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1 ma2) and epsilon-productive transcripts (VDJ-Cepsilon).
2 hese events was activation of protein kinase Cepsilon.
3 m involving increased direct CSR from Cmu to Cepsilon.
4 ely from Cmu to Cgamma1, and subsequently to Cepsilon.
5 g through beta2 integrins and protein kinase Cepsilon.
6 transcriptions and repress CSR to Cgamma and Cepsilon.
7 to Ras, mediates activation of phospholipase Cepsilon.
8 rference screen, we identified phospholipase Cepsilon 1 (PLCepsilon1) as a crucial regulator of strom
10 tely 80% reduction in hepatic protein kinase Cepsilon activation, and increased hepatic insulin sensi
12 tide-specific phospholipases (phospholipases Cepsilon and Cgamma1) in coordinating certain intracellu
13 oA and Rac1), phospholipases (phospholipases Cepsilon and Cgamma1), and phosphoinositide 3-kinase, in
14 AR2 was colocalized with protein kinase (PK) Cepsilon and PKA in a subset of dorsal root ganglia neur
15 he cooperative effects of protein kinase (PK)Cepsilon and PKCdelta and leads to AKT-FOXO3a phosphoryl
16 the TPA-induced activation of protein kinase Cepsilon and prevented subsequent activation of c-Jun NH
19 h agents inhibited S6 kinase, protein kinase Cepsilon, and glycogen synthase kinase 3 alpha and beta.
23 g(10) guanidinium Czeta atom and the Lys(13) Cepsilon atom are close to the lipid (31)P (4.0-4.2 A),
28 n of antiapoptotic effectors (protein kinase Cepsilon, endothelial and inducible NO synthase isoforms
30 transduce intracellular signals that lead to Cepsilon gene transcription independently of its associa
33 and gene expression of T-cell markers and of Cepsilon germline transcript, reflecting antibody isotyp
35 if(-/-) B cells completely failed to express Cepsilon germline transcripts (GLT) and secrete IgE.
36 4 and IL-13 play a critical role in inducing Cepsilon germline transcripts and IgE isotype switching
39 e 1 (Jak1) activation, STAT6 activation, and Cepsilon germline transcripts in human B cell line BJAB.
41 Myd88(-/-) B cells had normal expression of Cepsilon GLT but reduced IgE secretion in response to LP
42 PS plus IL-4 stimulation selectively blocked Cepsilon GLT expression and IgE secretion but had little
43 epsilon-Cmu, Imu-Cgamma4, Igamma-Cmu, Igamma-Cepsilon, Iepsilon-Cgamma, and Igamma4-Calpha1 transcrip
44 es of chimeric Ig germ-line transcripts (Imu-Cepsilon, Iepsilon-Cmu, Imu-Cgamma4, Igamma-Cmu, Igamma-
45 4 induces CSR from Cmu to Cgamma1 (IgG1) and Cepsilon (IgE), the latter of which contributes to the p
46 presses constitutively active protein kinase Cepsilon in the heart and slowly develops a dilated card
48 ost mature peripheral B cells undergo CSR to Cepsilon indirectly, namely from Cmu to Cgamma1, and sub
51 , providing evidence that the productive VDJ-Cepsilon mRNA was derived from a transcriptionally activ
52 of products is initiated by cleavage of the Cepsilon-NdeltaH2+ bond, yielding urea and L-ornithine(H
53 rt halogen bond increases the flexibility of Cepsilon of MET146, whereas the rest of the residue fail
55 Cmu to a downstream Ch (for example, Cgamma, Cepsilon or Calpha), thereby switching expression from I
56 (cCSR) substitutes the Cmu gene with Cgamma, Cepsilon, or Calpha, thereby generating IgG, IgE, or IgA
57 for beta2-AR antagonism of the phospholipase Cepsilon pathway that may contribute to the known protec
58 ular epithelial cells express protein kinase Cepsilon (PKCepsilon ), an oncoprotein that coordinately
59 ing in a 3.6-fold increase in protein kinase Cepsilon (PKCepsilon) activation (P < 0.01) and a subseq
60 h functional coupling between protein kinase Cepsilon (PKCepsilon) and mitochondria has been implicat
63 Our recent work identified protein kinase Cepsilon (PKCepsilon) as a critical and causative player
64 protein complex of activated protein kinase Cepsilon (PKCepsilon) bound to RACK1, a receptor for act
65 usly shown that activation of protein kinase Cepsilon (PKCepsilon) in male rats induces a chronic, lo
67 ed by PD98059, rottlerin, and protein kinase Cepsilon (PKCepsilon) inhibitor peptide, suggesting that
69 activation and inhibition of protein kinase Cepsilon (PKCepsilon) mimicked and prevented, respective
72 fic methylation occurs at the protein kinase Cepsilon (PKCepsilon) promoter of the babies born of mot
73 We have previously shown that protein kinase Cepsilon (PKCepsilon) protects breast cancer cells from
74 androgen receptor, c-Myc, and protein kinase Cepsilon (PKCepsilon) proteins are overrepresented in mo
76 ment induced translocation of protein kinase Cepsilon (PKCepsilon) to the plasma membrane of these ne
78 Furthermore, activation of protein kinase Cepsilon (PKCepsilon) was necessary for length recovery,
82 We previously observed that protein kinase Cepsilon (PKCepsilon), a member of the protein kinase C
84 teroids were found to express protein kinase Cepsilon (PKCepsilon), an oncogenic protein capable of p
85 Here, we used protein kinase A (PKA) and Cepsilon (PKCepsilon), as well as ribosomal S6 kinase II
86 )P]orthophosphate in UGTs and protein kinase Cepsilon (PKCepsilon), following treatment of LS180 cell
87 e, induced activation of Akt, protein kinase Cepsilon (PKCepsilon), mitogen-activated protein kinase
88 ografts (a) the expression of protein kinase Cepsilon (PKCepsilon), phosphatidylinositol 3-kinase, ph
89 ptor) or direct activation of protein kinase Cepsilon (PKCepsilon), the pronociceptive effects of PGE
90 4 (a primary HA receptor) and protein kinase Cepsilon (PKCepsilon), which regulates a number of human
91 lyFn assembly is regulated by protein kinase Cepsilon (PKCepsilon), which translocates rapidly and in
92 gh constitutive expression of protein kinase Cepsilon (PKCepsilon), while phorbol 12-myristate 13-ace
94 ften involves an outgrowth of protein kinase Cepsilon (PKCepsilon)-positive cells in recurrent prosta
98 , Epac2, and the Epac effector phospholipase-Cepsilon (PLCepsilon) in airway inflammation and remodel
106 hase and the translocation of protein kinase Cepsilon to the plasma membrane, were observed with SWIP
107 n basal germ line Igamma-Cgamma and Iepsilon-Cepsilon transcriptions and repress CSR to Cgamma and Ce
110 sulin resistance, and hepatic protein kinase Cepsilon was activated, providing a potential mechanism
111 hat IQGAP1 is a substrate for protein kinase Cepsilon, which catalyzes phosphorylation on Ser-1443.