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 y gluconeogenetic enzyme phosphoenolpyruvate carboxykinase.

4 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

5 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

6 nd the cytosolic form of phosphoenolpyruvate carboxykinase.

7 lucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

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

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

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

11 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase 1 (PCK1) has negative consequences for blo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 Phosphoenolpyruvate carboxykinase activity is comparable to mature animals a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 Phosphoenolpyruvate carboxykinase catalyzes the reversible decarboxylation o

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

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

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

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

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

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

61 ver gluconeogenic enzyme phosphoenolpyruvate carboxykinase expression and activity.

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

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

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

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

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

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

68 3 (gAF3) elements in the phosphoenolpyruvate carboxykinase gene glucocorticoid response unit.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 to down-regulate hepatic phosphoenolpyruvate carboxykinase mRNA expression.

95 fold increase in hepatic phosphoenolpyruvate carboxykinase mRNA levels.

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

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

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

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

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

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

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

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

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

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

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

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

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

109 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PCK1) expression, key regulators of hepat

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

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

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

113 -6-phosphatase (G6P) and phosphoenolpyruvate carboxykinase (PEPCK) activities were investigated in sh

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

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

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

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

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

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

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

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

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

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

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

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

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

127 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the first committed step

128 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the first committed step

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Phosphoenolpyruvate carboxykinase (PEPCK) is regulated solely by alterations

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 4-(13)C]oxaloacetate via phosphoenolpyruvate carboxykinase (PEPCK), forward TCA cycle flux of [4-(13)

191 8 and increase levels of phosphoenolpyruvate carboxykinase (PEPCK), glucose-6-phosphatase, and peroxi

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

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

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

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

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

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

198 6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (Pepck), two gluconeogenetic genes, along

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

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

201 patic gluconeogenic gene phosphoenolpyruvate carboxykinase (PEPCK).

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

203 1alpha (PGC-1alpha) and phosphoenolpyruvate carboxykinase (PEPCK).

204 increased expression of phosphoenolpyruvate carboxykinase (PEPCK).

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

206 uconeogenesis, including phosphoenolpyruvate carboxykinase (PEPCK).

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

208 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

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

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

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

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

213 cluding both isoforms of phosphoenolpyruvate carboxykinase (pepck).

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

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

216 the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

232 er the regulation of the phosphoenolpyruvate carboxykinase promoter.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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