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1 C) has recently been identified as the Golgi casein kinase.
2 clear translocation of PER2 are regulated by casein kinase.
3 ity 20C (Fam20C), is the physiological Golgi casein kinase.
4 ubiquitylation were blocked by disruption of casein kinase 1 (CK1) activity, and mass spectrometry an
5 lation was reduced by specific inhibitors of casein kinase 1 (CK1) and casein kinase 2 (CK2) (10 muM
6 such as phosphorylation of clock proteins by casein kinase 1 (CK1) and glycogen synthase kinase 3 (GS
7  ligase complex upon dual phosphorylation by casein kinase 1 (CK1) and glycogen synthase kinase 3beta
8  under physiological conditions and identify Casein Kinase 1 (CK1) as an upstream effector that bidir
9 rylation and that both were inhibited by the casein kinase 1 (CK1) delta/epsilon inhibitor IC261.
10 lated in vitro and in vivo by members of the casein kinase 1 (CK1) family and by glycogen synthase ki
11 dies to show that Ser-247 is a target of the casein kinase 1 (CK1) family of protein kinases.
12                                    Here, the casein kinase 1 (CK1) Hrr25 is shown to be an endocytic
13                                              Casein kinase 1 (CK1) is one such enzyme; it stimulates
14                                              Casein kinase 1 (CK1) was identified as the major kinase
15 at Ser680 promotes Ser683 phosphorylation by casein kinase 1 (CK1), and these phosphorylation events
16         Phosphorylation of the COPII coat by casein kinase 1 (CK1), Hrr25, contributes to the directi
17 nes; rephosphorylation by kinases, including casein kinase 1 (CK1), restores NFAT to its latent state
18 elsr1, Prickle1, FZD3, FZD7, Dvl2, Dvl3, and casein kinase 1 (CK1)-epsilon are upregulated in B lymph
19 er-174 and Ser-175 by the nuclear isoform of casein kinase 1 (CK1).
20 ent manner by the plasma membrane-associated casein kinase 1 (CK1).
21                         Two such regulators, casein kinase 1 (CKI) and F-box and leucine-rich repeat
22 ts G2 mode by blocking Srs2 DNA helicase and Casein Kinase 1 (Hhp1).
23                                 We also show casein kinase 1 (Hrr25) is a key kinase that phosphoryla
24                          Strikingly, loss of casein kinase 1 activity causes constitutive activation
25                                              Casein kinase 1 alpha (CK1 alpha) was shown to directly
26  protein stability of FOXO3A is regulated by Casein Kinase 1 alpha (CK1alpha) in an oncogenic RAS-spe
27                         Here, we report that casein kinase 1 alpha (CK1alpha) phosphorylates Cdc25A o
28                                We found that casein kinase 1 alpha (Csnk1a1), a serine-threonine kina
29 ung cancer (NSCLC) cell lines, we identified casein kinase 1 alpha (CSNK1A1, CK1alpha).
30              Our results describe a role for casein kinase 1 as a direct regulator of sterol homeosta
31 nstrated that Ser(568) was phosphorylated by casein kinase 1 both in vitro and in vivo.
32                                         Both casein kinase 1 delta (CK1delta) and epsilon (CK1epsilon
33                                              Casein kinase 1 delta (CK1delta) and its closest homolog
34                                Inhibition of casein kinase 1 delta (CK1delta) blocks primary ciliogen
35                                              Casein kinase 1 epsilon (CK1epsilon) and its closest hom
36 requires both non-canonical Wnt5a ligand and casein kinase 1 epsilon (CK1varepsilon), and that this e
37  self-renewal, by inducing the expression of casein kinase 1 epsilon.
38 be our isolation and characterization of the casein kinase 1 family member Hhp2 as a novel regulator
39                          We demonstrate that Casein kinase 1 family members, including isoforms of Ta
40 he Hedgehog pathway are redundant with other Casein kinase 1 family members.
41                                 Depletion of casein kinase 1 gamma (CSNK-1) in Caenorhabditis elegans
42  a multifaceted approach, we have found that casein kinase 1 gamma 1 (CK1gamma1) carries out this fun
43        We further evaluated whether D4476, a casein kinase 1 inhibitor, would exhibit selective antil
44                                      Because casein kinase 1 is associated with sites of polar growth
45                                Inhibition of casein kinase 1 may also contribute to the antitumoral a
46 in 90 and glycogen synthase kinase 3 but not casein kinase 1 nor LATS in YAP-mediated TAZ loss.
47 ists of two independent domains that contain casein kinase 1 phosphorylation sites.
48 depends on the ubiquitin ligase Rsp5 and the casein kinase 1 redundant pair Yck1/Yck2.
49                         Deregulation of CK1 (casein kinase 1) activity can be involved in the develop
50 ing protein (IQGAP); and three NFAT kinases, casein kinase 1, glycogen synthase kinase 3, and dual sp
51 e sensitive to pharmacological inhibition of Casein kinase 1, suggesting the possibility of shared cl
52                    Csnk1e, the gene encoding casein kinase 1-epsilon, has been implicated in sensitiv
53  involves SOD1-mediated stabilization of two casein kinase 1-gamma (CK1gamma) homologs, Yck1p and Yck
54 psis (Arabidopsis thaliana) CK1 member named casein kinase 1-like 6 (CKL6) associates with cortical m
55 iotic division is coordinated by a conserved casein kinase 1.
56 y for calcineurin and decreased affinity for casein kinase 1.
57     In this study, we determined the role of casein kinase-1 (CK1) in regulating NMDAR activity in th
58     Arsenite also recruited a TDP-43 kinase, casein kinase-1 (CK1), to GADD34.
59 ut not other PI3Kdelta inhibitors, inhibited casein kinase-1 epsilon (CK1epsilon).
60         CK1delta, a member of the ubiquitous casein kinase-1 family, is implicated in the progression
61                                 We show that casein kinase-1 inhibition increases NMDA receptor activ
62                       Our data indicate that casein kinase-1 tonically regulates NMDA receptor activi
63 clock, a protein complex of frequency (FRQ), casein kinase 1a (CK1a), and the FRQ-interacting RNA Hel
64  the ability of FRQ to interact with WCC and casein kinase 1a.
65 t lenalidomide induces the ubiquitination of casein kinase 1A1 (CK1alpha) by the E3 ubiquitin ligase
66                                          The casein kinase 1A1 gene (CSNK1A1) is a putative tumor sup
67  Here we report that both screens identified casein kinase 1alpha (CK1alpha) as a bifunctional regula
68  report purification and characterization of casein kinase 1alpha (CK1alpha) as a bona fide major IFN
69                                We identified casein kinase 1alpha (CK1alpha) as a direct target of mi
70 iRNA kinome screen, we identify and validate casein kinase 1alpha (CK1alpha) as being responsible for
71  caused by GLIPR1-mediated redistribution of casein kinase 1alpha (CK1alpha) from the Golgi apparatus
72  demonstrate that RAS-dependent elevation of casein kinase 1alpha (CK1alpha) negatively regulates aut
73 trate that the destruction complex component casein kinase 1alpha (CK1alpha) phosphorylates Jade-1 at
74                 Previous studies showed that casein kinase 1alpha (CK1alpha) stably associates with M
75 and metastasis in vivo via downregulation of casein kinase 1alpha (CK1alpha), a suppressor of pro-met
76                          Here we report that casein kinase 1alpha (CK1alpha), a ubiquitously expresse
77 nhibitor), adenomatous polyposis coli (APC), casein kinase 1alpha (CK1alpha), and glycogen synthase k
78 inc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kinase 1alpha (CK1alpha), and the translation ter
79 IFN in the context of intestinal knockout of casein kinase 1alpha (CK1alpha), which controls the ubiq
80                         Finally, we identify casein kinase 1alpha as a possible candidate for KLP10A
81 o impacted by lenalidomide, which suppressed casein kinase 1alpha expression while augmenting glycoge
82                         We thus propose that Casein kinase 1alpha is essential to allow beta-Catenin
83 ion in the beta-Catenin degradation complex, Casein Kinase 1alpha mutant cells accumulate beta-Cateni
84 , we could not detect any effect of the same Casein Kinase 1alpha mutation on Hedgehog signaling.
85 mor suppressor adenomatous polyposis coli or casein kinase 1alpha uncovered new regulatory features a
86 in-related protein 2, and the protein kinase Casein kinase 1alpha.
87 rvinium as a novel, potent (IC50, 10 nmol/L) casein kinase-1alpha (CK1alpha) agonist.
88 lycogen synthase kinase-3beta (GSK3beta) and casein kinase-1alpha (CK1alpha) are multifunctional kina
89 as carried out by the combined activities of casein kinase 1delta (CK1 delta) and casein kinase 1epsi
90                                              Casein kinase 1delta (CK1delta) and 1epsilon (CK1epsilon
91                                              Casein kinase 1delta (CK1delta) family members associate
92 89, while also enhancing Sid4's affinity for casein kinase 1delta (CK1delta).
93   Given the role of mammalian Hhp2 homologs, casein kinase 1delta and 1epsilon, in regulation of the
94                We and others have shown that casein kinase 1delta and epsilon (CK1delta/epsilon) are
95 ermined whether pharmacological targeting of casein kinase 1delta and epsilon (CK1delta/epsilon), key
96 n correlated with neurite outgrowth and that casein kinase 1delta, one of the enzymes that mediate Wn
97 ithin Rec8 as well as two different kinases, casein kinase 1delta/epsilon (CK1delta/epsilon) and Dbf4
98                                              Casein kinase 1delta/epsilon (CK1delta/epsilon) and thei
99                  Earlier work has implicated casein kinase 1delta/epsilon as responsible for the Dvl
100             This activity was inhibited by a casein kinase 1delta/epsilon inhibitor, suggesting a rol
101                                              Casein kinases 1delta and epsilon are closely related cl
102  liver nuclei all three PERs, both CRYs, and Casein Kinase-1delta (CK1delta) are present together in
103 ties of casein kinase 1delta (CK1 delta) and casein kinase 1epsilon (CK1epsilon) and was antagonized
104                  Specifically, we found that casein kinase 1epsilon (CK1epsilon) is highly expressed
105          In the present study, we found that casein kinase 1epsilon (CK1epsilon) was increased signif
106  pigment aggregation signaling also involved casein kinase 1epsilon (CK1epsilon), that both enzymes w
107 its vulnerability to degradation mediated by casein kinase 1epsilon (CSNK1E) is increased.
108 earing a short-period mutation in the enzyme casein kinase 1epsilon (tau mutation), which accelerates
109  Fat-Hippo signaling requires the Drosophila Casein kinase 1epsilon encoded by discs overgrown (Dco),
110     Here, we show that fission yeast Cki3 (a casein kinase 1gamma homolog) is a critical regulator to
111 es with thapsigargin (10 mum), inhibition of casein kinase 2 (4,5,6,7-tetrabromobenzotriazole; 10 mum
112 ific inhibitors of casein kinase 1 (CK1) and casein kinase 2 (CK2) (10 muM D4476, 100 muM CK2-inhibit
113 effects of mutant M1 spastins on FAT involve casein kinase 2 (CK2) activation.
114 rt inhibition as a consequence of endogenous casein kinase 2 (CK2) activation.
115                                  We focus on casein kinase 2 (CK2) and demonstrate that the regulator
116                 In this study, we identified casein kinase 2 (CK2) as a critical modulator of NADPH o
117                                  We identify casein kinase 2 (CK2) as a key regulator of temperature
118 ave identified polo-like kinase 1 (Plk1) and casein kinase 2 (CK2) as two kinases of CLIP-170 and map
119                                              Casein kinase 2 (CK2) binds to the NHE3 C-terminus and c
120  Our previous results highlighted a role for casein kinase 2 (CK2) in the modulation of dopamine D1 r
121 iated stimulation, PTEN is phosphorylated by casein kinase 2 (CK2) in the Ser380-Thr382-Thr383 cluste
122 tified serine 358 as a specific site used by casein kinase 2 (CK2) in vitro and in vivo.
123 7 -: tetrabromobenzotriazole (TBB), a potent casein kinase 2 (CK2) inhibitor, as a strong suppressor
124                           The protein kinase casein kinase 2 (CK2) is a pleiotropic and constitutivel
125                                              Casein kinase 2 (CK2) is a typical serine/threonine kina
126                      Although protein kinase casein kinase 2 (CK2) is readily detected in MKs and pla
127              Previous research suggests that casein kinase 2 (CK2) may be a promising therapeutic tar
128     Previous in vitro studies indicated that casein kinase 2 (CK2) mediated the phosphorylation of NS
129                We have previously shown that casein kinase 2 (CK2) negatively regulates dopamine D1 a
130   We demonstrated that increased activity of casein kinase 2 (CK2) observed in HPC and in MDSC could
131 w that murine caspase-9 is phosphorylated by casein kinase 2 (CK2) on a serine near the site of caspa
132 at shock and antioxidants induced Hsp90, and casein kinase 2 (CK2) phosphorylated INrf2Thr55.
133                                              Casein kinase 2 (CK2) phosphorylates the NR2B subunit wi
134 The MRE11-PIH1D1 interaction is dependent on casein kinase 2 (CK2) phosphorylation of two acidic sequ
135     The Foxc2 amino terminus has a consensus casein kinase 2 (CK2) phosphorylation site at serine 124
136 ariant of the formin FHOD3 that introduces a casein kinase 2 (CK2) phosphorylation site.
137  the C terminus, which was predicted to be a casein kinase 2 (CK2) phosphorylation site.
138 ) of MDC1, which contains multiple consensus casein kinase 2 (CK2) phosphorylation sites.
139 and overexpression experiments, we show that casein kinase 2 (CK2) promotes stress granule dynamics.
140 that phosphorylation of recombinant TFIIF by casein kinase 2 (CK2) reduces or eliminates some of the
141  serine residues 16 and 18, which are within casein kinase 2 (CK2) sites, and serine residue 114, whi
142 ctivated through pharmacologic inhibition of casein kinase 2 (CK2) to eradicate disease in high-risk
143 sh1 is phosphorylated by the Cka2 subunit of casein kinase 2 (CK2) to promote its E3 activity for Cse
144                                CD5 activates casein kinase 2 (CK2), a serine/threonine kinase that co
145 ere, we report that Brg1 is also a target of casein kinase 2 (CK2), a serine/threonine kinase, in pro
146 wn previously to require the Cka2 subunit of casein kinase 2 (CK2), a ubiquitous enzyme with multiple
147                                              Casein kinase 2 (CK2), a ubiquitous kinase, regulates se
148 nsists of Daz interacting protein 1 (Dzip1), casein kinase 2 (CK2), and B56 containing protein phosph
149 on was dependent on XRCC1 phosphorylation by casein kinase 2 (CK2), enhancing XRCC1's interaction wit
150 on events catalyzed first by MEK and then by casein kinase 2 (CK2), followed by interaction with impo
151 e, and this phosphorylation was catalyzed by casein kinase 2 (CK2), the levels of which were dramatic
152 a striking resemblance to that of eukaryotic casein kinase 2 (CK2), which also exhibits dual nucleoti
153 d51 phosphorylation at threonine 13 (T13) by casein kinase 2 (CK2), which in turn triggers direct bin
154                  Wnt stimulation induces the casein kinase 2 (CK2)-dependent phosphorylation of LRP6
155                      We have also noted that casein kinase 2 (CK2)-directed phosphorylation of Pax7 a
156  the unsuspected tyrosine kinase activity of casein kinase 2 (CK2).
157 ISA analyses and Western blotting to measure casein kinase 2 (CK2).
158  by the disease-relevant signalling protein, casein kinase 2 (CK2).
159 orylated on conserved serines 487 and 491 by casein kinase 2 (CK2).
160 t human cytomegalovirus pUL84 interacts with casein kinase 2 (CK2).
161  various kinases, including GPCR kinases and casein kinase 2 (CK2).
162 minal kinase; (ii) inhibition of calpain and casein kinase 2 activity; and (iii) induction of fibrobl
163                                              Casein kinase 2 alpha phosphorylates PDCD5 at Ser-119 to
164 lation sites and two putative GRIP1 kinases, casein kinase 2 and cyclin-dependent kinase 9.
165 molecular events of this modulation involved casein kinase 2 and the synaptic vesicle rapid endocytos
166 posttranslationally regulated by TNF-induced casein kinase 2 catalytic subunit (CK2alpha') phosphoryl
167                These data support a role for casein kinase 2 in regulation of protein synthesis by do
168                          We report here that casein kinase 2 phosphorylates a conserved threonine res
169                   Upon hypertrophic stimuli, casein kinase 2 phosphorylates DPF3a at serine 348.
170                            We also show that casein kinase 2 phosphorylates G3BP1 at serine 149 in vi
171 a physical interaction between S6KII and the casein kinase 2 regulatory subunit (CK2beta), suggesting
172     We now show that TFIIF phosphorylated by casein kinase 2 remains competent to support PIC assembl
173                                              Casein kinase 2 stimulates the biogenesis of Tom22 and T
174 an interacting protein, protein kinase C and casein kinase 2 substrate in neurons 1 (PACSIN1).
175             The PACSIN (protein kinase C and casein kinase 2 substrate in neurons) adapter proteins c
176            This activity, and the ability of casein kinase 2 to use GTP as a phosphate donor, may be
177 ine 424 by protein kinase CK2 (also known as casein kinase 2) activated the HDAC3 in vitro.
178 ylation of calmodulin by protein kinase CK2 (casein kinase 2) rapidly and reversibly modulated KCNQ2
179 overed that murine Arl13b is a substrate for casein kinase 2, a contaminant in our preparation from h
180           Protein kinase CK2 (CK2) (formerly casein kinase 2, a protein Ser/Thr kinase signal that is
181 ation of ErbB2 or loss of the betasubunit of casein kinase 2, shifted the whole population toward a f
182 uired Rab11-dependent trafficking and FAM20C/casein kinase 2-dependent C-terminal phosphorylation of
183 required for insulin induction of Sort1 in a casein kinase 2-dependent manner and that inhibition of
184                                              Casein kinase 2-mediated phosphorylation at VHL N-termin
185                                 ERK promotes casein kinase 2-mediated phosphorylation of alpha-cateni
186 t we identified as substrates for Erk1/2 and casein kinase 2.
187 I, whereas Ca(V)1.1-T1579 is a substrate for casein kinase 2.
188 c but not the cardiac CCRK with cyclin H and casein kinase 2.
189 nts indicate that phosphorylation of TLE1 by casein kinase-2 (CK2) at Ser-239 and Ser-253 is necessar
190                                              Casein kinase-2 (CK2) promotes cell survival and is upre
191                                  Conversely, casein kinase-2 (CK2)-inhibitor increases Ikaros functio
192 s NMDA receptor activity by interacting with casein kinase-2 and protein phosphatases in the hypothal
193 r localization of Atx3 was not affected by a casein kinase-2 inhibitor or by mutating a predicted nuc
194 he protein phosphatase 1/2A, calcineurin, or casein kinase-2 inhibitor.
195       Some interesting cross reactivity with casein kinase-2 was also identified, and structural feat
196  M1-type muscarinic receptors and occur in a casein kinase-2-dependent manner.
197           In this study, we explored whether casein kinase 2alpha (CK2alpha), the human homolog of Ck
198 ated protein 1 (MRP1), is regulated by yeast casein kinase 2alpha (Cka1p) via phosphorylation at Ser2
199 se kinase-3beta and an increase in levels of casein kinase 2alpha, and led to increased cyclin-D1, an
200 orylation status of the downstream molecules casein kinase-2alpha and histone deacetylase 2 were sign
201 x1 regulates normal cardiac function via p27/casein kinase-2alpha/histone deacetylase 2 and indicate
202 e U.S. Food and Drug Administration-approved casein kinase activator, pyrvinium) in C57Bl/6J mice res
203                              NUCKS1 (nuclear casein kinase and cyclin-dependent kinase substrate 1) i
204 kDa enamelin that is phosphorylated by Golgi casein kinase and is thought to mediate calcium binding.
205 " with Axin, glycogen synthase kinase 3, and casein kinase, APC targets sscatenin (sscat) for phospho
206 e interacting proteins were found to contain casein kinase (CK) 2, phosphokinase (PK)C phosphorylatio
207  acidic amino acids, is regulated in vivo by casein kinase (CK) Idelta and/or CKIepsilon, but not by
208 R2 is phosphorylated on Ser-662 and flanking casein kinase (CK) sites in vivo.
209 g peptide, we established a pivotal role for casein kinase (CK)-2-mediated circadian BMAL1-Ser90 phos
210  HDAC inhibitors transcriptionally activated casein kinase (CK)2alpha expression through increased as
211                          Increased levels of casein kinase (CK1 and CK2), which are associated with T
212                                              Casein kinase CK2 is an essential enzyme in higher organ
213 s of ataxia-telangiectasia-mutated (ATM) and casein kinases (CKs) 1 and 2.
214 y mechanistic target of rapamycin (mTOR) and casein kinase (CSNK)-2.
215                                          The casein kinase family of serine/threonine kinases regulat
216 r axonemes has implicated the protein kinase casein kinase I (CK1) in regulation of dynein.
217                        To assess the role of casein kinase I (CK1) in the regulation of dopamine sign
218                      Although members of the casein kinase I (CKI) family phosphorylate alphaSyn at S
219 to growth signals, and in collaboration with casein kinase I (CKI), generates a phosphodegron that bi
220 biquitination and destruction of VEGFR2 in a casein kinase I (CKI)-dependent manner.
221 -induced phosphorylation of its prodomain by casein kinase I (Yck1/2).
222 dation requires phosphorylation of PHLPP1 by casein kinase I and glycogen synthase kinase 3beta (GSK-
223 r a critical requirement for the centrosomal casein kinase I delta (CKIdelta) in centrosome transloca
224              Activating beta-catenin through Casein Kinase I inhibition or Wnt3A addition increased b
225 es, we show that Hrr25p, an isoform of yeast casein kinase I, phosphorylates Tif6p both in vitro and
226 ucleation pathway were identified as well as casein kinase I, which had a similar morphological RNAi
227 res downstream assistance from an inhibitory casein kinase I, Yck3.
228  When HOPS is phosphorylated by the vacuolar casein kinase I, Yck3p, tethering only takes place when
229                                              Casein kinase I-alpha (CKI-alpha) was identified as an N
230 Set8 for ubiquitination and degradation in a casein kinase I-dependent manner, which is activated by
231        We identify the PI-4,5-P(2)-sensitive casein kinase Ialpha (CKIalpha) as a protein kinase resp
232                                              Casein kinase Ialpha (CKIalpha) directly phosphorylated
233             Following these changes, loss of Casein kinase Ialpha and induction of chronic DNA damage
234 (PER) proteins, which is highly dependent on casein kinase Idelta/epsilon (CKIdelta/epsilon; termed D
235                                              Casein kinases Idelta and Iepsilon (CKIdelta/epsilon) ca
236 ks, including three compounds that inhibited casein kinase Iepsilon in vitro and a unique benzodiazep
237 f Drosophila Doubletime (DBT) and vertebrate casein kinase Iepsilon/delta (CKIepsilon/delta) produce
238 f the gilgamesh (gish) gene, which encodes a casein kinase Igamma homolog that is preferentially expr
239 t sites by at minimum two different kinases, casein kinase II (CK II) and tousled-like kinase (tlk).
240  for phosphorylation by protein kinase C and casein kinase II (CK-II).
241 ar substrates of human protein kinases (e.g. casein kinase II (CK2) and Akt), that implicated several
242 s presented here identify the protein kinase casein kinase II (CK2) as a BMP receptor type Ia (BRIa)
243                                              Casein kinase II (CK2) has been shown to act as a positi
244             Here we uncover a novel role for casein kinase II (CK2) in the cellular response to hyper
245  calmodulin-dependent kinase II (CaMKII) and casein kinase II (CK2) inhibition.
246 -dione derivatives were synthesized as human casein kinase II (CK2) inhibitors.
247  that the conserved serine/threonine kinase, casein kinase II (CK2), promotes miRISC function in Caen
248 y, Brd4 association with p53 is modulated by casein kinase II (CK2)-mediated phosphorylation of a con
249   The N-terminal phosphorylation by cellular casein kinase II (CKII) at S21, T32, and S43, and other
250 roaches, we have identified a novel role for casein kinase II (CKII) in the modification of the polym
251                    We have demonstrated that casein kinase II (CKII) is involved in the phosphorylati
252 n intact pocket protein binding domain and a casein kinase II (CKII) phosphorylation motif.
253 ed the phosphorylation of Dgk1 DAG kinase by casein kinase II (CKII).
254 s work, we show that Pah1 is a substrate for casein kinase II (CKII); its phosphorylation was time- a
255                                              Casein kinase II (formerly known as CK2), a ubiquitous S
256 damage in a manner dependent on TCOF1 and on casein kinase II and ATM, which are known to modify TCOF
257           In vitro studies support roles for casein kinase II and PKC in this modification, consisten
258 this repression by directly interacting with Casein Kinase II and preventing it from activating HDAC3
259 phorylated by two EVI1 interactome proteins, casein kinase II and protein phosphatase-1alpha.
260  Thr1704-sites of phosphorylation by PKA and casein kinase II at the interface between the proximal a
261 RNA designed to knock down expression of the casein kinase II beta-subunit gene family lengthens peri
262 t with previous reports of a short period in casein kinase II beta-subunit overexpressors.
263  phosphatase calcineurin (TAX-6), and of the casein kinase II homologue KIN-10.
264  preincubation of RBCs with DMAT, a specific casein kinase II inhibitor.
265 dition, our data indicate that inhibition of casein kinase II or GSK3beta significantly reduced hnRNP
266 uniquely possess lysine residues following a casein kinase II phosphorylation motif which is critical
267 he nuclei of infected cells, indicating that casein kinase II phosphorylation of S186 occurs in the n
268                             Mutations of the casein kinase II phosphorylation site caused a complex p
269  region identified IE63 S186 as a target for casein kinase II phosphorylation.
270  serine 72 and pharmacological inhibition of casein kinase II reduced GTPCH-1 phosphorylation and blu
271 ll three members of the protein kinase C and casein kinase II substrate in neurons (PACSIN) family an
272 ously reported that the protein kinase C and casein kinase II substrate in neurons (PACSIN) forms a c
273 his report we identify CK2 (formerly termed "casein kinase II") as the kinase responsible for phospho
274 ned the role of protein kinase CK2 (formerly casein kinase II) in increased N-methyl-d-aspartate rece
275 ng 1 (YY1) in vitro and in vivo by CK2alpha (casein kinase II), a multifunctional serine/threonine pr
276 se A/calcium calmodulin-dependent kinase II, casein kinase II, and proline-directed kinase, indicatin
277 Ser184 of Geminin could be phosphorylated by Casein kinase II, resulting in the enhanced binding to H
278 trated that Ser(10) can be phosphorylated by casein kinase II, Ser(21) can be phosphorylated by prote
279 on of myosin light chain kinase (P<0.05) and casein kinase II-alpha (P=0.06).
280    EGF enhanced secretion of AMF through its casein kinase II-mediated phosphorylation.
281 , which in turn increases enzyme activity of casein kinase II.
282 ivity) is inactivated via phosphorylation by casein kinase II.
283  P<0.0001) through a mechanism that includes casein kinase II.
284 ain binding to Asf1-T(270) phosphorylated by casein kinase II.
285        Dual mutation of Ser1700 and a nearby casein-kinase II site (Thr1704) caused accelerated hyper
286 and signaling pathways, including CaMK, PKA, Casein kinase-II, and the Raf-MEK-ERK and PI-3K-Akt path
287 RNA synthesis through the phosphorylation of casein kinase IIalpha (CK2alpha) on a threonine residue
288                                              Casein kinase Ivarepsilon phosphorylates the S102 in thi
289                                              Casein kinase levels were not altered after treatment wi
290 e WC complex in the nucleus by promoting the casein kinases-mediated WC phosphorylation.
291 n HapMap cell lines was protein kinase C and casein kinase substrate in neurons 2 (PACSIN2).
292 or by coexpression with protein kinase C and casein kinase substrate in neurons 3 (PACSIN3), a regula
293 eletions of YCK3, encoding a vacuolar type I casein kinase; SVP26, encoding an endoplasmic reticulum
294                          Fam20C is the Golgi casein kinase that phosphorylates secretory pathway prot
295               Fam20C appears to be the Golgi casein kinase that phosphorylates secretory pathway prot
296            Fam20C is the physiological Golgi casein kinase, which phosphorylates many secreted protei
297                 We also show that the type-I casein kinases Yck1 and Yck2 phosphorylate Ubr1 on Ser(3
298            We report here that the redundant casein kinases Yck1p and Yck2p phosphorylate sites withi
299 e requires its phosphorylation by the type 1 casein kinase Yck3.
300                                    The yeast casein kinases (Ycks) are key players in this pathway.

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