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1 quency-dependent activation of PKC(epsilon) (protein kinase C epsilon).
2 andin E(2), emergence of novel dependence on protein kinase C epsilon.
3 hrome b561, glutathione s-transferase a4 and protein kinase C-epsilon.
4 noprecipitated from smooth muscle cells with protein kinase C-epsilon.
8 lowering hepatic diacylglycerol content and protein kinase C epsilon activation through decreased SR
9 t-induced hepatic insulin resistance through protein kinase C epsilon activation, we next sought to u
10 sistance was accompanied by elevated hepatic protein kinase C-epsilon activation and blunted insulin-
12 me when mitogen-activated protein kinase and protein kinase C-epsilon are targeted to the plasmalemma
13 um pathway and promotes translocation of the protein kinase C epsilon (epsilonPKC) isozyme and whethe
18 otein kinase C delta activation increased in protein kinase C epsilon knock-out myocytes without alte
20 ncentration, green fluorescent protein (GFP)-protein kinase C-epsilon mutants were tracked during pha
23 TnI was replaced with cTnI phosphorylated by protein kinase C-epsilon or mutated to cTnI-S43E/S45E/T1
24 protein kinase C-alpha and -zeta, but not of protein kinase C-epsilon, overexpressed in insect cells.
26 se require eicosanoid-mediated activation of protein kinase C epsilon (PKC epsilon) and that the majo
28 metastatic squamous cell carcinoma (mSCC) in protein kinase C epsilon (PKC epsilon) transgenic mice w
34 ith a blockade within hematopoietic cells of protein kinase C-epsilon (PKC-epsilon) up-regulation and
36 e selective down-regulation in K562 cells of protein kinase C-epsilon (PKC-epsilon), which has recent
43 stress to the fetus and results in decreased protein kinase C epsilon (PKCepsilon) expression in the
46 oll-like receptor 4 (TLR4) and signaling via protein kinase C epsilon (PKCepsilon) in common, whereas
48 y pull-down assays, we found that myocardial protein kinase C epsilon (PKCepsilon) is physically asso
49 c increase in mRNA and protein levels of the protein kinase C epsilon (PKCepsilon) isozyme in primary
52 enhanced capsaicin-evoked responses involve protein kinase C epsilon (PKCepsilon) or phosphatidylino
53 We have previously shown that mice lacking protein kinase C epsilon (PKCepsilon) show decreased eth
55 ere we demonstrated that mutant mice lacking protein kinase C epsilon (PKCepsilon) were more sensitiv
59 (PKA) alone or through a combination of PKA, protein kinase C epsilon (PKCepsilon), and extracellular
60 duced by agonists at receptors that activate protein kinase C epsilon (PKCepsilon), occurs in male bu
61 D9 revealed a fragment of the gene, encoding protein kinase C epsilon (PKCepsilon), that was then sho
62 d to determine whether SIRT5 is activated by protein kinase C epsilon (PKCepsilon)-mediated increases
64 xplored the sensitizing effects of epidermal protein kinase C epsilon (PKCepsilon)expression in the h
65 ycerol-mediated (DAG-mediated) activation of protein kinase C-epsilon (PKCepsilon) and the consequent
66 tabotropic glutamate receptor-5 (mGluR5) and protein kinase C-epsilon (PKCepsilon) expression in the
67 atrial fibrillation (AF), is mediated via a protein kinase C-epsilon (PKCepsilon)-dependent mechanis
69 nes (SKH-1 hairless mice, wild-type FVB, and protein kinase C epsilon (PKCvarepsilon)-overexpressing
71 ing the locus containing the gene coding for protein kinase C-epsilon, previously implicated in model
72 d because of its phosphorylation mediated by protein kinase C epsilon (PRKCE) and ATM serine/threonin
73 nerated that overexpressed an epitope-tagged protein kinase C epsilon (T7-PKCepsilon) in their epider
74 press (approximately 18-fold) epitope-tagged protein kinase C-epsilon (T7-PKCepsilon) protein in the
75 phosphates and induces the translocation of protein kinase C epsilon to the myocyte membrane, consis
77 on, direct activation of protein kinase A or protein kinase C epsilon, two pathways that mediate infl