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1 e kinase domains of AKT and was dependent on AMP-activated kinase.
2 crease in the active, phosphorylated form of AMP-activated kinase.
3 ates nonhistone proteins, including Snf1, an AMP-activated kinase.
4 polarization was also partially dependent on AMP-activated kinase.
5 AMP/ATP ratio that is sufficient to activate AMP-activated kinase.
6 3 significantly inhibited viniferin-mediated AMP-activated kinase activation and diminished the neuro
7  CD8 T cells lacking TRAF6 display defective AMP-activated kinase activation and mitochondrial fatty
8            We found that myostatin represses AMP-activated kinase activation in the heart via transfo
9 n VHL(+) cells was likely due to the reduced AMP-activated kinase activity in these cells.
10 ma membrane GLUT1 levels, possibly involving AMP-activated kinase activity.
11                           Treatment with the AMP-activated kinase agonist, AICAR, increases V(max) fo
12 kinase alpha, as compound C, an inhibitor of AMP-activated kinase alpha, abrogated endorepellin-media
13          Endorepellin functioned upstream of AMP-activated kinase alpha, as compound C, an inhibitor
14 e oxygen species (ROS) and the activation of AMP-activated kinase alpha1 (AMPK-alpha1).
15 e and in mice deficient in both apoE and the AMP-activated kinase alpha1 subunit (AMPK-alpha1) (Apoe(
16 n of cAMP-dependent protein kinase (PKA) and AMP activated kinase (AMPK) was increased in the brain,
17 d PGC1alpha and low adenosine monophosphate (AMP)-activated kinase (AMPK) activity.
18   Adenosine monophosphate-activated protein (AMP)-activated kinase (AMPK) is a highly conserved kinas
19  originating from mitochondria that sustains AMP-activated kinase (AMPK) activation and the metabolic
20 nilotinib up-regulated the phosphryaltion of AMP-activated kinase (AMPK) and protein phosphatase PP2A
21 -deficient mice also exhibit enhanced muscle AMP-activated kinase (AMPK) and reduced liver stearoyl-C
22                         The metabolic sensor AMP-activated kinase (AMPK) binds to and phosphorylates
23 tide 3-kinase-dependent activation of the 5'-AMP-activated kinase (AMPK) by peroxynitrite (ONOO-) and
24 AK1/NUAK2) and related to the PAR-1 and SNF1/AMP-Activated kinase (AMPK) families.
25   Salt-inducible kinase 2 (SIK2) is the only AMP-activated kinase (AMPK) family member known to inter
26                                              AMP-activated kinase (AMPK) has been implicated in regul
27 mines the role of protein kinase C (PKC) and AMP-activated kinase (AMPK) in acetaminophen (APAP) hepa
28       Our results show a rapid activation of AMP-activated kinase (AMPK) in macrophages upon exposure
29                                Activation of AMP-activated kinase (AMPK) in skeletal muscle increases
30  We recently found that the metabolic sensor AMP-activated kinase (AMPK) inhibits the epithelial Na+
31                                              AMP-activated kinase (AMPK) is a fuel-sensing enzyme pre
32                                              AMP-activated kinase (AMPK) is a key player in energy se
33                                              AMP-activated kinase (AMPK) is a ubiquitous metabolic se
34                                              AMP-activated kinase (AMPK) is an evolutionarily conserv
35 overexpression of a constitutively active 5'-AMP-activated kinase (AMPK) mutant or a kinase-inactive
36 test whether the ubiquitous metabolic sensor AMP-activated kinase (AMPK) regulates ENaC, we examined
37                                          The AMP-activated kinase (AMPK) senses the energy status of
38 through the reactive oxygen species-mediated AMP-activated kinase (AMPK) signaling pathway.
39 ch, stimulates production of ROS to activate AMP-activated kinase (AMPK) to increase glucose uptake.
40                             In addition, the AMP-activated kinase (AMPK) was shown to be activated.
41                                              AMP-activated kinase (AMPK), a metabolic sensor, was act
42 yme thought to be activated during CR is the AMP-activated kinase (AMPK), a sensor of cellular energy
43 ction of leptin, concomitant with inhibiting AMP-activated kinase (AMPK), activates acetyl-CoA carbox
44                     Here, we report that the AMP-activated kinase (AMPK), an enzyme involved in respo
45 that Abeta42 oligomers trigger activation of AMP-activated kinase (AMPK), and its activation is incre
46 ucose on LCFA metabolism, assess the role of AMP-activated Kinase (AMPK), and to establish if changes
47 t to Akt, ONOO(-) significantly activated 5'-AMP-activated kinase (AMPK), as evidenced by its increas
48 lin-dependent protein kinase beta, activates AMP-activated kinase (AMPK), leading to increased glucos
49 d the AMP/ATP ratio, subsequently activating AMP-activated kinase (AMPK), leading to increased stress
50  Here we show that TPr stimulation activates AMP-activated kinase (AMPK), which in turn limits TPr-in
51 lowers serum glucose levels by activating 5'-AMP-activated kinase (AMPK), which maintains energy home
52 ins cellular energy resources and stimulates AMP-activated kinase (AMPK).
53 via activation of the cellular energy sensor AMP-activated kinase (AMPK).
54 to determine if free fatty acid inhibits the AMP-activated kinase (AMPK).
55 tes activate the intracellular energy sensor AMP-activated kinase (AMPK).
56                          Viniferin activates AMP-activated kinase and enhances mitochondrial biogenes
57                                 DAF-18/PTEN, AMP-activated kinase and fatty acid biosynthesis are als
58            Snf1 is the ortholog of mammalian AMP-activated kinase and is responsible for activation o
59                                              AMP-activated kinase and mammalian target of rapamycin c
60 67 expression by inducing phosphorylation of AMP-activated kinase and subsequent mTOR proproliferativ
61 rapamycin activated a protein kinase Calpha, AMP-activated kinase, and CREB-dependent vasculoprotecti
62 or calcium/calmodulin protein kinase kinase, AMP-activated kinase, and RhoA/ROCK.
63 rks--those centered on Ras/protein kinase A, AMP-activated kinase, and target of rapamycin complex I,
64             This regulation involved a novel AMP-activated kinase-dependent Sirt2 phosphorylation at
65  of an adenovirus encoding dominant-negative AMP-activated kinase diminished the improvement in limb
66  ATP hydrolysis, is associated with elevated AMP-activated kinase function, and, if triggered by this
67                             Mutations of the AMP-activated kinase gamma 2 subunit (AMPKgamma2), N488I
68 active oxygen species-mediated activation of AMP-activated kinase in Huh7.5 cells during HCV (JFH-1)-
69                                Inhibition of AMP-activated kinase in vivo rescued cardiac hypertrophy
70 involves phosphorylation of nutrient-sensing AMP-activated kinase, inhibition of rapamycin-sensitive
71       In this study, we identified MARK4, an AMP-activated kinase-related kinase, as a negative regul
72  in response to ischemic stress by promoting AMP-activated kinase signaling.
73 pletion, Mig1 is phosphorylated by the yeast AMP-activated kinase Snf1 and exported into the cytoplas
74 ng pathways, including Ras/protein kinase A, AMP-activated kinase, the high-osmolarity response mitog
75 of intracellular protein kinases, PKA, Snf1p/AMP-activated kinase, TOR, Gcn2p, and the cyclin-depende
76  mechanism for how metformin activates AMPK (AMP-activated kinase) was investigated in isolated skele
77 Vps34 is also inhibited by activation of the AMP-activated kinase, which inhibits mTOR/S6K1 in glucos

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