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Showing 1 to 4 of 4 for “"loss-of-imprinting"”.

  1. Large offspring syndrome, a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann

    Beckwith-Wiedemann syndrome (BWS) is a human loss-of-imprinting syndrome primarily characterized by macrosomia, macroglossia, and abdominal wall defects. BWS has been associated with misregulation of two clusters of imprinted genes. Children conceived with the use of assisted reproductive …

    missouri Repository record for Large offspring syndrome, a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann (opens in a new tab)

  2. Establishment of a phenotypical model of adverse outcomes associated with assisted reproductive technologies

    Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. BWS is speculated to occur primarily as the result of the misregulation of imprinted genes associated with two clusters on chromosome 11p15.5, namely the KvDMR1 and H19/IGF2. There is a similar overgrowth …

    missouri Repository record for Establishment of a phenotypical model of adverse outcomes associated with assisted reproductive technologies (opens in a new tab)

  3. The role of imprinting in embryonic development and tumorigenesis

    Imprinting is a mammalian adaptation that results in the mono-allelic expression of a subset of genes depending on their parental origin. It is believed that DNA methylation marks are responsible for maintaining imprinted gene expression patterns. The 'parental conflict' hypothesis was proposed to …

    mit Repository record for The role of imprinting in embryonic development and tumorigenesis (opens in a new tab)

  4. Regulation of the Kcnq1ot1 Imprinting Domain in Mouse

    Genomic imprinting is an epigenetic mechanism that controls gene expression based on parental-origin of an allele. The Kcnq1ot1 imprinting cluster consists of an imprinting control region (ICR), the Kcnq1ot1 ncRNA, and maternally expressed protein-coding genes. Truncation of the Kcnq1ot1 ncRNA or …

    uwo Repository record for Regulation of the Kcnq1ot1 Imprinting Domain in Mouse (opens in a new tab)