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

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

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

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

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

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

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

7 erestingly, metformin-induced stimulation of AMP-activated protein kinase (a nutrient deprivation sen

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

9 Here, we show that AMPK (AMP-activated protein kinase), activated in mouse metast

10 tate (phosphocreatine:ATP) and consequently, AMP activated protein kinase activation.

11 vels independently of energy stress-mediated AMP-activated protein kinase activation and possibly thr

12 A1 showed enhanced collagen content and AMP-activated protein kinase activation in the scar, inc

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

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

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

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

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

18 rinsic interaction between the expression of AMP-activated protein kinase alpha (AMPKalpha) and the i

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

20 reperfusion recovered poorly with no phospho-AMP-activated protein kinase alpha activation, decreased

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

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

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

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

25 AMP-activated protein kinase AMPK senses and regulates c

26 Several emerging examples include AMP-activated protein kinase AMPK, nutrient/energy senso

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

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

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

30 f the energy sensor adenosine monophosphate (AMP)-activated protein kinase (AMPK) is repressed in NAS

31 course experiments revealed that PF induces AMP-activated protein kinase (AMPK) activation before in

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

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

34 AMP-activated protein kinase (AMPK) activation triggered

35 AMP-activated protein kinase (AMPK) activation vasodilat

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

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

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

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

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

41 nduced activation of autophagy, or use of 5'-AMP-activated protein kinase (AMPK) agonists, promoted t

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

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

44 eraction with the master metabolic sensor 5' AMP-activated protein kinase (AMPK) and Folliculin, a pr

45 In RGCs expressing mutated Opa1, active 5' AMP-activated protein kinase (AMPK) and its autophagy ef

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

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

48 involving stress-responsive activation of 5'-AMP-activated protein kinase (AMPK) and neuroprotective

49 cancer development through the activation of AMP-activated protein kinase (AMPK) and p38alpha.

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

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

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

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

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

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

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

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

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

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

60 Target of rapamycin complex 1 (TORC1) and AMP-activated protein kinase (AMPK) antagonistically mod

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

62 Since the discovery of AMP-activated protein kinase (AMPK) as a central regulat

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

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

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

66 Yeast AMP-activated protein kinase (AMPK) directly phosphoryla

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

68 NUAK1/2 belong to the AMP-activated protein kinase (AMPK) family, whose member

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

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

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

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

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

74 that activation of the low-energy sensor 5'-AMP-activated protein kinase (AMPK) in hepatocytes and s

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

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

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

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

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

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

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

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

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

84 The AMP-activated protein kinase (AMPK) inhibitor dorsomorph

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

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

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

88 AMP-activated protein kinase (AMPK) is a fundamental com

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

90 AMP-activated protein kinase (AMPK) is a key energy sens

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

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

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

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

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

96 The cellular energy sensor AMP-activated protein kinase (AMPK) is a metabolic hub r

97 The cellular energy sensor AMP-activated protein kinase (AMPK) is a metabolic regul

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

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

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

101 The AMP-activated protein kinase (AMPK) is a molecular senso

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

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

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

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

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

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

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

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

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

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

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

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

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

115 urthermore, the mechanism by which activated AMP-activated protein kinase (AMPK) negatively regulates

116 this effect is primarily mediated through a AMP-activated protein kinase (AMPK) pathway and a novel

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

118 We found that the AMP-activated protein kinase (AMPK) pathway mediates lep

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

120 SG improved NAFLD significantly by enhancing AMP-activated protein kinase (AMPK) phosphorylation and

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

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

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

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

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

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

127 lmodulin-dependent kinase kinase (CaMKK) and AMP-activated protein kinase (AMPK) regulate metabolic a

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

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

130 Activation of AMP-activated protein kinase (AMPK) results in vasodilat

131 AMP-activated protein kinase (AMPK) senses energetic str

132 AMP-activated protein kinase (AMPK) senses energy status

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

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

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

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

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

138 ioning (PreCon) is decreased due to impaired AMP-activated protein kinase (AMPK) signaling.

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

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

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

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

143 Signaling by the master metabolic regulator AMP-activated protein kinase (AMPK) was a critical node

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

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

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

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

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

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

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

151 AMP-activated protein kinase (AMPK), a key energy stress

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

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

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

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

156 elial cell line, we investigated the role of AMP-activated protein kinase (AMPK), a master regulator

157 AMP-activated protein kinase (AMPK), a master regulator

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

159 Inactivation of AMP-activated protein kinase (AMPK), a sensor of cellula

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

161 ti-inflammatory signaling pathways involving AMP-activated protein kinase (AMPK), Akt and eNOS, and i

162 nt and anti-inflammatory signaling involving AMP-activated protein kinase (AMPK), Akt, endothelial ni

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

166 gy sensors, which include sirtuin-1 (SIRT1), AMP-activated protein kinase (AMPK), and hypoxia inducib

167 nt and oxygen deprivation-sirtuin-1 (SIRT1), AMP-activated protein kinase (AMPK), and hypoxia-inducib

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

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

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

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

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

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

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

175 pound berberine (BBR), a potent activator of AMP-activated protein kinase (AMPK), can reduce beta-cat

176 how that HSF1, a physiological substrate for AMP-activated protein kinase (AMPK), constitutively supp

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

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

179 orin signals via the energy sensing protein, AMP-activated protein kinase (AMPK), in the autophagic d

180 ynthesis and a well-established activator of AMP-activated protein kinase (AMPK), induces widespread

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

182 ng sirtuin 1 (SIRT1), forkhead box O (FoxO), AMP-activated protein kinase (AMPK), peroxisome prolifer

183 ted with a significant activation of hepatic AMP-activated protein kinase (AMPK), peroxisome prolifer

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

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

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

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

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

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

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

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

192 TDRD7 inhibited the virus-activated AMP-activated protein kinase (AMPK), which was essential

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

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

195 e extract enhances glycolysis and attenuates AMP-activated protein kinase (AMPK)-dependent inhibition

196 sed glucose uptake in skeletal muscles in an AMP-activated protein kinase (AMPK)-dependent manner, an

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

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

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

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

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

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

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

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

205 Host hedgehog signaling was modulated in an AMP-activated protein kinase (AMPK)-mammalian target of

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

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

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

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

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

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

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

213 metformin is mediated by the stimulation of AMP-activated protein kinase (AMPK).

214 2, forming a complex that interacts with the AMP-activated protein kinase (AMPK).

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

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

217 orrelated significantly with the activity of AMP-activated protein kinase (AMPK).

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

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

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

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

222 induced starvation-like behavior mediated by AMP-activated protein kinase (AMPK).

223 mitochondrial translocation of energy sensor AMP-activated protein kinase (AMPK).

224 on glucose availability or the energy sensor AMP-activated protein kinase (AMPK).

225 and activated by the cellular energy sensor AMP-activated protein kinase (AMPK).

226 ation of CaMKK2 and the downstream kinase 5' AMP-activated protein kinase (AMPK).

227 biopsy tissue revealed misregulation of the AMP-activated protein kinase (AMPK)/4E-binding protein 1

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

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

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

231 Function of the energy-sensing AMP-activated protein kinase, AMPK, is myristoylation de

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

233 tochondria for oxidation, which responded to AMP-activated protein kinase and acetyl-CoA carboxylase

234 through a stress-responsive induction of 5'-AMP-activated protein kinase and autophagy.

235 -derived oxidative stress and stimulation of AMP-activated protein kinase and downstream signaling pa

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

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

238 nd glucagon, the cellular master switches 5' AMP-activated protein kinase and mTOR, and also numerous

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

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

241 phagic flux - mammalian target of rapamycin, AMP-activated protein kinase and sirtuins are key regula

242 f downstream protein kinases - such as AMPK (AMP-activated protein kinase) and CAMK types I and IV.

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

244 tivation of the cellular energy sensor AMPK (AMP-activated protein kinase), and decreases EC prolifer

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

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

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

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

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

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

251 ACLS1 overexpression activated AMP activated protein kinase at baseline, but during TAC

252 acrophages in vitro, heme activates an AMPK (AMP-activated protein kinase)/ATF1 (activating transcrip

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

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

255 y in the synthesis of biologically important AMP-activated protein kinase deprived of any metal Pd co

256 scle cells have lower levels of ATP and have AMP-activated protein kinase dysfunction.

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

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

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

260 ociated with the negative regulator of mTOR, AMP-activated protein kinase, have higher translational

261 infection might initiate a cross talk among AMP-activated protein kinase-Hippo-TBK1 pathways, which

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

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

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

265 downstream insulin signalling and activated AMP-activated protein kinase in HFD placenta.

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

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

268 h glucose by stimulation of glycolysis by an AMP-activated protein kinase-independent mechanism throu

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

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

271 Both direct and indirect activation of AMP-activated protein kinase isolated to the distal axon

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

273 Sestrins affect multiple signaling pathways: AMP-activated protein kinase, mammalian target of rapamy

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

275 In particular, we observed that AMP-activated protein kinase-mediated phosphorylation at

276 Finally, we show that the deletion of the AMP-activated protein kinase ortholog-encoding gene SNF1

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

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

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

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

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

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

283 In addition, this result suggests AMP-activated protein kinase signaling pathway's role in

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

285 rk highlights the ability of acute localized AMP-activated protein kinase signaling to affect mitocho

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

287 oxidative fibres and decreased activation of AMP-activated protein kinase signalling in transgenics c

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

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

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

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

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

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

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

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 PR-1, in turn, stimulates phosphorylation of AMP-activated protein kinase, which leads to phosphoryla

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

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

300 Maternal exercise activates placental AMP-activated protein kinase, which was inhibited as a r