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Results: 1-25 |
Results: 25
Lack of association between N-ras gene mutations and clinical prognosis inBrazilian children with acute lymphoblastic leukemia
Authors: Clementino, NCD Yamamoto, M Viana, MB Figueiredo, MS Kerbauy, J Saad, STO Costa, FF
Citation: Ncd. Clementino et al., Lack of association between N-ras gene mutations and clinical prognosis inBrazilian children with acute lymphoblastic leukemia, LEUK LYMPH, 42(3), 2001, pp. 473-479
Increased risk for acute myeloid leukaemia in individuals with glutathioneS-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects
Authors: Arruda, VR Lima, CSP Grignoli, CRE de Melo, MB Lorand-Metze, I Alberto, FL Saad, STO Costa, FF
Citation: Vr. Arruda et al., Increased risk for acute myeloid leukaemia in individuals with glutathioneS-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects, EUR J HAEMA, 66(6), 2001, pp. 383-388
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patients
Authors: Bincoletto, C Perlingeiro, RCR Saad, STO Costa, FF Queiroz, MLS
Citation: C. Bincoletto et al., Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patients, HEMOGLOBIN, 25(1), 2001, pp. 1-7
Mdm2, and c-Myc overexpression is associated with a poor prognosis in aggressive non-Hodgkin's lymphomas, (vol 67, pg 84, 2001)
Authors: Pagnano, KBB Vassallo, J Lorand-Metza, I Costa, FF Saad, STO
Citation: Kbb. Pagnano et al., Mdm2, and c-Myc overexpression is associated with a poor prognosis in aggressive non-Hodgkin's lymphomas, (vol 67, pg 84, 2001), AM J HEMAT, 67(4), 2001, pp. 279-279
p53, Mdm2, and c-Myc overexpression is associated with a poor prognosis inaggressive non-Hodgkin's lymphomas
Authors: Pagnano, KBB Vassallo, J Lorand-Metze, I Costa, FF Saad, STO
Citation: Kbb. Pagnano et al., p53, Mdm2, and c-Myc overexpression is associated with a poor prognosis inaggressive non-Hodgkin's lymphomas, AM J HEMAT, 67(2), 2001, pp. 84-92
Walker tumor cells express larger amounts of the antiapoptotic protein Bcl-2 and presents higher resistance to toxic concentrations of Ca2+ than the tumor cells K 562
Authors: Milani, G Kowaltowski, AD Saad, STO Metze, K Vercesi, AE
Citation: G. Milani et al., Walker tumor cells express larger amounts of the antiapoptotic protein Bcl-2 and presents higher resistance to toxic concentrations of Ca2+ than the tumor cells K 562, DRUG DEV R, 52(4), 2001, pp. 508-514
Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria
Authors: de Carvalho, RF Arruda, VR Saad, STO Costa, FF
Citation: Rf. De Carvalho et al., Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria, BRAZ J MED, 34(6), 2001, pp. 763-766
The (A)gamma-195 (C -> G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
Authors: Schreiber, R Goncalves, MS Junqueira, ML Saad, STO Krieger, JE Costa, FF
Citation: R. Schreiber et al., The (A)gamma-195 (C -> G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro, BRAZ J MED, 34(4), 2001, pp. 489-492
beta-Spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism
Authors: Basseres, DS Duarte, ASS Hassoun, H Costa, FF Saad, STO
Citation: Ds. Basseres et al., beta-Spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism, BR J HAEM, 115(2), 2001, pp. 347-353
Expression of inducible nitric oxide synthase is increased in acute myeloid leukaemia
Authors: Brandao, MM Soares, E Salles, TSI Saad, STO
Citation: Mm. Brandao et al., Expression of inducible nitric oxide synthase is increased in acute myeloid leukaemia, ACT HAEMAT, 106(3), 2001, pp. 95-99
C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction
Authors: Annichino-Bizzacchi, JM Saad, STO Arruda, VR Ramires, JAF Siqueira, LH Chiaparini, LC Mansur, AP
Citation: Jm. Annichino-bizzacchi et al., C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction, J CARD RISK, 7(1), 2000, pp. 37-40
beta(0)-thalassemia resulting from a novel mutation: beta 66/u -> stop codon
Authors: Grignoli, CRE Carvalho, MH Kimura, EM Sonati, MF Arruda, VR Saad, STO Costa, FF
Citation: Cre. Grignoli et al., beta(0)-thalassemia resulting from a novel mutation: beta 66/u -> stop codon, EUR J HAEMA, 64(2), 2000, pp. 137-138
Association of the alpha-spectrin R28H mutation with allele alpha(LELY) and with alpha I/alpha II domain haplotypes in three Brazilian families
Authors: Basseres, DS Bordin, S Costa, FF Saad, STO
Citation: Ds. Basseres et al., Association of the alpha-spectrin R28H mutation with allele alpha(LELY) and with alpha I/alpha II domain haplotypes in three Brazilian families, EUR J HAEMA, 64(1), 2000, pp. 53-58
Cytoplasmic overexpression of p53 and p21(ras) in megaloblastic anemia
Authors: Schulz, E Arruda, VR Costa, FF Saad, STO
Citation: E. Schulz et al., Cytoplasmic overexpression of p53 and p21(ras) in megaloblastic anemia, HAEMATOLOG, 85(8), 2000, pp. 874-875
beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene
Authors: Arruda, VR Agostinho, MF Cancado, R Costa, FF Saad, STO
Citation: Vr. Arruda et al., beta-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene, AM J HEMAT, 63(4), 2000, pp. 230-230
Molecular heterogeneity of the A(3) subgroup
Authors: Barjas-Castro, ML Carvalho, MH Locatelli, MF Bordin, S Saad, STO
Citation: Ml. Barjas-castro et al., Molecular heterogeneity of the A(3) subgroup, CLIN LAB H, 22(2), 2000, pp. 73-78
alpha-globin genes: thalassemic and structural alterations in a Brazilian population
Authors: Wenning, MRSC Kimura, EM Costa, FF Saad, STO Gervasio, S de Jorge, SB Borges, E Silva, NM Sonati, MF
Citation: Mrsc. Wenning et al., alpha-globin genes: thalassemic and structural alterations in a Brazilian population, BRAZ J MED, 33(9), 2000, pp. 1041-1045
Decreased GATA3 mRNA expression in human T-cell lymphotropic virus type 1 (HTLV-1) infection
Authors: Gilli, SCO Salles, TSI Saad, STO
Citation: Sco. Gilli et al., Decreased GATA3 mRNA expression in human T-cell lymphotropic virus type 1 (HTLV-1) infection, SC J IN DIS, 32(2), 2000, pp. 161-163
Novel mutation in the MYOC gene in primary open angle glaucoma patients
Authors: Vasconcellos, JPC Melo, MB Costa, VP Tsukumo, DML Basseres, DS Bordin, S Saad, STO Costa, FF
Citation: Jpc. Vasconcellos et al., Novel mutation in the MYOC gene in primary open angle glaucoma patients, J MED GENET, 37(4), 2000, pp. 301-303
A recurrent frameshift mutation of the ankyrin gene associated with severehereditary spherocytosis
Authors: Gallagher, PG Ferreira, JDS Costa, FF Saad, STO Forget, BG
Citation: Pg. Gallagher et al., A recurrent frameshift mutation of the ankyrin gene associated with severehereditary spherocytosis, BR J HAEM, 111(4), 2000, pp. 1190-1193
Mutation analysis of the HFE gene in Brazilian populations
Authors: Agostinho, MF Arruda, VR Basseres, DS Bordin, S Soares, MCP Menezes, RC Costa, FF Saad, STO
Citation: Mf. Agostinho et al., Mutation analysis of the HFE gene in Brazilian populations, BL CELL M D, 25(21), 1999, pp. 324-327
Arginine 490 is a hot spot for mutation in the band 3 gene in hereditary spherocytosis
Authors: Lima, PRM Sales, TSI Costa, FF Saad, STO
Citation: Prm. Lima et al., Arginine 490 is a hot spot for mutation in the band 3 gene in hereditary spherocytosis, EUR J HAEMA, 63(5), 1999, pp. 360-361
Haematopoietic response and bcl-2 expression in patients with acute myeloid leukaemia
Authors: Bincoletto, C Saad, STO da Silva, ES Queiroz, MLS
Citation: C. Bincoletto et al., Haematopoietic response and bcl-2 expression in patients with acute myeloid leukaemia, EUR J HAEMA, 62(1), 1999, pp. 38-42
Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] andalpha-thalassemia-2 (-alpha(3.7))
Authors: Grignoli, CRE Wenning, MRSC Sonati, MF Kimura, EM Arruda, VR Saad, STO Costa, FF
Citation: Cre. Grignoli et al., Hb Rio Claro [beta 34(B16)Val -> Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha 47(CE5)Asp -> His] andalpha-thalassemia-2 (-alpha(3.7)), HEMOGLOBIN, 23(2), 1999, pp. 177-182
Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease
Authors: Perlingeiro, RCR Costa, FF Saad, STO Arruda, VR Queiroz, MLS
Citation: Rcr. Perlingeiro et al., Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease, AM J HEMAT, 61(1), 1999, pp. 40-45
Risultati: 1-25 |