ライフサイエンスコーパス: cell density

1 ental noise (e.g. varying stain intensity or cell density).

2 s using Scheimpflug imaging; and endothelial cell density.

3 equivalent, hyperopic shift, and endothelial cell density.

4 creted autoinducers as a proxy for bacterial cell density.

5 I-2 pathway is activated only at much higher cell density.

6 rend level, but decreased D3KO PL area glial cell density.

7 a to compensate for reduced retinal ganglion cell density.

8 cuits, which regulate transcription based on cell density.

9 n, coupled with increased glial and neuronal cell density.

10 rotocol was necessary to increase CA1 engram cell density.

11 logarithmic growth phase and a higher final cell density.

12 air cells without affecting the overall hair cell density.

13 es, seeded in decreasing number and constant cell density.

14 hotosynthetic capacity or increase mesophyll cell density.

15 apsulated cells depends on gel stiffness and cell density.

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

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

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

19 n primary Merkel cell carcinoma beyond the T-cell density.

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

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

22 es, on different substrates independently of cell density.

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

24 different subcellular sites with increasing cell density.

25 ased to numbers comparable to the inoculated cell density.

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

27 tiffer and correlates with higher epithelial cell density.

28 tested MPM cell lines when cultured at high cell density.

29 r to maintain biomolecule concentrations and cell density.

30 icantly associated with increased microglial cell density.

31 lar senescence are accompanied by changes in cell density.

32 ntly associated with IOP or retinal ganglion cell density.

33 n be reversed by acute physical reduction of cell density.

34 kness did not correlate with the endothelial cell density.

35 ities, but remain poorly understood at lower cell densities.

36 like arrest of epithelial monolayers at high cell densities.

37 ars, with an increased lag phase, but higher cell densities.

38 quations model that describes time-dependent cell densities.

39 is requires secondary signals and particular cell densities.

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

41 d stationary phase was obtained with similar cell densities.

42 d by antral and duodenal eosinophil and mast cell densities.

43 increasing function of the density at small cell densities.

44 ve phenotypes are only beneficial at certain cell densities.

45 . cholerae quorum-sensing transition at high cell densities.

46 ar resolution to systematically quantify OTR cell densities.

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

48 ortion of Faecalibacterium and low microbial cell densities(1,2), and its prevalence varies from 13%

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

50 s (34%; P < 0.001), and increased epithelial cell density (13%; P < 0.001).

51 e phosphorylated paxillin levels and reduced cell density (16% to 28%; P < 0.05) at confluence.

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

53 om wound healing assays with varying initial cell densities [2].

54 bacteria sense and respond to the status of cell density(2).

55 ation of migration and proliferation at high cell density (6 x 10(6) cells/ml) near the GelMA surface

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

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

58 e-specific density, we know little about how cell density affects cell function, how it is controlled

59 For example, in humans variability in cell density among cells of a given cell type is 100 tim

60 system exhibits gelation-like arrest at low cell densities, analogous to the glass-like arrest of ep

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

62 soil by inoculating the soil with different cell densities and using a quorum-sensing-deficient muta

63 y-smaller tissues develop a local minimum of cell density and a tissue-spanning vortex.

64 slices were evaluated by immunostaining for cell density and astrogliosis.

65 tein, whose localization varies according to cell density and Ca(2+) in the media.

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

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

68 cal communication that bacteria use to track cell density and coordinate gene expression across a pop

69 We evidence changes in epithelial cell density and distribution in C57/BL6J mice during th

70 a jamming-like phase diagram based on local cell density and EGF.

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

72 ice treated with MSU-42011 exhibited reduced cell density and fewer actively proliferating cells comp

73 yield quantitative predictions for the onset cell density and frequency in terms of measured single-c

74 By adulthood, neocortical glial cell density and gene expression were decreased, while G

75 nduction correlates with changes in multiple cell density and growth regulatory pathways including hy

76 ng leads to short-term decreased endothelial cell density and hexagonality, while the rest of morphol

77 BE to EAC was associated with reduced goblet cell density and increased levels of Notch expression.

78 asing reduction rate constants normalized by cell density and initial U(VI).

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

80 We measured goblet cell density and levels of Notch messenger RNAs in BE ti

81 re was an inverse correlation between goblet cell density and levels of NOTCH3 and JAG2 messenger RNA

82 activation in single cells while controlling cell density and ligand expression level, we show that c

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

84 ubsequently examine the relationship between cell density and mosaic regularity across recombinant in

85 weapons is shaped by many factors, including cell density and nutrient abundance, and how strains are

86 ession, gene expression signatures, CD8(+) T cell density and others.

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

88 responders had higher pretreatment tumor CD8 cell density and programmed death ligand 1 expression, w

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

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

91 ling techniques is complicated by increasing cell density and rapid embryo rotation, which hampers au

92 Alveolar Type II progenitor cell density and self-renewal were maintained per unit t

93 The present study compared neural cell density and serotonergic innervation of the amygdal

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

95 een the topographic distribution of ganglion cell density and the nonuniform spatial integration acro

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

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

98 safety included adverse events, endothelial cell density and vision.

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

100 ucted neuronal morphologies with appropriate cell densities, and then we connect neurons together bas

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

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

103 nversion depended neither on colony size nor cell density, and MECs did not exhibit "memory" of prior

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

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

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

107 ed cells, but our data suggest that such Trm cell densities are relatively uncommon in infected tissu

108 ow CD8+ and CD4+ tissue-resident T cell (Trm cell) density are unknown.

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

110 17.5) and peak (26.2 vs. 22.9) duodenal mast cell densities as compared those without nausea.

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

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

113 ukin 2 production in a manner dependent on T cell density as confirmed by in vivo modulation of this

114 Endothelial cell density at 1 month postoperatively was similar betw

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

116 r biomass and metabolite accumulation at low cell densities before diverting key metabolic fluxes tow

117 The difference in cell density between calcified and decalcified cells can

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

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

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

121 In the descending colon, eosinophil and mast cell densities both correlated with depression scores.

122 haviors as well as arrested motility at high cell densities, but remain poorly understood at lower ce

123 verse events (TEAEs) and corneal endothelial cell density (CECD).

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

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

128 y when cells formed a compact monolayer with cell densities comparable to those observed in vivo.

129 significantly increasing conjunctival goblet cell density compared with a standard diet.

130 Further, they vary little in cell density compared with neuronal cell densities withi

131 iated with a significant reduction in goblet cell density comparing nondysplastic regions of tissues

132 xhibit rhythmic oscillatory behavior in high cell-density continuous cultures.

133 (BSCVA), topography, refraction, endothelial cell density, corneal thickness, haze, intraocular press

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 cell type, some of which are observed to be cell density dependent.

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

138 the reporter genes are strongly induced in a cell density-dependent and reporter-independent fashion.

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

140 ates expression of many virulence genes in a cell density-dependent manner by using an intricate quor

141 regulates expression of dozens of genes in a cell density-dependent manner.

142 lial adherens junction-associated genes in a cell density-dependent manner.

143 rdinate virulence and biofilm formation in a cell density-dependent manner; thus, AHL-interfering enz

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

145 an CDVA, manifest refraction and endothelial cell density did not change.

146 Endothelial cell density did not differ significantly 12 months afte

147 study revealed serotonergic innervation and cell density differences among closely related macaque s

148 We demonstrate that cell density drives contact patterns downstream of singl

149 the second day and at 3 months: endothelial cell density (ECD in cells/mm), corneal transparency and

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

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

152 nditions), intraocular pressure, endothelial cell density (ECD) and patient impairment.

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

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

155 Donor endothelial cell density (ECD) decline was evaluated for 351 eyes of

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

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

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

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

160 Endothelial cell density (ECD) was measured without any additional m

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

162 corrected visual acuity (BSCVA), endothelial cell density (ECD), and graft survival.

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

164 corrected visual acuity (BSCVA), endothelial cell density (ECD), central corneal thickness (CCT) at 3

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

166 central corneal thickness (CCT), endothelial cell density (ECD), coefficient of variation in cell siz

167 cluding changes from baseline in endothelial cell density (ECD), coefficient of variation, and percen

168 -corrected visual acuity (BCVA), endothelial cell density (ECD), postoperative complications, and gra

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

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

171 When the corneal endothelial cells density (ECD) drops, the HCEC may decompensate to

172 ed visual acuity [BCVA], central endothelial cell density [ECD], and central corneal thickness [CCT])

173 evels (0-325 mumol photons m(-2) s(-1)), and cell density factor (1.0-4.0).

174 distributed and viable biomass with ultralow cell densities (fewer than 2,000 cells per cm(3)).

175 in some patients, the [Formula: see text] T cell density first decreases when moving in from the bou

176 rinsic mechanisms to maintain an appropriate cell density for normal tissue morphogenesis and homeost

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

178 Goblet Cell Density (GCD) was measured in 71 current or former

179 The main outcomes were: goblet cell density (GCD), limbal dendritic cell density (LDCD)

180 The EDA wave spreads across a mesenchymal cell density gradient, triggering pattern formation by l

181 Reducing cell density gradually up to 50-fold, we studied changes

182 Activation of RpoS promotes high cell density growth under nutrient-limiting conditions.

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

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

185 ysiologic parameters such as oxygen tension, cell density, growth factors, and pharmacotherapy with a

186 h both high SDom and high CD3(+) or CD8(+) T-cell density had markedly improved disease-specific surv

187 synthetic methylotroph that grows to a high cell density has been challenging.

188 CMs to proliferate is density-dependent, and cell density has no effect on the outcome of proliferati

189 ulting tumors were characterized by enhanced cell density, higher proliferation rates, and increased

190 A), refractive astigmatism (RA), endothelial cell density, immunologic rejection, herpetic recurrence

191 ss is one of scalability: would scaling down cell density impact a network's ability to reproduce cor

192 n Allee effect in cancer cells seeded at low cell densities in a controlled in vitro setting.

193 novo biosynthesis of palmitate is reduced by cell density in an Nf2/Merlin-dependent manner.

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 BAR1 agonist, L3740, selectively increased L-cell density in mouse and human intestinal organoids and

197 0.01), corresponding to areas with increased cell density in MRI (ADCmin, 0.89 vs. 1.59 x 10(-3) mm(2

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

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

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

201 CT DSP-Zn-NP significantly reduced microglia cell density in the retina, a hallmark of EAU in rats.

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

203 al nuclear migration as the tissue grows and cell density increases, and these defects can be reverse

204 y of TEAD proteins, is actively regulated by cell density independent of Lats, the key kinase of the

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

206 In this report, we show that high cell density induces ABCA1 expression in glioblastoma ce

207 omponents that enable them to integrate host cell density information into the lysis-lysogeny decisio

208 tes that maintenance of a cell type-specific cell density is important for cell function.

209 as a model, we find that spermatogenic stem cell density is tightly regulated by the supply of fibro

210 m images with experimentally realistic SBRs, cell densities, labeling methods, and cell shapes.

211 goblet cell density (GCD), limbal dendritic cell density (LDCD), subbasal corneal nerve inhomogeneit

212 We observed moderate reduction in cell density (<10%) at low EF amplitudes (<4 V/cm) and a

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

214 tes through the timely transfer of increased cell density mediated by cell proliferation, which contr

215 eir environment; responses to alterations in cell density might then be coordinated via changes in ge

216 ses are often manifested as increased mucous cell density (mucous cell metaplasia) associated with mu

217 ea is associated with increased mucosal mast cell density, non-gastrointestinal somatic symptoms, and

218 ct of sex and experience with a tutor on the cell densities of GAD65- and parvalbumin-expressing cell

219 We propose, given the low host cell densities of hot spring environments, that the TSPV

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

221 able of growing microalgae with high spatial cell densities of up to 10(9) cells mL(-1).

222 ) Cultures grew over periods of 3 to 8 mo to cell densities of up to 2 to 9 x 10(6) cells per mL(-1)

223 pecifically, we test the hypothesis that the cell density of reward-related regions is associated wit

224 f new technologies to accurately measure the cell density of single cells in suspension and in tissue

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

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

227 le V. cholerae to assess the total bacterial cell density of the vicinal community.

228 litudes (<4 V/cm) and a greater reduction in cell density of up to 25% at higher amplitudes (4-6.5 V/

229 We track single cells as agents, cell density on a coarser scale, and growth factor diffu

230 how that the quantitative dependence of stem cell density on FGF dosage, the biased localization of s

231 cal perturbations to show a direct effect of cell density on mitotic nuclear positioning.

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

233 Utilizing RUSD, we can detect extremely low cell densities (optical density [OD] >= 5 x 10-7) that c

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

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

236 sition (P = 0.001), 110% greater TGFbeta1(+) cell density (P = 0(.)04), 1.7-fold increase in TGFbeta1

237 nts with low SDom and low CD3(+) or CD8(+) T-cell density (P = 0.002 and P = 0.03, respectively).

238 Optimal conditions including cell density, passage number, and culture time were exam

239 -corrected visual acuity (BCVA), endothelial cell density, postoperative complications, and retranspl

240 ng state, dependent on cumulative history of cell density, predicted by extrinsic noise in transcript

241 r growth to provide spatially resolved tumor cell density predictions.

242 shelf size and increased palatal mesenchyme cell density prior to the time of normal palatal shelf e

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

244 in are present before committing to the high-cell-density QS mode, but it is, in fact, the broadly ma

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

246 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).

247 Cell density regulates many aspects of cell properties a

248 in mice and in silico modelling, we identify cell density regulation by three-dimensional tissue boun

249 unohistochemistry, we found that bronchiolar cell density remained stable with aging, but inferred ra

250 Topographic variations of ganglion cell density reveal a temporal area, a horizontal streak

251 Combining SDom with CD3(+) or CD8(+) T-cell density revealed three distinct prognostic groups w

252 shown that drug release is commensurate with cell density, revealing more effective cell killing when

253 Cell density shows very little variation within a given

254 ymphocyte and lamina propria CD138(+) plasma cell densities simultaneously proved to be a meaningful

255 20/25 or better and the average endothelial cell density (+/-standard deviation) was 2363.8+/-82.7 c

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

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

258 Cell density studies were performed on human embryonic k

259 , but not central, FGF1 increased islet beta-cell density, suggesting that peripheral FGF1 may induce

260 Endothelial cell density, suitability for transplantation based on t

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

262 e study group manifested a lower endothelial cell density than that of the control and the contralate

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

264 st this hypothesis, we determined microglial cell densities (the inverse of cell size) using immunocy

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

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

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

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

269 downstream effectors, resulted in increased cell density to a level similar to that seen on matrices

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

271 At lower, more commonly observed Trm cell densities, Trm cells must initiate a rapidly diffus

272 e glycol diacrylate (PEGDA) hydrogel at high cell density using an emulsion process.

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

274 ology, we sought to measure how the ganglion cell density varies across the retina of the Nubian ibex

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

276 ation profiles, we modeled the dynamics of T cell density via partial differential equations.

277 The corneal endothelial cell density was 2400 cells/mm(2) in both eyes 3 years a

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

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

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

281 Cell density was found to be a prominent source of heter

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

283 In IBS patients, rectosigmoid mast cell density was higher in those reporting pain relief w

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

287 Cell densities were correlated with morphometric data fo

288 In Set 1, endothelial cell densities were determined.

289 However, the final cell densities were similar for all media tested, indica

290 At high cell densities, when autoinducers have accumulated, biof

291 At low cell densities, when QS autoinducers are absent, V. chol

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

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

294 ooperative behavior among tumor cells at low cell densities with relevance to early stage growth patt

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

296 on assume exponential growth kinetics at low cell densities, with deviations to account for observed

297 ittle in cell density compared with neuronal cell densities within the cerebral cortex, across brain

298 Confocal microscopy revealed differences in cell density within microcolonies between the EmaA posit

299 o infected WIS rats, was loss of trophoblast cell density within the junctional zone of the placenta

300 Under conditions of low cell density, YAP is nuclear and associates with enhance