ライフサイエンスコーパス: stable transfectant

1 of the native PC12 cells used to prepare the stable transfectants.

2 sfected into CD44- Jurkat cells to establish stable transfectants.

3 ux in response to leukotriene (LT) D(4) with stable transfectants.

4 tase (DHFR) expression to allow selection of stable transfectants.

5 genized cassette from the genomic DNA of the stable transfectants.

6 aging studies of enhanced GFP-tagged RelA in stable transfectants.

7 by the androgen-liganded AR in transient and stable transfectants.

8 nter dotERalpha complexes were noted only in stable transfectants.

9 se activity declined in long term culture of stable transfectants.

10 PS-inducible expression of IL-6 and MCP-1 in stable transfectants.

11 ollow trafficking of mCD14 and BODIPY-LPS in stable transfectants.

12 T mutants, their parental cells, and an NPC1-stable transfectant allow us to present evidence that NP

13 owered plectin levels in astrocytoma-derived stable transfectants and plectin-positive fibroblasts.

14 By analyzing stable transfectants and transgenic animals, we demonstr

15 of plasminogen activator inhibitor utilizing stable transfectants, and the use of vitronectin as a su

16 skin epidermal JB6 P+ Cl41 cell line and its stable transfectants as well as on several human tumor c

17 sfection techniques, including production of stable transfectants; biochemical and other assays of pu

18 In the stable transfectants (BM3 cells) expressing a mutant bac

19 s of 4-OHT and raloxifene were lost in these stable transfectants, but antiestrogenic action was reta

20 The resulting stable transfectant clones expressing maspin/PAI-1 and P

21 The B2-targeted TRz was used to develop stable transfectant clones from an SV40-immortalized hep

22 Stable transfectant clones with 5-10-fold decreased leve

23 -1 and IL-6 were down-regulated in the MnSOD stable transfectants compared to the control cell lines.

24 f cells through the cell cycle, we find that stable transfectants constitutively overexpressing the w

25 ompared with vector-alone control cells, BLU stable transfectants, derived from poorly-differentiated

26 In contrast, c-Cbl knockdown stable transfectants differentiated slower than wt cells

27 of MEnT protein was induced with ZnCl2, the stable transfectants differentiated with kinetics that w

28 AhR overexpression in stable transfectants downregulated Oct4 and also decreas

29 Stable transfectants ectopically expressing c-Cbl underw

30 Stable transfectants expressed mRNA and the expected 74-

31 The resultant stable transfectants expressed vimentin- and keratin-pos

32 age FcgammaRIa as a model system, we created stable transfectants expressing a full-length or a CY de

33 - and CD44-deficient COS-7/M6 cell to create stable transfectants expressing CD74, CD44, and a trunca

34 perone association with MPO precursors using stable transfectants expressing cDNA encoding wild type

35 Three stable transfectants expressing exogenous FGF4 were stud

36 Using synthetic phosphopeptides, and stable transfectants expressing immunoreceptor tyrosine-

37 In contrast, leukocyte binding to stable transfectants expressing intercellular adhesion m

38 Stable transfectants expressing recombinant viruses were

39 Stable transfectants expressing similar levels of either

40 In two stable transfectants expressing survivin-specific short

41 sibly accounting for the inability to obtain stable transfectants expressing the protein.

42 Stable transfectants expressing these human splice varia

43 Stable transfectants expressing these scFvs then were ge

44 Stable transfectants expressing wild-type or mutant form

45 e involved in this shedding process, we used stable transfectants expressing WT L-selectin (on microv

46 We generated stable transfectants-expressing wild-type, K303R ERalpha

47 However, the stable transfectant failed to release a peptide with the

48 different organ environments, we engineered stable transfectants from RenCa mouse renal carcinoma ce

49 is of a HEL cDNA, were expressed as separate stable transfectants in a B cell lymphoma line.

50 COX-2 stable transfectants in LN-18 (LN-18-COX2) also induced

51 Intracerebral injection of antisense stable transfectants in nude mice produced no tumors or

52 Stable transfectants in rat PC12 cells showed distinct d

53 ure and proliferating state we have produced stable transfectants in the C19 MEL cell line that conta

54 PRs on protein expression were determined in stable transfectants in vivo.

55 rced BRCA2 expression in Skp2-overexpressing stable transfectants inhibited the migratory and growth

56 the low frequency of authentic wild-type p53 stable transfectants limits the power of this analysis,

57 Stable transfectant NIH3T3 clones expressing vIRF grew i

58 maximal expression occurring at about 36 h; stable transfectants normally can be generated within th

59 a cells (A-431 and MDA-MB-468), and EGFRvIII stable transfectants (NR-6M).

60 duced hematopoietic diseases, we generated a stable transfectant of Ba/F3 cells expressing EpoR and a

61 fusion protein into the helper cell-derived stable transfectant of TCRalpha cDNA resulted in translo

62 Evaluation of a stable transfectant of the KM12L4 cell line expressing c

63 When a helper Ts hybridoma or a stable transfectant of the same TCRalpha cDNA in a helpe

64 Upon stimulation with anti-CD3, a stable transfectant of the TCR-alpha cDNA formed OVA-spe

65 Studies with stable transfectants of 293 cells demonstrated recogniti

66 esponsible for their retention, we generated stable transfectants of a mu-negative pre-B cell line ex

67 the p53 inhibitor, pifithrin-alpha, or using stable transfectants of a v-MYC-immortalized, telomerase

68 In this study, we characterized stable transfectants of A2780 ovarian carcinoma cells.

69 Stable transfectants of baby hamster kidney (BHK) epithe

70 To track AML cells, stable transfectants of C1498 expressing DsRed2, a red f

71 ructed a tailless form of CD80 and generated stable transfectants of Chinese hamster ovary epithelial

72 To address this question, we have generated stable transfectants of early passage HDF, represented h

73 E2-stimulated increase in TGF-alpha mRNA in stable transfectants of ER-negative human breast cancer

74 To address the role of AF1, stable transfectants of ERalpha or D351YERalpha with an

75 s suggested that HCV core gene expression in stable transfectants of Huh-7 cells resulted in a basal

76 MAT1A on in vivo tumorigenesis, we generated stable transfectants of Huh7 cells overexpressing either

77 Using stable transfectants of human bronchial epithelial cells

78 Cloned stable transfectants of human embryonic kidney 293 cells

79 ated transcription factor TBX2, we generated stable transfectants of human embryonic kidney cells (29

80 Stable transfectants of human glioblastoma cells with a

81 uting to an IBC-like phenotype, we generated stable transfectants of human mammary epithelial cells o

82 We then isolated stable transfectants of Hut102/6TG cells that express th

83 Analysis of stable transfectants of LTR constructs showed that CDP b

84 d the interconverted phenotype by developing stable transfectants of MCF-7 human breast cancer cells,

85 sis of breast cancer in humans, we generated stable transfectants of MCF7 breast cancer cells negativ

86 ) mRNA was used as a gene target in situ for stable transfectants of MDA-MB-231 cells.

87 Stable transfectants of MDA-MB-435 cells that expressed

88 Herein we made stable transfectants of MM1 expressing active and Botuli

89 ponses in human monocytic THP-1 cells and in stable transfectants of mouse J774A.1 macrophages.

90 ng to cell cycle withdrawal were assessed in stable transfectants of murine erythroleukemia cells, in

91 tracrine signaling of HMW FGF-2, we produced stable transfectants of NIH 3T3 fibroblasts overexpressi

92 dependent on p53 status, we have established stable transfectants of p53 mutant 143Ala in two human c

93 When stable transfectants of p53-143ala were prepared in yeas

94 Stable transfectants of PC12 cells expressing bcl-2 or c

95 y Edg2 and Edg4 was further characterized in stable transfectants of rat HTC4 hepatoma cells.

96 erties of zinc alpha-2-glycoprotein further, stable transfectants of recombinant human zinc alpha-2-g

97 ogenous SOCS-3 mRNA expression is blocked in stable transfectants of SOCS-3 wild type or in dominant

98 ared in mice injected intraperitoneally with stable transfectants of TA3/St cells that overexpress so

99 Stable transfectants of the human glioblastoma cell line

100 n of c-Myc in hepatocyte sensitivity to TNF, stable transfectants of the rat hepatocyte cell line RAL

101 We therefore developed stable transfectants of the renal epithelial cell line,

102 The 55 kDa GIF peptide formed by stable transfectants of the TCR-alpha-tag cDNA bound to

103 We have engineered stable transfectants of these cells that produce either

104 Stable transfectants of these L(d)/Fc gamma1 and L(d)/Fc

105 of human colon cancer cells, we established stable transfectants of this isoenzyme in CaCo-2 cells.

106 Stable transfectants of this mutant c-jun in the two mor

107 at mediate these functions, we characterized stable transfectants of various E1A mutants in murine me

108 tegy for the isolation, from a population of stable transfectants, of clones with tightly regulated t

109 decreased S100A1 protein levels in all three stable transfectants (pAntisense clones) that expressed

110 In stable transfectants, pre-SCP-2 processing resulted in a

111 729HTLVRex- stable transfectants produced functional Tax, but undete

112 f GM-CSF in RAW 264 cells, and studies using stable transfectants revealed that colchicine impaired t

113 rn blot and immunofluorescence studies using stable transfectants revealed that EDL2a and EDL2b were

114 A stable transfectant (S2SN7) of p53-null SaOS-2 (human os

115 carcinoma cell lines, Jar, JEG and BeWo, the stable transfectants showed significantly reduced growth

116 o the ovarian carcinoma cell line SKOV3, the stable transfectants showed significantly reduced growth

117 Knocking out PTTG in STAT3-C HCT116 stable transfectants strongly decreased tumor metastases

118 ing PTTG expression by siRNA in STAT3 HCT116 stable transfectants suppressed cell growth and colony f

119 The stable transfectants synthesized and secreted IL-16 prot

120 In stable transfectants, tetracycline-induced expression of

121 These data suggest that stable transfectants that overexpress BAX may be sensiti

122 elanoma cell line, WM35, we have established stable transfectants that overexpress RhoC (called WM35R

123 Stable transfectants that overexpressed Akt were also re

124 t in Pgp-negative MCF-7 cells and MCF-7/MDR1 stable transfectants that were established and maintaine

125 A Bax stable transfectant, the K/Bax cell line, expressed more

126 to HL-60 cells and their WT or mutant c-Cbl stable transfectants, the c-Cbl/Vav/Slp-76 complex is al

127 cted with S and AS plasmids for selection of stable transfectants using Geneticin, and the presence o

128 nitude greater accumulation in NR-6-EGFRvIII stable transfectants versus parental NR-6 cells.

129 g Wnt5A, we compared gain-of-function (WNT5A stable transfectants) versus loss-of-function (siRNA kno

130 2 cells, which do not express Bcl-2, and two stable transfectants, W.Hb13 and W.Hb12.

131 The level of PI10 expression in the stable transfectants was found to correlate with their r

132 ion in Chinese hamster ovary cells, pools of stable transfectants were analyzed for qualitative or qu

133 Six stable transfectants were cloned.

134 duced apoptosis of human colon cancer cells, stable transfectants were created that express an activa

135 hether DcR3 promotes tumor growth, CT26-DcR3 stable transfectants were established.

136 Ras in nontransformed lung epithelial cells, stable transfectants were generated in RL-65 cells, a sp

137 Two stable transfectants were made using a tumorigenic human

138 Stable transfectants were obtained through selection wit

139 Stable transfectants were produced in the pRb-lacking Sa

140 Stable transfectants were selected by use of the appropr

141 Stable transfectants were selected for overexpression of

142 Stable transfectants were studied for their response to

143 ansfected with the human G-CSF receptor, and stable transfectants were studied.

144 The stable transfectants were then tested for: (1) colony fo

145 ties among the parental MDA-MB-435 cells and stable transfectants which express increased levels of p

146 Using a stable transfectant with high expression of PCFT, physio

147 a p70-negative mouse fibroblast line yielded stable transfectants with a flattened, less refractile m

148 not significantly different from that of the stable transfectants with a kinase-deficient EGF recepto

149 not significantly different from that of the stable transfectants with a kinase-deficient EGF recepto

150 To increase the probability of obtaining stable transfectants with adequate expression of effecto

151 l line, which is devoid of the EGFR, and its stable transfectants with either wild-type EGFR (B82L) o

152 Stable transfectants with expression of small interferin

153 ent of the Cdc25B2-green fluorescent protein stable transfectants with vanadate inhibited the cell cy