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Six-week-old male mice were divided into two groups and fed an MCDD

Furthermore, specific KOs s were found to be more abundant in each treatment group, uniquely, when compared to T1, particularly in T5 (68 KOs), where they were mainly encoding for proteins involved in the biosynthesis of cofactors ( AKR1A1 , ALDH , bioB , phoA , menB , pdxB ) and glycosaminoglycan degradation ( hya and HEXA_B )