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Showing 1 to 4 of 4 for “"Globin gene regulation"”.

  1. Analysis Of The Mouse p100H Mutation: Implications For Two Disease Related Genes: P and Sox6

    My dissertation is focused on the genetics analyses of a mouse mutation, p100H. This mutation is caused by a radiation-induced chromosomal inversion that disrupts both the p gene and Sox6. The human counterparts of these two murine genes are either known to cause human disease (human P gene) or …

    arizona-thes Repository record for Analysis Of The Mouse p100H Mutation: Implications For Two Disease Related Genes: P and Sox6 (opens in a new tab)

  2. The Roles of Krüppel-like Transcription Factors KLF1 and KLF2 in Mouse Embryonic and Human Fetal Erythropoiesis

    Hemoglobinopathies are some of the most common monogenic disorders in the world, affecting millions of people and representing a growing burden on health systems worldwide. Although the pathophysiology of sickle cell anemia and beta-thalassemia, two of the most common hemoglobinopathies, have been …

    vcu Repository record for The Roles of Krüppel-like Transcription Factors KLF1 and KLF2 in Mouse Embryonic and Human Fetal Erythropoiesis (opens in a new tab)

  3. Investigating the function of DNA G-quadruplex structures in human enhancers

    … 3D folding of interphase chromosomes to regulate gene transcription. However, the functional relevance of G4 structures at non- coding enhancer elements remains poorly understood. In this thesis, I explore the folding of G4 structure in 3D chromatin interactions, and dissect the function of a G4 …

    cambridge Repository record for Investigating the function of DNA G-quadruplex structures in human enhancers (opens in a new tab)