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Through bioinformatic analyses, metabolomics, and molecular, cellular and in vivo characterizations, we demonstrate that HNF4 plays a central role in controlling hepatic SAA metabolism and dictating sensitivity to methionine restriction in liver cancer both in vivo and in vitro
See, for example, the Nobel Prize Nomination Database: Mothers and daughters of invention: notes for a revised history of technology
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398, ISBN 0-12-181977-9
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