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This is unsurprising since oncogenesis requires multiple mutations including both oncogene induction and tumor suppressor attenuation." [13] History [edit] Dihexa was developed by Joseph Harding and his team at Washington State University

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Its converted into succinic acid via a B12-dependent enzyme

The Ramachandran plot analysis showed that 93.1% of the residues (352 aa) located in favored region, 5.8% of the residues (22 aa) located in allowed region and only 1.1% of the residues (4 aa) located in outlier region, suggesting high quality of the protein model (Figure 1B)