ライフサイエンスコーパス: galactosidase

1 mobilization and controlled released of beta-galactosidase.

2 nzymatic hydrolisis by Escherichia coli beta-galactosidase.

3 ymatic assays confirmed its activity of beta-galactosidase.

4 eptococcus, a bacterial surface-exposed beta-galactosidase.

5 at 95% lactose depletion for K. lactis beta-galactosidase.

6 lective artificial protein receptor for beta-galactosidase.

7 a prodrug converted into Daunorubicin by ss-galactosidase.

8 ry beta-lactoglobulin but too small for beta-galactosidase.

9 only exons 1-4 were expressed, fused to beta-galactosidase.

10 rference with the enzymatic activity of beta-galactosidase.

11 ity-based probes that target retaining alpha-galactosidases.

12 inetic binding studies with substituted beta-galactosidases.

13 erization is not a universal feature of beta-galactosidases.

14 support for the immobilization of model beta-galactosidases.

15 idase 1 (Neu1), neuraminidase 3 (Neu3), beta-galactosidase 1 (Glb1), and hexosaminidase B (HexB), pos

16 ly, no method is available to identify alpha-galactosidase A (agalA) mutations determining clinically

17 d lysosomal storage disorder caused by alpha-galactosidase A (alpha-GAL A) deficiency.

18 Clinical assessments, alpha-galactosidase A (alpha-GalA) activities, glycosphingolip

19 neumoniae mutants deficient in NanA and beta-galactosidase A (BgaA) failed to form biofilms in vivo d

20 A gene knockout (Gla KO) mice have no alpha-galactosidase A activity and progressively accumulate GL

21 ype observed in patients with residual alpha-galactosidase A activity.

22 ase is caused by deficient activity of alpha-galactosidase A and subsequent accumulation of glycosphi

23 isease caused by deficient activity of alpha-galactosidase A and the resultant systemic accumulation

24 torage disorder caused by a deficit in alpha-galactosidase A enzyme activity leading to glycosphingol

25 Leukocyte alpha-galactosidase A enzyme activity was mildly reduced in 19

26 caused by the absence or reduction of alpha-galactosidase A enzyme activity.

27 alpha-Galactosidase A gene knockout (Gla KO) mice have no alph

28 of the N215S (c.644A>G [p.Asn215Ser]) alpha-galactosidase A gene variant.

29 We studied whether cardio-specific alpha-galactosidase A gene variants are misinterpreted as hype

30 inked Fabry disease (FD) caused by GLA(alpha-galactosidase A gene) mutations encoding p.D322E (family

31 alpha-Galactosidase A genotype N215S does not lead to the deve

32 orage disorder caused by deficiency of alpha-galactosidase A, resulting in glycosphingolipid accumula

33 r caused by a deficiency of the enzyme alpha-galactosidase A, which results in the progressive accumu

34 mulation and deletion of iNKT cells in alpha-galactosidase A-deficient (alphaGalA(-/-)) mice (human F

35 b3Cer) in the kidneys of wild-type and alpha-galactosidase A-knockout (Fabry) mice was possible at ab

36 se, which is caused by a deficiency in alpha-galactosidase A.

37 deficient activity of lysosomal enzyme alpha-galactosidase A.

38 increases in senescence associated (SA) beta-galactosidase, a known marker of cellular senescence.

39 beta-galactosidase, a lysosomal protein, was elevated 3.6-5.7

40 en fluorescent protein (GFP)-AAP2BR and beta-galactosidase-AAP2BR fusion proteins, respectively, and

41 X-gal analysis has shown strong beta-galactosidase activities in the prostate, brain, and few

42 ere imaged with and without a stain for beta-galactosidase activity (S-Gal + ferric ammonium citrate)

43 We also found high beta-galactosidase activity accompanying tension wood differe

44 he gene responsible for the majority of beta-galactosidase activity against xyloglucan.

45 the induction of senescence-associated beta-galactosidase activity and cell morphology.

46 Analysis of beta-galactosidase activity and controlled release reveals th

47 the induction of senescence-associated beta-galactosidase activity and flat cell morphology.

48 by an increase in senescence-associated beta-galactosidase activity and formation of senescence-assoc

49 s effectively demonstrated in vitro for beta-galactosidase activity and in vivo in a mouse model of i

50 totic but displayed senescence associated-ss-galactosidase activity and upregulated p16, indicating p

51 spectively, which by their lacZ encoded beta-galactosidase activity convert the inactive prodrug Daun

52 rmination of the fusion protein via its beta-galactosidase activity found 8.3 and 9.8 ng/mug (nanogra

53 porter assay linking LasR function with beta-galactosidase activity gave results consistent with thos

54 taGal sensitively detects intracellular beta-galactosidase activity in several ovarian cancer lines.

55 in Escherichia coli yields significant beta-galactosidase activity in vivo from a lacZ gene containi

56 Some cerebral LLC exhibited beta galactosidase activity indicating a senescence phenotype

57 e was assessed as senescence-associated beta-galactosidase activity using flow cytometry, oxidative s

58 beta-Galactosidase activity was detected in osteocytes of sos

59 e senescence, as indicated by increased beta-galactosidase activity, elevated CDKN1A mRNA expression,

60 ined by a rise in senescence-associated beta-galactosidase activity, higher abundance of CDKN1A/P21 a

61 splayed increased senescence-associated beta-galactosidase activity, lower average telomere lengths b

62 induced increased senescence-associated beta-galactosidase activity, oxidative stress, early phosphor

63 arkers (increased senescence associated-beta galactosidase activity, p16, and p53 expression and lowe

64 ed with decreased senescence-associated beta-galactosidase activity, preserved telomere length, reduc

65 erative capacity, senescence-associated beta-galactosidase activity, the known senescence-inducing pa

66 e, as assessed by senescence-associated beta-galactosidase activity, was induced by the passaging of

67 sing the novel phenotype of periplasmic beta-galactosidase activity, we show that the periplasmic cha

68 ll morphology and senescence-associated beta-galactosidase activity.

69 y become senescent, as determined by SA-beta-galactosidase activity.

70 est and increased senescence-associated beta-galactosidase activity.

71 cence and express senescence-associated beta-galactosidase activity.

72 equence caused an 8.6-fold reduction in beta-galactosidase activity.

73 Cellular senescence was monitored by beta-galactosidase activity.

74 criptional fusion norA-lacZ for altered beta-galactosidase activity.

75 gy, and increased senescence-associated beta-galactosidase activity.

76 oviruses (genogroup III) interact with alpha-galactosidase (alpha-Gal) carbohydrates, and murine noro

77 s possibly involved in apple softening, beta-galactosidase, alpha-arabinofuranosidase, polygalacturon

78 and 4 inhibit the two human retaining alpha-galactosidases alphaGal A and alphaGal B covalently and

79 beta-Galactosidase also exhibited glycoproteineous properties

80 0 xyl1 double mutant, deficient in both beta-galactosidase and alpha-xylosidase.

81 cts of ganglioside hydrolases, e.g., of beta-galactosidase and beta-hexosaminidases, and of GM2-activ

82 an only be detected and qualified after beta-galactosidase and beta-N-acetylhexosaminidase digestion.

83 beta-Galactosidase and beta-N-acetylhexosaminidase were used

84 needle-mediated intradermal delivery of beta-galactosidase and formaldehyde-inactivated botulinum tox

85 exposure and hydrolysis by exoglycosidases (galactosidase and hexosaminidase).

86 -ON probes for detection and imaging of beta-galactosidase and hydrogen peroxide.

87 e markers, namely senescence-associated beta-galactosidase and increased p16(INK4a)/p19(ARF) expressi

88 en shown to restore activity of mutant alpha-galactosidase and is currently in clinical trial for tre

89 We studied the enzymatic reaction for beta-galactosidase and its substrate (resorufin-beta-D-galact

90 increased senescence-associated markers beta-galactosidase and p16 mRNA in aged CPCs.

91 e of a complex between Escherichia coli beta-galactosidase and the cell-permeant inhibitor phenylethy

92 nzymatic activity of the cargo proteins beta-galactosidase and the enzymatic subunit of Clostridium b

93 onstrated with the accurate modeling of beta-galactosidase and TRPV1 proteins at 3.2 A and 3.4 A reso

94 en labeled with an enzyme (streptavidin-beta-galactosidase), and single enzymes associated with these

95 hexosaminidase, galactosylceramidase, alpha-galactosidase, and beta-galactosidase) mediating glycosp

96 vered intracistronic complementation in beta-galactosidase, and investigated the role of cAMP in Esch

97 luding p16, EGFP, senescence-associated beta-galactosidase, and the senescence-associated secretory p

98 40-50% with B. circulans and A. oryzae beta-galactosidases, and at 95% lactose depletion for K. lact

99 e a fluctuation type of distribution of beta-galactosidase appearance in a growing culture, consisten

100 hydrolysis of RFOs increase the Cicer alpha-galactosidase application in food processing industries.

101 solution structure of Escherichia coli beta-galactosidase ( approximately 465 kDa), solved at approx

102 panies the use of senescence-associated beta-galactosidase as a collection of semiselective markers t

103 ed with adenoviruses containing A20 (or beta-galactosidase as a control) were allografted into major

104 ssful intracellular delivery of bioactive ss-galactosidase as a model enzyme was also demonstrated us

105 Using beta-galactosidase as a reporter for the null gene, developme

106 nhibition of the hydrolytic activity of beta-galactosidase (Aspergillus oryzae) was evaluated.

107 we established a senescence associated beta-galactosidase assay as a screening platform to rapidly i

108 d dramatically the dynamic range of the beta-galactosidase assay for cadBA activation.

109 staining reaction than the traditional beta-galactosidase assay in mouse embryos.

110 Using Northern hybridization and beta-galactosidase assays of an ace promoter-lacZ fusion, we

111 cytotoxicity and senescence-associated beta-galactosidase assays, which were compared with dissolved

112 osomal enzymes (alpha-glucosidase (AG), beta-galactosidase (B-GAL) and beta-N-acetylglucosamidase (B-

113 uring treatment with several commercial beta-galactosidases (Bacillus circulans, Kluyveromyces lactis

114 ant was also 'leaking' as revealed by a beta-galactosidase-based assay employing a membrane impermeab

115 pithelial cells (PI-MECs)-are marked by beta-galactosidase (beta Gal) expression following pregnancy

116 the DeltabioR DeltabioBFDA mutant), the beta-galactosidase (beta-Gal) activity of three plasmid-borne

117 h amounts of galactose and considerable beta-galactosidase (beta-Gal) activity was observed.

118 beta-galactosidase (beta-gal) and beta-glucuronidase (beta-gl

119 was implemented into the procedure with beta-galactosidase (beta-gal) as the detection enzyme.

120 iated lysis was used to release endemic beta-galactosidase (beta-gal) from the bound bacterial cells;

121 In these animals, staining for beta-galactosidase (beta-gal) identifies cells in which NF-ka

122 We demonstrate that when beta-galactosidase (beta-gal) is expressed in LECs, beta-gal-

123 k, specific immobilization of 6-phospho-beta-galactosidase (beta-Gal) on a self-assembled monolayer (

124 es, namely pectin methylesterase (PME), beta-galactosidase (beta-Gal), endo-1,4-beta-D-glucanase (EGa

125 mbinant A20 adenovirus (rAd.A20) or rAd.beta-galactosidase (beta-gal), implanted, harvested 4 weeks a

126 12, which expresses the omega-domain of beta-galactosidase (beta-gal).

127 ngineered with lacZ operon encoding for beta-galactosidase (beta-gal).

128 mes resulted in increased expression of beta-galactosidase(beta-gal) plasmid in rat brain tissue in c

129 osidase/beta-xylosidase that also shows beta-galactosidase, beta-fucosidase, alpha-arabinofuranosidas

130 reduction or absence of lysosomal acid beta-galactosidase (betagal) activity.

131 Using beta-galactosidase (betagal) as a model system, we have emplo

132 to cell fate reporter mice that express beta-galactosidase (betagal) in cells of AEC lineage.

133 Mice expressing beta-galactosidase (betagal) on a retina-specific promoter (b

134 ew model of memory inflation based on a beta-galactosidase (betagal)-recombinant adenovirus vector.

135 ides 7a-e and 8 were found to be modest beta-galactosidase (bGal) inhibitors.

136 Galectin-9 (Gal9), a beta-galactosidase-binding protein expressed by T-regs, is ke

137 ses, BoMan26A and BoMan26B, and a GH36 alpha-galactosidase, BoGal36A.

138 xhibit trans-alpha-xylosidase and trans-beta-galactosidase (but not trans-alpha-fucosidase) activitie

139 ent analytes (Pd(0/2+), H(2)O(2), F(-), beta-galactosidase) can be created from the same core structu

140 elastin-binding protein/spliced form of beta-galactosidase chaperone, enhancing secretion.

141 e tit1+ and tit1-Delta cells by using a beta-galactosidase codon-swap reporter whose catalytic activi

142 In the current study we used a beta-galactosidase complementation method to screen a selecti

143 We used a beta-galactosidase complementation method to screen several t

144 PCR assay to detect NWM SFV DNA, and a beta-galactosidase-containing indicator cell line to assay re

145 Importantly, endo-beta-galactosidase coupled with MALDI-MS allowed these two ep

146 ith LC-MS/MS, indicating that Chick pea beta-galactosidase (CpGAL) is a heterodimer.

147 ase, an X-linked disorder of lysosomal alpha-galactosidase deficiency, leads to substrate accumulatio

148 ansport of a model therapeutic enzyme (alpha-galactosidase, deficient in lysosomal Fabry disease).

149 ies provide an enhanced alternative for beta-galactosidase detection in expression and cell fate stud

150 cheal delivery of AAV1 was confirmed by beta-galactosidase detection in the distal pulmonary vasculat

151 gene and lacz reporter cDNA coding for beta-galactosidase directed by the CerS6 promoter.

152 ein G domain but delays that of a large beta-galactosidase domain as a result of kinetic trapping of

153 beta-Galactosidase, encoded by lacZ, is usually detected usin

154 l of oligonucleotides to the surface of beta-galactosidase enhances its cellular uptake of by up to a

155 Monastrell wines were also treated with beta-galactosidase enzyme addition and commercial enzyme addi

156 ques (cold pre-fermentative maceration, beta-galactosidase enzyme addition and enzymatic preparation

157 d by hydrolyzing native guar gum using alpha-galactosidase enzyme.

158 beta-Galactosidase enzymes are used in the dairy industry to

159 genic AlbuminCreXRosa26 mice expressing beta-galactosidase exclusively in hepatocytes.

160 nic green fluorescence protein (GFP) or beta-galactosidase expressed from the ROSA26 locus was used t

161 beta-galactosidase expression was predominantly found in mous

162 istinct profile of senescence including beta-galactosidase expression, autofluorescence, growth inhib

163 ting in decreased senescence-associated beta-galactosidase expression, increased self-renewal potenti

164 vasive imaging of Hmox1 expression, and beta-galactosidase for high-resolution mapping of expression

165 t 50 of the 67 participants had mutant alpha-galactosidase forms suitable for targeting by migalastat

166 The initial assay of mutant alpha-galactosidase forms that we used to categorize 67 patien

167 andomly assigned patients (with mutant alpha-galactosidase forms that were suitable or not suitable f

168 alysis, involving patients with mutant alpha-galactosidase forms that were suitable or not suitable f

169 The level of beta-galactosidase from a gerA-lacZ fusion in superdormant sp

170 hia coli l-arabinose promoter and bgaB (beta-galactosidase from Bacillus stearothermophilus) to creat

171 (putrescine transaminase) activity and beta-galactosidase from cells with patA-lacZ transcriptional

172 ageously used to optimally immobilise a beta-galactosidase from chick pea onto alkylamine glass using

173 A beta-galactosidase from Cicer arietinum seeds has been purifi

174 ctans from acacia gum by a galactan-beta-1,3-galactosidase from family GH43; however, while B. thetai

175 Solubilisation of beta-galactosidase from Kluyveromyces lactis in Aerosol-OT wa

176 ese results indicate that (i) levels of beta-galactosidase from lacZ fusions to operons encoding germ

177 The separation of beta-galactosidase from the test protein beta-lactoglobulin w

178 ifferent GOS profiles of the commercial beta-galactosidases from Bacillus circulans, Kluyveromyces la

179 alCer-beta-galactosylceramidase and GM1-beta-galactosidase functions in the degradation of lactosylce

180 Expression of the kazrin-beta-galactosidase fusion protein faithfully reported endogen

181 using six cryo-EM structures of TRPV1, beta-galactosidase, gamma-secretase, ribosome-EF-Tu complex,

182 as able to image cells transfected with beta-galactosidase gene by chemiluminescence microscopy.

183 type RIMD2210633 strain marked with the beta-galactosidase gene lacZ (WBWlacZ), the mutant colonized

184 rpoE mutant and the WT marked with the beta-galactosidase gene lacZ (WBWlacZ), the mutant strain was

185 arahaemolyticus strains marked with the beta-galactosidase gene lacZ demonstrated that the DeltatoxRS

186 either the BMP inhibitor noggin or the beta- galactosidase gene under the control of a BMP-responsive

187 of the human coagulation factor IX and alpha-galactosidase genes into endogenous genomic loci with hi

188 n (Psap), Niemann Pick type C2 (Npc2), alpha-galactosidase (Gla), are up-regulated in early adipogene

189 is approach (0.5L) using the commercial beta-galactosidase Godo-YNL2.

190 alpha-galactosidase has been shown to reduce gas production an

191 livery to the mouse brain of functional beta-galactosidase, human IgG and IgM, and two antibodies tha

192 Transport of beta-galactosidase, IgG, IgM, and antibodies against amyloid

193 ructures confirmed the utility of a beta-1,3-galactosidase in Bifidobacterium longum subsp. infantis

194 orm, we could investigate the levels of beta-galactosidase in cells grown under different nutrient co

195 y induce expression of Fgfr2(S252W) and beta-galactosidase in either the neural crest or mesoderm of

196 were able to visualize the activity of beta-galactosidase in embryos at stages when the customary X-

197 se factors on the performance of enzyme beta-galactosidase in formulations for reduction of levels of

198 eling in Pw1(nLacZ+/-) mouse expressing beta-galactosidase in PW1(+) cells and in differentiated cell

199 The distribution of neurons expressing beta-galactosidase in the brain and the relative intensity of

200 luate the efficacy and tolerability of alpha-galactosidase in the treatment of gas-related symptoms i

201 ion of the endogenous activity of both alpha-galactosidases in cell extracts, thereby providing a mea

202 infect and express transgenes (hGM-CSF, beta-galactosidase) in tumor-associated vascular endothelial

203 e, stabilizes specific mutant forms of alpha-galactosidase, increasing enzyme trafficking to lysosome

204 f treated cells also stain positive for beta-galactosidase, indicating senescence.

205 ounds, 4-epi-fagomine (2b) was the best beta-galactosidase inhibitor, and it also prevented LPS-media

206 d using gene targeted mice with nuclear beta-galactosidase inserted into the Islet-1 locus.

207 ose-free food and controlled release of beta-galactosidase into lactose-intolerant individuals.

208 beta-d-Galactosidase is an important enzyme in the dairy indust

209 a genetic circuit in which synthesis of beta-galactosidase is under control of the arsenite-derepress

210 ide and a constant amount of the enzyme beta-galactosidase, is produced at frequencies in excess of 1

211 n (EBP), a spliced variant of lysosomal beta-galactosidase, is the primary receptor of elastin peptid

212 ein G, ovalbumin, bovine serum albumin, beta-galactosidase, lactoferrin) on the EIG with initial capt

213 ostin (sost) gene was replaced by the beta-D-galactosidase (lacZ) gene in the germ line.

214 beta-Galactosidase (lacZ) has bifunctional activity.

215 Using mice expressing beta-galactosidase (lacZ) under the control of seven repeated

216 completely account for the increase in beta-galactosidase levels in mutT lacZamber cultures, without

217 cts, elevation of senescence-associated beta-galactosidase levels, and changes in gene expression clo

218 pe IV collagen was investigated, but no beta-galactosidase-like activity capable of collagen modifica

219 , accumulated the senescence-associated beta-galactosidase marker, and increased P16 protein expressi

220 positive for the senescence-associated beta-galactosidase marker, suggesting that cells have lost th

221 sylceramidase, alpha-galactosidase, and beta-galactosidase) mediating glycosphingolipid hydrolysis we

222 function observed for the more severe alpha-galactosidase mutants could be enhanced by combining pha

223 ely affected by protein aggregation of alpha-galactosidase mutants, revealing a qualitative differenc

224 domized to receive placebo (n = 25) or alpha-galactosidase (n = 27).

225 examined STOML1 null mutant mice with a beta-galactosidase-neomycin cassette gene-trap reporter drive

226 nctional vascular graft by immobilization of galactosidase on the graft surface.

227 arly, pretreating neutrophils with endo-beta-galactosidase or neuraminidase converted ANCA assay resu

228 ts treated with a control AAV1 carrying beta-galactosidase or saline.

229 on with rats administered AAV1 carrying beta-galactosidase or saline.

230 etected in immune cells of C57BL/6, BRE-beta-galactosidase, or BMP-4(betagal/+) mice.

231 hibit an elevated VEGF, localization of beta-galactosidase outside the subventricular zone (SVZ), sub

232 shows that the glucose binding site of beta-galactosidase played an important role in lac operon evo

233 reduced telomerase activity, increased beta-galactosidase-positive cells, upregulation of the senesc

234 sed the number of senescence-associated beta-galactosidase-positive HSCs and decreased alpha-smooth m

235 hese mice resulted in the generation of beta-galactosidase-positive liver progenitor cells, demonstra

236 lactulose was performed with commercial beta-galactosidase preparations from Aspergillus oryzae, Kluy

237 beta-Galactosidase promotes the isomerization by means of an

238 t with the deglycosylating enzyme, endo-beta-galactosidase, reduced the mass of neutrophil hLAMP-2 to

239 AR2 and PDI1 mRNAs, and expression of a beta-galactosidase reporter activated by Hac1(i) Phosphorylat

240 t mice overexpressing human HB-EGF with beta-galactosidase reporter exhibit an elevated VEGF, localiz

241 Expression of the bacterial beta-galactosidase reporter gene (lacZ) in the vector used fo

242 tion of the intronic CArG region from a beta-galactosidase reporter gene abolished transgene expressi

243 5'UTR clearly decreased expression of a beta-galactosidase reporter in a proportional manner, a delet

244 lly conferred thermoregulation upon the beta-galactosidase reporter in E. coli.

245 ed pCTEN-Cre:R26R mice by crossing R26R beta-galactosidase reporter mice with pCTEN-Cre transgenic mi

246 a premature UAG stop codon located in a beta-galactosidase reporter.

247 splicing, induction of KAR2, PDI1, and beta-galactosidase reporters, and survival of ER stress, but

248 DNA-functionalized beta-galactosidase retains its ability to catalyze the hydrol

249 S) production and senescence-associated beta-galactosidase (SA-beta-gal) activity but an increase in

250 Senescence-associated beta-galactosidase (SA-beta-Gal) activity was investigated by

251 n; an increase in senescence-associated beta-galactosidase (SA-beta-Gal) activity, a marker of cellul

252 rked by increased senescence-associated beta-galactosidase (SA-beta-Gal) staining and gammaH2AX-posit

253 lat, enlarged and senescence-associated beta-galactosidase (SA-beta-Gal)-positive cells.

254 (DDR) signaling, senescence-associated beta-galactosidase (SA-betagal) activity, increased expressio

255 ers p21(CIP1/WAF1), senescence-associated ss-galactosidase (SA-ss-gal), and p16(INK4a) were increased

256 d found that only senescence-associated beta-galactosidase (SAbetagal) activity is specifically enric

257 An anti-beta-galactosidase scFv:MOG fusion protein (scFv GL117:MOG) s

258 als are needed to confirm this result, alpha-galactosidase seems to be a safe, well tolerated and eff

259 (addition of enzymatic preparation and beta-galactosidase separately and dry ice addition) may affec

260 ignment of CpGAL with other known plant beta-galactosidase showed high amino acid sequence homology.

261 alpha-galactosidase significantly reduced global distress (p =

262 ation of DC before adoptive transfer of beta-galactosidase-specific T cells dramatically increased se

263 was evaluated by senescence-associated beta-Galactosidase staining and by Western blot analysis of p

264 ver tissue and by senescence-associated beta-galactosidase staining in a culture-based model of insul

265 KLK4 protein levels in rat enamel and beta-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ) mou

266 By beta-galactosidase staining, a subpopulation of Cdc42-null NC

267 ce, determined by senescence-associated beta-galactosidase staining, was obviously attenuated by p38-

268 By beta-galactosidase staining, we demonstrated that Mig-6 was u

269 senescence activation, as indicated by beta--galactosidase staining.

270 quantification of senescence-activated beta-galactosidase staining.

271 fundi harbors a model polyextremophilic beta-galactosidase that functions in cold, hypersaline condit

272 7 is an exo-acting 3,6-anhydro-alpha-(1,3)-L-galactosidase that removes the 3,6-anhydrogalactose from

273 te based on a substituted enzyme (G794A-beta-galactosidase) that traps allolactose.

274 e Cre-loxP system allowed to direct the beta-galactosidase to proximal dendrites, and in particular t

275 s exoglycosidases, one of which is BgaC beta-galactosidase, to deglycosidate host surface glycolconju

276 th reduced co-localisation of the viral beta-galactosidase transgene with MAdCAM-1+ sinus-lining endo

277 We found that beta-galactosidase translocation is driven only by the negati

278 sed approach to quantify pep-1-mediated beta-galactosidase translocation.

279 02 in the LHb previously transfected with ss-galactosidase under control of the FosB promoter.

280 Daun02 in the dlBST previously expressing ss-galactosidase under control of the FosB/DeltaFosB promot

281 6/lacZ reporter mouse strain expressing beta-galactosidase under the control of the Mig-6 gene promot

282 we used RRas2-knockout mice expressing beta-galactosidase under the regulation of the endogenous RRa

283 , as evidenced by senescence-associated beta-galactosidase upregulation, decreased self-renewal poten

284 hydrolysis by the immobilized K. lactis beta-galactosidase using genipin as a crosslinker was 87%.

285 wn mRNA of a selected chromosomal gene (beta-galactosidase) using an artificial miniCRISPR locus.

286 aximum GOS concentration with K. lactis beta-galactosidase was achieved in 1 and 5h at 40 and 4 degre

287 Initially, beta-galactosidase was employed as a detectable model for BT

288 Expression of senescence-associated beta-galactosidase was greatly induced in hepatocytes exposed

289 Cicer alpha-galactosidase was immobilized onto functionalized graphe

290 Escherichia coli beta-galactosidase was incubated in the presence of the slow-

291 gle enzyme molecule of Escherichia coli beta-galactosidase was measured using a capillary electrophor

292 Finally, the expression level of beta-galactosidase was significantly higher when point mutati

293 ke growth factor binding protein 7, and beta-galactosidase were able to distinguish the severe neurol

294 Here we focus on beta-galactosidase, which is overexpressed in primary ovarian

295 wn of some lactose and the provision of beta-galactosidase, which remains active in the gastrointesti

296 alytic ability of the hydrolytic enzyme beta-galactosidase, which serves as the protein core, despite

297 cells with HHV-8 induces expression of beta-galactosidase, which was used to determine TCID50 levels

298 Among patients with suitable mutant alpha-galactosidase who received migalastat for up to 24 month

299 ect enzyme activity for the reaction of beta-galactosidase with p-aminophenyl-galactopyranoside (PAPG

300 Kanzi apples had lower activity of beta-galactosidase, with no decline in the extent of branchin