ライフサイエンスコーパス: filtrate

1 tinocytes (HKs) are in contact with a plasma filtrate.

2 ecular weight substances into the glomerular filtrate.

3 proximal tubules reclaim from the glomerular filtrate.

4 tuberculosis (SapM) localized to the culture filtrate.

5 s of metagenomes recovered from geyser water filtrate.

6 ular weight polypeptides from the glomerular filtrate.

7 d that filters blood to form primary urinary filtrate.

8 ation and remodelling compared to WT culture filtrate.

9 L1 uptake from the circulation or glomerular filtrate.

10 ction was two-times higher than that of whey filtrate.

11 cytosing urinary albumin from the glomerular filtrate.

12 rier to macromolecular flow into the urinary filtrate.

13 ntrifugation, O-glycans are recovered in the filtrate.

14 l and were not detected in the extracellular filtrate.

15 mal catabolism of proteins captured from the filtrate.

16 us suppresses the re-uptake of P(i) from the filtrate.

17 s), from environmental samples and a biofilm filtrate.

18 nd is mainly present as a monomer in culture filtrates.

19 cted diverse bacterial DNA signatures in the filtrates.

20 ts were autoclaved or converted into sterile filtrates.

21 y commonly observed in S. marcescens culture filtrates.

22 doenzyme from Diplococcus pneumoniae culture filtrates.

23 ls analysis of fabric digests and wash water filtrates.

24 The 3 kDa filtrate (1 mg/ml), that demonstrated highest ACE-I inhi

25 Subsequent HPLC fractionation of plasma filtrate (10-kd MWt cutoff) by sequential column chromat

26 tric monitoring of the concentrations of the filtrates (214 nm).

27 ing activity in Rhizobium meliloti cell-free filtrates, a plant response dependent on the bacterial n

28 Furthermore, sonication of the filtrates abolished their ability to elevate [Ca(2+)](i)

29 fumigatus vaccine preparations (sonicate and filtrate) administered intranasally and subcutaneously w

30 The condensed materials in the filtrated aerogel particles can be squeezed and washed o

31 e protective immunogen (cryptococcal culture filtrate Ag + heat-killed cryptococci-CFA), or controls,

32 th shed cryptococcal products (C. neoformans filtrate Ag) but not other nonspecific stimuli.

33 e protective immunogen (cryptococcal culture filtrate Ag-CFA), in contrast to the nonprotective immun

34 The C. albicans culture filtrates also induced migration of PMNs across confluen

35 ges of carbohydrates were identified in whey filtrate and in all second fractions, where galactose wa

36 itinase enzyme activity found in SEs culture filtrate and in cellular extracts of developing SE and h

37 ration of Aspergillus fumigatus cell culture filtrate and OVA.

38 lbumin, which were secreted into the primary filtrate and reabsorbed by proximal tubular cells, resul

39 igh molecular weight proteins into the blood filtrate and urine, a condition called proteinuria.

40 trated that Sepp1 passed into the glomerular filtrate and was specifically taken up by proximal tubul

41 g of the three chlorobenzenes in the 1.5 mum filtrate, and the partitioning behavior did not follow t

42 The hydrolysate was ultra-filtrated, and the fractions were evaluated for antioxid

43 (85-kDa antigen complex, "short-term culture filtrate," and peptides from the ESAT-6 protein), as wel

44 ity (DTH) reactivity to cryptococcal culture filtrate antigen (CneF) can be either protective or nonp

45 mmunized with a soluble cryptococcal culture filtrate antigen (CneF) emulsified in complete Freund's

46 antigen preparations, one a soluble culture filtrate antigen (CneF) in complete Freund's adjuvant (C

47 showed that GXM or the cryptococcal culture filtrate antigen CneF directly induces L-selectin loss f

48 ing heat-killed whole C. neoformans, culture filtrate antigen, C. neoformans lysate, and purified cry

49 tion of genes encoding several early culture filtrate antigens (ESAT-6-like proteins), ribosomal prot

50 s, there is a well-defined subset of culture filtrate antigens that elicits antibodies during noncavi

51 Since this IMS was reactive to culture filtrate antigens, several of these proteins were cut fr

52 were prepared against the 10 x -concentrated filtrate antigens.

53 chemoattractant in Candida albicans culture filtrates appeared to act through the formyl peptide rec

54 The carbohydrates in the filtrate are then derivatized with 1-phenyl-3-methyl-5-p

55 lbumin-sized nanoparticles reach the primary filtrate, are captured by proximal tubule cells, and are

56 Using mouse brain filtrate as substrate, both brain sulfotransferases were

57 We found that crude ETEC culture filtrates, as well as purified ETEC toxins, did potentia

58 nd hyphae in response to serum or to a serum filtrate but does form pseudohyphae.

59 ied MnP proteins in C. subvermispora culture filtrates, but none in P. chrysosporium cultures.

60 Analysis of culture filtrate by double immunodiffusion yielded a single line

61 ron are reabsorbed daily from the glomerular filtrate by kidney proximal tubule cells (PT), requiring

62 Analysis of the filtrate by SDS-PAGE showed a major band at approximatel

63 reabsorption of proteins from the glomerular filtrate by the renal proximal tubule.

64 by active reabsorption of nearly 99% of that filtrate by the tubules creates vulnerability in both co

65 To prevent recontamination of the filtrate by zinc in this type of experiment, Candida alb

66 urified to apparent homogeneity from culture filtrates by ammonium sulfate precipitation and ion-exch

67 These filtrates caused no damage to mouse small intestinal epi

68 a 32-kDa putative glyoxalase in the culture filtrate (CF) of growing M. tuberculosis (originally ann

69 testing including measurement of MTB culture filtrate (CF)-stimulated interferon gamma (IFN-gamma) an

70 ntigens (whole-cell [WC] antigen and culture filtrate [CF] antigen) of B. pseudomallei The ELISAs wer

71 study, we found that a cryptococcal culture filtrate (CneF), when injected into the bloodstream of m

72 oformans strain B3501, we prepared a culture filtrate (CneF-Cap67) similar to that used for preparing

73 retention changes were demonstrated by large filtrate concentration reductions at all temperatures te

74 mbrane surface area or membrane fouling, the filtrate concentrations behaved according to a barrier b

75 tures for C. difficile and cytotoxin B fecal filtrate concentrations.

76 The filtrate contained pure streptavidin.

77 The particle free filtrate containing the growth media is suitable for rec

78 We demonstrate that the presence of the filtrate containing these enzymes prevents ATP-induced m

79 We investigated whether sterile fecal filtrates (containing bacterial debris, proteins, antimi

80 tron microscopy (IEM) in an infectious stool filtrate derived from an outbreak of gastroenteritis in

81 fatty acids at the same concentration as the filtrates did not.

82 inaceous elicitor called sclerotinia culture filtrate elicitor1 (SCFE1) from the necrotrophic fungal

83 s are concentrated inside the oral cavity as filtrate exits between the rakers, but particles are not

84 The culture filtrate exponentially decreased the viscosity of a pect

85 ndicated that the major component in culture filtrate extracts of the mutant was less polar and small

86 ative gene disruption construct, and culture filtrate extracts of the mutant were assayed for the pre

87 graphic fractionation of S. meliloti culture filtrate extracts revealed at least three peaks with AHL

88 size-exclusion HPLC analysis of the ethanol filtrate for low molecular weight components.

89 obulin binding proteins, we examined culture filtrates for their ability to induce endothelial cell a

90 E in renal structure and regulation of renal filtrate formation, single-nephron GFR, proximal tubular

91 Analysis of virus-like particles from a filtrate found to reduce symptoms of CDI showed a comple

92 ed lipids from the cell envelope and culture filtrate from 52 isolates of Mycobacterium species, anal

93 w cell densities, was rescued by the culture filtrate from a high cell density tup1Delta culture and

94 When mice are vaccinated with a culture filtrate from Cryptococcus neoformans (CneF), they mount

95 Thrombin, trypsin, tryptase, a filtrate from degranulated mast cells, and peptides corr

96 Microbiota analysis was performed on fecal filtrate from donors and stool samples from FT recipient

97 the presence of an intestinal content fluid filtrate from gnotobiotic pigs.

98 hyperfiltration, hypertrophy, and outflow of filtrate from subpodocyte spaces.

99 o P13 the pigs were inoculated with a tissue filtrate from the corresponding pig in the previous pass

100 ferns, their enriched leaf pockets and water filtrate from the surrounding ditch established that bac

101 Filtrate from toxic strains of Pfiesteria spp. in bacter

102 osed over the course of 5 weeks with culture filtrate from wild-type (WT), Asp f 5 null (5) or Asp f

103 ovine leukocytes were incubated with culture filtrates from a mutant strain of P. haemolytica that do

104 y and validated the assays using (i) culture filtrates from a panel of clinical C. difficile isolates

105 ents with CDI shows that transfer of sterile filtrates from donor stool (FFT), rather than fecal micr

106 Culture filtrates from Helicobacter pylori promote the transfer

107 33 but not at 37 degrees C, and only culture filtrates from infected monolayers incubated at 33 degre

108 The culture filtrates from isogenic mutants were devoid of hemolytic

109 ass spectrometer for the analysis of culture filtrates from Mycobacterium marinum.

110 Culture filtrates from selected M. ovis field isolates demonstra

111 harveyi but exhibited no response to culture filtrates from V. harveyi mutants defective in BAI-2 syn

112 ined by electron microscopy, whereas culture filtrates from wild-type Aeromonas caused complete destr

113 osensor responded to the addition of culture filtrates from wild-type Vibrio harveyi but exhibited no

114 lly, 29%; sonicate given subcutaneously, 0%; filtrate given intranasally, 75%; and filtrate given sub

115 y, 0%; filtrate given intranasally, 75%; and filtrate given subcutaneously, 50%.

116 essed form of MTB12 protein found in culture filtrates has a molecular mass of 12.5 kDa.

117 Serratia marcescens culture filtrates have been reported to be cytotoxic to mammalia

118 reabsorption of Me-4FDG from the glomerular filtrate in wild-type mice and the absence of reabsorpti

119 nd that bovine S. aureus M60 and its culture filtrates induce a 3- to 10-fold increase in urokinase-t

120 Culture filtrates induced similar levels of endothelial cell apo

121 en deleted strains, in particular 13 culture filtrate, induced significantly less airway inflammation

122 sistent with transtubular backleak of 57% of filtrate (inulin) in sustained ARF.

123 adium catalyst is removed by filtration, the filtrate is blown dry with an inert gas, and the dried p

124 tration, and a renal tubule, along which the filtrate is modified.

125 ugal filtration, and digested HA left in the filtrate is quantified by electrospray ionization mass s

126 of piGC, the force opposing the formation of filtrate, is predominantly or uniquely responsible for t

127 rovides a paracellular pathway through which filtrate leaks back in sustained allograft ARF.

128 c intranasal exposure to the three different filtrates led to comparable airway hyper-reactivity and

129 te, leading to poor size cut-off properties, filtrate loss within the membranes, and low transport ra

130 ation of ultrafiltration and flow-associated filtrate modification that is central to CKD etiology is

131 Instead, a filtrate (molecular mass, <1 kDa) devoid of serum albumi

132 three distinct urinary spaces through which filtrate must pass before reaching the proximal convolut

133 te (NOMr, Mw = 691,000 g/mol) and 98 wt % of filtrate (NOMf, Mw = 12,800 g/mol).

134 reabsorption of insulin from the glomerular filtrate occurs by binding to as yet unidentified sites

135 Purification of the enzymes from the culture filtrate of 7H9-grown M. bovis BCG cells and determinati

136 incubation with trypsin or with the culture filtrate of a P. aeruginosa lasAdelta mutant.

137 in relevant biological samples, the culture filtrate of A. niger grown on wheat straw.

138 enged intranasally on days 0, 3 and 6 with a filtrate of Alternaria alternata.

139 alactosidase A was purified from the culture filtrate of an over-producing strain of Aspergillus nige

140 tethered ligand), mast cell tryptase, and a filtrate of degranulated mast cells stimulated a prompt

141 Interestingly, a cell culture filtrate of FB17 suppressed flg22-induced MAMPs-activate

142 pure solvent and spiked into fungal culture filtrate of Fusarium graminearum respectively.

143 urifying polypeptides present in the culture filtrate of M. tuberculosis and evaluating these molecul

144 ow here that *MtCM secretes into the culture filtrate of M. tuberculosis.

145 Polypeptide Ags present in the culture filtrate of Mycobacterium tuberculosis were purified and

146 on was illustrated by demonstrating that the filtrate of plasma (10-kd MWt cutoff) could supply compo

147 rioferritin was more abundant in the culture filtrate of the live vaccine strain.

148 xidase was much more abundant in the culture filtrate of the virulent clinical isolate, whereas bacte

149 blood of infected mice, we used a cell-free filtrate of their blood to immunize congenic naive mice.

150 Culture filtrates of a MAT1-1 strain contained an activity that

151 nferred a cytotoxic phenotype on the culture filtrates of a nonpathogenic Escherichia coli strain.

152 cterized the proteins present in the culture filtrates of a virulent recent clinical isolate and the

153 rotease activity on external substrates, and filtrates of AAV virus preparations also showed no prote

154 undertaken to define the antigens in culture filtrates of actively replicating Mycobacterium tubercul

155 inity purification studies were performed on filtrates of bacteria incubated in human serum and plasm

156 It has been reported that culture filtrates of clinically derived strains of B. cepacia ar

157 chitinase had been isolated from the culture filtrates of Coccidioides immitis endosporulating spheru

158 n Circumdati, ochratoxin was not detected in filtrates of cultures grown in various media.

159 Gnotobiotic calves inoculated with fecal filtrates of each group B rotavirus developed diarrhea,

160 Interestingly, while filtrates of fatty acid solutions evoked CCK secretion a

161 11 ng of trans-zeatin per liter from culture filtrates of four PPFM leaf isolates (from Arabidopsis,

162 mpare the repertoires of antigens in culture filtrates of in vitro-grown Mycobacterium tuberculosis t

163 ntibodies detected no antigen in the culture filtrates of M. avium and other nontuberculous mycobacte

164 tected Rv1681 protein in lysates and culture filtrates of M. tuberculosis and immunoprecipitated it f

165 Fractionation of filtrates of M. tuberculosis cultures has yielded an abu

166 To identify and purify novel proteins in the filtrates of M. tuberculosis cultures, a bacteriophage l

167 stimulated by whole cell lysates and culture filtrates of Mycobacterium tuberculosis and Mycobacteriu

168 orobenzene to COC for both 1.5 mum and 1 kDa filtrates of PE was investigated using the gas-stripping

169 Serum-free culture filtrates of six Candida species and Saccharomyces cerev

170 h those from rapidly prepared noncentrifuged filtrates of sputum (r(s) = 0.94).

171 ive proteins partially purified from culture filtrates of strain N4-7.

172 Culture filtrates of strains expressing HopPtoD2 were able to de

173 ixty-five Gn pigs were inoculated with fecal filtrates of the NoV/GII/4/HS66/2001/US strain or with p

174 amined for inflammatory responses to culture filtrates of the outbreak strain.

175 lucanase, pectinase, and xylanase in culture filtrates of the Tox2(+) ccsnf1 mutant were reduced by 5

176 cine formulations prepared as either culture filtrate or partially purified toxoid.

177 overed from the factory, warehouse, solution filtrate, or unopened solution bottles; production of im

178 lp determine the water profile direction and filtrate outlets for different food materials based on t

179 Heat inactivation of H. somnus culture filtrates partially reduced the apoptotic effect on endo

180 icity was significantly reduced when culture filtrates prepared from wild-type strains were pretreate

181 nsisted of 2-week-old fission arthroconidial filtrates produced in Pine's broth at 37 degrees C.

182 A fumigatus culture filtrates profoundly inhibited the differentiation, migr

183 ed Mycobacterium tuberculosis 10-kDa culture filtrate protein (CFP)10 is a potent T cell Ag that is r

184 The 10-kDa culture filtrate protein (CFP-10) and 6-kDa early secretory anti

185 tigenic target (ESAT-6) and a 10-kDa culture filtrate protein (CFP-10), that is essential for virulen

186 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP-10) antigens via the Salmonella

187 we confirm the DND captured antigen is cell filtrate protein 10 (CFP-10) because its Mascot analysis

188 Culture filtrate protein 10 (CFP-10) from Mycobacterium tubercul

189 ic target 6-kDa protein (ESAT-6) and culture filtrate protein 10 (CFP-10), was therefore investigated

190 00-amino-acid protein referred to as culture filtrate protein 10 (CFP-10).

191 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP-10).

192 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP10).

193 ese clones, the Ag was identified as culture filtrate protein 10 (CFP10)/Mtb11, a 10.8-kDa protein no

194 rived macrophages (BMDM) compared to culture filtrate protein 10 kDa (CFP10) and antigen 85A.

195 agnitude of ex vivo reactivity, with culture filtrate protein 10 kDa being most dominant, followed by

196 rly secreted antigenic target 6 kDa, culture filtrate protein 10 kDa, Rv2031c, Rv2654c, and Rv1038c.

197 rly secretory antigenic target 6 and culture filtrate protein 10, for 18 mo after cessation of tuberc

198 y compatible with current ESAT-6 and culture filtrate protein 10-based diagnostics.

199 he secreted proteome of Histoplasma, culture filtrate protein 4 (Cfp4) is a heavily glycosylated fact

200 A native 37-kDa culture filtrate protein and a 55-kDa mycelial glycoprotein (gp5

201 The mycobacterial culture filtrate protein MPT64 was expressed as a chimeric prote

202 ESAT-6 and its molecular chaperone, culture filtrate protein of 10 kDa (CFP10), on the capacity of h

203 e of one of the new genes encoding a culture filtrate protein of 310 amino acid (aa) residues.

204 mulated ex vivo with M. tuberculosis culture filtrate protein was delayed in ApoE(-/-) HC mice, and t

205 ith Mycobacterium tuberculosis H37Rv culture filtrate protein was higher than that of CD4(+) T cells

206 1 prevented secretion of the CFP-10 (culture filtrate protein, 10 kilodaltons)/ESAT-6 virulence facto

207 with the M. tuberculosis-specific Ag culture filtrate protein-10 (CFP-10).

208 CD8(+) T cells specific for culture filtrate protein-10 (CFP10) are found in purified protei

209 early secretory antigenic target-6, culture filtrate protein-10, and PPD as stimulatory antigens wer

210 Culture filtrate proteins (CFP) of Mycobacterium tuberculosis ha

211 ained and recall immune responses to culture filtrate proteins (CFP) of Mycobacterium tuberculosis we

212 in M. tuberculosis lysate but not in culture filtrate proteins (CFP), indicating that it is not a sec

213 ion of mice with Mycobacterium bovis culture filtrate proteins (CFP), prepared in a variety of adjuva

214 mild adjuvant admixed with purified culture filtrate proteins and enhanced by the cytokine interleuk

215 s confirmed by using M. tuberculosis culture filtrate proteins and fractions from infected macrophage

216 sis, are among the bacterium's major culture filtrate proteins in actively growing cultures.

217 lectrophoresis, detailed maps of the culture filtrate proteins of M. tuberculosis H37Rv were generate

218 Lipoarabinomannan-free culture filtrate proteins of M. tuberculosis were fractionated b

219 nary antibodies directed against the culture filtrate proteins of M. tuberculosis, MPT 32, and the 81

220 e with Leishmania major promastigote culture filtrate proteins plus Corynebacterium parvum confers re

221 Normal reabsorption of glomerular filtrate proteins probably requires recycling of the end

222 A number of the culture filtrate proteins secreted by Mycobacterium tuberculosis

223 terogeneous, our studies with native culture filtrate proteins show that the antibody responses in TB

224 Finally, we expressed the major culture filtrate proteins that are promising vaccine candidates

225 B patients recognized 26 of the >100 culture filtrate proteins, and the repertoire changed with disea

226 as several other well-characterized culture filtrate proteins, including members of the 85B complex.

227 all extract, and Mycobacterium bovis culture filtrate proteins.

228 s were obtained for three additional culture filtrate proteins; however, these did not yield signific

229 he effectiveness of DNA-HSP65 or CpG/culture filtrated proteins (CFP) immunotherapy.

230 Filtrate PRP collected from an optimally-designed CIF de

231 responses that were triggered by crude ETEC filtrates, purified STa, and the peptide hormone guanyli

232 r (h), instantaneous volumetric flow rate of filtrate (Q), and cumulative volume of water produced (V

233 was immunoscreened by using an anti-culture filtrate rabbit antiserum.

234 ofile direction and the anolyte to catholyte filtrate ratio.

235 s and times of Staphylococcus aureus culture filtrate revealed a single dose- and time-dependent diff

236 ivated sludge process (ASP)), tertiary (sand filtrated (SF)), or advanced (chlorine dioxide (ClO(2)),

237 Parent WT and 5 culture filtrates showed high protease activity, whilst protease

238 Proteome analyses of selected FFT filtrates showed no obvious protein candidates associate

239 Chemical analysis of low-pH culture filtrates showed that the proteins encoded by the ompATb

240 tRNA hydrolysates in addition to the culture filtrates, suggesting that secreted trans-zeatin resulte

241 is protective antigens released into culture filtrate supernatant (CFS), a bacterial growth system wa

242 as abundant proteins in Phytophthora culture filtrates that have the capacity to elicit hypersensitiv

243 or two known components of the early culture filtrate, the secreted 45/47-kDa antigen complex and the

244 on artifacts; and (2) the direct delivery of filtrate to dedicated bottle sets for specific analytes.

245 ognized in the glomerulus conducting primary filtrate to the proximal convoluted tubule has been Bowm

246 protein components of mycobacterial culture filtrates to develop subunit vaccines and immunodiagnost

247 n that the ability of C(10), C(12) and C(14) filtrates to elevate [Ca(2+)](i) decayed with time was c

248 ed the cytotoxicity of S. marcescens culture filtrates towards HeLa cells, suggesting the involvement

249 e series to investigate the effects of fecal filtrate transfer (FFT) in 5 patients with symptomatic c

250 bridizations, immunoblot analyses of culture filtrates using both CTS1-specific murine antiserum and

251 omotes retrieval of iron from the glomerular filtrate via its ferrireductase activity and modulates k

252 ing from application of F. oxysporum culture filtrate was also reduced in lbd20 leaves relative to th

253 aked in acidified ethanol, filtered, and the filtrate was cleaned by solid phase extraction using sil

254 ield through samples between two electrodes, filtrate was discharged mainly towards the anode in OJ s

255 nto the SPRi chip surface covalently and the filtrate was flowed over the sensor surface.

256 and the most abundant protein in the culture filtrate was identified as the only family 7 glycoside h

257 ture and the active molecule in this culture filtrate was identified to be an oligopeptide composed o

258 The response to tryptase and the mast cell filtrate was inhibited by the tryptase inhibitor BABIM,

259 vity, whilst protease activity in 13 culture filtrate was low.

260 nd chemotaxis toward the C. albicans culture filtrate was not inhibited by an FPR antagonist (t-butox

261 ignificant HOC-COC partitioning to the 1 kDa filtrate was observed with organic carbon-normalized par

262 to remove small particles and bacteria; the filtrate was transferred to patients in a single adminis

263 oGastro Cd assay and 200 microl of the stool filtrate was used for the TOX-B CCCNA.

264 The hemolytic activity of the culture filtrates was attenuated after heat treatment.

265 fter stimulation with Pseudomonas aeruginosa filtrates was not greater in CF cells in the absence of

266 ulations, but reappearance of toxin in fecal filtrates was observed in 28% of vancomycin-treated pati

267 efense eliciting activity present in culture filtrates was recovered and purified by ultrafiltration

268 Using GII.4 huNoV positive stool filtrates, we demonstrated limited huNoV replication in

269 FH), and the generated 3 kDa and 10 kDa MWCO filtrates were assessed for their in vitro ACE-I inhibit

270 order to better define these anomalies, the filtrates were collected in sequential fractions of 7.5

271 activity was restored when the same culture filtrates were incubated with zinc divalent cations, whi

272 MPT63, purified from M. tuberculosis culture filtrates, were indistinguishable in serological assays.

273 us humor is a clear fluid, primarily a blood filtrate, which circulates through the anterior chamber