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1 ndent kinases, cyclin-dependent kinase 4 and cyclin-dependent kinase 6.
4 Although fisetin has been cocrystalized with cyclin-dependent kinase 6 and inhibits its activity, thi
7 ed protein, the checkpoint suppressor 1, the cyclin-dependent kinase 6, and a protein tyrosine phosph
8 be inhibition of cyclin-dependent kinase 4, cyclin-dependent kinase 6, and cyclin D1, and accumulati
10 rted previously that the G(1) phase-specific cyclin-dependent kinase 6 (CDK6) also blocks erythroid d
12 introduction of cell cycle molecules such as cyclin-dependent kinase 6 (cdk6) and cyclin D1, but thei
13 lar alterations including down-regulation of cyclin-dependent kinase 6 (CDK6) and integrin beta1 (ITG
14 STAT activation and downstream activation of cyclin-dependent kinase 6 (Cdk6) and MycNol3(-/-) MPN Th
17 I3C selectively abolished the expression of cyclin-dependent kinase 6 (CDK6) in a dose- and time-dep
20 has previously been demonstrated to activate cyclin-dependent kinase 6 (Cdk6) to induce the phosphory
21 CR results in rapid transport of cytoplasmic cyclin-dependent kinase 6 (cdk6) to nuclei, where it ass
22 -specific amplification of the gene encoding cyclin-dependent kinase 6 (CDK6), an observation not pre
23 fects may be mediated by targeting of HMGA2, cyclin-dependent kinase 6 (CDK6), and other predicted mi
28 s is because of the known ability of vCyclin/cyclin-dependent kinase 6 complex to resist p21 and p27
29 NK4a), p27(KIP1), cyclin-dependent kinase 4, cyclin-dependent kinase 6, glycogen synthase kinase 3bet
30 ue to each class, including amplification of cyclin-dependent kinase 6 in UV-treated cohort, a findin
31 d no effect on cyclin-dependent kinase 2 and cyclin-dependent kinase 6 levels during this time period
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