ライフサイエンスコーパス: glyceraldehyde-3-phosphate dehydrogenase

1 -C but had no effect on beta-actin or GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

2 and an internal manufacturer control, GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

3 in O) and plr (encoding the plasmin receptor/glyceraldehyde-3-phosphate dehydrogenase).

4 SC70, protein disulfide isomerase ERp60, and glyceraldehyde 3-phosphate dehydrogenase.

5 ersulfidation leads to decreased activity of glyceraldehyde 3-phosphate dehydrogenase.

6 ein, the promyelocytic leukemia protein, and glyceraldehyde 3-phosphate dehydrogenase.

7 drogenase ExaC, arginine deiminase ArcA, and glyceraldehyde 3-phosphate dehydrogenase.

8 our system: alpha-synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase.

9 itrosylation of the major apoptotic effector glyceraldehyde-3-phosphate dehydrogenase.

10 an operon that encode the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

11 A 39-kDa species was identified as glyceraldehyde-3-phosphate dehydrogenase.

12 vels of Rb, E2F, dihydrofolate reductase, or glyceraldehyde-3-phosphate dehydrogenase.

13 We have identified one of these proteins as glyceraldehyde-3-phosphate dehydrogenase.

14 ion levels similar to the housekeeping gene, glyceraldehyde-3-phosphate dehydrogenase.

15 g protein, and Grb2), DnaJ-like protein, and glyceraldehyde-3-phosphate dehydrogenase.

16 One, gapdh, encodes the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

17 ng the non-secreted proteins gamma-actin and glyceraldehyde 3'-phosphate dehydrogenase.

18 unknown function, gapC, with similarities to glyceraldehyde-3-phosphate dehydrogenases.

19 xoplasma gondii egresses from the host cell, glyceraldehyde-3-phosphate dehydrogenase 1 (GAPDH1), whi

20 Although glyceraldehyde 3-phosphate dehydrogenase (a huntingtin b

21 Glyceraldehyde-3-phosphate dehydrogenase (a constitutive

22 phosphopeptide, including nitrate reductase, glyceraldehyde- 3-phosphate dehydrogenase, a calcium-dep

23 tose phosphate pathway by ADPr inhibition of glyceraldehyde-3-phosphate dehydrogenase, a central enzy

24 EGF or ammonia prolonged the half-life of glyceraldehyde-3-phosphate dehydrogenase, a classic subs

25 o 42 h circadian patterns in the activity of glyceraldehyde-3-phosphate dehydrogenase, a common clock

26 influential role for the nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase, a cytosolic en

27 We also show that glyceraldehyde-3-phosphate dehydrogenase, a gene induced

28 ngerprinting and peptide sequencing included glyceraldehyde-3-phosphate dehydrogenase, a glycolytic e

29 IGFBP-4, a structurally related protein, or glyceraldehyde-3-phosphate dehydrogenase, a housekeeping

30 covalent inhibitors of Plasmodium falciparum glyceraldehyde-3-phosphate dehydrogenase, a validated ta

31 -NSAID prodrug inhibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and tr

32 Both decreased glyceraldehyde-3-phosphate dehydrogenase activity and in

33 e maintenance of NAD(+) pools sufficient for glyceraldehyde-3-phosphate dehydrogenase activity and Wa

34 rst that hyperglycemia induced a decrease in glyceraldehyde-3-phosphate dehydrogenase activity in bov

35 Heparan sulfate was also capable of inducing glyceraldehyde-3-phosphate dehydrogenase aggregation, bu

36 or catalysis or FeS cluster binding, such as glyceraldehyde-3-phosphate dehydrogenase, aldehyde dehyd

37 ajor glycated amino acids) of serum albumin, glyceraldehyde-3-phosphate dehydrogenase, aldolase, and

38 erythrocytes were stained with antibodies to glyceraldehyde-3-phosphate dehydrogenase, aldolase, phos

39 exin A1/A3/A4/A5/A6, clathrin heavy chain 1, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,

40 (ATP) synthase, alphaB-crystallin, galectin, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,

41 east homologues of Hsp70 proteins), Tdh2/3p (glyceraldehyde-3-phosphate dehydrogenase, an RNA-binding

42 ve hippocampal content of glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and pyruvate de

43 ce protein of group A streptococci, has both glyceraldehyde-3-phosphate dehydrogenase and ADP-ribosyl

44 Overexpression of the secretory protein glyceraldehyde-3-phosphate dehydrogenase and ATP synthas

45 abolic enzymes, including nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase and beta-glucos

46 Nuclear complex of glyceraldehyde-3-phosphate dehydrogenase and DNA repair

47 ase, Akt kinase, phospho-BAD (inactive), and glyceraldehyde-3-phosphate dehydrogenase and increased t

48 h muscle actin protein or the mRNA levels of glyceraldehyde-3-phosphate dehydrogenase and interleukin

49 ion of proteins with a KFERQ motif including glyceraldehyde-3-phosphate dehydrogenase and Pax2.

50 demonstrated an increased ability to degrade glyceraldehyde-3-phosphate dehydrogenase and ribonucleas

51 splayed an increased ability to degrade both glyceraldehyde-3-phosphate dehydrogenase and ribonucleas

52 lic enzymes that are sensitive to oxidation, glyceraldehyde-3-phosphate dehydrogenase and the sodium-

53 rase, glucose-6-phosphate dehydrogenase, and glyceraldehyde-3-phosphate dehydrogenase) and their resp

54 rprisingly, p38 represents a nuclear form of glyceraldehyde-3-phosphate dehydrogenase, and binding to

55 her macromolecules including Tau, ubiquitin, glyceraldehyde-3-phosphate dehydrogenase, and glycosamin

56 le expression level such actin, tubulin, and glyceraldehyde-3-phosphate dehydrogenase are frequently

57 Preexisting stable mRNAs (e.g., GAPDH [glyceraldehyde-3-phosphate dehydrogenase]) are rapidly d

58 We have obtained soluble recombinant sperm glyceraldehyde-3-phosphate dehydrogenase as a heterotetr

59 Of the latter, we confirmed glyceraldehyde-3-phosphate dehydrogenase as a key target

60 Colell et al. identify the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase as a potent inh

61 ocytes, and identified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most sel

62 with micromolar to submicromolar potency in glyceraldehyde-3-phosphate dehydrogenase assays, an impr

63 We found that the HKGs glyceraldehyde-3-phosphate dehydrogenase, beta actin and

64 Glyceraldehyde 3-phosphate dehydrogenase binds tightly t

65 e, while spermadhesin-1, gelsolin, tubulins, glyceraldehyde-3-phosphate dehydrogenase, calmodulin, AT

66 gs indicate that the HMGB1-HMGB2-HSC70-ERp60-glyceraldehyde 3-phosphate dehydrogenase complex detects

67 in prefibrillar species, the heparin-induced glyceraldehyde-3-phosphate dehydrogenase early oligomers

68 In addition, we found that the chloroplast glyceraldehyde-3-phosphate dehydrogenase enzyme activity

69 in vitro the early oligomers present in the glyceraldehyde-3-phosphate dehydrogenase fibrillation pa

70 of the light-activated pea leaf chloroplast glyceraldehyde-3-phosphate dehydrogenase form a disulfid

71 vailability of the structure of the extended glyceraldehyde-3-phosphate dehydrogenase from the archae

72 tein with significant sequence similarity to glyceraldehyde-3-phosphate dehydrogenases from other org

73 the activity of the oxidatively inactivated glyceraldehyde-3-phosphate dehydrogenase (G-3PD) in H2O2

74 uctase (GR), thioredoxin reductase (TR), and glyceraldehyde-3-phosphate dehydrogenase (G3PD) activiti

75 nzymes involved in the generation of ATP are glyceraldehyde-3-phosphate dehydrogenase (G3PD) and phos

76 ase (GR)-specific activity and a 24% loss in glyceraldehyde-3-phosphate dehydrogenase (G3PD)-specific

77 reatine kinase, aldolase A and an isoform of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed

78 sp-Glu-Ala-Asp) box polypeptide, beta-actin, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexi

79 study based on the single-copy nuclear gene glyceraldehyde 3-phosphate dehydrogenase (G3pdh).

80 Binding of glyceraldehyde-3-phosphate dehydrogenase (G3PDH) and ald

81 ocytes, suggesting limited flux throught the glyceraldehyde-3-phosphate dehydrogenase (G3PDH) step in

82 argeted hAuNP exhibited high specificity for glyceraldehyde 3-phosphate dehydrogenase (GADPH) mRNA in

83 , which encodes the B subunit of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GADPH) of Arab

84 yphal wall protein-1 (Hwp1); enolase (Enol); glyceraldehyde-3-phosphate dehydrogenase (Gap1); and pho

85 onstituted by the combined activities of the glyceraldehyde 3-phosphate dehydrogenases GapA/GapB and

86 t encode the A and B subunits of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GAPA and GAPB)

87 The cytosolic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPC) catalyze

88 A cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPC) was iden

89 nduce the nuclear translocation of cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPC), but its

90 thaliana) plastidial glycolytic isoforms of glyceraldehyde-3-phosphate dehydrogenase (GAPCp) in phot

91 e show that the cytosolic glycolytic enzymes glyceraldehyde-3-phosphate dehydrogenases (GAPCs) intera

92 ects and report association with SNPs in the glyceraldehyde-3-phosphate dehydrogenase (GAPD) gene.

93 Successful single cell analysis of the glyceraldehyde 3 phosphate dehydrogenase (GAPDH) gene in

94 ity of two commonly used housekeeping genes, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and 18S

95 complete recovery of oxidatively inactivated glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glu

96 lvin cycle by forming a ternary complex with glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and pho

97 Phosphoribulokinase (PRK) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) are ess

98 olved in this DNA-protein complex identified glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as a co

99 e identified the mammalian glycolysis enzyme glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as an N

100 These acyloxy nitroso compounds inhibit glyceraldehyde 3-phosphate dehydrogenase (GAPDH) by form

101 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has bee

102 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is a gl

103 elta12 desaturase, superoxide dismutase, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) mRNA wi

104 hat the P39 peptide is a structural mimic of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) on the

105 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) plays a

106 A chicken glyceraldehyde 3-phosphate dehydrogenase (GAPDH) process

107 ase 1, Lupus Ku autoantigen protein p70, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) protein

108 Arginine kinase (AK) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were de

109 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a cell

110 Here, we demonstrate that glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a conv

111 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a prot

112 ol) and measured for total protein quantity, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), citrat

113 ly reported specific interaction of cellular glyceraldehyde 3-phosphate dehydrogenase (GAPDH), the ke

114 n 1 (Nramp1), ceruloplasmin, hephaestin, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH), were m

115 The glyceraldehyde 3-phosphate dehydrogenase (GAPDH)-normali

116 n, aggregation, and nuclear translocation of glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

117 ose-1,6-bisphosphate aldolase (aldolase) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

118 ive oxygen species accumulate and inactivate glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

119 itated glucose transport into the cytoplasm; glyceraldehyde 3-phosphate dehydrogenase (GAPDH; a glyco

120 Tetrameric rabbit muscle glyceraldehyde 3-phosphate dehydrogenase (GAPDH; EC 1.2.

121 ulin), elongation factor 1 alpha (EF1alpha), glyceraldehyde-3 phosphate dehydrogenase (GAPDH), 40 S r

122 hat is, PML-RAR alpha mRNA copies divided by glyceraldehyde-3'-phosphate dehydrogenase (GAPDH) mRNA c

123 etoxification via synergistic interaction of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and a m

124 Rab2 requires glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and aty

125 orms an inactive supramolecular complex with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and pho

126 identified as possibly acetylated, including glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Rpa

127 hat are regulated by S-nitrosylation such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the

128 pathway initiated by the interaction between glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the

129 cting proteins to be the glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and tri

130 The glycolytic enzymes aldolase and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) are als

131 y experimental approaches, we identified the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a C1

132 us and processed for RT-PCR and qrtPCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an e

133 quantitative reverse transcription-PCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as cont

134 We found that I/R induces glyceraldehyde-3-phosphate dehydrogenase (GAPDH) associa

135 ), a NO+ donor, modified the thiol groups of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) by S-ni

136 ix and Bcl-xL proteins decreased relative to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) control

137 ose-1,6-bisphosphate aldolase (aldolase) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) followe

138 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from hu

139 Translocation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from th

140 The enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from th

141 The structure of glycosomal glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from th

142 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from th

143 Sequence analysis of two nuclear-encoded glyceraldehyde-3-phosphate dehydrogenase (GAPDH) genes i

144 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) has bee

145 Recently, a surface-bound glyceraldehyde-3-phosphate dehydrogenase (GAPDH) has bee

146 ir ability to perform molecular targeting of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in huma

147 The translocation and accumulation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in the

148 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a cl

149 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a gl

150 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ke

151 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a mu

152 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a mu

153 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ub

154 NAD-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ub

155 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an a

156 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an e

157 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is cova

158 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is ofte

159 In a second pathway, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate

160 ling cascade involving nitric oxide (NO) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate

161 bservations suggested that the length of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA 3'

162 All results were normalized according to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA in

163 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) partici

164 ow that, unexpectedly, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) physica

165 METH also increases glyceraldehyde-3-phosphate dehydrogenase (GAPDH) protein

166 malization of cDNA templates was achieved by glyceraldehyde-3-phosphate dehydrogenase (GAPDH) quantif

167 n kinase C iota/lambda (aPKCiota/lambda) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) recruit

168 Using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) silenci

169 yzed the mechanism of NADH-channeling from D-glyceraldehyde-3-phosphate dehydrogenase (GAPDH) to L-la

170 mide gel electrophoresis, and phosphorylated glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide

171 regulated telomere-binding proteins, nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide

172 protein of 362 amino acids with identity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was obt

173 dual photooxidizable residues in the protein glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were ex

174 ar SMCs that involves interaction of nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with ap

175 id (KA) is a selective covalent inhibitor of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a crit

176 nown to serve as receptors for Plg including glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a cyto

177 ontrolled gene, ccg-7, showing similarity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a glyc

178 P-ribosyl)ation of the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a modi

179 a natural product that specifically inhibits glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a rate

180 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), an imp

181 s adenylate kinase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and en

182 ei glycosomal phosphoglycerate kinase (PGK), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and gl

183 g transcription of the cyclophilin A (PPIA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and se

184 Its ability to protect citrate synthase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th

185 otein kinase C iota/lambda (PKCiota/lambda), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th

186 lity, some common housekeeping genes such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a

187 GSTP1, and GSTT1) and three reference gene [glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a

188 Commonly used glyceraldehyde-3-phosphate dehydrogenase (Gapdh), beta-a

189 two major proteins, creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), confor

190 h neurotoxicity may be sufficient to inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH), experi

191 yotic translation elongation factor 2 (EF2), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), hypoxa

192 ion and inhibition of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), in vit

193 numbers of a constitutively expressed gene, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), were a

194 Superoxide inhibits glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

195 gical concentrations, nitroalkenes inhibited glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

196 ssion and the involvement in this process of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

197 dy, we have discovered that Escherichia coli glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

198 ent, pathways have been uncovered: (1) a p53-glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-BAX pat

199 cycle enzymes phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

200 es fructose bisphosphate aldolase (FBPA) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

201 o oxidative stress: creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

202 We focused on one of these, glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

203 nown association with NFTs; one of these was glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

204 esicles also contained the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

205 forms of all six mammalian Prx isoforms and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

206 s (VTCs) where PKCiota/lambda phosphorylates glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

207 e identified as low micromolar inhibitors of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

208 to Rab2 also contained the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

209 ellar neurons involves the overexpression of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

210 degree of homology to the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

211 huntingtin protein and the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

212 n of nitric oxide (NO), which S-nitrosylates glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

213 keeping genes beta-2 microglobulin (B2M) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

214 ar localization of the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

215 bind directly to the L1 interaction partner glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

216 otein 1 (NSAP1), ribosomal protein L13a, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

217 lated a 37-kDa AUBP, which was identified as glyceraldehyde-3-phosphate dehydrogenase (GAPDH).To summ

218 e [IA, an inhibitor of the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH)] on end

219 ipt [0.24 versus 0.008% relative to 100% for glyceraldehyde-3-phosphate dehydrogenase (GAPDH)], the r

220 olar concentrations of palmitoyl-CoA inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.

221 en reading frame of gap genes for glycolytic glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.

222 Glyceraldehyde-3-phosphate dehydrogenases (GAPDH) from t

223 s the abundance of glycolytic enzymes (e.g., glyceraldehyde-3-phosphate dehydrogenase [GAPDH]) and tr

224 We report the cloning and sequence of the glyceraldehyde-3-phosphate dehydrogenase gene (GAP) from

225 ry metabolic growth under the control of the glyceraldehyde-3-phosphate dehydrogenase gene promoter,

226 designed to target the histidine kinase and glyceraldehyde-3-phosphate dehydrogenase genes of B. der

227 s on several genes including c-myc, p21, and glyceraldehyde-3-phosphate dehydrogenase genes, indicati

228 lytic domain of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) in whi

229 of tropomyosin, arginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenase (GPDH), calcium

230 Sperm glyceraldehyde-3-phosphate dehydrogenase has been shown

231 ggregation of malate dehydrogenase (MDH) and glyceraldehyde-3-phosphate dehydrogenase heated to 45 de

232 or bovine serum albumin, choriogonadotropin, glyceraldehyde-3-phosphate dehydrogenase, Herceptin, and

233 inity-purified proteins we identified actin, glyceraldehyde-3-phosphate dehydrogenase, HSP27, protein

234 calcium channels; DC, dendritic cell; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; IFN-gamma, int

235 s a heterotetramer with the Escherichia coli glyceraldehyde-3-phosphate dehydrogenase in a ratio of 1

236 Two crystal structures of L. mexicana glyceraldehyde-3-phosphate dehydrogenase in complex with

237 b proteins, alpha-synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase in cultured hip

238 is inhibited by iodoacetate, an inhibitor of glyceraldehyde-3-phosphate dehydrogenase in glycolysis.

239 l respiratory chain enzymes, inactivation of glyceraldehyde-3-phosphate dehydrogenase, inhibition of

240 ucose, koningic acid (10 microM), a specific glyceraldehyde-3-phosphate dehydrogenase inhibitor, incr

241 ent of glucose metabolism via iodoacetate, a glyceraldehyde-3-phosphate dehydrogenase inhibitor, is s

242 Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic

243 with dithiobispropionimidate indicated that glyceraldehyde-3-phosphate dehydrogenase is a near neigh

244 ression levels, we found that beta-actin and glyceraldehyde-3-phosphate dehydrogenase levels fluctuat

245 sin-beta4, alpha-tubulin, alphaB-crystallin, glyceraldehyde-3-phosphate dehydrogenase, metallothionei

246 metastases and on normalization to 5 x 10(6) glyceraldehyde-3'-phosphate dehydrogenase mRNA copies, n

247 hamtreated rats (kidney, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati

248 us 0.58 +/- 0.04; liver, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati

249 ERbeta mRNA steady-state levels (relative to glyceraldehyde-3-phosphate dehydrogenase mRNA) were sign

250 HeLa cell surface copurified with authentic glyceraldehyde-3-phosphate dehydrogenase (muscle form) (

251 ng cytosolic creatine kinase, tropomyosin 1, glyceraldehyde-3-phosphate dehydrogenase, myosin light c

252 6 arbitrary units, respectively, relative to glyceraldehyde-3-phosphate dehydrogenase (n = 5, p = non

253 re we report a mechanism by which glycolytic glyceraldehyde-3-phosphate dehydrogenase of Arabidopsis

254 nin, and Tmod) but did not affect endogenous glyceraldehyde-3-phosphate dehydrogenase or expression f

255 apparently unrelated to vesicular transport (glyceraldehyde-3-phosphate dehydrogenase or lactic dehyd

256 g reduced levels of the Calvin cycle enzymes glyceraldehyde-3-phosphate dehydrogenase or ribulose-1,5

257 Cytosolic Oryza sativa glyceraldehyde-3-phosphate dehydrogenase (OsGAPDH), the

258 eleton), protein 4.1, protein 4.2, aldolase, glyceraldehyde-3-phosphate dehydrogenase, phosphofructok

259 r) had C-terminal lysine residues and three (glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera

260 osphoglucose isomerase, phosphofructokinase, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera

261 chromosome 4 (heterochromatic) and the human glyceraldehyde-3-phosphate dehydrogenase promoter (euchr

262 ry metabolic growth under the control of the glyceraldehyde-3-phosphate dehydrogenase promoter.

263 cle pyruvate kinase, malate dehydrogenase 1, glyceraldehyde-3-phosphate dehydrogenase, proteoglycan 4

264 ere, we use RNA-seq to identify three genes (GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE (PvGAPC1), ORGA

265 Catfish L-lactate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, pyruvate kinas

266 e with hyperplastic polyps (median IFN-gamma/glyceraldehyde-3-phosphate dehydrogenase ratio x 100,000

267 ted no significant effect of furosemide (NCC/glyceraldehyde-3-phosphate dehydrogenase ratios: group 1

268 ction of siRNA(GAPDH) [small interfering RNA(glyceraldehyde 3-phosphate dehydrogenase)] reduces PLCbe

269 ructures of human somatic and sperm-specific glyceraldehyde-3-phosphate dehydrogenase revealed few di

270 nces in amounts of WDNM1, epsilon-casein, or glyceraldehyde-3-phosphate dehydrogenase RNA were observ

271 c peptides independently confirmed actin and glyceraldehyde-3-phosphate dehydrogenase S-thiolation du

272 Glyceraldehyde 3-phosphate dehydrogenase-S (GAPDS) is th

273 1), penicillin-binding protein 2b (SAG0765), glyceraldehyde-3-phosphate dehydrogenase (SAG0823), and

274 of cocaine are mediated by the nitric oxide-glyceraldehyde-3-phosphate dehydrogenase signaling pathw

275 re determined by measuring the ratio of OP-1/glyceraldehyde 3-phosphate dehydrogenase signals for eac

276 establish the blockade of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step as the cen

277 eads to the attenuation of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step due to the

278 f glycolytic intermediates before and at the glyceraldehyde 3-phosphate dehydrogenase step, promoting

279 decreased glycolytic intermediates after the glyceraldehyde 3-phosphate dehydrogenase step, thereby r

280 to attenuation of glycolysis by blocking the glyceraldehyde 3-phosphate dehydrogenase step.

281 ever, further detailed analysis of the sperm glyceraldehyde-3-phosphate dehydrogenase structure revea

282 t difference compared with published somatic glyceraldehyde-3-phosphate dehydrogenase structures that

283 E. coli and demonstration that the resulting glyceraldehyde-3-phosphate dehydrogenase, the normal tar

284 e, after which glutathione S-transferase and glyceraldehyde-3-phosphate dehydrogenase then ATPases un

285 re determined by (1)H NMR spectroscopy using glyceraldehyde 3-phosphate dehydrogenase to trap the fir

286 o observed on binding of a metabolic enzyme, glyceraldehyde-3-phosphate dehydrogenase, to cdAE1.

287 dentified four points in central metabolism (Glyceraldehyde 3-phosphate dehydrogenase, transaldolase,

288 y untargeted glycolytic enzymes, aldolase A, glyceraldehyde 3-phosphate dehydrogenase, triose phospha

289 A +142-Da delta(m) on glyceraldehyde-3-phosphate dehydrogenase was automatical

290 he mRNA abundance for lipoprotein lipase and glyceraldehyde-3-phosphate dehydrogenase was elevated in

291 The GPD gene encoding glyceraldehyde-3-phosphate dehydrogenase was isolated fr

292 Glyceraldehyde-3-phosphate dehydrogenase was used as a h

293 ression of other genes, such as p21, p53, or glyceraldehyde-3-phosphate dehydrogenase, was not reduce

294 of human, T. brucei, and Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase, we designed ad

295 the intrinsic beta-actin, alpha-tubulin, and glyceraldehyde 3-phosphate dehydrogenase, which are usua

296 Fluoride decreased expression of glyceraldehyde-3-phosphate dehydrogenase, which acts to

297 of multifunctional, cell-surface-associated glyceraldehyde-3-phosphate dehydrogenases, which not onl

298 ed with an siRNA for the housekeeping enzyme glyceraldehyde-3-phosphate dehydrogenase, wild-type HSV

299 itution of malonylated lysine residue 184 in glyceraldehyde 3-phosphate dehydrogenase with glutamic a

300 enhanced the rate of S-glutathionylation of glyceraldehyde-3-phosphate dehydrogenase with GSSG or S-