA expression in CD34+ cells of patients with myelodysplatic syndrome by RNA microarray analysis
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Identification of intronic RNA expression in CD34+ cells of patients with myelodysplatic syndrome by RNA microarray analysis

Mariana O. Baratti Yuri B Moreira; Fabiola Traina; Luciene Borges; Fernando F Costa; Sergio Verjovski-Almeida; Sara T. O Saad; Annual Meeting of the American Society of Hematology (49. 2007 Atlanta)

Blood Washington v. 110, n. 11, p. 715A res. 2423, 2007

Washington 2007

Item não circula. Consulte sua biblioteca.(Acessar)

2
Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin
Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin
Material Type:
Artigo 		Adicionar ao Meu Espaço

Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin

T. Takahashi R Schreiber; Jose Eduardo Krieger; S. T. O Saad; F. F Costa

European Journal of Haematology Oxford v. 71, n. 6, p. 418-424, 2003

Oxford 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

3
Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin
Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin
Material Type:
Artigo 		Adicionar ao Meu Espaço

Analysis of the mechanism of action of the Brazilian type (Agama-195C-G) of hereditary persistence of fetal hemoglobin

T. Takahashi R Schreiber; Jose Eduardo Krieger; S. T. O Saad; F. F Costa

European Journal of Haematology Oxford v. 71, n. 6, p. 418-424, 2003

Oxford 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

4
DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation
DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation

Juliana T. N. Martins Silvana Bordin; Dulcinéia M. de Albuquerque; Sara T. O Saad; Fernando F Costa

Hemoglobin Philadelphia v. 29, n. 1, 85-89, 2005

Philadelphia 2005

Item não circula. Consulte sua biblioteca.(Acessar)

5
DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation
DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

DNAase I hypersensitive site 3' to the 'beta'-globin gene cluster containing two TAA insertions and a G'seta'A polymorphism is predominantly associated with the 'beta''POT.x'-thalassemia IVS-I-6 (T'seta'C) mutation

Juliana T. N. Martins Silvana Bordin; Dulcinéia M. de Albuquerque; Sara T. O Saad; Fernando F Costa

Hemoglobin Philadelphia v. 29, n. 1, 85-89, 2005

Philadelphia 2005

Item não circula. Consulte sua biblioteca.(Acessar)

6
Stathmin 1 expression in plasma cell neoplasms. [Carta]
Stathmin 1 expression in plasma cell neoplasms. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Stathmin 1 expression in plasma cell neoplasms. [Carta]

João Agostinho Machado Neto Fernando Vieira Pericole; Fernando Ferreira Costa; Fabiola Traina; Sara Teresinha Olalla Saad

Revista Brasileira de Hematologia e Hemoterapia Rio de Janeiro v. 39, n. 2, p. 183-185, 2017

Rio de Janeiro 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2920120 Estantes Deslizantes )(Acessar)

7
The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
Material Type:
Artigo 		Adicionar ao Meu Espaço

The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro

R. Schreiber M. S Gonçalves; M. L Junqueira; S. T. O Saad; José Eduardo Krieger; F. F Costa

Brazilian Journal of Medical and Biological Research v. 34(4), p. 489-492, 2001

São Paulo 2001

Item não circula. Consulte sua biblioteca.(Acessar)

8
Molecular characterization of hemoglobin alpha-D chain from geochelone carbonaria and geochelone denticulata land turtles
Molecular characterization of hemoglobin alpha-D chain from geochelone carbonaria and geochelone denticulata land turtles
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular characterization of hemoglobin alpha-D chain from geochelone carbonaria and geochelone denticulata land turtles

M B. Melo Silvana Bordin; A S Duarte; S H Ogo; M Torsoni; S T O Saad; F F Costa

Comparative Biochemistry v. 134, p.389-395, 2003

2003

Item não circula. Consulte sua biblioteca.(Acessar)

9
Risk factors for conjunctival and retinal vessel alterations in sickle cell disease
Risk factors for conjunctival and retinal vessel alterations in sickle cell disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Risk factors for conjunctival and retinal vessel alterations in sickle cell disease

Carmen S. P. Lima Eduardo Melani Rocha; Nadia M Silva; Maria F Sonatti; Fernando F Costa; Sara T. O Saad

Acta Ophthalmologica Scandinavica Copenhagen v. 84, p. 234-241, 2006

Copenhagen 2006

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1533399 )(Acessar)

10
The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
Material Type:
Artigo 		Adicionar ao Meu Espaço

The Ay-195 (C-G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro

R. Schreiber M. S Gonçalves; M. L Junqueira; S. T. O Saad; José Eduardo Krieger; F. F Costa

Brazilian Journal of Medical and Biological Research v. 34(4), p. 489-492, 2001

São Paulo 2001

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Saad, S
  2. Costa, F
  3. Traina, F
  4. Machado Neto, J
  5. Lorand-Metze, I

Neste Assunto:

  1. Doenças Hematológicas
  2. Leucemia
  3. Expressão Gênica
  4. Fisiologia
  5. Neoplasias

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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