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

4 rategy for generating and maintaining acinar cells in culture.

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

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

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

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

9 receptor as essential for the growth of ALCL cells in culture and as patient-derived xenografts.

10 L inhibits cell growth and survival of T-ALL cells in culture and blocks disease progression in a mur

11 mote short-term maintenance of primitive AML cells in culture, no work to date has examined whether a

12 EhVs), both of which display variation among cells in culture and in natural populations.

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

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

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

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

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

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

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

20 ues for the analysis of individual bacterial cells in culture.

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

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

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

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

25 Cancer cells in culture rely on glutamine as an anaplerotic sub

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

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

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

29 ir functional interaction with breast cancer cells in culture and in mice.

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

31 model acquired resistance by exposing cancer cells in culture to gradually increasing concentrations

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

33 doxorubicin, selectively kills liver cancer cells in culture, as the selectivity of the aptamer bind

34 tes resistance to ferroptosis in lung cancer cells in culture and in mouse tumour xenografts.

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

36 ex ligand 20A causes growth arrest of cancer cells in culture and in a HeLa cell xenografted mouse mo

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

38 minates the proliferation capacity of cancer cells in culture, and enhances tumour growth inhibition

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

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

41 markedly enhance the invasiveness of cancer cells in culture.

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

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

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

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

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

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

48 tions were assessed on primary human cardiac cells in culture.

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

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

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

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

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

54 ifferent subpopulations of bovine chromaffin cells in culture.

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

56 retion of IL10, and extended survival of CLL cells in culture.

57 eract with docetaxel and cabazitaxel on CRPC cells in culture and implanted into nude mice.

58 down of LINC00346 inhibited invasion of cSCC cells in culture and suppressed growth of human cSCC xen

59 issue sections and functional assays of cSCC cells in culture showed that LINC00346 expression is dow

60 ily infects murine macrophages and dendritic cells in culture.

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

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

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

64 re selectively retained in actively dividing cells in culture, whereas mCHH is depleted.

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

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

67 he development of hyperplasia of endometrial cells in culture.

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

69 expression on human dermal blood endothelial cells in culture.

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

71 sections and to human glomerular endothelial cells in culture.

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

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

74 oliferation of latently infected endothelial cells in culture, but not their uninfected counterparts.

75 gulated during KSHV infection of endothelial cells in culture.

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

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

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

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

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

81 LINC complex of fibroblastic and epithelial cells in culture.

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

83 196 lincRNAs in murine intestinal epithelial cells in culture.

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

85 5-fold elevated in CF IB3-1 lung epithelial cells in culture, compared with control IB3-1/S9 cells.

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

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

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

89 ted phenotypes in retinal pigment epithelial cells in culture.

90 acterial adherence to respiratory epithelial cells in culture.

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

92 n inhibit gonococcal adherence to epithelial cells in culture.

93 Mice or renal proximal tubular epithelial cells in culture were exposed to cisplatin-induced acute

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

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

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

99 ponential growth phase released 220 exosomes/cell in culture medium.

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

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

102 We choose to use primary human fibroblasts cells in culture (foreskin, FSK) as a physiological mode

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

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

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

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

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

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

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

110 that in human neuronal precursors and glial cells in culture, ZIKV infection activates both mTOR com

111 ilencing AVIL nearly eradicated glioblastoma cells in culture, and dramatically inhibited in vivo xen

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

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

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

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

116 ed gene expression and reduced growth of HCC cells in culture and xenografts of HCC tumors, suggestin

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

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

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

120 endently of adhesive cues in flattened human cells in culture.

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

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

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

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

125 st viral infection in diverse types of human cells in culture.

126 eight upregulated LTRs into recipient human cells in culture showed robust and heterogenous activati

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

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

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

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

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

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

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

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

135 cylation-induced mitochondrial superoxide in cells in culture and in the retina.

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 ureus lipases, prevents activation of innate cells in culture.

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

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

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

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

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

146 at may not be evident from studying isolated cells in culture or bulk tissue.

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

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

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

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

151 and, along with studies of human neuron-like cells in culture, implicates LINC00473 as a CREB effecto

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

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

154 influence their interactions with macrophage cells in culture.

155 domain to promote toxicity against mammalian cells in culture and lethality during mouse bacteremia.

156 R-20, promotes USP-46 abundance in mammalian cells in culture and in C. elegans neurons in vivo Inhib

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

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

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

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

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

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

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

164 FR suppressed the proliferation of melanoma cells in culture and inhibited the growth of Galpha(q)-d

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

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

167 w pentobarbital affects BV2 mouse microglial cells in culture.

168 reshly isolated peripheral blood mononuclear cells in culture.

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

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

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

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 neralization of human arterial smooth muscle cells in culture, as shown by Alizarin red and van Kossa

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

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

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

178 is differentially regulated in GATA3 mutant cells in culture and in tumors bearing similar mutations

179 eved synthetic lethality in multiple myeloma cells in culture and prevented HK1(-)HK2(+) multiple mye

180 llular vesicles (EVs) are secreted by myriad cells in culture and also by unicellular organisms, and

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

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

183 PARP-1 protein in dopaminergic-like neuronal cells in culture.

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

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

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

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

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

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

197 ription factor MYC, and the proliferation of cells in culture, as well as reduced tumor growth in a m

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

201 uman seminal plasma and its toxic effects on cells in culture limit the ability to study in vitro vir

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

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

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

205 rapy-resistant growth of fusion-positive PCa cells in culture and in mice.

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

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

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

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

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

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

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

213 e in infectious virus and fewer RSV-positive cells in cultures after neutrophil exposure than in pree

214 ystal treatment of oligodendrocyte precursor cells in culture resulted in oligodendrocyte maturation

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 The basal keratinocyte progenitor cells in cultured epithelial autografts (CEAs) regenerat

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

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

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

223 recruited to maturing phagolysosomes in RPE cells in culture.

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

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

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

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

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

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

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

231 Here we show that mouse and human SCLC cells in culture and in vivo can grow cellular protrusio

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

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

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

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

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

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

238 Embryonic stem cells in culture self-organise to form spatial patterns

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

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

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

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

243 sed differentiation and helped maintain stem cells in culture.

244 regulators of pluripotency in mammalian stem cells in culture.

245 gulate the function of a broad range of stem cells in culture and in tissue.

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

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

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

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

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 y CD8(+) T cells; we confirmed that CD8(+) T cells in culture targeted these HDV epitopes.

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

255 ive approach to reactivate latent HIV from T cells in culture, it can cause deleterious cytokine dysr

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

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

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

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

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

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

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

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

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 ycan features of a mature tissue rather than cells in culture.

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

268 allenges of generating and maintaining these cells in culture.

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

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

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

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

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

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

275 The sensor by itself is nontoxic to cells in culture and has been used to monitor the real-t

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

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

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

279 However, the use of transformed cells in culture does not provide the same environment t

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

281 e, and suppressor function of long-term Treg cells in culture with EVR were similar to those with RAP

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

288 vins are able to activate p53 and kill 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 o sufficient to alter proliferation of tumor cells in culture, but not that of normal lymphatic cells

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

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

294 ssed the proliferation of B-Raf(V600E) tumor cells in culture and in vivo, including their B-Raf inhi

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

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

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

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

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

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