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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
11 tion under conditions of persistent PKC (and protein kinase D) activity.
12  by expression of a dominant-negative mutant protein kinase D, an enzyme implicated in regulating con
13                           A kinase defective protein kinase D and a phospholipase C beta inhibitor bl
14       Our results suggest that activation of protein kinase D and Akt1 are approaches to promote axon
15 esis confirmed telethonin as a substrate for protein kinase D and Ca(2+)/calmodulin-dependent kinase
16 ion, IL-2 production, and phosphorylation of protein kinase D and IkappaB.
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.
19                         Protein kinase C and protein kinase D are potently activated by agonist-evoke
20 tant mice that lacked the Rho-GEF and/or the protein kinase D-binding domains.
21 of p53 by recombinant protein kinase CK2 and protein kinase D, both associated with CSN3.
22 telethonin as an interaction partner for the protein kinase D catalytic domain.
23 lular locations, causes phospholipase C- and protein kinase D-dependent vesiculation of the Golgi in
24                                          The protein kinase D family of serine/threonine kinases, par
25 the protein kinase C-dependent activation of protein kinase D induced by these agonists.
26     Using mass spectrometry, we identified a protein kinase D-interacting substrate of 220 kD (Kidins
27       Using mass spectrometry, we identified protein kinase D-interacting substrate of 220 kDa (Kidin
28                            The kinase PRKD2 (protein kinase D) is a crucial regulator of tumor cell-e
29       Protein kinase Cmu (PKCmu), also named protein kinase D, is an unusual member of the PKC family
30                              We identify the protein kinase D-mediated phosphorylation of serine 92 o
31                                              Protein kinase D/PKCmu is a member of the protein kinase
32                Serine 351 is a substrate for protein kinase D (PKD [also known as PKCmu]) in vitro an
33  relay pathway in which the serine/threonine protein kinase D (PKD) activates the NF-kappaB transcrip
34                                        Rapid protein kinase D (PKD) activation and phosphorylation vi
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
38             We evaluated the contribution of protein kinase D (PKD) and Gbetagamma to this process.
39       Here we demonstrate a critical role of protein kinase D (PKD) and histone deacetylase 5 (HDAC5)
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
44       This study identifies a novel role for protein kinase D (PKD) as an in vivo cardiac CREB-Ser(13
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
48                                              Protein kinase D (PKD) binds to a pool of diacylglycerol
49                   Protein kinase C (PKC) and protein kinase D (PKD) coordinate and regulate many fund
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
52                                              Protein kinase D (PKD) exists as a family of structurall
53                                          The protein kinase D (PKD) family consists of three serine/t
54                                          The protein kinase D (PKD) family consists of three serine/t
55              Treatment of the cells with the protein kinase D (PKD) family inhibitors CRT0066101 and
56                                          The protein kinase D (PKD) family is a recent addition to th
57                                              Protein kinase D (PKD) family members (PKD1, 2, and 3) h
58                           The members of the protein kinase D (PKD) family of serine/threonine kinase
59 or family of small G-proteins (ARFs) and the protein kinase D (PKD) family of serine/threonine kinase
60                                          The protein kinase D (PKD) family of serine/threonine kinase
61                            The serine kinase protein kinase D (PKD) has a cysteine-rich domain (CRD)
62                        In nonneuronal cells, protein kinase D (PKD) has an important role in stabiliz
63 apidly and transiently induces activation of protein kinase D (PKD) in aortic smooth muscle cells.
64             Use of a novel, highly selective protein kinase D (PKD) inhibitor and a nonphosphorylatab
65                                          The protein kinase D (PKD) inhibitor Go6976 blocked both bas
66          Blockade of DRAK2 activity with the protein kinase D (PKD) inhibitor Go6976 or expression of
67            Cells were pretreated or not with protein kinase D (PKD) inhibitors.
68                                              Protein kinase D (PKD) is a cytosolic protein, which upo
69                                              Protein kinase D (PKD) is a cytosolic serine-threonine k
70                                              Protein kinase D (PKD) is a family of novel diacylglycer
71                                              Protein kinase D (PKD) is a family of stress-responsive
72                                              Protein kinase D (PKD) is a member of the AGC family of
73                                              Protein kinase D (PKD) is a nodal point in cardiac hyper
74                                              Protein kinase D (PKD) is a novel family of serine/threo
75                                              Protein kinase D (PKD) is a protein serine kinase that i
76                                              Protein kinase D (PKD) is a serine kinase whose myocardi
77                                              Protein kinase D (PKD) is a serine/threonine kinase that
78                                              Protein kinase D (PKD) is a serine/threonine kinase with
79                                              Protein kinase D (PKD) is a serine/threonine protein kin
80                                              Protein kinase D (PKD) is a serine/threonine protein kin
81                                              Protein kinase D (PKD) is a serine/threonine protein kin
82                                              Protein kinase D (PKD) is a stress-responsive kinase tha
83                                              Protein kinase D (PKD) is an antigen receptor-activated
84 tive stress, and the serine/threonine kinase protein kinase D (PKD) is critical for signal relay to N
85                                              Protein kinase D (PKD) is known to be involved in Golgi-
86                                              Protein kinase D (PKD) is recruited to the trans-Golgi n
87                                              Protein kinase D (PKD) isoforms are effectors in signali
88                                              Protein kinase D (PKD) isoforms are involved in controll
89                                              Protein kinase D (PKD) isoforms are protein kinase C (PK
90                                              Protein kinase D (PKD) isoforms are protein kinase C eff
91                                              Protein kinase D (PKD) isoforms are protein kinase C eff
92                                              Protein kinase D (PKD) mediates signal transduction down
93                                              Protein kinase D (PKD) mediates signals from the platele
94                          We examined whether protein kinase D (PKD) overexpression in Swiss 3T3 cells
95                                              Protein kinase D (PKD) participates in activation of the
96           Further analysis showed downstream protein kinase D (PKD) phosphorylation and phosphatase a
97                                              Protein kinase D (PKD) plays a critical role at the tran
98            In the present study we show that protein kinase D (PKD) plays an important role in the fo
99                                              Protein kinase D (PKD) potentiates cellular DNA synthesi
100                           Here, we show that protein kinase D (PKD) regulates Bit1 apoptotic function
101                                              Protein kinase D (PKD) regulates many diverse cellular f
102                                          The protein kinase D (PKD) serine/threonine kinases are acti
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
105                                              Protein kinase D (PKD) transduces an abundance of signal
106 d by cell treatments with H(2)O(2) activates protein kinase D (PKD) via a protein kinase C (PKC)-depe
107                     Persistent activation of protein kinase D (PKD) via protein kinase C (PKC)-mediat
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
110                     We also demonstrate that protein kinase D (PKD), a downstream effector of PKC, di
111                                              Protein kinase D (PKD), a downstream effector of protein
112 ,13-dibutyrate led to striking activation of protein kinase D (PKD), a member of a novel family of se
113                                              Protein kinase D (PKD), a newly described serine/threoni
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
116       Our previous studies demonstrated that protein kinase D (PKD), a serine/threonine kinase implic
117                                              Protein kinase D (PKD), a serine/threonine kinase, is ex
118                                              Protein kinase D (PKD), a serine/threonine kinase, is re
119 satory increase (32.6%) in the activation of protein kinase D (PKD), an alternate HDAC5 kinase.
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
125                                     Although protein kinase D (PKD), like protein kinase C (PKC), pos
126             The BCR, but not CD40, activates protein kinase D (PKD), while CD40, but not the BCR, emp
127 C) isoforms-alpha and -delta and may involve protein kinase D (PKD).
128 ation complex for the lipid-dependent enzyme protein kinase D (PKD).
129 of nuclear calcium and activation of nuclear protein kinase D (PKD).
130 ell as phosphorylation of serine residues by protein kinase D (PKD).
131 against the optimal phosphorylation motif of protein kinase D (PKD).
132                                              Protein kinase D (PKD)/protein kinase C (PKC) mu is a se
133                                              Protein kinase D (PKD)/protein kinase C mu is a serine/t
134 at S. rectivirgula induces the activation of protein kinase D (PKD)1 in lung cells in vitro and in vi
135 e is known about the serine/threonine kinase protein kinase D (PKD)1 in mast cells.
136 e present study, we investigated the role of protein kinase D (PKD)1 in the proinflammatory responses
137                                              Protein kinase D (PKD, also known as PKCmu) is closely r
138               When a kinase inactive form of Protein Kinase D (PKD-K618N) was expressed in HeLa cells
139                                              Protein kinase D (PKD/PKCmu) immunoprecipitated from COS
140                                              Protein kinase D (PKD/PKCmu) immunoprecipitated from COS
141 on loop phosphorylation in the regulation of protein kinase D (PKD/protein kinase C (PKC) mu) activit
142                                              Protein kinase D (PKD; also known as PKCmicro) is a seri
143           Although protein kinase C-mediated protein kinase D(PKD)activation was implicated in the re
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
148                  Remarkably, the activity of protein kinase D, the kinase that mediates nuclear expor
149                     We provide evidence that protein kinase D, which is phosphorylated and activated

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