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1 phosphorylation of specific sites on axin by casein kinase I.
2 ties of the purified kinase identified it as casein kinase I.
3 a consensus sequence for phosphorylation by casein kinase I.
4 hia coli could be phosphorylated in vitro by casein kinase I.
5 inactivated by Cki1, the S. pombe homolog of casein kinase I.
6 evidence is presented indicating that it is casein kinase I.
7 e identify the major phosphorylation site of casein kinase I.
9 ulted in the amplification of cDNAs encoding casein kinase I-alpha and -gamma, while an in-gel casein
12 dation requires phosphorylation of PHLPP1 by casein kinase I and glycogen synthase kinase 3beta (GSK-
13 ce, and the prospective Ser residue-specific casein kinase I and II phosphorylation sites for this pu
14 endent protein kinase, casein kinase II, and casein kinase I and not at all phosphorylated by MAPK.
16 ctivity; phosphopeptide analysis showed that casein kinase I and the connexin49 protein kinase activi
17 ation of optimal peptide substrates of CDK5, casein kinases I and II, NIMA, calmodulin-dependent kina
18 nt galectin-3 was phosphorylated in vitro by casein kinase I, and separated from the native species b
19 horylates Fas ligand, in which two conserved casein kinase I binding sites regulate NFAT activation a
20 n49 was shown to be a substrate for purified casein kinase I but not for casein kinase II; the endoge
21 us of Rho, as observed by phosphorylation by casein kinase I, but did not affect phosphorylation by R
29 ested the ability of the acidotropic kinases casein kinase I (CKI) and casein kinase II (CKII) to pho
37 is established that Ser45 phosphorylation by casein kinase I (CKI) initiates phosphorylation at Thr41
40 veral approaches were used to determine that casein kinase I (CKI) is physically anchored in the flag
42 osophila melanogaster, mutations affecting a casein kinase I (CKI) ortholog called doubletime (dbt) c
43 iew these roles, including recent results on casein kinase I (CKI) phosphorylation and activation of
46 Here we show that protein kinase A (PKA) and casein kinase I (CKI) regulate Smo cell-surface accumula
47 to growth signals, and in collaboration with casein kinase I (CKI), generates a phosphodegron that bi
50 utation in a phosphorylation site within the casein kinase I (CKI)-binding domain of the human PER2 g
53 ycolytic enzymes, phosphorylation of CDB3 by casein kinase I could conceivably impact erythrocyte str
54 ytic region of the mammalian protein kinase, casein kinase I delta (CKI delta), has been solved by X-
56 r a critical requirement for the centrosomal casein kinase I delta (CKIdelta) in centrosome transloca
58 Set8 for ubiquitination and degradation in a casein kinase I-dependent manner, which is activated by
60 ant for phosphorylation of Drosophila PER by casein kinase I epsilon (CKI epsilon; doubletime protein
61 ns, the cryptochromes (mCRY1 and mCRY2), and casein kinase I epsilon (CKIepsilon) form multimeric com
63 The Drosophila double-time gene product, a casein kinase I epsilon (CKIepsilon) homolog, has been r
67 has suggested that phosphorylation of Dsh by Casein Kinase I epsilon (CKIepsilon) may act as a molecu
70 (CSNK1 epsilon, encoding the Ser/Thr kinase casein kinase I epsilon; DLG1, encoding a membrane-assoc
74 ne MTA1s-interacting proteins, we identified casein kinase I-gamma 2 (CKI-gamma2, a ubiquitously expr
77 hemical evidence suggests involvement of the casein kinase I homolog doubletime (dbt) in the Drosophi
79 of the interaction between FRQ and CK-1a (a casein kinase I homolog) results in the hypophosphorylat
86 to vertebrate epsilon and delta isoforms of casein kinase I, is essential for circadian rhythmicity
87 scription-PCR using total ovine lens RNA and casein kinase I isoform-specific oligonucleotide primers
88 her, upon Fas ligand-mediated costimulation, casein kinase I phosphorylates Fas ligand, in which two
89 es, we show that Hrr25p, an isoform of yeast casein kinase I, phosphorylates Tif6p both in vitro and
92 this sequence not only showed two consensus casein kinase I phosphorylation sites, but also provided
96 protein kinase A, CDK2, Erk2, twitchin, and casein kinase I, provide a structural basis for the subs
97 expressed in Chinese hamster ovary cells and casein kinase I readily phosphorylated the immunopurifie
100 a 12-amino acid leader sequence containing a casein kinase I serine phosphorylation site, which is pr
101 phosphorylation of CIITA by GSK3 relies on a casein kinase I site three amino acids C-terminal to the
102 lens membranes with KCl was inhibited by the casein kinase I-specific inhibitor, N-(2-aminoethyl)-5-c
104 ucleation pathway were identified as well as casein kinase I, which had a similar morphological RNAi
108 When HOPS is phosphorylated by the vacuolar casein kinase I, Yck3p, tethering only takes place when
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