ライフサイエンスコーパス: primary culture

1 n were decreased in PAH smooth muscle cells (primary culture).

2 es in recombinant systems and rat neurons in primary culture.

3 s, SCFAs raised cytosolic Ca2+ in L cells in primary culture.

4 f keratin filaments in skin keratinocytes in primary culture.

5 ventricular myocytes and those in short-term primary culture.

6 s for Arc overexpression were performed from primary cultures.

7 ased dendritic arborization and soma size in primary cultures.

8 Nes-S impairs the survival of DRG neurons in primary cultures.

9 n cell samples from both muscle biopsies and primary cultures.

10 creases in mitotic defects and aneuploidy in primary cultures.

11 tanyl, and DAMGO function as morphine in the primary cultures.

12 whereas CN neurons were from postnatal mouse primary cultures.

13 r dendritic spine density in rat hippocampal primary cultures.

14 and differentiation of human fibroblasts in primary cultures.

15 RNA populations in terminally differentiated primary cultures.

16 thalamic cell line mHypoE-N41 and ARC neuron primary cultures, 2) likewise blocked by a peroxisome pr

17 JIP3 knockout mouse neuron primary cultures accumulate lysosomes within focal axona

18 from C57BL/6 transgenic mice were studied in primary cultures, allowing for visualization of soma and

19 e, NHE5 depletion in rat cortical neurons in primary culture also inhibits neurite formation.

20 Commercial and primary culture AMSCs and commercial BMSCs demonstrated

21 th commercial AMSCs and BMSCs as compared to primary culture AMSCs, suggesting primary cultures have

22 ventricular cardiomyocytes were incubated in primary culture and exposed to isoproterenol (1 mumol/L)

23 glioblastoma multiforme cells maintained in primary culture and following knockdown of one of the co

24 nic and neuroprotective potential in ex vivo primary culture and in vivo zebrafish and mouse models.

25 WDR73 p.Phe296Leufs*26 proliferate poorly in primary culture and senesce early.

26 ochondrial architecture was observed both in primary cultures and brown adipose tissue from cold-expo

27 hat NuMA was overexpressed in tumour tissue, primary cultures and cell lines compared to normal ovari

28 and potentiator combinations were tested in primary cultures and conditionally reprogrammed cells ge

29 arkers were investigated in 25 human CCAs in primary cultures and established cell lines.

30 Bmal1 expression promoted neuronal death in primary cultures and in mice treated with a chemical ind

31 microglial responses to myelin pathology in primary cultures and in the cuprizone mouse model of mul

32 stable cell lines, low-grade glioma-derived primary cultures and NSCs.

33 re, in hippocampal pyramidal neurons of both primary cultures and slices, we triggered a unique form

34 n human lung fibroblasts were examined using primary cultures and the MRC5 cell line in vitro.

35 non-O157 STEC (n = 8) isolates, although the primary cultures and toxin assays were frequently negati

36 We expressed the mutation in cell lines and primary cultures, and we evaluated the putative morpholo

37 to late in their embryogenesis to establish primary cultures, as these eggs contain cells that are p

38 ound by the phosphorylated forms of CRYAB in primary cultured astrocytes, we show that there is clear

39 activated caspase 3 and induced apoptosis in primary cultured astrocytes, which was prevented by casp

40 alent cation-sensitive permeation pathway in primary cultured astrocytes.

41 TNF-alpha augmented the contraction of primary cultured bladder smooth muscle cells through upr

42 Finally, in a cortical neuron primary culture, both Nanobodies were able to inhibit en

43 prove salivary gland cell differentiation in primary cultures by using a combination of L1 and a feed

44 e the axon maintenance function of NMNAT2 in primary cultures, can also correct developmental defects

45 ositol 4,5-bisphosphate (PIP2) levels in the primary cultured cardiomyocytes from adult rats.

46 This protocol is suitable for producing primary culture cells from organs and tissues of small v

47 Experiments were also done ex vivo and with primary cultured cells in vitro.

48 We found that in primary cultures derived from human haematopoietic proge

49 Primary cultures derived from retinoblastoma tumors can

50 High-throughput screening of primary cultures derived from those xenografts identifie

51 in multiple glioma patient specimens, glioma primary cultures derived from tumors taken at surgery an

52 ithelial cultures, termed "mini-intestines." Primary cultures developed from isolated intestinal cryp

53 R-126 upregulation increased angiogenesis of primary cultured endothelial cells from patients with de

54 ys a floating, solid-walled enclosure as the primary culture environment, providing greater potential

55 In primary cultures, epithelial-mesenchymal transition mark

56 In primary culture, Esl-1(-/-) osteoclast progenitors show

57 sufficient cell lines for a large scale HTS, primary cultured fibroblasts from MLD patients were tran

58 Here, we found that EC cells in mouse primary cultures fired spontaneous bursts of action pote

59 HGFs were primary cultured from human gingiva specimens.

60 We have also studied primary cultures from 10 spontaneous canine OSAs.

61 HR status was determined in primary cultures from ascitic fluid in 50 chemotherapy-n

62 Furthermore, in primary cultures from atherosclerotic human aorta lesion

63 ificant deficits in TRPV1 desensitization in primary cultures from beta-arrestin-2 knock-out mice com

64 unction in rat septal cholinergic neurons in primary cultures from E18.5 embryos and in the adult bra

65 We established primary cultures from follicular epithelium in human hom

66 d with established cell lines were seen with primary cultures from fresh tumors.

67 Primary cultures from murine cancers derived from prosta

68 ytes, oligodendrocytes, and microglia) using primary cultures from postnatal d 1 rat cortex.

69 ested the effect of SU6656 on differentiated primary cultures from severe asthma.

70 ompared to primary culture AMSCs, suggesting primary cultures have a slower growth rate than commerci

71 Primary-culture hBECs from subjects with mild to severe

72 ation with P300 antibody, in HepG2 and human primary culture hepatocytes.

73 phagy both in the in vivo mouse liver and in primary cultured hepatocytes.

74 Primary cultured HSCs isolated from WT, SODmu, and NOX1

75 candidate gene mutations were determined in primary culture human tracheobronchial epithelial cells

76 ssenger RNA (mRNA) and protein expression in primary cultured human hepatocytes, and stimulated MDR3

77 X2 is up-regulated in lungs, distal PAs, and primary cultured human PASMCs isolated from PAH and comp

78 Klotho protein (KL) is expressed in primary cultured human RPE, and regulates pigment synthe

79 From 65 patients, 27 primary cultures, including several from patients with s

80 Primary cultures, initiated from testes, were treated wi

81 Among 61 primary culture isolates (25 study group and 36 control

82 tically reduces sequencing error, to analyze primary cultured isolates phenotypically resistant to ri

83 KT restored normal Na+/K+-ATPase activity in primary cultured lens cells and reduced lens pressure in

84 lated reporter-tagged Mbp mRNA granules from primary cultured mammalian oligodendrocytes to show that

85 ieux), a chromogenic medium, to conventional primary culture medium for evaluation of urine specimens

86 ion changes that occur during development of primary cultured megakaryocytes (MEG) and primary erythr

87 A rat ENS primary culture model confirmed this expression.

88 trigger the activation of ATM or ATR in our primary culture model.

89 cterized TDP-43 localization and dynamics in primary cultured motor neurons.

90 strong inhibitory effect on adipogenesis in primary cultured mouse ADSVFCs and human ADSCs.

91 We performed global expression profiling of primary cultured mouse and human macrophages, sampling a

92 expression profile of their synthases in the primary cultured mouse bone marrow derived macrophages (

93 ve role against APAP-induced hepatotoxicity, primary cultured mouse hepatocytes and green fluorescent

94 In primary cultured mouse hepatocytes and HepG2 cells, the

95 various essential autophagy-related genes in primary cultured mouse hepatocytes and in mouse liver.

96 Furthermore, primary cultured mouse motor neurons showed axonal degen

97 we examined PLN stability and degradation in primary cultured mouse neonatal cardiomyocytes (CMNCs) a

98 AVP stimulated GLP-1 and PYY release from primary cultured murine and human colonic cells and was

99 of TRAIL on IL-33 expression was assessed in primary cultured murine hepatocytes.

100 into axons is required for axon survival in primary culture neurites and axon extension in vivo.

101 live-cell imaging of axonal transport in SCG primary culture neurons, we find that Nmnat2 is bidirect

102 e with an essential axon maintenance role in primary culture neurons.

103 e and boosts its axon protective capacity in primary culture neurons.

104 N1 protected primary cultured neurons against toxicity and cell death

105 d enhances aggregation of alpha-synuclein in primary cultured neurons and in dopaminergic neurons of

106 ated oxidative stress-mediated cell death in primary cultured neurons at nanomolar concentrations.

107 ta load in neuroblastoma cells as well as in primary cultured neurons derived from Tg2576 mice.

108 t ubiquitination of endogenous Bax comparing primary cultured neurons from WT and parkin KO mice and

109 We show that increased E6AP expression in primary cultured neurons leads to a reduction in dendrit

110 Furthermore, in primary cultured neurons, a proportion of UCH-L1(M) does

111 o mammalian-cultured cells, yeast, bacteria, primary cultured neurons, Drosophila melanogaster larval

112 In primary cultured neurons, NES mutations increase nuclear

113 tide in multiple mammalian cell lines and in primary cultured neurons.

114 vation and reduced spine density and size in primary cultured neurons.

115 in the murine hippocampus and in hippocampal primary culture, neurons of the CA1 region and the denta

116 In vitro BBB models have been developed from primary culture of brain endothelial cells of several ma

117 Primary culture of cells allowed us to analyze their rel

118 t cells of human colon epithelial tissue and primary culture of colonic epithelial cells.

119 PGD2 levels were determined in a medium of primary culture of ENS and neuro-glial coculture model t

120 PGD2 levels were significantly increased on primary culture of ENS treated with LPS.

121 S induced higher levels of neuritogenesis in primary culture of enteric neurons, compared with contro

122 as breathing tumors by xenografting and as a primary culture of epithelial cells.

123 ta1 inhibitor, on the morphologic changes of primary culture of hGE cells were examined in vitro.

124 Here, we have used 14 d in vitro primary culture of hippocampal neurons and ex vivo prepa

125 ossibility by using the 25-57 Dpl peptide in primary culture of mouse embryo cortical neurons and fou

126 he mouse lungs and airway cells, including a primary culture of mucus-covered human airway epithelium

127 Here we establish a sustainable primary culture of Oct3/4(+)/Nanog(+) lung CSCs fed with

128 d in HeLa cells or endogenously expressed in primary culture of pancreatic beta-cells.

129 ingle chemicals and as complex mixtures in a primary culture of rainbow trout (Oncorhynchus mykiss) h

130 rapid and highly selective protocol for the primary culture of Schwann cells in vitro from freshly d

131 umour epithelial cells by almost two-fold in primary culture of tumour cells from Apc(Min/+) mice.

132 ascular cell adhesion molecule-1 (VCAM-1) in primary culture of tumour endothelial cells.

133 e potency and/or efficacy of DOR agonists in primary cultures of adult rat peripheral sensory neurons

134 We show here that in well-differentiated primary cultures of airway epithelial cells from human d

135 igate the expression levels of chemokines in primary cultures of ASM cells from asthmatics vs healthy

136 tases from eight craniotomy specimens and in primary cultures of astrocyte-enriched glial cells.

137 Infected mixed primary cultures of astrocytes and microglia had higher

138 increases the level of mRNA encoding xCT in primary cultures of astrocytes isolated from mouse corte

139 In vitro studies using primary cultures of bone marrow monocyte-derived macroph

140 In primary cultures of bone marrow, we showed that GW9508,

141 Primary cultures of bovine retinal pericytes were cultur

142 When astrocytes were cocultured with primary cultures of brain vascular endothelial cells, st

143 GDF15 was found upregulated in situ and in primary cultures of CAF from prostate cancer.

144 rleukin (IL)8 messenger RNA by AGS cells and primary cultures of canine parietal and mucus cells.

145 on or siRNA-mediated silencing of PKCzeta in primary cultures of cardiac cells and in neonatal cardio

146 In primary cultures of cardiomyocytes, overexpression of mi

147 In vitro, primary cultures of CB1 receptor-deficient KC released i

148 In response to IL-1beta, primary cultures of central nervous system ECs produce G

149 However, acute deletion of Sox2 from primary cultures of CGNPs with constitutive Shh signalin

150 Using serum-free primary cultures of chick lens epithelial cells (DCDMLs)

151 nalyze the function of RBPMS2 in vivo and in primary cultures of chicken SMCs.

152 aling in colorectal cancer cell lines and in primary cultures of colorectal cancer metastases.

153 tion of heparan sulfate was also detected in primary cultures of cortical neural cells, especially as

154 A reduced endogenous P2X7 receptor levels in primary cultures of cortical neurons and astrocytes.

155 n A under global hypoxia without ischemia in primary cultures of cortical neurons and in neonatal and

156 ecreased capacity to infect and replicate in primary cultures of cortical neurons, a property depende

157 ot seen when astrocytes were cocultured with primary cultures of cortical neurons.

158 Its addition to primary cultures of differentiating oligodendrocyte prec

159 ctrophysiological activity was recorded from primary cultures of dissociated rat cortical neurons pla

160 photosensitivity and functioning of HCs from primary cultures of embryonic retinas at day 15 by using

161 In primary cultures of endothelial cells, vascular endothel

162 rheas, (R)-BPO-27 blocked fluid secretion in primary cultures of enteroids from human small intestine

163 Primary cultures of esophageal fibroblasts and muscle ce

164 n heterologous F508-CFTR-expressing cells or primary cultures of F508/F508 human bronchial epithelia.

165 SF was used to stimulate primary cultures of fibroblast-like synoviocytes (FLS) a

166 For functional analyses, primary cultures of fibroblasts were obtained from 11 pa

167 We show in primary cultures of glioma stemlike cells that EGR1 cont

168 Primary cultures of hepatocytes and LPCs from AlfpCre(+)

169 Primary cultures of hepatocytes derived from wild-type o

170 Primary cultures of HGFs were grown on Type I collagen m

171 ant protein and induced neurite outgrowth in primary cultures of hippocampal and cerebellar granule n

172 Overexpression of miR-132 in primary cultures of hippocampal neurons or delivered dir

173 Primary cultures of hippocampal neurons were used to sel

174 observed in mammalian cell lines as well as primary cultures of hippocampal neurons.

175 In well-differentiated primary cultures of human airway epithelial cells from n

176 e wild-type MV spread in well-differentiated primary cultures of human airway epithelial cells.

177 2, inhibit its expression, and are active in primary cultures of human cutaneous cells.

178 d DeltaF508-CFTR-mediated Cl(-) transport in primary cultures of human cystic fibrosis airway epithel

179 In contrast, in primary cultures of human fetal kidney cells, which main

180 Primary cultures of human GFs and PDLFs were isolated.

181 Primary cultures of human gingival fibroblasts (HGFs) we

182 Primary cultures of human hepatocyte spheroids are a pro

183 define the complex protein mixtures found in primary cultures of human intrahepatic biliary epithelia

184 In this report, we used primary cultures of human iris stroma (HIS) cells derive

185 nd stimulates repair-associated responses in primary cultures of human keratinocytes and fibroblasts,

186 In primary cultures of human monocytes or alveolar type 2 c

187 (PPP) on osteoblastic differentiation using primary cultures of human periodontal ligament stem cell

188 Primary cultures of human saphenous vein endothelial cel

189 and endocrine regulation of sex steroids by primary cultures of human skin epidermal keratinocytes a

190 g analysis of conditioned media derived from primary cultures of human trabecular meshwork (HTM) cell

191 n profile of prostaglandin (PG) receptors in primary cultures of human trabecular meshwork (TM) and S

192 Primary cultures of human trabecular meshwork (TM) cell

193 of TGF-beta1 on VE-cadherin was confirmed in primary cultures of human trophoblast cells.

194 By contrast, primary cultures of invasive breast cancer cells convert

195 In primary cultures of isolated human ASM, we identified mR

196 4 (TLR4)-mediated signaling was assessed in primary cultures of Kupffer cells from ethanol- and pair

197 phological changes to the lipid membranes of primary cultures of living human trabecular meshwork cel

198 ut proliferating precursors were detected in primary cultures of lung tissue.

199 l and tumour tissues, ovarian cell lines and primary cultures of malignant cells derived from ovarian

200 ces of removing the beta1-integrin gene from primary cultures of mammary epithelial cells in situ, us

201 Influenza A virus (IAV) is a lytic virus in primary cultures of many cell types and in vivo.

202 origin of BDNF in platelets, we established primary cultures of megakaryocytes, the progenitors of p

203 Although primary cultures of mesothelial cells or submesothelial

204 Using primary cultures of microglia isolated from mouse brains

205 In primary cultures of mouse bone marrow-derived macrophage

206 Treatment of primary cultures of mouse cortical astrocytes with the n

207 to knock down individual DNMT expression in primary cultures of mouse embryonic cardiomyocytes.

208 R-dependent ATP release was also observed in primary cultures of mouse epididymal epithelial cells.

209 Primary cultures of mouse hepatocytes were exposed to ty

210 In primary cultures of mouse hepatocytes, ChREBP overexpres

211 resses TNF-alpha and caspase-3 expression in primary cultures of mouse hepatocytes.

212 d time-dependent neuronal hyperexcitation in primary cultures of mouse hippocampal neurons.

213 itionally, felodipine inhibition of LTCCs in primary cultures of mouse lens epithelial cells resulted

214 erstood, we addressed this issue with use of primary cultures of mouse mesencephalic dopaminergic neu

215 a phosphorylation-null Thr84 SV2A mutant in primary cultures of mouse neurons.

216 r RFS-associated kappaLCs (RFS-kappaLCs) and primary cultures of mouse PT cells exposed to low doses

217 cipates in interkeratin disulfide bonding in primary cultures of mouse skin keratinocytes.

218 In vitro studies where strain was applied to primary cultures of mouse tibia-derived osteoblastic cel

219 In this paper, using primary cultures of mouse tracheal epithelial cells, we

220 experiments in C2C12 and MC3T3-E1 cells and primary cultures of murine bone marrow-derived mesenchym

221 ANKRD55 was produced by primary cultures of murine hippocampal neurons and micro

222 ptide bond, and when pre-mixed with IL-23 in primary cultures of murine splenocytes inhibits IL-23-me

223 es such as cell migration were not affected, primary cultures of N-WASP-deficient podocytes revealed

224 cursor miR-181c (or a scrambled sequence) in primary cultures of neonatal rat ventricular myocytes.

225 n against cytotoxicity in cardiomyocytes and primary cultures of neuronal cells exposed to H2O2 speci

226 Human cell lines and rat primary cultures of neurons and astrocytes were treated

227 Primary cultures of neurons and glial cells from Npc1(-/

228 the expression of the MCU channel subunit in primary cultures of neurons expressing a genetically enc

229 ocks alpha-synuclein-induced cytotoxicity in primary cultures of nigral dopaminergic neurons, and rec

230 ced inflammatory responses were evaluated in primary cultures of non-CF versus CF AMs.

231 We confirmed in primary cultures of normal human bronchial epithelial ce

232 Primary cultures of normal human bronchial epithelial ce

233 t treatment, oxygen concentration, etc.), in primary cultures of normal human dermal fibroblasts expo

234 tributed to a direct action of galectin-8 on primary cultures of osteoblasts that secrete the osteocl

235 tagonist mifepristone each acted directly on primary cultures of parietal epithelial cells, inhibitin

236 with baseline expression of alphavbeta3, but primary cultures of peritoneal macrophages (PMo) require

237 human nectin-4 at promoting MV infection in primary cultures of porcine airway epithelia.

238 After repetitive passages, primary cultures of porcine aortic endothelial cells exh

239 Primary cultures of porcine RPE cells were differentiate

240 Analysis of Pi transport in primary cultures of proximal tubular cells or in freshly

241 Using primary cultures of pure motoneurons or astrocytes from

242 OCs, as well as immature mononuclear OCs, in primary cultures of RANKL-stimulated bone marrow cells.

243 A, miR-487b, was further investigated, using primary cultures of rat aortic and human umbilical cord

244 embranes in LBs and LBPs freshly secreted by primary cultures of rat ATII cells has been compared wit

245 Immunoblot analysis of DIC and OGC in primary cultures of rat cerebellar granule neurons (CGNs

246 analyze microtubule plus-end orientations in primary cultures of rat hippocampal and cortical neurons

247 Using primary cultures of rat hippocampal neurons as a model s

248 Using primary cultures of rat hippocampal neurons as a quantit

249 Here, we use primary cultures of rat hippocampal neurons to show that

250 atically analyze microtubule organization in primary cultures of rat hippocampal neurons, dentate gra

251 2-R by the reversible antagonist PSB-0739 in primary cultures of rat inner medullary CD cells potenti

252 copy and quantitative immunocytochemistry in primary cultures of rat neocortical neurons.

253 in both the PC3 human prostate cell line and primary cultures of rat prostate fibroblasts, supporting

254 Primary cultures of rodent sensory neurons are widely us

255 se have been limited by the lack of extended primary cultures of the epithelium.

256 cytotoxicity of bFGF-NP were evaluated with primary cultures of the left ventricular (LV) cardiomyoc

257 Analysis of primary cultures of TMJ articular chondrocytes from wild

258 ed the invasiveness of HTR-8/SVneo cells and primary cultures of trophoblast cells.

259 unctional study of variants at this locus in primary cultures of vascular smooth muscle and endotheli

260 was performed on medial tissue extracts and primary cultures of VSMCs of human thoracic aneurysms (n

261 Analyses of primary cultures of VSMCs showed that the 9p21 risk geno

262 s were infected with MeV and then applied to primary cultures of well-differentiated airway epithelia

263 e have developed an in vitro BBB model using primary cultured porcine brain endothelial cells (PBECs)

264 slices from PS conditional knockout mice and primary cultured postnatal hippocampal neurons, in which

265 itotoxic stimulus in rat cortical neurons in primary culture promotes cyclin B1 accumulation in the m

266 s a correlation of apoD's ability to protect primary cultured rat cardiomyocytes from hypoxia/reoxyge

267 Primary cultured rat hepatocytes were transfected with s

268 teric small arteries, and Ca2+ signalling in primary cultured rat hippocampal neurones.

269 tion of a heteromeric TRPV4-C1-P2 complex in primary cultured rat mesenteric artery endothelial cells

270 ines, and during in vitro differentiation of primary cultured rat oligodendrocytes.

271 dependently up-regulated TRPC6 expression in primary cultured rat PASMCs, and this was accompanied wi

272 eterogeneity, as is generally encountered in primary cultures, reduces measurement yield and limits t

273 RNA-mediated knockdown of beta-arrestin-2 in primary cultures resulted in a significant increase in b

274 Conditional genetic ablation of Tpx2 in primary cultures resulted in deficient microtubule nucle

275 IF of primary cultures revealed that high NuMA levels at mitot

276 erentiation to syncytiotrophoblast (SynT) in primary culture, revealed that members of miR-515 family

277 In primary cultured rodent and human macrophages, CB1R acti

278 novirus 12 - SV40 hybrid (BEAS-2B) cells and primary cultures], roflumilast enhanced fluticasone prop

279 Using primary cultured Schwann cells, we analyze the upstream

280 Using primary cultured Sertoli cells as an in vitro model that

281 Similar experiments with primary cultures showed protection and survival of perip

282 Here we describe an in vitro primary culture system for Caenorhabditis elegans germli

283 cell differentiation, we set up a controlled primary culture system to differentiate human naive B ce

284 Both in tissue slices and primary cultures, the NOP-eGFP receptors appear througho

285 debridement and in rabbit corneal epithelial primary cultures through scratch injury.

286 In primary cultures treated with cyclosporin A, renal tubul

287 Conventional methods to extend the life of primary cultures typically utilize viral oncogenes.

288 ons, or induction of cell differentiation in primary cultures upregulated the number of cells permiss

289 gnant human myometrial cell line PHM1-41 and primary cultured uterine myocytes responded to Toll-like

290 Aneuploidy status in primary cultures was determined by FACS analysis.Affymet

291 Serial transfer of material from several primary cultures was maintained and has led to the isola

292 Using behavioral, electrophysiological, and primary culture, we now demonstrate that reduced dopamin

293 20) and normal mucosa (Controls, n = 15) in primary culture were analyzed by global proteomic approa

294 Glioma cell lines and low passage primary cultures were analyzed.

295 GBM cell lines and primary cultures were found to express CD97.

296 Primary cultures were initiated in modified Leibovitz's

297 In vitro scratch assays of primary cultures were used to evaluate cell migration.

298 a specimens and in high-grade glioma-derived primary cultures, whereas remaining low in glioblastoma

299 ed Nmnat2 to preserve transected neurites in primary culture, while re-targeting the strongly protect

300 lastoma specimens, including patient-derived primary cultures, xenografts, genetically engineered gli