ライフサイエンスコーパス: immortalize

1 Immortalized and malignant EBV-carrying B-cell lines wer

2 expression and silencing studies of FOSL1 in immortalized and primary HPMEC demonstrated that baselin

3 c sonoporation method to deliver plasmids to immortalized and primary human cell types, based on pore

4 ted T-cell lines promote KSHV infectivity in immortalized and primary human oral epithelial cells.

5 We show, using immortalized and primary keratinocytes, that S. aureus p

6 ted T-cell lines promote KSHV infectivity in immortalized and primary oral epithelial cells.

7 ) and upregulation of interleukin (IL)-17 in immortalized and primary patient-derived malignant and n

8 cells from two people exposed to DENV4 were immortalized and screened to identify DENV-specific clon

9 to increased autophagic flux in both normal-immortalized and tumor-derived cell lines.

10 derived nonneuronal cell lines (cancerous or immortalized) and found significant subpopulations that

11 ones, histone variants, and PTMs in primary, immortalized, and transformed cells.

12 1970s when Georges Kohler and Cesar Milstein immortalized antibody-producing mouse B-lymphocytes by f

13 Here, we used immortalized Arabidopsis cell suspensions to sort replic

14 induced chromatin relaxation and observed in immortalized as compared to normal cellular states.

15 Engagement of both the BCR and CR3, on immortalized as well as primary murine B cells and human

16 o escape contact inhibition, and transformed immortalized astrocytes, supporting AVIL being a bona fi

17 t lipoprotein particle standards produced by immortalized astrocytes.

18 V-2 isolates, compromised in the capacity to immortalize B cells, infect CD3(+) T cells ex vivo and p

19 for HPA-1a, named 26.4, was derived from an immortalized B cell from an alloimmunized woman who had

20 We utilized immortalized B cells (IBCs) from 32 childhood asthmatics

21 In immortalized B cells from these patients, the D427ins17

22 NFkappaB and is critical for survival of EBV-immortalized B cells.

23 te adhesion deficiency (LAD) patient-derived immortalized B lymphocytes, where nearly 70% of alleles

24 e used iPSCs derived from Epstein-Barr virus-immortalized B-lymphocytes to verify that the hyperexcit

25 EBV infects and immortalizes B cells in vitro and in vivo.

26 We exposed preneoplastic, hTERT-immortalized Barrett's cell, CP-C and CP-A, to the oncog

27 ls; this can be replicated using LAE and SAE immortalized basal cell lines derived from healthy nonsm

28 99.52% of BCa cells, but only 47.47% of the immortalized benign bladder epithelial cells.

29 Cai and adenosine were measured in fresh or immortalized blood lymphocytes incubated with 0-10 mM 4-

30 circadian manner and is induced during both immortalized bone marrow derived stromal cell (iBMSC) as

31 ween miR-181a and the circadian machinery in immortalized bone marrow stromal cells and adipose deriv

32 DR77 in breast cancer cell lines relative to immortalized breast epithelial cells.

33 ntial to enhance the cell viability of human immortalized bronchial epithelial cell line of Beas-2B.

34 red the inducible activation of oncogenes in immortalized bronchial epithelial cells.

35 ensitivity to otherwise resistant telomerase-immortalized bronchial epithelial cells.

36 ma cells, stable overexpression of BAP1 into immortalized but non-transformed melanocytes did suppres

37 orced expression of MCM8 in RWPE1 cells, the immortalized but non-transformed prostate epithelial cel

38 estricted to keratinocyte-derived cell lines immortalized by HPV due to the lack of experimental syst

39 Immortalized cancer cell lines are widely used in cancer

40 umor immunotherapy models have reconstituted immortalized cancer cell lines with immune components, o

41 ayed culture wound closing in three types of immortalized cancer cell lines.

42 HMMR over-expression in immortalized cancer cells induces phenotypes consistent

43 AS activation does not cooperate with MA4 to immortalize CD34(+) HSPCs.

44 ophagy in HTLV-1-transformed T cells and Tax-immortalized CD4 memory T cells.

45 fection, but this has mostly been limited to immortalized cell culture models.

46 to rodent models, we explored the use of an immortalized cell line derived from human dorsal root ga

47 Here, we use Oli-neu cells, an immortalized cell line derived from primary murine oligo

48 resident immune cells of the brain, and the immortalized cell line of human microglia-SV40.

49 ally, we have demonstrated the utility of an immortalized cell line to produce a high yield of exosom

50 studies in UB/OC-1 cells, an organ of Corti immortalized cell line, showed that R-PIA reduced cispla

51 sosomal phenotypes and cell toxicity in both immortalized cell lines and neurons.

52 rence detector in situ assay in a variety of immortalized cell lines and primary human airway smooth

53 -based ontology that contains information of immortalized cell lines and relevant experimental compon

54 ral nervous tissue or exogenously expressing immortalized cell lines as common mechanisms throughout

55 Ectopically expressed NLRP2 in immortalized cell lines assembles an inflammasome and in

56 In the 'Immortalized cell lines column, the 'Expansion/Scalabili

57 Research in transformed immortalized cell lines indicates the cadherin-related f

58 ansforming primary human CD4(+) T cells into immortalized cell lines indistinguishable from patient-d

59 We generated mixed immortalized cell lines that stably maintained their cha

60 ng (ChIP-seq) analyses have focused on a few immortalized cell lines whose activities and physiology

61 ads from 46 primary cell types, 42 cancer or immortalized cell lines, and 26 tissues.

62 cell culture tools, including primary cells, immortalized cell lines, human stem cells, and their mor

63 ition characteristic of fibroblasts and many immortalized cell lines.

64 h were recurrently affected in the set of 25 immortalized cell lines.

65 ompetent primary sheep endothelial cells and immortalized cell lines.

66 ial agents when delivering genes to multiple immortalized cell lines.

67 n transform primary human B lymphocytes into immortalized cell lines.

68 sing stably expressed non-native proteins in immortalized cell lines.

69 y murine choroid plexus epithelial cells and immortalized cell lines.

70 protein nephrin, and colocalizes with it in immortalized cell lines.

71 (BCL-2) to early-infected (MCL-1/BCL-2) and immortalized cells (BFL-1).

72 The immortalized cells differentiate efficiently into mature

73 cells is smaller than that produced in other immortalized cells due to cleavage.

74 In addition, in contrast to drug-treated, immortalized cells in vitro, mature motor neurons rarely

75 esent at attenuated levels, in spontaneously immortalized cells provide insights into the role of oxi

76 t 100-fold more selective for AML than solid immortalized cells such as HEK293 or human peripheral bl

77 the prevailing mutation type in the treated immortalized cells was A:T->C:G transversion, with a uni

78 Notably, unlike immortalized cells, all treated cell populations eventua

79 models tested (e.g., between primary cells, immortalized cells, and in cocultures of immortalized hu

80 ere genetically stable, highly attenuated in immortalized cells, had defects in replication and sprea

81 nd swine influenza viruses replicated in the immortalized cells, which generally yielded higher-titer

82 hotosensitization-induced mutagenesis in the immortalized cells, which were present at attenuated lev

83 n vivo and ex vivo, but is not needed in non-immortalized cells, while PAK4 overexpression in untrans

84 ose frequency was intensified in the treated immortalized cells.

85 nd differentiation potential, or have become immortalized cells.

86 as shown to induce tumorigenic phenotypes in immortalized cells.

87 nvironment, which impacts viral infection in immortalized cells.

88 established as a potent hCAR deactivator in immortalized cells; whether it inhibits hCAR activity un

89 GAs present several limitations due to their immortalized characteristics, and NHAs represent an inno

90 heir ability to increase the permeability of immortalized choroid plexus epithelium monolayers in vit

91 ty, we have developed multiple conditionally immortalized clonal preadipocyte lines from white adipos

92 Here we successfully "pseudo-immortalized" cochlear progenitor cells using the "condi

93 senescent cells which was augmented in their immortalized counterparts.

94 n complex, partially restores TERC levels in immortalized DKC1 mutant cells, but it remains unknown i

95 In contrast, immortalized DPCs have high resemblance to intact dermal

96 MVA biomanufactured on an immortalized duck cell line shows potential for very lar

97 We have taken an alternative approach, immortalizing early adult erythroblasts generating a sta

98 d a lack of viral replication in primary and immortalized EFB-derived cell lines.

99 idbody (cytokinesis) during cell division in immortalized epithelial cells as well as breast, ovarian

100 differentiation of an enucleation-competent immortalized erythroblast cell line (BEL-A) support both

101 ablish the use of reticulocytes derived from immortalized erythroblasts as a powerful model system to

102 on of AKT signaling in cancer cell lines and immortalized esophageal epithelial cells.

103 The immortalized expression proved a powerful confirmation o

104 For example, when analyzing the same immortalized F2 rice population genotypic data examined

105 lecules were evaluated for two conditionally immortalized fetal NSC lines derived from the cortical a

106 Viral entry into TAg-immortalized fibroblasts could largely be rescued by PDG

107 a overexpression in either HeLa cells or TAg-immortalized fibroblasts, suggesting additional restrict

108 Here, we show that EBV-immortalized FSHD lymphoblastoid cell lines express DUX4

109 ld-type YAP, or constitutively active YAP in immortalized FTSECs, induced cell proliferation, migrati

110 Primary and immortalized GAR22beta(-/-) Sertoli cells moved faster t

111 erior pituitary cells and Asic1 and Asic2 in immortalized GH3 pituitary cells.

112 .3 and 3.4 muM), was evaluated in telomerase immortalized gingival keratinocytes (TIGKs) by measuring

113 this hypothesis, primary rat hepatocytes or immortalized H4IIEC3 rat hepatoma cells were treated wit

114 We observed that knockdown of AE2 sensitized immortalized H69 human cholangiocytes to not only bile s

115 single-cell movement and signaling in human immortalized HaCaT keratinocytes treated with soluble or

116 able tissues from genetically engineered and immortalized HEK293 cells with well-characterized electr

117 the mechanism by which that occurs, using an immortalized hematopoietic progenitor cell line, EML-C1,

118 rogression, we performed in vitro studies on immortalized hepatic stellate cells (LX-2).

119 An immortalized hepatocyte cell line (HHL-17) stably expres

120 ing positive-strand RNA virus replication in immortalized hepatocytes and identified an unexpected ro

121 ach, we generated and subsequently subjected immortalized heterozygous R349P desmin knock-in myoblast

122 Here, we found that TGFbeta treatment of immortalized HSCs (i.e. LX-2 cells) induces phosphorylat

123 Primary human HSCs and immortalized HSCs (LX2 cells) were incubated with condit

124 lthough the MLL-CHD fusion protein failed to immortalize HSPCs in myeloid conditions in vitro, it cou

125 In immortalized human airway smooth muscle (ASM) cells, Sul

126 ls, immortalized cells, and in cocultures of immortalized human and murine cells).

127 tion thrombin directly injured conditionally immortalized human and rat podocytes.

128 ty of (a) an in vitro model using hTERT/Cdk4 immortalized human bronchial epithelial cell lines to id

129 d a quantitative global proteome analysis of immortalized human bronchial epithelial cells (HBEC3-KT)

130 Telomerase immortalized human bronchial epithelial cells (HBECs) wi

131 In contrast, NuLi-1 immortalized human bronchial epithelial cells did expres

132 The data support the hypothesis that immortalized human cardiomyocytes exposed to Ketoprofen

133 Ketoprofen in comparison with Diclofenac in immortalized human cardiomyocytes.

134 owever, have been hampered by the lack of an immortalized human cell line derived from oligodendrocyt

135 ne, mirrored their Neuro-2a activity in four immortalized human cell lines and in a human neuroprogen

136 sing for the identified compounds in several immortalized human cell lines as well as normal diploid

137 from karyotypically normal primary and hTERT-immortalized human cell lines to catalog NORs in terms o

138 Ectopic expression of PGBD5 in primary immortalized human cells was sufficient to promote cell

139 e pluripotent, primary, differentiating, and immortalized human cells, and demonstrate that a class o

140 on the integrity of tight monolayers of the immortalized human cerebral microvascular endothelial ce

141 hour MMC treatment of primary and telomerase immortalized human corneal limbal epithelial (HCLE) cell

142 We derived immortalized human DPC lines from balding (BAB) and non-

143 Herein we describe the generation of an immortalized human endometrial stromal cell line that us

144 ignaling proteins in decidualized telomerase-immortalized human endometrial stromal cells (dT-HESCs)

145 A workflow was established using telomerase-immortalized human epithelial cells that revealed highly

146 ypersensitivity to oxidative stress in hTERT-immortalized human foreskin fibroblasts (HFF-hTERT).

147 nse of pocket epithelium-derived, telomerase-immortalized human gingival keratinocytes (TIGKs) to mic

148 he current study establishes the response of immortalized human glomerular endothelial cells (GEnC) t

149 Primary or immortalized human hepatic stellate (LX2) cells were exp

150 epatocellular carcinoma (HepG2) cell line or immortalized human hepatocytes (IHH) and activation of i

151 r Ab-dependent cell-mediated cytotoxicity of immortalized human hepatocytes in the presence of CD55-b

152 CV-infected hepatoma cells (Huh7.5 cells) or immortalized human hepatocytes inhibited C3 convertase a

153 Hepatoma cell line and immortalized human hepatocytes transiently transfected o

154 TRPV3 channels endogenously expressed in an immortalized human keratinocyte cell line (HaCaT) and in

155 Incubation of primary or immortalized human keratinocytes with Leishmania infantu

156 reas the effects are much less pronounced in immortalized human keratinocytes.

157 omotes breast cancer initiation in models of immortalized human mammary epithelial cells (HMECs).

158 xpression promotes tumorigenic phenotypes in immortalized human mammary epithelial MCF10A cells and,

159 found that compared with normal primary and immortalized human melanocytes, SIRT3 is significantly o

160 umbilical vein endothelial cells (HUVEC) and immortalized human microvascular endothelial cells (HMEC

161 Using immortalized human myoblasts with a titratable DUX4 tran

162 Using immortalized human myoblasts, we performed RNA-seq analy

163 Using immortalized human myometrial (hTERT-HM) cells stably ex

164 blastoma multiforme (GBM) model derived from immortalized human neural stem/progenitor cells (hNSCs)

165 Rac exchange factor 2 (PREX2) using the same immortalized human NRAS(G12D) melanocytes as the origina

166 Expression of P5P6 in immortalized human pancreatic duct epithelial (HPDE) cel

167 owth and drives PanIN to PDAC progression in immortalized human pancreatic ductal cells.

168 In the present article, using immortalized human podocytes in vitro and a mouse model

169 tide exchange factors that activate Cdc42 in immortalized human podocytes.

170 nt to provide IL-2-independent growth of Tax-immortalized human T cells and increase the tumor format

171 s from wild-type and Elf3 knockout mice, and immortalized human T/C-28a2 and murine ATDC5 cell lines

172 leading to a TFG-RET fusion which transforms immortalized human thyroid cells in a kinase-dependent m

173 TRPV4 to the plasma membrane of primary and immortalized human TM (hTM) cells, and to human and mous

174 LIN28-let-7 axis regulates genes in immortalized human trophoblast cells by targeting the AR

175 study showing regulation of let-7 targets in immortalized human trophoblast cells by the ARID3B-compl

176 KSHV replication, we xeno-grafted telomerase-immortalized human umbilical vein endothelial cells that

177 AE immortalizes human CD34(+) cord blood cells in long-term

178 xpression in human umbilical cord, HUVECs or immortalized HUVECs (HUV-ST).

179 An allopolyploid can be viewed as an immortalized hybrid, with the opportunity to select and

180 vity is not required for PEDV replication in immortalized, IFN-deficient Vero cells, but is important

181 terovirus 71 (EV71), and that contrary to an immortalized intestinal cell line, enteroids induced ant

182 In the first model, an immortalized keratinocyte cell line (NIKS) was used, in

183 normal human epidermal keratinocytes and the immortalized keratinocyte cell line, N/TERT-1.

184 immune genes was confirmed in an ano-genital immortalized keratinocyte cell line, N/Tert-1.

185 tastatic melanoma cell line (SKMEL- 147) and immortalized keratinocyte cells (HaCaT).

186 expression and DNA methylation using normal immortalized keratinocyte lines, NIKS, NIKS-16, NIKS-18,

187 ed cell populations of normal, spontaneously immortalized keratinocytes (NIKS) and NIKS stably transf

188 e expression profiles in human spontaneously immortalized keratinocytes (NIKs) expressing the early g

189 , rare cells positive for Lgr6 expression in immortalized keratinocytes and show that their frequency

190 otypic rafts, and human papillomavirus (HPV)-immortalized keratinocytes are altered in the presence o

191 rometric analysis of conditioned medium from immortalized keratinocytes showed that alpha3beta1 regul

192 in natural lesions and in rafts derived from immortalized keratinocytes.

193 tiation of squamous carcinoma cells and TERT-immortalized keratinocytes.

194 Observations were confirmed in an immortalized line (BEAS-2B) by QRT-PCR and protein assay

195 Telomerase-immortalized lines of control and R258C human dermal fib

196 Primary human LSECs (HLSECs) and immortalized liver endothelial cells (TMNK-1) were expos

197 orroborated in human lung cancer tissues and immortalized lung cancer cell lines via indirect immunof

198 e in multiple lung cell lines, including the immortalized lung cell BEAS-2B.

199 ng cancer driver, its expression transformed immortalized lung epithelial cells while a transgenic mo

200 vels modulate KRAS-induced transformation of immortalized lung epithelial cells.

201 man cancers and transform B lymphocytes into immortalized lymphoblastoid cell lines in vitro.

202 were increased in proband versus control EBV-immortalized lymphoblastoid cell lines.

203 These conditionally immortalized macrophages (CIMs) retain characteristics o

204 ected in the membrane-containing fraction of immortalized macrophages after caspase-11 activation by

205 noclonal antibodies (mAbs) manufactured from immortalized mammalian cell lines are becoming increasin

206 Depleting HOXA5 in immortalized MCF10A or transformed MCF10A-Kras cells red

207 otential of Hs294T melanoma cells and normal immortalized Mel-ST melanocytes.

208 PARP1 also transformed TERT-immortalized melanocytes expressing BRAF(V600E).

209 and tracked DAT's postendocytic itinerary in immortalized mesencephalic cells.

210 iopsies (n = 13), and primary peritoneal and immortalized mesothelial cells (MeT5A) by immunohistoche

211 ture models, such as SVG-A cells (SVGAs), an immortalized, mixed population of glial cells transforme

212 zed with EBV gp350 is capable of efficiently immortalizing monkey B cells in vitro and reproduces acu

213 xpression, and adhesion of human primary and immortalized monocytes (Mono Mac 6) were measured.

214 fer NAI resistance in avian viruses grown in immortalized monolayer cells, especially those of the N3

215 We report that overexpression of HSPB8 in immortalized motor neurones decreased the accumulation o

216 yR2/phospholamban hyperphosphorylation in an immortalized mouse atrial cardiomyocyte cell-line (HL-1-

217 We developed an immortalized mouse embryonic fibroblast (iMEF) line in w

218 ogene-induced transformation using G0s2-null immortalized mouse embryonic fibroblasts (MEF).

219 de CRISPR/Cas9 knockout screen in Kras(G12D) immortalized mouse embryonic fibroblasts (MEFs) to searc

220 its functions in cells, we deleted ELMOD2 in immortalized mouse embryonic fibroblasts and discovered

221 We have found that in an immortalized mouse hepatocyte cell line in which efficie

222 We report here that in an immortalized mouse hepatocyte cell line, AML12HBV10, in

223 ethanol-induced lipophagy was studied in an immortalized mouse hepatocyte line, AML12.

224 Using immortalized mouse hippocampal neuronal cells as an in v

225 describe a genome-wide CRISPR/Cas9 screen in immortalized mouse macrophages aiming at the unbiased id

226 tterns of AP-1 family members in primary and immortalized mouse macrophages.

227 enriched in mouse Schwann cells compared to immortalized mouse motor neurons (MN-1), and is predicte

228 Here, we describe an immortalized mouse neuronal astrocyte cell line (C8D1A)

229 Pkm-knockdown immortalized mouse podocytes had higher levels of toxic

230 c podocyte injury promoted CFH expression in immortalized mouse podocytes in vitro.

231 In immortalized mouse podocytes, JAK2 knockdown decreased T

232 DHPS or DOHH induced tolerance to anoxia in immortalized mouse renal proximal cells.

233 of a GFP-based NF-kappaB reporter system in immortalized murine bone marrow-derived macrophages (iBM

234 The spontaneously immortalized murine calvarial cell line MC3T3-E1 and its

235 to induce phagocytic uptake into primary or immortalized murine cells.

236 n-related gene and protein expression in the immortalized murine cementoblast cell line OCCM-30 after

237 Immortalized murine cementoblasts were exposed to variou

238 e chromosomes 9, 10, 12, or 14 in tetraploid immortalized murine embryonic fibroblasts.

239 aracterized an in vitro system of transduced immortalized murine macrophages expressing either WT or

240 showed a significant increase in LPS-treated immortalized murine microglial cell line BV2 cells in an

241 human dental pulp stem cells (hDPSCs) and an immortalized murine odontoblast cell line (MDPC-23), to

242 We show here that cell fusion between immortalized myoblasts and transformed fibroblasts, thro

243 s in mdx muscles, isolated myofibers and DMD immortalized myoblasts.

244 blasts but is downregulated by H-Ras(V12) in immortalized NIH 3T3 cells through a mechanism involving

245 tial while not altering the proliferation of immortalized, noncancerous human peripheral airway cells

246 We developed an in vivo assay based on the immortalized nontumorigenic breast cell line MCF10A and

247 epletion was selectively lethal to tumor and immortalized normal cells expressing the mutant kinase B

248 epletion of Cx43 increased cell migration in immortalized normal EEC.

249 down in ESCC cell lines (KYSE450 and T.Tn), immortalized normal esophageal epithelial cell lines (NE

250 in depletion can selectively induce death of immortalized normal fibroblasts IMR90E1A when combined w

251 In immortalized normal human astrocytes (NHAs) and syngenei

252 ate that PML depletion in U2OS cells or TERT-immortalized normal human diploid fibroblasts results in

253 an papillomavirus 16 (HPV 16) E6 and E7 gene-immortalized normal human epidermal keratinocytes, we de

254 ssed in normal prostate epithelial cells and immortalized normal human prostate epithelial cells (RWP

255 dent of immortalization, as human telomerase-immortalized normal oral keratinocytes supported robust

256 xpressing pancreatic cancer cells and spares immortalized normal pancreatic duct cells, hTERT-HPNE.

257 arian cancer cell lines relative to those in immortalized normal surface epithelial cells and that su

258 ar subtypes of breast cancer, as well as two immortalized ("normal") human breast cell lines.

259 into telomerase reverse transcriptase (TERT) immortalized oral keratinocytes (NOKs) that are capable

260 26 ovarian cancer cell lines, HGSOC tumours, immortalized ovarian surface epithelial cells and fallop

261 ation 873 EFO-CLO aligned and 344 EFO unique immortalized permanent cell lines.

262 sibility of inactivating PERV activity in an immortalized pig cell line.

263 16 (IFI16) as the major DNA sensors in human immortalized podocytes.

264 and chromatin opening during adipogenesis of immortalized preadipocytes derived from mouse brown adip

265 Immortalized primary bronchial epithelial cell line (BEA

266 An immortalized primary human lung EC (HPMEC-im) line was g

267 differentiation program, which culminates in immortalized, proliferating cells that partially resembl

268 Introduction of FOXA1 and HOXB13 into an immortalized prostate cell line reprogrammed the AR cist

269 pheroid culture from normal human primary or immortalized prostate epithelial cells, and their differ

270 Here, we utilized primary and immortalized PSC obtained from mice and patients with CP

271 ve rafts but little to no replication in HPV-immortalized rafts.

272 y generated monoclonal line of conditionally immortalized rat atrial myocytes.

273 Immortalized rat renal proximal tubular cells (IRPTCs) a

274 nucleoprotein F (hnRNP F) in their RPTCs and immortalized rat renal proximal tubular cells (IRPTCs) w

275 that displays strong regulatory activity in immortalized rat Schwann (S16) cells.

276 ney effectively and reproducibly using mixed immortalized renal cells, and showed their application f

277 meshifted, from an intracellular location in immortalized renal epithelial cells of a patient affecte

278 laced DAs from the interphase centrosomes of immortalized retina pigment epithelial (RPE1) cells.

279 Human IgG/M binding to primary RMEC, immortalized RMEC (iRMEC), and iRMEC-deficient in B4GALN

280 d-type and various mutant forms of Merlin in immortalized Schwann cells.

281 e applied CRISPR/Cas9 technology to generate immortalized sialylation-deficient podocytes (asialo-pod

282 -stimulated cell transformation of the HaCaT immortalized skin cell line and mutation of NFAT3 at Ser

283 Similarly, mitofusin depletion in immortalized spermatocytes or germ cells in vivo results

284 system of gastric organoids co-cultured with immortalized stomach mesenchymal cells (ISMCs).

285 IB formation is observed in a conditionally immortalized striatal neuron model of HD, and IB formati

286 nd tracheal respiratory epithelial cells and immortalized swine nasal epithelial cells (siNEC) and tr

287 We have developed immortalized swine respiratory epithelial cells that ret

288 low cytometry following transfection into an immortalized T-cell line and compared to that of a refer

289 tion and invasion compared to commonly used, immortalized TB cell lines and primary cells from term p

290 Although immortalized, these cells nonetheless retain normal grow

291 ng the establishment of EBV infection in HPV-immortalized tissues, we showed an HPV-induced interrupt

292 g a model of direct EBV infection into HPV16-immortalized tonsillar cells grown in organotypic raft c

293 uPA expression in TSC2-null tumor cells and immortalized TSC2-null angiomyolipoma cells, but not in

294 is, chromosome missegregation was induced in immortalized tubal epithelial cells, which proved acutel

295 We propose that in an immortalized ("undead") model of AiP, signaling back and

296 ntigen deletions were cultured in cell lines immortalized using simian virus 40 (SV40) T antigen, sug

297 s [PBMCs], CD14(+) monocytes, and telomerase-immortalized vascular endothelial [TIVE] cells), from vi

298 blastoma cell proliferation, including cells immortalized via the telomerase-independent ALT mechanis

299 In culture, GR-deficient primary or immortalized white and brown preadipocytes showed severe

300 Conditionally immortalized, young adult mouse colonic (YAMC) epithelia