ライフサイエンスコーパス: viable cell

1 cel (ranging from 6.0 x 10(4) to 5.6 x 10(5) viable cells).

2 sposon mutagenesis data, failed to produce a viable cell.

3 ed low levels of radiolabeled nucleoside per viable cell.

4 ry, a necessary step in the development of a viable cell.

5 regress, leaving a repolarized monolayer of viable cells.

6 tion of ROS by N-acetyl cysteine led to more viable cells.

7 5% to over 94% with a recovery of 73% of the viable cells.

8 ect 200 dead cells in a population of 10,000 viable cells.

9 ntly authenticated DNA to date obtained from viable cells.

10 tects protease activity restricted to intact viable cells.

11 e-binding protein that bridges apoptotic and viable cells.

12 ring membrane proteins into the membranes of viable cells.

13 ins, followed by their binding to surface of viable cells.

14 evidence for direct inhibition of uptake by viable cells.

15 fficiently obtain highly pure populations of viable cells.

16 in to air for 8 h resulted in recovery of no viable cells.

17 tosolic aggregation of GFP-nCLU was found in viable cells.

18 Similarly, EO6 binds apoptotic cells but not viable cells.

19 neither cell cycle kinetics nor recovery of viable cells.

20 tigated to maximize total RNA extracted from viable cells.

21 lorimetric method to determine the number of viable cells.

22 therapy because of an insufficient number of viable cells.

23 e cathepsin B was secreted pericellularly by viable cells.

24 e analysis of beta-glucuronidase activity in viable cells.

25 2 were passageable, resulting in up to 10(7) viable cells.

26 to detect HIV-1 gene expression in infected viable cells.

27 ing, and the decrease in the total number of viable cells.

28 orm elevated spherical structures containing viable cells.

29 trating that this reaction occurs in situ in viable cells.

30 he germination/ outgrowth process to produce viable cells.

31 ning, and measurement of the total number of viable cells.

32 orescent staining, and molecular delivery to viable cells.

33 the skin and low penetration into the skin's viable cells.

34 ctionalities they offer and their effects on viable cells.

35 ation peak at about 750 mV that accounts for viable cells.

36 ryopreserved tissue and from fewer than four viable cells.

37 y greater than that of THP-1 cells at day 5 (viable cells: 17 [8%] THP-1 vs 73% [4%] RPE; P < .05).

38 ylation of cell surface membrane proteins in viable cells, (2) affinity enrichment using streptavidin

39 conds resulted in a significant reduction in viable cells (69.69% +/- 16.34% at 30 seconds compared w

40 Since surface calreticulin is also found on viable cells, a mechanism preventing inadvertent uptake

41 e of therapy-induced cytotoxic edema because viable cells act as a diffusion barrier in tissue.

42 LY 294002 decreased the number of viable cells after 18 h of treatment; therefore, the inh

43 tion of STI571 needed for a 50% reduction in viable cells after a 3-day exposure was on average 10 ti

44 The fractions of viable cells after exposure were allowed to grow in fres

45 unt of protein release and the percentage of viable cells after the operation.

46 w cytometry, this technique does not rely on viable cells allowing measurement of frozen samples in a

47 wed a significant reduction in the number of viable cells, an increase in the number of apoptotic cel

48 various intervals for quantitation of total viable cell and heat-resistant spore counts on taurochol

49 ces demonstrated that all capsules contained viable cells and 20 of 21 devices released basal and nic

50 ntitated by a tetrazolium staining assay for viable cells and by measurement of DNA content.

51 roteolytic activities associated with intact viable cells and cells that have lost membrane integrity

52 firmed a lack of histone immunoreactivity in viable cells and demonstrated co-localization of histone

53 y maintained significantly higher numbers of viable cells and exhibited less cell death during G-CSF

54 etin and the retraction ATPase can result in viable cells and found that these cells display paradoxi

55 ons, U0126 or iloprost reduced the number of viable cells and increased caspase-3 activity, which cou

56 In contrast, the number of viable cells and invasive cells was decreased in sFRP3 m

57 BMX associates with BAK in viable cells and is the first kinase to phosphorylate th

58 not alter the compound's ability to permeate viable cells and localize in mitochondria.

59 ered following introduction of the TFOs into viable cells and photoactivation of the psoralen.

60 lysozyme allowed the cwlD spores to produce viable cells and showed that they have normal heat resis

61 inhibitor, leading to a decreased number of viable cells and suggesting an antiapoptotic role for NF

62 To reveal active repulsion of viable cells and to seek specific capture or 'tethering'

63 s of 60 to 66 degrees C, both TUNEL-positive viable cells and TUNEL-positive nonviable cells were obs

64 Indeed, tryptase was found in the nucleus of viable cells and was shown to cleave core histones in th

65 subjects had antibodies to native antigen on viable cells, and antibody assays with this specificity

66 locations are labor intensive, often require viable cells, and are biased toward known IGH fusions.

67 ergone apoptosis are physically smaller than viable cells, and our device exploits this fact to achie

68 rations of DSF alone decreased the number of viable cells, and the addition of CuCl(2) significantly

69 arge fraction of these 15 sarcomas contained viable cells, and this impression was confirmed histolog

70 ell competition, which is a process in which viable cells are actively eliminated by more competitive

71 rosophila follicular epithelia, aberrant but viable cells are eliminated through cell competition, an

72 ponse to apoptotic stimuli and suppressed in viable cells are largely unknown.

73 changes is related to their viability; live (viable) cells are more voluminous than the dead ones, an

74 Using a viable cell arginase assay, B. anthracis arginase increa

75 At later times, viable cells arrest in G1/G0.

76 lular viability, assessed as a percentage of viable cell-associated NTHI, were measured.

77 ssociated with the increase in the number of viable cells at the initial density used (10(7) per plat

78 ic material admixed with few macrophages and viable cells at their outer rim.

79 In viable cells, Bax associates with Bcl-2, Bcl-x(L) and Mc

80 es C, cells died predominantly by apoptosis; viable cells became TUNEL positive, indicating degradati

81 ent process, and that this process begins in viable cells before they detach from the culture dish.

82 light was observed to increase the number of viable cells, biofilm biomass, and thickness relative to

83 Here, we outline a viable cell-biological model for generating synaptic spe

84 to inhibit cell death and generate enhanced viable cell biomass.

85 by phosphatidylserine (PS) on the surface of viable cells both in vitro and in vivo then slowly relea

86 introduce transcriptionally active DNA into viable cells but approaches to deliver functional protei

87 throughout and spheres with an outer rim of viable cells but necrotic cells centrally.

88 can induce the proliferation of neighboring viable cells, but how this is controlled is not clear.

89 caspase-3 was undetectable in the cytosol of viable cells, but was recovered in subcellular fractions

90 etermine manganese speciation within intact, viable cells, but we here report that this speciation ca

91 s targeted, this causes cell death, reducing viable cells by a factor of 10(8).

92 Jurkat cells are enriched to high purity of viable cells by a factor of 185-fold.

93 vents phagocyte ingestion of closely apposed viable cells by transmitting 'detachment' signals, and w

94 This apparent binding of 7E11 to viable cells can be accounted for by a 5-7% subpopulatio

95 10(7)cells/ml, indicating that the amount of viable cells can be accurately quantified.

96 Drosophila, it has been known for years that viable cells can be eliminated by their neighbours throu

97 shed after terminal differentiation, whereas viable cells can be shed by classical apoptosis with the

98 The general notion is that, in viable cells, caspase-3 is found as a cytosolic inactive

99 Multivariate analysis confirmed that viable cells comprise independent risk factor for LTP (P

100 lls lacking the La protein homolog Lhp1p are viable, cells containing a mutation that disrupts the an

101 Since the metabolic activity of viable cells could be detected directly on the support m

102 er, (+/-)-2 was able to significantly reduce viable cells count, endothelial cell migration, and tube

103 he effect of anti-CD95 MoAbs was measured by viable cell counting, flow cytometry, and CFU-C assays.

104 tosis of PHPs measured by flow cytometry and viable cell counting.

105 density measurements or quantitatively using viable cell counting.

106 within the pneumocytes and we determined by viable-cell counting that a small percentage of the inoc

107 The biofilm viable cell counts and total protein concentration incre

108 hesis concurrent with the taking of standard viable cell counts of the plaque samples.

109 Using viable cell counts to assess proliferation after 14 d of

110 concentration, a decrease of 4log cycles in viable cell counts was observed at 10h, against four of

111 ced apoptosis of B-CLL cells is confirmed by viable cell counts, annexin V/propidium iodide and tetra

112 Viable cell counts, proliferation, and apoptosis were de

113 s reflected by a decrease of A578 values and viable cell counts.

114 The level of viable cell coverage was therefore determined in human d

115 tify key sub-dynamics that are essential for viable cell cycle control, as well as identifying the su

116 wth compared to a reference regarded as 100% viable cells; data analysis was inspired by that in quan

117 (18)F-FBnTP cellular uptake in viable cells declined linearly with the increasing durat

118 low growth rate and failure to meet required viable cell density (VCD).

119 xperimental data, both at the cell cycle and viable cell density levels, was observed.

120 t candidate for oncoming economical in-field viable-cell detection systems, fully integrable with sop

121 to pseudo-bipolar spindles, thereby ensuring viable cell division.

122 roblasts results in significant reduction of viable cells due to induction of programmed cell death.

123 Elevated numbers of viable cells during G-CSF treatment were also observed i

124 n D allowed us to identify four populations: viable cells, early apoptotic cells, late apoptotic and/

125 ctional exogenous membrane-bound proteins to viable cells encapsulated within a lipid templated silic

126 re or composition will be required to enable viable cell encapsulation, the functionalized injectable

127 ng the clumps, then diluting and plating for viable cell enumeration.

128 and necrotic targets may permit neighboring viable cells, especially non-migratory epithelial cells,

129 al change, apoptotic death may enable nearby viable cells, especially nonmigratory epithelial cells,

130 During transdermal delivery, the first viable cells exposed to the oligonucleotides are the ker

131 In all cases, we isolated viable cells expressing only the mutant actin.

132 In this two-color fluorescence assay, viable cells fluoresce green, and the nuclei of nonviabl

133 disorders by exploring why microglia destroy viable cells following viral infection.

134 capsular bags contain a large population of viable cells for many years after cataract surgery.

135 reast tumors and provide adequate numbers of viable cells for studying and manipulating their functio

136 ated a progressive increase in the burden of viable cells for the first 24 h of development.

137 However, extraction of viable cells, fractionation of lineages, and in vitro an

138 -35 to SK-N-SH cells decreased the number of viable cells from 5% at 3 h to 35% at 15 h when compared

139 d enables efficient, label-free isolation of viable cells from mixed samples containing 10(6) cells/m

140 for the purpose of patterning and isolating viable cells from small cell samples.

141 apoptosis (anoikis), inhibited detachment of viable cells from substratum and reduced tumorigenicity.

142 ns of fresh human brain and (ii) cultures of viable cells grown from human meningiomas.

143 However, chromosome targeting in viable cells has not been demonstrated, and in vitro exp

144 However, fabricating PEMs on viable cells has proven challenging owing to the high cy

145 The viable cells have an elongated helical morphology with n

146 nhibited cells had a significant fraction of viable cells (herein termed "rescued" cells) that failed

147 Elimination of individual gene pairs yields viable cells; however, attempts at double knock-outs res

148 escent protein-labeled HB1.F3 cells (200,000 viable cells in 3 microl of PBS) when stereotaxically tr

149 t by itself to determine the distribution of viable cells in 3D.

150 n on the engulfing cell, permitted uptake of viable cells in a calreticulin/LRP-dependent manner.

151 les (NPs) are observed to be toxic or reduce viable cells in a population of bacteria, we observed th

152 anumycin was shown to decrease the number of viable cells in all six of the cell lines though to a le

153 ated via the secretion of soluble factors by viable cells in hCVAM and that these factors are protein

154 in the ovary or fallopian tube), Peritoneal (viable cells in peritoneal fluid), and Metastatic (cells

155 yde-fixed corneal cells were as effective as viable cells in preventing corneal graft rejection.

156 L-4 mAb dramatically decreased the number of viable cells in the CD28-/- cultures but had little effe

157 ity between the amount of GPdh and number of viable cells in the cultures.

158 e truncated huIL-2R beta with percentages of viable cells in the G0/G1, S, and G2/M phases similar to

159 in and a further reduction in the numbers of viable cells in the presence of both bleomycin and Cu(2+

160 However, Bax expression decreased in viable cells in the presence of these cytokines and the

161 ion of CaLas DNA, but a higher proportion of viable cells, in the asymptomatic tissues.

162 The number of foci per viable cell increases linearly from approximately 0.17 x

163 Viable cells incubated in 50 mM trehalose, then lyophili

164 Exosome release by viable cells is a feature of activated cell types, inclu

165 The enrichment of viable cells is an essential step to obtain effective pr

166 iable cells separately or in the vicinity of viable cells is of great importance for many fundamental

167 nd an intracellular epitope of PSMA that, in viable cells, is not available for binding.

168 Hepatocytes (10(6) viable cells) isolated from congeneic mice ([ROSA]26 C57

169 on content of nucleic acids, a biomarker for viable cells, isolated from size-fractionated particles

170 Floating "spheres" of viable cells, known to contain an abundance of normal SC

171 For viable cells, larger pores resealed more quickly than sm

172 an increase in keratin 19 expression in all viable cell layers.

173 a plasma membrane-bound receptor present in viable cells, leading to a conformational rearrangement

174 Furthermore, ISG15 was released from viable cell lines of monocyte, T lymphocyte, B lymphocyt

175 transformants of the U1 and U2 loci produced viable cell lines.

176 dpoint was telomerase enzymatic activity per viable cell, measured at baseline and after 3 months.

177 by mass spectrometry that in comparison with viable cells, membranes of cells undergoing apoptosis co

178 DEP can discriminate between viable and non-viable cells minimizes the number of false positives com

179 erial replication to occur, the phagocytosed viable cells must be grown to a low cell density and the

180 (3)H-FDG remains a generally valid marker of viable cell number after cancer chemotherapy.

181 the relationship between (3)H-FDG uptake and viable cell number can become disjointed, with transient

182 When values were normalized for viable cell number in three clones of each type, there w

183 reatment for 48 and 72 h caused decreases in viable cell number of 70% and 65%, respectively.

184 ensions (40% partial pressure) decreased the viable cell number of the mutant further, and the mutant

185 th; however, GDNF dose-dependently increased viable cell number under serum-free culture conditions.

186 ffect of individual or combined compounds on viable cell number was also evaluated using the Trypan b

187 se II inhibitor) was synergistic in reducing viable cell number, and was associated with a reduction

188 rabead DO concentration (AIDO) and the total viable cell number, as well as between AIDO and the radi

189 l in vivo homeostatic mechanisms controlling viable cell number, but these constraints could be overr

190 ve promoter, light output in part depends on viable cell number, so that changes in bioluminescence i

191 of doxorubicin was investigated by counting viable cell number.

192 compounds provided the strongest decrease in viable cell number.

193 uptake experiments and determination of the viable cell number.

194 isolation of cells (4-6 h), determination of viable cell numbers (approximately 30 min) and growth in

195 nonreplicating cells, causing a reduction in viable cell numbers below the detection limit after 24 h

196 inhibitors resulted in a marked reduction of viable cell numbers in medulloblastoma cell lines and pr

197 e combinations resulted in a net increase in viable cell numbers of 50% to 100% whereas total cell nu

198 The peak current increased at viable cell numbers ranging from 3 x 10(5) to 1.6 x 10(7

199 ylated poly(4-vinylpyridine), the numbers of viable cells of another Gram-positive bacterium, Staphyl

200 electrochemical responses of viable and non-viable cells of C. albicans and Saccharomyces cerevisiae

201 luorescence microscopy technique for imaging viable cells of Magnetospirillum magneticum strain AMB-1

202 ion across the stratum corneum (SC) and into viable cells of skin.

203 onductance as well as sorting nonviable from viable cells of the budding yeast Saccharomyces cerevisi

204 are highly unlikely, therefore, to reach the viable cells of the epidermis or beyond.

205 competent, particularly since the number of viable cells of the suppressed strain increased during t

206 apsular bags contained a large population of viable cells on the capsular surfaces.

207 Removal of apoptotic cells by neighboring viable cells or professional phagocytes is essential for

208 Viable cells or purified LPS from an msbB mutant had a 1

209 confirms the selectivity of deoxyglucose for viable cells over necrotic regions and for hypoxic cells

210 he protease substrate reagents do not damage viable cells over the course of the assay, thus the meth

211 0 can be localized to the plasma membrane of viable cells, particularly antigen-presenting cells, pro

212 formation of l-sorbose-utilizing mutants per viable cell per day ranged from 10(-6) at the initial ti

213 structure and cell viability (percentage of viable cells per microsphere) were correlated with micro

214 s from mouth (buccal) epithelium may contain viable cells, permitting assay of gene expression for di

215 ayed resistance to killing by chlorine, with viable cells persisting for >30 min in 2 mg/L free chlor

216 the CD4+CD127(lo/-)CD25+ T-cells represent a viable cell population for cellular therapy in this auto

217 The ability to isolate specific, viable cell populations from mixed ensembles with minima

218 completion of cytokinesis and generation of viable cell progeny.

219 Upon cell death, the viable cell protease marker becomes inactive.

220 lum levels for 7 days after application, and viable cell quantities determined by PMA real-time PCR w

221 rvival during ATP depletion was indicated by viable cells recovered 24 hours later.

222 Viable cells recovered from excised grafts were seeded a

223 C with 5H7 mAb induced a marked reduction in viable cell recovery (VCR) of T cells (<10% VCR), NK cel

224 PCD was assessed by viable cell recovery (VCR) with trypan blue, ethidium br

225 e cell population in hyperoxia (doubling the viable cells), reduced the percentage that were activate

226 Viable cells remained in the coil lumen.

227 h of glutamate exposure, respiration of the viable cells remained near basal and protonophore stimul

228 s and to discriminate between viable and non-viable cells, respectively.

229 this study can be used to enrich and detect viable cells simultaneously within 24h.

230 We used multiparameter flow cytometry and viable cell sorts from phenotypically defined CD8(+) T-c

231 similar to those of hBMSCs; hence, they were viable cell sources for bone engineering.

232 Extensions include the tracking of multiple viable cell species populations through a continuum diff

233 TRG better than the percentage of viable cells stratified patient prognosis: 5-year surviv

234 sing cells failed to stimulate engulfment of viable cells, suggesting that uPAR enhances recognition

235 ionarily conserved, and resident normally in viable cells (SUPER).

236 stress in such dense packing, extrusions of viable cells take place several days after seeding.

237 when added after LF has already entered the viable cell targets.

238 20-fold greater number of transformants per viable cell than that observed after 0.5 Gy x-irradiatio

239 (1) growth arrest and apoptosis with loss of viable cells that is accompanied by a marked decrease in

240 The 3DFC contains viable cells that secrete angiogenic growth factors and

241 on sulforhodamine B assays for the number of viable cells, the NQO1 clones showed increased sensitivi

242 eir progeny stopped dividing but remained as viable cells throughout 140 h of observation.

243 consisted of 2 submorphologies: spheres with viable cells throughout and spheres with an outer rim of

244 mally invasively deliver a large quantity of viable cells to a tissue of interest with high engraftme

245 elf-renewal as evidenced by the inability of viable cells to form secondary tumor spheres.

246 sphate by intracellular acid phosphatases in viable cells to produce p-nitrophenol.

247 dial infarction (MI) include the delivery of viable cells to replace necrotic cardiomyocytes.

248 SC population using a process that maximizes viable cell transplantation.

249 For nonfixed, viable cells, tumor cell recovery ranged from 72.5% to 9

250 ustering can only be quantified by gating on viable cells under physiological conditions.

251 ted mutagenesis, and 14C-labeling studies in viable cells unequivocally demonstrate that these compou

252 ession of multiple genes in fixed as well as viable cells using molecular beacon imaging technology.

253 thelial cells were determined by quantifying viable cells using the MTT assay.

254 Intracellular delivery of molecules into viable cells was also achieved with high efficiency.

255 esence of CH11, p24 production per number of viable cells was decreased as compared with the same PBM

256 The fraction of viable cells was determined using 3-(4,5-dimethylthiazol

257 The number of viable cells was evaluated by ATP measurements.

258 ls in culture, while VEGF release (pg/10,000 viable cells) was significantly reduced.

259 In viable cells, we found BAK complexed with mitochondrial

260 concomitant (123)I-MIBG scans, 4 tumors with viable cells were (123)I-MIBG-negative but were successf

261 urprisingly, large and stable populations of viable cells were also recovered from the cecum and larg

262 Only viable cells were capable of inducing these characterist

263 tion, and after 20h of ultrasonic treatment, viable cells were hardly found.

264 Viable cells were labeled with calcein acetoxymethyl, vi

265 3DFCs with or without viable cells were sized to the damaged area, implanted i

266 d from the encapsulated drug, the numbers of viable cells were still significantly smaller for the en

267 FNA samples yielded greater numbers of viable cells when compared to core needle biopsies.

268 nM dexamethasone (Dex), with 10-20-fold more viable cells when compared to the parental CEM-C7-14 clo

269 of EtOH-H2O showed significant reduction of viable cells when EtOH-H2O concentration exceeded 25% (P

270 und 5 produced a reduction in the numbers of viable cells when incubated in the presence of bleomycin

271 aced by a dense peripheral ring of primarily viable cells, whereas inner cells are mostly necrotic.

272 er, yet hypoxic zones in solid tumors harbor viable cells which are particularly resistant to treatme

273 es unique capabilities to study functions of viable cells, which are beyond the capabilities of other

274 duced a dose- and time-dependent decrease in viable cells, which was not blocked by the soluble guany

275 length and telomerase enzymatic activity per viable cell with those at baseline, and assessed their r

276 Deletion of both yeast genes results in a viable cell with undetectable esterified sterol.

277 Deletion of both genes resulted in a viable cell with undetectable esterified sterol.

278 ransducer enables the selective detection of viable cells with a limit of detection of 3 x 10(2) cfu/

279 Eighteen hours after implantation, viable cells with depolarized mitochondria in quarter-si

280 were removed after 6 months, they contained viable cells with minimal cell loss and gave CNTF output

281 cal system capable of specifically detecting viable cells with the simple sample preparation and dete

282 mal epithelial surface is composed mainly of viable cells, with nonviable cells making up a small per

283 normal epithelial surface consists mainly of viable cells, with only a small percentage of nonviable

284 Entrapment of viable cells within hydrogels, followed by lysis, could

285 lm viability and the spatial distribution of viable cells within the biofilm.

286 tion of DPH1, DPH2, DPH4, and DPH5 generated viable cells without diphthamide.