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F F Costa

Showing results (201-210 of 228) with videos related to

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International Journal of Laboratory Hematology|June 1, 2018
First report of εγδβ<sup>0</sup> -thalassemia in a Brazilian familyR D Ferreira, N O Mota, G A Pedroso, et al.
Archives of Biochemistry and Biophysics|December 5, 2017
Understanding the molecular basis of the high oxygen affinity variant human hemoglobin CoimbraS E Jorge, M Bringas, A A Petruk, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 6, 2000
alpha-globin genes: thalassemic and structural alterations in a Brazilian populationM R Wenning, E M Kimura, F F Costa, et al.
Human Heredity|November 1, 1994
Sickle cell disease in a Brazilian population from Sao Paulo: a study of the beta s haplotypesM S Goncalves, J F Nechtman, M S Figueiredo, et al.
Journal of Thrombosis and Haemostasis : JTH|July 24, 2012
Hydroxyurea is associated with reductions in hypercoagulability markers in sickle cell anemiaM P Colella, E V De Paula, N Conran, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|May 26, 2010
Death switch for gene therapy: application to erythropoietin transgene expressionD S Souza, D M Spencer, T S I Salles, et al.
British Journal of Haematology|May 22, 2008
The deletion of SOX8 is not associated with ATR-16 in an HbH family from BrazilM A C B Bezerra, A S Araujo, M Phylipsen, et al.
Leukemia|August 7, 2012
miR-433 is aberrantly expressed in myeloproliferative neoplasms and suppresses hematopoietic cell growth and differentiationX Lin, K L Rice, M Buzzai, et al.
Tropical and Geographical Medicine|October 1, 1992
Growth and sexual maturation of Brazilian patients with sickle cell diseasesM A Zago, J Kerbauy, H M Souza, et al.
American Journal of Hematology|January 1, 1994
Beta S-gene-cluster haplotypes in sickle cell anemia patients from two regions of BrazilF F Costa, V R Arruda, M G Gonçalves, et al.
Pageof 23

Showing results (201-210 of 228) with videos related to

Sort By:
Pageof 23
International Journal of Laboratory Hematology|June 1, 2018
First report of εγδβ<sup>0</sup> -thalassemia in a Brazilian familyR D Ferreira, N O Mota, G A Pedroso, et al.
Archives of Biochemistry and Biophysics|December 5, 2017
Understanding the molecular basis of the high oxygen affinity variant human hemoglobin CoimbraS E Jorge, M Bringas, A A Petruk, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 6, 2000
alpha-globin genes: thalassemic and structural alterations in a Brazilian populationM R Wenning, E M Kimura, F F Costa, et al.
Human Heredity|November 1, 1994
Sickle cell disease in a Brazilian population from Sao Paulo: a study of the beta s haplotypesM S Goncalves, J F Nechtman, M S Figueiredo, et al.
Journal of Thrombosis and Haemostasis : JTH|July 24, 2012
Hydroxyurea is associated with reductions in hypercoagulability markers in sickle cell anemiaM P Colella, E V De Paula, N Conran, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|May 26, 2010
Death switch for gene therapy: application to erythropoietin transgene expressionD S Souza, D M Spencer, T S I Salles, et al.
British Journal of Haematology|May 22, 2008
The deletion of SOX8 is not associated with ATR-16 in an HbH family from BrazilM A C B Bezerra, A S Araujo, M Phylipsen, et al.
Leukemia|August 7, 2012
miR-433 is aberrantly expressed in myeloproliferative neoplasms and suppresses hematopoietic cell growth and differentiationX Lin, K L Rice, M Buzzai, et al.
Tropical and Geographical Medicine|October 1, 1992
Growth and sexual maturation of Brazilian patients with sickle cell diseasesM A Zago, J Kerbauy, H M Souza, et al.
American Journal of Hematology|January 1, 1994
Beta S-gene-cluster haplotypes in sickle cell anemia patients from two regions of BrazilF F Costa, V R Arruda, M G Gonçalves, et al.
Pageof 23