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1 of Nod-factor-induced calcium spiking and a calcium/calmodulin-dependent protein kinase.
2 DMI3 encodes a calcium/calmodulin-dependent protein kinase.
3 ococcal uptake; one of them encoded CaMK4, a calcium/calmodulin-dependent protein kinase.
4 omain of CCaMK with the crystal structure of calcium/calmodulin-dependent protein kinase 1 suggests t
5 s upstream kinase liver kinase B1 (LKB1) and calcium/calmodulin-dependent protein kinase 2 (CaMKK2).
6 -dependent and is prevented by inhibitors of calcium/calmodulin-dependent protein kinase 2, phosphati
8 l profiling studies demonstrated that Cn and calcium/calmodulin-dependent protein kinase activate dis
9 ed transcription by calcium signals requires calcium/ calmodulin-dependent protein kinases and is dep
10 need for new protein synthesis and required calcium/calmodulin-dependent protein kinases and the nuc
11 pharmacological inhibition with the specific calcium/calmodulin-dependent protein kinase beta inhibit
12 thanol tolerance, as did mutants in the gene calcium/calmodulin-dependent protein kinase (caki), enco
13 lowing oxidant injury, whereas inhibition of calcium-calmodulin-dependent protein kinase, calcineurin
14 Calcium-dependent protein kinase C (PKC) and calcium-calmodulin-dependent protein kinase (CAM K) have
16 e--which are deficient in a component of the calcium calmodulin-dependent protein kinase (CaMK) pathw
17 gh a posttranslational mechanism mediated by calcium, calmodulin-dependent protein kinase (CaMK), and
18 which is localized to the nucleus, and that calcium-calmodulin-dependent protein kinase (CaMK)-depen
20 dent on downstream signaling via calmodulin, calcium/calmodulin-dependent protein kinase (CaMK) and e
21 calcium signal is transduced in part by the calcium/calmodulin-dependent protein kinase (CaMK) casca
22 on DeltaPsi Here, we characterize a role for calcium/calmodulin-dependent protein kinase (CaMK) I in
23 ediate postretrieval bilateral inhibition of calcium/calmodulin-dependent protein kinase (CaMK) II in
27 The Ca(2+)-dependent binding of S100B to the calcium/calmodulin-dependent protein kinase (CaMK)-type
28 have shown that the cytoplasmically oriented calcium/calmodulin-dependent protein kinase (CaMK)Ialpha
29 are required for RANK-mediated activation of calcium/calmodulin-dependent protein kinase (CaMK)II and
31 , beta, gamma, and delta isoforms of type II calcium/calmodulin-dependent protein kinase (CaMKII), al
32 pase Cbeta, diacylglycerol (DAG) kinase, and calcium/calmodulin-dependent protein kinase (CaMKII), ha
33 ular calcium, resulting in the modulation of calcium-calmodulin-dependent protein kinases (CaMKs).
36 ced lateral root development in Populus in a calcium/calmodulin-dependent protein kinase (CCaMK)-depe
37 e D (PKD) family is a recent addition to the calcium/calmodulin-dependent protein kinase group of ser
38 enetic protein-2/4) or constitutively active calcium/calmodulin-dependent protein kinase I and/or cal
41 ickening, the amount of PSD-associated alpha-calcium calmodulin-dependent protein kinase II (alpha- C
42 found to signal neuronal cells and activate calcium calmodulin-dependent protein kinase II (CaMKII)
44 mTOR and increasing dendritic translation of calcium calmodulin-dependent protein kinase II alpha and
45 ssociates with mRNA, e.g. encoding GluR1 and calcium calmodulin-dependent protein kinase II alpha.
46 hyl-d-aspartate receptors, and inhibitors of calcium calmodulin-dependent protein kinase II and (ii)
47 mics in myocytes from arrhythmia-susceptible calcium calmodulin-dependent protein kinase II delta C (
52 ogical blockade of protein kinase C (PKC) or calcium-calmodulin-dependent protein kinase II (CaMK II)
53 F), cAMP response-element-binding (CREB) and calcium-calmodulin-dependent protein kinase II (CAMKII)
56 be dependent on NMDA receptor and subsequent calcium-calmodulin-dependent protein kinase II (CaMKII)
61 lement-binding protein (CREB), phospho-CREB, calcium-calmodulin-dependent protein kinase II (CAMKII),
62 s activation of the calcium-sensitive kinase calcium-calmodulin-dependent protein kinase II (CaMKII).
63 stinct sites by protein kinase A (Ser-7) and calcium-calmodulin-dependent protein kinase II (Ser-13)
65 revent neuronal death, whereas inhibitors of calcium/ calmodulin-dependent protein kinase II did not.
67 e diacylglycerol lipase-alpha (DGLalpha) and calcium/calmodulin dependent protein kinase II (CaMKII).
68 tain other brain regions, using Thy1-Cre and calcium/calmodulin dependent protein kinase II alpha-Cre
69 process is critically regulated by the alpha-calcium/calmodulin-dependent protein kinase II (alpha-Ca
70 tial coding rely on the alpha-isoform of the calcium/calmodulin-dependent protein kinase II (alphaCaM
72 piperazine (KN-62), a selective inhibitor of calcium/calmodulin-dependent protein kinase II (CaM kina
74 results from phosphorylation of Thr-1940 by calcium/calmodulin-dependent protein kinase II (CaM kina
76 ions of cyclin-dependent kinase 5 (cdk5) and calcium/calmodulin-dependent protein kinase II (CaMK II)
78 d to quantify the phosphopeptide produced by calcium/calmodulin-dependent protein kinase II (CaMK II)
80 Pyramidal cells were identified by using calcium/calmodulin-dependent protein kinase II (CaMK) im
81 used as a marker for cholinergic terminals; calcium/calmodulin-dependent protein kinase II (CaMK) wa
82 neurons that exhibited immunoreactivity for calcium/calmodulin-dependent protein kinase II (CaMK).
83 were selectively labeled with antibodies to calcium/calmodulin-dependent protein kinase II (CaMK); p
86 activity is downstream of Dalpha7 nAChRs and Calcium/calmodulin-dependent protein kinase II (CaMKII)
87 ions significantly increased the activity of calcium/calmodulin-dependent protein kinase II (CaMKII)
91 tion of calmodulin, but was not dependent on calcium/calmodulin-dependent protein kinase II (CaMKII)
93 by phosphorylation at serine 73, a conserved calcium/calmodulin-dependent protein kinase II (CaMKII)
94 ice showed increased prefrontal cortex (PFC) calcium/calmodulin-dependent protein kinase II (CaMKII)
101 eceptor-mediated calcium influx and possibly calcium/calmodulin-dependent protein kinase II (CaMKII)
102 f free calcium that activates members of the calcium/calmodulin-dependent protein kinase II (CaMKII)
103 ions of tetrodotoxin, omega-conotoxin MVIIC, calcium/calmodulin-dependent protein kinase II (CaMKII)
104 ss or suppress kinase activity, we find that calcium/calmodulin-dependent protein kinase II (CaMKII)
108 In the present study, we examined whether calcium/calmodulin-dependent protein kinase II (CaMKII)
111 the hippocampus during synaptic plasticity, calcium/calmodulin-dependent protein kinase II (CaMKII)
113 or glutamic acid decarboxylase 67 (GAD67) or calcium/calmodulin-dependent protein kinase II (CAMKII)
121 in egg extracts or specific inactivation of calcium/calmodulin-dependent protein kinase II (CaMKII)
123 e, whereas in potentiated synapses the major calcium/calmodulin-dependent protein kinase II (CaMKII)
124 entiation (LTP) or increased activity of the calcium/calmodulin-dependent protein kinase II (CaMKII)
125 a continuing search for proteins that target calcium/calmodulin-dependent protein kinase II (CaMKII)
127 mine, we treated wild-type C57BL/6 mice with calcium/calmodulin-dependent protein kinase II (CaMKII)
131 -D-aspartate (NMDA) receptor activation, and Calcium/calmodulin-dependent protein kinase II (CaMKII)
135 ting in reduced activation of PLCgamma-alpha-calcium/calmodulin-dependent protein kinase II (CaMKII)
136 rin directly associates with and targets the calcium/calmodulin-dependent protein kinase II (CaMKII)
139 l segments depends on their interaction with calcium/calmodulin-dependent protein kinase II (CaMKII),
140 e examined its effects on phosphorylation of calcium/calmodulin-dependent protein kinase II (CaMKII),
144 significant increase in hippocampal phospho-calcium/calmodulin-dependent protein kinase II (CaMKII),
145 ation site matched the consensus sequence of calcium/calmodulin-dependent protein kinase II (CaMKII),
146 2N1 and CaMK2N2 are endogenous inhibitors of calcium/calmodulin-dependent protein kinase II (CaMKII),
147 stently reduces FRET between the NMDARcd and calcium/calmodulin-dependent protein kinase II (CaMKII),
148 is new pathway is a kinase cascade involving calcium/calmodulin-dependent protein kinase II (CaMKII),
149 5-phosphono pentanoic acid; the inhibitor of calcium/calmodulin-dependent protein kinase II (CaMKII),
150 We sought to determine how activation of calcium/calmodulin-dependent protein kinase II (CaMKII),
151 w that in cultured rat hippocampal neurons a calcium/calmodulin-dependent protein kinase II (CaMKII)-
153 e metabolism regulates oocyte cell death via calcium/calmodulin-dependent protein kinase II (CaMKII)-
154 alcium channels and requires the activity of calcium/calmodulin-dependent protein kinase II (CaMKII).
155 res the subsequent activation of presynaptic calcium/calmodulin-dependent protein kinase II (CaMKII).
156 teins in the postsynaptic density, including calcium/calmodulin-dependent protein kinase II (CaMKII).
157 cytosolic Ca2+ and concomitant activation of calcium/calmodulin-dependent protein kinase II (CaMKII).
158 e inhibitory phosphorylation of caspase-2 by calcium/calmodulin-dependent protein kinase II (CaMKII).
159 of the Wnt-Ca2+ pathway: Ca2+ flux, PKC, and calcium/calmodulin-dependent protein kinase II (CamKII).
160 1, a substrate of protein kinase C (PKC) and calcium/calmodulin-dependent protein kinase II (CaMKII).
161 nal plasticity are thought to be mediated by calcium/calmodulin-dependent protein kinase II (CaMKII).
162 h the key NMDAR downstream signaling protein calcium/calmodulin-dependent protein kinase II (CaMKII).
164 elonged to principal or local-circuit cells, calcium/calmodulin-dependent protein kinase II (CAMKIIal
165 tion factor DeltaFosB and the brain-enriched calcium/calmodulin-dependent protein kinase II (CaMKIIal
166 e we demonstrate that the delta B isoform of calcium/calmodulin-dependent protein kinase II (CaMKIIde
167 rea mAb 24.3.1 and acute chorea sera induced calcium/calmodulin-dependent protein kinase II activity
168 receptor 1 (GluR1) subunit can be driven by calcium/calmodulin-dependent protein kinase II activity
170 artic acid) receptor activation, calcium and calcium/calmodulin-dependent protein kinase II activity,
171 N-methyl-d-aspartate receptor activation and calcium/calmodulin-dependent protein kinase II activity.
173 show that mice devoid of IFNAR1 signaling in calcium/calmodulin-dependent protein kinase II alpha (Ca
174 (MRov mice) by using the forebrain-specific calcium/calmodulin-dependent protein kinase II alpha pro
176 ybridization to mRNA of the alpha subunit of calcium/calmodulin-dependent protein kinase II and incre
177 pe Ca(2+) currents were dependent in part on calcium/calmodulin-dependent protein kinase II and IP(3)
178 that mimic the calmodulin binding domain of calcium/calmodulin-dependent protein kinase II and its 1
179 to cognitive deficits via altered levels of calcium/calmodulin-dependent protein kinase II and N-met
180 were associated with reduced levels of total calcium/calmodulin-dependent protein kinase II and N-met
181 appear to be independent of their effects on calcium/calmodulin-dependent protein kinase II and PKA,
184 evelopment and function, including Titin and calcium/calmodulin-dependent protein kinase II delta (Ca
185 study the mechanical effects of the kinases calcium/calmodulin-dependent protein kinase II delta (Ca
186 tial novel mechanism that regulates neuronal calcium/calmodulin-dependent protein kinase II function.
189 -219 in NMDA receptor signaling, we identify calcium/calmodulin-dependent protein kinase II gamma sub
190 ch as extracellular signal-regulated kinase, calcium/calmodulin-dependent protein kinase II gamma, an
192 eta (PTK2B, also referred to as Pyk2) and of calcium/calmodulin-dependent protein kinase II in wild-t
193 y 80% to 90% (P<0.05) by STAT1 deficiency or calcium/calmodulin-dependent protein kinase II inhibitio
194 otein synthesis, nor are protein kinase C or calcium/calmodulin-dependent protein kinase II involved
196 neurotrophic factor and the alpha subunit of calcium/calmodulin-dependent protein kinase II mRNA in h
198 e, whereas phosphorylation of substrates for calcium/calmodulin-dependent protein kinase II was uncha
199 RPP-32, synapsin I, and the alpha subunit of calcium/calmodulin-dependent protein kinase II were meas
200 ranes, and is accompanied by altered CaMKII (calcium/calmodulin-dependent protein kinase II) and flot
201 ased activity of the protein kinases CaMKII (calcium/calmodulin-dependent protein kinase II), PKA, an
203 ion sites for cAMP-dependent protein kinase, calcium/calmodulin-dependent protein kinase II, and S6 k
204 e intracellular protein mediators Homer1b/c, calcium/calmodulin-dependent protein kinase II, and the
205 ess in a manner requiring cytosolic calcium, calcium/calmodulin-dependent protein kinase II, and toll
206 tsynaptic activation of protein kinase A and calcium/calmodulin-dependent protein kinase II, as well
208 roteins, synapsin I and the alpha subunit of calcium/calmodulin-dependent protein kinase II, did not
209 including postsynaptic density-95 and alpha-calcium/calmodulin-dependent protein kinase II, normally
210 s and was blocked by HA1004, an inhibitor of calcium/calmodulin-dependent protein kinase II, protein
211 e for both cAMP-dependent protein kinase and calcium/calmodulin-dependent protein kinase II, whereas
212 al cells were labeled by using antibodies to calcium/calmodulin-dependent protein kinase II, whereas
213 cium, in turn, led to the phosphorylation of calcium/calmodulin-dependent protein kinase II, which pr
215 ted Sim1 after birth using CaMKII-Cre (alpha-calcium/calmodulin-dependent protein kinase II-Cre) line
216 ple tg mice using the CaMKIIalpha-Cre (alpha-calcium/calmodulin-dependent protein kinase II-Cre) syst
217 and egl-2 expression can be upregulated in a calcium/calmodulin-dependent protein kinase II-dependent
218 CA1 pyramidal neuron dendrites by activating calcium/calmodulin-dependent protein kinase II-mediated
219 lly, we used 1 Hz optogenetic stimulation of calcium/calmodulin-dependent protein kinase II-positive
224 te that FTO interacts with three isoforms of calcium/calmodulin-dependent protein kinase II: alpha, b
225 OD plasticity, but was absent in adult alpha-calcium/calmodulin-dependent protein kinase II;T286A (al
227 m chelator EGTA, or a specific inhibitor for calcium/calmodulin-dependent protein kinase-II (CaMKII).
228 Studies of the structural organization of calcium/ calmodulin-dependent protein kinase IIalpha (Ca
229 opsin-3 (Arch)-mediated optical silencing of calcium/calmodulin-dependent protein kinase IIalpha (CAM
230 l PGC-1alpha knock-out mice (BalphaKO) using calcium/calmodulin-dependent protein kinase IIalpha (CaM
231 icity, including Thr(286) phosphorylation of calcium/calmodulin-dependent protein kinase IIalpha (CaM
232 functional role of dendritic translation of calcium/calmodulin-dependent protein kinase IIalpha (CaM
233 how that a regulator of synaptic plasticity, calcium/calmodulin-dependent protein kinase IIalpha (CaM
235 horing protein (alphakap) encoded within the calcium/calmodulin-dependent protein kinase IIalpha (CAM
236 ice expressing Cre-recombinase driven by the calcium/calmodulin-dependent protein kinase IIalpha prom
237 , reduced cardiomyocyte apoptosis, fibrosis, calcium/calmodulin-dependent protein kinase IIdelta phos
238 ctivated by inflammatory signals that induce calcium/calmodulin-dependent protein kinase IIgamma (CaM
239 s death receptor through a pathway involving calcium/calmodulin-dependent protein kinase IIgamma (CaM
240 lamban form could serve as substrate for the calcium-calmodulin-dependent protein kinase in vitro.
241 en-activated protein kinase is downstream of calcium/calmodulin-dependent protein kinase in a signali
242 learn more about the targets of Cn (Cn) and calcium/calmodulin-dependent protein kinase in cardiac m
243 cytosolic calcium has been shown to activate calcium/calmodulin-dependent protein kinase in muscle.
245 which is the predominant nuclear isoform of calcium/calmodulin-dependent protein kinases in heart mu
246 plored the mechanistic role of the family of calcium/calmodulin-dependent protein kinases in mediatin
247 here that MtNIN is essential for autoactive calcium/calmodulin-dependent protein kinase-induced nodu
248 cription factor-2, which were blocked by the calcium/calmodulin-dependent protein kinase inhibitor KN
249 tal NF-AT reporter gene was abrogated by the calcium/calmodulin-dependent protein kinase inhibitor KN
250 an autoactive form of a nodulation-specific calcium/calmodulin-dependent protein kinase is sufficien
260 nt reactive oxygen species (ROS) production, calcium/calmodulin-dependent protein kinase IV (CaMKIV)
261 is process have been identified, such as the calcium/calmodulin-dependent protein kinase IV (CaMKIV),
262 an internal regulatory domain responsive to calcium/calmodulin-dependent protein kinase IV (CaMKIV),
263 tudy, we describe a novel mechanism in which calcium/calmodulin-dependent protein kinase IV (CaMKIV),
264 cies and is commonly activated in neurons by calcium/calmodulin-dependent protein kinase IV (CaMKIV).
265 letal muscle a constitutively active form of calcium/calmodulin-dependent protein kinase IV (CaMKIV*)
267 eceptor-gamma coactivator-1alpha and -1beta, calcium/calmodulin-dependent protein kinase IV, and nitr
268 ate that KN93, a small-molecule inhibitor of calcium/calmodulin-dependent protein kinase IV, targeted
269 of mammalian target of rapamycin (mTOR) via calcium calmodulin-dependent protein kinase kinase (CaMK
271 st mammalian homologue of yeast Pak1 kinase, calcium-calmodulin-dependent protein kinase kinase beta,
273 RLC in the mitotic spindle is dependent upon calcium/calmodulin-dependent protein kinase kinase (CamK
275 as partially reduced by the application of a calcium/calmodulin-dependent protein kinase kinase 2 inh
276 e mechanistic target of rapamycin complex 1, calcium/calmodulin-dependent protein kinase kinase 2, an
278 phosphate activation of protein kinase A and calcium/calmodulin-dependent protein kinase kinase 2.
279 A-mediated knockdown of the key AMPK kinase, calcium/calmodulin-dependent protein kinase kinase beta,
280 PK phosphorylation in pathways involving the calcium/calmodulin-dependent protein kinase kinase beta.
281 vation loop alpha-Thr(172) via inhibition of calcium/calmodulin-dependent protein kinase kinase-alpha
282 m levels and promoted AMPK activation by the calcium/calmodulin-dependent protein kinase kinase-beta.
283 utative progenitor markers [doublecortin and calcium/calmodulin-dependent protein kinase-like 1 (Dcam
285 ibroblasts that shares 80% homology to a rat calcium/calmodulin-dependent protein kinase phosphatase
286 ylated site (Ser16) of PLB (p16-PLB) and the calcium/calmodulin-dependent protein kinase-phosphorylat
288 ylation of CREB, including protein kinase A, calcium/calmodulin-dependent protein kinase, protein kin
289 alpha, was markedly increased by Cn, but not calcium/calmodulin-dependent protein kinase, providing o
291 lase (GLO)-1, glutathione reductase (GSR)-1, calcium/calmodulin-dependent protein kinase type (CAMK)-
292 m exchanger, phospholamban, calcineurin, and calcium/calmodulin-dependent protein kinase type II (CaM
294 ed with an antibody directed against CaMKII (calcium/calmodulin-dependent protein kinase type II, alp
295 class of IC neurons that strongly expressed calcium/calmodulin-dependent protein kinase type II, alp
300 -inhibition approaches, we demonstrated that calcium/calmodulin-dependent protein kinase type IV, whi