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1 e structure of the catalytic domain of human Cdc25 phosphatase.
2 ologues of the catalytic domain of the human Cdc25 phosphatase.
3 ted by Wee1-related kinases and activated by Cdc25 phosphatase.
4  activities of the Wee1/Myt1 kinases and the Cdc25 phosphatase.
5 ted by Wee1 tyrosine kinase and activated by Cdc25 phosphatase.
6 eracting activities of Wee1/Myt1 kinases and Cdc25 phosphatases.
7 ical inhibitors of Wee1 and Myt1 kinases and Cdc25 phosphatases.
8 of MPF is regulated by Wee1/Myt1 kinases and Cdc25 phosphatases.
9 ved arginine, which is also present in human Cdc25 phosphatases.
10 idue Cys75 are unchanged with respect to the Cdc25 phosphatases.
11 hat employ Chk1 and Chk2 Ser/Thr kinases and Cdc25 phosphatases.
12 p is not a phosphatase but is a homologue of CDC25 phosphatases.
13 s driven by downregulation of the activating Cdc25 phosphatases.
14 tive, and partially competitive inhibitor of Cdc25 phosphatases.
15 PF through the activating phosphorylation on Cdc25 phosphatases.
16 ternal mRNAs, string and twine, which encode Cdc25 phosphatases.
17 ate reductases form, together with the known Cdc25 phosphatases, a well-defined subfamily of the rhod
18                                              Cdc25 phosphatases activate cyclin-dependent kinases (Cd
19                                              Cdc25 phosphatases activate the cell division kinases th
20 string and twine; and (4) consequent loss of Cdc25 phosphatase activity allows inhibitory phosphoryla
21         We propose that direct inhibition of Cdc25 phosphatase activity by Chk1, as demonstrated in v
22                   Although the regulation of CDC25 phosphatase activity has been elucidated both bioc
23 idues in the active site motif abolished the Cdc25 phosphatase activity.
24 ontrolled by Cdk1, which is activated by the Cdc25 phosphatase and inhibited by Wee1 tyrosine kinase,
25               At the MBT, down-regulation of Cdc25 phosphatase and the resulting inhibitory phosphory
26                       Chk1 downregulates the Cdc25 phosphatases and concomitantly upregulates the Wee
27 e that triggers G2/M arrest and inhibits the Cdc25 phosphatase, and many compounds that synergize wit
28 f a key family of cell cycle regulators, the CDC25 phosphatases, and have identified four genes.
29 ) kinase dephosphorylation and activation by Cdc25 phosphatase are essential for mitotic entry.
30 with poor prognosis in many diverse cancers, Cdc25 phosphatases are attractive targets for anticancer
31                                              Cdc25 phosphatases are dual specificity phosphatases tha
32                                              Cdc25 phosphatases are key activators of the eukaryotic
33  dual specificity, low-molecular-weight, and Cdc25 phosphatases, are key mediators of a wide variety
34                                              Cdc25 phosphatases, as activators of the Cdk/cyclins, pl
35                                              Cdc25 phosphatases belong to the family of protein tyros
36 coding the Drosophila homologue of the yeast CDC25 phosphatase, contributes to the G2 cell cycle dela
37  be useful in further clarifying the role of Cdc25 phosphatase-dependent pathways in checkpoint contr
38                   In yeast and animal cells, CDC25 phosphatase dephosphorylates the CDK releasing cel
39 activates Wee1 and Myt1 kinases and inhibits Cdc25 phosphatase during the M to G1 transition.
40 t can be used to discover new members of the CDC25 phosphatase family.
41 st species, the G(2) checkpoint prevents the Cdc25 phosphatase from removing inhibitory phosphate gro
42 will focus on the role of Plk3 in regulating Cdc25 phosphatase function and its effect on the cell cy
43 s is accomplished in part by maintaining the Cdc25 phosphatase in a phosphorylated form that binds 14
44 e improves our understanding of the roles of CDC25 phosphatases in CDK regulation and may inform the
45 Like DA3003-1, JUN1111 selectively inhibited Cdc25 phosphatases in vitro in an irreversible, time-dep
46  most potent reported synthetic inhibitor of Cdc25 phosphatases in vitro.
47 phila embryos, zygotic expression of the stg(cdc25) phosphatase in G2 activates cyclin/cdc2 kinases a
48                                              Cdc25 phosphatase induces mitosis by dephosphorylating t
49                      Many of the more potent Cdc25 phosphatase inhibitors reported to date are quinon
50                            Because selective Cdc25 phosphatase inhibitors would be valuable biologica
51 ng that protein substrate recognition by the Cdc25 phosphatases is an essential and evolutionarily co
52 ession levels, the intracellular activity of Cdc25 phosphatases is determined by their subcellular di
53                                              CDC25 phosphatases play a critical role in the regulatio
54                                          The Cdc25 phosphatases play key roles in cell-cycle progress
55                                          The Cdc25 phosphatase promotes entry into mitosis by removin
56                                          The Cdc25 phosphatase promotes entry into mitosis by removin
57                                          The Cdc25 phosphatase promotes entry into mitosis through th
58                                              CDC25 phosphatase promotes progression through the eukar
59                                              Cdc25 phosphatases propel cell cycle progression by acti
60                                       Active Cdc25 phosphatase released Cdc2-cyclin B from the deterg
61                                      Because Cdc25 phosphatases remove this phosphate, Cdc25 activity
62 Cdk1, a fraction of total cyclin B1, and the Cdc25 phosphatases reside predominantly in the cytoplasm
63                                    Dampening Cdc25 phosphatases simultaneously with Wee1 and Myt1 inh
64 A), regulator of cyclin A1 (rca1) and string/cdc25 phosphatase (stg), and the microtubule destabilizi
65                                          The cdc25 phosphatase string (stg) has been proposed to cont
66 ays and exerts its effect via suppression of CDC25 phosphatase String expression.
67       These genes include the G2/M regulator Cdc25 phosphatase, String; a regulator of the APC ubiqui
68 lated Cys-dependent hydrolases and rhodanese/Cdc25 phosphatases), suggesting that neither secondary s
69 d were abolished in cells overexpressing the Cdc25 phosphatase, suggesting a role for the Cdc2 cyclin
70 s, a well-defined subfamily of the rhodanese/Cdc25 phosphatase superfamily, characterized by a 7-amin
71 ses, which, in turn, belong to the rhodanese/Cdc25 phosphatase superfamily.
72 uch knowledge of the basic enzymology of the Cdc25 phosphatases that may aid in the development of sp
73  late times, we observed accumulation of the Cdc25 phosphatases that remove the inhibitory phosphates
74 ve-site motif CE[F/Y]SXXR that characterizes Cdc25 phosphatase, the novel CALSQ[Q/V]R motif is also c
75 hosphorylates and suppresses the activity of Cdc25 phosphatase: the resulting failure to remove inhib
76                                   Similar to Cdc25 phosphatase, these proteins are likely involved in
77 r gastrulation and require downregulation of Cdc25 phosphatase, which was previously attributed to th
78 rylating activity of Cpd 5, it might inhibit Cdc25 phosphatases, which contain a cysteine in the cata
79                                          The Cdc25 phosphatases, which control cell cycle progression
80                           In particular, the Cdc25 phosphatases, which dephosphorylate cyclin-depende
81 ns are homologous to the catalytic domain of Cdc25 phosphatases, which, in turn, belong to the rhodan
82 structure, specificity, and mechanism of the Cdc25 phosphatases with a special focus on the activity
83 ases with a special focus on the activity of Cdc25 phosphatases with native protein substrates.
84 e a valuable reagent to probe the actions of Cdc25 phosphatases within cells and may also be useful s