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1 hosphorylation events that release activated protein kinase D.
2 n by Ca(2+)-calmodulin protein kinase II and protein kinase D.
3 R (Bin-amphiphysin-Rvs) domain proteins, and protein kinase D.
4 pathway involving specific LPA receptors and protein kinase D.
5 olgi-targeted beta(1)gamma(2) also activates protein kinase D.
6 way, one that involves novel PKCs (nPKC) and protein kinase D.
7 ed in part via a PKC-dependent activation of protein kinase D.
8 on events and also serine phosphorylation by protein kinase D.
9 that erythropoietin regulates GATA1 through protein kinase D activation, promoting histone deacetyla
10 in (F-actin) disassembly and an elevation in protein kinase D activity that altered Golgi organizatio
12 by expression of a dominant-negative mutant protein kinase D, an enzyme implicated in regulating con
15 esis confirmed telethonin as a substrate for protein kinase D and Ca(2+)/calmodulin-dependent kinase
17 cytosis (e.g., expression of kinase-inactive protein kinase D and low temperature incubation) cause a
18 ers on cell spreading requires activation of protein kinase D and the subsequent activation of Akt1.
23 lular locations, causes phospholipase C- and protein kinase D-dependent vesiculation of the Golgi in
26 Using mass spectrometry, we identified a protein kinase D-interacting substrate of 220 kD (Kidins
33 relay pathway in which the serine/threonine protein kinase D (PKD) activates the NF-kappaB transcrip
35 A2 domains of PLC are required for long term protein kinase D (PKD) activation and subsequent inducti
36 hways to lysophosphatidic acid (LPA)-induced protein kinase D (PKD) activation, we tested the effect
37 n rat cardiac myocytes by phosphorylation of protein kinase D (PKD) and expression of collagens (COL1
40 phosphorylated by the CSN-associated kinase protein kinase D (PKD) and its expression is decreased u
41 inhibited by Goedecke 6976, an inhibitor of protein kinase D (PKD) and PKCalpha, but not with GF1092
42 The results presented here demonstrate that protein kinase D (PKD) and PKCeta transiently coexpresse
43 Since both OSBP and PI4KB are substrates for protein kinase D (PKD) and PKD is known to be involved i
45 ignaling pathway together with BCR-activated protein kinase D (PKD) as important cooperative factors
46 pproaches, we identified the upstream kinase protein kinase D (PKD) as the primary kinase targeting H
47 We show that tyrosine phosphorylation of protein kinase D (PKD) at Y463 in the Pleckstrin Homolog
50 etween the GTPase RhoA and the serine kinase protein kinase D (PKD) during thymocyte development.
51 Dependent on their cellular localization, Protein Kinase D (PKD) enzymes regulate different proces
59 or family of small G-proteins (ARFs) and the protein kinase D (PKD) family of serine/threonine kinase
63 apidly and transiently induces activation of protein kinase D (PKD) in aortic smooth muscle cells.
84 tive stress, and the serine/threonine kinase protein kinase D (PKD) is critical for signal relay to N
103 kout approach to interrogate the function of protein kinase D (PKD) serine/threonine kinases in lymph
104 ted kinase, ribosomal protein S6 kinase, and protein kinase D (PKD) that increase cAMP binding respon
106 d by cell treatments with H(2)O(2) activates protein kinase D (PKD) via a protein kinase C (PKC)-depe
108 omoter, whereas the combination of XBP-1 and protein kinase D (PKD) was required for efficient activa
109 ues show that AKAP-Lbc couples activation of protein kinase D (PKD) with the phosphorylation-dependen
112 ,13-dibutyrate led to striking activation of protein kinase D (PKD), a member of a novel family of se
114 How these stimuli interact at the level of protein kinase D (PKD), a nodal point in cardiac hypertr
115 B) led to a rapid and striking activation of protein kinase D (PKD), a novel serine/threonine protein
120 that the downstream target of Gbetagamma is protein kinase D (PKD), an isoform of protein kinase C.
121 VAMP3 is bound by the contraction-activated protein kinase D (PKD), and contraction and VAMP3 overex
122 y active PLCepsilon, sustained activation of protein kinase D (PKD), and nuclear translocation of NF-
123 hich can inhibit protein kinase C as well as protein kinase D (PKD), blocked H2O2- but not TNF-induce
124 treatment led to activation of PKCmicro, or protein kinase D (PKD), but not PKCalpha/beta, PKCzeta/l
134 at S. rectivirgula induces the activation of protein kinase D (PKD)1 in lung cells in vitro and in vi
136 e present study, we investigated the role of protein kinase D (PKD)1 in the proinflammatory responses
141 on loop phosphorylation in the regulation of protein kinase D (PKD/protein kinase C (PKC) mu) activit
144 endogenous signaling pathways revealed that protein kinase D/protein kinase Cmicro (PKD/PKCmicro) an
145 rylation of MAPKs and the phosphorylation of protein kinase D/protein kinase Cmu and protein kinase C
146 tein kinase C-Zetalambda-Thr538 and phosphor-protein kinase D-Ser744-748 were reduced, whereas messen
147 Protein kinase D/PKCmu is a member of the protein kinase D serine/threonine kinase family that exh
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