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1 d CaMKIK beta are also capable of activating CaM kinase IV.
5 n of a transcriptional program that involves CaM kinase IV and CREB-mediated signaling to the nucleus
6 ng via calcium/calmodulin-dependent protein (CaM) kinase IV and microtubule-associated protein (MAP)
7 n be induced by activation of CaM kinase II, CaM kinase IV, and protein kinase A, but not by activati
12 ible for persistent CREB phosphorylation and CaM kinase IV (CaMKIV) responsible for phosphorylating t
17 inhibitors, a constitutively active form of CaM kinase IV induces dendritic growth in the absence of
18 ession of constitutively active or wild-type CaM kinase IV inhibited Ca2+ stimulation of adenylyl cyc
24 esults in the calcium-mediated activation of CaM kinase IV, phosphorylation of CREB, increased expres
26 titutively active mutants of CaM kinase I or CaM kinase IV specifically blocks nuclear targeting of C
27 lular stimulation, and a kinase-dead form of CaM kinase IV suppresses dendritic growth induced by cal
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