ライフサイエンスコーパス: cell line

1 ation in a BRAF(V600E)-mutant human melanoma cell line.

2 s) and integrins, in a gp96-deficient murine cell line.

3 sitions in the AGM region and supportive OP9 cell line.

4 ZIKV isolate in a FcgammaRII-expressing K562 cell line.

5 of the IL-6-dependent B9 mouse plasmacytoma cell line.

6 n the estrogen-responsive MCF7 breast cancer cell line.

7 tacts in live cells from a monkey fibroblast cell line.

8 uantitatively determined and unique for each cell line.

9 n co-transfection experiments in a human RPE cell line.

10 in the human acute myeloid leukemia MOLM-13 cell line.

11 .3 nM) against a large number (93) of cancer cell lines.

12 and long-term rapamycin treatment in sarcoma cell lines.

13 erns in parental and NOTCH1-expressing C2C12 cell lines.

14 erative activities in acute myeloid leukemia cell lines.

15 lastoma and atypical teratoid rhabdoid tumor cell lines.

16 tory papillary and follicular thyroid cancer cell lines.

17 those that reduced viability of 6 human CCA cell lines.

18 genome-wide landscapes in a series of human cell lines.

19 sues as well as pancreatic and breast cancer cell lines.

20 oth endometriotic and endometrial epithelial cell lines.

21 d conjugate was studied in normal and cancer cell lines.

22 pressed in primary ATC samples and human ATC cell lines.

23 rowth inhibition in multiple patient-derived cell lines.

24 losing in three types of immortalized cancer cell lines.

25 ts in C57BL/6 mice in vivo and hematopoietic cell lines.

26 thout significantly affecting EGFR wild-type cell lines.

27 also measured expression by 15 human cancer cell lines.

28 using stably transfected, inducible isogenic cell lines.

29 inhibition of cell growth in acute leukemia cell lines.

30 oid precursor protein transgenic mice and AD cell lines.

31 6(+intron 2)) transcripts in CRC tissues and cell lines.

32 ase I hypersensitivity in one or more ENCODE cell lines.

33 t, and cell death in sensitive breast cancer cell lines.

34 ed and 344 EFO unique immortalized permanent cell lines.

35 poptosis and proliferation inhibition in AML cell lines.

36 ibroblast), and RAW 264.7 (mouse macrophage) cell lines.

37 ssibility were similar across hiPSC and hESC cell lines.

38 on was observed in MCC tumor tissues and MCC cell lines.

39 T and HDAC pathway blockade in hematological cell lines.

40 ased MAP3K13 mRNA in HNSCC tumor samples and cell lines.

41 aortic endothelial cells and lymphoblastoid cell lines.

42 , and induced cytotoxicity in a panel of AML cell lines.

43 xpression profiles for different tissues and cell-lines.

44 A photoreceptor cell line, 661W, derived from a mouse retinal tumor that

45 nd 4 have shown low cytotoxicity activity in cell line A-431 and low green staining in cells.

46 Treatment of human melanoma cell lines (A375, Hs294t, SK-Mel28 and SK-Mel119) with c

47 ct hundreds of transcripts in lymphoblastoid cell lines across three African populations.

48 tive behaviour was conserved among different cell-lines: all nuclei showed a softer and more viscous

49 k-in of mutant PIK3CA (H1047R) in the MCF10A cell line, an important cell model for studying oncogeni

50 drove proliferation of a human cholangiocyte cell line and demonstrated potent wound healing in mice.

51 iRNA-mediated knockdown of KIF20B in a human cell line and fixed and live imaging, we show that KIF20

52 h alters enhancer activity in a mouse atrial cell line and in embryonic zebrafish and differentially

53 Ca(2+) concentration of HCT116 colon cancer cell line and modified the cytosolic Ca(2+) oscillations

54 RCA2 loss in a non-transformed human mammary cell line and see increased replication stress due to un

55 Nonetheless, systematic differences between cell line and tumor proteomes were apparent, attributabl

56 Dual-auristatin ADCs imparted activity in cell line and xenograft models that are refractory to AD

57 e datasets to survey a total of 1,056 cancer cell lines and 9,250 primary tumors.

58 dy, using acute myeloid leukemia (AML) human cell lines and a custom CRISPR/Cas9 screening platform,

59 t KuQs are highly active toward the analyzed cell lines and almost nontoxic for healthy cell, indicat

60 r of STS subtypes, making development of STS cell lines and animal models representative of the diver

61 -Cas9 essentiality screens across 342 cancer cell lines and applied CERES to this data set.

62 on simulated data as well as prostate cancer cell lines and cfDNA obtained from castration-resistant

63 It was then used to treat cell lines and compared with cisplatin and carboplatin a

64 entified gene were measured in 9 human liver cell lines and compared with expression profiles of its

65 omparison of protein scavenging rates across cell lines and conditions.

66 alpha pathway was also observed in human HCC cell lines and datasets.

67 phate (GTP) in untransformed and transformed cell lines and determine this phenomenon depends on the

68 human embryonic and induced pluripotent stem cell lines and have potential applications for both dise

69 ure to infer MAE for genes in lymphoblastoid cell lines and human fetal brain tissue.

70 displayed increased uptake in two different cell lines and improved proteolytic stability.

71 y predict the fitness costs of passengers in cell lines and in human breast cancers.

72 titutively in a panel of basal breast cancer cell lines and in more than one third of basal tumors.

73 cardiac stress response using bioengineered cell lines and mouse models containing either isoform of

74 cted in preclinical studies, typically using cell lines and mouse models.

75 n effectively promotes apoptosis in leukemia cell lines and patient samples while sparing healthy cel

76 Both alterations are also detectable in PDAC cell lines and patient specimens.

77 In multiple glioma cell lines and patient-derived glioma stem cells (GSCs),

78 n compared to commonly used, immortalized TB cell lines and primary cells from term placenta.

79 in expression induced chemoresistance of AML cell lines and primary cells in vitro and in vivo.

80 We expressed the mutation in cell lines and primary cultures, and we evaluated the pu

81 gy and in vitro culture of murine fibroblast cell lines and primary fibroblasts and human epithelial

82 In studies of hepatoma cell lines and primary human hepatocytes, we found that

83 ases CD20 levels in established B-cell tumor cell lines and primary malignant cells.

84 le and female transgenic mice in vivo and in cell lines and primary neuronal culture derived from tim

85 AZ20 caused proliferation inhibition in AML cell lines and primary patient samples.

86 Suppression of GnT-III in EOC cell lines and primary tumor-derived cells resulted in a

87 gy that contains information of immortalized cell lines and relevant experimental components.

88 s overexpressed in a panel of ovarian cancer cell lines and that MICU1 overexpression correlates with

89 lated in human papillomavirus (HPV)-infected cell lines and tissues.

90 potentially applicable to other pluripotent cell lines and to generating other forms of muscle.

91 signature drove clustering of breast cancer cell lines and tumors into the common subtypes and corre

92 and Western blotting-in several nonprostatic cell lines and xenografts of melanoma and small cell lun

93 tant lacking only this alpha-helix in stable cell lines and Xenopus laevis photoreceptors.

94 the epithelioma papulosum cyprini [EPC] fish cell line) and in vivo (using rainbow trout fry) in a do

95 ific methylation and nucleosome occupancy in cell lines, and colon and tumor samples, and by benchmar

96 mouse models of colorectal cancer (CRC), CRC cell lines, and mouse and human normal and cancer colono

97 mphocytic leukaemia and mantle cell lymphoma cell lines, and patients treated with idelalisib, but no

98 enchymal transition in human prostate cancer cell lines, and stable overexpression of miR-194 enhance

99 bs) manufactured from immortalized mammalian cell lines are becoming increasingly important as therap

100 investigate the biology of HGSC, and the ID8 cell lines are freely available to researchers.

101 erimental models: the human-derived RPE-like cell line ARPE-19, cultured murine primary RPE cells, an

102 Using the mouse endothelial-derived EOMA cell line as a model of HE, we explored the regulatory e

103 ent drug response data for a large cohort of cell lines as a heterogeneous network.

104 re we demonstrate, using a variety of cancer cell lines as well as activated primary T cells, that cy

105 heir endogenous forms were detected in human cell lines as well.

106 ecretion in mouse neuroblastoma and striatal cell lines, as well as in primary neurons.

107 differentially required in subsets of these cell lines at a threshold of six SDs from the mean.

108 h has been hampered by limited human sarcoma cell line availability and the large number of STS subty

109 Transgenic- and cell line-based experiments have identified 5'-flanking

110 Here, we developed 3D cell-line-based models of human syncytiotrophoblasts, ce

111 V replication and oncolysis in all resistant cell lines but only partially improve the susceptibility

112 ed cytotoxic activity against HeLa and HT-29 cell lines, but were inactive towards MRC-5 and MCF7.

113 ly quantify parasite infection of hepatocyte cell lines by flow cytometry.

114 (CO) reduced GSH/GSSG in three breast cancer cell lines by inhibiting CBS.

115 lular cholesterol content in prostate cancer cell lines by inhibiting the activation of sterol regula

116 the effect of anti-cancer drugs in cultured cell lines by monitoring phosphatidylserine translocatio

117 reduces the toxicity of Taxol towards cancer cell lines by over 200-fold.

118 In this study, we present a novel reporter cell line capable of detecting live ebolaviruses.

119 Cancer cell lines carrying genetic aberrations that impair the

120 Using MCF 10A cell line cells as an example, we demonstrated how to on

121 ll assays using Madin-Darby canine kidney II cell line cells stably expressing specific uptake and/or

122 th 5 x 10(6) rat colorectal liver metastasis cell line cells.

123 nduce similar transcriptional changes across cell lines, changes induced by drugs that inhibit intra-

124 viruses produced by transformed lymphocytic cell lines chronically infected with HTLV-1, particularl

125 alyzed a panel of 17 KRAS mutant lung cancer cell lines classified as K-Ras-dependent or -independent

126 ifferences in BER capacity across a panel of cell lines collected from healthy individuals, and to ge

127 pression data newly generated for 448 cancer cell lines, combined with publicly available datasets to

128 terfering RNA (P < 0.01-0.001 for responding cell lines), compared with vehicle treatment.

129 t HepAD38 cells, a widely-used HBV-inducible cell line, contain cell clones with diverse permissivene

130 for tumor tissue cores (R2 = 0.42-0.91) and cell line cores (R2 = 0.83-0.97) by quantitative immunof

131 In addition, both cell lines cultured on the T-MOC showed increased resist

132 for the FUT6 variant rs78060698 using HepG2 cell line demonstrated strong allele-specific promoter a

133 Analyses of these cell lines demonstrated that the epithelial cells with s

134 Prostate cancer cell lines derived from HiMyc tumors (HMVP2 and derivati

135 B-468) than normal breast cells (MCF-10A) or cell lines derived from other tumor types.

136 study, we examined the AR cistrome in a PCa cell line-derived CRPC model using integrated bioinforma

137 Glial cell line-derived neurotrophic factor (GDNF) binds GDNF

138 IFICANCE STATEMENT Delivery of ectopic glial cell line-derived neurotrophic factor (GDNF) promotes th

139 The UL46-expressing cell lines did not activate interferon-stimulated gene (

140 arboring a different oncogenic driver (K-562 cell line) did not result in selective growth inhibition

141 extracted from human lung and breast cancer cell lines, discriminating between the cancer-positive a

142 ived from HiMyc tumors (HMVP2 and derivative cell lines) displayed increased protein expression of bo

143 it most prominently reduces the workload of cell-line editing, which may be completed within 4 weeks

144 ss all major types of cancer from the Cancer Cell Line Encyclopedia, which provides genetic and expre

145 ing NAPRT levels in a BRCA2-deficient cancer cell line exacerbated DNA damage in response to chemothe

146 d to be over-expressed in all ovarian cancer cell lines examined and upregulated by mutated TP53, a g

147 e of RB-intact basal-like type breast cancer cell lines exhibited a similar phenotype following RB de

148 The rho0 cell lines exhibited increased sensitivity to PLX4720 co

149 tate the VLP platform, we generated a stable cell line expressing high levels of ZIKV prM-E proteins

150 hat constitutively produce VLPs as well as a cell line expressing ZIKV C-prM-E proteins for RVP produ

151 te this question, we developed breast cancer cell lines expressing an inducible, constitutively activ

152 inate between normal and human breast cancer cell lines (fibrocystic and metastatic states) as well a

153 d following cisplatin- or Taxol-treatment in cell lines from both cancer types and was associated wit

154 Text labels of cell lines from both ontologies were verified by biologi

155 c and 7 non-fibrotic conjunctival fibroblast cell lines from patients with and without previous glauc

156 r AsiDNA treatment was validated in 43 tumor cell lines from various tissues and 15 models of cell- a

157 cal-scale protocol to generate BK-specific T cell lines from viremic KTR.

158 Overall, the BCa cell line genomic aberrations were concordant with those

159 When CBL was knocked down in the mutant cell line H1975 (erlotinib-resistant), it became sensiti

160 ibition of cell growth in the drug-resistant cell line H1975, without significantly affecting EGFR wi

161 ively inhibits cell growth in human leukemia cell lines harboring MLL translocations and is >40 times

162 an isogenic pair of human colorectal cancer cell lines harboring mutant or wild-type KRAS.

163 ts with colon, breast, or ovarian cancer and cell lines harboring specific oncogenic mutations and re

164 ubcellular organelles and the lack of stable cell lines have prevented routine application of this te

165 Many of these cell lines have publicly available, high-quality DNA, RN

166 ear cells] and epithelial and iNKT-hybridoma cell lines) have been used to determine the immunologica

167 d compared the results with a drug resistant cell line, HCC1954.

168 types (the human brain capillary endothelial cell line hCMEC/D3 and human umbilical vein endothelial

169 50 = 369 muM), high efficiency against other cell lines (HCT 116 and HeLa), and possible activation b

170 ver, by utilizing the human embryonic kidney cell line HEK293T, it was possible to demonstrate that P

171 noglycosides G418 and gentamicin in hepatoma cell lines (HepG2, Hep3B and Hepa1-6) and in experimenta

172 fects using a human hepatocellular carcinoma cell line, HepG2 cells.

173 sent study, in vitro cell models using a HCC cell line, HepG2, and human endothelial cells, HUVECs, a

174 enteric windows (ex vivo) and the human mast cell line HMC-1.

175 basophil cell line KU812 and the human mast cell line HMC-1.

176 ting cAMP signaling in the mouse hippocampal cell line HT-22 leading to an increase in CREB phosphory

177 man cells, we established several human stem cell lines: human embryonic stem cell (hESC) line carryi

178 Evaluation of CRPC cell lines identified resistant vs sensitive in vitro mo

179 n Caenorhabditis elegans and in chondrogenic cell lines implicated variants in genes necessary for tr

180 showed there was a tendency to describe the cell line in accordance with the description in the cite

181 nts, reduced the invasion of prostate cancer cell lines in 3D in vitro assays.

182 ivities often improves the stratification of cell lines in response to drug treatment.

183 variant libraries in transfectable mammalian cell lines in two steps.

184 imary cancer specimens in vivo and in cancer cell lines in vitro.

185 (9b-9n, 10) were evaluated on various cancer cell lines including, MCF-7 breast, HL-60 leukemia, MIA

186 Many different human cell lines, including both normal and cancer cells, appe

187 In cell lines, including HIV-1 latency models, increased HI

188 imary human CD4(+) T cells into immortalized cell lines indistinguishable from patient-derived ALK+ A

189 etic parameters vary significantly among the cell lines investigated.

190 The utility of cancer cell lines is affected by the similarity to endogenous t

191 ulation in metastatic tumors and mesenchymal cell lines is coordinated to that of collagen.

192 tant 4R-Tau isoform in neuroblastoma SH-SY5Y cell lines is sufficient to induce monopolar spindles.

193 Utilizing a reporter cell-line it was confirmed that LCM activated TLR4.

194 q data of the human chronic myeloid leukemia cell line K562 in response to shRNA knockdown of the RNA

195 se drugs on the growth of the human basophil cell line KU812 and the human mast cell line HMC-1.

196 or inhibition of endogenous TAK1 in hepatoma cell lines leads to an upregulation of HBV replication,

197 Expression of MAN2A1-FER in 4 cell lines led to epidermal growth factor receptor activ

198 EK293-RXFP1 cAMP assay and the human hepatic cell line LX-2.

199 detection from real samples of breast cancer cell line, MCF-7.

200 nt at inhibiting the growth of breast cancer cell lines (MCF7, MCF7/VP16, BT474, T47D, ZR-75-1, SKBR3

201 For in vivo studies, a human breast cancer cell line (MDA-231) was implanted in five mice per group

202 oss of function mutations in human and mouse cell lines measured by FLAER labelling.

203 expression in a mouse insulin-secreting PNET cell line, MIN6, downregulates c-Met expression.

204 By continuously exposing the gastric cancer cell line MKN45 to 5-FU for >100 passages, we establishe

205 CA11 overexpression in a t(4;14)-negative MM cell line, MM1.S, demonstrated enhanced reactive oxygen

206 overexpression, knockdown and Pak1 knockout cell line models showed that Pak1 confers protection to

207 Coculture of the AML cell lines MOLM-4, THP-1 or primary AML cells with donor

208 ic and extrahepatic cholangiocarcinoma (CCA) cell lines, Mz-ChA-1, TFK-1, SG231, CCLP, HuCCT-1, and H

209 Indeed, after transduction, the NK cell line NK-92 became TCR positive and reacted against

210 es from a nontumorigenic prostate epithelial cell line (NMVP cells).

211 However, in a motor neuron cell line, NSC34, E478G mutant of OPTN but not E50K and

212 e growth of multiple RAS-mutant human cancer cell lines of diverse tissue origin by blockade of nucle

213 % growth inhibition = 0.2 mum) in almost all cell lines of the National Cancer Institute (NCI)-60 cel

214 targeting JAK for ALK- ALCL, we treated ALK- cell lines of various histological origins with JAK inhi

215 The Cell Ontology (CL) and Cell Line Ontology (CLO) have long been established as r

216 The Cell Line Ontology (CLO) is an OBO community-based ontol

217 However, due to the lack of any stable flea cell line or a published flea genome sequence, little is

218 -expressing hepatocellular carcinoma (HepG2) cell line or immortalized human hepatocytes (IHH) and ac

219 ared to monolayer cultures of ovarian cancer cell lines or primary cells.

220 and primary fibroblasts and human epithelial cell lines or primary human epithelial cells exposed to

221 xamine the effect of these haplotypes on CRC cell lines, our results suggest that inflammation and et

222 DNA damage was studied in two ovarian cancer cell lines (OVCAR3 and A2780), normal hamster ovary cont

223 n against the National Cancer Institute's 60-cell line panel and allowed us to obtain an X-ray co-cry

224 ap subunit of the TIP60 complex, both in the cell line panel and in a human tumor data set.

225 Experiments involving a human cancer cell line panel and mouse xenografts revealed that 6OTD

226 lls, was severely down-regulated in vitiligo cell line PIG3V and skin biopsy samples from vitiligo pa

227 echanistic analyses revealed that each tumor cell line presented AH1, a common endogenous retroviral

228 None of the studied BC cell lines presented hypermethylation of the BRCA1 promo

229 in a cohort of low-passage pancreatic cancer cell lines, primary patient-derived xenografts, and panc

230 ly enhanced by co-culture of leukocytes with cell lines prior to molecular and immunologic tests.

231 mice bearing LNCaP and PC-3 (prostate cancer cell line; PSMA-negative) tumors.

232 f TCR signaling restoration in LAT-deficient cell lines reconstituted with a synthetic LAT gene beari

233 rooted in defective glycine uptake in DLBCL cell lines, rendering them uniquely dependent upon SHMT

234 y studies in human tumors, cancer models and cell lines reveal transcriptional reprogramming that sup

235 as established in human NF1-associated MPNST cell lines (S462, T265, NSF1), and functional effects on

236 es of the National Cancer Institute (NCI)-60 cell line screen and relatively selective cytotoxicity a

237 logical investigation of 2-5 on human cancer cell lines showed enhancement of antiproliferative effec

238 ssion of GFP-tagged POMP10 in inducible RNAi cell lines shows that its mitochondrial localization dep

239 ase inhibition with CB-839 or BPTES, the RCC cell lines SN12PM-6-1 (SN12) and 786-O exhibited decreas

240 We found significant, coherent and non-cell line specific changes in fatty acids, glycerophosph

241 e peptide (GLP-1), using the enteroendocrine cell line, STC-1.

242 ppress let-7 target genes in multiple cancer cell lines such as HMGA2 and MYC.

243 TF binding is transferable across TFs and/or cell lines suggesting there are a set of universal "rule

244 ERK phosphorylation and growth in a melanoma cell line, suggesting that it may provide a highly selec

245 KPNA4 reduces cell migration in multiple PCa cell lines, suggesting a role of KPNA4 in PCa progressio

246 , and SIN3A from the cell lysate of the TNBC cell line SUM149.

247 ndividual haploid mouse embryonic stem (mES) cell lines targeting 16,970 genes with genetically barco

248 esponses in primary human lymphoid cells and cell lines that express CXCR4.

249 Cell lines that expressed MAN2A1-FER had increased proli

250 examine in mouse and in a mouse limb-derived cell line the dynamic events that activate and restrict

251 Cells lining the proximal tubule (PT) of the kidney are

252 rve that depletion of BICD2 in the monocytic cell line THP-1 results in an induction of IFN-stimulate

253 th a low or high FcRn-expressing endothelium cell line to clearly define the FcRn involvement, intrac

254 A robust cell line to study the novel molecular biology of ascovi

255 the proteomes of 10 human pancreatic cancer cell lines to a depth of >8,700 quantified proteins.

256 rect and indirect assays in 12 breast cancer cell lines to estimate the spontaneous occurrence of sin

257 ssion levels were quantified on 20 different cell lines to identify appropriate model cells for in vi

258 ic and epigenomic study in patient-derived B-cell lines to investigate the genome-scale effects of DN

259 y driven by experimental variables including cell lines to organize and describe the diverse experime

260 provides genetic and expression data of 496 cell lines together with their response to 24 common ant

261 Recently developed osteocytic cell lines-together with new genome editing tools-has al

262 ed actin depolymerization and apoptosis, and cell line transfection.

263 47-dependent phosphoproteome in the Jurkat T cell line upon treatment with T cell stimulating agents.

264 d pharmacogenomic data in cancer tissues and cell lines using a global statistical model connecting p

265 e sensitive and Pgp overexpressing resistant cell lines was found to correlate directly with an impac

266 mprehensive phosphoproteome analysis of ALCL cell lines was performed in the presence or absence of N

267 from PGE2-G response-positive and -negative cell lines was subjected to transcriptome-wide RNA seque

268 One difference between native cells and cell lines was the time absent from a fluid-phase comple

269 ically, using the RAW 264.7 mouse macrophage cell line we show that whole OSPW containing naphthenic

270 For 95 MHC homozygous cell lines we assembled, de novo, a set of high-fidelity

271 melanocytes and a highly pigmented melanoma cell line, we demonstrate that reduced expression of eit

272 For each cell line, we monitored constitutive PARP activation, sp

273 Besides cell lines, we could observe chromatin interactions by a

274 h genomic analysis of colorectal cancers and cell lines, we find frequent loss of heterozygosity and

275 ce of genetic dependencies observed in human cell lines, we performed a secondary screen in a syngene

276 their human TERC knockout-derived ALT human cell lines, we show that ALT cells harbor more fragile t

277 ining lysates from an insulin-producing beta-cell line were implanted subcutaneously in autoimmune di

278 y was demonstrated in acute myeloid leukemia cell lines, where significant impairment of proliferatio

279 We generated Huh7 cell lines which ectopically express wild-type and NEDDy

280 infected with HTLV-1, particularly the MT-2 cell line, which harbors truncated proviruses and expres

281 on; a common choice of calibrator is the 8E5 cell line, which is assumed to be stable and to contain

282 Removal of stroma enables outgrowth of PKD cell lines, which exhibit defects in PC1 expression and

283 CL2L11 or CDH9 will enhance the migration of cell lines, which provides evidence that these two genes

284 tenance under growth factor supplements into cell lines, which usually takes >6 months and results in

285 NK1 were observed in a human collecting duct cell line, while SPAK was unaltered.

286 riety of TLR-transfected human embryonic 293 cell lines, while the PF-deficient mutants lacked the ab

287 ncogenic KRAS derived from a murine isogenic cell line with a coexpression network derived by integra

288 screened a library of 60,000 shRNAs using a cell line with a MeCP2 reporter on the Xi and found 30 g

289 in vitro and in vivo proliferation rates of cell lines with aberrant activation of the Hedgehog sign

290 rotein synthesis in patient-derived melanoma cell lines with acquired resistance to combined treatmen

291 Similarly, human colorectal cancer cell lines with increased KRAS mutant allele frequency w

292 incubated with MIR21 inhibitors, and stable cell lines with inducible expression of MIR21.

293 AIR-overexpressing ovarian and breast cancer cell lines with PNAs decreased invasion and increased ch

294 reduced viability of two basal breast cancer cell lines with pronounced endogenous overexpression of

295 r metabolic profiles of four prostate cancer cell lines with varying degrees of aggressiveness.

296 Transfection of cell lines with ZNHIT3 expression vectors showed that th

297 atment of MLL-fusion leukaemia cells (MV4;11 cell line) with the BET bromodomain inhibitor I-BET151 r

298 etween hiPSCs and hESCs, and clustering of 4 cell lines within each time point demonstrated that chan

299 e in vitro results were confirmed in various cell line xenograft and patient-derived xenograft mouse

300 d to extend animal survival to >90 days in a cell-line xenograft model of disseminated ovarian cancer