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Loss of Imprinting of IGF2 Sense and Antisense Transcripts in Films' Tumor Thanh H. VU, Nguyen V. Chosen, Tao Li, et al. Cancer Res 2003;63:1900-1905. Updated Version Access the most recent version
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Loss of imprinting refers to the phenomenon in which one of the two parental alleles fails to undergo normal epigenetic modifications during gametogenesis or early development.
Loss of imprinting report should be filed by researchers or organizations studying epigenetics or genetic inheritance patterns.
The loss of imprinting report should include detailed information about the specific gene or genes affected, experimental methods used, and any observed changes in gene expression or phenotype.
The purpose of studying loss of imprinting is to better understand the role of epigenetic modifications in gene regulation and inheritance, and to identify any potential implications for human health and disease.
The loss of imprinting report should include details such as the gene or genes affected, the specific epigenetic modifications that are aberrant or absent, and any associated changes in gene expression or phenotypic outcomes.
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