ライフサイエンスコーパス: glucuronidase

1 cherichia coli gene encoding the enzyme beta-glucuronidase).

2 modified enzyme was superior to native beta-glucuronidase.

3 and could label bystander proteins near beta-glucuronidase.

4 F-alpha-responsive, heparan sulfate-specific glucuronidase.

5 to its unconjugated counterpart by sulfatase/glucuronidase.

6 atal injection of an AAV vector expressing b-glucuronidase.

7 ivated by the oncologically significant beta-glucuronidase.

8 hol drug surrogates under the action of beta-glucuronidase.

9 he lysosomal hydrolases cathepsin D and beta-glucuronidase.

10 uidA, an E. coli-specific gene encoding beta-glucuronidase.

11 was based on a loop unique to bacterial beta-glucuronidases.

12 resent in microbial, but not mammalian, beta-glucuronidases.

13 beta-glucuronidase-activated FITC-TrapG did not interfere wit

14 n by strain B301D and reduced levels of beta-glucuronidase activities of the sypA::uidA and syrB1::ui

15 2 promoter as measured by a decrease in beta-glucuronidase activity after treatment.

16 us and BG, have been reported to encode beta-glucuronidase activity among human colonic bacteria.

17 ssed in guard cells as shown by promoterbeta-glucuronidase activity and by whole-genome microarray.

18 vated FITC-TrapG did not interfere with beta-glucuronidase activity and could label bystander protein

19 ue-specific expression when analyzed by beta-glucuronidase activity assays, differences in gusA mRNA

20 on-sorbitol fermenting and negative for beta-glucuronidase activity but serotyped O nontypeable:H25 (

21 the BOS1-beta-glucuronidase transgene, beta-glucuronidase activity could be detected only after inhi

22 ransgenic Arabidopsis, with the highest beta-glucuronidase activity detected in pollen.

23 Here we detected an increase in beta-glucuronidase activity in faecal samples from obese volu

24 t the upstream sequence of POTH1 drives beta-glucuronidase activity in response to light and in assoc

25 n) of (18)F-FEAnGA also correlated with beta-glucuronidase activity in the same brain regions.

26 rrhiza (TFG), can significantly enhance beta-glucuronidase activity in vitro.

27 provide a valuable tool for visualizing beta-glucuronidase activity in vivo.

28 Finally, we show that BtGH115A alpha-glucuronidase activity is necessary for the sequential d

29 ersions of the AtSUS2:promoter fused to Beta-glucuronidase activity revealed an internal 421 bp regio

30 ed only the BG gene gave relatively low beta-glucuronidase activity that was not induced by 4-nitroph

31 lates that possessed only the gus gene, beta-glucuronidase activity was induced.

32 of near-IR (NIR) probes for imaging of beta-glucuronidase activity would be ideal to allow estimatio

33 on of root elongation, promotion of DR5-beta-glucuronidase activity, and reduction of Aux/IAA protein

34 two fluorescent probes for detection of beta-glucuronidase activity, one for the NIR range (containin

35 ic plants were functionally assayed for beta-glucuronidase activity.

36 robably the result of reduced bacterial beta-glucuronidase activity.

37 h displays glucuronoxylan alpha-(4-O-methyl)-glucuronidase activity.

38 t be associated with elevated levels of beta-glucuronidase, an enzyme previously associated with blad

39 expression using northern and promoter-beta-glucuronidase analyses and found overlapping but distinc

40 ome analysis are supported by promoter::beta-glucuronidase analyses of CHX genes and by other methods

41 Promoter-beta-glucuronidase analyses revealed that SHM1 is predominant

42 RT-PCR and beta-glucuronidase analyses showed that LTP5 is present in po

43 AtHAK5 promoter-beta-glucuronidase and -green fluorescent protein fusions sho

44 he influence of carbohydrate quality on beta-glucuronidase and cancer activity, deserve further scrut

45 ns were enzymatically deconjugated with beta-glucuronidase and extracted by a solid-phase extraction

46 pression pattern of recombinant ProBTS::beta-GLUCURONIDASE and found that it is expressed in developi

47 by expressing in soybean roots promoter beta-glucuronidase and green fluorescent protein fusions.

48 moter, when fused to the reporter genes beta-glucuronidase and green fluorescent protein, directed bi

49 udy sheds new light on the mechanism of beta-glucuronidase and helps to make industrial production of

50 hibition can be mimicked by recombinant beta-glucuronidase and is associated with proteolytic degrada

51 In addition, the use of mixtures of beta-glucuronidase and sulfatase enzymes from different sourc

52 promoter and protein fusions using the beta-glucuronidase and the green fluorescent protein, respect

53 idase, the auxin-sensitive reporter DR5:beta-glucuronidase, and auxin-dependent growth defects.

54 several digestive enzymes (acid lipase, beta-glucuronidase, and cathepsins B and D).

55 e without inhibiting purified mammalian beta-glucuronidase, and they do not impact the survival of ei

56 us, by probing the actions of microbial beta-glucuronidases, and by understanding which substrate glu

57 additionally hydrolysed enzymatically (beta-glucuronidase/arylsulphatase, cellulase), the compounds

58 tant (fls2) as the scion and ALMT1(pro):beta-glucuronidase as the rootstock revealed that both COR an

59 the help of a single accessory enzyme (alpha-glucuronidase) as revealed by the sugar release assay.

60 b in roots were revealed by a promoter::beta-glucuronidase assay, with atU2AF35b expressed strongly i

61 alyses of the syrB1::uidA reporter with beta-glucuronidase assays.

62 tive real time-PCR, GGPPS promoter-GUS (beta-glucuronidase) assays and publicly available microarray

63 ytic kinetics catalyzed by bovine liver beta-glucuronidase at interstitial pH = 7.4 fit the Michaelis

64 ng a whole-gene translational fusion to beta-glucuronidase, AtSUC9 expression was found in sink tissu

65 MPS VII is due to deficiency in beta-glucuronidase (beta-glu) enzymatic activity, which leads

66 beta-galactosidase (beta-gal) and beta-glucuronidase (beta-glucur) are both produced by E. coli

67 The direct inhibition of bacterial beta-glucuronidase (betaG) activity is expected to reduce the

68 that there is an increase in release of beta-glucuronidase by activated microglia into the extracellu

69 more, selective disruption of bacterial beta-glucuronidases by small molecule inhibitors alleviates t

70 hanol while incubating our samples with beta-glucuronidase, confirming that the methyl protons of EtG

71 , expression analysis of a PLP promoter-beta-glucuronidase construct in transgenic plants and in situ

72 ess ABA induction of the HVA22 promoter-beta-glucuronidase construct, while OsWRKY72 and -77 synergis

73 Furthermore, AtLETM2 promoter beta-glucuronidase constructs displayed exclusive maternal ex

74 aphy (HPLC) showed that the activity of beta-glucuronidase could be increased by 2.66-fold via the ad

75 charidosis type VII (MPS VII) caused by beta-glucuronidase deficiency.

76 We used the beta-glucuronidase-deficient nonobese diabetic/severe combine

77 cture of one inhibitor bound to E. coli beta-glucuronidase demonstrates that it contacts and orders o

78 ation study, coadministration with oral beta-glucuronidase derived from Escherichia coli and pretreat

79 n of auxin redistribution using the DR5:beta-glucuronidase (DR5:GUS) auxin-responsive reporter showed

80 able to detect an increased release of beta-glucuronidase during neuroinflammation.

81 Urine samples are incubated with beta-glucuronidase (E. coli K12) and then analyzed by liquid

82 mutant alleles in the same codon of the beta-glucuronidase-encoding GUS transgene.

83 sidase enzyme (beta-gly) and W492G in a beta-glucuronidase enzyme (beta-gluc), in which we engineer i

84 In the GI tract, the microbiota express beta-glucuronidase enzymes that remove the glucuronic acid as

85 ve been conventionally studied by using beta-glucuronidase enzymes to release the phase I metabolites

86 Bacterial beta-glucuronidases expressed by the symbiotic intestinal mic

87 apped on purified beta-glucuronidase or beta-glucuronidase-expressing CT26 cells (CT26/mbetaG) but no

88 but not on bovine serum albumin or non-beta-glucuronidase-expressing CT26 cells used as controls.

89 e to nucleophilic moieties located near beta-glucuronidase-expressing sites.

90 erse transcription PCR, promoter-driven beta-glucuronidase expression in transgenic plants, and Affym

91 Promoter-beta-glucuronidase expression of one transcription factor can

92 Promoter::beta-glucuronidase expression studies show that individual At

93 beta-Glucuronidase expression was detected in mature pollen r

94 a delay in the asymmetric auxin-induced beta-glucuronidase expression with gravistimulation as compar

95 of hydrogen peroxide-responsive AoPR10-beta-glucuronidase expression, suppression of plant stress/de

96 terologous in vivo Pv-ALF/phas-GUS (for beta-glucuronidase) expression system in transgenic Arabidops

97 iferase, green fluorescent protein, and beta-glucuronidase) facilitated in vivo profiling at the whol

98 Beta-glucuronidase from both Escherichia coli and bovine live

99 rations from different sources, such as beta-glucuronidase from Escherichia coli, were found to conta

100 Therefore, the use of beta-glucuronidase from H. pomatia combined with an enzyme "b

101 s (urine and plasma) were studied using beta-glucuronidase from Helix pomatia.

102 under different light treatments using beta-glucuronidase fusion constructs with the promoters of bo

103 sing both reverse transcription-PCR and beta-glucuronidase fusion constructs.

104 Promoter-beta-glucuronidase fusion experiments showed that MEDIATOR15

105 rabidopsis plants containing the AtHD2C:beta-glucuronidase fusion gene revealed that AtHD2C was const

106 Arabidopsis plants containing the HDA19:beta-glucuronidase fusion gene revealed that HDA19 was expres

107 F-Y complexes, we have created promoter:beta-glucuronidase fusion lines for all 36 Arabidopsis genes.

108 -type and ABA response mutants, an ABI8-beta-glucuronidase fusion protein is localized primarily to t

109 y a promoter::green fluorescent protein-beta-glucuronidase fusion revealed strong gene expression in

110 at similar levels, and the two promoter-beta-glucuronidase fusion transgenes show very similar expres

111 The promoter:beta-glucuronidase fusions also demonstrated that RAP2.6L exp

112 Expression patterns of SWEET2-beta-glucuronidase fusions confirmed that SWEET2 accumulates

113 RAP2.6L promoter:beta-glucuronidase fusions demonstrated that the up-regulatio

114 P (green fluorescent protein) and NaKR1-beta-glucuronidase fusions driven by the native promoter.

115 , transgenic plants expressing ProRPL10:beta-glucuronidase fusions show that, while AtRPL10A and AtRP

116 dopsis lines carrying AtWRKY30 promoter-beta-glucuronidase fusions showed transcriptional activity in

117 lting in increased activity of secreted beta-glucuronidase fusions that result from gene trap integra

118 independently validated using promoter:beta-glucuronidase fusions with the MtCRE1 CK receptor gene a

119 idate genes was performed using promoterbeta-glucuronidase fusions, and all of these showed embryo sa

120 on of each GGT in plants containing GGT:beta-glucuronidase fusions, the temporal and spatial pattern

121 using data mining and promoter-reporter beta-glucuronidase fusions.

122 beta-Glucuronidase-fusions to full-length ARR2, ARR12, and AR

123 d Cy5.5 was the red channel acceptor for the glucuronidase gene (uidA) target.

124 cteriaceae) and approximately 9% higher beta-glucuronidase gene abundance compared with nonresponders

125 ression of two reporter constructs: the beta-glucuronidase gene driven by the GA-inducible Amy32b alp

126 mulated lateral root production and DR5-beta-glucuronidase gene expression.

127 gnature sequencing, and promoter-driven beta-glucuronidase gene expression.

128 ed for the transgenic expression of the beta-glucuronidase gene fused to a synthetic auxin-inducible

129 nthase-like1 (MtCBS1), using a promoter-beta-glucuronidase gene fusion, which revealed expression in

130 nes in Arabidopsis thaliana by promoter-beta-glucuronidase gene fusions and by quantitative RT-PCR an

131 fusion of the GhCTL2 promoter to the beta -d-glucuronidase gene showed preferential reporter gene act

132 The Lactobacillus gasseri ADH beta-glucuronidase gene, gusA, was cloned previously and foun

133 processed as predicted by bovine liver beta-glucuronidase, generating 2-aminoethylGdDO3A, 2.

134 alyses using a complete set of promoter-beta-glucuronidase/green fluorescent protein reporter lines f

135 Here, RNA analysis and SWEET17-beta-glucuronidase/-GREEN FLUORESCENT PROTEIN fusions express

136 expression patterns as shown by DAO1pro:beta-glucuronidase (GUS) activity and DAO1pro:YFP-DAO1 signal

137 of VHA-c1, monitored by promoter-driven beta-glucuronidase (GUS) activity was responsive to light or

138 e and protein levels was analyzed using beta-glucuronidase (GUS) activity, quantitative reverse trans

139 s lines were constructed expressing the beta-glucuronidase (GUS) and green fluorescence protein (GFP)

140 PCR and transcriptional fusions to both beta-glucuronidase (GUS) and green fluorescent protein (GFP).

141 eam of these two genes was confirmed by beta-glucuronidase (GUS) assays.

142 etics of wild-type and in vitro evolved beta-glucuronidase (GUS) at the single molecule level.

143 An inherited deficiency of beta-glucuronidase (GUS) causes mucopolysaccharidosis type VI

144 ently reported that PerT-GUS, a form of beta-glucuronidase (GUS) chemically modified to eliminate its

145 mon manifestation of MPS VII because of beta-glucuronidase (GUS) deficiency.

146 For Arabidopsis research, beta-glucuronidase (GUS) enhancer-trap lines have been create

147 The gut microbiota harbor diverse beta-glucuronidase (GUS) enzymes that liberate glucuronic aci

148 proof-of-principle experiments, a 35S::beta-glucuronidase (GUS) expression cassette was introduced i

149 Here we show that beta-glucuronidase (GUS) expression from sense T-strands is m

150 dentified multiple lines that exhibited beta-glucuronidase (GUS) expression in the micropylar end of

151 sion patterns, as monitored by promoter-beta-glucuronidase (GUS) fusion and RT-PCR experiments.

152 Promoter-beta-glucuronidase (GUS) fusion experiments and seed mRNA loc

153 At5g23960 and At5g44630 promoter-beta-glucuronidase (GUS) fusion experiments demonstrated that

154 Furthermore, promoter-beta-glucuronidase (GUS) fusion transgenics were generated fo

155 fusion assay of RIE1 promoter with the beta-glucuronidase (GUS) gene.

156 Inheritance analyses using beta-glucuronidase (GUS) histochemical staining revealed that

157 nsgene with three direct repeats of the beta-glucuronidase (GUS) open reading frame (ORF) is associat

158 promoter and a coding region for either beta-glucuronidase (Gus) or glyphosate acetyltransferase (Gat

159 d region (UTR) was used to drive either beta-glucuronidase (GUS) or green fluorescent protein (GFP) e

160 1av1 promoter sequence was fused to the beta-glucuronidase (GUS) reporter gene and two varieties of A

161 system, we analyzed the activation of a beta-glucuronidase (GUS) reporter gene by enhancers contained

162 m tumefaciens strain AGL1 harboring the beta-glucuronidase (GUS) reporter gene driven by the cauliflo

163 Transcriptional regulatory region-beta-glucuronidase (GUS) reporter gene fusions introduced int

164 med with the RTE1 promoter fused to the beta-glucuronidase (GUS) reporter gene revealed that RTE1 exp

165 and enhancer trap vectors carrying the beta-glucuronidase (GUS) reporter gene were inserted into the

166 gulator (ARR)5 gene promoter fused to a beta-glucuronidase (GUS) reporter gene, and cytokinin oxidase

167 NAC promoter elements were fused to the beta-glucuronidase (GUS) reporter gene, and spatial and tempo

168 5830 promoter activity, measured with a beta-glucuronidase (GUS) reporter gene, was primarily found i

169 containing a PG11a promoter fused to a beta-glucuronidase (GUS) reporter gene.

170 taining an INPACT cassette encoding the beta-glucuronidase (GUS) reporter had negligible background e

171 ltransferase (UGT) operates in opposition to glucuronidase (GUS) to control activity of diverse metab

172 onsive Em promoter from wheat linked to beta-glucuronidase (GUS) to determine whether ABI3/VP1, trans

173 nic Arabidopsis lines bearing promoter::Beta-glucuronidase (GUS) transcriptional fusions as well as s

174 Seven of 10 single-crossover beta-glucuronidase (GUS) transcriptional reporters in genes c

175 Using glucuronidase (GUS) transformed tobacco as a model syste

176 examined the differential expression of beta-glucuronidase (GUS) transgenes under the control of the

177 ransgenic plants harboring an SOB5:SOB5-beta-glucuronidase (GUS) translational fusion under the contr

178 irect the evolution of Escherichia coli beta-glucuronidase (GUS) variants with increased beta-galacto

179 pression of the reporter construct EBS: beta-glucuronidase (GUS) was detected in Arabidopsis root tip

180 d the minor activity, and ARGAH1-driven beta-glucuronidase (GUS) was expressed throughout the seedlin

181 Treatment of human beta-glucuronidase (GUS) with sodium metaperiodate followed b

182 te the fact that the uidA gene product, beta-glucuronidase (GUS), was produced only when the cells we

183 tivated variants of the reporter enzyme beta-glucuronidase (GUS).

184 d nonphosphorylated (NP) forms of human beta-glucuronidase (GUS).

185 resulting from inherited deficiency of beta-glucuronidase (GUS).

186 infection with Agrobacterium carrying a beta-glucuronidase (GUS, uidA) gene with an artificial intron

187 o regulate expression of uidA (encoding beta-glucuronidase; GUS) and the cytokinin-biosnythetic gene

188 mal storage disease caused by deficient beta-glucuronidase (GUSB) activity resulting in defective cat

189 cer and Transferrin receptor (TFRC) and beta-Glucuronidase (GUSB) in pancreatic cancer were identifie

190 The lysosomal enzyme beta-glucuronidase (Gusb) is a key regulator of Lyme-associat

191 ion of severe cardiac manifestations in beta-glucuronidase (GUSB) null mice BM-transplanted i.v. as n

192 ach, we identified the lysosomal enzyme beta-glucuronidase (GUSB), a member of a large family of core

193 ability to ferment sorbitol and express beta-glucuronidase have complicated its detection and identif

194 cells express low levels of the endo-beta-D-glucuronidase heparanase that increase upon NK cell acti

195 d the distribution of recombinant human beta-glucuronidase (hGUS) and reduction in storage by weekly

196 were unchanged compared to control (DR5:beta-glucuronidase), however, in the seedlings expressing the

197 exane (2 ml/5 ml) and an overnight sulfatase/glucuronidase hydrolysis.

198 n resistance, ectopically expressed DR5:beta-glucuronidase in developing embryos, and defective respo

199 gher activity of the auxin reporter DR5-beta-glucuronidase in lateral root apices.

200 -C1 induces chemotaxis and secretion of beta-glucuronidase in peripheral blood neutrophils with a pot

201 cted, incubation of these prodrugs with beta-glucuronidase in the culture medium led to much more eff

202 Bacterial beta-glucuronidase in the human colon plays an important role

203 and Thi1.2 [thionin]) or SA (PR1 [PR1a-beta-glucuronidase in tobacco]) signaling when both signals w

204 express the reporter gusA gene encoding beta-glucuronidase in transgenic tobacco seeds relative to th

205 nhibitors that inhibit Escherichia coli beta-glucuronidase in vitro with Ki values between 180 nM and

206 ties from drug metabolites by bacterial beta-glucuronidases in the GI lumen can significantly damage

207 structural basis of selective microbial beta-glucuronidase inhibition, which may improve human drug e

208 ect of Klotho on NaPi-2a was blocked by beta-glucuronidase inhibitor but not by protease inhibitor.

209 Here we characterize novel microbial beta-glucuronidase inhibitors that inhibit Escherichia coli b

210 Potent bacterial beta-glucuronidase inhibitors were identified by high-through

211 protein fusion, beta-galactosidase, and beta-glucuronidase) into the F14.5L, J2R (encoding thymidine

212 g of the abscission marker, Pro(PGAZAT):beta-glucuronidase, into the mutant reveals that while floral

213 with A. tumefaciens cells carrying the beta-glucuronidase intron reporter gene.

214 beta-glucuronidase is an attractive reporter and prodrug-conv

215 beta-glucuronidase is involved in the hydrolysis of glycosami

216 beta-Glucuronidase is the key enzyme in the biotransformation

217 sion of the auxin-induced reporter (DR5-beta-glucuronidase) is reduced in initiating lateral roots an

218 n patterns inferred from these promoter:beta-glucuronidase lines for roots, light- versus dark-grown

219 GPA1 promoter::beta-glucuronidase lines indicate that the GPA1 promoter is a

220 r-adapted vectors with three reporters, beta-glucuronidase, luciferase, and green fluorescent protein

221 the untranslated regions of StBEL5 to a beta-glucuronidase marker, translation in tobacco (Nicotiana

222 beta-glucuronidase-mediated hydrolysis of the glucuronyl bond

223 Therefore, beta-glucuronidase might be a biomarker for ongoing neurodege

224 t are non-sorbitol fermenting (NSF) and beta-glucuronidase negative (GUD(-)) carry a large virulence

225 ent common ancestor of the contemporary beta-glucuronidase-negative, non-sorbitolfermenting STEC O157

226 apG was selectively trapped on purified beta-glucuronidase or beta-glucuronidase-expressing CT26 cell

227 herapy of necrotic tumors that liberate beta-glucuronidase or for antibody-directed enzyme prodrug th

228 The Vp1 promoter fused to beta-glucuronidase or green fluorescent protein reproduced th

229 mporal characterization, using Pro(HWS):beta-glucuronidase or Pro(HWS):green fluorescent protein fusi

230 ting stable transgenic lines expressing beta-glucuronidase plus (GUSplus), green fluorescent protein

231 55:H7 (sorbitol fermenting [SOR(+)] and beta-glucuronidase positive [GUD(+)]), through sequential gai

232 The beta-glucuronidase-positive O157 variants, although phylogene

233 It is well-known that hydrolysis with beta-glucuronidase presents some limitations that may result

234 RT-PCR and beta-glucuronidase-promoter fusion analyses demonstrated GPAT

235 brain microvasculature, indicating that beta-glucuronidase reached brain parenchyma via the perivascu

236 cause ISL could reduce the Km and Ea of beta-glucuronidase reacting with GL.

237 tracer (18)F-FEAnGA was able to detect beta-glucuronidase release during neuroinflammation in a rat

238 Green fluorescent protein and beta-glucuronidase reporter analyses indicated that NRT1.11 a

239 studies with an ABA-INSENSITIVE2 (ABI4)-beta-glucuronidase reporter construct revealed that in root,

240 ProOskn2:beta-glucuronidase reporter expression was down-regulated by

241 Beta-glucuronidase reporter expression, driven by YSL1 and YS

242 AGP31 promoter-beta-glucuronidase reporter gene analysis showed expression i

243 In an Arabidopsis-protoplast beta-glucuronidase reporter gene assay, as well as in a heter

244 on analyses and promoter fusions to the beta-glucuronidase reporter gene confirmed the expression of

245 genes were variably induced in planta; beta-glucuronidase reporter gene expression analysis of a sub

246 ression pattern, determined by promoter-beta-glucuronidase reporter gene expression, is associated wi

247 irmed in transgenic plants expressing the ss-glucuronidase reporter gene fused to the NtPDR1 promoter

248 Expression analysis of the beta-glucuronidase reporter gene fused to the NtSCP1 transcri

249 alyses of the WAKL4 promoter fused with the -glucuronidase reporter gene have shown that WAKL4 expres

250 ion start site direct expression of the beta-glucuronidase reporter gene primarily in the vascular ti

251 ression of the RPT2 promoter fused to a beta-glucuronidase reporter gene shows differential expressio

252 established to be root-specific using a beta-glucuronidase reporter gene strategy.

253 expression of the auxin-responsive DR5:beta-glucuronidase reporter gene, suggesting a perturbation i

254 four copies of the GCC-box fused to the beta-glucuronidase reporter gene, we showed that the GCC-box

255 ed in C. reinhardtii chloroplasts using beta-glucuronidase reporter genes, and the nearly identical C

256 oriented green fluorescent protein and beta-glucuronidase reporter genes, both transcripts and prote

257 ZATION SIGNAL-GREEN FLUORESCENT PROTEIN/beta-GLUCURONIDASE reporter lines throughout the life cycle,

258 Through microarray analysis and beta-glucuronidase reporter lines, we showed that the gene is

259 he gene expression patterns in promoter:beta-glucuronidase reporter lines.

260 auxin influx facilitator expression in beta-glucuronidase reporter plants revealed that AUXIN RESIST

261 dition, primer extension analyses and a beta-glucuronidase reporter system were used to quantitate tr

262 fection using both quantitative PCR and beta-glucuronidase reporter transgenic lines.

263 and tags mutant pollen grains with the beta-glucuronidase reporter.

264 len, as indicated from a promoter::GUS (beta-glucuronidase) reporter analysis and expression profilin

265 OsGZF1 can down-regulate a GluB-1-GUS (beta-glucuronidase) reporter and OsGZF1 was also able to sign

266 the expression pattern of the GL2::GUS (beta-glucuronidase) reporter gene.

267 OTH1 when fused to an expression marker beta-glucuronidase, repressed its translation in tobacco prot

268 and biological evaluation of the first beta-glucuronidase-responsive albumin-binding prodrug designe

269 ief incubation of the plasma with sulfatases/glucuronidases results in complete deconjugation of conj

270 2.66-fold via the addition of ISL to a beta-glucuronidase solution that contained GL at a 3:10 molar

271 As evaluated by beta-glucuronidase staining and independently confirmed by ot

272 In the flower, beta-glucuronidase staining occurred throughout the pistil, e

273 -polymerase chain reaction and promoter:beta-glucuronidase studies indicate that all AtGT genes are t

274 Promoter:beta-glucuronidase studies show that ECA3 is expressed in a r

275 The delivery of heparanase, the endo-beta-D-glucuronidase that degrades HS, accelerated the acquisit

276 diarrhea caused by symbiotic bacterial beta-glucuronidases that reactivate the drug in the gut.

277 ion of main chain xylanases as well as alpha-glucuronidases that release the alpha- (1-->2)-linked (M

278 ization of the provascular marker Athb8:beta-glucuronidase, the auxin-sensitive reporter DR5:beta-glu

279 herapy with antibodies that can deliver beta-glucuronidase to target tumor cells.

280 n transgenic plants expressing the BOS1-beta-glucuronidase transgene, beta-glucuronidase activity cou

281 markers such as a viviparous1 promoter-beta-glucuronidase transgene.

282 We used both promoter-beta-glucuronidase transgenic plants and immunolocalization t

283 e-specific accumulation of an OBP3:OBP3-beta-glucuronidase translational fusion is regulated by light

284 sed 6 weeks after gene transfer in AAV4 beta-glucuronidase-treated MPS VII mice.

285 reduced by either chondroitinase ABC or beta-glucuronidase treatment.

286 etions, were fused to the reporter gene beta-glucuronidase (uidA) and analyzed in transgenic Nicotian

287 erpes simplex virus type 2 (HSV-2) UL24 beta-glucuronidase (UL24-betagluc) insertion mutant was deriv

288 ivo functional assay using the reporter beta-glucuronidase under the auxin-inducible DR5 promoter con

289 which can be rescued by expressing SUF4-beta-glucuronidase under the control of the SUF4 promoter.

290 otoplasts inhibited nuclear import of a beta-glucuronidase-VirD2 nuclear localization signal fusion p

291 ction affinity for the lysosomal enzyme beta-glucuronidase was also much lower (K(d) = 54 microm) as

292 Thus, an enzymatic deconjugation with beta-glucuronidase was optimized.

293 IGF-II fused to the C terminus of human beta-glucuronidase was taken up by MPS VII fibroblasts in a m

294 beta-Glucuronidase was used to remove nonreducing-terminal gl

295 Recombinant AAV4 vectors encoding beta-glucuronidase were injected unilaterally into the latera

296 Family GH115 contains alpha-glucuronidases where several members have been shown to

297 ed with BC share an enzymatic activity, Beta-Glucuronidase, which may promote breast cancer.

298 and gusA3, were recovered that produced beta-glucuronidase with increased activity in neutral pH rang

299 All compounds are selective for E. coli beta-glucuronidase without inhibiting purified mammalian beta

300 r proteins, and the enzymes AguA (GH67 alpha-glucuronidase), XynA2 (GH10 endoxylanase), and XynB (GH4