AAAAAA

   
Results: 1-25 | 26-32
Results: 1-25/32
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
High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia
Authors: Borges, E Wenning, MRSC Kimura, EM Gervasio, SA Costa, FF Sonati, MF
Citation: E. Borges et al., High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia, BRAZ J MED, 34(6), 2001, pp. 759-762
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
The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome
Authors: Camargo, AA Samaia, HPB Dias-Neto, E Simao, DF Migotto, IA Briones, MRS Costa, FF Nagai, MA Verjovski-Almeida, S Zago, MA Andrade, LEC Carrer, H El-Dorry, HFA Espreafico, EM Habr-Gama, A Giannella-Neto, D Goldman, GH Gruber, A Hackel, C Kimura, ET Maciel, RMB Marie, SKN Martins, EAL Nobrega, MP Paco-Larson, ML Pardini, MIMC Pereira, GG Pesquero, JB Rodrigues, V Rogatto, SR da Silva, IDCG Sogayar, MC Sonati, MDF Tajara, EH Valentini, SR Alberto, FL Amaral, MEJ Aneas, I Arnaldi, LAT de Assis, AM Bengtson, MH Bergamo, NA Bombonato, V de Camargo, MER Canevari, RA Carraro, DM Cerutti, JM Correa, MLC Correa, RFR Costa, MCR Curcio, C Hokama, POM Ferreira, AJS Furuzawa, GK Gushiken, T Ho, PL Kimura, E Krieger, JE Leite, LCC Majumder, P Marins, M Marques, ER Melo, ASA Melo, M Mestriner, CA Miracca, EC Miranda, DC Nascimento, ALTO Nobrega, FG Ojopi, EPB Pandolfi, JRC Pessoa, LG Prevedel, AC Rahal, P Rainho, CA Reis, EMR Ribeiro, ML da Ros, N de Sa, RG Sales, MM Sant'anna, SC dos Santos, ML da Silva, AM da Silva, NP Silva, WA da Silveira, RA Sousa, JF Stecconi, D Tsukumo, F Valente, V Soares, F Moreira, ES Nunes, DN Correa, RG Zalcberg, H Carvalho, AF Reis, LFL Brentani, RR Simpson, AJG de Souza, SJ
Citation: Aa. Camargo et al., The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome, P NAS US, 98(21), 2001, pp. 12103-12108
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
Low incidence of human herpesvirus 8 in bone marrow samples from Brazilianpatients with multiple myeloma
Authors: Cunha, A Costa, SC Lima, CSP Ortega, M Costa, FF
Citation: A. Cunha et al., Low incidence of human herpesvirus 8 in bone marrow samples from Brazilianpatients with multiple myeloma, ACT HAEMAT, 105(4), 2001, pp. 247-248
HLA-DRB1 alleles and the prognosis of rheumatoid arthritis in Brazilian patients
Authors: Bertolo, MB Costallat, LTL Persoli, LB Costa, FF
Citation: Mb. Bertolo et al., HLA-DRB1 alleles and the prognosis of rheumatoid arthritis in Brazilian patients, JCR-J CLIN, 6(4), 2000, pp. 233-235
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
Hb Campinas [alpha 26(B7)Ala -> Val]: a novel, electrophoretically silent,variant
Authors: Wenning, MRSC Silva, NM Jorge, SB Kimura, EM Costa, FF Torsoni, MA Ogo, SH Sonati, MF
Citation: Mrsc. Wenning et al., Hb Campinas [alpha 26(B7)Ala -> Val]: a novel, electrophoretically silent,variant, HEMOGLOBIN, 24(2), 2000, pp. 143-148
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
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
The genome sequence of the plant pathogen Xylella fastidiosa
Authors: Simpson, AJG Reinach, FC Arruda, P Abreu, FA Acencio, M Alvarenga, R Alves, LMC Araya, JE Baia, GS Baptista, CS Barros, MH Bonaccorsi, ED Bordin, S Bove, JM Briones, MRS Bueno, MRP Camargo, AA Camargo, LEA Carraro, DM Carrer, H Colauto, NB Colombo, C Costa, FF Costa, MCR Costa-Neto, CM Coutinho, LL Cristofani, M Dias-Neto, E Docena, C El-Dorry, H Facincani, AP Ferreira, AJS Ferreira, VCA Ferro, JA Fraga, JS Franca, SC Franco, MC Frohme, M Furlan, LR Garnier, M Goldman, GH Goldman, MHS Gomes, SL Gruber, A Ho, PL Hoheisel, JD Junqueira, ML Kemper, EL Kitajima, JP Krieger, JE Kuramae, EE Laigret, F Lambais, MR Leite, LCC Lemos, EGM Lemos, MVF Lopes, SA Lopes, CR Machado, JA Machado, MA Madeira, AMBN Madeira, HMF Marino, CL Marques, MV Martins, EAL Martins, EMF Matsukuma, AY Menck, CFM Miracca, EC Miyaki, CY Monteiro-Vitorello, CB Moon, DH Nagai, MA Nascimento, ALTO Netto, LES Nhani, A Nobrega, FG Nunes, LR Oliveira, MA de Oliveira, MC de Oliveira, RC Palmieri, DA Paris, A Peixoto, BR Pereira, GAG Pereira, HA Pesquero, JB Quaggio, RB Roberto, PG Rodrigues, V Rosa, AJD de Rosa, VE de Sa, RG Santelli, RV Sawasaki, HE da Silva, ACR da Silva, AM da Silva, FR Silva, WA da Silveira, JF Silvestri, MLZ Siqueira, WJ de Souza, AA de Souza, AP Terenzi, MF Truffi, D Tsai, SM Tsuhako, MH Vallada, H Van Sluys, MA Verjovski-Almeida, S Vettore, AL Zago, MA Zatz, M Meidanis, J Setubal, JC
Citation: Ajg. Simpson et al., The genome sequence of the plant pathogen Xylella fastidiosa, NATURE, 406(6792), 2000, pp. 151-157
Shotgun sequencing of the human transcriptome with ORF expressed sequence tags
Authors: Neto, ED Correa, RG Verjovski-Almeida, S Briones, MRS Nagai, MA da Silva, W Zago, MA Bordin, S Costa, FF Goldman, GH Carvalho, AF Matsukuma, A Baia, GS Simpson, DH Brunstein, A de Oliveira, PSL Bucher, P Jongeneel, CV O'Hare, MJ Soares, F Brentani, RR Reis, LFL de Souza, SJ Simpson, AJG
Citation: Ed. Neto et al., Shotgun sequencing of the human transcriptome with ORF expressed sequence tags, P NAS US, 97(7), 2000, pp. 3491-3496
Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags
Authors: de Souza, SJ Camargo, AA Briones, MRS Costa, FF Nagai, MA Verjovski-Almeida, S Zago, MA Andrade, LEC Carrer, H El-Dorry, HFA Espreafico, EM Habr-Gama, A Giannella-Neto, D Goldman, GH Gruber, A Hackel, C Kimura, ET Maciel, RMB Marie, SKN Martins, EAL Nobrega, MP Paco-Larson, ML Pardini, MIMC Pereira, GG Pesquero, JB Rodrigues, V Rogatto, SR da Silva, IDCG Sogayar, MC Sonati, MD Tajara, EH Valentini, SR Acencio, M Alberto, FL Amaral, MEJ Aneas, I Bengtson, MH Carraro, DM Carvalho, AF Carvalho, LH Cerutti, JM Correa, MLC Costa, MCR Curcio, C Gushiken, T Ho, PL Kimura, E Leite, LCC Maia, G Majumder, P Marins, M Matsukuma, A Melo, ASA Mestriner, CA Miracca, EC Miranda, DC Nascimento, ALTO Nobrega, FG Ojopi, EPB Pandolfi, JRC Pessoa, LG Rahal, P Rainho, CA da Ro's, N de Sa, RG Sales, MM da Silva, NP Silva, TC da Silva, W Simao, DF Sousa, JF Stecconi, D Tsukumo, F Valente, V Zalcberg, H Bretani, RR Reis, LFL Dias-Neto, E Simpson, AJG
Citation: Sj. De Souza et al., Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags, P NAS US, 97(23), 2000, pp. 12690-12693
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
Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patients
Authors: Nogueira, E Arruda, VR Bizzacchi, JMA Costa, FF Ozelo, MC Rossi, CL Costa, SCB
Citation: E. Nogueira et al., Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patients, ACT HAEMAT, 103(2), 2000, pp. 73-77
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
Risultati: 1-25 | 26-32