ライフサイエンスコーパス: phosphoenolpyruvate carboxykinase

1 luconeogenic genes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

2 explained by increased expression of hepatic phosphoenolpyruvate carboxykinase.

3 uconeogenic genes, glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

4 RNA levels of the key gluconeogenetic enzyme phosphoenolpyruvate carboxykinase.

5 uconeogenic enzymes glucose-6-phosphtase and phosphoenolpyruvate carboxykinase.

6 coneogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

7 cose-6-phosphatase and the cytosolic form of phosphoenolpyruvate carboxykinase.

8 ls for the enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

9 eased transcription of the gene that encodes phosphoenolpyruvate carboxykinase 1 (a protein involved

10 re detail and indicated that the activity of phosphoenolpyruvate carboxykinase 1 (AT4G37870), a key e

11 nhibited hepatic gluconeogenic genes such as phosphoenolpyruvate carboxykinase 1 (Pck-1) and glucose

12 g2 and Yy1 induced key gluconeogenic enzymes phosphoenolpyruvate carboxykinase 1 (PCK1) and glucose-6

13 ts as a coactivator for transcription of the phosphoenolpyruvate carboxykinase 1 (PCK1) gene to incre

14 nic enzymes glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase 1 (PCK1) has negative

15 erosis/cataplerosis via genetic knockdown of phosphoenolpyruvate carboxykinase 1 (Pck1) prevented fat

16 D3/ICOS beads were rescued by overexpressing phosphoenolpyruvate carboxykinase 1 (PCK1), a PEP regula

17 Here, we investigate the role of phosphoenolpyruvate carboxykinase 1 (PCK1), an enzyme in

18 cluding liver glycogen phosphorylase (PYGL), phosphoenolpyruvate carboxykinase 1 (PCK1), and the gluc

19 rcinoma (HCC) cells phosphorylates cytosolic phosphoenolpyruvate carboxykinase 1 (PCK1), the rate-lim

20 ing PEP production through overexpression of phosphoenolpyruvate carboxykinase 1 (PCK1), which bolste

21 ticoid regulated kinase 2 (SGK2) to activate phosphoenolpyruvate carboxykinase 1 (PEPCK1) and glucose

22 leled by elevated serum glucagon and hepatic phosphoenolpyruvate carboxykinase 1 (PEPCK1) expression,

23 Phosphoenolpyruvate carboxykinase 1 (PEPCK1) is the crit

24 e-6-phosphatase catalytic subunit (G6Pc) and phosphoenolpyruvate carboxykinase 1 (PEPCK1).

25 We determined MNR effects on fetal liver phosphoenolpyruvate carboxykinase 1 (protein, PEPCK1; ge

26 Furthermore, this treatment normalizes phosphoenolpyruvate carboxykinase 1 contents without aff

27 d dexamethasone-induced transcription of the phosphoenolpyruvate carboxykinase 1 gene was strikingly

28 t with TCPOBOP or PB decreased the levels of phosphoenolpyruvate carboxykinase 1 mRNA in mice but not

29 ith a glucocorticoid response element in the phosphoenolpyruvate carboxykinase 1 promoter in a hormon

30 l hepatic levels of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase 1 were increased in hP

31 EDV administration increased mRNA levels for phosphoenolpyruvate carboxykinase 1, argininosuccinate s

32 the rate-limiting enzyme in gluconeogenesis, phosphoenolpyruvate carboxykinase 1, is regulated throug

33 ify downregulation of metabolism transcripts Phosphoenolpyruvate carboxykinase-1, 4-Hydroxyphenylpyru

34 ally, Lin28a directly bound to mitochondrial phosphoenolpyruvate carboxykinase 2 ( Pck2) mRNA and inc

35 hosphoenolpyruvate carboxykinase (PEPCK) and phosphoenolpyruvate carboxykinase 2 (PCK2) to reprogram

36 with shizukaol F decreased the expression of phosphoenolpyruvate carboxykinase 2 (PEPCK), glucose-6-p

37 king this novel process with an inhibitor of phosphoenolpyruvate carboxykinase (3-mercaptopicolinic a

38 lucose levels and hepatic mRNA expression of phosphoenolpyruvate carboxykinase, a well known rate-lim

39 lectron transfer flavoprotein subunit alpha, phosphoenolpyruvate carboxykinase, aconitate hydratase,

40 A pckA mutant lacked detectable phosphoenolpyruvate carboxykinase activity and grew poor

41 Phosphoenolpyruvate carboxykinase activity is comparable

42 Highly related IRSs from the phosphoenolpyruvate carboxykinase and apolipoprotein CII

43 a not only with the rPDK4 gene but also with phosphoenolpyruvate carboxykinase and CPT-1a (carnitine

44 PST administration in KO mice stimulated phosphoenolpyruvate carboxykinase and G6Pase mRNA abunda

45 atic expression of the gluconeogenic enzymes phosphoenolpyruvate carboxykinase and G6Pase mRNAs was r

46 vates expression of gluconeogenic, including phosphoenolpyruvate carboxykinase and glucose-6-phosphat

47 ession of key gluconeogenic genes, including phosphoenolpyruvate carboxykinase and glucose-6-phosphat

48 of hepatic mRNA for the cytosolic isoform of phosphoenolpyruvate carboxykinase and glucose-6-phosphat

49 ctivate key genes of gluconeogenesis such as phosphoenolpyruvate carboxykinase and glucose-6-phosphat

50 major regulators of hepatic gluconeogenesis, phosphoenolpyruvate carboxykinase and glucose-6-phosphat

51 Suppressed mRNA abundance of phosphoenolpyruvate carboxykinase and glucose-6-phosphat

52 ssion of two critical gluconeogenic enzymes, phosphoenolpyruvate carboxykinase and glucose-6-phosphat

53 epatocyte genes involved in gluconeogenesis (phosphoenolpyruvate carboxykinase and glycogen synthase)

54 We show that lack of phosphoenolpyruvate carboxykinase and isocitrate lyase,

55 orrelation between dynamics and catalysis in phosphoenolpyruvate carboxykinase and other enzymes in w

56 Specifically, we determined that phosphoenolpyruvate carboxykinase and synthase do not ca

57 n of the expression of two key genes: PEPCK (phosphoenolpyruvate carboxykinase) and SREBP-1c (sterol

58 e expression of liver gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, and fructose-1,6-bisp

59 Expression of liver glycogen synthase, phosphoenolpyruvate carboxykinase, and glucose-6-phospha

60 y acid synthase, liver-type pyruvate kinase, phosphoenolpyruvate carboxykinase, and type I deiodinase

61 malate dehydrogenase, isocitrate lyase, and phosphoenolpyruvate carboxykinase are induced.

62 pyruvate kinase), and gluconeogenic enzymes (phosphoenolpyruvate carboxykinase), as well as the diet-

63 coneogenic enzymes glucose-6 phosphatase and phosphoenolpyruvate carboxykinase, as well as a marked i

64 Phosphoenolpyruvate carboxykinase catalyzes the reversib

65 The pckA gene, encoding phosphoenolpyruvate carboxykinase, catalyzes the reversi

66 ugh pyruvate carboxylation (anaplerosis) and phosphoenolpyruvate carboxykinase (cataplerosis) and dec

67 the nematode analog of the cytosolic form of phosphoenolpyruvate carboxykinase caused a marked extens

68 te (PEP) and oxaloacetate (OAA) by cytosolic phosphoenolpyruvate carboxykinase (cPEPCK) were investig

69 ng to the cAMP response element found in the phosphoenolpyruvate carboxykinase-cytosolic (PEPCK-C) pr

70 Transcripts encoding phosphoenolpyruvate carboxykinase did not appear to be r

71 , transaldolase, fructose bisphosphatase and phosphoenolpyruvate carboxykinase (encoded by ICL1, MAS1

72 n increase in the liver gluconeogenic enzyme phosphoenolpyruvate carboxykinase expression and activit

73 In addition, increased phosphoenolpyruvate carboxykinase expression in DHet mou

74 orrelated well with the observed increase in phosphoenolpyruvate carboxykinase expression, type IA fi

75 to regulate major metabolic genes including phosphoenolpyruvate carboxykinase, fatty acid synthase,

76 gluconeogenic enzymes glucose-6-phosphatase, phosphoenolpyruvate carboxykinase, fructose-1,6-phosphat

77 locomplex and regulates expression of PEPCK (phosphoenolpyruvate carboxykinase), G6P (glucose-6-phosp

78 receptor substrate-1 (IRS-1), and it reduces phosphoenolpyruvate carboxykinase gene expression in a p

79 factor 1 (gAF1) and 3 (gAF3) elements in the phosphoenolpyruvate carboxykinase gene glucocorticoid re

80 rifampicin effects were also observed in the phosphoenolpyruvate carboxykinase gene that contains a f

81 The repression of hormone-activated phosphoenolpyruvate carboxykinase gene transcription by

82 cessory factor for the complete induction of phosphoenolpyruvate carboxykinase gene transcription by

83 ng response elements for insulin (in the rat phosphoenolpyruvate carboxykinase gene), glucocorticoids

84 By using the promoter for the phosphoenolpyruvate carboxykinase gene, conditional, tis

85 glucose production and hepatic expression of phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

86 vity in the liver of L-iNOS-Tg mice, whereas phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

87 oid-regulated hepatic gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

88 The expression of genes encoding phosphoenolpyruvate carboxykinase, glycogen synthase, an

89 iption of the gene for the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (EC ) (PEPCK-C).

90 Phosphoenolpyruvate carboxykinase (GTP) (EC 4.1.1.32) (P

91 lear factor I (NFI) binds to a region of the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene pro

92 Nuclear factor-I (NFI) binds to the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene pro

93 iption of the gene for the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (4.1.1

94 aining a chimeric gene in which the cDNA for phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (EC 4.

95 n of the gene encoding the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C).

96 iption of the gene for the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C).

97 coneogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase in the leptin-infused

98 ts metabolism and discuss the role played by phosphoenolpyruvate carboxykinase in this process.

99 f ROR target genes, including Glc-6-Pase and phosphoenolpyruvate carboxykinase, in an ROR-dependent m

100 acted by mercaptopicolinate, an inhibitor of phosphoenolpyruvate carboxykinase, indicating that it is

101 enic enzymes fructose-1,6-bisphosphatase and phosphoenolpyruvate carboxykinase, is repressed by gluco

102 sat1 and Psph) and the gluconeogenic enzyme, phosphoenolpyruvate carboxykinase-M (Pck2/PEPCK-M), incr

103 pogenesis but fails to down-regulate hepatic phosphoenolpyruvate carboxykinase mRNA expression.

104 n resulted in a 2-3-fold increase in hepatic phosphoenolpyruvate carboxykinase mRNA levels.

105 cokinase mRNA was decreased, whereas that of phosphoenolpyruvate carboxykinase mRNA was increased com

106 ed cAMP response element binding protein and phosphoenolpyruvate carboxykinase mRNA were profoundly r

107 Liver pyruvate kinase and phosphoenolpyruvate carboxykinase mRNA were unchanged by

108 (4 h) suppressed hepatic glucose production, phosphoenolpyruvate carboxykinase mRNA, and plasma FFA t

109 vity of the key gluconeogenic pathway enzyme phosphoenolpyruvate carboxykinase (Pck) also increased u

110 e (NAD) phosphate malic enzyme (NADP-ME) and phosphoenolpyruvate carboxykinase (PCK) photosynthetic p

111 Although phosphoenolpyruvate carboxykinase (Pck)-1 expression was

112 n a bacterial verterbrate-type GTP-dependent phosphoenolpyruvate carboxykinase (PCK).

113 intermediates and this relies on the enzyme phosphoenolpyruvate carboxykinase (PCK).

114 Phosphoenolpyruvate carboxykinase (Pck; EC 4.1.1.32) is

115 ate weak interactions between MDH2 and yeast phosphoenolpyruvate carboxykinase (PCK1) and between MDH

116 pression of the hepatic gluconeogenic genes, phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-p

117 n regulating glucose metabolism by targeting phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-p

118 elates with glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PCK1) expression, key

119 known to regulate the activity of cytosolic phosphoenolpyruvate carboxykinase (PCK1), a key enzyme i

120 these, acetylation sites (Lys19 and 514) of phosphoenolpyruvate carboxykinase (Pck1p) were determine

121 Here we show that mitochondrial phosphoenolpyruvate carboxykinase (PCK2), the hub molecu

122 ges lacking the initial gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PCK2, mitochondrial i

123 Tissue glucose-6-phosphatase (G6P) and phosphoenolpyruvate carboxykinase (PEPCK) activities wer

124 Phosphoenolpyruvate carboxykinase (PEPCK) activity (carb

125 The extracts significantly inhibited phosphoenolpyruvate carboxykinase (PEPCK) and accelerate

126 amme of key gluconeogenic enzymes, including phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-

127 gluconeogenetic and glycogenolytic enzymes, phosphoenolpyruvate carboxykinase (Pepck) and glucose-6-

128 es that encode gluconeogenic enzymes such as phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-

129 lycemia was associated with normal levels of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-

130 d to increased transcriptional expression of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-

131 patic expression of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) and impairs in

132 The insulin response elements (IREs) of the phosphoenolpyruvate carboxykinase (PEPCK) and insulin-li

133 pts for archetypical decarboxylation enzymes phosphoenolpyruvate carboxykinase (PEPCK) and malic enzy

134 ncer cells utilize the gluconeogenic enzymes phosphoenolpyruvate carboxykinase (PEPCK) and phosphoeno

135 nvestigate the effect of decreased cytosolic phosphoenolpyruvate carboxykinase (PEPCK) and plastidic

136 transcriptional regulation of Glc-6-Pase and phosphoenolpyruvate carboxykinase (PEPCK) by apoA-IV was

137 c DNA vaccine encoding Leishmania glycosomal phosphoenolpyruvate carboxykinase (PEPCK) by EP and agai

138 The enzyme phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

139 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

140 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

141 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

142 ructural studies of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) demonstrate th

143 Here, we reveal two discrete phosphoenolpyruvate carboxykinase (PEPCK) enzymes in the

144 response in two independent assays: reducing phosphoenolpyruvate carboxykinase (PEPCK) expression in

145 Phosphoenolpyruvate carboxykinase (PEPCK) expression pla

146 While little change was evident for phosphoenolpyruvate carboxykinase (PEPCK) expression, py

147 TP binding motif and takes a fold similar to phosphoenolpyruvate carboxykinase (PEPCK) from Escherich

148 human CYP7A1 gene in bile acid synthesis and phosphoenolpyruvate carboxykinase (PEPCK) gene in glucon

149 TTG sequence, which is the core motif of the phosphoenolpyruvate carboxykinase (PEPCK) gene IRS.

150 The phosphoenolpyruvate carboxykinase (PEPCK) gene is a case

151 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is induce

152 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is induce

153 Transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene is regula

154 ide here such an example by showing that the phosphoenolpyruvate carboxykinase (PEPCK) gene knockout

155 cyclic AMP response element (CRE) of the rat phosphoenolpyruvate carboxykinase (PEPCK) gene promoter

156 etinoic acid response element (RARE1) in the phosphoenolpyruvate carboxykinase (PEPCK) gene promoter

157 The phosphoenolpyruvate carboxykinase (PEPCK) gene promoter

158 Glucocorticoid induction of the phosphoenolpyruvate carboxykinase (PEPCK) gene requires

159 Activation of phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

160 rticoids cause a 10-fold increase in hepatic phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

161 The in vivo pattern of induction of phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

162 ucocorticoid and cAMP-stimulated increase in phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

163 ular mechanisms underlying increased hepatic phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

164 ated transgenic (TG) mice overexpressing the phosphoenolpyruvate carboxykinase (PEPCK) gene under con

165 increase in the rate of transcription of the phosphoenolpyruvate carboxykinase (PEPCK) gene, which en

166 activate the complex native promoter in the phosphoenolpyruvate carboxykinase (PEPCK) gene.

167 ly 1 kilobase pair upstream of the cytosolic phosphoenolpyruvate carboxykinase (PEPCK) gene.

168 y in mice to determine the role of cytosolic phosphoenolpyruvate carboxykinase (PEPCK) in hepatic ene

169 ic gluconeogenesis through downregulation of phosphoenolpyruvate carboxykinase (PEPCK) in wild-type (

170 h enhanced activation of Akt, which inhibits phosphoenolpyruvate carboxykinase (PEPCK) induction, cau

171 Phosphoenolpyruvate carboxykinase (PEPCK) is a gluconeog

172 The gene encoding cytosolic phosphoenolpyruvate carboxykinase (PEPCK) is a PPARgamma

173 Phosphoenolpyruvate carboxykinase (PEPCK) is a rate-cont

174 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) is activated b

175 Phosphoenolpyruvate carboxykinase (PEPCK) is an essentia

176 Phosphoenolpyruvate carboxykinase (PEPCK) is present in

177 Phosphoenolpyruvate carboxykinase (PEPCK) is regulated s

178 Transcription of the gene for phosphoenolpyruvate carboxykinase (PEPCK) is stimulated

179 Phosphoenolpyruvate carboxykinase (PEPCK) is well known

180 ion of glucocorticoid receptor (GR) mRNA and phosphoenolpyruvate carboxykinase (PEPCK) mRNA (and acti

181 Liver-specific phosphoenolpyruvate carboxykinase (PEPCK) null mice, whe

182 be identical with one present in the enzyme phosphoenolpyruvate carboxykinase (PEPCK) of the organis

183 ic mice that express rabbit CRP from the rat phosphoenolpyruvate carboxykinase (PEPCK) promoter in re

184 aling in renal epithelial cells, we used the phosphoenolpyruvate carboxykinase (PEPCK) promoter to ge

185 The phosphoenolpyruvate carboxykinase (PEPCK) promoter was u

186 The insulin response sequence (IRS) of the phosphoenolpyruvate carboxykinase (PEPCK) promoter, loca

187 antigen (TAg), each under the control of the phosphoenolpyruvate carboxykinase (PEPCK) promoter, were

188 Expression was driven by the phosphoenolpyruvate carboxykinase (PEPCK) promoter, whic

189 e pH dependence of the reaction catalyzed by phosphoenolpyruvate carboxykinase (PEPCK) provides signi

190 e structures of the rat cytosolic isoform of phosphoenolpyruvate carboxykinase (PEPCK) reported in th

191 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) requires two d

192 of both glucose-6-phosphatase (Glc-6-P) and phosphoenolpyruvate carboxykinase (Pepck) to an extent s

193 Here we report gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) transcription

194 Avian mitochondrial phosphoenolpyruvate carboxykinase (PEPCK) was incubated

195 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) was rapidly in

196 eport crystal structures of the human enzyme phosphoenolpyruvate carboxykinase (PEPCK) with and witho

197 utes to TCDD suppression of transcription of phosphoenolpyruvate carboxykinase (PEPCK), a key regulat

198 The gene for phosphoenolpyruvate carboxykinase (PEPCK), a target of C

199 We provide evidence that phosphoenolpyruvate carboxykinase (PEPCK), an enzyme inv

200 receptor gamma coactivator-1 alpha (PGC-1), phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6

201 tion, expression of key gluconeogenic genes, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6

202 vestigated the role of glycerol kinase (GK), phosphoenolpyruvate carboxykinase (PEPCK), and pyruvate

203 decarboxylation of [4-(13)C]oxaloacetate via phosphoenolpyruvate carboxykinase (PEPCK), forward TCA c

204 d) could activate p38 and increase levels of phosphoenolpyruvate carboxykinase (PEPCK), glucose-6-pho

205 The key gluconeogenic enzyme, phosphoenolpyruvate carboxykinase (PEPCK), has been show

206 ough the insulin-responsive sequences of the phosphoenolpyruvate carboxykinase (PEPCK), IGFBP-1, and

207 receptor gamma co-activator-1a (PGC-1alpha), phosphoenolpyruvate carboxykinase (PEPCK), pyruvate carb

208 Regulation of phosphoenolpyruvate carboxykinase (PEPCK), the key gene

209 ted glucocorticoid induction of the gene for phosphoenolpyruvate carboxykinase (PEPCK), the rate-limi

210 Expression of phosphoenolpyruvate carboxykinase (PEPCK), the rate-limi

211 pression of glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (Pepck), two gluconeog

212 In phosphoenolpyruvate carboxykinase (PEPCK)-GFP mice, seri

213 nic genes glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

214 ces expression of hepatic gluconeogenic gene phosphoenolpyruvate carboxykinase (PEPCK).

215 on of glucose-6-phosphatase (Glc-6-Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

216 r gamma co-activator 1alpha (PGC-1alpha) and phosphoenolpyruvate carboxykinase (PEPCK).

217 duced expression of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

218 ed, in part, through increased expression of phosphoenolpyruvate carboxykinase (PEPCK).

219 zymes glucose-6-phosphatase (Glc-6-Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

220 volved in hepatic gluconeogenesis, including phosphoenolpyruvate carboxykinase (PEPCK).

221 cAMP stimulate transcription of the gene for phosphoenolpyruvate carboxykinase (PEPCK).

222 f the gene encoding the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

223 expression of gluconeogenic enzymes, such as phosphoenolpyruvate carboxykinase (PEPCK).

224 be identical with one present in the enzyme phosphoenolpyruvate carboxykinase (PEPCK).

225 rowth factor binding protein-1 (IGFBP-1) and phosphoenolpyruvate carboxykinase (PEPCK).

226 tic glycogen or induce the cytosolic form of phosphoenolpyruvate carboxykinase (PEPCK).

227 AMP-stimulated transcription of the gene for phosphoenolpyruvate carboxykinase (PEPCK).

228 to sugar feeding, including both isoforms of phosphoenolpyruvate carboxykinase (pepck).

229 erated in the glycosomes by kinases, such as phosphoenolpyruvate carboxykinase (PEPCK).

230 pyruvate dehydrogenase kinase 4 (pdk4), and phosphoenolpyruvate carboxykinase (pepck).

231 nic genes glucose-6-phosphatase (G6pase) and phosphoenolpyruvate carboxykinase (Pepck).

232 ME), NAD-dependent malic enzyme (NAD-ME) and phosphoenolpyruvate carboxykinase (PEPCK).

233 We previously identified Leishmania phosphoenolpyruvate carboxykinase (PEPCK, a gluconeogeni

234 creased gluconeogenic flux through cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) and associat

235 The cytosolic form of the phosphoenolpyruvate carboxykinase (PEPCK-C) gene is sele

236 tigated whether the mitochondrial isoform of phosphoenolpyruvate carboxykinase (PEPCK-M) is the GTPas

237 Mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M), encoded by

238 Expression profiles of selected genes (phosphoenolpyruvate carboxykinase - PEPCK, glucocorticoi

239 ROP (repressor of phosphoenolpyruvate carboxykinase, PEPCK) is a methanol-

240 colinic acid (3-MPA), a classic inhibitor of phosphoenolpyruvate carboxykinase, photosynthetic O(2) e

241 coneogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase, presumably, because o

242 ge-dependent phosphoenolpyruvate carboxylase/phosphoenolpyruvate carboxykinase process that decreases

243 essing rabbit CRP (CF1-CRP) regulated by the phosphoenolpyruvate carboxykinase promoter such that lev

244 SV40 T-Antigen in liver under control of the phosphoenolpyruvate carboxykinase promoter were generate

245 Diabetic mice that expressed the phosphoenolpyruvate carboxykinase promoter-driven BMP-7

246 it CRP (CF1-CRP) under the regulation of the phosphoenolpyruvate carboxykinase promoter.

247 diate complexes of the reaction catalyzed by phosphoenolpyruvate carboxykinase provide direct structu

248 ive human TGF-beta1 under control of the rat phosphoenolpyruvate carboxykinase regulatory sequences d

249 e, transaldolase, alcohol dehydrogenase, and phosphoenolpyruvate carboxykinase) that indicate the pot

250 rboxylic acid (TCA) cycle first and then use phosphoenolpyruvate carboxykinase to initiate gluconeoge

251 of expression of several HNF3 target genes (phosphoenolpyruvate carboxykinase, transferrin, tyrosine

252 rget genes such as glucose-6-phosphatase and phosphoenolpyruvate carboxykinase, two key targets for F

253 regulated by insulin such as those encoding phosphoenolpyruvate carboxykinase, tyrosine aminotransfe

254 ulation of PPARgamma-inducible genes such as phosphoenolpyruvate carboxykinase was maintained when ce

255 psin, aldolase B, alcohol dehydrogenase, and phosphoenolpyruvate carboxykinase, was also affected in

256 Levels of cytosolic and the mitochondrial phosphoenolpyruvate carboxykinase were elevated after 24

257 decarboxylase systems (NADP-malic enzyme and phosphoenolpyruvate carboxykinase) were critical for mat

258 gluconeogenic enzymes, isocitrate lyase and phosphoenolpyruvate carboxykinase, were also degraded in

259 and the gluconeogenesis controller, hepatic phosphoenolpyruvate carboxykinase, were significantly el

260 egulation of the first gluconeogenic enzyme, phosphoenolpyruvate carboxykinase, when acetate was the