ライフサイエンスコーパス: culture condition

1 ip under laminar flow compared to the static culture condition.

2 nities rather than activity under a specific culture condition.

3 appears to be dependent on cell type and/or culture condition.

4 C formed polarized acinar structures in a 3D-culture condition.

5 give rise to photoreceptors under a defined culture condition.

6 a case-by-case basis, for each cell line and culture condition.

7 ntially expressed genes (DEG), regardless of culture condition.

8 analyze MS datasets from various strains and culture conditions.

9 quires TCTP in MCF-7 cells under normal cell culture conditions.

10 Xi) of primed hESCs was reactivated in naive culture conditions.

11 ompared to cells cultured in standard tissue culture conditions.

12 AML cells in BM stroma-derived and standard culture conditions.

13 that improve cell growth and survival under culture conditions.

14 d structures were shown to proliferate under culture conditions.

15 below the limit of quantification under both culture conditions.

16 recursors, as well as APC, under appropriate culture conditions.

17 both strains, which was dependent on growth culture conditions.

18 omolog proximity that increases in saturated culture conditions.

19 ed yeast strains in four parallel switchable culture conditions.

20 ystems to import cholesterol in the analysed culture conditions.

21 cell lineage from Th17 cells under in vitro culture conditions.

22 can usually be mitigated by optimizing cell culture conditions.

23 eal cell type and parasite isolates, and the culture conditions.

24 nerational lineage tracking under controlled culture conditions.

25 spare glycolytic capacity (SGC) under normal culture conditions.

26 argely determined by host cell genotypes and culture conditions.

27 s under both in vitro aqueous and in situ co-culture conditions.

28 tured population while precisely controlling culture conditions.

29 lar metabolite distributions under different culture conditions.

30 ells (cardiomyocytes) is highly sensitive to culture conditions.

31 cells to chemically defined hypomethylating culture conditions.

32 between KCs and inflammatory cells under co-culture conditions.

33 dherent stem cell types and across different culture conditions.

34 ontrasting differentiation efficiency of the culture conditions.

35 ucing Microcystis strains under mono- and co-culture conditions.

36 ts are often not detectable under laboratory culture conditions.

37 tem (iPS) cells that uses defined serum-free culture conditions.

38 leatum viability under standard aerobic cell culture conditions.

39 mammals and maintained under identical cell culture conditions.

40 e stage at which they were derived and their culture conditions.

41 t stem cell states stabilized with different culture conditions.

42 xpression and function in cells under normal culture conditions.

43 carefully monitored with any changes in cell culture conditions.

44 ufficient amounts of NAR and NR under normal culture conditions.

45 les, genetic perturbations and assessment of culture conditions.

46 -dimensional (2D) and three-dimensional (3D) culture conditions.

47 ells growing slowly due to environmental and culture conditions.

48 rs are not expressed under common laboratory culture conditions.

49 000 genes required for optimal fitness under culture conditions.

50 n LGR5(+ve) cells from the hERM in xeno-free culture conditions.

51 s upregulated in 3D vs traditional monolayer culture conditions.

52 aggregates (or spheroids) under non-adherent culture conditions.

53 differentially expressed under the specified culture conditions.

54 dized the size of cardiospheres by modifying culture conditions.

55 ed by different functional maturation due to culture conditions.

56 he two-cell embryo (2C)-like state under ESC culture conditions.

57 ntal samples, without the need for anaerobic culture conditions.

58 as (GBM) and that have never known any serum culture conditions.

59 nterior cortex-like structures under minimal culture conditions.

60 ace for at least 2 weeks under in vitro cell culture conditions.

61 GLN1 is significantly impaired under hypoxic culture conditions.

62 variation, partly reflecting disparities in culture conditions.

63 ocytic lineage using feeder-free and defined culture conditions.

64 spensable for iPSC formation under optimized culture conditions.

65 nd apoptosis under both hypoxic and normoxic culture conditions.

66 ng EcSOD expression in HMEC under these cell culture conditions.

67 observed for soluble proteins under the same culture conditions.

68 e from environmental specimens under aerobic culture conditions.

69 C. difficile type strain ATCC 9689 under 768 culture conditions.

70 aried greatly among different cell lines and culture conditions.

71 ancer-related genes and implicated selective culture conditions.

72 ncremental pulsatile stretching, and optimal culture conditions.

73 ction in an organ-on-a-chip incorporating 3D culture conditions.

74 hibited a more constant drug response across culture conditions.

75 ents were maintained ex vivo under optimized culture conditions.

76 es yield under both monolayer and suspension culture conditions.

77 os, and in both primed and naive pluripotent culture conditions.

78 slets rapidly deteriorate under conventional culture conditions.

79 reconditioning in interpreting results under culture conditions.

80 is are frequently dispensable under standard culture conditions.

81 als compared to those for standard multiwell culture conditions.

82 in secretion for up to 6 days under normoxic culture conditions.

83 ise not to assume stability across different culture conditions.

84 -like cells (hALCs) using chemically defined culture conditions.

85 behave similarly when placed under distinct culture conditions.

86 genes during rapid proliferation in constant culture conditions.

87 in a wide range of assays and different cell culture conditions.

88 tivity have been replaced with fully defined culture conditions.

89 cytometry; fluid dynamic modelling validates culture conditions.

90 mmitment in contrast to osteogenic and basal cultured conditions.

91 mpared to the wild-type strain under aerobic culturing conditions.

92 ross-species co-culture as well as long-term culturing conditions.

93 expression was induced by three-dimensional culture conditions, activated Src, was reversible, and w

94 Hypoxic stress in the culture conditions also regulates limbal stem cell growt

95 is, addition of a ROS scavenger or anaerobic culture conditions also worked to promote L-form growth

96 te-derived EVs (ADEVs) generated in specific culture conditions and ADEVs that are engineered to carr

97 pared with control MVEC (n = 8) under static culture conditions and after 24, 72, and 120 hours of HS

98 duced protein 10 were measured under control culture conditions and after stimulation with cytokines.

99 ht into functional differences that exist in culture conditions and among ebolavirus glycoproteins.

100 in regenerants derived under distinct tissue culture conditions and analysed via Taguchi statistics.

101 . These features are dependent on lipid-free culture conditions and are lost upon lipid exposure, whe

102 l culture with multifunctional monitoring of culture conditions and control of cell behaviour.

103 uced cytotoxicity was retained under hypoxic culture conditions and during coculture with mesenchymal

104 d K562 cells were examined under normal cell culture conditions and during exposure to curcumin, a na

105 PDAC cells grown in variant culture conditions and exposed to extracellular lumican

106 ifferentiation in microColonies and standard culture conditions and find that in microColonies, above

107 higher levels of bmm mRNA both under normal culture conditions and in response to starvation, a lipo

108 hUTCs support neurite outgrowth under normal culture conditions and in the presence of the growth-inh

109 precisely controlled in standard cell/tissue culture conditions and in vivo.

110 limited due to the requirement of anaerobic culture conditions and microbiological expertise.

111 reness and early diagnosis using appropriate culture conditions and molecular techniques are importan

112 erted cancer cell-induced myotube wasting in culture conditions and mouse models.

113 -dimensional (2D) and three-dimensional (3D) culture conditions and orthotopic xenografts.

114 The association is effective under cell culture conditions and produces large changes in dye opt

115 can generate various cell types depending on culture conditions and raises the possibility of transit

116 n help control for biases introduced by cell-culture conditions and the microenvironment in mouse mod

117 group was different in different strains and culture conditions and the relevance of the unknown func

118 asiveness, were assessed both under standard culture conditions and under conditions of stress (i.e.,

119 aging of recombinant HEK293 cells at varying culture conditions and validate its ability to generate

120 ed to a fluorescent protein (FP) under basal culture conditions and validate our analysis by testing

121 hia coli strains were subjected to different culture conditions and were distinguishable with 88% acc

122 typic microscale systems that facilitate the culture, conditioning and manipulation of cells.

123 ned wall-less cell arrays for the mapping of culturing conditions and demonstrated the potential of t

124 ome in culture has been studied under normal culture conditions, and it is not known how DAMPs signal

125 ssion does not change in response to varying culture conditions, and thus, it appears to be constitut

126 Finally, FS cell culture conditions applied to human naive cells or embry

127 We observe that standard culture conditions are associated with a rapid and selec

128 Our data demonstrate that culture conditions are decisive for the expansion of hAF

129 noid esters that accumulate in non-stressful culture conditions are identified in Aphanotece microsco

130 Embryonic stem cell (ESC) culture conditions are important for maintaining long-te

131 most of these cell lines when standard cell culturing conditions are used.

132 ed the solubility of the protein also in the culture condition at 37 degrees C.

133 that under standard serum-containing tissue culture conditions, ATSP-7041 achieves intracellular acc

134 xicity in microfluidics compared with static culture conditions based on data obtained in our previou

135 s contaminating cells was influenced by iPSC culture conditions before differentiation.

136 This creates an increasing need for tissue culture conditions better adapted to live-cell imaging.

137 Under standard culture conditions BMP4 acts as a morphogen but this req

138 vity to proteasome inhibitors under adherent culture conditions, but acquired resistance as spheroids

139 h vincristine and LDHA inhibition under cell culture conditions, but this combination was ineffective

140 created a bioartificial adrenal with 3D cell culture conditions by encapsulation of bovine adrenocort

141 logy and immunocytochemistry, and optimizing culture conditions by use of growth curve assays with a

142 rformed controls under in vitro and ex vitro culture conditions (callus biomass, shoot production, an

143 indings again highlight the impact that cell culture conditions can have on the product quality of re

144 ronment (exometabolomics) over time in batch culture conditions can provide rich phenotypic data that

145 ains exhibit high fitness under a variety of culture conditions, compared with that of wild-type V st

146 expressed in the deletion mutant under both culture conditions conformed to a pattern resembling can

147 nt exhibited no growth defect under standard culture conditions, consistent with nonessentiality in t

148 Here we report that in in vitro low stress culture conditions consisting of a fibroblast feeder lay

149 The temporal evolution of culture conditions could be monitored for days, before a

150 The cell culture conditions did not affect cell killing, the abil

151 ion, we illustrated the formation of hypoxic culture conditions due to limited diffusion of oxygen th

152 diance and radiant exposure, as well as cell culture conditions (e.g., serum concentration, cell conf

153 In suitable culture conditions, EC form two-dimensional (2D) branche

154 ultured in conventional two-dimensional (2D) culture conditions, EcSOD protein expression was observe

155 h hAFSCs cultivated in multipotent stem cell culture conditions expressed OCT4A, and that the OCT4A p

156 Under standard culture conditions, expression of several heat shock pro

157 Modifications to enteroid culture conditions facilitated robust human cytokine res

158 Standard cell culture conditions fail to recapitulate the original tum

159 iously we reported that under procontractile culture conditions, fibronectin fibrillar matrix assembl

160 g in the identification of ideal strains and culture conditions for a specific application, saving an

161 overcome this problem recently and developed culture conditions for adult stem cells that allow the l

162 We first investigated the culture conditions for both cell types to optimize their

163 fits over standard platforms when optimizing culture conditions for cell-based screening and achieve

164 forces the importance of optimizing in vitro culture conditions for drug evaluation in mycobacteria,

165 Our results emphasize the importance of culture conditions for epigenomic studies, and reveal th

166 de possible by defining the first successful culture conditions for ex vivo maintenance of rHpScs con

167 Optimization of culture conditions for human limbal epithelial stem/prog

168 However, current culture conditions for human pancreatic slices (HPSs) ha

169 tromal cell interactions and to optimize HLE culture conditions for potential therapeutic application

170 However, despite intense research, culture conditions for robust maintenance of HSCs are st

171 population-level phenomenon, we established culture conditions for stable oscillations at the cellul

172 We first reconstituted the 2D culture conditions for stem cell fate control within 3D

173 bes, whose growth is unsupported by standard culture conditions for this specimen.

174 rogel scaffolds and maintained under dynamic culture conditions for up to 12 weeks.

175 e compared to those of CDBB (under anaerobic culture conditions) for the recovery of C. difficile fro

176 few genes were actively expressed in a given culture condition in expanded multigene families, sugges

177 several neural crest derivatives in minimal culture conditions in vitro or ectopic locations in vivo

178 n vivo-like perfusion and stable oxygenation culture conditions in vitro semi-independently of one an

179 Furthermore, under Th1 culture conditions in vitro, as well as in an IFN-gamma-

180 rich foamy macrophages but not under regular culture conditions in vitro, underscoring Msh1's importa

181 t in vivo and under differentiation-inducing culture conditions in vitro.

182 Culture conditions in which hematopoietic stem cells (HS

183 t physiology or primary human hepatocytes in culture conditions in which they rapidly lose their hepa

184 d loss of viability of rHBs, even though the culture conditions, in the absence of the agonists, were

185 as enhanced by p53 knockdown and appropriate culture conditions including hypoxia.

186 ret similarity scores and modulation of cell culture conditions, including substratum elastic modulus

187 ultures of naive human CD4+ T cells in iTreg culture conditions increased FOXP3 expression.

188 REIMS is sufficiently specific to serve as a culture condition-independent tool for the identificatio

189 human breast tissues, suggesting that the 2D-cultured condition induces a repressive status of EcSOD

190 manipulations and is widely adaptable across culture conditions, infection protocols, and downstream

191 in red Grenache grapes derived from organic culture conditions influence the bioavailability and met

192 f stool antigen CIDTs versus truly optimized culture conditions is unknown.

193 Here, we show that with appropriate 3D culture conditions, it is possible to support long-term

194 When transferred to differentiation culture conditions, Kdm5b-depleted adult NSCs migrated f

195 We show that under normal culture conditions, LDs are amorphous and that they tran

196 of human MSC and chondrocytes under standard culture conditions leads to improved extracellular matri

197 Furthermore, culture conditions like temperature or osmolality can be

198 However, in culture conditions, matrigel directly signals to cancer

199 Expansion in these culture conditions may be feasible for Lgr5(+) cells fro

200 ts of radiation in two-dimensional (2D) cell culture conditions may not recapitulate tissue responses

201 Experimental assays of chemotaxis towards culture conditioned media confirm this hypothesis.

202 Exosomes were isolated from the culture-conditioned media and delivered to athymic rats

203 efore evaluated the effects of O. formigenes culture conditioned medium (CM) on apical (14)C-oxalate

204 nduces sCD55 expression in HCV-infected cell culture-conditioned medium and inhibits C3 convertase ac

205 In suspended cell culture conditions, metastatic breast cancer cells exhib

206 Under normal culture conditions, MFS CMs show a lower beat-to-beat va

207 Naive culture conditions minimize epigenetic fluctuation, pote

208 TMJ discs were measured under varying tissue culture conditions (n = 40 discs), and mechanical strain

209 ediates cap-dependent translation under cell culture conditions of 1% oxygen (to mimic tumor microenv

210 gnaling could provide a strategy to optimize culture conditions of germline stem cells from other spe

211 ripotent stem cells using established neural culture conditions often exhibit functional deficits.

212 testing the effects of normoxic and hypoxic culture conditions on healthy and tumorigenic breast epi

213 However, the effects of culture conditions on RS-hAFSCs have not been determined

214 We also assess the impact of in vitro culture conditions on stromal cell gene expression and p

215 However, the effect of different culture conditions on the underlying mutation rate is un

216 in adult lung epithelial cells, but typical culture conditions only support cell proliferation for 3

217 which lack antimicrobial activity under cell culture conditions, only inhibit macrophage activation b

218 tral composite design statistical models for culture condition optimisation predicted a 464.2 U/ml of

219 t GFP-tagged yeast strains in one switchable culture condition or 24 different GFP-tagged yeast strai

220 oaches focus on chemical screening to adjust culture conditions or culture media.

221 n in real time without the use of artificial culture conditions or gene manipulations.

222 degradation of WGA-labeled GCX under UF cell culture conditions or in Balb/C mice and led to an over

223 evious FAO analyses involve nonphysiological culture conditions or lack adequate quantification.

224 Adaptation to culture conditions or selection with a toxic compound re

225 man primed embryonic stem cells by modifying culture conditions or through transgenic modification.

226 mass of single or multiple adherent cells in culture conditions over days with millisecond time resol

227 With the additional use of specific culture conditions, overexpression of Sox9 facilitated t

228 ic exposure was reduced compared to normoxic culture conditions (P < 0.01).

229 itutively active in PEL, but that under cell culture conditions, PEL rapidly became independent of th

230 nstrate a direct evaluation of several naive culture conditions performed in the same laboratory, the

231 In a high-density culture condition, podoplanin expression can be triggere

232 ro propagation, as well as the environmental culture conditions, present serious challenges to genome

233 In confluent monolayers, low mitogenic culture conditions preserved corneal endothelial cell st

234 Cleavage under standard cell culture conditions rarely exceeded 35% of total L2.

235 vitro two-dimensional, relatively disordered culture conditions recapitulate the development of in vi

236 d by an AhR-dependent mechanism because both culture conditions resulted in repression of its downstr

237 ced down-regulation of TbHrg in heme-limited culture conditions resulted in slower proliferation, dec

238 clusters from procontractile to promigratory culture conditions results in cell dispersal out of clus

239 agnetic levitation system under conventional culturing conditions results in the formation of three-d

240 omparative transcriptome analysis from three culture conditions revealed the landscape of gene-altere

241 ygen levels and suppressed under oxygen-rich culture conditions routinely used for IVOC.

242 However, depending on culture conditions some strains are more unstable than o

243 ted hundreds of independent radiations under culture conditions spanning a variety of productivities,

244 Culture conditions stimulated cellular differentiation i

245 his research direction is the improvement of culture conditions, such as oxygen supply, in the engine

246 of Smad2 phosphorylation under steady-state culture conditions, suggesting a chronic compensation.

247 ntaneous mutation (T544I) specific to tissue culture conditions, suggesting that it has no role in pa

248 increased with passage number under standard culture conditions, suggesting that the P53 mutations co

249 34(+) HSPCs was observed, none of the tested culture conditions supported the expansion or maintenanc

250 R-T cells polarized and expanded under a Th9-culture condition (T9 CAR-T) have an enhanced antitumor

251 x porci are coccoidal or spherical under the culture conditions tested, in contrast with the usual he

252 chnology to identify a defined and optimized culture condition that supports the derivation and propa

253 inhibition of EGF/MAPK signaling and define culture conditions that direct differentiation to the en

254 oblasts (CAFs) and required physiopathologic culture conditions that improved tumor cell survival and

255 Upon removal of culture conditions that maintain an undifferentiated sta

256 an brain cancer cell lines under 3 different culture conditions that maintain low, medium, and high H

257 ung complementation required newly developed culture conditions that maintained the developmental pot

258 sion, this work highlights the importance of culture conditions that modulate response to EGFR pathwa

259 from human blastocysts can be used to define culture conditions that more closely recapitulate the em

260 n-coated microchannels, allowing independent culture conditions that permitted cellular migration and

261 d retains its attenuated genotype under cell culture conditions that readily select for reversion in

262 her they apply to humans, due to the lack of culture conditions that recapitulate prostate gland arch

263 Here, we describe culture conditions that support schistosome sexual devel

264 Hutchins and co-workers is likely caused by culture conditions that support suboptimal growth rates.

265 Here, we developed culture conditions that support the maintenance of CD34(

266 intain their stem cell properties even under culture conditions that would otherwise induce different

267 involved in gene delivery, cell adhesion and culturing conditions that promote cell survival.

268 Under standard culture conditions, the distribution of PSII complexes i

269 Under normal culture conditions, the mitochondrial membrane potential

270 With optimization of CTC culture conditions, this strategy may help identify the

271 accomplish this goal, we have developed cell culture conditions to closely mimic events occurring dur

272 baeus and studied its growth under different culture conditions to elucidate pathways of carbon (C) a

273 a cell lines under normal and sphere-forming culture conditions to enrich for tumor cell progenitors.

274 Furthermore, we describe culture conditions to maintain mitochondrial-depleted ce

275 y, aerosol exposure technique, and bacterial culture conditions to optimize the spray factor (SF), a

276 ge populations, we have optimized serum-free culture conditions to permit robust survival of highly r

277 characteristics relative to those of static culture conditions under both baseline conditions and wi

278 Culture conditions under which steady-state growth and c

279 Moreover, we found that culture conditions used for the assay contributed to bac

280 large-scale cell production under xeno-free culture conditions using current matrices.

281 ing spermatogonial stem cells (SSCs) in cell culture conditions, using zebrafish testicular hyperplas

282 The impact of culture conditions was further seen when inhibitory effe

283 By tailoring delivery platforms and culture conditions we overcame these barriers and provid

284 Through improvements of culture conditions, we achieved efficient propagation of

285 Exploiting these new culture conditions, we explore the process of male-stimu

286 In common culture conditions, we found that small molecule inhibit

287 Culture conditions were developed based on those for the

288 The culture conditions were optimised for maximum chitinase

289 ty and specificity of CDBB-TC (under aerobic culture conditions) were compared to those of CDBB (unde

290 nding protein (21% normoxia or standard cell culture conditions), where eIF4E2 is the dominant cap-bi

291 sting the adaptation of the cells to the new culture conditions, which was also reflected by the expr

292 expression and sphere formation in stem cell culture conditions, which were rescued by re-introductio

293 ty to expand primary NHBE cells in different culture conditions while maintaining their 3D culture ch

294 We optimized the medium and culture conditions with continuous electrical stimulatio

295 Supplementing defined stroma- and serum-free culture conditions with recombinant DPT protein improved

296 duced PSCs (iPSCs), under chemically defined culture conditions, with ex vivo cultures for the induct

297 cted using LX-2 cell RNA derived from MLH co-culture conditions, with or without HCV and HIV infectio

298 reference for humidity levels under standard culture conditions, worms displayed a strong preference

299 Under such culture conditions, yeast colonies grow vertically and o

300 in endothelial and smooth muscle cells upon culture conditions, yielding a "vascular disease-like" p