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

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

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

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

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

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

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

14 actors promoted the activation of the Ca(2+)/calmodulin-dependent kinase II (CaMKII) and the phosphor

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

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

17 diseases, we have targeted the host calcium/calmodulin-dependent kinase II (CaMKII) for inhibition.

18 Calcium-calmodulin-dependent kinase II (CaMKII) has an important

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

20 Calmodulin-dependent kinase II (CaMKII) has long been kn

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

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 Calcium/calmodulin-dependent kinase II (CaMKII) plays a key role

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

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

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

29 )JPH2 overexpressing myocytes caused calcium/calmodulin-dependent kinase II activation and altered my

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

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

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

33 the extrasynaptic cell surface, in a calcium/calmodulin-dependent kinase II and protein kinase G-depe

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

35 arbors a phosphorylation site for the Ca(2+)/calmodulin-dependent kinase II at serine 315.

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

37 ng protein phosphorylated at Ser133, calcium-calmodulin-dependent kinase II phosphorylated at Thr286,

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

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

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

41 CaMKII (Ca(2+)/calmodulin-dependent kinase II) enhances I(Na,L) in resp

42 Unlike the CaMKII (Ca(2+)/calmodulin-dependent kinase II)-dependent JNK2 action in

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

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

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

46 lele with a cre mouse line driven by calcium/calmodulin-dependent kinase IIalpha promoter also elimin

47 Polymorphisms in the region of the calmodulin-dependent kinase isoform D (CaMK1D) gene are

48 Calcium/calmodulin-dependent kinase kinase (CaMKK) and AMP-activ

49 Here we find calcium/calmodulin-dependent kinase kinase (CaMKK2) to be highly

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

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

52 he Aurora kinases, Polo kinases, and calcium/calmodulin-dependent kinase kinases.

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

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

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

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

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

58 ctivated phosphatase calcineurin in a Ca(2+)/calmodulin-dependent manner, preventing beta-arrestin re

59 denylyl cyclase synthesizes cAMP in a Ca(2+)/calmodulin-dependent manner, serving as a coincidence de

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

61 sponse to hypoxia-induced cell swelling in a calmodulin-dependent manner.

62 ke Legionella effector, SidJ, in an ATP- and calmodulin-dependent manner.

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

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

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

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

67 del predicted new crosstalks between calcium/calmodulin-dependent pathways and upstream signaling of

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

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

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

71 The Ca(2+)/calmodulin-dependent phosphatase calcineurin is a key re

72 The ubiquitous Ca(2+) /calmodulin-dependent phosphatase calcineurin is a key re

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

74 ion by inhibiting the activity of the Ca(2+)/calmodulin-dependent phosphatase calcineurin toward nucl

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

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

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

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

79 Calcium-calmodulin dependent protein kinase II (CaMKII) regulate

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

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

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

83 CaMKII (Ca(2+)-Calmodulin dependent protein kinase) deltaC activation i

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

85 ndent phosphorylation by members of the Ca2+/calmodulin-dependent protein kinase (CaMK) group.

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

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

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

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

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

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

92 ral root development in Populus in a calcium/calmodulin-dependent protein kinase (CCaMK)-dependent ma

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

94 tion by the liver kinase B1 or by the Ca(2+)/calmodulin-dependent protein kinase 2 (CaMKK2).

95 am kinase liver kinase B1 (LKB1) and calcium/calmodulin-dependent protein kinase 2 (CaMKK2).

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

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

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

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

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

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

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

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

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

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

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

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

108 Ca(2+)/calmodulin-dependent protein kinase II (CAMK2) is a key

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

110 Ca2+/calmodulin-dependent protein kinase II (CaMKII) accounts

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

112 Ca(2+) oscillations and consequent Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activati

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

114 Calcium/calmodulin-dependent protein kinase II (CaMKII) and calc

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

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 tein kinase A (PKA) at Ser(16) and by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) at Thr(1

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

122 The many variants of human Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) differ i

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

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

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

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

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

128 The calcium calmodulin-dependent protein kinase II (CaMKII) is a dod

129 Calcium/calmodulin-dependent protein kinase II (CaMKII) is a mul

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

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

132 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is an ol

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 Ca(2+)/calmodulin-dependent protein kinase II (CaMKII), an adre

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

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

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

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

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

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

159 In addition, calcium/calmodulin-dependent protein kinase II (CaMKII), protein

160 d for activation of a MAPK cascade utilizing calmodulin-dependent protein kinase II (CaMKII), Raf, an

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

162 ts depends on their interaction with calcium/calmodulin-dependent protein kinase II (CaMKII), which i

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

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

165 reased intracellular Ca(2+) through a Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-mediated

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

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

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

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

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 to principal or local-circuit cells, calcium/calmodulin-dependent protein kinase II (CAMKIIalpha) imm

178 Activation of the Ca(2+)/calmodulin-dependent protein kinase II (CaMKIIdelta) is

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

180 , PKA regulatory subunit type II, and Ca(2+)/calmodulin-dependent protein kinase II across cardiomyoc

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

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

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

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

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

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

187 t mice devoid of IFNAR1 signaling in calcium/calmodulin-dependent protein kinase II alpha (CaMKIIalph

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

189 ) currents were dependent in part on calcium/calmodulin-dependent protein kinase II and IP(3) pathway

190 mic the calmodulin binding domain of calcium/calmodulin-dependent protein kinase II and its 1-amino-a

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

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

193 It is also acknowledged that calcium/calmodulin-dependent protein kinase II and protein kinas

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

195 , cardiac stress protein biomarkers, such as calmodulin-dependent protein kinase II and the transcrip

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

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

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

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

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

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

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

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

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

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

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

207 tracellular signal-regulated kinase, calcium/calmodulin-dependent protein kinase II gamma, and CREB2,

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

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

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

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

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

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

219 xygen species signaling, and oxidized Ca(2+)/calmodulin-dependent protein kinase II signaling were in

220 mellitus and counteracts pathological Ca(2+)/calmodulin-dependent protein kinase II signaling.

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

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

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

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

225 Increased CaMKII (Ca/calmodulin-dependent protein kinase II) activity has bee

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

227 1 pathway, phospho-alphaCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hip

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

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

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

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

232 kinases, including protein kinase C, Ca(2+)/calmodulin-dependent protein kinase II, and extracellula

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

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

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

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

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

238 l fragment of HDAC4 but also promoted Ca(2+)/calmodulin-dependent protein kinase II-mediated phosphor

239 ent of HDAC4, which was attenuated by Ca(2+)/calmodulin-dependent protein kinase II-mediated phosphor

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

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

242 lease channel-ryanodine receptor-2, PKA, and calmodulin-dependent protein kinase II-were activated in

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

244 by calcium influx and activation of calcium/calmodulin-dependent protein kinase II.

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

246 ning of GABA(A) receptor synapses via Ca(2+)/calmodulin-dependent protein kinase II.

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

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

249 control (dependent largely on CaMKII [Ca(2+)/calmodulin-dependent protein kinase II] activity).

250 rotein (alphakap) encoded within the calcium/calmodulin-dependent protein kinase IIalpha (CAMK2A) gen

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

252 ization of beta-actin mRNA but not of Ca(2+)/calmodulin-dependent protein kinase IIalpha (CaMKIIalpha

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

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

255 essing Cre-recombinase driven by the calcium/calmodulin-dependent protein kinase IIalpha promoter.

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

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

258 Because SN inhibits CaMKIIdelta (Ca(2+)/calmodulin-dependent protein kinase IIdelta) activity, w

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

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

261 Calcium/calmodulin-dependent protein kinase IV (CaMKIV) activati

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

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

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

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

266 Calcium/Calmodulin-dependent Protein Kinase Kinase 2 (CAMKK2) ac

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

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

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

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

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

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

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

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

275 The calcium-calmodulin-dependent protein kinase kinase-2 (CaMKK2) is

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

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

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

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

280 Calcium/calmodulin-dependent protein kinase type II delta (CaMKI

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

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

283 gh saturated fat diet activates CaMK (Ca(2+)/calmodulin-dependent protein kinase) in the heart, which

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

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

286 CaMKII (Ca(2+)/calmodulin-dependent protein kinase-II) protein-expressi

287 ms like those associated with CaMKII (Ca(2+)/calmodulin-dependent protein kinase-II), NLRP3 (NACHT, L

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

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

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

291 cations, MEF2D is an effector for the Ca(2+)/calmodulin-dependent protein phosphatase calcineurin (Ca

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

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

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

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

296 including transcripts encoding Cask (calcium/calmodulin-dependent serine protein kinase) and Madd (MA

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

298 d protein from yeast to humans, is a calcium-calmodulin-dependent serine-threonine-specific phosphata

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