ライフサイエンスコーパス: cell viability

1 nd (iii) the ND coatings selectively promote cell viability.

2 posure to collagenase digestion and preserve cell viability.

3 val for at least 7 d without any decrease in cell viability.

4 RF1, thereby protecting genome stability and cell viability.

5 nergy metabolism rewiring, protecting cancer cell viability.

6 necrosis is crucial for the determination of cell viability.

7 stain plasma membrane integrity, and prolong cell viability.

8 ranscription and secretion without affecting cell viability.

9 show that Rpn11-siRNA knockdown decreases MM cell viability.

10 tion dose-dependently but minimally affected cell viability.

11 nd outgrowth, without an immediate effect on cell viability.

12 ssembled nanofilms was assessed by measuring cell viability.

13 stress within 5.0 g/cm(2) did not influence cell viability.

14 aspases and RIPK3 did not completely restore cell viability.

15 nt cell retention device that also maintains cell viability.

16 act with the MTKI sunitinib to decrease GBM cell viability.

17 cell type to be resolved with no impact upon cell viability.

18 zaragozic acid reducing the impact of PLO on cell viability.

19 ly compromised protein synthesis and reduced cell viability.

20 occupancy, HIF-dependent gene expression and cell viability.

21 hibition improves mitochondrial function and cell viability.

22 ses that acts by regulating inflammation and cell viability.

23 e, we identify FOXO4 as a pivot in senescent cell viability.

24 to synergistic inhibition of human leukemia cell viability.

25 it correlates with enzymatically determined cell viability.

26 n-covalent insertion, while maintaining high cell viability.

27 tabolism and ER proteostasis that influences cell viability.

28 showed that induction of Cx50P59A decreased cell viability.

29 24 to reduce the Bcl-x(L)/(s) mRNA ratio and cell viability.

30 e C alpha expression, and ultimately reduced cell viability.

31 er due to the changes in ZO-1 expression nor cell viability.

32 whereas the presence of cholesterol rescued cell viability.

33 e transcription factor NFkappaB, and reduced cell viability.

34 ilization without significantly compromising cell viability.

35 glutathione depletion, resulting in loss of cell viability.

36 catastrophic effects on genome stability and cell viability.

37 cellular calcium mobilization or endothelial cell viability.

38 els in response to doxorubicin and protected cell viability.

39 hanced reversible sonoporation and preserved cell viability.

40 n TQ46 was added, the TQ416 had no effect on cell viability.

41 ion of the sequence has an adverse effect on cell viability.

42 VCP/p97 and proteasome inhibitions decrease cell viability.

43 containing eIF2alpha phosphatases to control cell viability.

44 t regions of the protein, thereby regulating cell viability.

45 -based cell sorting with molecular labels of cell viability.

46 in order to maintain optimal iron levels for cell viability.

47 ards dopamine as well as selectively promote cell viability.

48 verse the process of necroptosis and restore cell viability.

49 (2+) stores and their detrimental effects on cell viability.

50 sma membrane, but they all result in reduced cell viability.

51 tant biofilms on 3-D cells without affecting cell viability.

52 osis, altered cell morphology, and decreased cell viability.

53 ance of potassium homeostasis is crucial for cell viability.

54 SBB treatment does not significantly affect cell viability.

55 was responsible for the observed decrease in cell viability.

56 in depletion in the cell membrane and affect cell viability.

57 channeling into toxic structures threatening cell viability.

58 9 and Raw264.7 cells, substantially reducing cell viability.

59 of the CIA factors NUBP2 or FAM96A, reduced cell viability.

60 lowed by DTX treatment notably increased the cell viability ( 1.3 fold) markedly (p < 0.05) in 3D mod

61 novel Ca(2+) pre-coating step enhanced beta-cells viability (89 +/- 6%) and metabolic activity since

62 ption of the xCT antiporter greatly improves cell viability after glucose withdrawal, because conserv

63 This process was nondestructive with >95% cell viability after sampling, enabling long-term analys

64 characteristics of the hydrogel, as well as cell viability after treatment with the hydrogel contain

65 Knockdown of A3A or A3G could promote cell viability, along with the lower frequency of A/T in

66 (+31%) and bioprotective capacity (+25% for cell viability and +30% for LDH leakage) were observed i

67 gainst oxidative stress, with improvement in cell viability and a reduction of intracellular ROS.

68 with Grisu(R) alone caused an improvement of cell viability and a reduction of ROS production on epit

69 ed from FBCs-doped fuels shows a decrease in cell viability and alterations in the global gene expres

70 so implies that TRIM32 is a key regulator of cell viability and apoptosis in cardiomyocytes via simul

71 2+) signaling, hormone expression/secretion, cell viability and apoptosis) in pituitary adenomas (n =

72 a are intracellular organelles essential for cell viability and are characterized by the presence of

73 decipher the capacity of GATA2 in regulating cell viability and capillary formation.

74 ole of mcoln1 in embryonic development, hair cell viability and cellular maintenance.

75 novel role for calcium in supporting tumour cell viability and clarify the synthetic lethal interact

76 NLS induced a significant decrease in cell viability and clonogenic growth in a dose-dependent

77 25 mul of peripheral blood while maintaining cell viability and compatibility with downstream charact

78 As conventional methods to preserve cardiac cell viability and contractile function following ischem

79 g the injury of Triticum aestivum gliadin on cell viability and cytoskeleton reorganization.

80 ibition of tumour growth, circulating tumour cell viability and decreased metastasis.

81 umor cell motility and invasion, cancer stem cell viability and differentiation, resistance to anoiki

82 e expression of miR-210, along with promoted cell viability and differentiation.

83 Inhibition of PIM kinases decreases RS cell viability and disrupts signaling circuits that link

84 ntiviral-mediated ChR2 expression may affect cell viability and electrophysiological property of neon

85 Finally, reduced cell viability and elevated response to stressors is not

86 MEK inhibitors significantly inhibited both cell viability and ERK activation compared to treatment

87 was included to observe the preservation of cell viability and function.

88 TMEJ thus helps to sustain cell viability and genome stability by rescuing chromoso

89 ting further ethanol production were reduced cell viability and glucose uptake by D5A and not loss of

90 of miR-22 significantly suppresses leukaemic cell viability and growth in vitro, and substantially in

91 gatory nutritional process that impacts both cell viability and growth.

92 iple stress responses, reduced biosynthesis, cell viability and growth; and (6) ethanol-adapted E. co

93 drugs have additional effects that modulate cell viability and homeostasis.

94 DNA/RNA helicase that is essential for yeast cell viability and homologous to human senataxin, has be

95 Cell viability and IL-6/TNFalpha production were determi

96 As proof-of-principle, cell viability and immune responses after short-term exp

97 ion, including reductions in cell growth and cell viability and in the regulation of Akt downstream t

98 to KCNK9-expressing carcinoma cells reduces cell viability and increases cell death.

99 ATRA treatment specifically decreased cell viability and induced apoptosis of mutant IDH1 blas

100 levant concentrations of bupivacaine reduced cell viability and inhibited cellular proliferation and

101 n, resulting in suppression of neuroblastoma cell viability and inhibition of tumor growth associated

102 dithiothreitol (DTT), a reagent that reduces cell viability and interferes with further sputum analys

103 levated IL30 in supporting the breast cancer cell viability and invasive migration.

104 iomarkers for cellular health and integrity: cell viability and lactate dehydrogenase (LDH) leakage.

105 ndogenous levels of ARC is critical for beta-cell viability and maintenance of normal islet structure

106 ctive effects on beta-cells, preserving beta-cell viability and mass.

107 Both MTT and PrestoBlue assays showed higher cell viability and metabolism scores in fibroblasts trea

108 (TD-NMR) were respectively used to evaluate cell viability and microstructural changes during osmoti

109 hibitors initially block cell proliferation, cell viability and migration in some cancer cells are qu

110 d synaptic genes, mitochondrial function and cell viability and mitochondrial number in DDQ-treated a

111 lly prevented CB2 agonist-induced effects on cell viability and motility.

112 nd N-butyryl homoserine lactone (C4-HSL), on cell viability and mucus secretion in LS174T cells.

113 lipid biosynthesis is required for adipocyte cell viability and normal metabolic function and that re

114 ium phenylbutyrate, another HDACI, recovered cell viability and overall mitochondrial metabolism in m

115 ce that vIL-6 promotes latently infected PEL cell viability and proliferation and also viral producti

116 Silencing LZK reduced cell viability and proliferation of HNSCC cells with 3q

117 entiates the vorinostat inhibitory effect on cell viability and proliferation.

118 Nrf2 factor and restoration of the impaired cell viability and proliferation.

119 Increased cell viability and resistance to specific drug classes i

120 ntribute to cellular transformation, promote cell viability and resistance upon therapy, and have tum

121 tivity and the method was applied to monitor cell viability and screen susceptibility of metabolicall

122 s, we identify that BCL6 is required for GBM cell viability and that BCL6 overexpression is associate

123 alpha-Glucosidase inhibition activity, cell viability and thermal stability of Aglaonema extrac

124 impossible to perform due to disruptions in cell viability and tissue architecture from freeze-thaw

125 This exercise-mediated suppression of cell viability and tumor formation was completely blunte

126 g dominant active KRAS (mt) caused increased cell viability and tumor growth.

127 able formulations, maintaining high embedded cell viability and tunable cell behavior.

128 GMPS by RNA interference resulted in reduced cell viability and was sufficient to trigger cellular se

129 ne, TQ416) significantly affected recovering cells viability and mucin secretion.

130 Importantly, the receptor 1 showed excellent cells viability and was successfully applied for the det

131 al) and ten combination forms via hemolysis, cell viability, and AnnexinV-FITC/PI staining assays.

132 enced by decreased colony formation, reduced cell viability, and increased sub-G1 fractions.

133 Both TRES and RES inhibited cell viability, and induced apoptosis of pancreatic canc

134 d POL5551's effects on CXCR4 ligand binding, cell viability, and migration.

135 Both variables were able to affect cell viability, and the release of soluble molecules (fr

136 t accumulation of autophagosomes compromised cell viability, and this effect was alleviated by deplet

137 cantly inhibited cell proliferation, reduced cell viability, and was directly cytotoxic, whereas the

138 ted with supporting human mammary epithelial cell viability, and, moreover, preventing replication st

139 Cell cultures were tested for cell viability, apoptosis, alpha-smooth muscle actin (SM

140 cells were exposed to PgPE and assessed for cell viability, apoptosis, and proinflammatory gene expr

141 lly and in combination on the proliferation, cell viability, apoptosis, cell cycle distribution, and

142 eatment in PDL-CD105(+) cells did not affect cell viability, apoptosis, or osteogenic differentiation

143 al and highly regulated process required for cell viability, architecture, and division.

144 ne (NE) could directly inhibit breast cancer cell viability, as well as tumor growth in vivo EPI and

145 Biophysical characterizations and a cell viability assay revealed distinct effects of Lys an

146 ical density at 600nm (OD600) method and the cell viability assay were employed as standard reference

147 unctionality of our device, we carried out a cell viability assay with adherent and nonadherent cells

148 assay and no significant cytotoxicity in the cell viability assay, suggesting that it may be amenable

149 iazol-2-yl)-2,5-diphenyl-tetrazolium-bromide cell viability assay, the lactate dehydrogenase membrane

150 n of both compounds showed potent synergy in cell viability assays and cooperatively induced apoptosi

151 y, immunohistochemistry, immunofluorescence, cell viability assays and optical electrical mapping.

152 Cell viability assays confirm the low toxicity of A towa

153 performed limiting dilution, transwell, and cell viability assays to study the functional effects of

154 Cell viability assays were used to demonstrate the compl

155 Ralpha in-cell westerns, ERE-luciferase, and cell viability assays, with 2 (GDC-0810/ARN-810) used fo

156 Cell-viability assays indicated that the NHC-Au(I) -apta

157 AUC-ROC]=0.89) than traditional endpoints of cell viability (AUC-ROC for ATP=0.78; AUC-ROC for cell c

158 Mitochondrial DNA (mtDNA) is essential for cell viability because it encodes subunits of the respir

159 died for cytotoxicity and found to have high cell viability before and after surface modification.

160 Krtap5-5 depletion did not impact cell viability but reduced cell motility and extracellul

161 ar assembly, motility, bulk endocytosis, and cell viability but required for parasite virulence.

162 ow that the NreA protein is not required for cell viability but that loss of NreA (or replacement of

163 ons underpin the core reactions required for cell viability, but their contributions and relationship

164 ssing KRAS (mt) tumor cells caused increased cell viability by decreasing SMAD2 phosphorylation.

165 2-HSL but not C4-HSL significantly decreased cell viability by inducing mitochondrial dysfunction and

166 olin fragment enhances TRAIL-induced loss of cell viability by inhibiting phosphorylation of Akt and

167 signaling is essential for sustaining cancer cell viability by stimulating both mitochondrial biogene

168 The compounds likely enhanced cell viability by suppressing the formation of reactive

169 A549 cells via Crispr/Cas9 greatly promotes cell viability, colony formation, and invasion of cancer

170 /mL) significantly prevented the decrease in cell viability compared to control stress with H2O2 (5mM

171 ides a much faster, label-free assessment of cell viability compared with traditional approaches that

172 n of mcr-1 results in decreased growth rate, cell viability, competitive ability and significant degr

173 trol, we tested effects of HC-HA/PTX3 on the cell viability (cytotoxicity), proliferation (EGF + FGF-

174 Most importantly, cell viability data after camptothecin treatment showed

175 Our results showed that cell viability decreased with the increase of circulatin

176 Lung and immune cells viability decreased after 24 h of exposure only at

177 Pretreatment with oxytocin increased cell viability, decreased the cell damage against oxidat

178 nt critical to maintain genome integrity and cell viability, demonstrate SbcC-SbcD-ExoI acts before R

179 o mechanical loading had significantly lower cell viability, destruction of sarcomeres, smaller actio

180 logous gene in yeast (ppa2Delta) compromises cell viability due to the loss of mitochondria.

181 me measurement of RNA and DNA as proxies for cell viability during exposure to various noxious stimul

182 No significant effect was observed on the cell viability during the cell attachment to the surface

183 fold less potent than PLTX in reducing HaCaT cells viability (EC50 = 1.1 x 10(-9) M vs 1.8 x 10(-11)

184 lease interleukin-1 (IL-1) while maintaining cell viability, endowing these cells with potent aptitud

185 loped a mathematical model, parameterized by cell viability experiments under Nilotinib treatment and

186 patibility was demonstrated through in-vitro cell viability experiments, while acute in vivo characte

187 and studied the effects of these changes on cell viability, Fab yield and display on filamentous pha

188 lecule inhibitors resulted in an increase in cell viability, Figure 2B, which reported that RAF inhib

189 ion of differences in corticosteroid-treated cell viability following siRNA knockdown of 2 TFs and di

190 ric high-content imaging method, we evaluate cell viability, formation of reactive oxygen species, mi

191 ate and propionate failed to prevent loss of cell viability from glucose deprivation.

192 ion and efflux was similar with no effect on cell viability, function or proliferation under optimise

193 with DNA damage, apoptosis and inhibition of cell viability, glucose consumption, lactate production

194 ell retention, high IgG1 recovery (>99%) and cell viability (>97%).

195 for conducting 3D cell culture and analyzing cell viability has been developed towards a high through

196 liver cancer cells is sufficient to decrease cell viability; however, it is not known whether blockin

197 gf1R, suggesting adiponectin stimulates beta cell viability/hyperplasia in the context of PCOS.

198 ly target the viral genome without affecting cell viability.IMPORTANCE Smallpox was one of the most d

199 of fresh nerve tissue while maintaining high cell viability, improving yields and minimizing fibrobla

200 ntation is not sufficient to prevent loss of cell viability in a subset of glucose-deprived melanoma

201 (5hmC) modification, and effectively inhibit cell viability in AML with high expression of TET1 (i.e.

202 tion in autophagosome synthesis could affect cell viability in cell models expressing mutant huntingt

203 tin1 bias and reduced CB1 protein levels and cell viability in HD cells.

204 viral uptake, intracellular trafficking and cell viability in human endothelial cells of brain (hCME

205 g., cisplatin and radiation) decreased tumor cell viability in LKB1-deficient NSCLC cells.

206 To this end, a thorough characterization of cell viability in optical trapping environments was perf

207 monstrate biomedical applications and verify cell viability in our platform, whose multiplexing and i

208 sport, activation of signalling pathways and cell viability in relation to blood pressure regulation.

209 lly, we observed that Sirt2 deletion reduced cell viability in response to iron deficiency.

210 and that the absence of UBE2W does not alter cell viability in response to various stressors.

211 MicroRNA 26a (miR-26a) reduces cell viability in several cancers, indicating that miR-2

212 in individual cells was used as a measure of cell viability in the frozen state and this metric agree

213 pedance measurement in order to quantify the cell viability in the hydrogel.

214 A-MB-231 (hormone-insensitive) breast cancer cell viability in vitro by 11% to 19% and reduced tumori

215 quired to produce a comparative reduction in cell viability in vitro, when used in combination with g

216 inflammatory effects of LPS, and improve the cell viability in vitro.

217 dentified 36 compounds that inhibited cancer cell viability including 6 compounds that were previousl

218 We demonstrated that cell viability increased with an increase in fiber lengt

219 tration-dependently activated eNOS, improved cell viabilities, increased NO generations, and reduced

220 its SET domain, is critical for maintaining cell viability, indicating a novel catalytic-independent

221 phases of papaya ripening markedly decreased cell viability, induced necroptosis, and delayed culture

222 the ErbB3 receptor, significant reduction in cell viability, induction of apoptosis were observed whe

223 Additionally, cell viability is improved up to six fold on alloy fibre

224 CNTD2 overexpression increased lung cancer cell viability, Ki-67 intensity and clonogenicity and pr

225 miRNA-10b - a master regulator of metastatic cell viability - leads to elimination of distant metasta

226 bioprotective capacity was determined using cell viability, membrane integrity and nitric oxide (NO)

227 The results showed that SFN decreased HUVEC cell viability, migration and tube formation, all of whi

228 esults show how IL30 regulates breast cancer cell viability, migration, and gene expression to promot

229 duced NE differentiation, and opposed cancer cell viability, migration, invasion, and survival, point

230 and middle region of eL19 are essential for cell viability, most likely functioning in ribosome asse

231 e MIPs were not cytotoxic and did not affect cell viability; neither was the cells morphology affecte

232 g NCL-1 and NCD-38 significantly reduced the cell viability, neurosphere formation and induced apopto

233 intracellular potassium depletion or reduced cell viability occurred.

234 This subsequently yielded a cell viability of 82.90+/-0.78% against hydrogen peroxid

235 (EPS) composition, which in turn affects the cell viability of both biofilm and detached clusters.11

236 OX azide by showing significantly decreasing cell viability of breast cancer cells in a CL dose-depen

237 treated DCs with the PNVs, we found that the cell viability of DCs was unaffected, up to 200 mug/ml.

238 The cell viability of lactic acid bacteria and yeast was eva

239 d 5-FU/SDT treatment produced a reduction in cell viability of over 50% when tested against a panel o

240 injected with human K562 leukemia cells and cell viability of primary leukemia cells from human pati

241 the conjugates had no significant effect on cell viability of RAW 264.7 but conjugates 1 and 3 led t

242 ade solvents, and they effectively inhibited cell viability of the cancer cell lines investigated.

243 idues 1-70) in the presence of TRAIL impairs cell viability of TRAIL resistant transformed human hepa

244 Cell viability of two human hepatoma cell lines (Huh7 an

245 ogically relevant solvent, without affecting cell viability, opens the door to a wide range of biomed

246 MGO-treated collagen did not affect cell viability or apoptosis.

247 PgPE treatment (2 mug/mL) did not affect cell viability or survival but induced a significant inc

248 uman dental pulp, with no adverse effects on cell viability, or on their subsequent osteogenic capabi

249 onded with trypsinogen activation, decreased cell viability, organelle damage manifest by mitochondri

250 In this study, we examined effects of OA on cell viability, osteogenic differentiation in MSCs, and

251 issociation, 99% recovery of large clusters, cell viabilities over 87% and greater than five-log depl

252 O-nanostructures showed over 4-times greater cell viability over ZnO due to MZO releasing 4-times low

253 orous structure was stable and achieved high cell viability (over 90%).

254 ing of 15 fluorophore-conjugated Abs and one cell viability probe to immune cells isolated from synge

255 iability and productivity issues such as low cell viability, product retention, and an increased cont

256 Cell viability, proliferation and migration of ovarian c

257 e found that restoring MLK4 activity reduced cell viability, proliferation, and colony formation in v

258 e temperature was adjusted not to affect the cell viability/proliferation.

259 Mitochondrial membrane potential (DeltaPsi), cell viability, reactive oxygen species (ROS), and secre

260 ccinate, fumarate, and PBS have no effect on cell viability, regardless of cell lineage.

261 Cell viability results showed that MPM cells were highly

262 in static culture when evaluated in terms of cell viability, sarcomeric structure, action potentials

263 Inhibitors produced dose-dependent decreased cell viability similar to the combined administration of

264 ration (15% w/v) and stiffness enhanced OD21 cell viability, spreading and proliferation, as well as

265 Cell viability studies showed that some compounds specif

266 of release profiles and cellular-uptake and cell viability studies.

267 r neurites than control neurons, but similar cell viability, suggesting a causal link between pretang

268 uppressive effects of Akt2 deficiency on CRC cell viability, survival, migration and actin polymeriza

269 er or comparable to the minimum doses in the cell viability tests (0.1 mug/mL), at which acute cytoto

270 Cell viability tests confirmed the unevenness of the PEF

271 A variety of cell viability tests were performed after treatment with

272 ssed over time by studying the instantaneous cell viability, the colony-forming unit count, the conce

273 We demonstrate that LB100 decreases cell viability through caspase activation and G2/M cell-

274 othelial cells in terms of cell poration and cell viability to establish the imaging and therapeutic

275 1 or G2 lacking the signal peptide inhibited cell viability, triggered phosphorylation of stress-indu

276 enes are high-light induced and required for cell viability under excess light.

277 Extracellular Glu sustained cell viability under hypoglycemic conditions and increas

278 rocess in maintaining energy homeostasis and cell viability under starvation conditions, suggesting t

279 f stress responsive proteins, which controls cell viability via antioxidant activity and regulation o

280 Although cell viability was >80% at the concentrations tested, in

281 Considerable loss of cell viability was detected under light excitation, whil

282 -Al2O3 nanocomposite modified electrode, the cell viability was determined by monitoring the bioelect

283 Cell viability was determined by MTT reduction or LDH re

284 Cell viability was evaluated, and expression levels of R

285 We show that in vitro cell viability was maintained over a three-day period, t

286 ne Caco-2 and they showed no toxicity as the cell viability was more than 80% at 10times or higher di

287 Furthermore, the cell viability was not changed upon treatment with CDs p

288 bated with DOX azide and (68)Ga, after which cell viability was quantified using an assay.

289 Lowest cell viability was seen at 4 degrees C.

290 y of Mahogunin RING finger 1 (MGRN1) affects cell viability, we uncovered a novel role for its intera

291 Mitochondrial function and cell viability were maintained in AD neurons treated wit

292 ant role in maintaining genome integrity and cell viability when cells experience replication stress.

293 s that interfere with cellular functions and cell viability when exposed to light.

294 d normalized CB1 protein levels and improved cell viability, whereas CP55,940 and THC displayed beta-

295 g yields quantitative, online information on cell viability, which complements and supports other met

296 noma cell line (INS-1) resulted in decreased cell viability, which was restored in the presence of ph

297 ngival and PDL fibroblasts displayed reduced cell viability with increasing concentrations of CSE and

298 very of miR-34a and rubone decreased PC3-TXR cell viability with increasing paclitaxel concentration.

299 GMs exhibit a biocompatibility of 80% cell viability with primary fibroblast lung cells after

300 ting that it boosted protein homeostasis and cell viability without directly interfering with the eff