ライフサイエンスコーパス: decarboxylase

1 se, 2-oxoglutarate dehydrogenase and glycine decarboxylase).

2 lipoylation of the photorespiratory glycine decarboxylase.

3 pression level of Cmoxdc1 coding for oxalate decarboxylase.

4 uccinate than the pathway via 2-oxoglutarate decarboxylase.

5 t demonstrated for the classical MVA pathway decarboxylase.

6 nd characterization of any phosphomevalonate decarboxylase.

7 D1R, D2R, AMPAR, GABA(B)R and glutamic acid decarboxylase.

8 n be used by a parasite that lacks ornithine decarboxylase.

9 ehydrogenase and a subsequent glutaconyl-CoA decarboxylase.

10 synthesized putrescine via a SpeC ornithine decarboxylase.

11 synthase reaction involves a glycyl radical decarboxylase.

12 70 interacts with TH and aromatic amino acid decarboxylase.

13 dependent regulation of S-adenosylmethionine decarboxylase 1 (AMD1) stability.

14 ed conditional null alleles of Glutamic acid decarboxylase 1 (Gad1) and Resistant to dieldrin (Rdl),

15 enic mouse lines that suppress glutamic acid decarboxylase 1 (GAD1) in either cholecystokinin (CCK)-

16 used by epigenetic upregulation of glutamate decarboxylase 1 (GAD1), a regulator of the GABA neurotra

17 a-aminobutyric acid (GABA) and glutamic acid decarboxylase 1 (GAD1), the enzyme that synthesizes GABA

18 ), which is a suicide inhibitor of ornithine decarboxylase 1 (ODC1), and diethylnorspermine (DENSpm),

19 Interaction with ornithine decarboxylase 1 (ODC1), the rate-limiting enzyme of poly

20 Phosphatidylserine decarboxylase 1 (Psd1p), an ancient enzyme that converts

21 zyme that generates PE is phosphatidylserine decarboxylase 1 (Psd1p).

22 te and GABA, glutaminase (Gls) and glutamate decarboxylase 1 and 2 (Gad1 and Gad2).

23 deficits in the induction of GAD1 (glutamate decarboxylase 1) protein expression.

24 ynaptosomal-associated protein 29, glutamate decarboxylase 1, metabotropic glutamate receptor 1, and

25 n antizyme-mediated degradation of ornithine decarboxylase-1 and a resulting reduction in cellular po

26 to endosomes, and decarboxylation by PtdSer decarboxylase 2 (Psd2p) to produce phosphatidylethanolam

27 ne released from neurons expressing tyrosine decarboxylase 2 (Tdc2) signal directly to astrocytes to

28 In contrast, the silencing of glutamic acid decarboxylase 2-positive interneurons, which include the

29 ed autoantigens [proinsulin or glutamic acid decarboxylase 65 (GAD)] delayed T1D onset, but published

30 l as thyroperoxidase (TPO) and glutamic acid decarboxylase 65 (GAD65) Abs.

31 Glutamic acid decarboxylase 65 (GAD65) and autoantibodies specific for

32 ed, including orexin cells and glutamic acid decarboxylase 65 (GAD65) cells, but their interplay in o

33 on cerebellar ataxia (CA) with glutamic acid decarboxylase 65 antibodies (GAD65-Abs) is based on case

34 globulin, and the autoantigens glutamic acid decarboxylase 65, heat shock protein 60, and tyrosine ph

35 diabetes-related autoantigens (glutamic acid decarboxylase 65, insulin, heat shock protein 60, and ty

36 rologic study results revealed glutamic acid decarboxylase 65-IgG in all cases (median value, 754 nmo

37 4 classic; 5 variant; 66% were glutamic acid decarboxylase 65-IgG positive) and 1 with progressive en

38 (PMP) antibody positivity; and glutamic acid decarboxylase 65-kDa isoform (GAD65) antibody positivity

39 cond GABA-synthesizing enzyme, glutamic acid decarboxylase 65-kDa isoform (GAD65), remains unclear.

40 ssenger RNA interference targeting glutamate decarboxylase 65/67 (GAD65/67) gene expression in the nu

41 lsed with preproinsulin (PPI), glutamic acid decarboxylase (65-kDa isoform; GAD65), and insulinoma-as

42 expression of GABAergic marker glutamic acid decarboxylase 67 (GAD67) and the number of GABAergic GAD

43 nsity protein 95 (PSD95) and lower glutamate decarboxylase 67 (GAD67) expression in GluD1 KO.

44 sion levels of parvalbumin and glutamic acid decarboxylase 67 (GAD67) in schizophrenia subjects but n

45 istently found lower levels of glutamic acid decarboxylase 67 (GAD67) messenger RNA (mRNA) in the pre

46 f the GABA-synthesizing enzyme glutamic acid decarboxylase 67-kDa isoform (GAD67) in the PFC have bee

47 ytochemical markers, including glutamic acid decarboxylase-67 (GAD67), somatostatin, and neuropeptide

48 lpha-amino-beta-carboxymuconic--semialdehyde decarboxylase, a class III amidohydrolase, with a single

49 o C12 and C18 are decarboxylated by sirohaem decarboxylase, a heterodimeric enzyme composed of AhbA a

50 chanisms, with reduced aromatic L-amino acid decarboxylase (AAAD) activity closely related to the app

51 The aromatic L-amino-acid decarboxylase (AADC) defect appears to be consistently s

52 Aromatic l-amino acid decarboxylase (AADC) deficiency is an inborn error of mo

53 Aromatic l-amino acid decarboxylase (AADC) deficiency is an inherited disease

54 ygous mutations in the aromatic l-amino acid decarboxylase (AADC) gene result in a severe depletion o

55 containing the enzyme aromatic l-amino acid decarboxylase (AADC) occur not only near the central can

56 o its decarboxylation by aromatic amino acid decarboxylase (AADC), an enzyme overexpressed in these m

57 sine hydroxylase (TH), aromatic l-amino acid decarboxylase (AADC), and GTP cyclohydrolase I (GCH1) tr

58 lly express the enzyme aromatic L-amino acid decarboxylase (AADC), which synthesizes trace amines dir

59 We also show that pyruvate decarboxylase (AceE), the E1 component of pyruvate dehyd

60 The UbiD family of reversible decarboxylases act on aromatic, heteroaromatic, and unsa

61 te with enhanced aconitase and cis-aconitate decarboxylase activities by controlling the expression o

62 The recombinant Slr1099 protein displayed decarboxylase activity and catalyzed in vitro the decarb

63 vin mononucleotide (FMN)-binding protein, no decarboxylase activity has been detected.

64 Purified Cr-rPFO exhibits a specific decarboxylase activity of 12 micromol pyruvate min(-)(1)

65 vel flavin-derived cofactor required for the decarboxylase activity of UbiD.

66 the recombinant Sll0936 protein did not show decarboxylase activity regardless of the conditions used

67 rement of the enzyme responsible for in vivo decarboxylase activity remained unclear.

68 The second enzyme exhibits a decarboxylase activity that has never been directly attr

69 Inhibition of ornithine decarboxylase activity using small interfering RNA or th

70 Hydroxycinnamate decarboxylase activity was measured by the ability to tr

71 It was also observed that the decarboxylase activity was partially recovered in a hete

72 naptic dopamine synthesis capacity (ie, DOPA decarboxylase activity).

73 dc1 is solely responsible for the reversible decarboxylase activity, and that it requires a new type

74 ved to be initiated by a change in glutamate decarboxylase activity, but the underlying mechanisms ar

75 me are critical for proenzyme processing and decarboxylase activity.

76 lus cadaverine (CF) indicated biofilm lysine decarboxylase activity.

77 permidine biosynthesis: S-adenosylmethionine decarboxylase (AdoMetDC) and spermidine synthase (SpdSyn

78 s of Trypanosoma brucei S-adenosylmethionine decarboxylase alone and in functional complex with its c

79 pyruvoyl cofactor of S-adenosyl-L-methionine decarboxylase (AMD1) is dynamically controlled by intrac

80 glycyl radical enzyme 4-hydroxyphenylacetate decarboxylase, an enzyme involved in the fermentative pr

81 made possible by the evolution of a pyruvate decarboxylase, analogous to that in brewer's yeast and t

82 ways for polyamine biosynthesis via arginine decarboxylase and agmatinase were activated to rescue co

83 dE resulted in very high levels of glutamate decarboxylase and almost complete protection against aci

84 mtPE by RNAi silencing of phosphatidylserine decarboxylase and chronic reduction of mtPE in PSB-2 cel

85 lso analyzed the expression of the Histidine decarboxylase and ECP by flow cytometry and fluorescence

86 patients express higher levels of histidine decarboxylase and ECP than those from healthy volunteers

87 in H. volcanii of both the phosphomevalonate decarboxylase and isopentenyl phosphate kinase reactions

88 e show that cholangiocytes express histidine decarboxylase and its inhibition reduces CCA growth.

89 ania donovani have shown that both ornithine decarboxylase and spermidine synthase, two enzymes of th

90 4-mutant cells expressed high levels of DOPA decarboxylase and the dopamine transporter, two markers

91 g of 6-[(18) F]fluorodopa (FD; reflects dopa decarboxylase) and [(11) C]dihydrotetrabenazine (DTBZ; r

92 ichia coli induce expression of CadA (lysine decarboxylase) and CadB (lysine/cadaverine antiporter) i

93 rt (73%, P<0.01), the abundance of ornithine decarboxylase, and nitric oxide synthase (NOS3) proteins

94 Autoantibodies to insulin, glutamic acid decarboxylase, and the insulinoma-associated-2 (IA-2) mo

95 through the pro-tumorigenic enzyme ornithine decarboxylase, and this flux increases 2-fold following

96 Four patients also had high glutamic acid decarboxylase antibodies (>1000 U/ml), and one had high

97 y, many patients with SPS have glutamic acid decarboxylase antibodies (GAD-ab), but these 2 disorders

98 Little is known of glutamic acid decarboxylase antibodies (GAD-abs) in the paraneoplastic

99 espite the persistence of anti-glutamic acid decarboxylase antibodies following auto-HSCT suggests th

100 Two anti-glutamic acid decarboxylase antibody-positive patients with SPS had an

101 ornithine and polyamine synthesis, ornithine decarboxylase appeared to be the rate-limiting enzyme fo

102 Arginase, arginine deiminase and arginine decarboxylase are potential enzymes that may be used for

103 Inducible amino acid decarboxylases are known to promote adaptation to acidic

104 syltransferase and orotidine-5-monophosphate decarboxylase, are fused in a multi-domain enzyme and ar

105 A (CoA) transferase, and YfdU, an oxalyl-CoA decarboxylase, are required for the adaptation effect bu

106 techols, employing 3,4-dihydroxybenzoic acid decarboxylases (AroY) that belong to the UbiD enzyme fam

107 rom incomplete catalysis by TpcK (a putative decarboxylase), as its deletion results in a nearly 10-f

108 ge, sex, disease duration, and glutamic acid decarboxylase autoantibody titers.

109 8)F]FMT; a substrate for aromatic amino acid decarboxylase), baseline D2/3 receptor-binding potential

110 athogens (FBPs) was investigated in tyrosine decarboxylase broth (TDB) using HPLC.

111 Independent of the 2-oxoglutarate decarboxylase bypass, the gamma-aminobutyrate shunt is a

112 res provide molecular insights into malonate decarboxylase catalysis.

113 of triarylmethanols, and (3) benzoylformate decarboxylase-catalyzed enantioselective benzoin condens

114 Ferulic acid decarboxylase catalyzes the decarboxylation of phenylacr

115 Coproheme decarboxylase catalyzes two sequential oxidative decarbo

116 e 4-phosphate dehydrogenase (PdxA) oxidative decarboxylase, class II aldolase, or ribulose 1,5-bispho

117 ABCD) and syntrophic terephthalate-degrading decarboxylase complexes.

118 dC imports Glu into the cytoplasm, where Glu decarboxylases consume a cytoplasmic proton, which ends

119 PSDs are unusual decarboxylase containing a pyruvoyl prosthetic group wit

120 Cysteinesulfinic acid decarboxylase (CSAD) was induced at both the mRNA (8-fol

121 acterized clostridial p-hydroxyphenylacetate decarboxylase (CsdBC).

122 Diaminopimelate decarboxylase (DAPDC) catalyzes the final step in the di

123 genes in Drosophila encode the enzymes dopa decarboxylase (Ddc) and tyrosine hydroxylase (ple).

124 l-carbidopa, which is known to inhibit DOPA decarboxylase (DDC), a key protein in Parkinson's diseas

125 identified one dopamine synthesis gene, DOPA decarboxylase (DDC), as a suppressor of tau toxicity in

126 uences of tyrosine hydroxylase (TH) and dopa decarboxylase (DDC), two key enzymes in the biosynthesis

127 in, and trace amines, relies in part on DOPA decarboxylase (DDC, AADC), an enzyme that is required fo

128 Knockdown of MC histidine decarboxylase decreased cholangiocyte and HSC proliferat

129 These data confirm histidine decarboxylase deficiency as a rare cause of TS and ident

130 house assay for PGD of aromatic L-amino acid decarboxylase deficiency, based on an amplification refr

131 Histidine decarboxylase-deficient mice (HDCKO), which lack systemi

132 congeners originates from the activity of a decarboxylase-dehydrogenase enzyme with high similarity

133 , low levels of PE in the phosphatidylserine decarboxylase deletion mutant (psd1Delta) cause decrease

134 (a-FMHis), a suicide inhibitor of histidine decarboxylase, displayed impaired IA memory when tested

135 he polyamine biosynthetic pathway, ornithine decarboxylase, diverting the iNOS substrate l-arginine t

136 idoxal phosphate (PLP)-dependent l-aspartate decarboxylase encoded by MJ0050, the same enzyme that wa

137 The activity of the reversible decarboxylase enzyme Fdc1 is dependent on prenylated FMN

138 t through direct activation of glutamic acid decarboxylase enzyme isoforms that convert glutamate to

139 Fdc1 is a decarboxylase enzyme that requires the novel prenylated

140 atidylserine catalyzed by phosphatidylserine decarboxylase enzymes (PSD) as a suitable target for dev

141 POMC neurons, as these encode the glutamate decarboxylase enzymes GAD67 and GAD65, respectively.

142 Deltasll1981 strain, lacking 2-oxoglutarate decarboxylase, exhibited a succinate level that was 60%

143 ed here indicate that dedicated oxaloacetate decarboxylases exist in eukaryotes.

144 line expressing cre recombinase in histidine decarboxylase-expressing neurons (Hdc-Cre) followed by a

145 and a subsequent decrease of both ornithine decarboxylase expression and polyamine levels, accompani

146 at members of the beta-hydroxyacid reductive decarboxylase family employ different active site featur

147 n NAD-ME, suggesting that NAD-ME was the key decarboxylase for CAM.

148 cterization studies of a novel phenylacetate decarboxylase from an anaerobic, sewage-derived enrichme

149 ctural studies on the mevalonate diphosphate decarboxylase from E. faecalis (MDDEF).

150 ependent, irreversible inactivator of lysine decarboxylase from Hafnia alvei.

151 i xylonate dehydratase (yjhG), a 2-keto acid decarboxylase from Pseudomonas putida (mdlC) and native

152 tyric acid synthesizing enzyme glutamic acid decarboxylase (GAD) and choline acetyltransferase (ChAT)

153 th region-specific changes in glutamate acid decarboxylase (GAD) and vesicular GABA transporter expre

154 The human neuroendocrine enzyme glutamate decarboxylase (GAD) catalyses the synthesis of the inhib

155 ed by enzymes derived from two glutamic acid decarboxylase (GAD) genes, GAD1 and GAD2, both of which

156 (Fos) of GABAergic neurons and glutamic acid decarboxylase (GAD) mRNA expression in the aBST.

157 hosphate-diaphorase (NADPH-d), glutamic acid decarboxylase (GAD), cytochrome oxidase (CO), and calret

158 e parvalbumin-, calbindin-, or glutamic acid decarboxylase (GAD)-67-positive.

159 (GABA) transporter (vGAT) and glutamic acid decarboxylase (GAD)65 in the GABAergic contacts that the

160 Additionally, glutamic acid decarboxylase (GAD)65-loaded tolDCs from well-controlled

161 , we study the distribution of glutamic acid decarboxylase (GAD)67 and GLY transporter 2 (T2) in axon

162 2; VGluT2) and GABA signaling (glutamic acid decarboxylase; GAD, and vesicular GABA transporter; VGaT

163 orters (vglut1, vglut2.1, vglut3), glutamate decarboxylases (gad1, gad2), and choline acetyltransfera

164 ntional GABA-synthesizing enzymes, glutamate decarboxylases GAD65 and GAD67.

165 slet antigen (IA)-2, IA-2beta, and glutamate decarboxylase (GAD65) are major autoantigens in type 1 d

166 UT1) and the 65 kDa isoform of glutamic acid-decarboxylase (GAD65) as markers of, respectively, Ia af

167 beled for the 65 kD isoform of glutamic acid decarboxylase (GAD65), PV and the GABA(A) receptor alpha

168 nding reductions in this region of glutamate decarboxylase (GAD65/67) and markers of dendritic spines

169 oded 67-kDa protein isoform of glutamic acid decarboxylase (GAD67) is a hallmark of schizophrenia.

170 evels of the 67 kDa isoform of glutamic acid decarboxylase (GAD67) protein, the enzyme responsible fo

171 ssion of the 67-kDa isoform of glutamic acid decarboxylase (GAD67), a key enzyme for GABA synthesis,

172 vels of tyrosine hydroxylase (TH), glutamate decarboxylase (GAD67), and vesicular glutamate transport

173 tibody responses to insulin (IAA), glutamate decarboxylase (GADA), IA-2, IA-2beta, and ZnT8 were anal

174 no acid glutamate by the action of glutamate decarboxylases (GADs).

175 Gly decarboxylase (GDC) is the key component of photorespira

176 photosynthesizing tissue is used for glycine decarboxylase (GDC), necessary for the high-flux photore

177 phosphate dikinase-independent (but glycine decarboxylase (GDC)-dependent) manner, and recuperates p

178 H), and the glycine cleavage system (glycine decarboxylase [GDC]).

179 partate semialdehyde dehydrogenase, arginine decarboxylase gene activator, GTP cyclohydrolase I and a

180 omato plants over-expressing mouse ornithine decarboxylase gene under the control of fruit-specific p

181 es an upregulation of the insect's ornithine decarboxylase gene, which sequesters arginine for polyam

182 pression and activity of three tea glutamate decarboxylase genes (CsGAD1, 2, and 3), and their encode

183 Glycine decarboxylase (GLDC) acts in the glycine cleavage system

184 hydroxymethyltransferase (SHMT2) and glycine decarboxylase (GLDC) are highly expressed in the pseudop

185 e, catalase, superoxide dismutase, ornithine decarboxylase, glutamate receptor, and ammonia transport

186 Wild-type (WT) and l-histidine decarboxylase (Hdc(-/-)) mice were fed a control diet or

187 Histidine decarboxylase (HDC) and histamine receptor (HR) expressi

188 Histidine decarboxylase (HDC) deficiency has been shown to promote

189 in one integrated device to detect histidine decarboxylase (HDC) gene directly from human white blood

190 carboxypeptidase A3 (CPA3), and L-histidine decarboxylase (HDC) gene expression; and serum markers (

191 ure termination codon in the human histidine decarboxylase (Hdc) gene has been identified in a family

192 Histidine decarboxylase (HDC) is the main enzyme involved in hista

193 Histidine decarboxylase (HDC) is the unique enzyme responsible for

194 ased histamine, made by the enzyme histidine decarboxylase (HDC), enhances wakefulness.

195 A mutation in histidine decarboxylase (Hdc), the key enzyme for the biosynthesis

196 ematopoietic progenitors marked by histidine decarboxylase (Hdc).

197 the histamine-synthesizing enzyme histidine decarboxylase (HDC-KO) or acutely depleted of histamine

198 crystal structure of a Pseudomonas malonate decarboxylase hetero-tetramer, as well as biochemical an

199 The malonate decarboxylase holoenzyme contains four subunits, having

200 antigens are established (insulin, glutamate decarboxylase, IA2, and zinc transporter-8), but the mol

201 legans, RNAi depletion of phosphatidylserine decarboxylase in dopaminergic neurons expressing alpha-s

202 tant cells, in which panD encoding aspartate decarboxylase in E. coli had been knocked out, thus conf

203 the GABA-synthesizing enzyme, glutamic acid decarboxylase in EC were confirmed by immunostaining and

204 c protein-immunocytochemistry, glutamic acid decarboxylase in situ hybridization, and parvalbumin-imm

205 n addition, we identified TbPSD as type I PS decarboxylase in the mitochondrion and found that it is

206 expression of a recombinant mutant pyruvate decarboxylase in the RARE strain.

207 at least one bacterium encoding a tryptophan decarboxylase in their gut community.

208 bunit of the photorespiratory enzyme glycine decarboxylase, increased accumulation of glycine and gly

209 amine analog and potent S-adenosylmethionine decarboxylase inhibitor, decreases HIV expression in mon

210 ce treated with saline, histamine, histidine decarboxylase inhibitor, or cromolyn sodium.

211 The characterization of sirohaem decarboxylase is reported in molecular detail.

212 dual function enzyme, mevalonate 5-phosphate decarboxylase is unable to carry out the first phosphory

213 ne biosynthetic enzyme, S-adenosylmethionine decarboxylase, is regulated by heterodimer formation wit

214 romoter regulatory elements of glutamic acid decarboxylase isoforms (Gad1 and Gad2), which regulate G

215 also improved by overexpression of keto-acid decarboxylases (KDC) and alcohol dehydrogenase (ADH).

216 uring oral hygiene restriction (OHR), lysine decarboxylase (LDC) in dento-gingival biofilms converts

217 Pase RavA and the decameric inducible lysine decarboxylase LdcI-is reconstructed by cryo-electron mic

218 ng vagal activation of aromatic L-amino acid decarboxylase, leading to the production of dopamine in

219 5-Carboxyvanillate decarboxylase (LigW) catalyzes the conversion of 5-carbo

220 the promoter of the gene encoding glutamate decarboxylase-like protein 1 (GADL1) in 94 patients who

221 identified the pyridoxal phosphate-dependent decarboxylase-like proteins in the translated proteome o

222 ntify a novel family within the acetoacetate decarboxylase-like superfamily with divergent active sit

223 Mice deficient for malonyl CoA decarboxylase (MCD(-/-)), a mouse model of reduced fat o

224 Malonyl-CoA decarboxylase (MCD) has been a target of investigation b

225 SIRT4 deacetylates and inhibits malonyl CoA decarboxylase (MCD), an enzyme that produces acetyl CoA

226 cteria contain a biotin-independent malonate decarboxylase (MDC), which allows them to use malonate a

227 with a distinct prosthetic group, as well as decarboxylase (MdcD-MdcE) and acyl-carrier protein trans

228 ay by phosphorylating mevalonate diphosphate decarboxylase (MDD) at Ser(96).

229 zyme in this pathway, mevalonate diphosphate decarboxylase (MDD), acts on mevalonate diphosphate (MVA

230 form of Tourette syndrome due to L-histidine-decarboxylase mutation, with similar features in human a

231 The alternative malate decarboxylase, NADP-ME, did not appear to compensate for

232 olled by the rate-limiting enzymes ornithine decarboxylase (ODC) and spermidine-spermine N(1)-acetylt

233 ls (RWPE-1) with overexpression of ornithine decarboxylase (ODC) and used it for in vitro and in vivo

234 ornithine uptake and metabolism by ornithine decarboxylase (ODC) for survival.

235 Ornithine decarboxylase (ODC) is the sentinel enzyme in polyamine

236 Inhibition of ornithine decarboxylase (ODC) using low-dose eflornithine (DFMO, C

237 erated by the rate-limiting enzyme ornithine decarboxylase (ODC), in gastric carcinogenesis.

238 activity and protein abundance of ornithine decarboxylase (ODC), the committed enzyme for polyamine

239 we demonstrate that inhibition of ornithine decarboxylase (ODC), the rate-limiting enzyme in polyami

240 Ornithine decarboxylase (ODC), the rate-limiting enzyme in polyami

241 The plasma levels of arginase I, ornithine decarboxylase (ODC), transforming growth factor beta (TG

242 axis leading to the translation of ornithine decarboxylase (ODC).

243 matic decarboxylation; however, oxaloacetate decarboxylases (ODx) were so far not identified in eukar

244 e deletion of the orotidine 5'-monophosphate decarboxylase (OMPDC) and uridine phosphorylase (UP) gen

245 for activation of orotidine 5'-monophosphate decarboxylase (OMPDC) by interactions of side chains fro

246 Orotidine 5'-monophosphate decarboxylase (OMPDC) catalyzes the decarboxylation of 5

247 double mutant of orotidine 5'-monophosphate decarboxylase (OMPDC) from Saccharomyces cerevisiae that

248 to insulin, autoantibodies to glutamic acid decarboxylase or insulinoma-associated antigen 2, or dia

249 Oxalate decarboxylase (OxDC) catalyzes the Mn-dependent conversi

250 Oxalate decarboxylase (OxDC) catalyzes the Mn-dependent conversi

251 partate is a pyruvoyl-containing l-aspartate decarboxylase (PanD), the enzyme in M. jannaschii is a p

252 d, in microorganisms, the action of pyruvate decarboxylase (PDC) and pyruvate formate lyase (PFL)-enz

253 This enzyme, phosphomevalonate decarboxylase (PMD), exhibits strong inhibition by 6-flu

254 Microorganisms - CCDM 824 and CCDM 946) with decarboxylase positive activity in a model system of Dut

255 in the ganglion cell layer is glutamic acid decarboxylase-positive and shows the morphology of widef

256 control rats, there were fewer glutamic acid decarboxylase-positive neurons in the former cultures.

257 e describe here, mevalonate 3,5-bisphosphate decarboxylase, produces isopentenyl phosphate.

258 ay by an inhibitor of arginase and ornithine decarboxylase protected the mice from AD-like pathology

259 ine hydroxylase (TH) and aromatic amino acid decarboxylase, providing a novel mechanism for dopamine

260 double RNAi depletion of phosphatidylserine decarboxylase (psd-1) and choline/ETA phosphotransferase

261 , we demonstrate that the phosphatidylserine decarboxylase Psd1, located in the inner mitochondrial m

262 of a key pathway enzyme, phosphatidylserine decarboxylase Psd1, which generates phosphatidylethanola

263 Phosphatidylserine decarboxylase (PSDs) play a central role in the synthesi

264 Phosphatidylserine decarboxylases (PSDs) are central enzymes in phospholipi

265 This first-time study of the phenylacetate decarboxylase reaction constitutes an important step in

266 eat adaptation that uses rose phenylpyruvate decarboxylase (RyPPDC) as a novel enzyme.

267 erase (ScTIM), yeast orotidine monophosphate decarboxylase (ScOMPDC), and human liver glycerol 3-phos

268 cultured MCs were transfected with histidine decarboxylase short hairpin RNA to decrease histamine se

269 nations thereof, deficient in 2-oxoglutarate decarboxylase (Sll1981), succinate semialdehyde dehydrog

270 l1797) and two 4-hydroxy-3-solanesylbenzoate decarboxylases (slr1099 and sll0936).

271 85% are present in the malonate semialdehyde decarboxylase subgroup.

272 obutyric acid pathway or alpha-ketoglutarate decarboxylase/succinic semialdehyde dehydrogenase) plays

273 positive to antibodies against glutamic acid decarboxylase, suggesting that they use gamma-aminobutyr

274 struction of the rhamnose-regulated arginine decarboxylase system allowed us to render S. Typhi acid

275 ly equivalent to that of the native arginine decarboxylase system.

276 Transamination and the two decarboxylase systems (NADP-malic enzyme and phosphoenol

277 by inserting Shigella glutaminase-glutamate decarboxylase systems coexpressed with S. sonnei form I

278 ucei PS synthase 2 (TbPSS2) and T. brucei PS decarboxylase (TbPSD), two key enzymes involved in amino

279 zymes required for their synthesis, tyrosine decarboxylase (TDC) and tyramine beta-hydroxylase (TBH).

280 drion is synthesized by a phosphatidylserine decarboxylase (TgPSD1mt) of the type I class.

281 toacyl acyl-carrier protein, and ShMKS1 is a decarboxylase that converts the resulting 3-ketoacids to

282 bacteria have a biotin-independent malonate decarboxylase that is crucial for their utilization of m

283 al malic enzymes (ME2 and ME3) are oxidative decarboxylases that catalyse the conversion of malate to

284 revealed colocalization of DA, l-amino acid decarboxylase, the DA transporter, and vesicular monoami

285 ntibodies directed against the glutamic acid decarboxylase, the rate-limiting enzyme for the producti

286 Degradation of ornithine decarboxylase, the rate-limiting enzyme of polyamine bio

287 g pathway regulates translation of ornithine decarboxylase, thereby enhancing polyamine biosynthesis

288 rreversibly catalyzed by UDP-glucuronic acid decarboxylase (UXS).

289 C supernatant fluids increased CCA histidine decarboxylase, vascular endothelial growth factor, and M

290 nerate mevalonate 3,5-bisphosphate and a new decarboxylase we describe here, mevalonate 3,5-bisphosph

291 pressing different isoforms of glutamic acid decarboxylase were found to have differential subregiona

292 y decreased by inhibition of the enzyme dopa decarboxylase, which converts (11)C-5-HTP to (11)C-serot

293 Phosphatidylserine decarboxylase, which is embedded in the inner mitochondr

294 e levels of mitochondrial phosphatidylserine decarboxylase, which is involved in the synthesis of mit

295 ic acid (GABA)-synthesizing enzyme glutamate decarboxylase, which is present in inhibitory afferents

296 racterization of a branched-chain amino acid decarboxylase, which would appear to be responsible for

297 oplasm, providing the substrate for arginine decarboxylases, which consume a cellular proton ending u

298 me complex that have evolved into a pyruvate decarboxylase, while other copies retained the essential

299 we also determine the structure of malonate decarboxylase with CoA in the active site of MdcD-MdcE.

300 Black is a specific aspartate decarboxylase with no activity on glutamate.