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

1 lently label a nonactive site residue in the cAMP-dependent protein kinase.

2 the protein kinases Akt and GSK3beta but not cAMP-dependent protein kinase.

3 rominent and was shown to depend on G(s) and cAMP-dependent protein kinase.

4 ctivation of the proapoptotic protein BAD by cAMP-dependent protein kinase.

5 /Ser(67) inhibitor-1 is a poor substrate for cAMP-dependent protein kinase.

6 ein kinase family members, Akt-1, PDK-1, and cAMP-dependent protein kinase.

7 phosphorylation of alpha-Ser(485/491) by the cAMP-dependent protein kinase.

8 volving G G proteins, adenylate cyclase, and cAMP-dependent protein kinase.

9 and docking (D/D) domain of the cyclic AMP (cAMP)-dependent protein kinase.

10 (i) proteins to control the adenylyl cyclase-cAMP dependent protein kinase A (PKA) pathway to regulat

11 e C (PKC) or cyclic adenosine monophosphate (cAMP)-dependent protein kinase A (PKA) activation.

12 tion between cyclic adenosine monophosphate (cAMP)-dependent protein kinase A (PKA) and A-kinase anch

13 ion of adenosine 3',5'-cyclic monophosphate (cAMP)-dependent protein kinase A (PKA) is sufficient and

14 In this paper, we report that cyclic AMP (cAMP)-dependent protein kinase A (PKA) promotes acinus f

15 uires cyclic adenosine 3', 5'-monophosphate (cAMP)-dependent protein kinase A (PKA) signaling, raisin

16 at Tregs use cyclic adenosine monophosphate (cAMP)-dependent protein kinase A pathway to inhibit HIV-

17 ate cancer cells by activating a cyclic AMP (cAMP)-dependent protein kinase A signaling pathway.

18 d to determine the role of PPT intracellular cAMP-dependent protein kinase A (cAMP-PKA) in the regula

19 Inhibition of cAMP-dependent protein kinase A (cAMP/PKA) by either 5 m

20 racts with the regulatory subunit of type II cAMP-dependent protein kinase A (PKA(RIIalpha)).

21 proteins involved in lipolysis during brief cAMP-dependent protein kinase A (PKA) activation.

22 In addition, cAMP-dependent protein kinase A (PKA) activity and agoni

23 tory function, thereby transiently enhancing cAMP-dependent protein kinase A (PKA) activity.

24 s of two major components of cAMP signaling, cAMP-dependent protein kinase A (PKA) and adenylate cycl

25 ity is known to depend on phosphorylation by cAMP-dependent protein kinase A (PKA) and CFTR-ATPase ac

26 was found to be differentially modulated by cAMP-dependent protein kinase A (PKA) and exchange prote

27 DA D(1) receptor(D(1)R) signaling, including cAMP-dependent protein kinase A (PKA) and extracellular

28 C1 and PDE4 modulate NDE1 phosphorylation by cAMP-dependent protein kinase A (PKA) and identify a nov

29 vates dopamine D2 autoreceptors to stimulate cAMP-dependent protein kinase A (PKA) and protein kinase

30 regulated through Ser-133 phosphorylation by cAMP-dependent protein kinase A (PKA) and related kinase

31 lpha catalytic subunit and comparable global cAMP-dependent protein kinase A (PKA) enzyme activity.

32 Hedgehog (Hh) proteins and cAMP-dependent protein kinase A (PKA) generally play opp

33 regulatory subunit 1-alpha (RIalpha) of the cAMP-dependent protein kinase A (PKA) holoenzyme.

34 factor that integrates signaling through the cAMP-dependent protein kinase A (PKA) in many eukaryotes

35 cAMP-dependent protein kinase A (PKA) is a ubiquitous en

36 cAMP-dependent protein kinase A (PKA) is a ubiquitously

37 cAMP-dependent protein kinase A (PKA) is important in pr

38 The extensively studied cAMP-dependent protein kinase A (PKA) is involved in the

39 The cAMP-dependent protein kinase A (PKA) is the prime examp

40 endent changes in the activity levels of the cAMP-dependent Protein Kinase A (PKA) on the formation o

41 The cAMP and cAMP-dependent protein kinase A (PKA) signaling cascade

42 gnificant role has been ascribed to the cAMP/cAMP-dependent protein kinase A (PKA) signaling pathway

43 ith both receptors: Binding to CXCR4 induces cAMP-dependent protein kinase A (PKA) signaling, which i

44 d humans with defects that lead to increased cAMP-dependent protein kinase A (PKA) signaling.

45 tes I-LTD induction via direct inhibition of cAMP-dependent protein kinase A (PKA) signaling.

46 postsynaptic and required the activation of cAMP-dependent protein kinase A (PKA) signaling.

47 on, localization and regulation of different cAMP-dependent protein kinase A (PKA) subunits account f

48 Activation of presynaptic cAMP-dependent protein kinase A (PKA) triggers presynapt

49 A single molecule of the catalytic domain of cAMP-dependent protein kinase A (PKA) was attached to a

50 phosphorylation was blocked by inhibitors of cAMP-dependent protein kinase A (PKA), an enzyme involve

51 ferentiation requires activation of CREB and cAMP-dependent protein kinase A (PKA), but the role of P

52 We evaluated cAMP-dependent protein kinase A (PKA), phospho-cyclic AM

53 cAMP-dependent protein kinase A (PKA), ubiquitously expr

54 on of Ksp1 is partially activated by the Ras/cAMP-dependent protein kinase A (PKA), which is another

55 omotes nucleotide excision repair (NER) in a cAMP-dependent protein kinase A (PKA)-dependent manner.

56 with cardiac ryanodine receptors (RyR2), and cAMP-dependent protein kinase A (PKA)-dependent phosphor

57 n of Rap1 by cyclic AMP (cAMP) can occur via cAMP-dependent protein kinase A (PKA)-independent and PK

58 was oligomycin-insensitive and contingent on cAMP-dependent protein kinase A (PKA)-induced lipolysis.

59 erization and docking (D/D) domain, RIIa, in cAMP-dependent protein kinase A (PKA).

60 D activity is mediated, at least in part, by cAMP-dependent protein kinase A (PKA).

61 th epsilon protein kinase C (epsilonPKC) and cAMP-dependent protein kinase A (PKA).

62 phores, melanosome transport is regulated by cAMP-dependent protein kinase A (PKA).

63 through a cAMP-signaling pathway, activating cAMP-dependent protein kinase A (PKA).

64 ter release that is selectively regulated by cAMP-dependent protein kinase A (PKA).

65 , a specific isoform of the second messenger cAMP-dependent protein kinase A (PKAalpha) rapidly phosp

66 onical pathway involving both an increase in cAMP-dependent protein kinase A activity and the GLI3R t

67 tion, but inhibition of either calmodulin or cAMP-dependent protein kinase A activity blunted the hyp

68 e heart cell surface and induced Ab-mediated cAMP-dependent protein kinase A activity.

69 based community maps of the kinase domain of cAMP-dependent protein kinase A allow for a molecular ex

70 ing a yeast two-hybrid screen, we identified cAMP-dependent protein kinase A anchoring protein 95 kDa

71 Phosphorylation of RyR2 by cAMP-dependent protein kinase A and by calmodulin-depend

72 T, and dmLT promote human Th17 responses via cAMP-dependent protein kinase A and caspase-1/inflammaso

73 7/gp78-reconstituted system with and without cAMP-dependent protein kinase A and PKC, two liver cytos

74 n of recombinant mouse PDE3A with PKB/Akt or cAMP-dependent protein kinase A catalytic subunits leads

75 ,3-a]quinoxalin-1-one but was insensitive to cAMP-dependent protein kinase A inhibition with H89 and

76 diating the dual effects of PTH, whereas the cAMP-dependent protein kinase A pathway appears to predo

77 7 may contribute to EPO regulation through a cAMP-dependent protein kinase A pathway.

78 rescued by increasing signaling through the cAMP-dependent protein kinase A pathway.

79 The classic cAMP-dependent protein kinase A signaling is involved in

80 h-affinity state and activated the canonical cAMP-dependent protein kinase A signaling pathway in car

81 40 through the activation of MAPK/Erk1/2 and cAMP-dependent protein kinase A signaling, respectively.

82 Reduction in GluR1 phosphorylation at its cAMP-dependent protein kinase A site by the synthetic pe

83 Thus, inhibition of cAMP-dependent protein kinase A was abolished, and stimu

84 cyclase VI and the catalytic subunit of the cAMP-dependent protein kinase A, were predicted as direc

85 increased phosphorylation of Hsp90alpha in a cAMP-dependent protein kinase A-dependent manner, and th

86 tivity and subsequent stimulation of CFTR by cAMP-dependent protein kinase A.

87 1 channels as a result of phosphorylation by cAMP-dependent protein kinase A.

88 levation of intracellular cAMP and activates cAMP-dependent protein kinase A.

89 cAMP-dependent protein kinase A/PKC-mediated phosphoryla

90 The AGC protein kinase family (cAMP-dependent protein kinases A, cGMP-dependent protein

91 and shift in DNA organization act through a cAMP-dependent protein-kinase A-coupled signaling pathwa

92 disrupting hippocampal protein synthesis and cAMP-dependent-protein kinase A after the reactivation o

93 Syt12 is phosphorylated by cAMP-dependent protein kinase-A at serine-97 in an activ

94 ophil apoptosis, as did inhibition of type I cAMP-dependent protein kinases activated downstream of P

95 However, submaximal cAMP-dependent protein kinase activation had less effect

96 of the G(alpha)s G-protein subunit and cAMP-cAMP-dependent protein kinase activation, the nitric oxi

97 governs the responsiveness of inhibitor-1 to cAMP-dependent protein kinase activation.

98 renol-stimulated cAMP production (p = 0.04), cAMP-dependent protein kinase activity (p < 0.0004), pho

99 This result was consistent with attenuated cAMP-dependent protein kinase activity and reduced cyclo

100 stimulation of steroidogenesis by increasing cAMP-dependent protein kinase activity in both primary i

101 These agents were used to monitor endogenous cAMP-dependent protein kinase activity in erythrocyte ly

102 aracterize the compartmentalized location of cAMP-dependent protein kinase activity in mitochondria.

103 ndent protein kinase II activity, but not on cAMP-dependent protein kinase activity or presynaptic me

104 xemplifies two different ways for regulating cAMP-dependent protein kinase activity through non-conse

105 acting AKAP and suggest a mechanism by which cAMP-dependent protein kinase-AKAP binding can be modula

106 ation of FoxO1 in endothelial cells requires cAMP-dependent protein kinase alpha (PKA-alpha).

107 only demonstrate cross-talk between the cAMP/cAMP-dependent protein kinase and AMPK signaling modules

108 tic mutants in the phosphorylation sites for cAMP-dependent protein kinase and Ca(2)(+)/calmodulin-de

109 that Ca(V)1.1-S1575 is a substrate for both cAMP-dependent protein kinase and calcium/calmodulin-dep

110 effects are dependent on phosphorylation by cAMP-dependent protein kinase and cyclin-dependent prote

111 ly important neuromodulator uses synergistic cAMP-dependent protein kinase and endoplasmic reticulum

112 ypoglycemia, and catecholamine signaling via cAMP-dependent protein kinase and phosphorylation of inh

113 PLM phosphorylation induced by cAMP-dependent protein kinase and protein kinase C activ

114 nus of NR2C, which is phosphorylated by both cAMP-dependent protein kinase and protein kinase C.

115 /dephosphorylation of serine 196 mediated by cAMP-dependent protein kinase and protein phosphatase.

116 l binding between the regulatory subunits of cAMP-dependent protein kinase and the anchoring domains

117 Here, using cAMP-dependent protein kinase as a representative model

118 se activity and prevented phosphorylation by cAMP-dependent protein kinase at the neighboring Ser res

119 protein phosphatase 1 when phosphorylated by cAMP-dependent protein kinase at Thr(35).

120 The catalytic subunit of cAMP-dependent protein kinase autophosphorylates Thr(197

121 Here, we investigated the cAMP-dependent protein kinase B (PKB)/Akt regulation of

122 s and via activation of adenylyl cyclase and cAMP-dependent protein kinase, but some alternative down

123 a single phosphate to the activation loop of cAMP-dependent protein kinase by comparing the wild type

124 Recently, we reported that cAMP-dependent protein kinase (cAMP/PKA) signaling negat

125 Protein kinase A (PKA) or cAMP-dependent protein kinase (cAPK) mediates the synerg

126 A transmembrane adenylyl cyclase cAMP-dependent protein kinase cascade modulated by PDE1C

127 The cAMP-dependent protein kinase catalytic (C) subunit is i

128 ites are highly conserved among AGC kinases (cAMP dependent Protein Kinase, cGMP dependent Protein Ki

129 This pathway together with cAMP-dependent protein kinase contributes to maximal bet

130 so show that the regulation is via cAMP/PKA (cAMP-dependent protein kinase)-dependent signaling and p

131 t decreased FAK Tyr-397 phosphorylation in a cAMP-dependent protein kinase-dependent manner.

132 Here, we have identified cAMP-dependent protein kinase-dependent phosphorylation

133 PTH induces the rapid cAMP-dependent protein kinase-dependent release of HDAC4

134 PRKX was identified as a novel type-I cAMP-dependent protein kinase gene expressed in multiple

135 -anchoring protein (AKAP) that scaffolds the cAMP-dependent protein kinase holoenzyme.

136 atically potentiated following activation of cAMP-dependent protein kinase in DT40-3KO cells transien

137 hosphorylated within its HMG box 1 (HMG1) by cAMP-dependent protein kinase in mitochondria.

138 drawal of 8-Br-cAMP and was inhibited by the cAMP-dependent protein kinase inhibitor H89 and the cyst

139 evels, as indicated by experiments using the cAMP-dependent protein kinase inhibitors H89 and PKI.

140 -3 induction by cAMP occurs independently of cAMP-dependent protein kinase, instead requiring the rec

141 Although the cAMP-dependent protein kinase is known to be present in

142 iotic maturation by differentially impacting cAMP-dependent protein kinase, MAPK, NF-kappaB, and phos

143 glycoprotein inhibition was attributable to cAMP-dependent protein kinase-mediated inhibition of the

144 c spinal cord by an electrical activity- and cAMP-dependent protein kinase-mediated pathway.

145 potentiation of the synaptic response via a cAMP-dependent protein kinase-mediated postsynaptic mech

146 ation, which requires phosphorylation by the cAMP-dependent protein kinase of Ser-261/Ser-262.

147 hat mutation of the phosphorylation site for cAMP-dependent protein kinase on DARPP-32 attenuates l-D

148 ich of the two main cAMP sensors is at play: cAMP-dependent protein kinase or exchange protein direct

149 RI and RII) of the regulatory (R) subunit of cAMP-dependent protein kinase or protein kinase A (PKA)

150 y activation of the beta-adrenergic receptor/cAMP-dependent protein kinase pathway and up-regulation

151 s the clinical and molecular genetics of the cAMP-dependent protein kinase pathway in human pituitary

152 a primary response to PTH signaling via the cAMP-dependent protein kinase pathway in vitro.

153 r713 phosphorylation through inhibition of a cAMP-dependent protein kinase/phosphatase-2A cascade.

154 cAMP-dependent protein kinase-phosphorylated RyR2-G230C

155 g protein mAKAP serves as a scaffold for the cAMP-dependent protein kinase PKA and the cAMP-specific

156 to a functional phosphorylation site for the cAMP-dependent protein kinase PKA.

157 C-Raf were both subject to inhibition by the cAMP-dependent protein kinase PKA.

158 Cyclic AMP (cAMP)-dependent protein kinase (PKA) and ribosomal S6 ki

159 control, the cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) holoenzyme typicall

160 gical state, cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) is a tetramer that

161 ) subunit of cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) is inhibited by two

162 ic responses require activity of cyclic AMP (cAMP)-dependent protein kinase (PKA).

163 c subunit of cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA).

164 prototypical cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA-RIalpha), for which

165 Cyclic 3'5' adenosine monophosphate (cAMP)-dependent-protein kinase (PKA) signaling is a fund

166 ic mechanism of phosphorylation catalyzed by cAMP-dependent protein kinase (PKA) a structure of the e

167 receptors and intracellular cAMP binding to cAMP-dependent protein kinase (PKA) act together to indu

168 Ca(2+) release through InsP(3)R-1 following cAMP-dependent protein kinase (PKA) activation.

169 and KIN-29 function is inhibited in turn by cAMP-dependent protein kinase (PKA) activation.

170 eases glucagon-stimulated cAMP accumulation, cAMP-dependent protein kinase (PKA) activity and downstr

171 tegrin function-blocking antibodies enhances cAMP-dependent protein kinase (PKA) activity and increas

172 We found that knockdown of cAMP-dependent protein kinase (PKA) activity in prestalk

173 udied the therapeutic potential of beta-cell cAMP-dependent protein kinase (PKA) activity in restorin

174 fusion transcript, which leads to increased cAMP-dependent protein kinase (PKA) activity in the inde

175 LH-induced increases in cAMP and cAMP-dependent protein kinase (PKA) activity mediated tr

176 educed, but the increases in cAMP levels and cAMP-dependent protein kinase (PKA) activity were unaffe

177 gulation required receptor signaling via the cAMP-dependent protein kinase (PKA) and a specific PKA c

178 NOS and also abrogated epinephrine-dependent cAMP-dependent protein kinase (PKA) and Akt activation.

179 During postmortem, phosphorylation of cAMP-dependent protein kinase (PKA) and AMP activated ki

180 ex that controls the opposing actions of the cAMP-dependent protein kinase (PKA) and CaN in regulatio

181 We examined the individual roles that cAMP-dependent protein kinase (PKA) and Epac (exchange p

182 t CL316,243 regulates lipolysis through both cAMP-dependent protein kinase (PKA) and ERK.

183 e majority of cAMP functions are mediated by cAMP-dependent protein kinase (PKA) and exchange protein

184 family of proteins (AKAPs), which target the cAMP-dependent protein kinase (PKA) and other enzymes to

185 Previous reports have implicated type I cAMP-dependent protein kinase (PKA) and p90 ribosomal S6

186 found in dendritic spines that recruits the cAMP-dependent protein kinase (PKA) and protein phosphat

187 horing protein (AKAP)79/150 targets both the cAMP-dependent protein kinase (PKA) and protein phosphat

188 These pathways involve the cAMP-dependent protein kinase (PKA) and Tor proteins, re

189 rotein directly activated by cAMP (EPAC) and cAMP-dependent protein kinase (PKA) are two intracellula

190 SynIII is phosphorylated by cAMP-dependent protein kinase (PKA) at a highly conserve

191 nNOS is phosphorylated by cAMP-dependent protein kinase (PKA) at serine(S)1412.

192 ion of the adenine ring selectively activate cAMP-dependent protein kinase (PKA) but not exchange pro

193 y isoproterenol (10 nmol/L), which activates cAMP-dependent protein kinase (PKA) but not PKD.

194 Previously, we described the inactivation of cAMP-dependent protein kinase (PKA) by direct oxidation

195 Subcellular compartmentalization of the cAMP-dependent protein kinase (PKA) by protein kinase A-

196 cal antagonism of NMDA receptors (NMDARs) or cAMP-dependent protein kinase (PKA) during post-MD sleep

197 trimeric G(s) protein, adenylyl cyclase, and cAMP-dependent protein kinase (PKA) for efficient signal

198 cellular model of memory storage, implicate cAMP-dependent protein kinase (PKA) in presynaptic and p

199 Here, we show that the cAMP-dependent protein kinase (PKA) in Saccharomyces cer

200 In contrast, the role of cAMP-dependent protein kinase (PKA) in the control of TT

201 le is known about the regulation of cAMP and cAMP-dependent protein kinase (PKA) in these cells.

202 t Ser(21) in GRK1 would be phosphorylated by cAMP-dependent protein kinase (PKA) in vivo.

203 ve found that ET1 stimulates the activity of cAMP-dependent protein kinase (PKA) in VSMC as profoundl

204 ptors, phosphorylation of CaV1.2 channels by cAMP-dependent protein kinase (PKA) increases channel ac

205 Phosphorylation of Ser-656 by cAMP-dependent protein kinase (PKA) inhibits Drp1, where

206 The catalytic subunit of cAMP-dependent protein kinase (PKA) is a member of the A

207 The catalytic (C) subunit of cAMP-dependent protein kinase (PKA) is a serine/threonin

208 Specificity for signaling by cAMP-dependent protein kinase (PKA) is achieved by both

209 In addition, the cAMP-dependent protein kinase (PKA) is involved in Kv2.1

210 Spatial regulation of the cAMP-dependent protein kinase (PKA) is required for chem

211 yses of the cAMP binding domains of Epac and cAMP-dependent protein kinase (PKA) lead to a model of E

212 We studied the effects of cAMP-dependent protein kinase (PKA) on proteolysis by th

213 dramatically increased by activation of the cAMP-dependent protein kinase (PKA) pathway, which is im

214 romyces cerevisiae is also controlled by the cAMP-dependent protein kinase (PKA) pathway.

215 l androgen biosynthesis by activating a cAMP/cAMP-dependent protein kinase (PKA) pathway.

216 However, upon cAMP-dependent protein kinase (PKA) phosphorylation of P

217 r study has revealed age-related increase in cAMP-dependent protein kinase (PKA) phosphorylation of t

218 ked G protein-coupled receptor activation of cAMP-dependent protein kinase (PKA) plays an important r

219 isualise these two processes by studying the cAMP-dependent protein kinase (PKA) potentiation of pres

220 Phosphorylation of GluA1 S845 by the cAMP-dependent protein kinase (PKA) primes extrasynaptic

221 cAMP-dependent protein kinase (PKA) regulates a myriad o

222 The cAMP-dependent protein kinase (PKA) regulates a wide arr

223 For many years, cAMP-dependent protein kinase (PKA) represented the only

224 Activation of endogenous cAMP-dependent protein kinase (PKA) rescued the depresse

225 Here, we identified cAMP-dependent protein kinase (PKA) signaling as respons

226 by FRET fluorescence ratio changes of tagged cAMP-dependent protein kinase (PKA) subunits expressed u

227 ases channel activity via phosphorylation by cAMP-dependent protein kinase (PKA) tethered to the dist

228 he well designed compartmentalization of the cAMP-dependent protein kinase (PKA) through its anchorin

229 A kinase anchor protein AKAP150 recruits the cAMP-dependent protein kinase (PKA) to dendritic spines.

230 kinase anchoring proteins (AKAPs) tether the cAMP-dependent protein kinase (PKA) to intracellular sit

231 inase anchoring proteins (AKAPs) that target cAMP-dependent protein kinase (PKA) to the channel.

232 damental cellular processes by directing the cAMP-dependent protein kinase (PKA) toward its intended

233 atio-temporal specificity for the omnipotent cAMP-dependent protein kinase (PKA) via high affinity in

234 In particular, the cAMP-dependent protein kinase (PKA) was found to control

235 ort, novel substrate-binding variants of the cAMP-dependent protein kinase (PKA) were used to identif

236 To determine the physiological role of the cAMP-dependent protein kinase (PKA), a mouse model was d

237 cAMP-dependent protein kinase (PKA), along with other ki

238 r mechanism of activation, dependence on the cAMP-dependent protein kinase (PKA), and the magnitude a

239 sensory neurons results in the activation of cAMP-dependent protein kinase (PKA), and this kinase pho

240 h the negative feedback loop formed by cAMP, cAMP-dependent protein kinase (PKA), and type 4 phosphod

241 the sites is predicted to be a substrate of cAMP-dependent protein kinase (PKA), and yeast expressin

242 inuing activity of adenylyl cyclase (AC) and cAMP-dependent protein kinase (PKA), as well as a scaffo

243 is a human anchoring protein that organizes cAMP-dependent protein kinase (PKA), Ca(2+)/calmodulin (

244 on of the c-fos gene conferred regulation by cAMP-dependent protein kinase (PKA), cGMP-dependent prot

245 kinetics of sites that are phosphorylated by cAMP-dependent protein kinase (PKA), even in highly homo

246 lated on threonine residue 35 (Thr35) by the cAMP-dependent protein kinase (PKA), inducing the potent

247 rements of global cAMP, general increases in cAMP-dependent protein kinase (PKA), or the activity of

248 Pretreatment with cAMP-dependent protein kinase (PKA), phosphoinositide 3-

249 To identify novel substrates of cAMP-dependent protein kinase (PKA), the PKA catalytic s

250 nels is subject to pronounced enhancement by cAMP-dependent protein kinase (PKA), which is scaffolded

251 cAMP-dependent protein kinase (PKA)-mediated phosphoryla

252 he PlexA GAP domain is phosphorylated by the cAMP-dependent protein kinase (PKA).

253 two isoforms of the catalytic subunit of the cAMP-dependent Protein Kinase (PKA).

254 at are independent of its traditional target cAMP-dependent protein kinase (PKA).

255 ase-2, prostaglandins, and activation of the cAMP-dependent protein kinase (PKA).

256 l human and mouse substrates of CK2alpha and cAMP-dependent protein kinase (PKA).

257 ther metabolic control of the proteasome via cAMP-dependent protein kinase (PKA).

258 fect that was abolished by the inhibition of cAMP-dependent protein kinase (PKA).

259 lure in targeting and regulation of axonemal cAMP-dependent protein kinase (PKA).

260 growth factors is disrupted by cAMP through cAMP-dependent protein kinase (PKA).

261 the effects were attenuated by inhibition of cAMP-dependent protein kinase (PKA).

262 ulation of cAMP and subsequent activation of cAMP-dependent protein kinase (PKA).

263 icular function occurs through regulation of cAMP-dependent protein kinase (PKA).

264 plex pathways that converge on activation of cAMP-dependent protein kinase (PKA).

265 ncodes the regulatory subunit R1alpha of the cAMP-dependent protein kinase (PKA).

266 es synaptic transmission presynaptically via cAMP-dependent protein kinase (PKA).

267 of D(1) receptor signaling and substrate of cAMP-dependent protein kinase (PKA).

268 required NR2B-mediated downregulation of the cAMP-dependent protein kinase (PKA)/cAMP response elemen

269 ve small-molecule regulators for type Ialpha cAMP-dependent Protein kinase (PKA-Ialpha), a protein co

270 KAPs) spatially constrain phosphorylation by cAMP-dependent protein kinases (PKA).

271 gnaling can regulate and be regulated by the cAMP-dependent protein kinase, PKA, although the molecul

272 t lead to an increase in the activity of the camp-dependent protein kinase, PKA, which triggers rapid

273 y, we reported that the catalytic subunit of cAMP-dependent protein kinase (PKAc) binds to the active

274 ondria the regulatory subunit RIalpha of the cAMP-dependent protein kinase (PKARIalpha); and the horm

275 In this work, we use murine cAMP-dependent protein kinase (protein kinase A) as the

276 Ras proteins and cAMP-dependent protein kinase (protein kinase A, PKA) ar

277 The catalytic (C) subunit of cAMP-dependent protein kinase [protein kinase A (PKA)] i

278 The cAMP-dependent protein kinase [protein kinase A (PKA)] m

279 a pathway that is sensitive to inhibitors of cAMP-dependent protein kinase [protein kinase A (PKA)].

280 al cells, serine/threonine kinases including cAMP-dependent protein kinase, protein kinase C and calm

281 and poor inhibition of other members of the cAMP-dependent protein kinase/protein kinase G/protein k

282 Inhibiting cAMP-dependent protein kinase reduced the secretory resp

283 nding of RSPH3 to the regulatory subunits of cAMP-dependent protein kinase, RIIalpha and RIIbeta, is

284 volving mitogen-activated protein kinase and cAMP-dependent protein kinase signaling modules, wherein

285 ilar level in TG-RLC(P-) and NTG, suggesting cAMP-dependent protein kinase signaling to these protein

286 nuclear localization during fasting and cAMP/cAMP-dependent protein kinase signaling, suggesting loca

287 CRE-binding protein (CREB) or activation of cAMP-dependent protein kinase significantly increased GL

288 C5a orthologs efflux cyclic nucleotides, and cAMP-dependent protein kinase (Sp-CAPK/PKA) is expressed

289 hosphorylation of Synapsin I/II at serine 9 (cAMP-dependent protein kinase substrate site), serine 62

290 somatic mutations in PRKACA, which encodes a cAMP-dependent protein kinase that acts as a repressor p

291 Ps), defined by their capacity to target the cAMP-dependent protein kinase to distinct subcellular lo

292 activate mechanisms in addition to cAMP and cAMP-dependent protein kinase to modulate retinal gangli

293 ceptors (betaAR) in adipocytes activates the cAMP-dependent protein kinase to promote liberation of f

294 of cAMP, in parallel with the stimulation of cAMP-dependent protein kinase, to drive ribosomal protei

295 ssion of a non-coding transcript of PRKAR1A (cAMP-dependent protein kinase type I-alpha regulatory su

296 member 4 precursor, zinc finger protein 432, cAMP-dependent protein kinase type I-beta regulatory sub

297 rotein kinases (Pim-1, Pim-2, and Pim-3) and cAMP-dependent protein kinase were measured and found to

298 ptors that increase cAMP levels and activate cAMP-dependent protein kinase, which phosphorylates mamm

299 ccessfully applied to detect the activity of cAMP-dependent protein kinase with a low detection limit

300 surprising peptidergic transmission requires cAMP-dependent protein kinase, with only a minor contrib