However, we could observe an increasing trend in K14Ac stoichiometry from CIC to CIM and from CIM to MIM that was mainly contributed by overall higher K14Ac stoichiometry in donors D160, D164, and D423.
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Change of histone H3 lysine 14 acetylation stoichiometry in human monocyte derived macrophages as determined by MS-based absolute targeted quantitative proteomic approach: HIV infection and methamphetamine exposure.
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