ライフサイエンスコーパス: subline

1 (including cisplatin and multidrug-resistant sublines).

2 relaxin is overexpressed in the LNCaP-R273H subline.

3 or and in the differentiation-resistant KG1a subline.

4 d SOCS1, that are up-regulated regardless of subline.

5 n of this transcript in the metastatic AT6.1 subline.

6 enerate gene signatures associated with each subline.

7 s increased in an androgen-independent LNCaP subline.

8 was high in each of the KIT-independent GIST sublines.

9 s in both vector-alone and Ku86-complemented sublines.

10 blines than in the Ku86-complemented XR-V15B sublines.

11 n of the locus were detected between the two sublines.

12 the Me32a cells than in the MeMNK and MeWND sublines.

13 ut not in the K-ras-disrupted HCT116-derived sublines.

14 mulated or differentiating agent-treated Nb2 sublines.

15 regard to prion susceptibility in tumor cell sublines.

16 the expression of vitiligo between SL and BL sublines.

17 n vitro model of MART CTL-resistant melanoma sublines.

18 including cisplatin- and multidrug-resistant sublines.

19 cer, we have established docetaxel-resistant sublines.

20 t has been previously reported for these MEC sublines.

21 sistant sublines relative to their sensitive sublines.

22 y aberrations that were not found in the T/F-sublines.

23 terns that were distinct from those of the U-sublines.

24 nsfected into novel PCFT(+) and PCFT(-) HeLa sublines.

25 ases, including 3 derived from highly inbred sublines.

26 lar levels in RA and PsA SM lining layer and sublining.

27 oth patient groups, but lower in PsA than RA sublining.

28 Heterozygous transgenic rats, including P23H sublines 2 and 3 and S334ter sublines 4 and 9, were rear

29 fied in S334ter (sublines 4 and 9) and P23H (sublines 2 and 3) rats.

30 d damage outcomes was identified in S334ter (sublines 4 and 9) and P23H (sublines 2 and 3) rats.

31 including P23H sublines 2 and 3 and S334ter sublines 4 and 9, were reared in dim cyclic light or in

32 e human breast cancer cell line, MDA-MB-231 (subline 4175) and a noninvasive breast epithelial cell l

33 both VES and alpha-TEA can induce A2780 and subline A2780/cp70 ovarian cancer cells to undergo DNA s

34 ll line Cal27, and their cisplatin resistant sublines A2780CisR and Cal27CisR.

35 ved from the same organism, clonal sublines, sublines adapted to grow under certain conditions).

36 704, EFO-21, EFO-27 and UKF-NB-3) and their sublines adapted to the anti-cancer drugs cisplatin (COL

37 RRIG1-transfected sublines also inhibited tumor development in nude mice.

38 uired the highly permissive Huh-7.5 hepatoma subline and adaptive amino acid substitutions in both NS

39 of 3 in methotrexate-resistant CCRF-CEM cell sublines and metabolite protection studies implicated DH

40 phorylated Akt increased in both the GOF p53 sublines and the control lines.

41 expressed separately in drug-selected MCF-7 sublines and transiently transfected HeLa cells.

42 um, as activated T cells migrate through the sublining and lining layer, T cell-derived IL-2 may acti

43 Expression levels of cathepsin K in the sublining and vascularized areas of inflamed synovia sho

44 tories' wild type Myxococcus xanthus DK1622 "sublines" and sequenced each to determine if they had ev

45 (T-series sublines) or fulvestrant (F-series sublines) and sublines unselected by drugs (U-series).

46 mals bearing EL-4 or EG.7 (an OVA-expressing subline), and repetitively imaged by microPET over sever

47 cing identified 29 variants between the nine sublines, and eight had at least one unique variant with

48 aneously, each line was represented by three sublines, and seeds were equal in age, these estimates a

49 ency and size of GLFG bodies vary among HeLa sublines, and we find that an increased level of Nup98 i

50 and activation of leukocytes in the synovial sublining, and the formation and behavior of the hyperpl

51 These results suggest that the T/F-sublines are derived from a common monoclonal progenitor

52 both c-Kit and tryptase, accumulated in the sublining area of proliferating synovial tissue from RA

53 In sublining areas, levels of TNFalpha and IL-15 were lower

54 The establishment of a series of tumorigenic sublines based on this parental cell line is described.

55 One subline (BLIN-4E) undergoes cell death in the absence of

56 Another subline (BLIN-4L) slowly proliferates in the absence of

57 Historically, Swiss Webster mice of the CFW subline, both inbred and random-bred stocks, have been c

58 f gene expression between parental cells and sublines by genome-wide cDNA microarray analysis reveale

59 We have generated SLPI-ablated epithelial sublines by stably transfecting the Ishikawa human endom

60 ia(AR) (a MiaPaCa2-derived anoikis-resistant subline) by culture in poly-2-hydroxyethylmethacrylate-c

61 localized to the nucleus, whereas in its AI subline C4-2, FlnA failed to cleave and remained cytopla

62 CaP cell lines DU145, PC3, LNCaP, and LNCaP sublines (C4, C4-2, and C4-2B), conferred cell growth in

63 e-derived androgen-independent PSA-producing subline, C4-2, we identified two cis-elements within the

64 more pronounced for the cisplatin resistant subline Cal27CisR.

65 These infected sublines can be compared to the cognate uninfected cultu

66 ctor-alone, as well as the Ku86-complemented subline cells, indicating both events are initiated by r

67 the immunoreactive protein was localized to sublining cells rather than the intimal lining synoviocy

68 Sublining cellular infiltration, lymphoid aggregation, a

69 c CEM cell line and two teniposide-resistant sublines, CEM/VM-1 and CEM/VM-1-5 ( approximately 40 and

70 oma 2008 cells and CLDN3 and CLDN4 knockdown sublines (CLDN3KD and CLDN4KD, respectively).

71 e levels of AR decreased in the four GOF p53 sublines compared with the control lines.

72 Examination of BBDP sublines congenic for the Iddm26.2 locus that includes P

73 erived from RXRalpha(-/-) embryos and an EMC subline constitutively expressing a dominant negative re

74 in PLC-gamma1 expression, while the J.gamma1 subline contains no detectable PLC-gamma1 protein.

75 liferation of both H520-Cyr61 and H460-Cyr61 sublines decreased remarkably compared with the cells st

76 Further analysis identified subline-dependent differences in the pro-inflammatory re

77 e identified conserved, breed-dependent, and subline-dependent innate immune responses to NDV infecti

78 were differentially expressed in a breed- or subline-dependent manner.

79 ive parental line and a stably DDP-resistant subline derived by in vitro selection, resistance to DDP

80 haracterized two novel, PLC-gamma1-deficient sublines derived from the Jurkat T-leukemic cell line.

81 4T07; these cells are thioguanine-resistant sublines derived from the parental population of 410.4 c

82 al tumor cell lines, 4T1 and 4T07, which are sublines derived from the parental population of 410.4 c

83 Conversely, sublines derived from the primary tumor in vivo at dista

84 epothilone-resistant human ovarian carcinoma sublines derived in a single-step selection with epothil

85 ain shedding deficiencies in two mutated CHO sublines designated M1 and M2.

86 Two sibling sublines, designated T(3)30 and T(3)31, were identified

87 fected with an hREV1 expression vector and 4 sublines developed in which the hREV1 mRNA level was inc

88 the parental BPH-1 cells and the BPH1(TETD) sublines did not.

89 mRNA expression profiles of the U-sublines differed significantly from those of the T/F-su

90 ive phenotypic traits we measured, with some sublines differing by several-fold.

91 genic human breast cell lines, as well as on sublines differing in their tendency to "home" to differ

92 d that although the Fas-resistant/refractory subline displayed significant metastatic ability, the pa

93 The P98 subline displays a >90% reduction in PLC-gamma1 expressi

94 ulture on BM stromal cells plus IL-7, BLIN-3 sublines emerged expressing mu heavy chain and VpreB on

95 Melanoma tumor cell sublines established from lymph node metastasis express

96 were conducted in two pairs of transfectant sublines established from the Ku86-deficient Chinese ham

97 -4, a p53-null ALL cell line, to establish a subline EU-4/p53-143.

98 Thus, the BLIN-4 sublines exhibit biological characteristics consistent w

99 These epothilone-resistant sublines exhibit impaired epothilone- and taxane-driven

100 The three DU145 sublines expressed epidermal growth factor (EGF) recepto

101 Two of the resistant sublines expressed high levels of transcriptionally inac

102 pancreatic cancer cell line and its derived subline expressing functional CFTR, we report that MUC4

103 vation of ERKs or causing proliferation in a subline expressing low levels of membrane estrogen recep

104 iminated, but it was restored in a corrected subline expressing the XPA cDNA.

105 Clonal sublines expressing different levels of NOS II were then

106 proliferation of Chinese hamster ovary (CHO) sublines expressing folate receptors (FRs) alpha or beta

107 We further show that Ishikawa sublines expressing low to undetectable SLPI have corres

108 The expression of Mcl-1 in sublining fibroblasts correlated with the degree of infl

109 the synovial lining and was increased in the sublining fibroblasts of patients with RA, compared with

110 g in the differentiation of perivascular and sublining fibroblasts that express CD90 (encoded by THY1

111 nded in RA synovia: THY1(CD90)(+)HLA-DRA(hi) sublining fibroblasts, IL1B(+) pro-inflammatory monocyte

112 A-1 and was observed in multiple independent sublines for both the endogenous alpha IIb gene and tran

113 WDs when at rest, compared with the C3HeB/Fe subline (four SWDs per hour).

114 We made a stable Mirk-inducible subline from nontransformed Mv1Lu lung epithelial cells

115 d fulvestrant, we established drug-resistant sublines from a single colony of hormone-dependent breas

116 In the highest CR-1-expressing subline, G4, 38% (12/31) of the multiparous animals aged

117 pattern of gene expression with the GI-101A subline GI-BRN, which was generated by repeated in vivo

118 orms were KIT oncoprotein-dependent, whereas sublines had loss of KIT oncoprotein expression, accompa

119 Genomic DNA of the U-sublines harbored many aberrations that were not found i

120 d 123-fold (CEM/BTZ200) bortezomib-resistant sublines harboring PSMB5 mutations.

121 CI.1u.Lyp) cohort and Iddm26.2 congenic BBDP sublines has revealed an association of Ptpn22 with T1D.

122 ty between two iso-clonal human colon cancer sublines HCT116 and HCT116b on their ability to undergo

123 2)O(2) were compared in four colon carcinoma sublines: HCT116, HCT116/E6, HCT116+ch3, and HCT116+ch3/

124 ryngeal), and KB-Vin (multidrug resistant KB subline) human cancer cell lines.

125 murine embryonic fibroblasts (CTR1+/+) and a subline in which both alleles of CTR1 were deleted (CTR1

126 cell line, M160-8, was selected from a HeLa subline in which the RFC gene was deleted and PCFT was h

127 Parental 4T1 cells and metastatic sublines in isolation showed random migration in EFs of

128 Evaluation of 6 against MTX-resistant sublines indicated that DHFR is not the major target of

129 In susceptible aphid genotypes, parasitized sublines infected with Hamiltonella generally showed inc

130 in D(9k) gene by injecting the E14.1 ES cell subline into the C57BL/6 host blastocysts and proved tha

131 B78H1, unlike B16F1 and B16F10 sublines, is also selectively devoid of TAP2 and low mol

132 The clonal resistant subline K/VP.5 contains reduced TOP2alpha/170 mRNA and p

133 ocarcinoma cells and the colchicine-selected subline KB-8-5-11 that overexpresses P-gp.

134 cancer cell line and its colchicine-selected subline KB-8-5-11.

135 ast (RASF) and macrophages in the lining and sublining layer of the tissue.

136 7/MX100, a breast cancer drug-resistant cell subline) levels of ABCG2 expression.

137 he DG75 Burkitt's lymphoma cell line and its sublines (LMP1 transfected and EBV infected), with the h

138 the AS PCa cell line LNCaP and that of an AI subline LNCaP(CS) generated by maintaining LNCaP in medi

139 en independence, we used two human CaP LNCaP sublines: LNCaP(nan), which is androgen dependent (AD),

140 erythrocytes was performed using a RAW 264.7 subline (LR5 cells) and bone marrow-derived macrophages

141 After 12 cycles, the cell subline LV12 was obtained.

142 tigen immortalized human prostate epithelial subline M12 by stable transfection with human wild-type

143 lines, P69SV40Tag (P69) and its tumorigenic subline, M12, and 11 prostate cancer cases.

144 vated in RA and osteoarthritis ST lining and sublining macrophages and endothelial cells compared wit

145 coexpressed on RA synovial tissue lining and sublining macrophages and endothelial cells.

146 The BLIN-4 sublines maintained the ring chromosome 4, but the triso

147 which have low invasive ability, with their sublines MCF7-I4 and MDA-MB453-I4 with high invasive abi

148 Next, we showed that an androgen-refractory subline (MDA-hr) of MDA PCa 2b cells also expressed high

149 man bone metastasis, to generate an invasive subline (MDA-I) using a Matrigel chamber.

150 ) that do not express either transporter and sublines molecularly engineered to express either ATP7A

151 gher in RA synovium and was localized to the sublining mononuclear cells and the intimal lining.

152 4 cells were an atypical multidrug-resistant subline (no overexpression of P-gp).

153 d to produce a heart-specific Cx43-deficient subline ("O-CKO" mice) in which the loss of Cx43 in the

154 We noted that one subline of B10.Q mice, B10.Q/J, was completely resistant

155 membrane molecules on a liver-metastasizing subline of B16 melanoma versus the parental B16-F0 revea

156 Using the D5 subline of B16 melanoma, we demonstrate that DCs pulsed

157 BL41-3, a spontaneously derived subline of BL41 Burkitt lymphoma cells, was found to hav

158 signaling pathways of a cetuximab-resistant subline of DiFi colorectal cancer cells (DiFi5) that was

159 A subline of HCT-116, HCT-116/VM46, resistant to many stan

160 145, PC-3, LNCaP, and an androgen-refractory subline of LNCaP.

161 A subline of MCF-7, made resistant to tamoxifen by a 6-mon

162 xenograft growth of this tamoxifen-resistant subline of MCF-7.

163 A subline of MOLT-4 cells, MOLT-4CpGR, was selected for ac

164 We also show that prions in this subline of N2a cells are transmitted primarily from moth

165 an hepatic derived cell line, and L cells, a subline of NCTC clone 929 mouse fibroblasts.

166 tively measured these competing effects in a subline of neuroblastoma (N2a) cells and propose a conco

167 In the present experiments, using a subline of NIH 3T3 cells that is relatively refractory t

168 and signaling was investigated in the PC6-3 subline of PC12 cells.

169 cific GTPase-activating protein domain, in a subline of RAW 264.7 cells, and challenged the transfect

170 Characterization of defects in a variant subline of RBL mast cells has revealed a biochemical eve

171 ifferent from the virus expressed by another subline of RIII mice, the BR6 mice.

172 As a result, a new subline of S91 cells capable of growing in free cell sus

173 lture, we established a chronically infected subline of the living cells remaining after the death of

174 ys an essential role in lumen formation in a subline of the nonmalignant human breast cell line (MCF1

175 ion assays were performed with C4-2 cells, a subline of the PSMA-positive cell line LNCaP (human lymp

176 ion was induced in a tumorigenic, metastatic subline of the SV40 large T-antigen immortalized human p

177 passage (normal) and late passage (adapted) sublines of a single HESC line, H7.

178 ssion after hormone treatment; these include sublines of ALVA-31 as well as the cell lines TSU-Pr1 an

179 We generated sublines of Ba/F3 cells in which either wild-type STAT5

180 FPGS relative to hcFPGS was observed in some sublines of CCRF-CEM with acquired MTX resistance sugges

181 genes were methylated in both the SL and BL sublines of chickens; therefore, methylation does not ap

182 Two sublines of human mammary adenocarcinoma MCF-7 cells wer

183 However, in CRPC sublines of LNCaP and CWR22, which strongly overexpress

184 ing immunocompromised mice and highly inbred sublines of Massachusetts General Hospital major histoco

185 phic markers; (2) the generation of congenic sublines of mice by repeated backcrossing of CAST with B

186 phenotype of Darc-knockout mice and congenic sublines of mice carrying small chromosomal segments fro

187 nsgenic RIP-Tag lines, and three polymorphic sublines of one, enabled us to investigate the effects o

188 Two independently maintained sublines of QT35 were found to be positive for Marek's d

189 Sublines of RAW 264.7 cells with reduced GPI-PLD express

190 functional validations in murine macrophage sublines of RAW264.7 cells.

191 nate immune genes to NDV infection in inbred sublines of the Fayoumi and Leghorn breeds known to diff

192 Here, we used organ-specific metastatic sublines of the MDA-MB-231 human breast cancer cell line

193 taneous fusion between bone- and lung-tropic sublines of the MDA-MB-231 human breast cancer cell line

194 s M4A4 and NM2C5 are spontaneously occurring sublines of the MDA-MB-435 cell breast tumor cell line t

195 effect of DDP was assessed using a panel of sublines of the MMR-deficient HCT116 colon carcinoma cel

196 regulation of the Muc4/SMC gene in the 13762 sublines of the rat mammary adenocarcinoma correlates wi

197 espite 25 years of selective breeding of the sublines of this colony.

198 and are prominent in the synovial lining and sublining of patients with rheumatoid arthritis (RA).

199 vived 21-day exposure to tamoxifen (T-series sublines) or fulvestrant (F-series sublines) and subline

200 nting the entire genus, yielding alloplasmic sublines, or cytolines were created.

201 the synovial intimal lining rather than the sublining (P < 0.01).

202 ells which have wt p53, in all PTX-resistant sublines p53 was functionally inactive.

203 iRNA in the paclitaxel-resistant cancer cell sublines partially sensitized these cells toward paclita

204 PC3 and the even more aggressive, metastatic subline PC3M assessed by hyperpolarized in vivo pyruvate

205 This resulted in three sublines per genotype: uninfected, +APSE8 and +APSE3.

206 tion process to isolate murine mammary tumor sublines possessing an enhanced ability to colonize the

207 The third subline presented a novel p53 pseudo-null phenotype as a

208 A methotrexate (MTX)-resistant HeLa subline (R5), developed in this laboratory, with impaire

209 Compared with the vector-alone sublines, radiation resistance was restored in the human

210 Accumulation of DDP in the resistant sublines ranged from 38 to 67% of that in the parental l

211 ostate cancer xenograft models with isogenic sublines reflecting the transition from androgen-depende

212 However, all tumor sublines regardless of their Fas and ICAM-1 levels compa

213 subcellular fractions of two drug-resistant sublines relative to their sensitive sublines.

214 Similarly, the BL41-3 subline remained viable for an extended period under con

215 Tumor sublines rendered both Fas incompetent and ICAM-1 incomp

216 stingly, both in vitro- and in vivo-produced sublines resembled the naturally occurring metastatic po

217 c eosinophil cell line, AML14.3D10, an AML14 subline resistant to Fas-mediated apoptosis.

218 paclitaxel selected human ovarian carcinoma sublines, resistant to paclitaxel due to acquired beta-t

219 taII into the differentiation-resistant KG1a subline restored the ability to undergo DC differentiati

220 None of the primary isolates or sublines revealed mutations in either the VHL or Ras gen

221 We have established one RIII subline (RIII/Sa) that shows a pattern of virus expressi

222 with the milk and mammary glands of another subline, RIIIS/J, revealed that they do not express MMTV

223 Disease expression in the SAMP1/YitFc subline (SAMP1/Fc) is partially inhibited by outcross to

224 Under a common garden experiment, each subline satisfied the phenotypic prerequisites for wild

225 ne but was significantly down-regulated in a subline selected for in vivo tumor formation in Balb/c m

226 ared DU145 humanprostate cancer cells with a subline selected for resistance to camptothecin.Differen

227 numbers of tumor nodules compared with tumor sublines separately expressing low levels of Fas or ICAM

228 Most T/F-sublines shared highly homogeneous genomic DNA aberratio

229 x (ECM), 786-O VHL(-) RCC cells and isogenic sublines stably expressing VHL gene products [VHL(+)] we

230 In the 2008/ATP7B subline, steady-state copper levels were decreased under

231 lines derived from the same organism, clonal sublines, sublines adapted to grow under certain conditi

232 A set of genes strongly expressed in the U-sublines successfully predicted metastasis-free survival

233 n methotrexate (MTX)-resistant CCRF-CEM cell sublines suggested that polyglutamylation was crucial fo

234 binant restoration of EMP2 expression in the subline suppressed its tumorigenicity, suggesting that l

235 induced damage, whereas retinas in the other sublines sustained damage within a sensitive region in t

236 astatic clone of K1735 cells, SW1-C, and its subline SW1-P2, which expresses an activating transcript

237 In the T6 generation, all progeny of one subline, T(3)30, expressed ubiquitin-driven bar and uidA

238 were transcriptionally silenced in the other subline, T(3)31.

239 tions of stable expression in the multi-copy subline, T3#30, but not in the other lines studied.

240 s exactly like those in an identical sibling subline, T3#31, which had significant reduction in trans

241 sitization were observed in the vector-alone sublines than in the Ku86-complemented XR-V15B sublines.

242 ates; (c) lack of potentiation in a CCRF-CEM subline that does not express the RFC; and (d) similarit

243 into glyB cells, a Chinese hamster ovary K1 subline that is deficient in the transport of folates in

244 glutamine utilization in the metastatic PC3M subline that led directly to sensitivity to glutaminase

245 atic parental line and to an in vivo-derived subline that was highly metastatic for growth in the lun

246 with a large excess of uncloned cells from a subline that was refractory to transformation markedly d

247 east adenocarcinoma cells (MCF-7E and MCF-7L sublines that are sensitive and resistant to VD3 compoun

248 ed IGF-I effects in MCF-7 breast cancer cell sublines that have been selected for loss of ERalpha (C4

249 esistance, we characterized MCF-7 monoclonal sublines that survived 21-day exposure to tamoxifen (T-s

250 unique panel of human DU145 prostate cancer sublines that vary in their invasive potential.

251 sed mainly of fibroblasts, with a lining and sublining that surround the joints.

252 d by at least a factor of three, and in some sublines the sensitive region was enlarged to include th

253 ed studies performed with a cloned committed subline, the A33 line, verified stable adipocyte lineage

254 -independent and highly malignant Nb2-SFJCD1 subline, the constitutive expression of HRPAP20 was mark

255 of Tiam1 in the migration of these migratory sublines, the parental SW480 cell line was transfected w

256 Passage of the non-silenced subline through in vitro culture recreated the silenced

257 The relative susceptibilities of each subline to damage by light were different, even within t

258 CMK sublines, transfected with the BST2 cDNA and incubated w

259 en shown that a subset of fibroblasts in the sublining undergoes a major expansion in rheumatoid arth

260 ines) or fulvestrant (F-series sublines) and sublines unselected by drugs (U-series).

261 in hormone-sensitive and hormonal-resistant sublines using Affymetrix Human Genome U133 Plus 2.0 Arr

262 he sarcoma model, a Fas-resistant/refractory subline was produced in vitro from the parental line by

263 FAK binding; additionally, a CD44(-) Jurkat subline was transfected with murine CD44, CD44 with a po

264 sed acquisition of surface pre-BCR in BLIN-3 sublines was associated with loss of DJ rearrangements a

265 Each of the 15 total sublines was first subjected to a parasitism assay to de

266 UM-UC-6dox, a doxorubicin resistant subline, was infected with Ad-MMAC to evaluate its role

267 disrupting the ORF MXAN7041 in two different sublines, we demonstrated substantial epistasis from the

268 The sublines were 1.3- to 1.7-fold resistant to the cytotoxi

269 The hREV1-transfected sublines were 1.5- to 1.8-fold better than the parental

270 Resistant sublines were 250- to 385-fold resistant to romidepsin a

271 5.1 nM), whereas their bortezomib-resistant sublines were 9- and 17-fold cross-resistant to salinosp

272 The four GOF p53 sublines were able to grow under androgen-depleted condi

273 We found that the sublines were at least 100-fold more susceptible to stra

274 Three aphid sublines were experimentally created from single aphid g

275 R-deficient) and HCT116+ch3 (MMR-proficient) sublines were exposed for varying periods of time to an

276 The initial tumor isolates and sublines were histologically reconfirmed to be RCCs, and

277 at differences in drug sensitivities between sublines were independent of PCFT transport.

278 Several sublines were obtained with statistically significantly

279 Metastatic sublines were produced in vitro from the primary tumor c

280 d ICAM-1 regulated malignant behavior, tumor sublines were produced that expressed either lower level

281 All T/F-sublines were resistant to the cytocidal effects of both

282 These transporter-proficient sublines were resistant to the cytotoxic effect of coppe

283 ution of paclitaxel resistance, three SKOV-3 sublines were selected during successive rounds of expos

284 The sublines were selected to represent early (0.003 micro M

285 These stable PC12 sublines were then used to examine potential AC isoform

286 that the organism was a member of a distinct subline which includes uncultured Corynebacterium MTcory

287 We exploited this heterogeneity to derive sublines which are highly susceptible to prion infection

288 differed significantly from those of the T/F-sublines, whose transcriptomal responsiveness to fulvest

289 te carcinoma cell line and a highly invasive subline, wild-type DU-145, derived from it.

290 udi cells, but not in an IFN-resistant DRST3 subline with a defective STAT3 signaling pathway.

291 rs generated by the MDA-MB-231 breast cancer sublines with characteristically different primary tumor

292 clusions because they worked with transgenic sublines with drifted transgene expression patterns.

293 The use of array analysis with SOMs in sublines with progressive paclitaxel resistance can succ

294 lay of mRNA expression in prostate carcinoma sublines with varying metastatic potential revealed over

295 howed the bacterium to be a hitherto unknown subline within a group of Actinomyces species which incl

296 d each group represents a previously unknown subline within Clostridium cluster XIII.

297 ach group may represent a previously unknown subline within the Bacteroides phylogenetic cluster.

298 e strains are closely related and form a new subline within the genus Corynebacterium.

299 distinct and represents a previously unknown subline within the Porphyromonas phylogenetic cluster.

300 was restored in the human Ku86-complemented sublines without alteration of cell cycle distributions.