ライフサイエンスコーパス: AMP-activated protein kinase

1 tivation of the kinase upstream of ULK1, the AMP-activated protein kinase.

2 but nitrite increased the phosphorylation of AMP-activated protein kinase.

3 ase, sirtuin 1 (SIRT1), the cAMP pathway, or AMP-activated protein kinase.

4 ent, and a 3-fold increase in phosphorylated AMP-activated protein kinase.

5 roves cardiac function in vivo by activating AMP-activated protein kinase.

6 ectly suppress both mouse and human OGG1 via AMP-activated protein kinase.

7 displayed increased activation of SIRT3 and AMP-activated protein kinase.

8 tion, have recently emerged as activators of AMP-activated protein kinase.

9 bust activation of skeletal muscle SIRT3 and AMP-activated protein kinase.

10 of LKB1 in suppressing ROS is independent of AMP-activated protein kinase, a canonical substrate of L

11 f human resistin inhibited the activation of AMP-activated protein kinase, a major sensor and regulat

12 Prevention of AMP-activated protein kinase activation by Compound C or

13 amide riboside served to study the impact of AMP-activated protein kinase activation on vascular perm

14 phosphorylation complexes, restored cardiac AMP-activated protein kinase activation, and improved my

15 intracellular reactive oxygen species level, AMP-activated protein kinase activation, and interleukin

16 ns leading to lean mice, as well as abnormal AMP-activated protein kinase activation, which were asso

17 nic gene expression, glucose production, and AMP-activated protein kinase activation.

18 vorably modulated renal oxidative stress and AMP-activated protein kinase activation.

19 At a molecular level, metformin increases AMP-activated protein kinase activity and increases anti

20 ymerase also reduce sirtuin, PGC-1alpha, and AMP-activated protein kinase activity.

21 ylation (acetyl-Lys)-dependent activation of AMP-activated protein kinase, AKT, and PKA kinases durin

22 rates that polymet-CDDP NPs can activate the AMP-activated protein kinase alpha (AMPKalpha) pathway a

23 evates SIRT1 levels and activity in an AMPK (AMP-activated protein kinase alpha)-dependent manner.

24 ine palmitoyltransferase-1, phosphorylated 5'AMP-activated protein kinase-alpha, and phosphorylated p

25 In addition, both AMP-activated protein kinase alpha1 (AMPKalpha1) express

26 Here we report that the AMP-activated protein kinase alpha1 (AMPKalpha1) in mono

27 nt of cigarette smoke, selectively activates AMP-activated protein kinase alpha2 (AMPKalpha2) in adip

28 following disassociation from its repressor AMP activated protein kinase (AMPK) and was elicited by

29 ere preceded by increased phosphorylation of AMP activated protein kinase (Ampk) at tyrosine 172 and

30 These changes activate AMP activated protein kinase (AMPK), which in turn direc

31 the energy-sensing adenosine monophosphate (AMP)-activated protein kinase (AMPK) is genetically requ

32 The adenosine monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway a

33 Sestrin 2-dependent AMP-activated protein kinase (AMPK) activation attenuate

34 content (-45% vs. M-ERRalphaWT) and enhanced AMP-activated protein kinase (AMPK) activation in M-ERRa

35 JNK phosphorylation downstream of AMP-activated protein kinase (AMPK) activation is requir

36 Mechanistically, AMP-activated protein kinase (AMPK) activation is requir

37 AMP-activated protein kinase (AMPK) activation triggered

38 HG) induces apoptosis of podocytes, inhibits AMP-activated protein kinase (AMPK) activation, inactiva

39 We ascribed the effects of aspirin to AMP-activated protein kinase (AMPK) activation, mTORC1 i

40 In contrast AMP-activated protein kinase (AMPK) activation, which ca

41 d an inhibitor of autophagy, is inhibited by AMP-activated protein kinase (AMPK) activation.

42 to modulate both ATP-citrate lyase (ACL) and AMP-activated protein kinase (AMPK) activity in rodents.

43 Our observations revealed high AMP-activated protein kinase (AMPK) activity in STC1 tra

44 creases in oxidative stress and decreases in AMP-activated protein kinase (AMPK) activity.

45 te for the first time that the activation of AMP-activated protein kinase (AMPK) alpha in sensory hai

46 EGFP reduction was normal in muscle-specific AMP-activated protein kinase (AMPK) alpha2-inactive tran

47 idney, metformin increased the activation of AMP-activated protein kinase (AMPK) and decreased inflam

48 The subsequent identification of AMP-activated protein kinase (AMPK) and its activation b

49 The conserved energy sensor AMP-activated protein kinase (AMPK) and its correspondin

50 CSEE enhanced the phosphorylation of AMP-activated protein kinase (AMPK) and its primary down

51 strate that the metabolic checkpoint kinases AMP-activated protein kinase (AMPK) and LKB1 are not req

52 The link between AMP-activated protein kinase (AMPK) and myogenesis remai

53 and AdipoR2, increases the activities of 5' AMP-activated protein kinase (AMPK) and peroxisome proli

54 e in muscle coordinated by signaling through AMP-activated protein kinase (AMPK) and peroxisome proli

55 channels is dependent on the protein kinases AMP-activated protein kinase (AMPK) and PKA.

56 n of TWEAK inhibited ( approximately 31%) 5' AMP-activated protein kinase (AMPK) and reduced ( approx

57 lation by PKG2 is triggered by activation of AMP-activated protein kinase (AMPK) and requires endothe

58 the signaling pathways of the CR mediators, AMP-activated protein kinase (AMPK) and sirtuin-1 are ac

59 nstrate that NT attenuates the activation of AMP-activated protein kinase (AMPK) and stimulates fatty

60 spontaneously activate the metabolic sensor AMP-activated protein kinase (AMPK) and that activation

61 The AMP-activated protein kinase (AMPK) and the Gsk3 kinase

62 AMP-activated protein kinase (AMPK) and the homologous y

63 t of rapamycin (mTOR) pathway, downstream of AMP-activated protein kinase (AMPK) and upstream of ribo

64 this study, we identify the metabolic sensor AMP-activated protein kinase (AMPK) as a beta1-integrin

65 ) analysis to identify the gamma1 subunit of AMP-activated protein kinase (AMPK) as an essential cont

66 In particular, activation of the host AMP-activated protein kinase (AMPK) by low energy could

67 Activation of AMP-activated protein kinase (AMPK) by metformin, inhibi

68 target of rapamycin (mTOR) or activation of AMP-activated protein kinase (AMPK) during the contracti

69 KO did not restore mTOR inhibition or alter AMP-activated protein kinase (AMPK) expression.

70 ne/threonine protein kinase belonging to the AMP-activated protein kinase (AMPK) family.

71 The AMP-activated protein kinase (AMPK) functions to monitor

72 Chronic activation of AMP-activated protein kinase (AMPK) has been proposed to

73 Hepatic AMP-activated protein kinase (AMPK) has been proposed to

74 AMP-activated protein kinase (AMPK) has been proposed to

75 AMP-activated protein kinase (AMPK) has been shown to ac

76 AMP-activated protein kinase (AMPK) has been suggested a

77 e synthesis through activation of the enzyme AMP-activated protein kinase (AMPK) has recently been ch

78 The AMP-activated protein kinase (AMPK) has recently been im

79 extracellular matrix proteins and activated AMP-activated protein kinase (AMPK) in a time- and dose-

80 nistically, SIRT2 maintained the activity of AMP-activated protein kinase (AMPK) in aged and Ang II-i

81 ibrotic effects and specifically the role of AMP-activated protein kinase (AMPK) in kidney tubular ep

82 m of this study was to determine the role of AMP-activated protein kinase (AMPK) in lipopolysaccharid

83 gly, stretch induced the acute activation of AMP-activated protein kinase (AMPK) in normal cardiomyoc

84 The role of AMP-activated protein kinase (AMPK) in promoting fatty a

85 , and matrix protein synthesis by inhibiting AMP-activated protein kinase (AMPK) in renal cells.

86 phosphorylation of the downstream substrate AMP-activated protein kinase (AMPK) in response to ionom

87 as essential for LKB1-mediated activation of AMP-activated protein kinase (AMPK) in response to oxida

88 We ruled out a role for AMP-activated protein kinase (AMPK) in the effect of met

89 resveratrol required activation of Sirt1 and AMP-activated protein kinase (Ampk) in this tissue to in

90 agents that indirectly or directly stimulate AMP-activated protein kinase (AMPK) including salicylate

91 ed aerobic glycolysis, a process mediated by AMP-activated protein kinase (AMPK) independently of HIF

92 isolated from HFD rats, which was blocked by AMP-activated protein kinase (AMPK) inhibition.

93 The 5'-AMP-activated protein kinase (AMPK) is a cellular energy

94 AMP-activated protein kinase (AMPK) is a central metabol

95 AMP-activated protein kinase (AMPK) is a conserved serin

96 The AMP-activated protein kinase (AMPK) is a conserved signa

97 AMP-activated protein kinase (AMPK) is a heterotrimeric

98 AMP-activated protein kinase (AMPK) is a heterotrimeric

99 AMP-activated protein kinase (AMPK) is a key regulator o

100 The AMP-activated protein kinase (AMPK) is a key regulator o

101 AMP-activated protein kinase (AMPK) is a key sensor and

102 AMP-activated protein kinase (AMPK) is a master sensor a

103 AMP-activated protein kinase (AMPK) is a metabolic senso

104 AMP-activated protein kinase (AMPK) is a metabolic stres

105 AMP-activated protein kinase (AMPK) is a molecular energ

106 AMP-activated protein kinase (AMPK) is a sensor of cellu

107 The AMP-activated protein kinase (AMPK) is a Ser/Thr kinase

108 AMP-activated protein kinase (AMPK) is an energy sensor

109 AMP-activated protein kinase (AMPK) is an energy-sensing

110 As a central regulator of metabolism, the AMP-activated protein kinase (AMPK) is an established th

111 The mammalian AMP-activated protein kinase (AMPK) is an obligatory alp

112 The energy-sensing AMP-activated protein kinase (AMPK) is known to be a maj

113 potential controls calcium homeostasis, and AMP-activated protein kinase (AMPK) is regulated, in par

114 RATIONALE: The AMP-activated protein kinase (AMPK) is stimulated by hyp

115 The AMP-activated protein kinase (AMPK) is stimulated by hyp

116 The AMP-activated protein kinase (AMPK) is the master regula

117 The LKB1-AMP-activated protein kinase (AMPK) kinase pathway targe

118 at inhibition of the metabolic stress sensor AMP-activated protein kinase (AMPK) led to deranged gluc

119 f beta-oxidation genes, greater reduction in AMP-activated protein kinase (AMPK) levels, and diminish

120 tiates the stimulating effect of LKB1 on the AMP-activated protein kinase (AMPK) metabolic sensor thr

121 We demonstrated that AMP-activated protein kinase (AMPK) modulates PXR transc

122 lso exhibit constitutive activation of liver AMP-activated protein kinase (AMPK) pathway and nuclear

123 osed to trehalose resisted trehalose-induced AMP-activated protein kinase (AMPK) phosphorylation and

124 over, Sirt3-/- osteoclast precursors reduced AMP-activated protein kinase (AMPK) phosphorylation thro

125 kinase B1 (LKB1) and its downstream effector AMP-activated protein kinase (AMPK) play critical roles

126 AMP-activated protein kinase (AMPK) plays a central role

127 egans larvae, the master metabolic regulator AMP-activated protein kinase (AMPK) plays a critical rol

128 AMP-activated protein kinase (AMPK) plays a major role i

129 AMP-activated protein kinase (AMPK) plays an essential r

130 AMP-activated protein kinase (AMPK) plays an important r

131 AMP-activated protein kinase (AMPK) regulates cellular e

132 The AMP-activated protein kinase (AMPK) regulates metabolism

133 We show here that AMP-activated protein kinase (AMPK) regulates neuronal a

134 Recent studies demonstrated that AMP-activated protein kinase (AMPK) regulates neuronal m

135 sion of cardiac autophagy, and activation of AMP-activated protein kinase (AMPK) restores cardiac aut

136 he PKM1/2 knockdown in H1299 cells activated AMP-activated protein kinase (AMPK) signaling and stimul

137 We show here that GOF mutp53s inhibit AMP-activated protein kinase (AMPK) signaling in head an

138 been recently proposed as activators of the AMP-activated protein kinase (AMPK) signaling pathway an

139 e in the AMP/ATP ratio and activation of the AMP-activated protein kinase (AMPK) signaling pathway in

140 background, cAMP/protein kinase A (PKA) and AMP-activated protein kinase (AMPK) signaling pathways a

141 that the gene encoding the gamma2 subunit of AMP-activated protein kinase (AMPK) strongly correlated

142 c checkpoint controlled by the energy sensor AMP-activated protein kinase (AMPK) that regulated mRNA

143 or glucose restriction (GR) regulate PKA and AMP-activated protein kinase (AMPK) to protect against D

144 In response to low energy, the cellular AMP-activated protein kinase (AMPK) triggers a physiolog

145 yclic AMP (cAMP) signalling independently of AMP-activated protein kinase (AMPK) via direct inhibitio

146 Recently, it has been demonstrated that AMP-activated protein kinase (AMPK) was deregulated in t

147 In this study, we have identified 5'-AMP-activated protein kinase (AMPK), a cellular energy s

148 Here, we show that AMP-activated protein kinase (AMPK), a central metabolic

149 Recent evidence suggests that AMP-activated protein kinase (AMPK), a central regulator

150 ort that BRAF is phosphorylated at Ser729 by AMP-activated protein kinase (AMPK), a critical energy s

151 AMP-activated protein kinase (AMPK), a critical sensor o

152 with increased pseudopodial activity of the AMP-activated protein kinase (AMPK), a critically import

153 However, loss of AMP-activated protein kinase (AMPK), a HDAC5 kinase, in

154 In eukaryotes, the AMP-activated protein kinase (AMPK), a highly conserved

155 show that apoptotic cells potently activate AMP-activated protein kinase (AMPK), a highly sensitive

156 This study demonstrates that AMP-activated protein kinase (AMPK), a key driver of cel

157 demonstrate that VPA is a novel activator of AMP-activated protein kinase (AMPK), a key regulator of

158 s a direct target for phosphorylation by the AMP-activated protein kinase (AMPK), a key sensor and re

159 ncer cell growth via the metabolic sensor 5'-AMP-activated protein kinase (AMPK), a kinase that class

160 Mechanistically, inhibiting VEGFR2 or AMP-activated protein kinase (AMPK), a major decorin-act

161 Here we show that AMP-activated protein kinase (AMPK), a metabolic checkpo

162 stressed microenvironments that activate 5'-AMP-activated protein kinase (AMPK), a ubiquitous regula

163 AMP-activated protein kinase (AMPK), an important downst

164 lin, mechanistic target of rapamycin (mTOR), AMP-activated protein kinase (AMPK), and autophagy pathw

165 and tensin deleted on chromosome 10 (PTEN), AMP-activated protein kinase (AMPK), and dsRNA dependent

166 activity, including the metabolic indicator AMP-activated protein kinase (AMPK), and Fox transcripti

167 coneogenesis, protein phosphatase 2A (PP2A), AMP-activated protein kinase (AMPK), and FoxO1 proteins.

168 (ADP-ribose) polymerases (PARPs), sirtuins, AMP-activated protein kinase (AMPK), and mechanistic tar

169 eotide monophosphate (NMP) levels, activates AMP-activated protein kinase (AMPK), and suppresses gluc

170 lated the essential metabolic stress sensor, AMP-activated protein kinase (AMPK), and targeting AMPK

171 in-dependent kinase kinase beta (CaMKKbeta), AMP-activated protein kinase (AMPK), and ULK1.

172 oy receptor 8 (IL-1R8) and the activation of AMP-activated protein kinase (AMPK), because both inhibi

173 Glucose deprivation activates AMP-activated protein kinase (AMPK), but it is unclear w

174 quired miR-33 targeting of the energy sensor AMP-activated protein kinase (AMPK), but not cholesterol

175 sensor of energy status in mammalian cells, AMP-activated protein kinase (AMPK), can also be activat

176 regulate both O-GlcNAc transferase (OGT) and AMP-activated protein kinase (AMPK), cooperatively conne

177 d its downstream effector, the energy sensor AMP-activated protein kinase (AMPK), in repressing Yki a

178 A key sensor of cellular energy status, AMP-activated protein kinase (AMPK), interacts allosteri

179 Compound-C, an inhibitor of AMP-activated protein kinase (AMPK), partially prevented

180 We report that AMP-activated protein kinase (AMPK), phosphatidylinositi

181 the budding yeast ortholog of the mammalian AMP-activated protein kinase (AMPK), plays a role in the

182 lity or starvation-regulated mechanisms like AMP-activated protein kinase (AMPK), reactive oxygen spe

183 utophagy in ECM-detached cells by activating AMP-activated protein kinase (AMPK), resulting in downst

184 Fluctuations in these pools can activate AMP-activated protein kinase (AMPK), the central regulat

185 Here, we showed that AMP-activated protein kinase (AMPK), the master metaboli

186 Because TZD is known to activate AMP-activated protein kinase (AMPK), we determined wheth

187 Particularly relevant to this process is 5'-AMP-activated protein kinase (AMPK), which functions as

188 epletion and activation of the energy sensor AMP-activated protein kinase (AMPK), which induces stabi

189 to determine the role in this process of the AMP-activated protein kinase (AMPK), which is intimately

190 Nisch binds to and inhibits the activity of AMP-activated protein kinase (AMPK), which regulates ene

191 ed activation of the metabolic stress enzyme AMP-activated protein kinase (AMPK), which was mediated

192 Phospho-AMP-activated protein kinase (AMPK)-alpha (T172) was red

193 plex 1 and laminin gamma1 accumulation in an AMP-activated protein kinase (AMPK)-dependent manner.

194 urrent study, we find that metformin, via an AMP-activated protein kinase (AMPK)-dependent mechanism,

195 originally postulated to be due to a hepatic AMP-activated protein kinase (AMPK)-dependent mechanism.

196 we show that nutrient starvation results in AMP-activated protein kinase (AMPK)-dependent phosphoryl

197 e beta-cell electrical activity by promoting AMP-activated protein kinase (AMPK)-dependent traffickin

198 glycolytic enzyme, is a critical mediator of AMP-activated protein kinase (AMPK)-driven Sirt1 activat

199 tion and/or activation of the adiponectin-5'-AMP-activated protein kinase (AMPK)-forkhead box O (FOXO

200 Here we revealed an AMP-activated protein kinase (AMPK)-independent mechanis

201 ate here that glucose deprivation results in AMP-activated protein kinase (AMPK)-mediated acetyl-CoA

202 exercising muscle likely is counteracted via AMP-activated protein kinase (AMPK)-mediated down-regula

203 turn governs autophagic response through an AMP-activated protein kinase (AMPK)-mediated feedforward

204 ession of GOF mutant p53 G245D decreases the AMP-activated protein kinase (AMPK)-mediated phosphoryla

205 Here, we demonstrate that the AMP-activated protein kinase (AMPK)-related protein Snf1

206 ch is mediated by the cellular energy sensor AMP-activated protein kinase (AMPK).

207 Kv2.1 surface expression is mediated by the AMP-activated protein kinase (AMPK).

208 echanistically associated with activation of AMP-activated protein kinase (AMPK).

209 se, ATP, and activation of the energy sensor AMP-activated protein kinase (AMPK).

210 1) and the downstream fuel-sensitive kinase, AMP-activated protein kinase (AMPK).

211 hosphorylation of liver kinase B1 (LKB1) and AMP-activated protein kinase (AMPK).

212 FD)-induced insulin resistance by activating AMP-activated protein kinase (AMPK).

213 er-binding protein alpha, and phosphorylated AMP-activated protein kinase (AMPK).

214 e cellular starvation response and activates AMP-activated protein kinase (AMPK).

215 OGT regulates SREBP-1 protein expression via AMP-activated protein kinase (AMPK).

216 mbryonic fibroblasts (MEFs) by targeting the AMP-activated protein kinase (AMPK).

217 2, forming a complex that interacts with the AMP-activated protein kinase (AMPK).

218 aintenance of energy homeostasis, largely by AMP-activated protein kinase (AMPK).

219 Here, we show that SOCE activates AMP-activated protein kinase (AMPK); its effector p38bet

220 In AMP-activated protein kinase (AMPK)alpha2 KO mice, subst

221 yceride lipase, acetyl-CoA carboxylase 2 and AMP-activated protein kinase (AMPK)gamma3 were higher in

222 The energy sensor AMP-activated protein kinases (AMPK) is thought to play

223 The AMP-activated protein kinase, AMPK, is an energy-sensing

224 unx2 knockdown cells displayed activation of AMP-activated protein kinase (AMPKalpha), the sensor of

225 The SNF1/AMP-activated protein kinases (AMPKs) function in energy

226 ltifaceted mechanism involving activation of AMP-activated protein kinase and downregulation of key r

227 e edema formation, including aquaporin-4 and AMP-activated protein kinase and its downstream effector

228 renal levels of the phosphorylated forms of AMP-activated protein kinase and its target acetyl-CoA c

229 We show that the Nmrk2 gene is an AMP-activated protein kinase and peroxisome proliferator

230 resulting in activation of the energy sensor AMP-activated protein kinase and phosphorylation of euka

231 the cell metabolism (IR-alpha, IR-beta, and AMP-activated protein kinase), and a stabilizing effect

232 including endothelial nitric oxide synthase, AMP-activated protein kinase, and the actin-binding MARC

233 ylation of CAR by metformin was primarily an AMP-activated protein kinase- and extracellular signal-r

234 Yeast cells lacking Snf1 (AMP-activated protein kinase) are hypersensitive to 2DG.

235 the patients but also critical to the use of AMP-activated protein kinase as a drug target.

236 erted its anti-inflammatory function through AMP-activated protein kinase as AMP kinase knockout or i

237 ion of liver kinase B1 and the energy sensor AMP-activated protein kinase, as well as enhanced fatty

238 As adenosine monophosphate (AMP)-activated protein kinase both controls cytoskeleton

239 LKB1 in Tregs is largely independent of the AMP-activated protein kinase, but is mediated by the MAP

240 icroglia/macrophage WAP domain protein in an AMP-activated protein kinase-dependent manner and favora

241 ved cardiac function in animals on HFD by an AMP-activated protein kinase-dependent mechanism.

242 utations in the regulatory gamma2-subunit of AMP-activated protein kinase (encoded by Prkag2 gene) ca

243 AMP-activated protein kinase exerts a protective action

244 ased ATP levels and increased phosphorylated AMP-activated protein kinase, exposing an energy deficie

245 N-acetyl-cysteine reduced the activation of AMP-activated protein kinase, extracellular signal-regul

246 ession in various cell types and is the only AMP-activated protein kinase family member known to inte

247 Snf1, a member of the AMP-activated protein kinase family, plays a critical ro

248 Snf1, the yeast ortholog of AMP-activated protein kinase, has been implicated in thi

249 th sets is regulated positively by the yeast AMP-activated protein kinase homolog, Snf1, in response

250 etabolism may have in chemotransduction; the AMP-activated protein kinase hypothesis and its current

251 The role of gamma2-AMP-activated protein kinase in cell growth also has bro

252 Finally, phosphorylation of AMP-activated protein kinase in response to adiponectin

253 ular ATP levels and concomitantly stimulated AMP-activated protein kinase in vitro and in vivo As an

254 f1, the Saccharomyces cerevisiae ortholog of AMP-activated protein kinase, in this process.

255 ) and humans (~40%), and this activation was AMP-activated protein kinase independent.

256 AMP-activated protein kinase is a master regulator of ce

257 RATIONALE: AMPK (AMP-activated protein kinase) is a heterotrimeric protei

258 AMP-activated protein kinase-KD failed to block adiponec

259 ed treatment with DHA and Physcion activates AMP-activated protein kinase, leading to synergistic inh

260 FF depletes intracellular ATP, activates the AMP-activated protein kinase-mammalian target of rapamyc

261 its cell growth is through activation of the AMP-activated-protein-kinase/mammalian-target-of-rapamyc

262 Finally, we found that the 5'-AMP activated protein kinase may regulate this EB1-media

263 lly activates p53 through distinct MDM2- and AMP-activated protein kinase-mediated mechanisms in a fe

264 t on phosphorylated adenosine monophosphate (AMP)-activated protein kinase (pAMPK) form and gene expr

265 get of rapamycin pathways and stimulated the AMP-activated protein kinase pathway in both muscles.

266 ic action through regulation of hypothalamic AMP-activated protein kinase pathway, leading to a decli

267 athway and activation of the liver kinase B1/AMP-activated protein kinase pathway.

268 ssibly through SERCA2-mediated activation of AMP-activated protein kinase pathway.

269 cute exposure of mice to wood smoke promoted AMP-activated protein kinase phosphorylation and express

270 binding to different AdipoR combinations on AMP-activated protein kinase phosphorylation and peroxis

271 itric oxide synthase (eNOS) phosphorylation, AMP-activated protein kinase phosphorylation, and sirtui

272 nal validation did not identify NF-kappaB or AMP-activated protein kinase phosphorylation, but uric a

273 ed kinases, increased the phosphorylation of AMP-activated protein kinase, reduced intracellular pota

274 F-3 directly drives the transcription of the AMP-activated protein kinase-related gene pig-1, which e

275 Moreover, activation of AMP-activated protein kinase restored sirtuin-3 activity

276 creased and the expression and activation of AMP-activated protein kinase signaling and cyclooxygenas

277 This AMP-activated protein kinase signaling is likely importa

278 ephropathy by regulating the liver kinase B1/AMP-activated protein kinase signaling pathway.

279 dependent, reactive oxygen species-sensitive AMP-activated protein kinase signaling with Jun N-termin

280 single daily dosage of MB does not activate AMP-activated protein kinase signaling, and no tumor reg

281 e uptake and ATP production, which inhibited AMP-activated protein kinase signaling.

282 d protein kinase activation by Compound C or AMP-activated protein kinase siRNA lessened the activati

283 stimulation of a signaling cascade involving AMP-activated protein kinase, sirtuin 1, PGC-1alpha, sir

284 uttle systems, NAD(+) concentrations and the AMP-activated protein kinase/sirtuin 1/peroxisome prolif

285 ional activation by Adr1 is dependent on the AMP-activated protein kinase Snf1 and is inhibited by bi

286 ack loop on protein kinase A mediated by the AMP-activated protein kinase Snf1 is coupled with a nega

287 The AMP-activated protein kinase (SNF1 in yeast) is a centra

288 signature includes 3 prominent features: (i) AMP-activated protein kinase subunit alpha (AMPKalpha) d

289 t caused an increase in the expression of 5'-AMP-activated protein kinase subunit gamma-2 (PKRAG2) an

290 otein kinase subunit gamma-2 (PKRAG2) and 5'-AMP-activated protein kinase subunit gamma-3 (PKRAG3) wh

291 ed level of ATP results in activation of the AMP-activated protein kinase that leads to reduced lipog

292 However, Rac1-dependent activation of AMP-activated protein kinase, the signaling phospholipid

293 t activation of mTORC2 via the energy sensor AMP-activated protein kinase to increased proliferation

294 y of protein phosphatase 2A, liver kinase B1/AMP-activated protein kinase/tuberous sclerosis complex,

295 Equally AMP-activated protein kinase was not required either for

296 romyces cerevisiae ortholog of the mammalian AMP-activated protein kinase was required for the full b

297 mTORC2 downregulated the energy sensor AMP-activated protein kinase, which led to activation of

298 SLC13A5 depletion promotes activation of the AMP-activated protein kinase, which was accompanied by d

299 RLIP76(-/-) mice had baseline activation of AMP-activated protein kinase, which was not further affe

300 cts <45 yr and >65 yr, and by stimulation of AMP-activated protein kinase, with respective means of 1