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Learn MoreTo characterize the translation defects in Maf1-/- samples, we used ribosome profiling on three WT and three Maf1-/- fed livers. Each sample was spiked with a fixed amount of Drosophila S2 Schneider cell material as an internal control for sample-to-sample normalization, and to allow detection of global changes in translation. SOURCE: Viviane Praz (viviane.praz@unil.ch) - Hernandez University of Lausanne
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