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cerevisiae in which the ATP consuming glucose-glycogen bypass pathway had been shut-down by deletion of the GBE achieved 3.1-fold higher ATP-generating activity and 1.7-fold higher GSH productivity compared with the control strain [15]

85, 86 Current data showed that the nuclear localization of CPTI existed exclusively in neoplastic cells, and HDAC1 and CPTI coimmunoprecipitats in nuclear extracts from MCF-7 cells