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Explore the molecular basis of human hereditary hemolytic anemias, bilirubin metabolism disorders, and the role of spectrin in cell function. Also, delve into animal genetics using microsatellite markers and mitochondrial genomes.
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Department of Biochemistry and Bioinformatics • Analysis of the molecular basis of common and unknown human hereditary hemolytic anemias • Research on the structure and function of normal and pathological red blood cell membrane
Department of Biochemistry and Bioinformatics • Co-inherited mutations intensifying clinical picture of hyperbilirubinemia and impair condition of patients with hemolytic anemia • Disorders of bilirubin metabolism
Department of Biochemistry and Bioinformatics • Study of thespectrin role in nonerytroid cells: • in cell-cell contact • in T cell activation, • in immunological synapse formation • in dynamics of actin in lamellipodia
Department of Biochemistry and Bioinformatics • Genetics of animals: • microsatellite markers • in population research ( Myotis myotis, Plecotus auricus) • mitochondrial genome for the genus Anguis,