ライフサイエンスコーパス: carboxykinase

1 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

2 ed expression of hepatic phosphoenolpyruvate carboxykinase.

3 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

4 y gluconeogenetic enzyme phosphoenolpyruvate carboxykinase.

5 glucose-6-phosphtase and phosphoenolpyruvate carboxykinase.

6 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

7 nd the cytosolic form of phosphoenolpyruvate carboxykinase.

8 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

9 of the gene that encodes phosphoenolpyruvate carboxykinase 1 (a protein involved in gluconeogenesis)

10 ted that the activity of phosphoenolpyruvate carboxykinase 1 (AT4G37870), a key enzyme in gluconeogen

11 coneogenic genes such as phosphoenolpyruvate carboxykinase 1 (Pck-1) and glucose 6-phosphatase (G6Pas

12 ey gluconeogenic enzymes phosphoenolpyruvate carboxykinase 1 (PCK1) and glucose-6 phosphatase (G6PC)

13 for transcription of the phosphoenolpyruvate carboxykinase 1 (PCK1) gene to increase liver gluconeoge

14 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase 1 (PCK1) has negative consequences for blo

15 via genetic knockdown of phosphoenolpyruvate carboxykinase 1 (Pck1) prevented fatty acid-induced rise

16 escued by overexpressing phosphoenolpyruvate carboxykinase 1 (PCK1), a PEP regulator.

17 investigate the role of phosphoenolpyruvate carboxykinase 1 (PCK1), an enzyme involved in gluconeoge

18 en phosphorylase (PYGL), phosphoenolpyruvate carboxykinase 1 (PCK1), and the glucose-6-phosphatase ca

19 phosphorylates cytosolic phosphoenolpyruvate carboxykinase 1 (PCK1), the rate-limiting enzyme in gluc

20 hrough overexpression of phosphoenolpyruvate carboxykinase 1 (PCK1), which bolstered effector functio

21 ase 2 (SGK2) to activate phosphoenolpyruvate carboxykinase 1 (PEPCK1) and glucose-6-phosphatase (G6Pa

22 rum glucagon and hepatic phosphoenolpyruvate carboxykinase 1 (PEPCK1) expression, without affecting i

23 Phosphoenolpyruvate carboxykinase 1 (PEPCK1) is the critical enzyme for gluc

24 lytic subunit (G6Pc) and phosphoenolpyruvate carboxykinase 1 (PEPCK1).

25 R effects on fetal liver phosphoenolpyruvate carboxykinase 1 (protein, PEPCK1; gene, PCK1 orthologous

26 his treatment normalizes phosphoenolpyruvate carboxykinase 1 contents without affecting glycogen leve

27 ced transcription of the phosphoenolpyruvate carboxykinase 1 gene was strikingly increased in cryptoc

28 decreased the levels of phosphoenolpyruvate carboxykinase 1 mRNA in mice but not in Car(-/-) mice.

29 response element in the phosphoenolpyruvate carboxykinase 1 promoter in a hormone-dependent manner,

30 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase 1 were increased in hPXR mice compared wit

31 ncreased mRNA levels for phosphoenolpyruvate carboxykinase 1, argininosuccinate synthase 1, sodium/gl

32 zyme in gluconeogenesis, phosphoenolpyruvate carboxykinase 1, is regulated through reversible acetyla

33 f metabolism transcripts Phosphoenolpyruvate carboxykinase-1, 4-Hydroxyphenylpyruvate dioxygenase, Di

34 y bound to mitochondrial phosphoenolpyruvate carboxykinase 2 ( Pck2) mRNA and increased its transcrip

35 arboxykinase (PEPCK) and phosphoenolpyruvate carboxykinase 2 (PCK2) to reprogram anabolic metabolism

36 reased the expression of phosphoenolpyruvate carboxykinase 2 (PEPCK), glucose-6-phosphatase (G6Pase)

37 ess with an inhibitor of phosphoenolpyruvate carboxykinase (3-mercaptopicolinic acid), metastatic, ER

38 patic mRNA expression of phosphoenolpyruvate carboxykinase, a well known rate-limiting enzyme of live

39 voprotein subunit alpha, phosphoenolpyruvate carboxykinase, aconitate hydratase, branched-chain alpha

40 mutant lacked detectable phosphoenolpyruvate carboxykinase activity and grew poorly in the absence of

41 Phosphoenolpyruvate carboxykinase activity is comparable to mature animals a

42 te carboxylase was low in muscle, and no PEP carboxykinase activity was detected.

43 ly related IRSs from the phosphoenolpyruvate carboxykinase and apolipoprotein CIII genes also are eff

44 rPDK4 gene but also with phosphoenolpyruvate carboxykinase and CPT-1a (carnitine palmitoyltransferase

45 on in KO mice stimulated phosphoenolpyruvate carboxykinase and G6Pase mRNA abundance and raised the b

46 he gluconeogenic enzymes phosphoenolpyruvate carboxykinase and G6Pase mRNAs was reduced by more than

47 ressed mRNA abundance of phosphoenolpyruvate carboxykinase and glucose-6-phosphatase (G6Pase) in KO m

48 the cytosolic isoform of phosphoenolpyruvate carboxykinase and glucose-6-phosphatase were reduced, tr

49 gluconeogenesis such as phosphoenolpyruvate carboxykinase and glucose-6-phosphatase when HNF4alpha i

50 l gluconeogenic enzymes, phosphoenolpyruvate carboxykinase and glucose-6-phosphatase, above the level

51 gluconeogenic, including phosphoenolpyruvate carboxykinase and glucose-6-phosphatase, and also activa

52 eogenic genes, including phosphoenolpyruvate carboxykinase and glucose-6-phosphatase.

53 hepatic gluconeogenesis, phosphoenolpyruvate carboxykinase and glucose-6-phosphatase.

54 lved in gluconeogenesis (phosphoenolpyruvate carboxykinase and glycogen synthase) and sinusoidal bile

55 We show that lack of phosphoenolpyruvate carboxykinase and isocitrate lyase, two enzymes necessar

56 ynamics and catalysis in phosphoenolpyruvate carboxykinase and other enzymes in which the transition

57 ally, we determined that phosphoenolpyruvate carboxykinase and synthase do not carry flux at these ex

58 of two key genes: PEPCK (phosphoenolpyruvate carboxykinase) and SREBP-1c (sterol regulatory element-b

59 r gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, and fructose-1,6-bisphosphatase was also

60 liver glycogen synthase, phosphoenolpyruvate carboxykinase, and glucose-6-phosphatase remained at nor

61 element-binding protein, phoshoenolpyruvate carboxykinase, and peroxisome proliferator-activated rec

62 er-type pyruvate kinase, phosphoenolpyruvate carboxykinase, and type I deiodinase but not hydroxymeth

63 e, isocitrate lyase, and phosphoenolpyruvate carboxykinase are induced.

64 d gluconeogenic enzymes (phosphoenolpyruvate carboxykinase), as well as the diet-responsive type I de

65 lucose-6 phosphatase and phosphoenolpyruvate carboxykinase, as well as a marked increase in hepatic n

66 Phosphoenolpyruvate carboxykinase catalyzes the reversible decarboxylation o

67 The pckA gene, encoding phosphoenolpyruvate carboxykinase, catalyzes the reversible decarboxylation

68 lation (anaplerosis) and phosphoenolpyruvate carboxykinase (cataplerosis) and decreased flux through

69 of the cytosolic form of phosphoenolpyruvate carboxykinase caused a marked extension of the life span

70 etate (OAA) by cytosolic phosphoenolpyruvate carboxykinase (cPEPCK) were investigated by the systemat

71 nse element found in the phosphoenolpyruvate carboxykinase-cytosolic (PEPCK-C) promoter.

72 Transcripts encoding phosphoenolpyruvate carboxykinase did not appear to be regulated by pCO(2) i

73 ctose bisphosphatase and phosphoenolpyruvate carboxykinase (encoded by ICL1, MAS1, TAL1, FBP1, and PC

74 ver gluconeogenic enzyme phosphoenolpyruvate carboxykinase expression and activity.

75 se activity and increased phosphenolpyruvate carboxykinase expression and correlated with increased p

76 In addition, increased phosphoenolpyruvate carboxykinase expression in DHet mouse liver was reverse

77 the observed increase in phosphoenolpyruvate carboxykinase expression, type IA fibers, and mitochondr

78 etabolic genes including phosphoenolpyruvate carboxykinase, fatty acid synthase, carnitine palmitoylt

79 s glucose-6-phosphatase, phosphoenolpyruvate carboxykinase, fructose-1,6-phosphatase, respectively, a

80 tes expression of PEPCK (phosphoenolpyruvate carboxykinase), G6P (glucose-6-phosphatase), and certain

81 (IRS-1), and it reduces phosphoenolpyruvate carboxykinase gene expression in a phosphoinositide 3-ki

82 3 (gAF3) elements in the phosphoenolpyruvate carboxykinase gene glucocorticoid response unit.

83 ere also observed in the phosphoenolpyruvate carboxykinase gene that contains a functional HNF-4-bind

84 he complete induction of phosphoenolpyruvate carboxykinase gene transcription by glucocorticoids.

85 ion of hormone-activated phosphoenolpyruvate carboxykinase gene transcription by glucose was not affe

86 for insulin (in the rat phosphoenolpyruvate carboxykinase gene), glucocorticoids, cAMP, and phorbol

87 ing the promoter for the phosphoenolpyruvate carboxykinase gene, conditional, tissue-specific express

88 nd hepatic expression of phosphoenolpyruvate carboxykinase, glucose-6-phosphatase, and fatty acid syn

89 c gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, glucose-6-phosphatase, and fructose 1,6-b

90 L-iNOS-Tg mice, whereas phosphoenolpyruvate carboxykinase, glucose-6-phosphatase, and proliferator-a

91 ession of genes encoding phosphoenolpyruvate carboxykinase, glycogen synthase, and factor IX was also

92 or the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (EC ) (PEPCK-C).

93 Phosphoenolpyruvate carboxykinase (GTP) (EC 4.1.1.32) (PEPCK) is a key enzym

94 binds to a region of the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene promoter adjacent to th

95 tor-I (NFI) binds to the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene promoter immediately 5'

96 or the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (4.1.1.32) during diabetes

97 ne in which the cDNA for phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (EC 4.1.1.32) was linked t

98 or the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C).

99 ng the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C).

100 atis GTP-dependent phosphoenolpyruvate (PEP) carboxykinase (GTP-PEPCK) were investigated.

101 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase in the leptin-infused fetuses were lower t

102 scuss the role played by phosphoenolpyruvate carboxykinase in this process.

103 including Glc-6-Pase and phosphoenolpyruvate carboxykinase, in an ROR-dependent manner.

104 cript abundance of PHOSPHOENOLPYRUVATE (PEP) CARBOXYKINASE increased during fruit ripening and was ne

105 olinate, an inhibitor of phosphoenolpyruvate carboxykinase, indicating that it is not due to increase

106 e-1,6-bisphosphatase and phosphoenolpyruvate carboxykinase, is repressed by glucose.

107 he gluconeogenic enzyme, phosphoenolpyruvate carboxykinase-M (Pck2/PEPCK-M), increased during treatme

108 g protein (P-CREB), and phosphoenol pyruvate carboxykinase, markers of glucagon action, rose dramatic

109 to down-regulate hepatic phosphoenolpyruvate carboxykinase mRNA expression.

110 fold increase in hepatic phosphoenolpyruvate carboxykinase mRNA levels.

111 creased, whereas that of phosphoenolpyruvate carboxykinase mRNA was increased compared with Leptin -.

112 ment binding protein and phosphoenolpyruvate carboxykinase mRNA were profoundly reduced compared with

113 iver pyruvate kinase and phosphoenolpyruvate carboxykinase mRNA were unchanged by the manipulation of

114 atic glucose production, phosphoenolpyruvate carboxykinase mRNA, and plasma FFA to a similar extent i

115 ally upregulated by HIF-1, including the PEP carboxykinase PCK-1, a rate-limiting mediator of glucone

116 oneogenic pathway enzyme phosphoenolpyruvate carboxykinase (Pck) also increased under these condition

117 lic enzyme (NADP-ME) and phosphoenolpyruvate carboxykinase (PCK) photosynthetic pathways was twofold

118 energy-conserving phosphoenolpyruvate (PEP) carboxykinase (pck), which normally functions in the rev

119 Although phosphoenolpyruvate carboxykinase (Pck)-1 expression was unchanged, its inhi

120 brate-type GTP-dependent phosphoenolpyruvate carboxykinase (PCK).

121 his relies on the enzyme phosphoenolpyruvate carboxykinase (PCK).

122 Phosphoenolpyruvate carboxykinase (Pck; EC 4.1.1.32) is the enzyme at the ce

123 s between MDH2 and yeast phosphoenolpyruvate carboxykinase (PCK1) and between MDH2 and fructose-1,6-b

124 metabolism by targeting phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-phosphatase (G6PC), k

125 tic gluconeogenic genes, phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-phosphatase (G6PC).

126 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PCK1) expression, key regulators of hepat

127 he activity of cytosolic phosphoenolpyruvate carboxykinase (PCK1), a key enzyme in gluconeogenesis, b

128 sites (Lys19 and 514) of phosphoenolpyruvate carboxykinase (Pck1p) were determined by tandem mass spe

129 beta-cell PKm1, PKm2, and mitochondrial PEP carboxykinase (PCK2) that generates mitochondrial PEP.

130 show that mitochondrial phosphoenolpyruvate carboxykinase (PCK2), the hub molecule linking tricarbox

131 tamine via the activity of mitochondrial PEP-carboxykinase (PCK2).

132 ial gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PCK2, mitochondrial isoform).

133 -6-phosphatase (G6P) and phosphoenolpyruvate carboxykinase (PEPCK) activities were investigated in sh

134 Phosphoenolpyruvate carboxykinase (PEPCK) activity (carboxylating) in Udotea

135 significantly inhibited phosphoenolpyruvate carboxykinase (PEPCK) and accelerated fibroblast cell mi

136 glycogenolytic enzymes, phosphoenolpyruvate carboxykinase (Pepck) and glucose-6-phosphatase (G6p).

137 ed with normal levels of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase (G6Pase)

138 Hepatic gene expression of P-enolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase (Glc-6-P

139 criptional expression of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase, catalyt

140 genic enzymes, including phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase, leading

141 neogenic enzymes such as phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase.

142 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) and impairs insulin signalling in

143 e elements (IREs) of the phosphoenolpyruvate carboxykinase (PEPCK) and insulin-like growth factor-bin

144 decarboxylation enzymes phosphoenolpyruvate carboxykinase (PEPCK) and malic enzyme (ME) did not chan

145 he gluconeogenic enzymes phosphoenolpyruvate carboxykinase (PEPCK) and phosphoenolpyruvate carboxykin

146 t of decreased cytosolic phosphoenolpyruvate carboxykinase (PEPCK) and plastidic NADP-dependent malic

147 lation of Glc-6-Pase and phosphoenolpyruvate carboxykinase (PEPCK) by apoA-IV was determined by lucif

148 ng Leishmania glycosomal phosphoenolpyruvate carboxykinase (PEPCK) by EP and again found that the int

149 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the first committed step

150 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the first committed step

151 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the rate-limiting step i

152 The enzyme phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the reversible conversio

153 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) demonstrate that PEPCK contains a

154 , we reveal two discrete phosphoenolpyruvate carboxykinase (PEPCK) enzymes in the parasite, one of wh

155 pendent assays: reducing phosphoenolpyruvate carboxykinase (PEPCK) expression in hepatocytes and acti

156 Phosphoenolpyruvate carboxykinase (PEPCK) expression plays a critical role i

157 e change was evident for phosphoenolpyruvate carboxykinase (PEPCK) expression, pyruvate kinase expres

158 takes a fold similar to phosphoenolpyruvate carboxykinase (PEPCK) from Escherichia coli as recently

159 bile acid synthesis and phosphoenolpyruvate carboxykinase (PEPCK) gene in gluconeogenesis.

160 is the core motif of the phosphoenolpyruvate carboxykinase (PEPCK) gene IRS.

161 The phosphoenolpyruvate carboxykinase (PEPCK) gene is a case in point.

162 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is induced by glucagon, actin

163 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is induced upon activation of

164 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is regulated by a variety of

165 mple by showing that the phosphoenolpyruvate carboxykinase (PEPCK) gene knockout ( pepck) leads to th

166 e element (RARE1) in the phosphoenolpyruvate carboxykinase (PEPCK) gene promoter confers approximatel

167 The phosphoenolpyruvate carboxykinase (PEPCK) gene promoter contains a glucocort

168 element (CRE) of the rat phosphoenolpyruvate carboxykinase (PEPCK) gene promoter is required for a co

169 rticoid induction of the phosphoenolpyruvate carboxykinase (PEPCK) gene requires a glucocorticoid res

170 rlying increased hepatic phosphoenolpyruvate carboxykinase (PEPCK) gene transcription and gluconeogen

171 pattern of induction of phosphoenolpyruvate carboxykinase (PEPCK) gene transcription by cAMP and its

172 Activation of phosphoenolpyruvate carboxykinase (PEPCK) gene transcription in response to

173 fold increase in hepatic phosphoenolpyruvate carboxykinase (PEPCK) gene transcription through two low

174 P-stimulated increase in phosphoenolpyruvate carboxykinase (PEPCK) gene transcription.

175 mice overexpressing the phosphoenolpyruvate carboxykinase (PEPCK) gene under control of its own prom

176 of transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene, which encodes a key gluconeo

177 x native promoter in the phosphoenolpyruvate carboxykinase (PEPCK) gene.

178 pstream of the cytosolic phosphoenolpyruvate carboxykinase (PEPCK) gene.

179 ne the role of cytosolic phosphoenolpyruvate carboxykinase (PEPCK) in hepatic energy metabolism.

180 hrough downregulation of phosphoenolpyruvate carboxykinase (PEPCK) in wild-type (WT) mouse liver.

181 n of Akt, which inhibits phosphoenolpyruvate carboxykinase (PEPCK) induction, causing severe hypoglyc

182 Phosphoenolpyruvate carboxykinase (PEPCK) is a gluconeogenic enzyme with a c

183 gene encoding cytosolic phosphoenolpyruvate carboxykinase (PEPCK) is a PPARgamma/RXR target gene in

184 Phosphoenolpyruvate carboxykinase (PEPCK) is a rate-controlling enzyme in he

185 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) is activated by Cr2+ as the sole a

186 Phosphoenolpyruvate carboxykinase (PEPCK) is an essential metabolic enzyme o

187 Phosphoenolpyruvate carboxykinase (PEPCK) is present in ripening tomato frui

188 Phosphoenolpyruvate carboxykinase (PEPCK) is regulated solely by alterations

189 cription of the gene for phosphoenolpyruvate carboxykinase (PEPCK) is stimulated by thyroid hormone (

190 Phosphoenolpyruvate carboxykinase (PEPCK) is well known for its role in gluc

191 d receptor (GR) mRNA and phosphoenolpyruvate carboxykinase (PEPCK) mRNA (and activity) are increased

192 Liver-specific phosphoenolpyruvate carboxykinase (PEPCK) null mice, when fasted, maintain n

193 ne present in the enzyme phosphoenolpyruvate carboxykinase (PEPCK) of the organisms Caenorhabditis el

194 rabbit CRP from the rat phosphoenolpyruvate carboxykinase (PEPCK) promoter in response to gluconeoge

195 elial cells, we used the phosphoenolpyruvate carboxykinase (PEPCK) promoter to generate transgenic mi

196 The phosphoenolpyruvate carboxykinase (PEPCK) promoter was used as a model syste

197 se sequence (IRS) of the phosphoenolpyruvate carboxykinase (PEPCK) promoter, located within the gluco

198 under the control of the phosphoenolpyruvate carboxykinase (PEPCK) promoter, were developed as an app

199 ession was driven by the phosphoenolpyruvate carboxykinase (PEPCK) promoter, which gives high level e

200 he reaction catalyzed by phosphoenolpyruvate carboxykinase (PEPCK) provides significant insight into

201 rat cytosolic isoform of phosphoenolpyruvate carboxykinase (PEPCK) reported in the PEPCK-Mn2+, -Mn2+-

202 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) requires two divalent cations for

203 hosphatase (Glc-6-P) and phosphoenolpyruvate carboxykinase (Pepck) to an extent similar to both AICAR

204 ort gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) transcription and associated trans

205 Avian mitochondrial phosphoenolpyruvate carboxykinase (PEPCK) was incubated with Co2+ and H2O2 t

206 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) was rapidly inactivated by micromo

207 ures of the human enzyme phosphoenolpyruvate carboxykinase (PEPCK) with and without bound substrates.

208 sion of transcription of phosphoenolpyruvate carboxykinase (PEPCK), a key regulator of gluconeogenesi

209 The gene for phosphoenolpyruvate carboxykinase (PEPCK), a target of CCAAT/enhancer-bindin

210 We provide evidence that phosphoenolpyruvate carboxykinase (PEPCK), an enzyme involved in malate meta

211 key gluconeogenic genes, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase

212 tivator-1 alpha (PGC-1), phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase express

213 of glycerol kinase (GK), phosphoenolpyruvate carboxykinase (PEPCK), and pyruvate phosphate dikinase (

214 4-(13)C]oxaloacetate via phosphoenolpyruvate carboxykinase (PEPCK), forward TCA cycle flux of [4-(13)

215 8 and increase levels of phosphoenolpyruvate carboxykinase (PEPCK), glucose-6-phosphatase, and peroxi

216 ey gluconeogenic enzyme, phosphoenolpyruvate carboxykinase (PEPCK), has been shown to provide metabol

217 ponsive sequences of the phosphoenolpyruvate carboxykinase (PEPCK), IGFBP-1, and G6Pase promoters.

218 tivator-1a (PGC-1alpha), phosphoenolpyruvate carboxykinase (PEPCK), pyruvate carboxylase, and glucose

219 Regulation of phosphoenolpyruvate carboxykinase (PEPCK), the key gene in gluconeogenesis,

220 nduction of the gene for phosphoenolpyruvate carboxykinase (PEPCK), the rate-limiting enzyme in gluco

221 Expression of phosphoenolpyruvate carboxykinase (PEPCK), the rate-limiting step in hepatic

222 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (Pepck), two gluconeogenetic genes, along

223 In phosphoenolpyruvate carboxykinase (PEPCK)-GFP mice, serial MPM found PEC-to-

224 phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

225 patic gluconeogenic gene phosphoenolpyruvate carboxykinase (PEPCK).

226 phatase (Glc-6-Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

227 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

228 1alpha (PGC-1alpha) and phosphoenolpyruvate carboxykinase (PEPCK).

229 increased expression of phosphoenolpyruvate carboxykinase (PEPCK).

230 phatase (Glc-6-Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

231 uconeogenesis, including phosphoenolpyruvate carboxykinase (PEPCK).

232 cription of the gene for phosphoenolpyruvate carboxykinase (PEPCK).

233 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

234 eogenic enzymes, such as phosphoenolpyruvate carboxykinase (PEPCK).

235 ne present in the enzyme phosphoenolpyruvate carboxykinase (PEPCK).

236 protein-1 (IGFBP-1) and phosphoenolpyruvate carboxykinase (PEPCK).

237 ce the cytosolic form of phosphoenolpyruvate carboxykinase (PEPCK).

238 cription of the gene for phosphoenolpyruvate carboxykinase (PEPCK).

239 cluding both isoforms of phosphoenolpyruvate carboxykinase (pepck).

240 omes by kinases, such as phosphoenolpyruvate carboxykinase (PEPCK).

241 ase kinase 4 (pdk4), and phosphoenolpyruvate carboxykinase (pepck).

242 phosphatase (G6pase) and phosphoenolpyruvate carboxykinase (Pepck).

243 alic enzyme (NAD-ME) and phosphoenolpyruvate carboxykinase (PEPCK).

244 ly identified Leishmania phosphoenolpyruvate carboxykinase (PEPCK, a gluconeogenic enzyme) as an immu

245 c flux through cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) and associated pathways.

246 he cytosolic form of the phosphoenolpyruvate carboxykinase (PEPCK-C) gene is selectively expressed in

247 mitochondrial isoform of phosphoenolpyruvate carboxykinase (PEPCK-M) is the GTPase linking hydrolysis

248 Mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M), encoded by the nuclear PCK2 gen

249 files of selected genes (phosphoenolpyruvate carboxykinase - PEPCK, glucocorticoid receptor - GR, and

250 ROP (repressor of phosphoenolpyruvate carboxykinase, PEPCK) is a methanol- and biotin starvati

251 , a classic inhibitor of phosphoenolpyruvate carboxykinase, photosynthetic O(2) evolution was reduced

252 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase, presumably, because of relative intrahepa

253 enolpyruvate carboxylase/phosphoenolpyruvate carboxykinase process that decreases as the parasite mat

254 F1-CRP) regulated by the phosphoenolpyruvate carboxykinase promoter such that levels could be altered

255 ver under control of the phosphoenolpyruvate carboxykinase promoter were generated.

256 mice that expressed the phosphoenolpyruvate carboxykinase promoter-driven BMP-7 transgene and nondia

257 er the regulation of the phosphoenolpyruvate carboxykinase promoter.

258 he reaction catalyzed by phosphoenolpyruvate carboxykinase provide direct structural evidence for the

259 under control of the rat phosphoenolpyruvate carboxykinase regulatory sequences developed fibrosis of

260 cohol dehydrogenase, and phosphoenolpyruvate carboxykinase) that indicate the potential mechanisms co

261 cycle first and then use phosphoenolpyruvate carboxykinase to initiate gluconeogenesis; and (v) (13)C

262 veral HNF3 target genes (phosphoenolpyruvate carboxykinase, transferrin, tyrosine aminotransferase) w

263 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase, two key targets for FoxO1 in the regulati

264 n such as those encoding phosphoenolpyruvate carboxykinase, tyrosine aminotransferase, and insulin-li

265 -inducible genes such as phosphoenolpyruvate carboxykinase was maintained when cellular protein synth

266 ralobular distribution of phosphenolpyruvate carboxykinase was unaltered, though overall increased ac

267 cohol dehydrogenase, and phosphoenolpyruvate carboxykinase, was also affected in some of the microcel

268 ic and the mitochondrial phosphoenolpyruvate carboxykinase were elevated after 24 hours of NMP, more

269 s (NADP-malic enzyme and phosphoenolpyruvate carboxykinase) were critical for matching ATP and reduce

270 es, isocitrate lyase and phosphoenolpyruvate carboxykinase, were also degraded in the vacuole via the

271 esis controller, hepatic phosphoenolpyruvate carboxykinase, were significantly elevated in response t

272 st gluconeogenic enzyme, phosphoenolpyruvate carboxykinase, when acetate was the carbon source, sugge

273 the citric acid cycle intermediates via PEP carboxykinase, whereas another could involve reversal of