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- W1978940448 abstract "Synthesis of normal human hemoglobin A, alpha 2 beta 2, is based upon balanced expression of genes in the alpha-globin gene cluster on chromosome 16 and the beta-globin gene cluster on chromosome 11. Full levels of erythroid-specific activation of the beta-globin cluster depend on sequences located at a considerable distance 5' to the beta-globin gene, referred to as the locus-activating or dominant control region. The existence of an analogous element(s) upstream of the alpha-globin cluster has been suggested from observations on naturally occurring deletions and experimental studies. We have identified an individual with alpha-thalassemia in whom structurally normal alpha-globin genes have been inactivated in cis by a discrete de novo 35-kilobase deletion located approximately 30 kilobases 5' from the alpha-globin gene cluster. We conclude that this deletion inactivates expression of the alpha-globin genes by removing one or more of the previously identified upstream regulatory sequences that are critical to expression of the alpha-globin genes." @default.
- W1978940448 created "2016-06-24" @default.
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- W1978940448 date "1990-12-01" @default.
- W1978940448 modified "2023-09-23" @default.
- W1978940448 title "Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene cluster." @default.
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- W1978940448 doi "https://doi.org/10.1073/pnas.87.23.9431" @default.
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