ライフサイエンスコーパス: cell in culture

1 Cells in culture are grown with amino acids containing l

2 PD-L2 mAb blockade of wild-type B-1 cells in culture significantly increased CD138 and Blimp

3 Using EGFR-overexpressing A431 and UMSCC-1 cells in culture, we found that radiation activated the

4 absorbed, metabolized and released by Caco-2 cells in culture media.

5 t form a tidy stacked brick pattern on HEp-2 cells in culture, which is definitive for EAEC.

6 )O(2)) was used to impose an insult on RGC-5 cells in culture.

7 rategy for generating and maintaining acinar cells in culture.

8 fatty acids (NEFAs) and adipokines on acinar cells in culture.

9 ments with intact mice and pancreatic acinar cells in culture, that ZnT2 participates in zinc transpo

10 he total mass of single or multiple adherent cells in culture conditions over days with millisecond t

11 Irisin acts on white adipose cells in culture and in vivo to stimulate UCP1 expressio

12 n both streptozotocin (STZ)-treated mice and cells in culture exposed to hyperglycemic conditions, ex

13 x balance model of heterotrophic Arabidopsis cells in culture, irrespective of the objective function

14 b1 induced an increase in the number of ARPE cells in culture, while VEGF release (pg/10,000 viable c

15 ced injury, as well as upon placement of AT2 cells in culture.

16 tigen-dependent activation of human memory B cells in culture.

17 ility of MHV68 to transform primary murine B cells in culture, the absence of a robust cell culture l

18 s in M2-driven expansion of primary murine B cells in culture.

19 n and colony-forming ability of neoplastic B cells in culture and growth as tumor xenografts in mice.

20 Treatment of naive splenic B cells in culture with anti-CD40 plus IL-4 induces IgH CS

21 Analysis of B cells in cultures may shed light on the interaction of g

22 atly increase production of mature red blood cells in cultures of both mouse fetal liver BFU-Es and m

23 BRET systems for ratiometric imaging of both cells in culture and deep-tissue small animal tumor mode

24 n bone in vivo, and the growth rates of both cells in culture were similar, suggesting a role of the

25 liferation and migration of a subset of BrCA cells in culture.

26 or antiproliferative activity against cancer cells in culture and, for selected, highly active compou

27 spontaneously secreted by normal and cancer cells in culture, and by Par-4 transgenic mice that are

28 ted the malignant phenotype of breast cancer cells in culture and in a xenograft mouse model.

29 In quiescent breast cancer cells in culture and in malignant tissue sections from E

30 the migration and invasion of breast cancer cells in culture.

31 bles, inhibits growth of human breast cancer cells in culture.

32 vitro and induces apoptotic death in cancer cells in culture and in mouse xenograft models.

33 vitro and induces apoptotic death in cancer cells in culture and in mouse xenograft models.

34 and their ability to induce death in cancer cells in culture.

35 h and survival of PRL-induced mammary cancer cells in culture and in vivo.

36 LMX1B strongly promotes migration of cancer cells in culture and promotes xenograft growth in nude m

37 (ROS), DNQ potently induces death of cancer cells in culture, with IC(50) values between 16 and 210

38 the proliferation of several types of cancer cells in culture.

39 markedly enhance the invasiveness of cancer cells in culture.

40 arms of the UPR in breast and ovarian cancer cells in culture and in a mouse xenograft.

41 bitors with gemcitabine in pancreatic cancer cells in culture and orthotopic implantation models.

42 a/b induced massive death of prostate cancer cells in culture and reduced both subcutaneous and ortho

43 s both cancer stem cells and non-stem cancer cells in culture.

44 erlotinib targeted both CSCs and bulk cancer cells in cultures of EGFR-expressing TNBC-derived cells.

45 nic properties of FABP5-expressing carcinoma cells in cultured cells and in vivo.

46 ally inhibited the proliferation of CD133(+) cells in cultures of established cell lines derived from

47 ession of ITGA4 on human BM derived Lin-CD34 cells in culture, which was associated with improved hom

48 l treatment of differentiating human CD34(+) cells in culture increases fetal hemoglobin production w

49 HCC samples and induced expansion of CD44(+) cells in culture.

50 of TAMs to promote sphere formation by CD44+ cells in culture and growth of xenograft tumors in mice.

51 ifferent subpopulations of bovine chromaffin cells in culture.

52 nts infected a higher proportion of ciliated cells in cultures of human airway epithelium than did vi

53 ice grow slowly and die earlier than control cells in culture.

54 ily infects murine macrophages and dendritic cells in culture.

55 as Slf is lethal and lyses P. dendritiformis cells in culture.

56 Importantly, both Tiam1-depleted cells in culture and Rac1-deficient epithelial cells in

57 Furthermore, serum-deprived cells in culture show an upregulated EGFR/JAK3/PLD2-PA s

58 s can be meaningfully reduced to dissociated cells in culture has been uncertain.

59 ly(A) landscape of both human and Drosophila cells in culture and observed outstanding overlap with e

60 vivo Using both DJ-1 knockdown in Drosophila cells in culture, and DJ-1beta knock-out flies, we could

61 f centrosomes and microtubules in Drosophila cells, in culture and in vivo, using a combination of li

62 he development of hyperplasia of endometrial cells in culture.

63 Endothelial cells in culture show that ET stimulates very rapid inte

64 expression on human dermal blood endothelial cells in culture.

65 we examined the ability of brain endothelial cells in culture to synthesize thrombin and showed that

66 sections and to human glomerular endothelial cells in culture.

67 IL-6 production in primary human endothelial cells in culture.

68 reversibly increases vWF mRNA in endothelial cells in culture and the rate of vWF secretion from them

69 d the proliferation of lymphatic endothelial cells in culture and the number of lymphatic sprouts and

70 on in human dermal microvascular endothelial cells in culture.

71 gulated during KSHV infection of endothelial cells in culture.

72 VEGF in the lungs and in primary endothelial cells in culture.

73 Plvap Ab/SOD bound to endothelial cells in culture with much lower efficacy than CD31 Ab/S

74 increases leukocyte adherence to endothelial cells in culture.

75 Mean CBLuc expression of treated endothelial cells in culture was 20-fold higher with cationic than w

76 creted from human umbilical vein endothelial cells in culture upon activation with thrombin or after

77 activated Cl- secretion by airway epithelial cells in culture, thereby disrupting ion and water balan

78 tivated Cl(-) secretion by airway epithelial cells in culture, thereby disrupting ion and water balan

79 d by infection of Stat1-/- airway epithelial cells in culture.

80 n this study, we exposed alveolar epithelial cells in culture and mice to fine particulate matter <2.

81 se of free FN in medium of amnion epithelial cells in culture.

82 Oncogenic transformation of human epithelial cells in culture can be triggered by activation of v-Src

83 Normal human epithelial cells in culture have generally shown a limited prolifer

84 196 lincRNAs in murine intestinal epithelial cells in culture.

85 broblast cells and macaque kidney epithelial cells in culture, which are representative of foreign an

86 5-fold elevated in CF IB3-1 lung epithelial cells in culture, compared with control IB3-1/S9 cells.

87 ulates the growth rate of mammary epithelial cells in culture.

88 roteomics analysis of human nasal epithelial cells in culture revealed the activation of the unfolded

89 WNV infection of epithelial cells in culture resulted in a decrease in the transepit

90 nd survival in primary pancreatic epithelial cells in culture and for Kras-driven pancreatic intraepi

91 ted phenotypes in retinal pigment epithelial cells in culture.

92 n inhibit gonococcal adherence to epithelial cells in culture.

93 not gH/gL, blocks viral entry to epithelial cells in culture.

94 ime-lapse recording of vertebrate epithelial cells in culture.

95 ng had been lost or altered in Zfp57-null ES cells in culture.

96 rate cardiomyocytes from embryonic stem (ES) cells in culture it is essential to identify key regulat

97 cells in the embryo and embryonic stem (ES) cells in culture represent the ground state for a mammal

98 played toxicity toward primary adherent ESFT cells in culture but not to CSC-enriched ESFT spheres.

99 ense RNA virus, replicates in all eukaryotic cells in culture, suggesting that the host requirements

100 n in glycerol and is cytotoxic to eukaryotic cells in culture.

101 onential growth phase released 220 exosomes/cell in culture medium.

102 were more potent in killing MDR1-expressing cells in culture.

103 ts that in true nondividing human fibroblast cells in culture, microgravity experienced in space has

104 tric fields, have recently been realized for cells in culture, the impact of in vivo temporal ligand

105 ermolecular interactions are mainly used for cells in culture and have limited use for the noninvasiv

106 t of high micromolar zinc concentrations for cells in cultures.

107 nhibitor reduced the level of sphere-forming cells in culture.

108 whole animals, from isolated islets and from cells in culture, which suggests a direct effect on the

109 ave other applications such as sampling from cells in culture.

110 ct on the hair cell and dorsal root ganglion cells in culture; (iv) SLV recycling is Ca(2+) sensitive

111 cells (NPCs), supported the survival of germ cells in culture, and cooperated with endogenous embryon

112 did not eliminate the growth of glioblastoma cells in culture and in vivo.

113 lly bind and inhibit the migration of glioma cells in culture.

114 ogenic growth and induces apoptosis of H295R cells in culture.

115 o 400-fold enhanced cytotoxicity toward H460 cells in culture under hypoxia versus their potency unde

116 ero cells was 5-fold more infectious for HAE cells in culture, confirming our hypothesis and indicati

117 en studied by transfecting neonatal rat hair cells in culture with a beta-actin-GFP fusion, and evide

118 ntamicin accumulation were decreased in hair cells in cultured organs of Corti from Va(J)/+ and Va(J)

119 drug release (via heat), and killing of HeLa cells in culture is investigated.

120 hese T cells killed GPC3-expressing hepatoma cells in culture and slowed growth of HCC xenograft tumo

121 limiting the propagation of aneuploid human cells in culture to preserve the diploid karyotype of th

122 that human geminin, when expressed in human cells in culture under a constitutive promoter, is exclu

123 g imported into mitochondria of living human cells in culture, these RNA induced a decrease of the pr

124 e-wide small interfering RNA screen of human cells in culture and identified multiple cellular genes

125 frog embryos, as well as chirality of human cells in culture.

126 mage to red blood cells or toxicity to human cells in culture.

127 Genetically identical cells in culture often exhibit significant variations, o

128 observed in flattening lung alveolar type II cells in culture are associated with down-regulation of

129 s included pH recovery from acidification in cells in culture expressing recombinant NHX-7, extracell

130 PMCA reactions and to enter and aggregate in cells in culture.

131 nal-regulated kinase phosphorylation both in cells in culture and in tumor xenografts.

132 ase A (PKA) biosensor as an example-first in cells in culture and then in hepatocytes in the liver of

133 he delivery of effective RNA interference in cells in culture, efficient transduction into hematopoie

134 date RBP-Jkappa and TEAD family occupancy in cells in culture and test the response of each of these

135 necessary for interferon (IFN) resistance in cells in culture.

136 nd nucleus in the z-dimension are uniform in cells in cultured monolayers compared to isolated cells.

137 ree viral microRNAs (miRNAs) in BFV-infected cells in culture and also in infected cattle.

138 her than sequentially ordered as in infected cells in culture.

139 y norovirus to date that efficiently infects cells in culture.

140 elivering plasmid DNA of different size into cells in culture, yielding high transfection rates and m

141 ed L1 mobility in NHPs is not limited to iPS cells in culture and may have also occurred in the germ

142 ayers, but appear to have no effect on islet cells in culture.

143 lipid interactions with its effects on islet cells in culture.

144 of sirolimus also appear beneficial to islet cells in culture and may be a useful strategy in improvi

145 ng animal models, human tissues and isolated cells in culture.

146 ous sized fragments, which when added to IVD cells in culture, caused a significant increase in MMP e

147 in murine kidney slices and in 786-O kidney cells in culture as determined by reverse transcription

148 Upregulation of autophagy protected kidney cells in culture from oxidative stress and reduced colla

149 specific structures and proteins in labeled cells in cultured and explanted neurons and in live Xeno

150 e can be confirmed on primary human leukemia cells in culture and in vivo, and is identical to that o

151 e tool for analyzing the composition of live cells in culture that has the potential to quantify, in

152 ulated the proliferation of human macrophage cells in culture and partially restored the number of ki

153 be used for analyses in individual mammalian cells in culture, in tissue slices and in intact organis

154 w them with the ability to bind to mammalian cells in culture and the properties of the cell surface

155 ially the proliferation of various mammalian cells in culture by an unknown mechanism.

156 when added to autologous patient bone marrow cells in culture.

157 s in the mouse respiratory tract versus MDCK cells in culture showed that the mutants displayed disti

158 and promotes growth of human medulloblastoma cells in culture and in murine xenografts.

159 and down-regulated cFLIP levels in melanoma cells in culture and in vivo.

160 y potently inhibit ROCK activity in melanoma cells in culture and in vivo.

161 h increasing malignant phenotype of melanoma cells in culture and human tissue samples.

162 ) signaling reduces invasiveness of melanoma cells in culture and strongly inhibits Brn-2 expression.

163 Treatment of mesothelial cells in culture with carboplatin resulted in a transien

164 oxin has a wide range of effects on metazoan cells in culture, including induction of apoptosis throu

165 w pentobarbital affects BV2 mouse microglial cells in culture.

166 reshly isolated peripheral blood mononuclear cells in culture.

167 budded from the plasma membrane of mosquito cells in culture.

168 f endocytic origin that are secreted by most cells in culture, but are also present in serum.

169 cellular milieu in senescent human and mouse cells in culture and in vivo.

170 tothenate after three passages of the murine cells in culture.

171 Furthermore, treatment of skeletal muscle cells in culture (C2C12 myotubes) with apocynin resulted

172 ork in cardiomyocytes and L6 skeletal muscle cells in culture.

173 , is downregulated in vascular smooth muscle cells in culture exposed to monotonous stretch cycles wh

174 lated growth of human vascular smooth muscle cells in culture.

175 erotic plaques and in vascular smooth muscle cells in culture.

176 to determine whether vascular smooth muscle cells in cultured microvascular networks maintain the ab

177 ly induced not only in WNV-infected neuronal cells in culture but also in the central nervous system

178 nd other lytic proteins in infected neuronal cells in culture.

179 cific silencing in neuronal and non-neuronal cells in culture and in the DRG of mice in vivo includin

180 Incubation of neuronal cells in culture with human prorenin and angiotensinogen

181 and lower levels of LacNAc than nonmalignant cells in culture and in vivo and that nuclear localizati

182 tected in significantly fewer nontransfected cells in cultures transfected with mature IGF-I compared

183 To test the method, normal rat kidney (NRK) cells in culture were allowed to take up SWNTs upon expo

184 Using complete nutrient deprivation of cells in culture as a simple model of stress, we have ad

185 itation in vivo or amino acid deprivation of cells in culture causes a signal transduction cascade co

186 is study we investigated whether exposure of cells in culture to AgNPs or Ag ions at subtoxic doses w

187 ults were observed after 10 h of exposure of cells in culture to hyperglycemic conditions.

188 ction by washed cells and inhibits growth of cells in culture when U(VI) is present, confirming a rol

189 onstructural protein (NSs) upon infection of cells in culture.

190 is phosphorylated during virus infection of cells in culture.

191 ming large-scale Stable Isotopic Labeling of Cells in Culture (SILAC) quantitative proteomics combine

192 f label-free and stable isotope labelling of cells in culture (SILAC) based proteomic strategies in t

193 ociates with the endo/lysosomal machinery of cells in culture, suggesting that it functions at these

194 ters secreted into the conditioned medium of cells in culture or into blood in vivo have shown to be

195 sion, mKate2, and increased total numbers of cells in culture, suggesting these chaperones partly rec

196 A population of cells in culture displays a range of phenotypic response

197 as for effects on the cytological profile of cells in culture.

198 sor for detection of proliferation status of cells in culture and in animals.

199 similar findings in humans, as do studies of cells in culture.

200 of cargo into live animals and a variety of cells in culture without the need for complicated geneti

201 s reversibility and the general viability of cells in culture.

202 Here we predict theoretically the effect on cells in culture of locally introduced biochemical signa

203 ted delivery of hCD59 to the RPE, cornea, or cells in culture protects those cells from human MAC dep

204 ezrin-mediated motility of osteosarcoma (OS) cells in culture.

205 expression analysis of human dermal papilla cells in culture and discovered very rapid and profound

206 -mediated phagocytosis of human SCLC patient cells in culture.

207 ic effects in reducing proliferation of PDAC cells in culture and growth of xenograft tumors in mice.

208 ic effects in reducing proliferation of PDAC cells in culture and the growth of xenograft tumours.

209 MicroRNA-218 prevents proliferation of PDAC cells in culture, and tumor growth and metastasis in nud

210 usly cross the plasma membrane and penetrate cells in culture, retaining HIV-1 inhibitory activity.

211 creased mitochondrial membrane potential per cell in cultured hepatocytes after hypoxia-reoxygenation

212 ically labeled forms is carried out by plant cells in culture, followed by careful fractionation.

213 gher concentrations killed long-lived plasma cells in cultured thymus cells from nine early-onset MG

214 nhanced chromosomal instability of polyploid cells in culture suggests that such cells contribute to

215 been demonstrated with cell lines or primary cells in culture, their collective responses in vitro ha

216 an CD34(+) hematopoietic stem and progenitor cells in culture ex vivo.

217 GF infection of nestin-tv-a brain progenitor cells in culture.

218 patocytes to dedifferentiate into progenitor cells in culture, and this may potentially have a signif

219 PT cells in culture up-regulate endocytic capacity in respo

220 In R28 retinal cells in culture, hyperglycemic conditions enhanced REDD

221 by half) of caveolin-1 protein levels in RPE cells in culture was sufficient to accelerate or impair

222 recruited to maturing phagolysosomes in RPE cells in culture.

223 iants of Drosophila melanogaster mtSSB in S2 cells in culture caused mtDNA depletion under conditions

224 so enhanced proliferation of mouse satellite cells in culture and maintained their ability to engraft

225 thors hypothesized that Schlemm's canal (SC) cells in culture respond to S1P by increasing actomyosin

226 n of matrix metallopeptidase 7 (MMP7) in SCC cells in culture.

227 y significantly delayed the migration of SCC cells in culture.

228 he proliferation of NF2-deficient schwannoma cells in culture and displayed potent anti-tumor activit

229 irs the proliferation of NF2-null schwannoma cells in culture and inhibits their ability to form tumo

230 een fluorescent protein as a means to select cells in culture that harbor latent virus.

231 ting M1-state capable of attacking senescent cells in culture, whereas proliferating p53-deficient st

232 ool to dissect signaling pathways for single cells in culture but has not previously been used to rev

233 or studying the actin cytoskeleton in single cells in culture, tissues, and multicellular organisms i

234 d volume throughout the cell cycle of single cells in culture and in zebrafish embryos showed that th

235 of UV on melanocytes and other types of skin cells in culture have been studied, but little is known

236 ous population containing both SP and non-SP cells in culture.

237 eotide treatment of human embryo kinase-sst2 cells in culture demonstrated that phosphorylated sst2 w

238 beads and introduced them to embryonic stem cells in culture.

239 -specific regulatory genes in embryonic stem cells in culture.

240 ned as embryonic stem cells or epiblast stem cells in culture.

241 clear how these physical cues influence stem cells in culture.

242 sed differentiation and helped maintain stem cells in culture.

243 regulators of pluripotency in mammalian stem cells in culture.

244 Recent work with pluripotent stem cells in culture has revealed a previously under-appreci

245 ayed implantation model and trophoblast stem cells in culture, we further demonstrate that a coordina

246 Stem cells in cultured tissue respond to insulin and orient t

247 ant Clec11a promoted osteogenesis by stromal cells in culture and increased bone mass in osteoporotic

248 ed osteogenesis by human bone marrow stromal cells in culture and in vivo.

249 ouse ventral medial neuron cultures, SH-SY5Y cells in culture, and isolated mouse lysosomes, we have

250 b blockade significantly increased IL-5(+) T cells in culture.

251 Activated CD4(+) T cells in culture with H. pylori-treated GECs were decrea

252 edominantly immortalizes/transforms CD4(+) T cells in culture.

253 edominantly immortalizes/transforms CD8(+) T cells in culture.

254 effective at generating Ag-specific human T cells in culture, including against complex peptide mixt

255 The novel finding that EBV-2 infects T cells in culture will provide a model to understand the

256 generally failed to readily infect mature T cells in culture.

257 activation-induced elevation of EMMPRIN on T cells in culture and in EAE mice, correspondent with red

258 cline affects the expression of EMMPRIN on T cells in culture and in mice afflicted with EAE.

259 cells, which induces CD4+Foxp3+ regulatory T cells in culture and contributes to immune tolerance med

260 tly promoted survival and proliferation of T cells in cultures from immunized animals, but only when

261 erent plant tissues, such as Arabidopsis T87 cells in culture and fenugreek (Trigonella foenum-graecu

262 lecules, such as DNA plasmids, into targeted cells in culture, yet only a narrow range of laser regim

263 c cells (DCs) are efficient inducers of Th17 cells in culture, including antigen-specific Th17 cells.

264 is study, therefore, we tried to induce Th17 cells in cultures of severely burned patient PBMC by sti

265 DNA during the proliferation of A. thaliana cells in culture.

266 her, these experimental results suggest that cells in culture biologically tune their membrane compos

267 ation and release of type IV collagen by the cells in culture.

268 allenges of generating and maintaining these cells in culture.

269 ticular characteristic of the state of these cells in culture and is not specific to the collagen VI

270 ct on the proliferation or survival of these cells in culture.

271 lable due to the short-lived nature of these cells in culture.

272 The ability to propagate these cells in culture while maintaining their intrinsic linea

273 lpha-synuclein that was exogenously added to cells in culture.

274 henomena were observed when ACE was added to cells in culture: 1) it bound to SMC and EC with high af

275 led that anti-ICAM NCs specifically bound to cells in culture, were internalized via CAM-mediated end

276 viral or lentiviral vectors and delivered to cells in culture or used to generate transgenic mice.

277 have been developed these are best suited to cells in culture and cannot be used in vivo To address t

278 e (env) is the oncogene, as it can transform cells in culture and induce tumors in animals.

279 the proliferation of Hoxa9/Meis1-transformed cells in culture and that loss of C/EBPalpha greatly imp

280 tion in the proliferation of the transformed cells in culture, suggesting that, at least in this cont

281 an virus 40 large T antigen (TAg) transforms cells in culture and induces tumors in rodents.

282 liferation or differentiation of trophoblast cells in culture.

283 Sca-1 mRNA was highly expressed in mouse TS cells in culture, we found that it was also expressed in

284 afforded nanomolar GI50 values against tumor cells in culture.

285 nvasion of MDA-MB-231 and BT-20 breast tumor cells in culture.

286 ing of a reporter gene (luciferase) in tumor cells in culture.

287 Compound 3 inhibited tumor cells in culture with GI50 <or= 10(-7) M.

288 ing Chinese hamster cells and human KB tumor cells in culture.

289 , oncolytic Ad (rAdDelta24) that lyses tumor cells in culture and generates oncolytic progeny virions

290 ive effects of shRNAs on the growth of tumor cells in culture versus in their native microenvironment

291 of Rpn11 that blocks proliferation of tumor cells in culture.

292 ty of the EGF-conjugated GemC18-NPs to tumor cells in culture was correlated to EGFR expression as we

293 umour burden in mice or in killing of tumour cells in culture, while MUC1 glycopeptide-Tetanus toxoid

294 re, we found that tubulogenesis of wild-type cells in culture was inhibited by both an inhibitor of C

295 Unlike cells in culture, the physiological fate of cells that d

296 In addition, results from studies using cells in culture will be used to provide a more complete

297 o affect the growth and viability of various cells in culture.

298 Infection of HEp-2 and Vero cells in culture depends largely on virion G protein bin

299 Experiments with cells in culture showed that treatment with hydrogen per

300 atomically intact tissue, rather than within cells in culture.