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While the expression of DNMT3B, DNMT3L, and TET1 is barely detectable in SCD erythroblasts, the expression of DNMT1, DNMT3A, TET2 or TET3 was not significantly changed at the mRNA or protein level after DMF treatment (Supplementary Fig

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By activating both GLP-1 and GIP receptors, it has produced more pronounced metabolic effects in clinical trials than single-agonist predecessors

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N.CiceroT

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MDR1, Multidrug Resistance 1

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