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1 ZIPK also binds and phosphorylates proapoptotic protein
2 ZIPK is regulated by multisite phosphorylation.
3 ZIPK mRNA and protein are abundant in heart tissue and i
4 onclude that a pool of constitutively active ZIPK is involved in regulation of vascular smooth muscle
7 , and inhibitory phosphorylation of MYPT1 by ZIPK requires "unlocking" of Par-4 by phosphorylation an
8 Mutation of Thr299 alone to alanine caused ZIPK to assume a diffuse cellular localization, whereas
9 ility of ZIPK to oligomerize and also caused ZIPK to relocalize from the cytoplasm to the nucleus in
10 13a is phosphorylated at Ser(77) by the DAPK-ZIPK cascade, but EPRS is phosphorylated only at Ser(999
13 atic applications, we have pinpointed DAPK3 (ZIPK) as a novel cancer-associated kinase with functiona
14 in kinase subdomain X is essential for full ZIPK autophosphorylation and activity toward exogenous s
15 have identified six phosphorylation sites in ZIPK that regulate both its enzyme activity and localiza
17 tation of the leucine zipper motif increased ZIPK activity toward exogenous substrates by severalfold
21 ibitor of zipper-interacting protein kinase (ZIPK) was used to examine the involvement of ZIPK in the
22 activates zipper-interacting protein kinase (ZIPK), culminating in L13a phosphorylation on Ser(77), L
26 egree of substrate specificity toward native ZIPK, both stoichiometrically phosphorylating the enzyme
27 ions of Moloney (PIM) virus 3 kinase but not ZIPK, had no effect on calyculin A-induced contraction o
28 of the leucine zipper reduced the ability of ZIPK to oligomerize and also caused ZIPK to relocalize f
32 ZIPK) was used to examine the involvement of ZIPK in the regulation of smooth muscle contraction.
35 small-interfering RNA-mediated reduction of ZIPK, Daxx, or Par-4 expression decreased activation of
37 sed substrate search performed with purified ZIPK on heart homogenates led to the discovery of a prom
41 association of Daxx with PODs, implying that ZIPK recruits Daxx to PODs via its catalytic activity.
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