ライフサイエンスコーパス: primary cell culture

1 less than 14 wk do not exhibit aneuploidy in primary cell culture.

2 Neurocan is also expressed by astrocytes in primary cell culture.

3 presenting cytotoxic effects on a non-tumour primary cell culture.

4 inal pigment epithelial cells was studied in primary cell culture.

5 tiffness of the cellular microenvironment in primary cell culture.

6 s) tracks cumulative population doublings in primary cell culture.

7 toxicity was evaluated using a porcine liver primary cell culture.

8 f pathogenesis and exhibit reduced growth in primary cell culture.

9 elial cells and fibroblasts were obtained by primary cell culture.

10 eterminant of efficient HSV-1 replication in primary cell culture.

11 e excitability in rat hippocampal neurons in primary cell culture.

12 ighly expressed on some tumor cell lines and primary cell cultures.

13 gs were made from rat hippocampal neurons in primary cell cultures.

14 mere length in chicken tissues as well as in primary cell cultures.

15 and their antagonists of Cai2+ in sheep lens primary cell cultures.

16 ansfer into several mammalian cell lines and primary cell cultures.

17 eliminated from tumor cell lines as well as primary cell cultures.

18 an block glial cell differentiation in mixed primary cell cultures.

19 e describe a method to generate EHE extended primary cell cultures.

20 essed using flow cytometry and microscopy on primary cell cultures.

21 imal medium for long-term growth of D. citri primary cell cultures.

22 d healthy controls (n = 25) were cultured as primary cell cultures.

23 s cell-autonomous as it was also observed in primary cell cultures.

24 a swine cell line (SK6) and swine macrophage primary cell cultures.

25 n both in vivo and in three-dimensional (3D) primary cell cultures.

26 ence in osteoclast precursors and GPR40(-/-) primary cell cultures.

27 fication or degradation and were nontoxic in primary cell cultures.

28 glia and can modulate microglial activity in primary cell cultures.

29 ents were performed on mouse small intestine primary cell cultures.

30 ceptor ligands on ICC numbers was studied in primary cell cultures.

31 arian surface epithelial cells in tissues or primary cell cultures.

32 regions on dengue virus replication in human primary cell cultures.

33 oscopy, resemble those of cells derived from primary cell cultures.

34 rradiated (30 Gy) and/or mitomycin C-treated primary cell cultures.

35 In other experiments, APR(4)s were placed in primary cell culture 4 days before eclosion in medium co

36 Development of these extended primary cell cultures allowed for single-cell profiling

37 Here, using a transgenic mouse model and primary cell cultures along with quantitative PCR, immun

38 Two culture systems, a primary cell culture and a cell line transformed with th

39 egration of nicotinic EPSPs were compared in primary cell culture and in the acutely isolated intact

40 S1P(1) was enriched on LSECs in vivo and in primary cell culture and that VPC23019 inhibited both sp

41 ghly specific inhibitors that can be used in primary cell culture and whole animals.

42 Using primary cell cultures and cell lines, we investigated th

43 to those found in late serous adenocarcinoma primary cell cultures and established ovarian cancer cel

44 Ns may limit the growth and spread of HCV in primary cell cultures and in the infected liver.

45 rradiation in the media from established and primary cell cultures and in the urine of irradiated mic

46 In the present work, we used primary cell cultures and isolated muscles from Trpc1(-/

47 muscle (PrSM), and prostate stromal (PrSt)] primary cell cultures and prostatic carcinoma cell lines

48 Herein, we used primary cell cultures and the intrastriatal alphaSyn pre

49 sense drugs singly and as cocktails, both in primary cell culture, and two in vivo delivery methods (

50 e and report editing activity in cell lines, primary cell cultures, and adult mice via nonviral deliv

51 nt in vitro models of VC (i.e., human serum, primary cell cultures, and tissue explants), and largely

52 Primary cell cultures are in general resistant to the tr

53 erning how relevant studies of senescence in primary cell cultures are to aging in whole animals.

54 lcium uptake in a mouse dorsal root ganglion primary cell culture assay.

55 d to selectively isolate genetically altered primary cell cultures based on the permanent activation

56 erum-stimulated human vascular smooth muscle primary cell cultures, bilirubin favors growth arrest, a

57 blocked the Shh-induced CGP proliferation in primary cell cultures, but also ameliorated aberrant CGP

58 ular meshwork (HTM) and Schlemm's canal (SC) primary cell cultures by Western blot analysis.

59 Primary cell cultures composed of photoreceptors, bipola

60 Analysis of primary cell cultures confirmed that astrocytes expresse

61 sis of follicular melanocytes in vivo and in primary cell culture demonstrated that pRB plays a cell-

62 human and monkey eyes, as well as organ and primary cell cultures derived from these eyes, were inve

63 Primary cell cultures displayed a transient increase in

64 Induction of RAE-1 occurred in primary cell cultures, embryonic brain cells in vivo, an

65 In addition, primary cell cultures enriched for human CD4+, monocytes

66 ced colony formation and proliferation in 3D primary cell cultures established from CYLD mutant tumou

67 ytosol and strongly reduced proliferation in primary cell cultures established from fibrotic membrane

68 Primary cell cultures established from normal and osteoa

69 ous biological samples including cell lines, primary cell cultures, ex vivo specimens, biopsy samples

70 Primary cell culture experiments also show that several

71 nsive analysis of T-cell cross-reactivity in primary cell cultures, facilitating the identification o

72 bly steps are expected to take 8 d, with the primary cells cultured for 12 d to form mature in vitro

73 ngival tissues were then processed to obtain primary cell cultures, for which proliferation rates wer

74 mation of oligodendrocytes were inhibited in primary cell culture from the furue mice.

75 ndrocyte differentiation also is observed in primary cell culture from this mutant.

76 d tyrosine kinome RNA interference screen in primary cell cultures from a genetically engineered, con

77 dr2(slie/slie) mice, and deletion of Ddr2 in primary cell cultures from dental pulp and PDL inhibited

78 In this article, we first show, using primary cell cultures from human lung adenocarcinoma, th

79 m, we previously developed three-dimensional primary cell cultures from infant bronchial epithelium t

80 Homogenous primary cell cultures from normal and glaucomatous human

81 Primary cell cultures from OA cartilage contained signif

82 r models, epicardial and subcutaneous stroma primary cell cultures from patients undergoing open hear

83 F) have been detected in tumor specimens and primary cell cultures from patients with head and neck s

84 We tested this hypothesis using primary cell cultures from the cortex and hippocampus of

85 to characterize the adipogenic phenotype in primary cell cultures from three tissue sources.

86 ypes where it establishes latency.IMPORTANCE Primary cells cultured in vitro currently provide the hi

87 assay involving mouse calvaria (skull bone) primary cell cultures, in which a large fraction of the

88 MHV infection of primary cell cultures indicates that hepatocytes are not

89 expressing corneal epithelial cell lines and primary cell culture is consistent with the notion that

90 re shortening in human and mouse tissues and primary cell cultures may be due to the absence of telom

91 We have developed a primary cell culture model of rabbit uroepithelium that

92 on and sFLT1 production, a human trophoblast primary cell culture model was established in which hypo

93 In contrast to prior work with primary cell cultures, MyoD did not activate the myogeni

94 ot assays in fresh human tissues (n = 8) and primary cell cultures (n = 6).

95 toxicity was evaluated using a porcine liver primary cell culture (non-tumour cells).

96 5-HT(2B) receptor activation in primary cell cultures obtained from PKCgamma(-/-) mice d

97 siological activation of sGC in context of a primary cell culture of human umbilical vein endothelial

98 We report aragonite crystallization in primary cell cultures of a hard coral, Pocillopora damic

99 tis virus) of different neurovirulences with primary cell cultures of brain immune cells (astrocytes

100 Primary cell cultures of human corneal epithelial cells

101 We infected primary cell cultures of human keratinocytes with KSHV/H

102 operiod melatonin signals (16 h exposure) on primary cell cultures of melatonin target cells of the o

103 Primary cell cultures of porcine trabecular meshwork (PT

104 Primary cell cultures of RA- and OA-derived synovial fib

105 sion of cathepsin K was also demonstrated in primary cell cultures of RA-SFs.

106 Mannose-GPs of primary cell cultures of rabbit corneal epithelium were

107 of Meis1-expressing cells, were observed in primary cell cultures of Rarb(-/-) LGE.

108 the intracellular concentrations of ROIs in primary cell cultures of rat retina and, in vivo, preven

109 report of oral microorganisms invading human primary cell cultures of the vasculature.

110 DeltaNp63a and keratin 3/12 was detected in primary cell cultures on the two substrates with no stat

111 In contrast, primary cells cultured on laminin/collagen mixtures do n

112 ter removal of the cytokine in the NOS2(-/-) primary cell culture only.

113 s recordings from cell populations either in primary cell cultures or in intact tissues.

114 he cellular environment of contact-inhibited primary cell cultures or the myocardium in vivo is suffi

115 tially improves image quality in live-imaged primary cell cultures, planarians, zebrafish and human c

116 imilar results were obtained in dissociated, primary cell cultures prepared from the ventral medulla,

117 This has led to the increasing use of primary cell cultures, primary tumour cell explants, ear

118 Primary cell culture remains useful, but large tumours a

119 ditional deletion of ILK both in vivo and in primary cell cultures resulted in defective differentiat

120 Infection studies in a primary cell culture revealed that Ifi27l2a(-/-) cerebel

121 icroarray analysis of RNA from neuroblastoma primary cell cultures revealed 10-fold higher MCM7 expre

122 High-content analysis of primary cell cultures revealed that T-DM1 is taken up by

123 ssfully applied to genomic DNA isolated from primary cell culture, sorted cells and fresh tissue from

124 ransporters (MCTs), we used a combination of primary cell culture studies, (13)C isotopic tracing, la

125 n and mRNA levels were determined in a sheep primary cell culture system by Western and Northern blot

126 ession during differentiation, and this lens primary cell culture system provides a valuable tool to

127 the three sheep connexin proteins in a lens primary cell culture system.

128 ptor that exhibited impaired activity in the primary cell culture system.

129 n immunodeficiency (SIV) macaque model and a primary cell-culture system to investigate the associati

130 y the progenitor to pre-B cell transition in primary cell culture systems and in the bone marrow in v

131 a variety of settings including cell lines, primary cell culture systems, ex vivo tissue preparation

132 In primary cell culture systems, forskolin not only down-re

133 data from mouse models, human HSE cases, and primary cell culture systems, we showed that microglia a

134 In primary cell cultures, the addition of TSLP led to an in

135 Using primary cell culture to screen for changes in neuronal m

136 fusion (I/R), genetically modified mice, and primary cell culture, to investigate the cell type-speci

137 Interestingly, treatment of primary cell cultures using aurothiomalate (ATM), which

138 ntargeted metabolomics analyses of serum and primary cell cultures using hyphenated ultra-high perfor

139 Acid secretion in primary cell cultures was measured by aminopyrine accumu

140 Using chick embryos and primary cell culture, we examined gene expression of the

141 cell sorting, single-cell RNA sequencing and primary cell culture, we have identified multiple subtyp

142 Using primary cell culture, we validated the ability of hepato

143 observation of telomere aberrations in those primary cell cultures, we are reasonably certain that ou

144 ls of ADPKD, including ADPKD patient-derived primary cell cultures, we demonstrate that treatment wit

145 Using an in vitro model of ccRCC primary cell cultures, we performed, for the first time

146 X-2 upregulation, gingival connective tissue primary cell cultures were established and challenged wi

147 Their viability was confirmed when primary cell cultures were established from isolated der

148 ll adhesion molecule], CD133, and CD13), and primary cell cultures were prepared.

149 Human PDL cells, derived from a primary cell culture, were transfected with simian virus

150 as replicated ex vivo by incubating podocyte primary cell cultures with low-dose ouabain.

151 treatment of TRPV5-expressing mouse DCT2/CNT primary cell cultures with the beta1-AR agonist dobutami