コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 -C but had no effect on beta-actin or GAPDH (glyceraldehyde-3-phosphate dehydrogenase).
2 in O) and plr (encoding the plasmin receptor/glyceraldehyde-3-phosphate dehydrogenase).
3 and an internal manufacturer control, GAPDH (glyceraldehyde-3-phosphate dehydrogenase).
4 SC70, protein disulfide isomerase ERp60, and glyceraldehyde 3-phosphate dehydrogenase.
5 ein, the promyelocytic leukemia protein, and glyceraldehyde 3-phosphate dehydrogenase.
6 drogenase ExaC, arginine deiminase ArcA, and glyceraldehyde 3-phosphate dehydrogenase.
7 ersulfidation leads to decreased activity of 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 One, gapdh, encodes the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.
12 A 39-kDa species was identified as glyceraldehyde-3-phosphate dehydrogenase.
13 vels of Rb, E2F, dihydrofolate reductase, or glyceraldehyde-3-phosphate dehydrogenase.
14 We have identified one of these proteins as glyceraldehyde-3-phosphate dehydrogenase.
15 ion levels similar to the housekeeping gene, glyceraldehyde-3-phosphate dehydrogenase.
16 g protein, and Grb2), DnaJ-like protein, and glyceraldehyde-3-phosphate dehydrogenase.
17 on pair, not unlike that found in papain and glyceraldehyde-3-phosphate dehydrogenase.
18 ng the non-secreted proteins gamma-actin and glyceraldehyde 3'-phosphate dehydrogenase.
19 unknown function, gapC, with similarities to glyceraldehyde-3-phosphate dehydrogenases.
20 xoplasma gondii egresses from the host cell, glyceraldehyde-3-phosphate dehydrogenase 1 (GAPDH1), whi
21 d to the identification of these proteins as glyceraldehyde-3-phosphate dehydrogenase (40 kDa), creat
24 phosphopeptide, including nitrate reductase, glyceraldehyde- 3-phosphate dehydrogenase, a calcium-dep
25 tose phosphate pathway by ADPr inhibition of glyceraldehyde-3-phosphate dehydrogenase, a central enzy
26 EGF or ammonia prolonged the half-life of glyceraldehyde-3-phosphate dehydrogenase, a classic subs
27 o 42 h circadian patterns in the activity of glyceraldehyde-3-phosphate dehydrogenase, a common clock
28 influential role for the nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase, a cytosolic en
30 ngerprinting and peptide sequencing included glyceraldehyde-3-phosphate dehydrogenase, a glycolytic e
31 IGFBP-4, a structurally related protein, or glyceraldehyde-3-phosphate dehydrogenase, a housekeeping
32 covalent inhibitors of Plasmodium falciparum glyceraldehyde-3-phosphate dehydrogenase, a validated ta
33 -NSAID prodrug inhibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and tr
35 rst that hyperglycemia induced a decrease in glyceraldehyde-3-phosphate dehydrogenase activity in bov
36 Heparan sulfate was also capable of inducing glyceraldehyde-3-phosphate dehydrogenase aggregation, bu
37 or catalysis or FeS cluster binding, such as glyceraldehyde-3-phosphate dehydrogenase, aldehyde dehyd
38 ajor glycated amino acids) of serum albumin, glyceraldehyde-3-phosphate dehydrogenase, aldolase, and
39 erythrocytes were stained with antibodies to glyceraldehyde-3-phosphate dehydrogenase, aldolase, phos
40 exin A1/A3/A4/A5/A6, clathrin heavy chain 1, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,
41 (ATP) synthase, alphaB-crystallin, galectin, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,
42 east homologues of Hsp70 proteins), Tdh2/3p (glyceraldehyde-3-phosphate dehydrogenase, an RNA-binding
43 ve hippocampal content of glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and pyruvate de
44 ce protein of group A streptococci, has both glyceraldehyde-3-phosphate dehydrogenase and ADP-ribosyl
46 abolic enzymes, including nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase and beta-glucos
48 ase, Akt kinase, phospho-BAD (inactive), and glyceraldehyde-3-phosphate dehydrogenase and increased t
49 h muscle actin protein or the mRNA levels of glyceraldehyde-3-phosphate dehydrogenase and interleukin
51 demonstrated an increased ability to degrade glyceraldehyde-3-phosphate dehydrogenase and ribonucleas
52 splayed an increased ability to degrade both glyceraldehyde-3-phosphate dehydrogenase and ribonucleas
53 lic enzymes that are sensitive to oxidation, glyceraldehyde-3-phosphate dehydrogenase and the sodium-
54 rase, glucose-6-phosphate dehydrogenase, and glyceraldehyde-3-phosphate dehydrogenase) and their resp
55 rprisingly, p38 represents a nuclear form of glyceraldehyde-3-phosphate dehydrogenase, and binding to
56 her macromolecules including Tau, ubiquitin, glyceraldehyde-3-phosphate dehydrogenase, and glycosamin
57 2, and the glycolytic enzymes aldolase B and glyceraldehyde-3-phosphate dehydrogenase, and liver pyru
58 le expression level such actin, tubulin, and glyceraldehyde-3-phosphate dehydrogenase are frequently
60 We have obtained soluble recombinant sperm glyceraldehyde-3-phosphate dehydrogenase as a heterotetr
61 Colell et al. identify the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase as a potent inh
62 ranscription-polymerase chain reaction using glyceraldehyde-3-phosphate dehydrogenase as an internal
63 ocytes, and identified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most sel
64 with micromolar to submicromolar potency in glyceraldehyde-3-phosphate dehydrogenase assays, an impr
67 gs indicate that the HMGB1-HMGB2-HSC70-ERp60-glyceraldehyde 3-phosphate dehydrogenase complex detects
68 in prefibrillar species, the heparin-induced glyceraldehyde-3-phosphate dehydrogenase early oligomers
69 In addition, we found that the chloroplast glyceraldehyde-3-phosphate dehydrogenase enzyme activity
70 in vitro the early oligomers present in the glyceraldehyde-3-phosphate dehydrogenase fibrillation pa
71 of the light-activated pea leaf chloroplast glyceraldehyde-3-phosphate dehydrogenase form a disulfid
72 vailability of the structure of the extended glyceraldehyde-3-phosphate dehydrogenase from the archae
73 tein with significant sequence similarity to glyceraldehyde-3-phosphate dehydrogenases from other org
74 the activity of the oxidatively inactivated glyceraldehyde-3-phosphate dehydrogenase (G-3PD) in H2O2
75 uctase (GR), thioredoxin reductase (TR), and glyceraldehyde-3-phosphate dehydrogenase (G3PD) activiti
76 nzymes involved in the generation of ATP are glyceraldehyde-3-phosphate dehydrogenase (G3PD) and phos
77 ase (GR)-specific activity and a 24% loss in glyceraldehyde-3-phosphate dehydrogenase (G3PD)-specific
78 reatine kinase, aldolase A and an isoform of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed
79 sp-Glu-Ala-Asp) box polypeptide, beta-actin, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexi
82 ocytes, suggesting limited flux throught the glyceraldehyde-3-phosphate dehydrogenase (G3PDH) step in
83 argeted hAuNP exhibited high specificity for glyceraldehyde 3-phosphate dehydrogenase (GADPH) mRNA in
84 , which encodes the B subunit of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GADPH) of Arab
85 yphal wall protein-1 (Hwp1); enolase (Enol); glyceraldehyde-3-phosphate dehydrogenase (Gap1); and pho
86 onstituted by the combined activities of the glyceraldehyde 3-phosphate dehydrogenases GapA/GapB and
87 t encode the A and B subunits of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GAPA and GAPB)
91 thaliana) plastidial glycolytic isoforms of glyceraldehyde-3-phosphate dehydrogenase (GAPCp) in phot
92 e show that the cytosolic glycolytic enzymes glyceraldehyde-3-phosphate dehydrogenases (GAPCs) intera
93 ects and report association with SNPs in the glyceraldehyde-3-phosphate dehydrogenase (GAPD) gene.
95 ity of two commonly used housekeeping genes, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and 18S
96 complete recovery of oxidatively inactivated glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glu
97 lvin cycle by forming a ternary complex with glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and pho
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
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
107 ase 1, Lupus Ku autoantigen protein p70, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) protein
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
120 hat is, PML-RAR alpha mRNA copies divided by glyceraldehyde-3'-phosphate dehydrogenase (GAPDH) mRNA c
121 etoxification via synergistic interaction of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and a m
123 orms an inactive supramolecular complex with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and pho
124 identified as possibly acetylated, including glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Rpa
125 hat are regulated by S-nitrosylation such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the
126 pathway initiated by the interaction between glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the
127 cting proteins to be the glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and tri
129 y experimental approaches, we identified the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a C1
130 us and processed for RT-PCR and qrtPCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an e
131 quantitative reverse transcription-PCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as cont
132 antisense riboprobes specific for c-fos and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as well
134 ), a NO+ donor, modified the thiol groups of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) by S-ni
135 ix and Bcl-xL proteins decreased relative to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) control
136 ose-1,6-bisphosphate aldolase (aldolase) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) followe
142 Sequence analysis of two nuclear-encoded glyceraldehyde-3-phosphate dehydrogenase (GAPDH) genes i
145 ir ability to perform molecular targeting of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in huma
157 In a second pathway, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate
158 ling cascade involving nitric oxide (NO) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate
159 bservations suggested that the length of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA 3'
160 All results were normalized according to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA in
161 b) or PDE4D (7.6 kb) were normalized against glyceraldehyde-3-phosphate dehydrogenase (GAPDH) or ribo
163 ow that, unexpectedly, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) physica
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
169 mide gel electrophoresis, and phosphorylated glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide
170 regulated telomere-binding proteins, nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide
171 protein of 362 amino acids with identity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was obt
172 dual photooxidizable residues in the protein glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were ex
173 ar SMCs that involves interaction of nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with ap
174 nown to serve as receptors for Plg including glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a cyto
175 ontrolled gene, ccg-7, showing similarity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a glyc
176 P-ribosyl)ation of the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a modi
178 s adenylate kinase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and en
179 ei glycosomal phosphoglycerate kinase (PGK), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and gl
180 g transcription of the cyclophilin A (PPIA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and se
181 otein kinase C iota/lambda (PKCiota/lambda), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th
182 Its ability to protect citrate synthase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th
183 lity, some common housekeeping genes such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a
184 GSTP1, and GSTT1) and three reference gene [glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a
186 two major proteins, creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), confor
187 h neurotoxicity may be sufficient to inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH), experi
188 ion and inhibition of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), in vit
189 11/11 with amino acids 67-77 of human liver glyceraldehyde-3-phosphate dehydrogenase (GAPDH), respec
190 numbers of a constitutively expressed gene, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), were a
192 gical concentrations, nitroalkenes inhibited glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which
193 ssion and the involvement in this process of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which
194 dy, we have discovered that Escherichia coli glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which
195 ent, pathways have been uncovered: (1) a p53-glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-BAX pat
212 lated a 37-kDa AUBP, which was identified as glyceraldehyde-3-phosphate dehydrogenase (GAPDH).To summ
213 e [IA, an inhibitor of the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH)] on end
214 ipt [0.24 versus 0.008% relative to 100% for glyceraldehyde-3-phosphate dehydrogenase (GAPDH)], the r
215 olar concentrations of palmitoyl-CoA inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.
216 en reading frame of gap genes for glycolytic glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.
218 s the abundance of glycolytic enzymes (e.g., glyceraldehyde-3-phosphate dehydrogenase [GAPDH]) and tr
219 We report the cloning and sequence of the glyceraldehyde-3-phosphate dehydrogenase gene (GAP) from
220 ry metabolic growth under the control of the glyceraldehyde-3-phosphate dehydrogenase gene promoter,
221 designed to target the histidine kinase and glyceraldehyde-3-phosphate dehydrogenase genes of B. der
222 s on several genes including c-myc, p21, and glyceraldehyde-3-phosphate dehydrogenase genes, indicati
223 lytic domain of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) in whi
224 of tropomyosin, arginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenase (GPDH), calcium
226 ggregation of malate dehydrogenase (MDH) and glyceraldehyde-3-phosphate dehydrogenase heated to 45 de
227 or bovine serum albumin, choriogonadotropin, glyceraldehyde-3-phosphate dehydrogenase, Herceptin, and
228 inity-purified proteins we identified actin, glyceraldehyde-3-phosphate dehydrogenase, HSP27, protein
229 calcium channels; DC, dendritic cell; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; IFN-gamma, int
230 s a heterotetramer with the Escherichia coli glyceraldehyde-3-phosphate dehydrogenase in a ratio of 1
232 b proteins, alpha-synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase in cultured hip
233 is inhibited by iodoacetate, an inhibitor of glyceraldehyde-3-phosphate dehydrogenase in glycolysis.
234 l respiratory chain enzymes, inactivation of glyceraldehyde-3-phosphate dehydrogenase, inhibition of
235 ucose, koningic acid (10 microM), a specific glyceraldehyde-3-phosphate dehydrogenase inhibitor, incr
236 ent of glucose metabolism via iodoacetate, a glyceraldehyde-3-phosphate dehydrogenase inhibitor, is s
239 with dithiobispropionimidate indicated that glyceraldehyde-3-phosphate dehydrogenase is a near neigh
240 ression levels, we found that beta-actin and glyceraldehyde-3-phosphate dehydrogenase levels fluctuat
241 sin-beta4, alpha-tubulin, alphaB-crystallin, glyceraldehyde-3-phosphate dehydrogenase, metallothionei
242 metastases and on normalization to 5 x 10(6) glyceraldehyde-3'-phosphate dehydrogenase mRNA copies, n
243 hamtreated rats (kidney, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati
244 us 0.58 +/- 0.04; liver, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati
245 ERbeta mRNA steady-state levels (relative to glyceraldehyde-3-phosphate dehydrogenase mRNA) were sign
247 HeLa cell surface copurified with authentic glyceraldehyde-3-phosphate dehydrogenase (muscle form) (
248 ng cytosolic creatine kinase, tropomyosin 1, glyceraldehyde-3-phosphate dehydrogenase, myosin light c
249 6 arbitrary units, respectively, relative to glyceraldehyde-3-phosphate dehydrogenase (n = 5, p = non
250 ect on the levels of mRNA for beta-actin and glyceraldehyde-3-phosphate dehydrogenase nor on levels o
251 nin, and Tmod) but did not affect endogenous glyceraldehyde-3-phosphate dehydrogenase or expression f
252 apparently unrelated to vesicular transport (glyceraldehyde-3-phosphate dehydrogenase or lactic dehyd
253 g reduced levels of the Calvin cycle enzymes glyceraldehyde-3-phosphate dehydrogenase or ribulose-1,5
255 this promoter in the following order: gapdh (glyceraldehyde-3-phosphate dehydrogenase), pgk (phosphog
256 eleton), protein 4.1, protein 4.2, aldolase, glyceraldehyde-3-phosphate dehydrogenase, phosphofructok
257 r) had C-terminal lysine residues and three (glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera
258 osphoglucose isomerase, phosphofructokinase, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera
259 chromosome 4 (heterochromatic) and the human glyceraldehyde-3-phosphate dehydrogenase promoter (euchr
262 cle pyruvate kinase, malate dehydrogenase 1, glyceraldehyde-3-phosphate dehydrogenase, proteoglycan 4
263 e with hyperplastic polyps (median IFN-gamma/glyceraldehyde-3-phosphate dehydrogenase ratio x 100,000
264 ted no significant effect of furosemide (NCC/glyceraldehyde-3-phosphate dehydrogenase ratios: group 1
265 ction of siRNA(GAPDH) [small interfering RNA(glyceraldehyde 3-phosphate dehydrogenase)] reduces PLCbe
266 ructures of human somatic and sperm-specific glyceraldehyde-3-phosphate dehydrogenase revealed few di
267 nces in amounts of WDNM1, epsilon-casein, or glyceraldehyde-3-phosphate dehydrogenase RNA were observ
268 c peptides independently confirmed actin and glyceraldehyde-3-phosphate dehydrogenase S-thiolation du
270 1), penicillin-binding protein 2b (SAG0765), glyceraldehyde-3-phosphate dehydrogenase (SAG0823), and
271 of cocaine are mediated by the nitric oxide-glyceraldehyde-3-phosphate dehydrogenase signaling pathw
272 re determined by measuring the ratio of OP-1/glyceraldehyde 3-phosphate dehydrogenase signals for eac
273 establish the blockade of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step as the cen
274 eads to the attenuation of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step due to the
275 f glycolytic intermediates before and at the glyceraldehyde 3-phosphate dehydrogenase step, promoting
276 decreased glycolytic intermediates after the glyceraldehyde 3-phosphate dehydrogenase step, thereby r
278 ever, further detailed analysis of the sperm glyceraldehyde-3-phosphate dehydrogenase structure revea
279 t difference compared with published somatic glyceraldehyde-3-phosphate dehydrogenase structures that
280 E. coli and demonstration that the resulting glyceraldehyde-3-phosphate dehydrogenase, the normal tar
281 e, after which glutathione S-transferase and glyceraldehyde-3-phosphate dehydrogenase then ATPases un
282 re determined by (1)H NMR spectroscopy using glyceraldehyde 3-phosphate dehydrogenase to trap the fir
283 o observed on binding of a metabolic enzyme, glyceraldehyde-3-phosphate dehydrogenase, to cdAE1.
284 dentified four points in central metabolism (Glyceraldehyde 3-phosphate dehydrogenase, transaldolase,
285 y untargeted glycolytic enzymes, aldolase A, glyceraldehyde 3-phosphate dehydrogenase, triose phospha
287 he mRNA abundance for lipoprotein lipase and glyceraldehyde-3-phosphate dehydrogenase was elevated in
290 ression of other genes, such as p21, p53, or glyceraldehyde-3-phosphate dehydrogenase, was not reduce
291 of human, T. brucei, and Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase, we designed ad
292 een only in liver, while creatine kinase and glyceraldehyde-3-phosphate dehydrogenase were absent fro
293 ptase and chymase mRNA normalized to that of glyceraldehyde-3-phosphate dehydrogenase were not apprec
294 important in glycolysis (pyruvate kinase and glyceraldehyde-3-phosphate dehydrogenase) were unaffecte
295 the intrinsic beta-actin, alpha-tubulin, and glyceraldehyde 3-phosphate dehydrogenase, which are usua
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-
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。