ライフサイエンスコーパス: phosphate dehydrogenase

1 ect on beta-actin or GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

2 anufacturer control, GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

3 inase and the rate-limiting enzyme glucose-6-phosphate dehydrogenase.

4 rginine deiminase ArcA, and glyceraldehyde 3-phosphate dehydrogenase.

5 sphate transport system and an sn-glycerol-3-phosphate dehydrogenase.

6 ific glycolytic proteins such as d-glucose-6-phosphate dehydrogenase.

7 a mutation of G6PD, which encodes glucose-6-phosphate dehydrogenase.

8 aminonicotinamide, an inhibitor of glucose-6-phosphate dehydrogenase.

9 within the endoplasmic reticulum by hexose-6-phosphate dehydrogenase.

10 ds to decreased activity of glyceraldehyde 3-phosphate dehydrogenase.

11 -synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase.

12 derived from the metabolic enzyme glucose-6-phosphate dehydrogenase.

13 he major apoptotic effector glyceraldehyde-3-phosphate dehydrogenase.

14 ncode the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

15 endoplasmic reticulum by the enzyme hexose-6-phosphate dehydrogenase.

16 codes the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

17 e dehydrogenase and heat-denatured glucose-6-phosphate dehydrogenase.

18 gresses from the host cell, glyceraldehyde-3-phosphate dehydrogenase 1 (GAPDH1), which is primary a g

19 malate/oxaloacetate shuttle and a glycerol-3-phosphate dehydrogenase 1(Gpd1p)-dependent shuttle are a

20 d with the PTS2-containing enzyme Glycerol-3-phosphate dehydrogenase 1, Gpd1.

21 ruvate dehydrogenase kinase 4 and glycerol 3-phosphate dehydrogenase 1, was acutely induced by a sing

22 in a conserved amino acid of the glycerol-3-phosphate dehydrogenase 1-like (GPD1-L) gene.

23 Here, we identify the enzyme glycerol-3-phosphate dehydrogenase 1-like (GPD1L) as a novel regula

24 of the mature miRNA, derepresses glycerol-3-phosphate dehydrogenase 1-like enzyme (GPD1L), a hypoxia

25 Recently, a novel mutation in the glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) disrupted t

26 blocked the mutant A280V GPD1-L (glycerol-3-phosphate dehydrogenase 1-like) effect on reducing I(Na)

27 dentified by mass spectrometry as glycerol-3-phosphate dehydrogenase 2 (Gpd2).

28 lciparum , the bifunctional enzyme glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase (PfGlu

29 inhibition of the parasite enzyme glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase, a key

30 thway by ADPr inhibition of glyceraldehyde-3-phosphate dehydrogenase, a central enzyme of glycolysis.

31 for the nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase, a cytosolic enzyme whose role i

32 rs of Plasmodium falciparum glyceraldehyde-3-phosphate dehydrogenase, a validated target for the trea

33 hibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and triggered significa

34 by inducing maximal mitochondrial glycerol-3-phosphate dehydrogenase activity in rat liver while havi

35 Glucose phosphate dehydrogenase activity that gives rise to NADP

36 ement mediating selection for high glucose-6-phosphate dehydrogenase activity.

37 as also capable of inducing glyceraldehyde-3-phosphate dehydrogenase aggregation, but chondroitin sul

38 eS cluster binding, such as glyceraldehyde-3-phosphate dehydrogenase, aldehyde dehydrogenase, aconita

39 no acids) of serum albumin, glyceraldehyde-3-phosphate dehydrogenase, aldolase, and aspartate aminotr

40 stained with antibodies to glyceraldehyde-3-phosphate dehydrogenase, aldolase, phosphofructokinase,

41 A6, clathrin heavy chain 1, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase, filamin-A, and h

42 olism (triosephosphate isomerase, glycerol-3-phosphate-dehydrogenase, alpha enolase and L-lactate deh

43 f Hsp70 proteins), Tdh2/3p (glyceraldehyde-3-phosphate dehydrogenase, an RNA-binding protein), Pdc1p

44 Hexose-6-phosphate dehydrogenase and 11 beta-hydroxysteroid dehyd

45 Two NAD-dependent dehydrogenases (glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydroge

46 homeostasis, which is regulated by glucose-6-phosphate dehydrogenase and AMP kinase.

47 on of the secretory protein glyceraldehyde-3-phosphate dehydrogenase and ATP synthase subunit alpha i

48 ncluding nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase and beta-glucosidase.

49 Nuclear complex of glyceraldehyde-3-phosphate dehydrogenase and DNA repair enzyme apurinic/a

50 s response, especially the roles of hexose-6-phosphate dehydrogenase and ER-anchored RING finger E3 l

51 oplast-targeted Plasmodium yoelii glycerol 3-phosphate dehydrogenase and glycerol 3-phosphate acyltra

52 es that catalyze their synthesis, glycerol-1-phosphate dehydrogenase and heptaprenylglyceryl phosphat

53 ntent of glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and pyruvate dehydrogenase subun

54 olving conversion to N(tz) ADPH by glucose-6-phosphate dehydrogenase and reoxidation to N(tz) ADP(+)

55 ncreased ability to degrade glyceraldehyde-3-phosphate dehydrogenase and ribonuclease A when the reac

56 sed ability to degrade both glyceraldehyde-3-phosphate dehydrogenase and ribonuclease A, substrates f

57 are sensitive to oxidation, glyceraldehyde-3-phosphate dehydrogenase and the sodium-potassium ATPase,

58 Evaluations for glucose-6-phosphate dehydrogenase and thiopurine S-methyltransfera

59 hosphate dehydrogenase, and glyceraldehyde-3-phosphate dehydrogenase) and their respective genetic va

60 glycerol synthesis gene, gpd1(+) (glycerol-3-phosphate dehydrogenase), and is independent of actin ca

61 l polymorphisms (ie, hemoglobin S, glucose-6-phosphate dehydrogenase, and alpha-thalassemia) were the

62 lucose 6-phosphate dehydrogenase, glycerol 3-phosphate dehydrogenase, and glucose oxidase.

63 mes (catechol-O-methyltransferase, glucose-6-phosphate dehydrogenase, and glyceraldehyde-3-phosphate

64 s including Tau, ubiquitin, glyceraldehyde-3-phosphate dehydrogenase, and glycosaminoglycans are rout

65 ce loci, glpABC, the anaerobic sn-glycerol-3-phosphate dehydrogenase, and plsB, an sn-glycerol-3-phos

66 el such actin, tubulin, and glyceraldehyde-3-phosphate dehydrogenase are frequently used as endogenou

67 ycerol-3-phosphate shuttle (Gut2, glycerol-3-phosphate dehydrogenase) are novel longevity factors in

68 stable mRNAs (e.g., GAPDH [glyceraldehyde-3-phosphate dehydrogenase]) are rapidly degraded.

69 d soluble recombinant sperm glyceraldehyde-3-phosphate dehydrogenase as a heterotetramer with the Esc

70 ntify the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase as a potent inhibitor of caspase

71 ified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most selective antiparasi

72 We found that the HKGs glyceraldehyde-3-phosphate dehydrogenase, beta actin and adenosine tripho

73 tially reduced the inactivation of glucose-6-phosphate dehydrogenase by 4-hydroxy-2-nonenal and malon

74 fied for the reaction catalyzed by glucose-6-phosphate dehydrogenase by comparing the 1-(13)C KIE wit

75 were silenced or up-regulated for sorbitol-6-phosphate dehydrogenase by using the CaMV35S promoter to

76 Transgenic plants with suppressed sorbitol-6-phosphate dehydrogenase compensated by accumulating sucr

77 nd that the glycolytic enzyme glyceraldehyde phosphate dehydrogenase constitutes a major cellular hem

78 olytic anaemia in individuals with glucose-6-phosphate dehydrogenase deficiency (G6PDd).

79 Other abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase d

80 idence interval {CI}, 0.52-0.90]), glucose-6-phosphate dehydrogenase deficiency in female children (R

81 Glucose-6-phosphate dehydrogenase deficiency serves as a prototype

82 ssemia, 0.3%; ABO group, 0.3%; and glucose-6-phosphate dehydrogenase deficiency, 0.5%) and the new po

83 eurotoxicity, such as prematurity, glucose-6-phosphate dehydrogenase deficiency, or hypoxia-ischemia.

84 alocytosis and two common forms of glucose-6-phosphate dehydrogenase deficiency.

85 relation with sickle cell trait or glucose-6-phosphate-dehydrogenase deficiency was observed.

86 pecies, the heparin-induced glyceraldehyde-3-phosphate dehydrogenase early oligomers might come in us

87 ncoded by glpK and suggest that a glycerol-3-phosphate dehydrogenase encoded by the upstream gpdABC o

88 Conditional expression of the glucose-6-phosphate dehydrogenase-encoding gene zwf, shown here to

89 Patients with glucose-6-phosphate dehydrogenase enzyme activity of less than 70%

90 licated falciparum malaria, normal glucose-6-phosphate dehydrogenase enzyme levels, and hemoglobin le

91 D or another oxidative PPP enzyme, glucose-6-phosphate dehydrogenase, exhibit non-immune hemolytic an

92 te for an enzyme, F(420)-dependent glucose-6-phosphate dehydrogenase (Fgd), found in few bacterial ge

93 er coenzyme for an F(420)-specific glucose-6-phosphate dehydrogenase (Fgd).

94 nly mediated by loss of a specific glucose-6-phosphate dehydrogenase (FGD1) or its deazaflavin cofact

95 ly oligomers present in the glyceraldehyde-3-phosphate dehydrogenase fibrillation pathway promote alp

96 e excess of ALDH3A1 also protected glucose-6-phosphate dehydrogenase from inactivation because of dir

97 redoxin reductase (TR), and glyceraldehyde-3-phosphate dehydrogenase (G3PD) activities, as well as th

98 ldolase A and an isoform of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed elevated oxidatio

99 ox polypeptide, beta-actin, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexin A2, triose phos

100 itochondrial glutathione (GSH) and glucose 6-phosphate dehydrogenase (G6-PD) was restored by SAC trea

101 iphenyltetrazolium bromide] (MTT), glucose-6-phosphate dehydrogenase (G6DP), and calcein AM and ethid

102 isocitrate dehydrogenase (IDH) or glucose-6-phosphate dehydrogenase (G6PD) activity in a single gene

103 Glucose-6-phosphate dehydrogenase (G6PD) activity is essential for

104 ATM activation induces glucose-6-phosphate dehydrogenase (G6PD) activity, the limiting en

105 Unexpectedly, Glucose-6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate de

106 xidation of G6P in the presence of glucose-6-phosphate dehydrogenase (G6PD) and nicotinamide adenine

107 tion, suggesting that intranuclear glucose-6-phosphate dehydrogenase (G6PD) can control NOX4 activity

108 ependent haemolysis in people with glucose-6-phosphate dehydrogenase (G6PD) deficiencies have limited

109 Individuals with glucose 6-phosphate dehydrogenase (G6PD) deficiency are at risk fo

110 halassaemia, ABO blood groups, and glucose-6-phosphate dehydrogenase (G6PD) deficiency encoded by the

111 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common hu

112 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is believed to

113 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most co

114 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most co

115 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most co

116 The global prevalence of X-linked glucose-6-phosphate dehydrogenase (G6PD) deficiency is thought to

117 by haemolysis in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency.

118 risk factors, and we also assessed glucose-6-phosphate dehydrogenase (G6PD) enzyme activity.

119 The inhibition of glucose-6-phosphate dehydrogenase (G6PD) expression by arachidonic

120 hondria, whereas chloroquine and a glucose-6-phosphate dehydrogenase (G6PD) inhibitor affected the cy

121 Glucose-6-phosphate dehydrogenase (G6PD) is a key enzyme in the pe

122 The reaction catalyzed by glucose-6-phosphate dehydrogenase (G6PD) is the first, rate-limiti

123 Glucose 6-phosphate dehydrogenase (G6PD) is the most common defici

124 Glucose-6-phosphate dehydrogenase (G6PD) is the principal source o

125 Glucose-6-phosphate dehydrogenase (G6PD) is the rate-limiting enzy

126 Glucose-6-phosphate dehydrogenase (G6PD) modulates vascular functi

127 roscopy and had normal function of glucose-6-phosphate dehydrogenase (G6PD) on colorimetric quantific

128 s exacerbated in erythrocytes from glucose-6-phosphate dehydrogenase (G6PD) patients and rescued by a

129 Glucose-6-phosphate dehydrogenase (G6PD) regulates production of t

130 ing ATM or its downstream effector glucose 6-phosphate dehydrogenase (G6PD) sensitizes AML cells to F

131 Glucose-6-phosphate dehydrogenase (G6PD) status was determined usi

132 ivo, pharmacological inhibition of glucose-6-phosphate dehydrogenase (G6PD) to decrease NADPH levels

133 tive capacity by overexpression of glucose-6-phosphate dehydrogenase (G6PD), a key enzyme for NADPH b

134 necessary for NET release because glucose-6-phosphate dehydrogenase (G6PD), an important enzyme from

135 ession and enzymatic activities of glucose-6-phosphate dehydrogenase (G6PD), glutathione reductase, a

136 rial pathogen Pseudomonas syringae Glucose-6-phosphate dehydrogenase (G6PD), the key enzyme of the ox

137 Here we show that glucose-6-phosphate dehydrogenase (G6PD), the rate-limiting enzyme

138 ity of another cytoplasmic enzyme, glucose-6-phosphate dehydrogenase (G6PD), was also measured.

139 gulates stress tolerance by activating Glc-6-phosphate dehydrogenase (G6PD), which is essential for m

140 lase (HDAC) inhibitors (HDACis) in glucose-6-phosphate dehydrogenase (G6PD)-deficient cells reinstate

141 NADPH by impairing the activity of glucose 6-phosphate dehydrogenase (G6PD).

142 lectively enhance transcription of glucose 6-phosphate dehydrogenase (G6PD).

143 In addition, glucose-6-phosphate-dehydrogenase (G6PD) deficiency, which is the

144 s in patients with a deficiency in glucose-6-phosphate dehydrogenase (G6PDd).

145 ake with a concomitant increase in glucose-6-phosphate dehydrogenase (G6PDH) activity, the key enzyme

146 ted the reactivation of aggregated glucose-6-phosphate dehydrogenase (G6PDH) by ClpB and its N-termin

147 Glucose-6-phosphate dehydrogenase (G6PDH) has been implicated in t

148 on enzymes such as NQO1 as well as glucose-6-phosphate dehydrogenase (G6PDH), a regulator of the pent

149 citrate dehydrogenase (NADP-ICDH), glucose-6-phosphate dehydrogenase (G6PDH), and, glutathione reduct

150 ibited high specificity for glyceraldehyde 3-phosphate dehydrogenase (GADPH) mRNA in live normal HEp-

151 n-1 (Hwp1); enolase (Enol); glyceraldehyde-3-phosphate dehydrogenase (Gap1); and phosphoglycerate kin

152 combined activities of the glyceraldehyde 3-phosphate dehydrogenases GapA/GapB and the malic enzymes

153 The cytosolic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPC) catalyzes a key reaction

154 A cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPC) was identified to bind to

155 dial glycolytic isoforms of glyceraldehyde-3-phosphate dehydrogenase (GAPCp) in photosynthetic and he

156 ytosolic glycolytic enzymes glyceraldehyde-3-phosphate dehydrogenases (GAPCs) interact with the plasm

157 ly used housekeeping genes, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and 18S ribosomal RNA (r

158 synergistic interaction of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and a major facilitator

159 Rab2 requires glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and atypical protein kin

160 supramolecular complex with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and phosphoribulokinase,

161 ming a ternary complex with glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and phosphoribulokinase.

162 sibly acetylated, including glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Rpa1177, a putative

163 by the interaction between glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the E3 ubiquitin lig

164 by S-nitrosylation such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and thereby contributes

165 be the glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and triose-phosphate iso

166 proaches, we identified the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a C1q partner when ex

167 for RT-PCR and qrtPCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an endogenous control

168 mammalian glycolysis enzyme glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as an NleB-interacting p

169 We found that I/R induces glyceraldehyde-3-phosphate dehydrogenase (GAPDH) association with mitocho

170 y nitroso compounds inhibit glyceraldehyde 3-phosphate dehydrogenase (GAPDH) by forming a reduction r

171 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from human pathogens Sta

172 single cell analysis of the glyceraldehyde 3 phosphate dehydrogenase (GAPDH) gene in human lymphocyte

173 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has been found down-regu

174 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) has been hypothesized as

175 form molecular targeting of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in human hepatocellular

176 ocation and accumulation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in the nucleus has close

177 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a classical glycolyti

178 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a glycolytic enzyme t

179 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is a glycolytic enzyme t

180 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a multifunctional enz

181 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ubiquitous and abun

182 NAD-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ubiquitous enzyme i

183 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an abundant metabolic

184 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an enzyme best known

185 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is often used as a stabl

186 hway, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediates a novel cell de

187 lving nitric oxide (NO) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediates cocaine's trans

188 , superoxide dismutase, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) mRNA with a concomitant

189 de is a structural mimic of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) on the sporozoite surfac

190 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) participates in a cell d

191 edly, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) physically associates wi

192 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) plays a key regulatory f

193 METH also increases glyceraldehyde-3-phosphate dehydrogenase (GAPDH) protein in the crude ves

194 utoantigen protein p70, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) proteins and that the si

195 ambda (aPKCiota/lambda) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) recruitment to VTCs.

196 Using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) silencing with small int

197 horesis, and phosphorylated glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was identified by matrix

198 mino acids with identity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was obtained.

199 Arginine kinase (AK) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were determined as the i

200 ble residues in the protein glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were examined.

201 lves interaction of nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with apurinic/apyrimidin

202 Here, we demonstrate that glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a conventional glycolyt

203 receptors for Plg including glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a cytoplasmic enzyme th

204 f the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a modification that inh

205 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a protein target used r

206 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), an important glycolytic

207 e, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and enolase, all of whi

208 o protect citrate synthase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and the restriction end

209 Commonly used glyceraldehyde-3-phosphate dehydrogenase (Gapdh), beta-actin (Actb), or b

210 for total protein quantity, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), citrate synthase (CS),

211 s, creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), conformationally affect

212 n of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), in vitro and in tissues

213 Superoxide inhibits glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which activates major p

214 ons, nitroalkenes inhibited glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which contains a critic

215 vered that Escherichia coli glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which is not known to b

216 olvement in this process of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which participates in i

217 f the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

218 the L1 interaction partner glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

219 ribosomal protein L13a, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

220 osphoribulokinase (PRK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

221 nd nuclear translocation of glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

222 s: creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

223 (NO), which S-nitrosylates glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

224 s accumulate and inactivate glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

225 a-2 microglobulin (B2M) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

226 Tetrameric rabbit muscle glyceraldehyde 3-phosphate dehydrogenase (GAPDH; EC 1.2.1.12) binds succe

227 ns of palmitoyl-CoA inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.1.12) enzyme acti

228 f glycolytic enzymes (e.g., glyceraldehyde-3-phosphate dehydrogenase [GAPDH]) and transcription facto

229 protein (Ucp1) and mitochondrial glycerol-3-phosphate dehydrogenase (Gdm) result in mice with increa

230 et the histidine kinase and glyceraldehyde-3-phosphate dehydrogenase genes of B. dermatitidis and H.

231 s including c-myc, p21, and glyceraldehyde-3-phosphate dehydrogenase genes, indicating reduced promot

232 We studied the contribution of glucose-6-phosphate dehydrogenase (Glc-6-PD), an important regulat

233 gene for the conserved aerobic sn-glycerol-3-phosphate dehydrogenase GlpD.

234 Sn-glycerol-3-phosphate dehydrogenase (GlpD) is an essential membrane

235 he integral membrane flavoenzyme, glycerol-3-phosphate dehydrogenase (GlpD), and the soluble redox fl

236 reaction utilizing three enzymes: glycerol 3-phosphate dehydrogenase, glycerol 3-phosphate acyltransf

237 s including alcohol dehydrogenase, glucose 6-phosphate dehydrogenase, glycerol 3-phosphate dehydrogen

238 phosphatase (PSP) motif fused to glycerol-3-phosphate dehydrogenase (GPD) domains.

239 ces cerevisiae has two homologous glycerol-3-phosphate dehydrogenases, Gpd1 and Gpd2, that are requir

240 e glycerol-producing PTS2 protein glycerol-3-phosphate dehydrogenase Gpd1p shows a tripartite localiz

241 Here we evaluate the effects of glycerol-3-phosphate dehydrogenase (Gpdh) and cytosolic malate dehy

242 of R269 lies at the surface of l-glycerol 3-phosphate dehydrogenase (GPDH) and forms an ion pair to

243 rginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenase (GPDH), calcium-binding protein,

244 Hexose-6-phosphate dehydrogenase (H6PD) generates NADPH, the cofa

245 Hexose-6-phosphate dehydrogenase (H6PD) is the initial component

246 hydrogenase type 1 (11betaHSD1) and hexose-6-phosphate dehydrogenase (H6PDH).

247 Sperm glyceraldehyde-3-phosphate dehydrogenase has been shown to be a successfu

248 lbumin, choriogonadotropin, glyceraldehyde-3-phosphate dehydrogenase, Herceptin, and ReoPro.

249 xylase (ScOMPDC), and human liver glycerol 3-phosphate dehydrogenase (hlGPDH) for catalysis of reacti

250 The R269A mutation of glycerol-3-phosphate dehydrogenase (hlGPDH) results in a 9.1 kcal/m

251 r with the Escherichia coli glyceraldehyde-3-phosphate dehydrogenase in a ratio of 1:3 and have solve

252 -synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase in cultured hippocampal neurons,

253 nd formate, and overexpression of sorbitol-6-phosphate dehydrogenase in lactate dehydrogenase-deficie

254 tabolism via iodoacetate, a glyceraldehyde-3-phosphate dehydrogenase inhibitor, is sufficient to indu

255 f the pentose phosphate pathway by glucose-6-phosphate dehydrogenase inhibitors and siRNA suppressed

256 Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic enzyme that can

257 vity of its ancillary subunit-the glycerol-3-phosphate dehydrogenase-like protein.

258 l 3-phosphate by mitochondrial sn-glycerol 3-phosphate dehydrogenase (mGPDH) is a major pathway for t

259 normalization to 5 x 10(6) glyceraldehyde-3'-phosphate dehydrogenase mRNA copies, normalized PSA copi

260 substrate glycolaldehyde (GLY) by glycerol 3-phosphate dehydrogenase (NAD (+), GPDH) saturated with N

261 to the gpdC gene of the putative glycerol-3-phosphate dehydrogenase operon (gpdABC), based on the fi

262 observe changes in the activity of glucose-6-phosphate dehydrogenase or in the pentose phosphate path

263 of the Calvin cycle enzymes glyceraldehyde-3-phosphate dehydrogenase or ribulose-1,5-bisphosphate car

264 Cytosolic Oryza sativa glyceraldehyde-3-phosphate dehydrogenase (OsGAPDH), the enzyme involved i

265 and a member of the 4-hydroxy-l-threonine 4-phosphate dehydrogenase (PdxA) oxidative decarboxylase,

266 that inhibit Plasmodium falciparum glucose-6-phosphate dehydrogenase (PfG6PD).

267 iculum Ca2+-ATPase, mitochondrial glycerol 3-phosphate dehydrogenase, PGC1alpha, CoxII, and mitochond

268 tants deficient in PavA, CodY, and glucose-6-phosphate dehydrogenase pointing to the robustness of th

269 erochromatic) and the human glyceraldehyde-3-phosphate dehydrogenase promoter (euchromatic), we show

270 se, malate dehydrogenase 1, glyceraldehyde-3-phosphate dehydrogenase, proteoglycan 4, minichromosome

271 PDH) [small interfering RNA(glyceraldehyde 3-phosphate dehydrogenase)] reduces PLCbeta-mediated calci

272 e acyltransferase or GLY1-encoded glycerol-3-phosphate dehydrogenase restored 18:1 levels in HRT ssi2

273 somatic and sperm-specific glyceraldehyde-3-phosphate dehydrogenase revealed few differences at the

274 nding protein 2b (SAG0765), glyceraldehyde-3-phosphate dehydrogenase (SAG0823), and an iron-binding p

275 ediated by the nitric oxide-glyceraldehyde-3-phosphate dehydrogenase signaling pathway.

276 METHODS AND Patients with normal glucose-6-phosphate dehydrogenase status with symptomatic P. vivax

277 ockade of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step as the central metabolic ba

278 uation of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step due to the reduced availabi

279 rmediates before and at the glyceraldehyde 3-phosphate dehydrogenase step, promoting carbon overflow

280 tic intermediates after the glyceraldehyde 3-phosphate dehydrogenase step, thereby reducing carbon fl

281 glycolysis by blocking the glyceraldehyde 3-phosphate dehydrogenase step.

282 ailed analysis of the sperm glyceraldehyde-3-phosphate dehydrogenase structure revealed sites in the

283 ared with published somatic glyceraldehyde-3-phosphate dehydrogenase structures that could be exploit

284 gene, gpdA, encoding a homolog of glycerol-3-phosphate dehydrogenase subunit A, were upregulated (8-

285 p is a cytosolic NAD(+)-dependent glycerol 3-phosphate dehydrogenase that also localizes to peroxisom

286 peS6PDH encodes a NADPH-dependent sorbitol-6-phosphate dehydrogenase, the key enzyme for biosynthesis

287 stration that the resulting glyceraldehyde-3-phosphate dehydrogenase, the normal target of pentalenol

288 (1)H NMR spectroscopy using glyceraldehyde 3-phosphate dehydrogenase to trap the first-formed product

289 ibitor (dehydroepiandrosterone) of glucose-6-phosphate dehydrogenase together established redundancy

290 ints in central metabolism (Glyceraldehyde 3-phosphate dehydrogenase, transaldolase, alcohol dehydrog

291 olytic enzymes, aldolase A, glyceraldehyde 3-phosphate dehydrogenase, triose phosphate isomerase, and

292 glycolaldehyde (GA) catalyzed by glycerol-3-phosphate dehydrogenase were determined over a 2100-fold

293 oxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase were initially implicated in thi

294 osolic isocitrate dehydrogenase or glucose-6-phosphate dehydrogenase, which also produce cytosolic NA

295 a-actin, alpha-tubulin, and glyceraldehyde 3-phosphate dehydrogenase, which are usually used as contr

296 has >80% amino acid homology with glycerol-3-phosphate dehydrogenase, which is involved in NAD-depend

297 for the housekeeping enzyme glyceraldehyde-3-phosphate dehydrogenase, wild-type HSV infection reduced

298 lated lysine residue 184 in glyceraldehyde 3-phosphate dehydrogenase with glutamic acid, a malonyllys

299 er-expressing zwf gene (coding for glucose-6-phosphate dehydrogenase), WX-zwf, produced the highest g

300 on glucose has been attributed to glucose-6-phosphate dehydrogenase (Zwf1p) and a cytosolic aldehyde