ライフサイエンスコーパス: enzyme required for

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1 25-hydroxyvitamin D 1alpha-hydroxylase, the enzyme required for 1,25-dihydroxyvitamin D3 (1,25(OH)2D

2 pacer regions, but the identities of several enzymes required for 18S rRNA release remain unknown.

3 ion, inactivation of Hs2st (which encodes an enzyme required for 2-O-sulfation of uronic acids in hep

4 Recent studies have identified the enzyme required for a critical step of jasmonate synthes

5 These efforts notwithstanding, APP and the enzymes required for Abeta production are synthesized by

6 e: mutants identical to WS, but defective in enzymes required for acetylation produced biofilms with

7 rized carboxymuconolactone decarboxylase, an enzyme required for aerobic growth with aromatic compoun

8 NO in susceptible larval stages may involve enzymes required for aerobic energy metabolism, since si

9 ective inhibitors of 5alpha-reductase, a key enzyme required for allopregnanolone synthesis.

10 uggest that M. lepromatosis has lost several enzymes required for amino acid synthesis whereas M. lep

11 ncludes the Escherichia coli AdhE enzyme, an enzyme required for anaerobic growth of E. coli.

12 sulfide (CoB-S-S-CoM) reductase (Hdr), a key enzyme required for anaerobic respiration in methane-pro

13 suring the rapid induction of genes encoding enzymes required for anaerobic metabolism.

14 e conclude that srtA and srtB encode sortase enzymes required for anchoring different subsets of prot

15 ctive antiandrogens, inhibitors of CYP17, an enzyme required for androgen synthesis, inhibitors of 5a

16 Steroidogenic enzymes required for androgen synthesis from cholesterol

17 ly, of previously unknown function, as novel enzymes required for AP synthesis.

18 atients with AML are deficient in a critical enzyme required for arginine synthesis, argininosuccinat

19 c acid as a result of a mutation in the last enzyme required for ascorbate biosynthesis.

20 t disrupts phosphoglycerate kinase (PGK), an enzyme required for ATP generation in the terminal stage

21 motif constitutes the catalytic core of the enzyme required for autopalmitoylation and palmitoyl tra

22 Dihydrodipicolinate synthase (DHDPS), an enzyme required for bacterial peptidoglycan biosynthesis

23 catB encodes muconate cycloisomerase, an enzyme required for benzoate catabolism.

24 ndance of DNA polymerase beta (beta-pol), an enzyme required for BER, which was almost absent in p53

25 ne-6-phosphate isomerase (Gln6PI), the first enzyme required for biosynthesis of N-acetylgalactosamin

26 pha-demethylase (CYP51) is a cytochrome P450 enzyme required for biosynthesis of sterols in eukaryoti

27 t GIBBERELLIN 20 OXIDASE 2, which encodes an enzyme required for biosynthesis of the growth regulator

28 en attributed to mutations in genes encoding enzymes required for biosynthesis of pigments and to ABC

29 Blmh and demonstrated that Blmh is the sole enzyme required for BLM deamination.

30 vation-induced cytidine deaminase (AID), the enzyme required for both CSR and SHM.

31 Ilv5p is a bifunctional yeast mitochondrial enzyme required for branched chain amino acid biosynthes

32 s cell-preferential accumulation of multiple enzymes required for C4 photosynthesis.

33 nclude that PAD3 almost certainly encodes an enzyme required for camalexin biosynthesis.

34 crophages genetically deficient in Dicer, an enzyme required for canonical microRNA (miRNA) biogenesi

35 dentical with mutants defective in metabolic enzymes required for carbon assimilation.

36 t TXNIP deficiency causes marked deficits in enzymes required for catabolism of branched chain amino

37 ritance of defects in the genes encoding the enzymes required for catabolism of GSLs within lysosomes

38 Cdc34 is an E2-conjugating enzyme required for catalyzing the polyubiquitination re

39 o knockouts of dopamine beta-hydroxylase, an enzyme required for catecholamine synthesis.

40 monstrate that keratinocytes express two key enzymes required for catecholamine (beta-AR agonist) syn

41 y PP2A-specific methyltransferase LCMT-1, an enzyme required for cell survival.

42 ules for the pathogen resistance pathway and enzymes required for cell wall modification and secondar

43 ollowing exposure to antibiotics that target enzymes required for cell wall synthesis, bacteria typic

44 bes exposed to saturated fats, inhibitors of enzymes required for ceramide synthesis enhance insulin

45 ulfur allele (su) of magnesium chelatase, an enzyme required for chlorophyll formation; and (2) the f

46 BPs) are transcription factors that regulate enzymes required for cholesterol and fatty acid synthesi

47 , we found that the fly genome lacks several enzymes required for cholesterol biosynthesis, ruling ou

48 luding the low-density lipoprotein receptor, enzymes required for cholesterol synthesis (3-hydroxy-3-

49 s, Sqle, Cyp51, Sc4mol and Ebp, which encode enzymes required for cholesterol synthesis, were highly

50 s that modulate expression of genes encoding enzymes required for cholesterol synthesis.

51 el increase in epidermal mRNA levels for the enzymes required for cholesterol, fatty acid, and cerami

52 e/CYP8B1 (12alpha-hydroxylase), the specific enzyme required for cholic acid synthesis.

53 l 12alpha-hydroxylase/CYP8b1 is the specific enzyme required for cholic acid synthesis.

54 tribute to telomerase, a medically important enzyme required for chromosome stability and long-term c

55 Activation-induced deaminase (AID) is an enzyme required for class switch recombination (CSR) and

56 xpression for lysyl oxidase, the determining enzyme required for collagen cross-linking, is down-regu

57 T is an inhibitor of the HIV proteinase, the enzyme required for correct processing of retroviral pre

58 dly, levels of mRNA for cyclooxygenase 2, an enzyme required for cumulus expansion, are increased.

59 ressing VrtK confirmed that VrtK is the sole enzyme required for cyclizing the geranyl moiety.

60 dihydroorotate dehydrogenase (DHODH), a host enzyme required for de novo pyrimidine biosynthesis, and

61 e [dihydroorotate dehydrogenase (DHODH)], an enzyme required for de novo pyrimidine biosynthesis, hav

62 transcarbamylase/dihydroorotase (CAD) is an enzyme required for de novo pyrimidine nucleotide synthe

63 pyr-1 encodes CAD, a trifunctional enzyme required for de novo pyrimidine synthesis, and py

64 s) that encode mitochondrial and peroxisomal enzymes required for de novo amino acid biosynthesis.

65 t mitochondria contain not only ACP, but all enzymes required for de novo fatty acid synthesis.

66 Enzymes required for de novo lipogenesis are induced in

67 rgdorferi has a reduced genome and lacks the enzymes required for de novo synthesis of purines for sy

68 phils deficient in glutaredoxin 1 (Grx1), an enzyme required for deglutathionylation of actin and tub

69 R controls bleach-mediated expression of two enzymes required for detoxification of reactive electrop

70 own of lipid biosynthetic enzymes identified enzymes required for division, which highly correlated w

71 e rhp6 gene product, a ubiquitin-conjugating enzyme required for DNA damage repair, promotes entry to

72 is an oncogene-encoded chromatin-remodeling enzyme required for DNA repair that possesses a poly(ADP

73 ses is that it is through an increase in the enzymes required for DNA synthesis, which include nucleo

74 hila Spo11 homolog that is proposed to be an enzyme required for DSB formation.

75 We disabled key enzymes required for each of the three pathways in M. sm

76 podia are membrane protrusions that localize enzymes required for ECM degradation.

77 the dsbA locus, which encodes a periplasmic enzyme required for efficient disulfide bond formation i

78 hylenetetrahydrofolate reductase (MTHFR), an enzyme required for efficient homocysteine metabolism, c

79 at mice lacking the Tec kinases Itk and Rlk, enzymes required for efficient activation of phospholipa

80 se is one of several recombination or repair enzymes required for efficient levels of pilin Av, and R

81 provide a platform for access of the various enzymes required for end processing and ligation.

82 ted levels of fatty acid synthase, the major enzyme required for endogenous fatty acid biosynthesis,

83 he efficacy of inhibitors targeting FabY, an enzyme required for FAS initiation in the absence of exo

84 lles in plant metabolism, containing all the enzymes required for fatty acid beta-oxidation.

85 nin and thereby induce the expression of key enzymes required for fatty acid beta-oxidation.

86 The RPE, like the liver, expresses enzymes required for fatty acid oxidation and ketogenesi

87 plant feedstocks could reduce the amount of enzymes required for feedstock pretreatment and hydrolys

88 cs gene, which encodes an acetate-scavenging enzyme required for fitness during periods of carbon sta

89 tase calcineurin as one Ca(2+)/CaM-dependent enzyme required for G(1) transit.

90 cine alpha-amidating monooxygenase (PAM), an enzyme required for generating amidated bioactive signal

91 aving enzyme 1 (BACE1) is the beta-secretase enzyme required for generating pathogenic beta-amyloid (

92 is a specialized chromosome end-replicating enzyme required for genome duplication in many eukaryote

93 illomaviruses lack most of the rate-limiting enzymes required for genome synthesis, they need to unco

94 teins act as phosphatidate phosphatase (PAP) enzymes required for glycerolipid biosynthesis, and also

95 ciated with loss of T-synthase but not other enzymes required for glycoprotein biosynthesis, demonstr

96 that affect individual proteoglycans or the enzymes required for glycosaminoglycan synthesis regulat

97 lutABC operon encodes iron sulfur-containing enzymes required for growth on lactate.

98 onine sulfoximine (BSO), an inhibitor of the enzyme required for GSH synthesis, or when cells were de

99 ansferase (GPRTase) from Giardia lamblia, an enzyme required for guanine salvage and necessary for th

100 We identified and validated several enzymes required for HCV replication, including class II

101 targets in this assay are viral and cellular enzymes required for HCV replication, which are monitore

102 pothesis, we created mice that lack Ext1, an enzyme required for heparan sulfate biosynthesis, in hep

103 e proteoglycan protein cores or biosynthetic enzymes required for heparan sulfate (HS) assembly.

104 Its effect is attributed to induction of the enzyme required for hepatic bilirubin elimination, UDP-g

105 We found that enzymes required for histone H3K4 methylation, both the

106 ransforming DNA into the chromosome involves enzymes required for homologous recombination.

107 , although the has operon, which encodes the enzymes required for hyaluronic acid synthesis, is highl

108 The yfcYX operon (renamed fadIJ) encodes enzymes required for hydration, oxidation, and thiolytic

109 The two enzymes required for hypusination were detected in pumpk

110 usine hydroxylase (DOHH), the dinuclear iron enzyme required for hypusine modification of the transla

111 identified ENOYL-COA HYDRATASE2 (ECH2) as an enzyme required for IBA response.

112 In addition, the level of the enzyme required for inositol biosynthesis, inositol-1-ph

113 gulation of the catalase KatG, an activating enzyme required for isoniazid sensitivity, and upregulat

114 Activation-induced cytidine deaminase, an enzyme required for isotype switching and somatic hyperm

115 compartments contains acid lipase (AL), the enzyme required for liberating cholesterol from choleste

116 w "PCP" genes we identified several kinases, enzymes required for lipid modification, scaffolding pro

117 Transcription of genes encoding enzymes required for lipogenesis is induced in hepatocyt

118 prolipoprotein signal peptidase A (lspA), an enzyme required for lipoprotein synthesis, to demonstrat

119 iciency in lysosomal acid lipase (Lipa), the enzyme required for lysosome lipid catabolism, leads to

120 G6PD is an essential myocardial antioxidant enzyme, required for maintaining cellular glutathione le

121 te, cytidyltransferase (CCTalpha), a crucial enzyme required for maintenance of cell membranes.

122 n essential and ubiquitous ribonucleoprotein enzyme required for maturation of tRNA.

123 s a mutation in a dicer-like1 homolog, a key enzyme required for microRNA (miRNA) biogenesis.

124 Dicer, a ribonuclease III enzyme required for microRNA processing, is also an E2-i

125 e effect of knocking out Dicer, an RNase III enzyme required for miRNA and small interfering RNA biog

126 conditional knock-out of Dicer, an RNase III enzyme required for miRNA maturation, previous studies h

127 miRNAs to pancreatic development, Dicer1, an enzyme required for miRNA processing, was conditionally

128 f mitochondrial Ribonuclease P (RNase P), an enzyme required for mitochondrial tRNA processing, but l

129 l cells by retinaldehyde dehydrogenase 2, an enzyme required for most fetal RA synthesis.

130 E235K) and pronounced activity of E214K, an enzyme required for "N-end rule" proteolysis; (iii) ATP-

131 molecule inhibitor of NAMPT, a rate-limiting enzyme required for NAD generation, to probe the pathway

132 s of protein-arginine deiminase 4 (PAD4), an enzyme required for NET formation, should enable clinica

133 The enzymes required for nitrate and nitrite assimilation ar

134 In Klebsiella oxytoca, enzymes required for nitrate assimilation are encoded by

135 In Klebsiella oxytoca (pneumoniae), enzymes required for nitrate assimilation are encoded by

136 Enzymes required for nitrate assimilation are encoded by

137 ertain whether NocL was the only N-oxidizing enzyme required for nocardicin A biosynthesis.

138 e of this screening was 2-fold: to implicate enzymes required for Nod factor-induced calcium spiking

139 ependent protein kinase (DNA-PK), a critical enzyme required for nonhomologous end-joining (NHEJ).

140 ding to cyclin-dependent kinase-2 (cdk2), an enzyme required for normal cell cycle progression; these

141 The GAL genes, which encode the enzymes required for normal galactose metabolism in yeas

142 In yeast, the GAL genes encode the enzymes required for normal galactose metabolism.

143 encoding protein O-fucosyltransferase 1, an enzyme required for Notch ligand binding and thus activa

144 otent, oral inhibitor of gamma-secretase, an enzyme required for Notch pathway activation.

145 NtdB, and NtdC, constitute a complete set of enzymes required for NTD synthesis, although their funct

146 ate expression of the transport proteins and enzymes required for nucleoside catabolism but also prov

147 ate expression of the transport proteins and enzymes required for nucleoside catabolism.

148 iochemically delineates the functions of the enzymes required for OCN modification and demonstrates t

149 hydrophobic pocket in the active site of the enzyme required for oseltamivir binding.

150 teracting protein, p135), a deubiquitinating enzyme required for p97/p47-mediated postmitotic Golgi m

151 ila Fat facets protein is a deubiquitinating enzyme required for patterning the developing compound e

152 ident sequestering of both Ipk1 and Mss4 (an enzyme required for phosphatidylinositol 4,5-bisphosphat

153 ssion of the pebAB operon, which encodes the enzymes required for phycoerythrobilin synthesis in the

154 s cerevisiae encodes a ubiquitin-conjugating enzyme required for postreplicational repair of UV-damag

155 f the mammalian SWI/SNF chromatin remodeling enzyme required for PPARgamma2 activation and adipogenic

156 Here we demonstrate that Ape1, an enzyme required for processing apurinic/apyrimidinic (kn

157 onfirming its role as the sole oxime-forming enzyme required for production of nocardicin A.

158 yrosyl protein sulfotransferase (TPST) is an enzyme required for production of the mature sulfated PS

159 at blocking either beta- or gamma-secretase, enzymes required for production of Abeta from amyloid pr

160 none of the copper protein lysyl oxidase, an enzyme required for proper cross-linking of collagen and

161 Cysteinyl-tRNA synthetase is an essential enzyme required for protein synthesis.

162 Lysyl-tRNA synthetase (KARS), an enzyme required for protein translation that was shown t

163 by elevated expression of PC-PLC or Mpl, the enzyme required for proteolytic activation of PC-PLC.

164 We found that although the enzyme required for RA production during early embryogen

165 dihydropteridine reductase (LmQDPR), the key enzyme required for regeneration and maintenance of H(4)

166 , an inhibitor of cathepsin K, an osteoclast enzyme required for resorption of bone matrix, is underw

167 diacylglycerol kinase is identified as a key enzyme required for response termination.

168 se H2 as a key mammalian genome surveillance enzyme required for ribonucleotide removal and demonstra

169 ation and results in increased expression of enzymes required for serine synthesis from the accumulat

170 vation of ytpB, encoding a C35 -PP utilizing enzyme required for sesquarterpenoid synthesis, leads to

171 haracterize the forms of selection acting on enzymes required for sialic acid scavenging and cataboli

172 polymerase IVb/Pol V, a multisubunit nuclear enzyme required for siRNA-mediated gene silencing of tra

173 This is the first time that a specific enzyme required for starch degradation has been identifi

174 protein tyrosine kinase ZAP-70 is a critical enzyme required for successful T lymphocyte activation.

175 Enzymes required for sulfur metabolism have been suggest

176 iscovered as were genes encoding the various enzymes required for SUMO processing, ligation, and rele

177 Ubc9 is an E2-conjugating enzyme required for sumoylation and has been implicated

178 double-mutant mice lacking both NPC1 and an enzyme required for synthesis of all complex ganglioside

179 gmhA encodes phosphoheptose isomerase, an enzyme required for synthesis of heptose, a conserved co

180 ne-beta-hydroxylase (DBH) is the penultimate enzyme required for synthesis of norepinephrine and is t

181 n of glutamate decarboxylase 65 (GAD65), the enzyme required for synthesis of the major inhibitory ne

182 ed reduction in the levels of mRNAs encoding enzymes required for synthesis of cholesterol, fatty aci

183 e include genes encoding myelin proteins and enzymes required for synthesis of normal myelin lipids.

184 accharomyces cerevisiae mitochondria contain enzymes required for synthesis of the phospholipids card

185 nowledge of the radical S-adenosylmethionine enzymes required for synthesis of these remarkable metal

186 termined whether the mRNA levels for the key enzymes required for synthesis of these three classes of

187 gnificantly decreased levels of RNase P, the enzyme required for the 5' maturation of all tRNA.

188 rgets in the pathway, FadD32 is an essential enzyme required for the activation of the long meromycol

189 rom an existing msbB mutant (msbB encodes an enzyme required for the acylation of lipid A).

190 As a result, the concentration of the enzyme required for the assay can be as low as 100 pM, p

191 e gene encoding for nitrate reductase, a key enzyme required for the assimilation of nitrate.

192 tearoyl-CoA desaturase (SCD) is a microsomal enzyme required for the biosynthesis of oleate and palmi

193 polyketide synthase gene (SpPks) encodes an enzyme required for the biosynthesis of the larval pigme

194 -1,4-galacturonosyltransferase (GalAT) is an enzyme required for the biosynthesis of the plant cell w

195 Cyclooxygenase (COX), the key enzyme required for the conversion of arachidonic acid t

196 ate dehydrogenase (IMPDH) is a rate-limiting enzyme required for the de novo synthesis of guanine nuc

197 Thioredoxin reductase (TrxR) is an essential enzyme required for the efficient maintenance of the cel

198 synthase (ALAS2; also known as ALAS-E), the enzyme required for the first step in haem biosynthesis.

199 lated, and expression of 5-lipoxygenase, the enzyme required for the first step in leukotriene synthe

200 in an X-linked gene, PIG-A, that encodes an enzyme required for the first step in the biosynthesis o

201 protein level of pyruvate oxidase(PoxL), an enzyme required for the generation of hydrogen peroxide

202 , expression of stearoyl-CoA desaturase, the enzyme required for the generation of mono-unsaturated f

203 -mannosyl transferase 1 (POMT1) is the first enzyme required for the glycosylation of alpha-dystrogly

204 ase epsilon (Pol epsilon) is a multi-subunit enzyme required for the initiation of chromosomal DNA re

205 ndiabetic mice expressed 5-lipoxygenase, the enzyme required for the initiation of leukotriene synthe

206 DNA gyrase is an essential bacterial enzyme required for the maintenance of chromosomal DNA t

207 nt formaldehyde dehydrogenase (FLD) is a key enzyme required for the metabolism of methanol as a carb

208 We conclude that Psd1p, the key enzyme required for the mitochondrial pathway of phospha

209 This work focuses on TyW1, the enzyme required for the most critical step of wyosine bi

210 defensin gene (DEFA5) and in mice lacking an enzyme required for the processing of mouse alpha-defens

211 ed that ecto-5'-nucleotidase (CD73) is a key enzyme required for the production of elevated adenosine

212 ate dehydrogenase (IMPDH), the rate-limiting enzyme required for the production of guanylyl metabolit

213 ough podocyte-specific knockout of Dicer, an enzyme required for the production of mature miRNAs (Nph

214 e phosphoribosyltransferase, a rate-limiting enzyme required for the regeneration of NAD(+) from nico

215 ylase Lsd1 (also known as Aof2 or Kdm1a), an enzyme required for the removal of the repressive histon

216 ion of T. brucei pyridoxal kinase (PdxK), an enzyme required for the salvage of vitamin B6, an essent

217 benzoate polyprenyl transferase) encodes the enzyme required for the second step of the final reactio

218 tes that JGT is the only glucosyltransferase enzyme required for the second step of the pathway.

219 g alpha-N-acetylglucosaminidase, a lysosomal enzyme required for the stepwise degradation of heparan

220 ine-6-sulfate sulfatase (GALNS), a lysosomal enzyme required for the stepwise degradation of keratan

221 Salmonella enterica, ThiI is a bifunctional enzyme required for the synthesis of both the 4-thiourid

222 Polyphosphate kinase (PPK), the principal enzyme required for the synthesis of inorganic polyphosp

223 Myoinositol monophosphatase (IMP) is a major enzyme required for the synthesis of myoinositol and the

224 ncoding UDP-glucose dehydrogenase (Ugdh), an enzyme required for the synthesis of the glycosaminoglyc

225 rt, and the nature and regulation of several enzymes required for the absorption, storage, activation

226 ospholipase C (PLC)-gamma were the signaling enzymes required for the alphaPDGFR to mediate PVR.

227 The concentration of the RT enzymes required for the assay can be as low as 1 pM, en

228 -CoA reductase (DCR) is one of the auxiliary enzymes required for the beta-oxidation of unsaturated f

229 perm storage parameters in females mutant in enzymes required for the biochemical synthesis of tyrosi

230 es of Listeria spp. encode all but one of 25 enzymes required for the biosynthesis of adenosylcobalam

231 ion and reconstitution of the minimum set of enzymes required for the biosynthesis of anhydrotetracyc

232 phila sugarless and sulfateless genes encode enzymes required for the biosynthesis of heparan sulfate

233 functional operon allows coregulation of two enzymes required for the biosynthesis of L-serine, pyrid

234 ilar to Escherichia coli lpx genes (encoding enzymes required for the biosynthesis of lipid A) have b

235 For years, we have known the enzymes required for the biosynthesis of peptidoglycan;

236 example by the expression of genes encoding enzymes required for the biosynthesis of phytochemicals

237 ooxygenases (COXs) are crucial rate-limiting enzymes required for the biosynthesis of prostaglandins.

238 hree unlinked gene clusters that encode five enzymes required for the conversion of 4-hydroxybenzoate

239 Cyanobacterial genes encoding enzymes required for the conversion of heme to 3Z-phycoc

240 Cyanobacterial genes encoding enzymes required for the conversion of heme to the natur

241 ted to cholesterol, implying that all of the enzymes required for the conversion of mevalonate to far

242 medaka eggs revealed selective deposition of enzymes required for the degradation of N-linked glycans

243 tyrosine kinase and phospholipase C-gamma2, enzymes required for the development of FoB from T2 B ce

244 an 16 carbons in length, suggesting that the enzymes required for the elongation of palmitic to stear

245 (TS) and ribonucleotide reductase (RR), two enzymes required for the entire de novo deoxyribonucleot

246 ectrometry, were shown to contain all of the enzymes required for the extension of a 2-carbon precurs

247 Additionally, two enzymes required for the final stages of barrier maturat

248 The trpAB genes encode the enzymes required for the final two steps in tryptophan b

249 Here, we investigated the enzymes required for the formation of these Ubl-protein

250 RNAi silencing of enzymes required for the indole and seco-iridoid (monote

251 ehydrogenase 6 (17beta-HSD6), one of several enzymes required for the interconversion of androstanedi

252 of alpha-N-acetylglucosaminidase, one of the enzymes required for the lysosomal degradation of hepara

253 e structures and enzymatic mechanisms of the enzymes required for the production of dTDP-Fucp3NAc.

254 DNA ligases are enzymes required for the repair, replication and recombi

255 was to determine the mechanism and specific enzymes required for the retroconversion step in human s

256 conserved core of SahR regulons includes all enzymes required for the SAM cycle: the SAH hydrolase Ah

257 ology and identify at least one new class of enzymes required for the suppression of cell shape defec

258 ng tissue was found to express steroidogenic enzymes required for the synthesis of corticosterone fro

259 rferon gamma decreases the expression of the enzymes required for the synthesis of these ultra long-c

260 se in interferon gamma by decreasing the key enzymes required for the synthesis of ultra long-chain c

261 tisera against octopamine, tyramine, and the enzymes required for their synthesis, tyrosine decarboxy

262 the Rv1079 gene showed it to encode the key enzyme required for this conversion, cystathionine gamma

263 e synthesized, indicating that the necessary enzymes required for this pathway are present in Arabido

264 imulate surrounding stromal cells to express enzymes required for tissue remodeling.

265 ases are essential ATP-dependent homodimeric enzymes required for transcription, replication, and chr

266 viding an opportunity to study the genes and enzymes required for tricarballylate catabolism.

267 PI3Ks are key signaling enzymes required for triggering many immunological funct

268 genes encoding matrix-degrading proteinases, enzymes required for tumor cell migration and invasion.

269 reductase activity of the elongase system of enzymes required for very long-chain fatty acid (VLCFA)

270 RR is an enzyme required for viral DNA synthesis and cytotoxicity

271 IV-1 integrase is one of the three essential enzymes required for viral replication and has great pot

272 mydomonas reinhardtii genome encodes all the enzymes required for vitamin C biosynthesis via the L-ga

273 -binding proteins were thought to be the key enzymes required for wall synthesis.

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