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1 DAG kinase (DGK) terminates DAG signaling by converting
2 DAG kinase activity was also significantly decreased (73
3 DAG kinase activity was monitored by DAG phosphorylation
4 DAG kinase and membrane PKC activities were higher in co
5 DAG kinase hypermorphs also suppressed the lethality cau
6 DAG kinases (DGKs) convert DAG into phosphatidic acid, r
7 DAG kinases (DGKs) metabolize DAG by converting it to ph
8 DAG kinases and phospholipase D, the enzymes that produc
9 DAG kinases play an important role in controlling intrac
10 ype, but the addition of DAG together with a DAG kinase inhibitor does not result in a wild-type phen
14 gh no differences were observed in the basal DAG kinase activity between control and diabetic rats.
15 pholipase C (PLC) enzymes and termination by DAG kinases (DGKs), as well as dysregulation in the acti
16 is thaliana) that target an Escherichia coli DAG kinase (DAGK) to each leaflet of each chloroplast en
18 of cyclooxygenase-2 (COX-2), diacylglycerol (DAG) kinase alpha (DGKalpha), and heme oxygenase-1 (HO-1
22 ubunit, phospholipase Cbeta, diacylglycerol (DAG) kinase, and calcium/calmodulin-dependent protein ki
24 ccharomyces cerevisiae, Dgk1 diacylglycerol (DAG) kinase catalyzes the CTP-dependent phosphorylation
25 y were enhanced by impairing diacylglycerol (DAG) kinase function by mutation (rdgA) or by restrictin
26 highlight recent studies of diacylglycerol (DAG) kinase (DGK) 5, an enzyme involved in PA biosynthes
27 we demonstrate that loss of diacylglycerol (DAG) kinase (Dgk) zeta, an enzyme which converts DAG int
28 he physiological function of diacylglycerol (DAG) kinase iota (DGKiota), which converts DAG to phosph
29 gkB, which encodes a soluble diacylglycerol (DAG) kinase required to recycle DAG to phosphatidylglyce
31 re, we report that targeting diacylglycerol (DAG) kinase zeta (DGKzeta), a negative regulator of DAG-
32 expression of leukocyte-type diacylglycerol (DAG) kinase alpha in PMN from LAP patients (4.6 +/- 1.7
35 alpha0 subunit) and DGK-1 (a diacylglycerol [DAG] kinase), both of which act in the ventral cord moto
37 ls mGluR1 response duration, and that graded DAG kinase levels correlate with systematic variation of
40 ressing cells showed a 7.7-fold reduction in DAG kinase activity; the reduced enzyme activity could b
41 Treatment with d-alpha-tocopherol increased DAG kinase activity in the glomeruli of both control and
43 al secondary bile acids, and colonic mucosal DAG kinase and PKC activities during different stages of
44 icle, we report that simultaneous absence of DAG kinase alpha and zeta causes severe defects in iNKT
45 ent significantly enhanced the activities of DAG kinase and total membrane PKC activities in colonic
46 In this report, we demonstrate expression of DAG kinase zeta (DGKzeta, the enzyme that catalyzes the
48 hese results have defined a novel isoform of DAG kinase, which may have important cellular functions
50 ibit any difference in the protein levels of DAG kinase alpha and gamma, the effect of d-alpha-tocoph
51 pathway, the activity and protein levels of DAG kinase alpha and gamma, which metabolize DAG to phos
52 AOM and fed HFCO showed increased levels of DAG kinase and membrane PKC activities in the colonic mu
56 Conversely, pharmacological inhibition of DAG kinases or expression of an inactive diacylglycerol
57 atment with inhibitors of phospholipase C or DAG kinase also altered SEB-induced TNF-alpha production
58 ous DAG, resulting from either DAG lipase or DAG kinase inhibition, completely prevented TRPC5 or TRP
60 both PMN transendothelial migration and PMN DAG kinase alpha signaling as disordered functions in LA
61 ng this balance is the apicomplexan-specific DAG-kinase-1, which interconverts PA and DAG, and whose
66 y of the phenotype caused by mutation of the DAG kinase, RDGA , indicating that Laza functions in opp
67 M) activated Icat in some cells, whereas the DAG kinase inhibitor R59949 (10 microM) never activated
68 ondary bile acids, colonic mucosal and tumor DAG kinase, and PKC that may play a role in colon carcin