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1 protein, 4E-BP1, and the activity of the p70 ribosomal protein S6 kinase.
2 tein kinase pathway, involving in particular ribosomal protein S6 kinase.
4 de evidence that IFNlambda activates the p90 ribosomal protein S6 kinase 1 (RSK1) and its downstream
8 signaling axis and downstream effectors, the ribosomal protein S6 kinase 1 (S6K1) and the translation
17 tes the mammalian target of rapamycin (mTOR)/ribosomal protein S6 kinase 1 (S6K1) signaling pathway i
18 Intriguingly, the homozygous deletion of ribosomal protein S6 kinase 1 (S6K1), an mTOR target, in
19 tor 4E-binding protein (4E-BP) and activates ribosomal protein S6 kinase 1 (S6K1), both of which stim
21 metabolic pathway via its downstream target ribosomal protein S6 kinase 1 (S6K1), which directly pho
28 ediated substrate phosphorylation (e.g., p70 ribosomal protein S6 kinase 1 [S6K1] and eukaryotic init
29 of tuberin is associated with an increase in ribosomal protein S6 kinase 1 and eukaryotic initiation
30 S6 kinase 1 inhibitor implicated a role for ribosomal protein S6 kinase 1 in IL-33-induced mTOR-depe
32 ed by mTOR-Raptor and mTOR-Rictor complexes (ribosomal protein S6 kinase 1 Thr(389) and Akt Ser(473),
33 of mammalian target of rapamycin complex 1, ribosomal protein S6 kinase 1, and eukaryotic translatio
34 with phosphorylation of the mTORC1 effector ribosomal protein S6 kinase 1, that the graft morphologi
36 ctivated phospho-ERK44/42, activated phospho-ribosomal protein S6 kinase-1 (RSK1) (a substrate of ERK
37 ion factor 4E-binding protein 1 (4E-BP1) and ribosomal protein S6 kinase-1 (S6K1), whereas HIF-1alpha
40 the T-loop of S6K1 alpha II (the 70-kDa 40 S ribosomal protein S6 kinase-1 alpha II isoform), and Thr
43 ponents of the mammalian target of rapamycin/ribosomal protein S6 kinase, 70 kDa, pathway and thereby
44 the oncogenic mammalian target of rapamycin/ribosomal protein S6 kinase, 70 kDa, pathway, and the im
47 inhibition resulted in TLR-4-mediated 70-kDa ribosomal protein S6 kinase activation and enhanced TNF-
48 urse experiment indicated that PI3K (AKT and ribosomal protein S6 kinase) activation occurred between
50 am target of the cyclooxygenase pathway, and ribosomal protein S6 kinase and eukaryotic translation i
51 nd p38 MAPK and suggested involvement of p90 ribosomal protein S6 kinase and mitogen and stress respo
52 ivated protein kinase (AMPK) and upstream of ribosomal protein S6 kinase and mTOR complex 1 (TORC1),
54 hey show constitutive phosphorylation of the ribosomal protein S6 kinase and the eukaryotic initiatio
55 lving extracellular signal-regulated kinase, ribosomal protein S6 kinase, and protein kinase D (PKD)
56 ene ESR1, and another involving the RPS6KB1 (Ribosomal protein S6 kinase beta-1) were recurrently exp
57 ith and inhibited B-Raf but did not activate ribosomal protein S6 kinase, indicating that farnesylati
60 ing and mammalian target of rapamycin/70-kDa ribosomal protein S6 kinase (mTOR/p70S6K) were not invol
61 ein kinase B on Ser(473), mTOR on Ser(2448), ribosomal protein S6 kinase on Thr(389), and eukaryotic
62 ied, phosphoinositide 3-kinase p110alpha and ribosomal protein S6 kinase p70(S6K1), plus the MAP kina
64 se (PI3-kinase) and their downstream targets ribosomal protein S6 kinase (p70(S6k)) and eukaryotic in
67 ucine also stimulated phosphorylation of the ribosomal protein S6 kinase, p70(S6k), resulting in incr
68 horylation state of two mTOR targets, 70-kDa ribosomal protein S6 kinase (p70S6K) and eukaryote initi
69 In the absence of ERK2, activation of the ribosomal protein S6 kinase (p70S6K) and its downstream
70 Akt/mammalian target of rapamycin (mTOR)/p70 ribosomal protein S6 kinase (p70S6K) and the extracellul
71 locking mTOR affects the activity of the 40S ribosomal protein S6 kinase (p70s6k) and the function of
72 tly attenuates phosphorylation of the 70 kDa ribosomal protein S6 kinase (p70S6K) in the basal state
74 The Akt/mammalian target of rapamycin (mTOR)/ribosomal protein S6 kinase (p70S6K) pathway is consider
78 mycin (i.e., phosphorylation of AMPK and p70 ribosomal protein S6 kinase, respectively) and IL-6/IL-6
79 lular signal-regulated kinase) and S6K-RPS6 (ribosomal protein S6 kinase-ribosomal protein S6) axes.
81 (MAP) kinase and the Mr = 90,000 isoform of ribosomal protein S6 kinase (Rsk) by approximately 1.5-2
82 of SKAR, which is mediated by either the p90 ribosomal protein S6 kinase (RSK) or p70 S6 kinase (S6K1
88 anslational signalling intermediates, 70 kDa ribosomal protein S6 kinase (S6k), ribosomal protein S6
89 d activity in vitro, decreased basal Akt and ribosomal protein S6 kinase (S6K1) activation, and decre
92 ent mammalian target of rapamycin (mTOR)/p70 ribosomal protein S6 kinase (S6K1)/eukaryotic initiation
94 st known to regulate translation through the ribosomal protein S6 kinases (S6Ks) and the eukaryotic t
95 leading to the stimulation of the 70/85 kDa ribosomal protein S6 kinases, substantially blocks the a
96 D relative to control subjects was found for ribosomal protein S6 kinase, which did not change after
97 eroxide each caused inhibition of the 70-kDa ribosomal protein S6 kinase, while arsenite activated it
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