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 RNA levels of the key gluconeogenetic enzyme phosphoenolpyruvate carboxykinase.

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

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

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

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

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

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

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

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

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

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

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

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

16 Phosphoenolpyruvate carboxykinase 1 (PEPCK1) is the crit

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

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

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

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

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

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

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

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

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

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

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

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

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

30 Phosphoenolpyruvate carboxykinase activity is comparable

31 Highly related IRSs from the phosphoenolpyruvate carboxykinase and apolipoprotein CII

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 Phosphoenolpyruvate carboxykinase catalyzes the reversib

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

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

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

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

57 Transcripts encoding phosphoenolpyruvate carboxykinase did not appear to be r

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

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

60 In addition, increased phosphoenolpyruvate carboxykinase expression in DHet mou

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 Liver pyruvate kinase and phosphoenolpyruvate carboxykinase mRNA were unchanged by

94 (4 h) suppressed hepatic glucose production, phosphoenolpyruvate carboxykinase mRNA, and plasma FFA t

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

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

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

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

99 Phosphoenolpyruvate carboxykinase (Pck; EC 4.1.1.32) is

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

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

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

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

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

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

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

107 Phosphoenolpyruvate carboxykinase (PEPCK) activity (carb

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

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

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

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

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

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

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

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

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

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

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

119 The enzyme phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

120 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

121 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

122 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

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

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

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

126 Phosphoenolpyruvate carboxykinase (PEPCK) expression pla

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

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

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

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

131 The phosphoenolpyruvate carboxykinase (PEPCK) gene is a case

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

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

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

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

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

137 The phosphoenolpyruvate carboxykinase (PEPCK) gene promoter

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

139 Activation of phosphoenolpyruvate carboxykinase (PEPCK) gene transcrip

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

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

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

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

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

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

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

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

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

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

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

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

152 Phosphoenolpyruvate carboxykinase (PEPCK) is a rate-cont

153 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) is activated b

154 Phosphoenolpyruvate carboxykinase (PEPCK) is an essentia

155 Phosphoenolpyruvate carboxykinase (PEPCK) is present in

156 Phosphoenolpyruvate carboxykinase (PEPCK) is regulated s

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

158 Phosphoenolpyruvate carboxykinase (PEPCK) is well known

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

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

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

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

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

164 The phosphoenolpyruvate carboxykinase (PEPCK) promoter was u

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

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

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

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

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

170 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) requires two d

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

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

173 Avian mitochondrial phosphoenolpyruvate carboxykinase (PEPCK) was incubated

174 Chicken liver phosphoenolpyruvate carboxykinase (PEPCK) was rapidly in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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