Hereditary spherocytosis (HS) belongs to the group of congenital hemolytic anemias
resulting from plasma membrane protein deficiency. When diagnosed too late, HS bares the …

In this minireview, we focus on advances in our knowledge of the human erythrocyte
proteome and interactome that have occurred since our seminal review on the topic …

Protein turnover through cullin-3 is tightly regulated by posttranslational modifications, the
COP9 signalosome, and BTB/POZ-domain proteins that link cullin-3 to specific substrates for …

Red blood cells have been extensively studied but many questions regarding membrane
properties and pathophysiology remain unanswered. Proteome analysis of red cell …

We overview recent advances in the theoretical modeling, in particular via numerical
simulation, of various vital human erythrocyte phenomena. The review is novel in how it …

Red blood cells are rather unique body cells, since they have lost all organelles when
mature, which results in lack of potential to replace proteins that have lost their function …

Erythrocytes undergo ineffective erythropoesis, hemolysis, and premature eryptosis in sickle
cell disease and thalassemia. Abnormal hemoglobin variants associated with …

İnsanlık tarihinin belki de en büyük ve sonuçları açısından en önemli projelerinden biri olan
İnsan Genom Projesi (Human Genome Project, HGP) ile elde edilen bilgilerin özellikle klinik …

Bacteriocins are antimicrobial peptides produced by several bacterial species. Among the
bacteriocins pediocin-like bacteriocins have a significant inhibitory activity on the foodborne …

Deficiency of glucose-6-phosphate dehydrogenase (G6PD) and sickle cell trait (SCT) are
described as the polymorphic disorders prevalent in erythrocytes. Both are considered the …