ライフサイエンスコーパス: culture condition

1 nities rather than activity under a specific culture condition.

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

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

4 give rise to photoreceptors under a defined culture condition.

5 lelically expressed in ESCs independently of culture condition.

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

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

8 mammals and maintained under identical cell culture conditions.

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

10 t stem cell states stabilized with different culture conditions.

11 xpression and function in cells under normal culture conditions.

12 carefully monitored with any changes in cell culture conditions.

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

14 les, genetic perturbations and assessment of culture conditions.

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

16 ells growing slowly due to environmental and culture conditions.

17 rs are not expressed under common laboratory culture conditions.

18 000 genes required for optimal fitness under culture conditions.

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

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

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

22 differentially expressed under the specified culture conditions.

23 dized the size of cardiospheres by modifying culture conditions.

24 ed by different functional maturation due to culture conditions.

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

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

27 nterior cortex-like structures under minimal culture conditions.

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

29 GLN1 is significantly impaired under hypoxic culture conditions.

30 variation, partly reflecting disparities in culture conditions.

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

32 spensable for iPSC formation under optimized culture conditions.

33 nd apoptosis under both hypoxic and normoxic culture conditions.

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

35 observed for soluble proteins under the same culture conditions.

36 e from environmental specimens under aerobic culture conditions.

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

38 aried greatly among different cell lines and culture conditions.

39 es that can grow under feeder-free stem cell culture conditions.

40 endrocytes) when cultured in differentiation culture conditions.

41 gent immediately followed by differentiating culture conditions.

42 d structures were shown to proliferate under culture conditions.

43 ith lumen under standard tridimensional (3D) culture conditions.

44 n as multicellular spheres under nonadherent culture conditions.

45 gy which provides high throughput testing of culture conditions.

46 ls are grown in HS, compared to standard FBS culture conditions.

47 dard embryonic or trophoblast stem (TS) cell culture conditions.

48 below the limit of quantification under both culture conditions.

49 esistance when cells are grown under routine culture conditions.

50 Identification was not affected by different culture conditions.

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

52 itutive or appeared to be unique to specific culture conditions.

53 gn Ag in normal mice without Th17-polarizing culture conditions.

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

55 ndent LNCaP cells under castration-simulated culture conditions.

56 ck rhythms are self-sustained under constant culture conditions.

57 cells (ECs) in response to defined media and culture conditions.

58 oliferation for more than 3 wk under hypoxic culture conditions.

59 eptible to apoptotic cell death under normal culture conditions.

60 ivate primary human ECs (hECs) in serum-free culture conditions.

61 omolog proximity that increases in saturated culture conditions.

62 , adipocytes, and chondrocytes under defined culture conditions.

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

64 ed yeast strains in four parallel switchable culture conditions.

65 ystems to import cholesterol in the analysed culture conditions.

66 ompared to cells cultured in standard tissue culture conditions.

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

68 can usually be mitigated by optimizing cell culture conditions.

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

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

71 nerational lineage tracking under controlled culture conditions.

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

73 argely determined by host cell genotypes and culture conditions.

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

75 tured population while precisely controlling culture conditions.

76 lar metabolite distributions under different culture conditions.

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

78 cells to chemically defined hypomethylating culture conditions.

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

80 dherent stem cell types and across different culture conditions.

81 ontrasting differentiation efficiency of the culture conditions.

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

83 ts are often not detectable under laboratory culture conditions.

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

85 at could provide information about microbial culturing conditions.

86 n indicative of cell stress even under basal culturing conditions.

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

88 Melanoma cells exposed to acidic culture conditions (7.0 < pH < 6.2) promptly accumulated

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

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

91 In both a monolayer culture condition and a three-dimensional Matrigel syste

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

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

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

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

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

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

98 t maintained levels of ATP under both normal culture conditions and following Abeta treatment.

99 ssential for vigorous growth under favorable culture conditions and for membrane lipid degradation wi

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

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

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

103 testing has been performed both in standard culture conditions and on chip at different concentratio

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

105 entified a set of miRNA that were induced by culture conditions and potentially able to bind to the B

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

107 ses entirely defined, feeder- and serum-free culture conditions and produces very consistent, pure, h

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

109 ing requires their adaptation to large-scale culture conditions and screening formats.

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

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

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

113 ) of procyclic form T. brucei under standard culture conditions and was lethal for this life cycle st

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

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

116 It was proved that the controlling of culturing conditions and the modifying of fermentation m

117 f an ideal host in terms of the growth rate, culture conditions, and available recombinant DNA tools.

118 oxylase is typically repressed under routine culture conditions, and for many live attenuated Salmone

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

120 can be raised at high densities, under clean culture conditions, and it lacks integumentary or skelet

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

122 li were quantified by an observer blinded to culture conditions, and tubules were phenotyped using sp

123 , we showed here that hAFSCs under selective culture conditions are able to give rise to functional S

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

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

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

127 ed a consistent increase of LC3-II in acidic culture conditions as compared with cells at normal pH.

128 hibition of cell proliferation, under tissue culture conditions as well as in vivo.

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

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

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

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

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

134 necrotic death prevails under standard cell culture conditions, but cells rescued from the necrosis

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

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

137 interaction in conventional two-dimensional culture conditions by using dominant mutants of Cdc42 in

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

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

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

141 e chambers of a microfluidic network so that culturing conditions can be independently controlled and

142 Depending on growth phase and culture conditions, cardiolipin (CL) makes up 5-15% of t

143 After 7 days, compared with the 2D culture condition, CM and FPCM markedly reduced amyloid

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

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

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

147 In the regular culture condition containing fetal bovine serum (FBS), C

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

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

150 oneidensis MR-1 cultures grown under various culture conditions displayed different DNA methylation p

151 reated ovarian cancer cells under suspension culture conditions drastically lost their ability of tum

152 More generally, these findings indicate that culture conditions during cellular reprogramming can str

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

154 Transfer into distinct culture conditions, each comprised of a specific mix of

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

156 s and hepatocytes in vitro, depending on the culture condition employed.

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

158 Advanced culture conditions facilitate the formation of three-dim

159 Standard cell culture conditions fail to recapitulate the original tum

160 We demonstrate here that hypoxic culture conditions favor the quiescence of satellite cel

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

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

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

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

165 ted in vivo and were independent of in vitro culture conditions for DC differentiation.

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

167 rization of ISCs and the absence of suitable culture conditions for expansion of ISCs in vitro.

168 ration and proplatelet production under live culture conditions for extended periods of time.

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

170 ace methodology was employed to optimise the culture conditions for kefiran production from kefir gra

171 approach can be used to efficiently optimize culture conditions for other algal species to improve gr

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

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

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

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

176 To address these issues, we developed culture conditions for the propagation and spontaneous m

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

178 e discovered that by removing serum from the culture conditions, GATA4 and GATA6 are each also able t

179 Remarkably, under hematopoietic serum-free culture conditions, hematopoietic outgrowth of Eng-expre

180 find that as an initial response to altered culture conditions, hESCs change their transcription pro

181 ammalian cell coculture under mammalian cell culture conditions; however, when the medium was modifie

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

183 e alternative gene transfer technologies and culture conditions in future studies to improve CAR expr

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

185 Upon manipulation of their culture conditions in vitro or transplantation into mice

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

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

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

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

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

191 The culture conditions include different carbon, nitrogen, p

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

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

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

195 simultaneous assessment of a large number of culture conditions influencing bacterial toxin productio

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

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

198 use 2-AEPn as a sole P source under standard culture conditions, it was able to use phosphite.

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

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

201 velopment and, in the case of miR-24, due to culture conditions, making this miRNA a candidate for sc

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

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

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

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

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

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

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

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

210 miR-503) expression in ECs is upregulated in culture conditions mimicking diabetes mellitus (high D-g

211 regarding growth and pigmentation in various culture conditions; most remarkably, it exhibited a gluc

212 Advances in culture conditions now allow for the establishment of in

213 upon reversion to the original feeder-based culture conditions, numerous transcription changes are n

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

215 We conclude that culture conditions of activated B cells before and at ea

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

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

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

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

220 Under all culture conditions, OPCs up-regulated expression of gene

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

222 t advances in manipulating cofactors include culture conditions or additive alterations, genetic modi

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

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

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

226 tic cell death phenomenon was independent of culture conditions or telomere shortening.

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

228 via heterologous expression, manipulation of culture conditions, or introduction of artificial glycos

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

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

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

232 ions do not induce cell death under standard culture conditions, p-tau-expressing neurons cultured un

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

234 acid (RA) in 2-dimensional and 3-dimensional culture conditions (physiomimetic organotypic culture).

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

236 id body, methods that cannot avoid undefined culture conditions, precluding analysis of the fate of i

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

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

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

240 In batch fermentation culture conditions, reductive conditions were obtained u

241 Hyperglycemic culture conditions rendered pericytes more susceptible t

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

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

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

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

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

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

248 We conclude that in vitro culture conditions significantly affect the transcriptom

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

250 Depending on cell types and culture conditions, such genetic alterations can lead to

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

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

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

254 spp. strains that were grown under identical culture conditions, suggesting that these processes are

255 long-term CD8 T cells ex vivo, by applying a culture condition that simulates an acute infection.

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

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

258 predict stem cell behavior under a number of culture conditions that emulate characteristics of 3D st

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

260 Upon removal of culture conditions that maintain an undifferentiated sta

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 own that expression of bba03 is increased by culture conditions that simulate tick feeding.

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 quires the expression of defined factors and culture conditions that support the self-renewal of embr

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

268 gh-salt intake can potentiate, in serum-free culture conditions, the differentiation of freshly-isola

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

270 Under normal culture conditions, the mitochondrial membrane potential

271 Under appropriate culture conditions, these progenitor cells adhered to an

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

273 multiplex nanoliter reactors under different culture conditions to assess the behavior of cells.

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

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

276 stem cells (mESCs) maintained under standard culture conditions to gain a better understanding of sel

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

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

279 investigated cell stress under a variety of culture conditions using three cell lines: parental HEK

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

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

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

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

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

285 for a short time, followed by sphere-forming culture conditions, we have established stem cell-like N

286 Culture conditions were applied for 24 hours, 4 days, an

287 Culture conditions were developed based on those for the

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

289 6A10 reduced spheroid growth in vitro under culture conditions where CA XII was active (i.e., alkali

290 We further established culture conditions where we can control glucose and mann

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

292 n serum-free medium supplemented with LIF, a culture condition which does not support induced pluripo

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

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

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 e expression level of miR-24 differed due to culture conditions, with lower levels detected in the IV

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