ライフサイエンスコーパス: calmodulin-dependent

1 Moreover, the NCAM antibody triggers calmodulin-dependent activation of nitric oxide synthase

2 ntracellular calcium up-regulated ERK1/2 via calmodulin-dependent activation of PI3K.

3 catalyzed by eEF2 kinase (eEF2K), a calcium/calmodulin-dependent alpha-kinase.

4 he costameric protein plasma membrane Ca(2+)/calmodulin-dependent ATPase (PMCA), and that its deletio

5 er, they were associated with reduced Ca(2+)/calmodulin-dependent auto-phosphorylation of eEF2 kinase

6 ave characterized two common forms of Ca(2+)/calmodulin-dependent endocytosis, i.e., slow clathrin-de

7 zures in zydeco mutants, suggesting a Ca(2+)/calmodulin-dependent glial signaling pathway underlies g

8 in cytosolic [Ca(2+)] and subsequent Ca(2+)/calmodulin-dependent inactivation of CaV1.3 channels.

9 The activation of the dodecameric Ca(2+)/calmodulin dependent kinase II (CaMKII) holoenzyme is cr

10 sible for dBest1 activation is likely Ca(2+)/calmodulin dependent kinase II (CaMKII), because specifi

11 ymbioses using three candidate genes: Ca(2+)/Calmodulin-Dependent Kinase (CCaMK), which plays a centr

12 autophosphorylation (activation) of calcium/calmodulin-dependent kinase 2 (CaMKII) and also that inh

13 The Ca(2+) and redox-sensing enzyme Ca(2+) /calmodulin-dependent kinase 2 (CaMKII) is a crucial and

14 mmon signaling pathway including the calcium/calmodulin-dependent kinase Doesn't Make Infection3 (DMI

15 They show that Ca(2+)/calmodulin-dependent kinase I (CaMKI) regulates thermal

16 We used alpha subunit of the calcium/calmodulin-dependent kinase II (alphaCaMKII) mutant mice

17 dynamin-related protein 1 (Drp1), by Ca(2+)/calmodulin-dependent kinase II (CaMKII) at a serine 616

18 The calcium/calmodulin-dependent kinase II (CaMKII) blocker, KN93, s

19 The multifunctional Ca(2+)/calmodulin-dependent kinase II (CaMKII) has been identif

20 onses were decreased by inhibition of Ca(2+)/calmodulin-dependent kinase II (CaMKII) in myocytes from

21 n resulted in increased expression of Ca(2+)/calmodulin-dependent kinase II (CaMKII) in the forebrain

22 Ca(2+)/calmodulin-dependent Kinase II (CaMKII) is a calcium-reg

23 glucagon-induced calcium signaling, calcium/calmodulin-dependent kinase II (CaMKII) phosphorylates O

24 rum show that synapsin is a target of Ca(2+) calmodulin-dependent kinase II (CaMKII) phosphorylation

25 a putative regulator of calmodulin and Ca2+/calmodulin-dependent kinase II (CaMKII) signaling, exclu

26 age-gated calcium channel EGL-19, and the Ca/calmodulin-dependent kinase II (CaMKII) UNC-43.

27 lar LTD depends on the activation of calcium/calmodulin-dependent kinase II (CaMKII).

28 lasmic reticulum Ca(2+) overload and calcium/calmodulin-dependent kinase II activation.

29 NK1 in vitro Inhibiting PKC, JNK, or calcium/calmodulin-dependent kinase II activity prevented the ef

30 y-dependent phosphorylation event on calcium-calmodulin-dependent kinase II alpha (CaMKIIalpha) at se

31 horylation directly through JNK1 and calcium/calmodulin-dependent kinase II and also by inducing expr

32 pulations suggest the involvement of calcium-calmodulin-dependent kinase II and calcium-activated pot

33 ed RyRs have a distinct modulation by Ca(2+)/calmodulin-dependent kinase II and reactive oxygen speci

34 Colocalization of Ca(2+)/calmodulin-dependent kinase II and RyR was not detectabl

35 of coupled RyRs was abolished by the Ca(2+)/calmodulin-dependent kinase II blockers autocamtide-2-re

36 a substrate for protein kinase D and Ca(2+)/calmodulin-dependent kinase II in vitro and identified S

37 m signaling, autoinhibition is reinforced by calmodulin-dependent kinase II phosphorylation of serine

38 FIP2 expression also increases alpha-calcium/calmodulin-dependent kinase II protein expression, and t

39 ts Nav1.5 and its regulatory protein calcium/calmodulin-dependent kinase II to the intercalated disc.

40 ude local synthesis of APP and alpha-calcium/calmodulin-dependent kinase II, a kinase that can phosph

41 e for ankyrin-dependent targeting of calcium/calmodulin-dependent kinase II-delta; however, betaIV-sp

42 y stimulation as a known activator of Ca(2+)/calmodulin-dependent kinase II.

43 nt and PKA-independent activation of calcium/calmodulin-dependent kinase II.

44 Ca(2+)/calmodulin-dependent kinase kinase beta (CaMKKbeta) emer

45 utophagy via a pathway that included calcium/calmodulin-dependent kinase kinase beta (CaMKKbeta), AMP

46 the cytoplasm, thereby activating a calcium/calmodulin-dependent kinase kinase-beta and 5' adenosine

47 ns of the excitatory neuron-specific Ca(2+) /calmodulin-dependent kinase subunit alpha (CaMKIIalpha)

48 ongation factor 2 kinase (eEF2K) is a Ca(2+)/calmodulin-dependent kinase that regulates translation e

49 Here we assessed the role of calcium/calmodulin-dependent kinase type II (CaMKII), in particu

50 ese cells, and in cells where calmodulin and calmodulin-dependent kinase were blocked pharmacological

51 n of antiapoptotic protein (c-IAP-2) through calmodulin-dependent kinase-II activation.

52 a member of the Arabidopsis thaliana Ca(2+)/calmodulin-dependent kinase-related kinase family.

53 rborization through interactions with Ca(2+)/calmodulin-dependent kinases (CaMKs) in rat hippocampal

54 he absence of Ca(2+) to activate CaMKII in a calmodulin-dependent manner.

55 pendent on the relative activities of Ca(2+)-calmodulin-dependent myosin light chain kinase (MLCK) an

56 endent on the relative activities of Ca(2+) /calmodulin-dependent myosin light chain kinase (MLCK) an

57 Ca(2+)/calmodulin-dependent myosin light chain kinase (MLCK) ph

58 ght chain (RLC) is phosphorylated by Ca(2+) /calmodulin-dependent myosin light chain kinase and depho

59 ends on the respective activities of Ca(2+) /calmodulin-dependent myosin light chain kinase and myosi

60 iated by L-type calcium channels and calcium/calmodulin-dependent myosin light-chain kinase.

61 thus enabling a more realistic simulation of calmodulin-dependent pathways.

62 These observations show that calcium- and calmodulin-dependent PDEs (PDE1A and PDE1C) and PDE3A mo

63 Scaffolding the calcium/calmodulin-dependent phosphatase 2B (PP2B, calcineurin)

64 otein phosphatase 2A isoform and the calcium-calmodulin-dependent phosphatase calcineurin (CaN) activ

65 n 1 (RCAN1) controls the activity of calcium/calmodulin-dependent phosphatase calcineurin (CaN), whic

66 esults also provide evidence that the Ca(2+)/calmodulin-dependent phosphatase calcineurin plays a rol

67 k1 signaling negatively regulates the Ca(2+)/calmodulin-dependent phosphatase, calcineurin, to enable

68 BAA signaling by calcineurin, a calcium- and calmodulin-dependent phosphatase, enables homeostatic ba

69 Calcineurin, the Ca(2+)/calmodulin-dependent phosphatase, is normally cytosolic

70 h and is dephosphorylated by the Ca(2+)- and calmodulin-dependent phosphoprotein phosphatase calcineu

71 ranslational control mechanism is the Ca(2+)/calmodulin-dependent phosphorylation of eukaryotic elong

72 glycerol lipase-alpha (DGLalpha) and calcium/calmodulin dependent protein kinase II (CaMKII).

73 er brain regions, using Thy1-Cre and calcium/calmodulin dependent protein kinase II alpha-Cre for abl

74 A protein with similarities to the Ca(2+)/ calmodulin dependent protein kinase II_association domai

75 The Ca(2+)-calmodulin dependent protein kinase kinase-2 (CaMKK2) is

76 Calcium/calmodulin-dependent protein kinase (CaMK) activation in

77 Psi Here, we characterize a role for calcium/calmodulin-dependent protein kinase (CaMK) I in the regu

78 f D-myo-inositol 1,4,5-trisphosphate/Ca(2+) /calmodulin-dependent protein kinase (CaMK) I. gamma-Amin

79 II could also induce the phosphorylation of calmodulin-dependent protein kinase (CaMK) II and cAMP r

80 ostretrieval bilateral inhibition of calcium/calmodulin-dependent protein kinase (CaMK) II in dorsal

81 +)-dependent binding of S100B to the calcium/calmodulin-dependent protein kinase (CaMK)-type domain o

82 2 model of Huntington disease and the Ca(2+)/calmodulin-dependent protein kinase (CaMK)/p25 double-tr

83 wn that the cytoplasmically oriented calcium/calmodulin-dependent protein kinase (CaMK)Ialpha regulat

84 gnaling in the inner ear is the type II Ca2+/calmodulin-dependent protein kinase (CaMK-II), which is

85 ore than 20 years, we have known that Ca(2+)/calmodulin-dependent protein kinase (CaMKII) activation

86 and the ensuing activation of the Ca(2+) and calmodulin-dependent protein kinase (CaMKII) are require

87 Mice with Ca(2+) -calmodulin-dependent protein kinase (CaMKII) constitutiv

88 lation of RyR2 phosphorylation at the Ca(2+)/calmodulin-dependent protein kinase (CaMKII) site (S2814

89 DLG1 can be phosphorylated by Ca(2+)/calmodulin-dependent protein kinase (CaMKII), resulting

90 prevent the arrhythmias induced by a Ca(2+) -calmodulin-dependent protein kinase (CaMKII)-dependent l

91 Calcium and Ca(2+)/calmodulin-dependent protein kinase (CCaMK) plays a crit

92 crease its activity in BTICs, whereas Ca(2+)-calmodulin-dependent protein kinase 2 (CAMK2) inhibited

93 hanistically, CaMKK2 signals through Ca(2+) /calmodulin-dependent protein kinase 4 (CaMKIV) to contro

94 Calcium/calmodulin-dependent protein kinase 4 (gene and transcri

95 d dysregulation of Na and Ca handling and Ca/calmodulin-dependent protein kinase and are especially p

96 ined increase in cytosolic Ca(2+), activated calmodulin-dependent protein kinase and the calpain-casp

97 cannabinoid type 1 (CB1) receptor and Ca(2+)/calmodulin-dependent protein kinase beta, activates AMP-

98 Here, we show that Ca2+/calmodulin-dependent protein kinase gamma (CaMKIIgamma)

99 plex dephosphorylates and inactivates Ca2(+)/calmodulin-dependent protein kinase I (CaMKI), an upstre

100 Mechanistically, calmodulin-dependent protein kinase I phosphorylates a R

101 oA activity in the cell body through calcium/calmodulin-dependent protein kinase I.

102 is critically regulated by the alpha-calcium/calmodulin-dependent protein kinase II (alpha-CaMKII), a

103 The alpha isoform of the calcium/calmodulin-dependent protein kinase II (alphaCaMKII) has

104 The alpha-Ca(2+)/calmodulin-dependent protein kinase II (alphaCaMKII) is

105 Since alpha calmodulin-dependent protein kinase II (alphaCaMKII), a

106 sion of glutamate receptor 2 and beta Ca(2+)/calmodulin-dependent protein kinase II (betaCaMKII).

107 Calcium/calmodulin-dependent protein kinase II (CAMK2) is one of

108 e Cl(-) currents can be attributed to Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activati

109 stically, this effect was mediated by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activati

110 tate (NMDA) receptor activation, and Calcium/calmodulin-dependent protein kinase II (CaMKII) activati

111 tamine exposure transiently increases Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) alpha ex

112 y (SOCE) and sequential activation of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) and Ca(2

113 reduced activation of PLCgamma-alpha-calcium/calmodulin-dependent protein kinase II (CaMKII) and PI3K

114 We show that phosphorylation by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) and Polo

115 In hypertrophy, Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) and prot

116 phorylated at serine 409 (Ser-409) by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) and prot

117 hibitory peptide (mAIP) selective for Ca2+ / calmodulin-dependent protein kinase II (CaMKII) and U012

118 cription factor DeltaFosB and protein kinase calmodulin-dependent protein kinase II (CaMKII) are co-r

119 The Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) assemble

120 Calcium/calmodulin-dependent protein kinase II (CaMKII) binds to

121 ulation; (5) inhibiting either PKA or Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) during b

122 imulation; (5) inhibiting either PKA or Ca2+/calmodulin-dependent protein kinase II (CaMKII) during b

123 lum (SR) Ca(2+) release that involves Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) effects

124 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) forms a

125 Calcium-calmodulin-dependent protein kinase II (CaMKII) has been

126 The Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) has rece

127 Ca(2+)-calmodulin-dependent protein kinase II (CaMKII) hyperact

128 ctly associates with and targets the calcium/calmodulin-dependent protein kinase II (CaMKII) in pancr

129 iew, the functions of multifunctional Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) in VSM p

130 The extent of calcium/calmodulin-dependent protein kinase II (CaMKII) inactiva

131 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is a cen

132 Calcium/calmodulin-dependent protein kinase II (CaMKII) is a syn

133 e heart; however, the multifunctional Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is also

134 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is an en

135 Calcium/calmodulin-dependent protein kinase II (CaMKII) is essen

136 Here we show that the activity of calcium/calmodulin-dependent protein kinase II (CaMKII) is incre

137 w that Ca(2+)-dependent activation of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is requi

138 Considerable evidence suggests that calcium/calmodulin-dependent protein kinase II (CaMKII) overacti

139 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) oxidatio

140 nhanced [(3) H]ryanodine binding and Ca(2+) /calmodulin-dependent protein kinase II (CaMKII) phosphor

141 Calcium/calmodulin-dependent protein kinase II (CaMKII) plays a

142 Calcium/calmodulin-dependent protein kinase II (CaMKII) plays a

143 Ca(2+)/Calmodulin-dependent protein kinase II (CaMKII) signalin

144 nel activity reduced EGF receptor (EGFR) and calmodulin-dependent protein kinase II (CAMKII) signalin

145 is downstream of Dalpha7 nAChRs and Calcium/calmodulin-dependent protein kinase II (CaMKII) signalin

146 treated wild-type C57BL/6 mice with calcium/calmodulin-dependent protein kinase II (CaMKII) specific

147 Here, we show that activated Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) strongly

148 Localization of the Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) to dendr

149 esulted in compromised signaling from Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) to myosi

150 which in turn requires binding of the Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) to the N

151 protein GW182 increases expression of a Ca2+/calmodulin-dependent protein kinase II (CaMKII) translat

152 In contrast, when the calcium/calmodulin-dependent protein kinase II (CaMKII) was bloc

153 In contrast, when the calcium-calmodulin-dependent protein kinase II (CaMKII) was bloc

154 nificantly increased the activity of calcium/calmodulin-dependent protein kinase II (CaMKII) while re

155 ought to determine how activation of calcium/calmodulin-dependent protein kinase II (CaMKII), a centr

156 CaMK2N2 are endogenous inhibitors of calcium/calmodulin-dependent protein kinase II (CaMKII), a key s

157 reduces FRET between the NMDARcd and calcium/calmodulin-dependent protein kinase II (CaMKII), a proce

158 following: 1) that autophosphorylated Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), an impo

159 triggers the exchange of subunits in Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), an olig

160 embranes, synGAP is phosphorylated by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), another

161 ono pentanoic acid; the inhibitor of calcium/calmodulin-dependent protein kinase II (CaMKII), autocam

162 vented by pharmacological blockade of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), it was

163 tream effector of WNT/Ca(2+) pathway, Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), led to

164 athway is a kinase cascade involving calcium/calmodulin-dependent protein kinase II (CaMKII), p38alph

165 tors of transient spine expansion, including calmodulin-dependent protein kinase II (CaMKII), RhoA, a

166 scular smooth muscle (VSM) expresses calcium/calmodulin-dependent protein kinase II (CaMKII)-delta an

167 ators of myocardial excitability, and Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-dependen

168 lism regulates oocyte cell death via calcium/calmodulin-dependent protein kinase II (CaMKII)-mediated

169 Although many studies have focused on Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-mediated

170 he hypotheses that (1) inhibition of Ca(2+) /calmodulin-dependent protein kinase II (CAMKII)-mediated

171 o the model reveal that inclusion of Ca(2+) /calmodulin-dependent protein kinase II (CAMKII)-mediated

172 ryanodine receptors or RyR2s) and the Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

173 lux (nSOC) and continuous activity of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

174 the caspase-2 prodomain by activated Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

175 tion of the calcium-sensitive kinase calcium-calmodulin-dependent protein kinase II (CaMKII).

176 cium flux triggered the activation of Ca(2+)-calmodulin-dependent protein kinase II (CaMKII).

177 y NMDAR downstream signaling protein calcium/calmodulin-dependent protein kinase II (CaMKII).

178 equired cell-autonomous activation of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

179 NMDA receptor-dependent activation of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

180 est was mediated by the activation of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

181 tor DeltaFosB and the brain-enriched calcium/calmodulin-dependent protein kinase II (CaMKIIalpha) are

182 Oxidized Ca(2+)/calmodulin-dependent protein kinase II (ox-CaMKII) was s

183 ites by protein kinase A (Ser-7) and calcium-calmodulin-dependent protein kinase II (Ser-13) and at m

184 Moreover, Carabin reduced Ca(2+)/calmodulin-dependent protein kinase II activation and pr

185 id) receptor activation, calcium and calcium/calmodulin-dependent protein kinase II activity, but not

186 increase in oxidation-dependent calcium and calmodulin-dependent protein kinase II activity, which c

187 -d-aspartate receptor activation and calcium/calmodulin-dependent protein kinase II activity.

188 Ca(2+)/calmodulin-dependent protein kinase II alpha (CaMKIIalph

189 Alcohol-sensitive proteins included calcium/calmodulin-dependent protein kinase II alpha (CaMKIIalph

190 ling molecules, calcineurin, Ras, and Ca(2+)/calmodulin-dependent protein kinase II and implicates Ca

191 itive deficits via altered levels of calcium/calmodulin-dependent protein kinase II and N-methyl-D-as

192 ociated with reduced levels of total calcium/calmodulin-dependent protein kinase II and N-methyl-D-as

193 lated to higher activation of nuclear Ca(2+)/calmodulin-dependent protein kinase II and nuclear expor

194 o be independent of their effects on calcium/calmodulin-dependent protein kinase II and PKA, respecti

195 rrhythmic manifestations, related to Ca(2+) /calmodulin-dependent protein kinase II and ryanodine rec

196 es and Thr-287 autophosphorylation of Ca(2+)/calmodulin-dependent protein kinase II beta (CaMKIIbeta)

197 However, double knockdown of pygo and Ca2+/calmodulin-dependent protein kinase II caused additional

198 The calcium/calmodulin-dependent protein kinase II delta (CAMK2D), w

199 nt and function, including Titin and calcium/calmodulin-dependent protein kinase II delta (Camk2d).

200 he mechanical effects of the kinases calcium/calmodulin-dependent protein kinase II delta (CaMKIIdelt

201 Ca(2+)/calmodulin-dependent protein kinase II delta (CaMKIIdelt

202 myocytes from arrhythmia-susceptible calcium calmodulin-dependent protein kinase II delta C (CaMKIIde

203 The multifunctional Ca(2+)/calmodulin-dependent protein kinase II delta-isoform (Ca

204 the LTP kinase dependency from PKA to Ca2(+)/calmodulin-dependent protein kinase II during synapse ma

205 Here, we show that calcium/calmodulin-dependent protein kinase II gamma (CAMK2gamma

206 Here, Ca(2+)/calmodulin-dependent protein kinase II gamma (CAMKIIgamm

207 Calcium/calmodulin-dependent protein kinase II gamma knockout mi

208 A null mutation of the Drosophila calcium/calmodulin-dependent protein kinase II gene (CaMKII) was

209 ion and subsequent activation of calcium and calmodulin-dependent protein kinase II has a causal role

210 eam signaling protein, PKC-alpha, and Ca(2+)/calmodulin-dependent protein kinase II in endothelial ce

211 2B, also referred to as Pyk2) and of calcium/calmodulin-dependent protein kinase II in wild-type brai

212 rolled firing rate adaptation whereas Ca(2+)/Calmodulin-dependent protein kinase II induced a delayed

213 ia inhibition of ryanodine receptors, Ca(2+)/calmodulin-dependent protein kinase II inhibition, or by

214 Development of organ-specific calcium and calmodulin-dependent protein kinase II inhibitors may re

215 ignal-regulated kinase activators and Ca(2+)/calmodulin-dependent protein kinase II inhibitors showed

216 Ca(2+)/calmodulin-dependent protein kinase II inhibitors suppre

217 rom transgenic mice expressing a calcium and calmodulin-dependent protein kinase II inhibitory peptid

218 Calcium/calmodulin-dependent protein kinase II is a prototypical

219 Ca(2+)/calmodulin-dependent protein kinase II is a synapse-enri

220 es including JNK, GSK3alpha/beta, and Ca(2+)/calmodulin-dependent protein kinase II is increased sign

221 p38 and Ca(2+)/calmodulin-dependent protein kinase II pathways were fou

222 on synapsin I, two of which are known Ca(2+)/calmodulin-dependent protein kinase II phosphorylation s

223 ignaling kinases protein kinase C and Ca(2+)/Calmodulin-dependent protein kinase II to AngII-mediated

224 In addition, phosphorylation of calcium/calmodulin-dependent protein kinase II was increased in

225 as phosphorylation of substrates for calcium/calmodulin-dependent protein kinase II was unchanged.

226 Pharmacologic inhibition of calcium and calmodulin-dependent protein kinase II with 2.5 microM o

227 stabilization of postsynaptic CaMKII (Ca(2+)/calmodulin-dependent protein kinase II) at inhibitory sy

228 1 pathway, phospho-alphaCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hip

229 mitochondrial recruitment of CaMKII (Ca(2+)/calmodulin-dependent protein kinase II), which decreases

230 phosphorylation at Ser16 and CaMKII (Ca(2+)/calmodulin-dependent protein kinase II)-dependent phosph

231 Inhibitors of calcium/calmodulin-dependent protein kinase II, a mitochondrial

232 ng protein, but not the activation of Ca(2+)/calmodulin-dependent protein kinase II, Akt or mitogen-a

233 mitogen-activated protein kinase, and Ca(2+)/calmodulin-dependent protein kinase II, and activators o

234 ellular protein mediators Homer1b/c, calcium/calmodulin-dependent protein kinase II, and the Alzheime

235 c activation of protein kinase A and calcium/calmodulin-dependent protein kinase II, as well as synap

236 a(2+) must first mobilize actin-bound Ca(2+)/calmodulin-dependent protein kinase II, freeing it for s

237 glutamate-mediated Ca(2+) signaling (Ca(2+)/calmodulin-dependent protein kinase II, PPP3CA, and VISL

238 Calcium and calmodulin-dependent protein kinase II, through phosphor

239 turn, led to the phosphorylation of calcium/calmodulin-dependent protein kinase II, which promoted b

240 2 expression can be upregulated in a calcium/calmodulin-dependent protein kinase II-dependent manner

241 at have the ryanodine receptor 2 calcium and calmodulin-dependent protein kinase II-dependent phospho

242 Genetic inhibition of Ca(2+)/calmodulin-dependent protein kinase II-mediated RyR2-S28

243 used 1 Hz optogenetic stimulation of calcium/calmodulin-dependent protein kinase II-positive principa

244 dent on calcium influx and linked to calcium/calmodulin-dependent protein kinase II.

245 nt downstream enzymes calcineurin and Ca(2+)-calmodulin-dependent protein kinase II.

246 sarcoplasmic reticulum and activated Ca(2+)/calmodulin-dependent protein kinase II.

247 FTO interacts with three isoforms of calcium/calmodulin-dependent protein kinase II: alpha, beta and

248 AT-C24 DAT) and thereby contained the Ca(2+)-calmodulin-dependent protein kinase IIalpha (CaMKIIalpha

249 a synapse-enriched protein kinase, Ca(2)(+)/calmodulin-dependent protein kinase IIalpha (CaMKIIalpha

250 is study, we investigated the role of Ca(2+)/calmodulin-dependent protein kinase IIalpha (CaMKIIalpha

251 Furthermore, calcium/calmodulin-dependent protein kinase IIalpha (CaMKIIalpha

252 ceptors, p600 associates with the calmodulin.calmodulin-dependent protein kinase IIalpha complex.

253 d cardiomyocyte apoptosis, fibrosis, calcium/calmodulin-dependent protein kinase IIdelta phosphorylat

254 as a direct inhibitor of CaMKIIdelta (Ca(2+)/calmodulin-dependent protein kinase IIdelta) activity, a

255 n vascular smooth muscle (VSM) cells, Ca(2+)/calmodulin-dependent protein kinase IIdelta2 (CaMKIIdelt

256 Here, we present evidence that the calcium/calmodulin-dependent protein kinase IV (CaMK4) is increa

257 ive oxygen species (ROS) production, calcium/calmodulin-dependent protein kinase IV (CaMKIV) activati

258 describe a novel mechanism in which calcium/calmodulin-dependent protein kinase IV (CaMKIV), through

259 Calcium/calmodulin-dependent protein kinase IV is involved in th

260 KN93, a small-molecule inhibitor of calcium/calmodulin-dependent protein kinase IV, targeted to CD4(

261 is regulated by the classical nuclear Ca(2+)/calmodulin-dependent protein kinase IV-CREB/CREB-binding

262 re, we report that the expression of Ca(2+) /calmodulin-dependent protein kinase kinase 2 (CaMKK2) is

263 ally reduced by the application of a calcium/calmodulin-dependent protein kinase kinase 2 inhibitor (

264 istic target of rapamycin complex 1, calcium/calmodulin-dependent protein kinase kinase 2, and protei

265 e expression of constitutively active Ca(2+)/calmodulin-dependent protein kinase kinase alpha (caCaMK

266 AMPK activation by aa is mediated by Ca(2+)/calmodulin-dependent protein kinase kinase beta (CaMKKbe

267 PK kinases liver kinase B1 (LKB1) and Ca(2+)/calmodulin-dependent protein kinase kinase beta (CaMKKbe

268 Activation of calmodulin-dependent protein kinase kinase beta was requ

269 Inhibition of Ca(2+)/calmodulin-dependent protein kinase kinase beta, a known

270 events were blocked by inhibition of Ca(2+)/calmodulin-dependent protein kinase kinase beta, an upst

271 n was significantly impaired by knockdown of calmodulin-dependent protein kinase kinase beta.

272 altered calcium signaling, transduced by the calmodulin-dependent protein kinase kinase cascade, medi

273 Calcium/calmodulin-dependent protein kinase regulates the PINK1/

274 alcineurin, Akt/protein kinase B, and Ca(2+)/calmodulin-dependent protein kinase signaling pathways i

275 O)-1, glutathione reductase (GSR)-1, calcium/calmodulin-dependent protein kinase type (CAMK)-IV, cAMP

276 which were abolished by inhibition of Ca(2+)/calmodulin-dependent protein kinase type 2.

277 ger, phospholamban, calcineurin, and calcium/calmodulin-dependent protein kinase type II (CaMKII) wer

278 -bisphosphate binding, protein kinase C- and calmodulin-dependent protein kinase type II phosphorylat

279 to remodeling pathways (e.g., Akt and Ca(2+)/calmodulin-dependent protein kinase type II) and develop

280 Calcium/calmodulin-dependent protein kinase type IV (CaMKIV) is

281 This process involves calcium/calmodulin-dependent protein kinase, matrix metalloprote

282 ngation factor 2 kinase (eEF2K), an atypical calmodulin-dependent protein kinase, phosphorylates and

283 Calmodulin expression (60%), Ca(2+)/calmodulin-dependent protein kinase-II (CaMKII) autophos

284 Ca(2+)/calmodulin-dependent protein kinase-II (CaMKII) phosphor

285 y AMPA-type glutamate receptors and required calmodulin-dependent protein kinase-mediated phosphoryla

286 uptake; one of them encoded CaMK4, a calcium/calmodulin-dependent protein kinase.

287 r new protein synthesis and required calcium/calmodulin-dependent protein kinases and the nuclear cal

288 We identified a role for calcium/calmodulin-dependent protein kinases II gamma isoform (C

289 he mechanistic role of the family of calcium/calmodulin-dependent protein kinases in mediating these

290 Multifunctional Ca(2+)/calmodulin-dependent protein kinases, including CaMKII,

291 We find that Iav activates the Ca(2+)/calmodulin-dependent protein phosphatase calcineurin, wh

292 pines, (3) required activation of the Ca(2+)/calmodulin-dependent protein-kinase II, (4) was restrict

293 or somatostatin-positive interneurons and of calmodulin-dependent, protein kinase-positive, principal

294 Calcineurin (CN) is a conserved Ca(2+)/calmodulin-dependent ser/thr phosphatase and the target

295 ongation factor 2 kinase (eEF2K), a Ca(2)(+)/calmodulin dependent serine/threonine kinase that phosph

296 h GluN2B and with the adaptor protein Ca(2+)/calmodulin-dependent serine protein kinase and kinesin K

297 G1 (discs-large homolog 1) and CASK (calcium/calmodulin-dependent serine protein kinase) interact at

298 ; membrane protein, palmitoylated 3; calcium/calmodulin-dependent serine protein kinase; membrane-ass

299 ere we provide evidence that the calcium and calmodulin-dependent serine/threonine protein kinase typ

300 Calcineurin encodes a calcium- and calmodulin-dependent serine/threonine protein phosphatas