Fernando Ferreira Costa
Fernando Ferreira Costa
UNICAMP,State university of Campinas,University of Campinas
E-mail confirmado em unicamp.br
Citado por
Citado por
The genome sequence of the plant pathogen Xylella fastidiosa
AJG Simpson, FC Reinach, P Arruda, FA Abreu, M Acencio, R Alvarenga, ...
Nature 406 (6792), 151-157, 2000
DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
G Lettre, VG Sankaran, MAC Bezerra, AS Araújo, M Uda, S Sanna, A Cao, ...
Proceedings of the National Academy of Sciences 105 (33), 11869, 2008
Sickle cell disease
GJ Kato, FB Piel, CD Reid, MH Gaston, K Ohene-Frempong, ...
Nature Reviews Disease Primers 4 (1), 1-22, 2018
The mutation Ala677--> Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.
VR Arruda, PM Von Zuben, LC Chiaparini, JM Annichino-Bizzacchi, ...
Thrombosis and haemostasis 77 (5), 818, 1997
Shotgun sequencing of the human transcriptome with ORF expressed sequence tags
E Dias Neto, R Garcia Correa, S Verjovski-Almeida, MRS Briones, ...
Proceedings of the National Academy of Sciences 97 (7), 3491, 2000
Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease.
VR Arruda, JM Annichino-Bizzacchi, MS Goncalves, FF Costa
Thrombosis and haemostasis 78 (6), 1430, 1997
Optical tweezers for measuring red blood cell elasticity: application to the study of drug response in sickle cell disease
MM Brandao, A Fontes, ML Barjas‐Castro, LC Barbosa, FF Costa, ...
European journal of haematology 70 (4), 207-211, 2003
Altered levels of cytokines and inflammatory mediators in plasma and leukocytes of sickle cell anemia patients and effects of hydroxyurea therapy
C Lanaro, CF Franco‐Penteado, DM Albuqueque, STO Saad, N Conran, ...
Journal of leukocyte biology 85 (2), 235-242, 2009
An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis
LM Hollanda, CSP Lima, AF Cunha, DM Albuquerque, J Vassallo, ...
Nature genetics 38 (7), 807-812, 2006
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion
N Conran, CF Franco-Penteado, FF Costa
Hemoglobin 33 (1), 1-16, 2009
The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome
AA Camargo, HPB Samaia, E Dias-Neto, DF Simão, IA Migotto, ...
Proceedings of the National Academy of Sciences 98 (21), 12103, 2001
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
WT Tse, MC Lecomte, FF Costa, M Garbarz, C Feo, P Boivin, D Dhermy, ...
The Journal of clinical investigation 86 (3), 909-916, 1990
Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3'beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus
JC Winkelmann, FF Costa, BL Linzie, BG Forget
Journal of Biological Chemistry 265 (33), 20449-20454, 1990
Prevalence of the mutation C677→ T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil
VR Arruda, LH Siqueira, MS Gonçalves, PM von Zuben, MCP Soares, ...
American Journal of Medical Genetics 78 (4), 332-335, 1998
El uso de los cuerpos
G Agamben, R Molina-Zavalía, F Costa
Adriana Hidalgo, 2017
ßS-Haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil
MS Gonçalves, GC Bomfim, E Maciel, I Cerqueira, I Lyra, A Zanette, ...
Brazilian Journal of Medical and Biological Research 36, 1283-1288, 2003
Chronic myeloid leukemia patients with the e13a2 BCR-ABL fusion transcript have inferior responses to imatinib compared to patients with the e14a2 transcript
CM Lucas, RJ Harris, A Giannoudis, A Davies, K Knight, SJ Watmough, ...
haematologica 94 (10), 1362, 2009
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: Relevance to …
VR Arruda, CE Grignolli, MS Gonçalves, MC Soares, R Menezes, ...
Clinical genetics 54 (3), 210, 1998
Effect of α‐thalassemia and β‐globin gene cluster haplotypes on the hematological and clinical features of sickle‐cell anemia in Brazil
MS Figueiredo, J Kerbauy, MS Gonçalves, VR Arruda, STO Saad, ...
American journal of hematology 53 (2), 72-76, 1996
DNA‐based typing of blood groups for the management of multiply‐transfused sickle cell disease patients
L Castilho, M Rios, C Bianco, J Pellegrino Jr, FL Alberto, STO Saad, ...
Transfusion 42 (2), 232-238, 2002
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