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Int J Nanomed (2018) 13:210728

Early research described it as relatively selective for GH release compared with some older secretagogues (Raun et al., 1998)

Kainate receptors are also tetrameric complexes of GluR57 and KA12 subunits

For example, leukemia cells treated with a histone deacetylase (HDAC) inhibitor showed an increased expression of the nuclear drug target, topoisomerase II (see Sec