Fernando Ferreira Costa
Fernando Ferreira Costa
UNICAMP,State university of Campinas,University of Campinas
E-mail confirmado em
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Sickle cell disease
GJ Kato, FB Piel, CD Reid, MH Gaston, K Ohene-Frempong, ...
Nature reviews Disease primers 4 (1), 1-22, 2018
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
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism
J Emmerich, FR Rosendaal, M Cattaneo, M Margaglione, V De Stefano, ...
Thrombosis and haemostasis 86 (09), 809-816, 2001
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
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
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
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 Leucocyte Biology 85 (2), 235-242, 2009
Analysis of the 677 C→ T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups
RF Franco, AG Araujo, JF Guerreiro, J Elion, MA Zago
Thrombosis and haemostasis 59 (01), 119-121, 1998
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 Methylenetetrahydrofolate Reductase TT677 Genotype Is Associated with Venous Thrombosis Independently of the Coexistence of the FV Leiden and the Prothrombin
M Margaglione, G D’Andrea, M d’Addedda, N Giuliani, G Cappucci, ...
Thrombosis and haemostasis 79 (05), 907-911, 1998
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
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
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
Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis
MBAJ KeiJzer, M Den Heijer, HJ Blom, GMJ Bos, HPJ Willems, ...
Thrombosis and haemostasis 88 (11), 723-728, 2002
Hydroxyurea and a cGMP-amplifying agent have immediate benefits on acute vaso-occlusive events in sickle cell disease mice
CB Almeida, C Scheiermann, JE Jang, C Prophete, FF Costa, N Conran, ...
Blood, The Journal of the American Society of Hematology 120 (14), 2879-2888, 2012
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
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