ライフサイエンスコーパス: cell density

1 and/or cell proliferation in regions of high cell density.

2 ence of the total killing rate on the target cell density.

3 No differences were found in endothelial cell density.

4 lved the use of ex vivo transduction at high cell density.

5 growth phase, and increase in frequency with cell density.

6 horizontal MGE spread by lowering the local cell density.

7 motes clonal growth in vitro but not at high cell density.

8 f matrix porosity was found to increase with cell density.

9 including secreted protease SpeB during high cell density.

10 more effective in decreasing viable biofilm cell density.

11 ion with a duration dependent on the initial cell density.

12 xpands at a constant rate independent of the cell density.

13 and an approach to account for variations in cell density.

14 ells die exponentially--is true only at high cell density.

15 l not well understood, in particular at high cell density.

16 l resistance factor, P2 area, or endothelial cell density.

17 othelial venules surrounded by high CD8(+) T-cell density.

18 he perseverance is inversely proportional to cell density.

19 ternalization in tumors of various sizes and cell density.

20 g to an age-dependent decline in endothelial cell density.

21 colour at 420 nm is directly proportional to cell density.

22 of gene expression in response to changes in cell density.

23 l equivalent, visual acuity, and endothelial cell density.

24 and that the sickled fraction increased with cell density.

25 d CrvA-dependent curvature increases at high cell density.

26 % [IQR 46.94-84.73]) reduction in the tumour cell density.

27 easured by assessment of reduction of tumour-cell density.

28 y mass and thus corresponds to a decrease in cell density.

29 at this front becomes unstable to changes in cell density.

30 hotosynthetic capacity or increase mesophyll cell density.

31 nd to promote CRISPR adaptation, all at high cell density.

32 ity than the control (grown at 42 degrees C) cell density.

33 es, on different substrates independently of cell density.

34 RNA biogenesis in BmN4 cells is regulated by cell density.

35 apsulated cells depends on gel stiffness and cell density.

36 different subcellular sites with increasing cell density.

37 ased to numbers comparable to the inoculated cell density.

38 is requires secondary signals and particular cell densities.

39 ve phenotypes are only beneficial at certain cell densities.

40 e killing saturates at higher CTL and target cell densities.

41 larger tracks (50-400 mum in width) at high cell densities.

42 d this acts to inhibit proliferation at high cell densities.

43 vity and promotes cell wall function at high cell densities.

44 thogens use QS to initiate infection at high cell densities.

45 d stationary phase was obtained with similar cell densities.

46 increasing function of the density at small cell densities.

47 PRP increased cartilage surface cell density 1.5-fold (P < 0.05), confirmed by bromodeox

48 ing Dehalococcoides were boosted to a higher cell density (1.2 x 10(8) to 1.3 x 10(8) cells per mL on

49 tral corneal thickness (CCT) and endothelial cell density 12 months postoperatively; and intraoperati

50 rences were identified in corneal Langerhans cell density (19.84 cells/mm2 for the controls vs 41.43

51 a more pronounced rate of change in ganglion cell density across the retina generally showed a higher

52 Here, we report a mechanism by which cell density activates the Hippo pathway, which in turn

53 hite and redox mediator, and the inoculation cell density all affect the characteristics of microbial

54 of Yap is tightly associated with different cell densities along the blastema proximal-distal axis,

55 etastatic cells in vivo, which achieves high cell densities and reduces the tumour burden within soli

56 hosphates IP7 and IP8, reach abnormally high cell densities and show decreased extracellular polyphos

57 Various tumor-cell densities and spatial cell distributions seen on hi

58 to initiate cell-cell signaling at moderate cell densities and to prime the LuxI/LuxR signaling syst

59 erived medium, Z. mobilis achieved a similar cell density and a slightly higher ethanol yield when su

60 on can be attributed to differences in local cell density and cell cycle.

61 een tissue growth and curvature, the role of cell density and cell vigor remains poorly understood.

62 creases, resulting in a decrease in the unit-cell density and concomitant disordering of the charge-t

63 l communication that bacteria use to monitor cell density and coordinate cooperative behaviors.

64 cal tension, conferred by a balancing act of cell density and cytoskeleton activity.

65 which is coincident with a region of higher cell density and E-cadherin expression.

66 al resolution based on peak retinal ganglion cell density and eye size ( approximately 6-12 mm in axi

67 Cell density and Hippo signaling have also been reported

68 gives rise to a linear relationship between cell density and intercellular tensile stress and forces

69 al quantitative imaging biomarker for tumour cell density and is widely used to detect early treatmen

70 en on multiple individuals and describes the cell density and its migration direction at every point

71 Tumor cell density and microvessel density correlated signific

72 erved tear secretion and conjunctival goblet cell density and mitigated inflammation and scarring of

73 Endothelial cell density and morphologic variables of both eyes of a

74 Changes in superficial epithelial cell density and morphology correlated strongly with cor

75 In this study we compare corneal endothelial cell density and morphometry measurements from two widel

76 This coincided with reduced cell density and myofibroblast formation.

77 in the tumor core during conditions of high cell density and oxygen deprivation by increasing glutat

78 ls a previously uncharacterized link between cell density and piRNA biogenesis, designates cell densi

79 t increase in apoptosis, with a reduction in cell density and proliferation in the outflow veins trea

80 quantify tissue-specific parameters such as cell density and proliferation.

81 etermine the association between endothelial cell density and suitability for transplantation in corn

82 etermine the association between endothelial cell density and suitability for transplantation in corn

83 rrent smokers, Schirmer I test value, goblet cell density and tear MUC5AC concentration were signific

84 moking might decrease tear secretion, goblet cell density and tear MUC5AC concentration.

85 d as scalar to compensate for differences in cell density and tissue thickness and the Pt/P ratios to

86 ion process called quorum sensing to monitor cell density and to alter behavior in response to fluctu

87 de [SpeB-inducing peptide (SIP)] during high cell density and uses the secreted peptide for cell-to-c

88 r of outcomes such as tear clearance, goblet cells density and corneal epithelial integrity, suggesti

89 e were beneficial to fungal mycelium growth, cell densities, and sporulation, which enhanced the dise

90 dual shapes, sizes, chemical concentrations, cell density, and 3D spatial distribution of multiple co

91 rical equivalent, visual acuity, endothelial cell density, and complications were evaluated.

92 rom the environment, describe the effects of cell density, and evaluate potential environmental inhib

93 by a glycerol fed-batch phase that increases cell density, and finally an induction phase for product

94 cluding photoreceptor distribution, ganglion cell density, and organization of interneurons.

95 gions of dense extracellular matrix and high cell density, and overall heterogeneity.

96 trated by increase in cell size, decrease in cell density, and squamous metaplasia.

97 rette smoking affects tear secretion, goblet cell density, and tear MUC5AC concentration.

98 re, glare, contrast sensitivity, endothelial cell density, anterior chamber depth, anterior chamber a

99 temporal area with maximum retinal ganglion cell density ( approximately 5,000-7,000 cells/mm(2) ) t

100 in humans, even small changes in endothelial cell density are relevant.

101 Importantly, Yap inactivation occurs in high cell density areas, conditional to F-actin distribution

102 e a generic mechanism for the instability in cell density around the defects that arises from the int

103 ell density and piRNA biogenesis, designates cell density as a critical variable in piRNA studies usi

104 cell system, and suggests the alteration of cell density as a useful tool to monitor piRNA biogenesi

105 Our findings show that increasing cell density, as might be seen in cancer, transforms gro

106 Conversely, diminishing cell density, as might occur at a wound front, leads to

107 cell morphology, molecular content and local cell density at single-cell resolution.

108 s 492+/-62.10 mum; postoperative endothelial cell density averaged 2026+/-397cells/mm(2) with a mean

109 quorum-sensing system is sufficient to probe cell density, bacteria frequently use multiple quorum-se

110 To measure their cell density, bacterial populations produce and detect d

111 Here we show that modulating the bulk cell density (BCD: cell number per culture volume) deter

112 ie, preculturing PBMCs for 2 days at a high cell density before initiation of antigenic stimulation)

113 rve fiber tortuosity, and corneal Langerhans cell density between healthy controls and patients with

114 e (a region lacking cells or with much lower cell density) between antagonist strains swarming toward

115 ngly associated with the formation of a high-cell density biofilm onto the polymer surfaces.

116 corneal tomography measurements, endothelial cell density, biomicroscopy, refraction, and intraoperat

117 thinning and a reduction in basal epithelial cell density, both previously have been documented in hu

118 egulated approximately 20-fold by increasing cell density but is up-regulated approximately 50-fold b

119 cell proliferation and increased epithelial cell density, but decreased epithelial cell size.

120 at the expansion rate increases with initial cell density, but the biophysical mechanisms involved re

121 decreased A. baumannii and S. aureus biofilm cell densities by (3.92 +/- 0.15) log and (2.31 +/- 0.12

122 sed anti-inflammatory mediators, increased T cell densities, caused mitochondrial dysfunction, altere

123 stically different change in the endothelial cell density (cells/mm(2)) at the end of the follow-up p

124 quantify the velocity field and the evolving cell density; cells not only concentrate at +1/2 defects

125 correlated positively (r=0.78, p<0.001) with cell density (cellsmm(-2)) which was higher in heterogra

126 With increasing bacterial cell densities, Cfree of solvent-spiked PAHs decreased w

127 P = 0.84), and the postoperative endothelial cell density changes were -3+/-10% (P = 0.07) and -10+/-

128 acteria alter gene expression in response to cell density changes.

129 A feedback between cell density, CIL, and cell-cell adhesion gives rise to

130 environments, focusing on mitotic activity, cell density, collagen content, osteogenic protein expre

131 he previous theoretical maximum using a high cell density continuous fermentation process.

132 Moreover, high dendritic cell density correlated with greater T cell proliferatio

133 cells (LSCs) are affected globally and basal cell density could be used as a parameter to measure LSC

134 on devices promote ischemia due to high beta cell densities creating prohibitively large diffusional

135 Using this low cell density culture model and HA as a control, we teste

136 There was a trend of basal cell density decline in more advanced stages of LSCD.

137 The basal cell density declined in the unaffected regions at a sim

138 Endothelial cell density decreased to a mean (SD) of 952 (366) and 7

139 bsequent vision loss ensues when endothelial cell density decreases below a critical threshold.

140 Expression was unrelated to cell density, depended on the secreted product's element

141 d monocyte osteoclastic differentiation in a cell-density dependent manner, with proliferating p38alp

142 We found that bacterial cell density-dependent gene expression termed "quorum se

143 ull mutant in S. venezuelae The mutant had a cell density-dependent growth phenotype and accumulated

144 Sporulation by Bacillus subtilis is a cell density-dependent response to nutrient deprivation.

145 ATF4 depletion decreases both cell-density-dependent transcription and adipocyte diffe

146 cardiac cells with varied 3D geometries and cell densities developed towards the goal of scale-up fo

147 and taken back up into the cells, mediating cell density-driven regulation.

148 ses with not only the stimulus, but also the cell density due to increased communication.

149 atypical process is essential to regulate CR cell density during growth, which in turn ensures the co

150 as well as the mechanisms regulating leader cell density during the migration process remain to be d

151 d RNCs are produced at high yield using high-cell-density E. coli growth conditions.

152 evaluate the long-term change in endothelial cell density (ECD) after the implantation of 2 types of

153 central corneal thickness (CCT), endothelial cell density (ECD) and complication rates.

154 Lower endothelial cell density (ECD) and higher corneal thickness (CT) at

155 lation time affect corneal donor endothelial cell density (ECD) and transplant suitability.

156 Endothelial cell density (ECD) at 3 years determined by a central im

157 t of donor-related parameters on endothelial cell density (ECD) decline and detachment rate in this g

158 examination revealed a decreased endothelial cell density (ECD) in patient 2, but no signs of corneal

159 croscope examination revealed an endothelial cell density (ECD) of 1532/mm(2) in patient 1 and 1620/m

160 ected visual acuity (BSCVA), and endothelial cell density (ECD) prior to DMEK and at 1, 3, 6, 12, and

161 nority of studies that evaluated endothelial cell density (ECD) reported an MMC-related decrease in E

162 nderwent trabeculectomy, corneal endothelial cell density (ECD) significantly decreased by 3.5% (P =

163 stablish a normative database of endothelial cell density (ECD) using in vivo specular microscopy in

164 -corrected visual acuity (BCVA), endothelial cell density (ECD), and complications.

165 central corneal thickness (CCT), endothelial cell density (ECD), and need for regraft.

166 corrected visual acuity (BSCVA), endothelial cell density (ECD), central corneal thickness (CCT) at 6

167 d distance visual acuity (CDVA), endothelial cell density (ECD), central corneal thickness (CCT), and

168 -corrected visual acuity (BCVA), endothelial cell density (ECD), central corneal thickness (CCT), gra

169 Endothelial cell density (ECD), hexagonal cell ratio (HEX) and coeff

170 -corrected visual acuity (BCVA), endothelial cell density (ECD), pachymetry, and intraoperative and p

171 ual acuity (BCVA), densitometry, endothelial cell density (ECD), pachymetry, and intraoperative and p

172 anation tonometer (GAT-IOP), and endothelial cell density (ECD), recorded at baseline and months 1, 3

173 thickness (CCT, micrometers) and endothelial cell density (ECD).

174 rected visual acuity (BSCVA) and endothelial cell density (ECD).

175 equivalent (MRSE), keratometry, endothelial cell density (ECD).

176 BSCVA), manifest refraction, and endothelial cell density (ECD).

177 In biopsy samples with high dendritic cell density, electron microscopy showed direct physical

178 Corneal endothelial cell density, endothelial cell viability, and epithelial

179 Endothelial cell density, endothelial failure, and endothelial survi

180 on-diffusion model describing the effects of cell density, EPS deposition and nutrient exposure on th

181 The rod bipolar cell density fell from 8,640 cells/mm(2) at 1 mm to 4,27

182 of sprouting activity (e.g., endothelial tip cell density, filopodia number) can be obtained.

183 Pseudomonas syringae pv. syringae cell densities fluctuate regularly during host plant col

184 abundance of a monitor protein and the local cell density for biologically relevant models of quorum

185 he retina (i.e., changes in retinal ganglion cell density from the retinal periphery to the center of

186 In contrast to stabilization at most cell densities, growth-independent fermentation inhibite

187 cell culture model to mimic PVR by defining cell density, growth factors, and cultivation time.

188 he Hippo pathway effector YAP in response to cell density human epithelial cells.

189 e ratio of intratumoral versus peritumoral T-cell densities (I/P ratio).

190 cell-cell interactions, indicating that low cell densities in vitro could be useful to help mitigate

191 Basal cell density in all locations was measured by 2 independ

192 highlight the prognostic value of dendritic cell density in allograft biopsy samples, suggest a new

193 Basal cell density in both central cornea and limbus decreases

194 hybridization, we detected higher Pax3 mRNA+ cell density in both young and aged satellite cell-deple

195 observe a significant increase in apoptotic cell density in Foxg1(-/-);Wnt8b(-/-) double mutants com

196 0.01), corresponding to areas with increased cell density in MRI (ADCmin, 0.89 vs. 1.59 x 10(-3) mm(2

197 er light scattering technology that measures cell density in real time.

198 Cell density in the area under each IOL was significantl

199 observations in a spreading MDCK colony, the cell density in the center increases as cells divide and

200 5AC concentration in tears depends on goblet cell density in the conjunctiva among office workers.

201 In the LSCD group, the mean basal cell density in the cornea decreased 31.0% (6389 +/- 182

202 The average VIP-tdTomato fluorescent cell density in the INL and GCL was 535 and 24 cells/mm(

203 In addition, we investigated the role of cell density in the kinetics of cell sickling.

204 easure leaf function, we show that increased cell density in the mesophyll of Arabidopsis can be used

205 ERMAL PATTERNING FACTOR (EPF) family altered cell density in the mesophyll.

206 for virulence gene expression when bacterial cell densities increase.

207 As cell density increased, the abundance of Piwi proteins a

208 lar polyphosphate concentrations increase as cell density increases, and if the concentration of poly

209 ial populations coordinate their behavior as cell density increases, using quorum sensing (QS) signal

210 cells were identical to the expected initial cell density, indicating that the reduction in CFU numbe

211 ated by increased HER2 expression and tumour-cell density involving microRNA-mediated progesterone re

212 The maximum ganglion cell density is 61,900/ mm(2) , comparable to Falconifor

213 Measurement of corneal endothelial cell density is important both for clinical diagnosis as

214 specific inhibition of TGF-beta signaling by cell density is restricted to polarized epithelial cells

215 rol, how it senses and responds to increased cell density is still unclear.

216 We found that CR cell density is sustained by an activity-dependent impor

217 ntal data, both at the cell cycle and viable cell density levels, was observed.

218 Median 5-year percent endothelial cell density loss was significantly greater in PK compar

219 Intratumoral immune cell densities (mDCs, CD8(+) T cells, neutrophils, macro

220 hether different instruments for endothelial cell density measurements give the same results and can

221 iments confirm this prediction, showing that cell density modulates the collective sensory response.

222 urnover of nitric oxide (NO) and N2 O at low cell densities of Nitrosomonas europaea (AOB) and Nitros

223 Cell densities of strain 83-1 with alginate as sole carb

224 Both the low animal cell density of bioreactors and their ability to post-tr

225 the limit of detection was at an approximate cell density of five cells per microliter (P < .01).

226 apsulated droplets (~78%), regardless of the cell density of input sample solutions.

227 A consequent increase in cell density of suprabasal layers results in a thicker t

228 layer V (CTIP2+) neurons, while the overall cell density of the cortex is unchanged.

229 The mean basal cell density of the normal group was 9264 +/- 598 cells/

230 Biofilms showed reproducible cell density on pegs of the biofilm device.

231 sensing causes the cell size decrease as the cell density on surfaces increases.

232 that allows for re-establishment of optimal cell density or sealing of the wound.

233 Rebubbling rates and endothelial cell density over a 3-month follow-up period analyzed by

234 The endothelial cell density (P = .053) and the change in spherical equi

235 el was constructed to determine the critical cell density parameter to maximize oxygen production, an

236 dhesive round-bottom microwells is the input cell density per microwell.

237 community-level defense requirements in high cell density populations and host fitness costs of basal

238 Bacteria commonly exist in high cell density populations, making them prone to viral pre

239 both effector and initiator caspases in high cell density, postconfluent CD44 knock-out (CD44KO), and

240 of FAK or Src in MCF-10A cells plated at low cell density prevented the activation of Yes-associated

241 posons decreased, suggesting that increasing cell density promotes piRNA biogenesis pathway and that

242 q) of wild-type V. cholerae and a locked low-cell-density QS-mutant strain identified 7,240 transcrip

243 significant negative correlation with goblet cell density (r = -0.174, P = 0.036) and tear MUC5AC con

244 ositive correlation with conjunctival goblet cell density (r = 0.181, P = 0.03).

245 95% CI, 0.26-0.78; P < .001) and with CD8+ T-cell density (r = 0.35; 95% CI, 0.11-0.59; P = .03).

246 The amacrine cell density ranged from 30,000 cells/mm(2) at 8 deg to

247 icrobial cell ratio decreases with microbial cell density, rather than remaining fixed.

248 tes, Golgb1 mutant embryos exhibit increased cell density, reduced hyaluronan accumulation and impair

249 reporters for competence, we found that the cell density required for differentiation was 100-fold h

250 ore, using mouse genetics, we showed that CR cell density severely affects the architecture of layer

251 enes are expressed under the control of both cell density signals via the Phr peptide system and nutr

252 cer cells revealed that given a fixed global cell density, significant differences in growth, prolife

253 Characterization of the high cell density-specific cell-free growth medium demonstrat

254 20/25 or better and the average endothelial cell density (+/-standard deviation) was 2363.8+/-82.7 c

255 ficantly higher OSDI score, basal epithelial cells density, stromal reflectivity and sub-basal nerve

256 ficantly higher OSDI score, basal epithelial cells density, stromal reflectivity, sub-basal nerves to

257 Cell density studies were performed on human embryonic k

258 ation and expression levels are sensitive to cell density, suggesting that it may crosstalk with Hipp

259 Main Outcomes and Measures: Endothelial cell density, suitability for transplantation based on t

260 Endothelial cell density, suitability for transplantation based on t

261 At high cell density the opposite occurs: LuxO is inactive, and

262 At high cell density, the Hippo pathway inhibits DNA damage-indu

263 ould not be attributed to differences in the cell density, the planktonic inoculum concentration or t

264 In Vibrio species, at low cell density, the sigma 54-dependent response regulator

265 dilution effect is strongest at high target cell densities; this can result in a peak in the depende

266 ng, analysis of bacterial cultures with high cell density (thousands of cells per frame) and complete

267 o measure spatially dependent differences in cell density, tissue organization, perfusion, and metabo

268 Here we focus on cell density to determine its role in collective migrati

269 which is amplified by cell proliferation and cell density, to directly promote cell migration.

270 ere removed and cell counting, viability and cell density under and outside the IOLs were evaluated.

271 Cell density under the single-piece IOL was not signific

272 +/- 0.12) log reduction in S. aureus biofilm cell densities upon 10 mM and 30 mM maltodextrin additio

273 topographic distribution of retinal ganglion cell density using stereology and retinal wholemounts.

274 onger ventilation led to reduced endothelial cell density: ventilation time >7 days (-46.5 cells/mm(2

275 crochannel resonator (SMR) to measure single-cell density, volume, and passage time through a narrow

276 Retinal ganglion cell density was 33% lower in glaucoma patients than in

277 nhibited mutualistic growth when the E. coli cell density was adequately high relative to that of R.

278 High dendritic cell density was associated with poor allograft survival

279 -linked immunoassay, and conjunctival goblet cell density was counted after Periodic-acid Schiff stai

280 Retinal ganglion cell density was estimated at the same test locations fr

281 up (P = 0.012), and no change in endothelial cell density was found (P = 0.355).

282 ion rate from pyruvate to CO2 normalized for cell density was found to increase by a factor of 12 due

283 Intratumoral CD8(+) T-cell density was high in smokers (P = 0.02) and TP53-mut

284 While the PYY cell density was increased in IBS-C relative to controls

285 Endothelial cell density was measureable in 6 cooperative children (

286 Endothelial cell density was measured with specular microscopy, and

287 Dendritic cell density was significantly higher in the DED group t

288 Goblet cell density was significantly lower in ABX treated grou

289 D. mccartyi cell densities were 10(13) and 10(12) 16S rRNA gene copi

290 Higher endothelial cell densities were found in eyes with FECD compared wit

291 kscatter, corneal thickness, and endothelial cell density were measured from confocal microscopy imag

292 ia to resolve up to two additional ranges of cell density when compared with bistable quorum-sensing

293 elial cell division occurs in regions of low cell density where cells are stretched.

294 a pronounced streak of high retinal ganglion cell density, whereas those favoring more enclosed micro

295 eous decrease in cell volume and increase in cell density, which occurs before autophagy initiation a

296 s behaviour, and we identify interactions of cell density with both cycle behaviour and Nanog.

297 Variation in dendritic field size and cell density with eccentricity was confirmed, and dendri

298 Higher parenchymatic cell density with higher content of alcohol insoluble re

299 uate the correlations of conjunctival goblet cell density with tear MUC5AC concentration and other oc

300 Smad1/5(dKO) thyroids had normal endothelial cell density yet impaired endothelial differentiation.