ライフサイエンスコーパス: calmodulin-dependent protein kinase

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

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

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

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

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

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

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

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

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

10 by NMDA receptor activation, requires Ca2+ /calmodulin-dependent protein kinase, and is mediated by

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

12 olerance, as did mutants in the gene calcium/calmodulin-dependent protein kinase (caki), encoding the

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

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

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

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

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

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

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

20 2 model of Huntington disease and the Ca(2+)/calmodulin-dependent protein kinase (CaMK)/p25 double-tr

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

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

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

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

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

26 Acute activation of calcium/calmodulin-dependent protein kinase (CaMKII) in permeabi

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

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

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

30 Ca(2+)/calmodulin-dependent protein kinases (CaMKs) are major d

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

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

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

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

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

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

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

38 sphorylation sites in Cx36 and evidence that calmodulin dependent protein kinase II (CaMKII) may pote

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 Whereas increased Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activity

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

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

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

58 Dys-/- had reduced expression of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) and CaMK

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

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

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

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

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

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

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

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

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

68 Ca(2)(+)/calmodulin-dependent protein kinase II (CaMKII) blockers

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

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

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

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

73 activation of the multifunctional Ca(2+) and calmodulin-dependent protein kinase II (CaMKII) favors m

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

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

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

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

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

79 o signal neuronal cells and activate calcium calmodulin-dependent protein kinase II (CaMKII) in neuro

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

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

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

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

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

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

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

87 The multifunctional Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is activ

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

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

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

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

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

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

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

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

96 ated Ca(2+) channels (VGCCs) leads to Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) phosphor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

144 age-gated Na(+) channel (Na(v)1.5) by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII).

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

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

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

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

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

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

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

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

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

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

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

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

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

158 bunit, Rpt6, by the plasticity kinase Ca(2+)/calmodulin-dependent protein kinase II alpha (CaMKIIalph

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

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

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

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

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

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

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

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

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

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

169 it that mediates dephosphorylation of Ca(2+)/calmodulin-dependent protein kinase II and tyrosine hydr

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

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

172 , inhibitors, and a dominant negative Ca(2+)/calmodulin-dependent protein kinase II construct block A

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 2B, also referred to as Pyk2) and of calcium/calmodulin-dependent protein kinase II in wild-type brai

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

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

190 This was abolished by the Ca(2+)/calmodulin-dependent protein kinase II inhibitor KN93, s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 The inhibition of Ca(2+)/calmodulin-dependent protein kinase II with 1-[N,O-bis(5

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

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

208 nd is accompanied by altered CaMKII (calcium/calmodulin-dependent protein kinase II) and flotillin-1

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

210 1 pathway, phospho-alphaCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hip

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

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

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

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

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

216 in cAMP, light-induced activation of Ca(2+) /calmodulin-dependent protein kinase II, and dopamine-ind

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

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

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

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

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

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

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

224 ice using the CaMKIIalpha-Cre (alpha-calcium/calmodulin-dependent protein kinase II-Cre) system to KD

225 2 expression can be upregulated in a calcium/calmodulin-dependent protein kinase II-dependent manner

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

257 se II inhibitor KN93, suggesting that Ca(2+)/calmodulin-dependent protein kinase IIdelta, a target of

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

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

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

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

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

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

264 sponse to membrane depolarization and Ca(2+)/calmodulin-dependent protein kinase IV (CaMKIV) activati

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

266 The calcium activated protein, calcium/calmodulin-dependent protein kinase IV (CaMKIV) phosphor

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

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

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

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

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

272 ersely, the DOR effect was reduced by Ca(2+)/calmodulin-dependent protein kinase kinase (CaMKK) inhib

273 alian target of rapamycin (mTOR) via calcium calmodulin-dependent protein kinase kinase (CaMKK).

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

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

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

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

278 e activation of protein kinase A and calcium/calmodulin-dependent protein kinase kinase 2.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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