The hematopoietic system provides one of the most attractive systems for studies
on development at both levels of molecular characterization and systems biology.
Among the single-gene related disorders, hemoglobinopathies ranked on top with
the prevalence of 4.83% in the world population (Urbinati et al., 2006). These
reasons underlined the need of discovering the mechanisms underlying hemoglobin
regulation and erythropoiesis. This thesis describes a journey beginning with an
attempt to establish an in vitro hematopoietic progenitor cell system, passing
through the transcriptional complexes regulating general aspects of erythropoiesis
including the regulation of globin gene expression. It ends with a proposal to select
patients with β-thalassemia for hydroxyurea treatment.
http://repub.eur.nl/res/pub/26726/111020_Esteghamat%20Hanzaei%2C%20Fatemehsadat%20-%20BEWERKT.pdf
http://repub.eur.nl/res/pub/26726/111020_Esteghamat%20Hanzaei%2C%20Fatemehsadat%20-%20BEWERKT.pdf
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