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These effects are in line with the reported loss of many LT muscles in msh mutants [13] and suggest that this loss may in part be due to the failure in the proper activation of these three muscle identity genes in their muscle founders.
These effects are in line with previous studies where it has been reported that there was a lack of globally increased histone H3 methylation after genetic ablation of KDM1 in murine ES cells [49], and following the suppression of KDM1 by T, or its knockdown by siRNA in human cervical cancer cell lines [48].
These effects are in line with data that showed PPARα-mediated downregulation of genes involved in hepatic amino acid metabolism [ 40, 63].
These effects are in line with earlier observations that the beta variant of C/EBP is important in the differentiation and maturation of adipocytes [ 13].
These long-term effects are in line with recommended alternate low-dose chemical safety testing approaches.
Further effects are in line with former analyses [ 23].
Both interaction effects are in line with the hypothesis.
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