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Expert Review of Hematology|November 19, 2010
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatmentKleber Yotsumoto Fertrin, Fernando Ferreira CostaBiochemistry Research International|April 15, 2011
Alpha-hemoglobin-stabilizing protein: an erythroid molecular chaperoneMaria Emília Favero, Fernando Ferreira CostaAnnals of Hematology|July 14, 2026
UGT1A1 polymorphisms and gallbladder-related outcomes in sickle cell disease in BrazilFernando Ferreira Costa, Kleber Yotsumoto FertrinJornal De Pediatria|September 16, 2008
The genetics of blood disorders: hereditary hemoglobinopathiesMaria de Fátima Sonati, Fernando Ferreira CostaHematology (Amsterdam, Netherlands)|July 16, 2005
AHSP and beta-thalassemia: a possible genetic modifierCamila Oresco dos Santos, Fernando Ferreira CostaAntioxidants (Basel, Switzerland)|December 30, 2025
Heme Modulates Bladder Contractility Through the HO-CO-sGC-cGMP Pathway: Insights into Sickle Cell Disease-Associated Bladder DysfunctionDalila Andrade Pereira, Fernando Ferreira Costa, Fábio Henrique SilvaIn Silico Biology|August 11, 2007
LyM: a tool to reach the best factor in gene expression comparisonTarcísio de Souza Peres, Fernando Ferreira Costa, Fernando Lopes AlbertoZoological Science|December 11, 2012
On the apterous line of the termite Velocitermes heteropterus (Isoptera: Termitidae): developmental pathways and cellulose digestionIves Haifig, Flávia Costa Leonardo, Fernando Ferreira Costa, et al.Biochimica Et Biophysica Acta|March 10, 2009
ARHGAP21 modulates FAK activity and impairs glioblastoma cell migrationCarolina Louzão Bigarella, Luciene Borges, Fernando Ferreira Costa, et al.Hematology (Amsterdam, Netherlands)|November 9, 2005
Granulocytic adhesive interactions and their role in sickle cell vaso-occlusionAndreia Averci Canalli, Fernando Ferreira Costa, Sara T O Saad, et al.Pageof 15