ライフサイエンスコーパス: be cultured

1 ymptoms and the causative organism could not be cultured.

2 er microbes, especially to those that cannot be cultured.

3 e through the Matrigel droplet in which they are cultured.

4 d polyacrylamide gels upon which these cells are cultured.

5 s and 14/31 (38.7%) air samples but no virus was cultured.

6 Bacterial and fungal isolates were cultured.

7 olution specimens collected from 16 patients were cultured.

8 as samples obtained from pet dogs and cats, were cultured.

9 Four matched pairs of hGFs and hPDLFs were cultured.

10 57BL/6 mice and resected human pancreata and were cultured.

11 sion, newborns were euthanized and specimens were cultured.

12 All platelet units had been cultured 24 hours after collection and released as

13 diagnosis was observed when three specimens were cultured (92%; 95% credible intervals, 79 to 100%).

14 cultured cells used for biomedical research are cultured adherently, and the requisite detachment pr

15 Primary murine lung fibroblasts (PLFs) were cultured +/- alcohol, miR-1946a mimic or inhibitor,

16 Representative Lb. plantarum isolates were cultured alone and in combination with acid-produci

17 hages or human monocytes (RAW264.7 or THP-1) were cultured alone or with breast cancer cells (mouse p

18 of mouse melanoma cells, can be selected by being cultured and grown in 3D soft fibrin gels.

19 Escherichia coli, our sentinel organism, was cultured and a single isolate from each sample teste

20 Swab and tissue specimens were cultured and analyzed by 16S ribosomal RNA polymera

21 were collected from mice; IECs and enteroids were cultured and analyzed by histology, immunoblots, ph

22 , analyzed by histology, and liver organoids were cultured and analyzed.

23 tes from MF patients and healthy individuals were cultured and differentiated into OCs.

24 Colon carcinoma HCT 116 cells were cultured and grown into three-dimensional cell cult

25 Mouse sensory neurons were cultured and incubated with biopsy supernatants and

26 ial cells (pNECs) collected during surgeries were cultured and injured under 3 conditions: (1) basal

27 Samples were cultured and isolates identified using matrix-assis

28 f cases of C. difficile infection, specimens were cultured and isolates underwent molecular typing.

29 Filoviruses were cultured and observed by EM in Antwerp, Belgium (In

30 Colonic explants were cultured and preserved ex vivo for 35 days and co-c

31 Isolated intra-allograft B cells were cultured and shown to synthesize multiple cytokines

32 onjunctival epithelial cells and fibroblasts were cultured and stimulated with IL-1beta, histamine, I

33 Isolates were cultured and their whole genome sequenced, and we u

34 rain microvascular endothelial cells (BMECs) were cultured and treated with Malat1 GapmeR before 16 h

35 Towards this goal, luteal cells were cultured and treated with VEGF A and FGF 2 and the

36 ently calved cows or clinical mastitis cases were cultured, and 181 isolates were identified by bioch

37 Tibiae and K-wires were cultured, and medians were reported as log10 colony

38 cytic leukemia macrophage (THP-1) cell lines were cultured, and RPE and THP-1 cells were exposed to a

39 Isolated myocytes can be cultured antibiotic free, with retained organized con

40 cells (SSCs) isolated from human bone marrow were cultured as high density micromass' using TGF-beta3

41 hree neuro- and glioblastoma cell lines that were cultured as monolayer and multicellular tumor spher

42 ntestinal bacterium, human jejunal enteroids were cultured as monolayers in microengineered fluidic-b

43 Cardia and forestomach tissues from mice were cultured as organoids and incubated with inhibitors

44 96%) or endotracheal aspirate (4%) specimens were cultured as per routine practice and also tested wi

45 iocytes, epithelial cells lining bile ducts, were cultured as polarized epithelia in a Transwell syst

46 e, n = 13 BOS) and healthy controls (n = 25) were cultured as primary cell cultures.

47 cells, including human cells, provided they are cultured at 30 degrees C.

48 els of these RNAs differ when M. sympodialis is cultured at normal human skin pH versus the elevated

49 When E681 was cultured at 20 degrees C or lower, it exhibited no v

50 on was restored in DeltaF508 CFTR when cells were cultured at 28 degrees C but only in the presence o

51 rease in global protein synthesis when cells were cultured at acidic pH.

52 NHBE cells were cultured at air-liquid interface and treated with i

53 atched DPCs from balding and occipital scalp were cultured at atmospheric (21%) or physiologically no

54 Porcine aortic endothelial cells were cultured at confluence on polyacrylamide gels of va

55 ed or did not recover at all after the cells were cultured at pH 7.2 for 8 weeks.

56 lls of control subjects and patients with AR were cultured at the air-liquid interface to study trans

57 Intraocular biopsy samples were cultured by standard methods.

58 age was performed and plastic-adherent cells were cultured, characterized and then delivered therapeu

59 Mouse bladder organoids can be cultured efficiently and genetically manipulated with

60 as of the Pacific Ocean, CRD1 and the yet-to-be cultured EnvB were the prevalent Synechococcus clades

61 defects persist even when Grn(-/-) microglia are cultured ex vivo.

62 st B-cell precursor ALL (BCP-ALL) cells that were cultured ex vivo or in vivo as patient-derived tumo

63 Murine alveolar macrophages (AMs) were cultured ex vivo with/without human MSC-derived EVs

64 ll mass for implantation within 72 hours can be cultured for 96 hours and longer to combine multiple

65 The cell line designated CTC-MCC-41 has been cultured for more than one year, and the cells have

66 ss is an important marine food fish that has been cultured for several decades in Asia Pacific.

67 RNA virus, vesicular stomatitis virus (VSV), was cultured for three passages on BHK host cells, and p

68 bioreactor that contained 10(6) HepG2 cells was cultured for up to 10 days in an incubator.

69 r cell-loaded IFN-DC from FL patients, which were cultured for 2 wk with autologous lymphocytes, led

70 d in each experiment prior to light exposure were cultured for 24 h as follows: Experiment 1) Normoxi

71 d human endometrial epithelial cells (hEECs) were cultured for 24 hours with and without recombinant

72 inct OvC types and one with a benign tumour, were cultured for 30 days in agitation-based culture sys

73 (3.5 x 10(4) cell clusters per cell chamber) were cultured for 4 days in the CCCM under cyclic mechan

74 blood mononuclear cells (PBMCs) of children were cultured for 48 h (anti-CD3/anti-CD28 stimulation o

75 ILC1, ILC2, and ILC3 cells were cultured for 5 days with RA, 1,25D3, and various cy

76 Single hiPSC-CMs were cultured for 5 to 7 days on a 0.4- to 0.8-mm thick

77 rate monocyte-derived macrophages, monocytes were cultured for 7 days, after which either vehicle con

78 Micropellets were cultured for 7-14 days in medium supplemented with

79 riptome of four P. vivax field isolates that were cultured for a short period ex vivo before using a

80 beta-cell numbers but included isolates that were cultured for a shorter duration.

81 ens from hospitalized patients with diarrhea were cultured for C. difficile.

82 Swabs were cultured for CPE until September 2017, when direct

83 mutational-signature generation, cell lines were cultured for extended periods and subsequently DNA

84 pper parts of the human hair follicles which were cultured for four weeks in a Dulbecco's Modified Ea

85 After aging, oocytes were cultured for maturation.

86 es and all samples from symptomatic patients were cultured for N gonorrhoeae, and resulting isolates

87 severity was assessed, and skin/nasal swabs were cultured for S aureus.

88 Said scaffolds were cultured for up to 21 days in a flow perfusion bior

89 Said scaffolds were cultured for up to 21 days in a flow perfusion bior

90 Corneas were cultured for up to 3 days and their green fluoresce

91 were significantly attenuated and could not be cultured from any tissue.

92 In humans, mast cells can be cultured from multipotent CD34(+) progenitor cells.

93 An Exophiala isolate was cultured from a biopsy specimen of a lesion on the f

94 A median of 1 Neisseria species was cultured from each participant (range, 1-4) with 10

95 Emmonsia sp. was cultured from skin biopsy (n = 20/28), mycobacterial

96 Salmonella Typhi and iNTS were cultured from 194 (1.4%) and 840 (5.9%), respective

97 In this study, DC were cultured from 2-14 days in a rotary cell culture sy

98 MRDOs were cultured from 3.2% of pre-procedure rectal swabs an

99 Porcine MSCs were cultured from abdominal fat, and EVs characterized

100 ured using broth enrichment; wound specimens were cultured from abscess cases.

101 e (n = 8) and nonsevere asthma (N-SA; n = 8) were cultured from endobronchial biopsies.

102 Stromal cells were cultured from human corneas (HCSC) and mouse cornea

103 MECs were cultured from lacrimal glands of C57BL/6J [wild typ

104 ssing skin-derived precursor (SKP) spheroids were cultured from murine back skin.

105 Legionella pneumophila serogroup 1 isolates were cultured from patient sputum (n = 3), endobronchial

106 Cancer cells were cultured from PDACs from mice and analyzed in cell

107 Mast cells were cultured from peripheral blood CD34(+) cells and ex

108 Goblet cells were cultured from rat conjunctiva.

109 erotype Typhi (S Typhi) and 94 iNTS isolates were cultured from the blood of 13 431 febrile patients.

110 In this study, fungi were cultured from the marine environment in the vicinit

111 MSCs were cultured from the umbilical cords of infants born t

112 Primary HSNECs were cultured from tissue explants.

113 Mast cells were cultured from wild-type and tryptase null mice, fol

114 MPP(+)-induced cell death when SH-SY5Y cells are cultured in a low glucose medium, as well as when di

115 when clonal three-dimensional (3D) spheroids are cultured in basement membrane, and one such state is

116 increased by Torin1 treatment or when cells are cultured in nutrient-deficient media, but not when c

117 appear fragile, and fuse in vivo when cells are cultured in oleic acid.

118 luctuations have similar kinetics when mESCs are cultured in standard conditions (serum plus leukemia

119 uorescence imaging of nonadherent cells that are cultured in suspension, such as Escherichia coli, ar

120 ound iNOS gene induction in macrophages that are cultured in tumour cell-conditioned media as well as

121 epithelial progenitor cells when these cells are cultured in two different, common culture approaches

122 The fact that they are cultured in vitro makes them easily accessible both

123 wever, about 95% of bacterial species cannot be cultured in labs.

124 are especially helpful when pathogens cannot be cultured in the lab.

125 iPSCs can be cultured in three dimensions to generate cerebral org

126 ts of unacylated ghrelin, dependent on cells being cultured in 3D in a biologically-relevant extracel

127 uent human fibroblast cells were fixed after being cultured in space for 3 and 14 d, respectively, to

128 hibit long term proliferation potential when being cultured in spheroids, have been shown to induce h

129 ells but not human skin fibroblasts, despite being cultured in the presence of serum and TNF.

130 Streptococcus pneumoniae was cultured in 33 episodes (51%) and H. influenzae in 1

131 Tissue was cultured in a short-term explant model.

132 As such, an ovarian cancer cell line, OV-90, was cultured in adherent and non-adherent conditions usi

133 ed, acutely but transiently, when the mutant was cultured in extracellular fluids from a WT culture,

134 ty mediated by ILY when S. intermedius PC574 was cultured in fetal bovine serum (FBS) than when it wa

135 Conversely, when strain PC574 was cultured in human plasma, no similar increase in hem

136 The organism was cultured in the 1960s and reclassified as Bartonella

137 Microcystis aeruginosa was cultured in the medium containing low and high conce

138 Blood was cultured in the presence of +/-25 uM resveratrol, +/

139 The human monocyte line THP-1 cell was cultured in vitro and differentiated into macrophage

140 Human subcutaneous fat was cultured in vitro to promote blood vessel outgrowth

141 Encapsulated LGG was cultured in vitro under the condition that mimicked

142 Cells were cultured in 2D and 3D systems.

143 HNSCC UM-SCC-1 and UM-SCC-47 cells were cultured in 2D monoculture and compared with: 2D co

144 Candida species were cultured in 40 cases (56.3%).

145 HRP were cultured in 5 mm normal glucose, 25 mm l- or d-gluc

146 contralateral L4 and L5 dorsal root ganglia were cultured in a compartmentalized system.

147 Here, retinal precursor cells were cultured in a microfluidic chip with multiple array

148 Cardiomyocytes were cultured in a novel microfluidic cardiac cell cultu

149 ns of the model coral Pocillopora acuta that were cultured in a recirculating aquaculture system (RAS

150 Neurons were cultured in a soma-soma or soma-axon configuration

151 ) and ventricular cells from the same embryo were cultured in a static condition for 4 days as contro

152 pithelial morphogenesis model in which cells were cultured in biochemically and mechanically defined

153 in this study with large T antigen deletions were cultured in cell lines immortalized using simian vi

154 transduce ASCs upon seeding, and constructs were cultured in chondrogenic conditions for 28 d.

155 INS-1 (832/13) cells were cultured in either a physiological (4 mm) or high (

156 ESCs and iPSCs were cultured in four specific stages under defined cond

157 associated herpesvirus (KSHV) infected cells were cultured in high glucose medium.

158 Organoids were cultured in hypoxic chamber with 0.1% O(2) for 24 h

159 tes released when T. harzianum and M. roreri were cultured in isolation and compared these to those p

160 ntrary to NO inhibition witnessed when MPhis were cultured in L-arginine.

161 Adult F. hepatica were cultured in lethal and sub-lethal doses of TCBZ and

162 ionally, CMT-93 cells, a cell line for IECs, were cultured in low glucose (LG, 5.5 mmol/L) or high gl

163 blast differentiation model, where myoblasts were cultured in low-serum medium to stimulate myogenic

164 In this study, five bacterial species were cultured in M9 minimal media containing a range of

165 , rat bone marrow-derived macrophages (BMMs) were cultured in media supplemented with soluble recepto

166 om human peripheral blood mononuclear cells, were cultured in medium containing TIMP-GLIA, anti-CD3 a

167 MLO-A5 murine osteoblasts were cultured in monolayer and subjected to two differen

168 od mononuclear cells from healthy volunteers were cultured in perioperative serum and CD14Human Leuko

169 Human CB-derived CD34+ cells were cultured in serum-free medium together with SCF, TP

170 Mouse or human islets were cultured in standard media +/-100 muM F573 and subs

171 HuMCs were cultured in stem cell factor with or without IL-6.

172 single biological system, CHO and xrs5 cells were cultured in T-175 cell culture flasks and irradiate

173 Cells encapsulated in the hydrogel were cultured in the microwells of a paper substrate.

174 tically diverse mouse cancer cell lines that were cultured in the presence of CTLs.

175 Osteoblasts and osteoclasts were cultured in the presence of elevated PA or OA level

176 Islets were cultured in the presence of F573, and F573 was admi

177 human intestinal Caco-2 cells when the cells were cultured in the presence of glucose.

178 ed circulating basophils from healthy donors were cultured in the presence of IL-3, IL-33, GM-CSF, th

179 mary T-ALLs were resistant to GCs when cells were cultured in the presence of IL-7, a cytokine that i

180 Cells were cultured in the presence of the short-acting beta2-

181 lized human meibomian gland epithelial cells were cultured in the presence or the absence of IGF-1, g

182 Caco-2 cells were cultured in the TEEI bioreactor under both flow and

183 th past PMD (n = 8) or control women (n = 9) were cultured in three experimental conditions: at vehic

184 e action of TIP39 in the dermis, fibroblasts were cultured in three-dimensional collagen gels, a proc

185 SARS-CoV-2 PCR positive samples were cultured in Vero C1008 cells and inspected daily fo

186 ovine granulosa cells from smaller follicles were cultured in vitro and after sub-confluency, cells w

187 dritic branching of hippocampal neurons that were cultured in vitro and for the proper ZBP1 dendritic

188 In addition, H9C2 rat cardiomyocytes were cultured in vitro and the phosphorylation of ERK1/2

189 Samples were cultured in vitro in osteogenic media (OM) for 13 d

190 S. epidermidis bacteria were cultured in vitro on the nanostructure modified sen

191 BMMSC and CPSC were cultured in vitro using a previously established co

192 Cells were cultured in vitro with four phthalate metabolites a

193 Pulmonary and monocyte-derived macrophages were cultured in vitro with NTHi.

194 Ishikawa cells were cultured in vitro, and a range of AEA concentration

195 obtained from men at ages 15, 23, 36 and 40 were cultured in vitro.

196 Some bioluminescent groups may be cultured, including some cnidarians, ctenophores, and

197 Fibroblasts were cultured; incubated with TGFbeta1 and/or LIGHT; and

198 hes, cancer cells and cancer cell aggregates were cultured individually or co-cultured with endotheli

199 For in vitro study, 3T3-L1 adipocytes were cultured, infected with adenovirus carrying AAT1 ge

200 l aggregation agents, fecal aerobic bacteria were cultured, isolated, and identified.

201 lid, Diaphorina citri Ca L. asiaticus cannot be cultured; its growth is restricted to citrus phloem a

202 model system of human trophoblast that could be cultured long term and differentiated to syncytiotrop

203 el of Ca(2+) overload, were lower when cells were cultured long-term under 5% compared with 18% O2.

204 tion and in whom surgical biological tissues were cultured (n = 429).

205 whereas it remains cytoplasmic when the CFbs are cultured on either 10 or 50 kPa static hydrogels.

206 Mammalian-derived cells are cultured on EM substrates, using optimized condition

207 Retinal pigment epithelium (RPE) cells are cultured on top of custom-made electrodes capable of

208 dless of the topographical feature they were being cultured on.

209 The sea cucumber Holothuria scabra was cultured on sediments under contrasting redox regime

210 Porphyromonas gingivalis W83 biofilm was cultured on titanium discs and reconstituted gingiva

211 When cells were cultured on a topography that mimics the epidermal-

212 tent stem cell (iPSC)-derived neuronal cells were cultured on chemically-defined poly(ethylene glycol

213 Cells were cultured on flat and wedge-shaped gels made from po

214 mber of functional myofibers than cells that were cultured on hydrogels with randomly distributed CNT

215 Samples were cultured on Lowenstein Jensen media and the BACTEC

216 c hydrogels, mammary epithelial cells (MECs) were cultured on methacrylated hyaluronic acid hydrogels

217 IECs (HT-29.cl19a) were cultured on microcarrier beads in simulated microgr

218 en spreading and PGE2 synthesis, fibroblasts were cultured on micropost arrays or hydrogels of varyin

219 ble resorption was observed when osteoclasts were cultured on mineral-deficient bone.

220 partment for clinically suspected keratitis, were cultured on non-nutrient agar examined by microscop

221 Single hPSC-CMs were cultured on polyacrylamide substrates of physiologi

222 Cells were cultured on profibrotic conditions including stiff

223 Fibroblasts were cultured on soft elastic hydrogels embedded with fl

224 line (NIH/3T3) and a tumor cell line (HepG2) were cultured on the 4-MBA modified SERS substrates.

225 Preosteoblasts (MC3T3-E1) were cultured on the bone samples for 24, 48, and 72 hou

226 DPSCs were cultured on the PCL+FA or the PCL scaffolds for up

227 Endothelial progenitor cells (EPCs) were cultured on the V-RDDs-anchoring scaffold and enhan

228 nt protein (GFP)-expressing Escherichia coli was cultured onto PAR4-AP-modified titanium with and wit

229 Cells were cultured onto plastic substrates containing selecti

230 Yet because these cells cannot be cultured or genetically manipulated, there are gaps i

231 ools for manipulating Wolbachia nor can they be cultured outside of host cells.

232 is important that samples analyzed with PCR are cultured, owing to higher-sensitivity drug susceptib

233 Stool specimens were cultured selectively for ciprofloxacin-resistant gr

234 es, collected 3 times over a 19-week period, were cultured selectively for E. coli.

235 only Mesomycetozoea fungal species that can be cultured, Sphaerothecum destruens, we obtained tracta

236 the observation that even if populations can be cultured, their in vitro and in vivo phenotypes diffe

237 Immortalised EA.hy926 endothelial cells were cultured through multiple passages under normoglyca

238 Embryonic mouse cortical tissue was cultured to form functional networks where spontaneo

239 HTBE) cells from donors without lung disease were cultured to determine pro-inflammatory and antivira

240 Primary embryonic (E18) rat cortical neurons were cultured to DIV (days in vitro) 14.

241 In addition, primary tubular cells were cultured to study the function and regulation of PI

242 Following IVF embryos were cultured to the blastocyst stage in vitro or transf

243 tions when wild-type and ylxM mutant strains were cultured together.

244 form xenogeneic reconstituted ovaries, which are cultured under an air-liquid interface condition for

245 f phycobilisome association A (RpaA), cannot be cultured under LD conditions.

246 nd the ability of mouse glioma cells (GC) to be cultured under stem cell conditions as compared with

247 rom the new species, although the population was cultured under controlled laboratory condition.

248 p-regulated by ten-fold when B. pseudomallei was cultured under high salt concentration.

249 t were strongly up-regulated when T. suecica was cultured under nitrogen starvation.

250 miliania huxleyi, a ubiquitous marine algae, was cultured under replete and Cu-limiting conditions to

251 Sterechinus neumayeri was cultured under the combined environmental stressors

252 0 generation, subsequent generations (F1-F5) were cultured under arsenite-free conditions.

253 The cells were cultured under different salinity conditions and sa

254 gingivalis-LPS were more evident when cells were cultured under high glucose conditions.

255 ignal-regulated kinase (ERK), and some cells were cultured under hypoxic conditions.

256 ENS cells were cultured under proliferation conditions leading to

257 Peripheral blood mononuclear cells were cultured unstimulated (U), with phorbol 12-myristat

258 rity of enzymes from organisms that have not been cultured untapped.

259 n that does not meet the sufficient dose can be cultured until this is reached after combination with

260 ith pathway network mapping in iPSC-CMs that were cultured until a late time point, day 200, in compa

261 HCEnCs from old donor corneas can be cultured using this method which may further lead to

262 Blood was cultured using the automated Bactec incubator system

263 al cells derived from endobronchial biopsies were cultured using a combination of mitotically inactiv

264 Specimens were cultured using Bactec MGIT liquid medium and Middle

265 presenting to 10 U.S. emergency departments were cultured using broth enrichment; wound specimens we

266 he spatially resolved metabolites, spheroids were cultured using HCT-116 colorectal cancer cells, tre

267 Specimens collected at 3 laboratories were cultured using the WASPLab CDM and plated to each s

268 blood progenitors from the same donor could be cultured with autologous leukocytes to generate a sam

269 potent stem cell-derived sensory neurons can be cultured with rat Schwann cells, and have produced fo

270 I) supplementation improved growth when cop- was cultured with Cu and this phenotype was dependent up

271 gnosis and after 2 and 4 weeks of treatment, was cultured with live Mycobacterium tuberculosis for 6

272 Furthermore, when LGG was cultured with the colonic luminal contents from heal

273 wley rats 1 week after collagenase injection were cultured with an antagonizing antibody against CD44

274 MACs from patients were cultured with and without 10 nM calcitriol, and fun

275 Peripheral blood mononuclear cells were cultured with atabecestat and its metabolites (diam

276 orescein diacetate succinimidyl ester (CFSE) were cultured with Bahia grass pollen.

277 A and mHA coated Mg and non-coated Mg plates were cultured with bone marrow derived mesenchymal stem

278 cells from C57BL/6J mice (8 to 10 weeks old) were cultured with CD40 ligand (CD40L) and the Toll-like

279 To find the components, germ cells were cultured with comprehensive natural plant extracts,

280 paired in normal mouse and human islets that were cultured with disease-relevant concentrations of ur

281 ionic colon explants from children with HSCR were cultured with GDNF and evaluated for neurogenesis.

282 e from the Australian Raine Study (n = 1374) were cultured with HDM extract (10 mug/ml).

283 Human tracheal epithelial cells (HTEpC) were cultured with IL-17A in the presence/absence of cig

284 Bovine cartilage explants were cultured with IL-1alpha to induce cartilage degrada

285 Human flow-sorted peripheral blood ILC2s were cultured with IL-33 and IL-2 and treated with the P

286 ) and PGI2 receptor-deficient (IP(-/-)) mice were cultured with IL-33 and treated with the PGI2 analo

287 biased toward collagen production when cells were cultured with induction media.

288 crophages (BMMs) from MCP-1(-/-) and WT mice were cultured with M-CSF, RANKL and/or MCP-1.

289 CD4(+) T cells were cultured with MC supernatant or control medium, aft

290 blood mononuclear cells from healthy donors were cultured with Mycobacterium tuberculosis and extrac

291 patible results were obtained when human CML were cultured with normal human hematopoietic progenitor

292 nal porcine epithelial cell 1 (IPEC-1) cells were cultured with or without EPA or DHA (6.25-25 mug/mL

293 e this, mouse bone marrow-derived mast cells were cultured with or without LA and activated with IL-3

294 Spleen B cells isolated from C57BL/6J mice were cultured with Porphyromonas gingivalis lipopolysacc

295 n healthy peripheral blood mononuclear cells were cultured with postoperative serum compared with pre

296 Sputum samples were cultured with PZA for up to 21 days at 37 degrees C

297 but formed significantly more OCs when they were cultured with RANKL and M-CSF.

298 ripheral T cells isolated from normal donors were cultured with TL1A.

299 solated peripheral blood naive and BND cells were cultured with various stimuli, and their activation

300 cell behaviors and dynamics while the cells are cultured within autofluorescent polymer scaffolds.