Hemoglobin, Sickle

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  Subject Areas on Research

  • Absence of Association Between Sickle Trait Hemoglobin and Placental Malaria Outcomes. 
  • Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure. 
  • Cerebral infarction in sickle cell trait. 
  • Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia. 
  • Effect of red blood cell variants on childhood malaria in Mali: a prospective cohort study. 
  • Effects of S-nitrosation on oxygen binding by normal and sickle cell hemoglobin. 
  • Functional properties of normal and sickle cell hemoglobins in polyethylene glycol 6000. 
  • Genetic polymorphisms associated with priapism in sickle cell disease. 
  • Haemoglobinopathies and the clinical epidemiology of malaria: a systematic review and meta-analysis. 
  • Heme redox properties of S-nitrosated hemoglobin A0 and hemoglobin S: implications for interactions of nitric oxide with normal and sickle red blood cells. 
  • Impaired cytoadherence of Plasmodium falciparum-infected erythrocytes containing sickle hemoglobin. 
  • MEK1/2 inhibitors reverse acute vascular occlusion in mouse models of sickle cell disease. 
  • Malaria parasites and red cell variants: when a house is not a home. 
  • Neurocognitive development of young children with sickle cell disease through three years of age. 
  • New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease. 
  • Nucleation of microtubule assembly. Experimental kinetics, computer fitting of models, and observations on tubulin rings. 
  • Patent foramen ovale in adults with sickle cell disease and stroke. 
  • Responses of normal and sickle cell hemoglobin to S-nitroscysteine: implications for therapeutic applications of NO in treatment of sickle cell disease. 
  • Screening of blood donors for sickle cell trait using a DNA-based approach: Frequency in a multiethnic donor population. 
  • Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review. 
  • Sickle-trait hemoglobin reduces adhesion to both CD36 and EPCR by Plasmodium falciparum-infected erythrocytes. 
  • Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. 
  • The clinical manifestations of cerebral malaria among Nigerian children with the sickle cell trait. 
  • The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia. 
  • The genomic analysis of erythrocyte microRNA expression in sickle cell diseases. 
  • The lung in sickle cell disease. 
  • Thermodynamic and kinetic aspects of assembly. 
  • Translocation of sickle cell erythrocyte microRNAs into Plasmodium falciparum inhibits parasite translation and contributes to malaria resistance. 
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  Keywords of People

  • Ibemere, Stephanie, Assistant Professor in the School of Nursing, School of Nursing
  • Shah, Nirmish Ramesh, Associate Professor of Medicine, School of Nursing