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 iated with the human oral cavity have yet to be cultured.

3 d polyacrylamide gels upon which these cells are cultured.

4 ilum rostratum and Cladosporium species have been cultured.

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

6 Four matched pairs of hGFs and hPDLFs were cultured.

7 obiota of women using DMPA for up to 2 years were cultured.

8 Bacterial and fungal isolates were cultured.

9 olution specimens collected from 16 patients were cultured.

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

11 Primary mouse cortical neurons were cultured 8 or 9 days in vitro (DIV), loaded with th

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

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

14 The remaining 5 KD samples were unable to be cultured and molecular typing showed either HAdV-C (n

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

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

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

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

19 H. pylori were cultured and antibiotic sensitivity was determined

20 Primary lung endothelial cells were cultured and assessed for mediators of inflammation

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

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

23 Samples were cultured and isolates identified using matrix-assis

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

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

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

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

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

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

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

31 Hippocampal slices were cultured and treated with micromolar concentrations

32 estosterone and estradiol, pancreatic tissue was cultured, and expression of key beta-cell developmen

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

34 The samples were cultured, and selected periodontal pathogens were t

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

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

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

38 96%) or endotracheal aspirate (4%) specimens were cultured as per routine practice and also tested wi

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

40 d functional in vitro only when the bacteria are cultured at 26 degrees C.

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

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

43 agated readily from the same cells when they were cultured at a physiologic oxygen concentration of 5

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

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

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

47 llow for sequencing of organisms that cannot be cultured, but generate highly variable coverage due t

48 lar matrix (ECM) composition upon which TSCs are cultured changes their differentiation potential fro

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

50 After being cultured, CTGF was increased in fibrocytes from pa

51 However, the majority of microbes have not been cultured, due in part to the difficulties of both i

52 coli O157:H7 with the outbreak PFGE pattern was cultured during July-August 2011, and presumptive ca

53 o address this issue, Pseudomonas aeruginosa was cultured during two Space Shuttle Atlantis missions:

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

55 ld type (WT) and miR-146a knockout (KO) mice were cultured ex vivo in the presence or absence of IL-1

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

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

58 tiated into multipotent stem cells when they were cultured ex vivo without basal stem cells.

59 d out within a few hours, and the tissue can be cultured for days for subsequent functional analyses.

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

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

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

63 ighteen RA synovial membrane MNC suspensions were cultured for 2 days or 5 days, either alone or in t

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

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

66 (3.5 x 10(4) cell clusters per cell chamber) were cultured for 4 days in the CCCM under cyclic mechan

67 es purified from healthy donor blood samples were cultured for 4 to 96 hours with media alone, a cros

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

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

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

71 PBMC were cultured for 7 d with staphylococcal enterotoxin B

72 The cells were cultured for 7 days in media or seeded at a density

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

74 al information was collected and the samples were cultured for C. difficile retrospectively.

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

76 Pharyngeal and food specimens were cultured for GAS by the MDH Public Health Laborator

77 ntation was most efficient when the monomers were cultured for longer periods (24-48 hr) in the prese

78 After aging, oocytes were cultured for maturation.

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

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

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

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

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

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

85 These fungi have been cultured from sputum of asthmatic and non-asthmatic

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

87 The virus was cultured from a patient's cerebrospinal fluid and id

88 Mycobacterium llatzerense was cultured from a subdiaphragmatic abscess.

89 hown by flow cytometry and replicating virus was cultured from exposed fetuses.

90 r of E. coli, the same kind of bacteria that was cultured from her urine when she was symptomatic wit

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

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

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

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

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

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

97 Primary human fibroblasts were cultured from endobronchial biopsy specimens obtain

98 CACs and CSCs were cultured from left atrial appendages and blood samp

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

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

101 Human EOCs were cultured from peripheral blood.

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

103 nderlying etiology, although Candida species were cultured from the prostatic fluid.

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

105 Primary HSNECs were cultured from tissue explants.

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

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

108 are rapidly selected when clinical isolates are cultured in fibroblasts.

109 rown cells, is restored in Huh7.5 cells that are cultured in HS.

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

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

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

113 al cells and microvascular endothelial cells are cultured in the microdevice with physiological flow

114 C9311 and Synechococcus sp. WH8102 when they are cultured in the presence of Synechococcus sp. CC9605

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

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

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

118 time over 2 d to create 3D cultures that can be cultured in the long term (>7 d).

119 ister sequence from an organism that has not been cultured in isolation, and it shows an ordered scis

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

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

122 h defects are most pronounced when S. aureus is cultured in chemically defined media with thiosulfate

123 P. aeruginosa was cultured in 1,714 (48%) subjects.

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

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

126 A urine sample was cultured in all patients, and those with ASB were id

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

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

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

130 Bone marrow from rat MB and LB was cultured in osteoblastic or osteoclastic differentia

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

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

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

134 thelial cells, fibroblasts, and/or myoblasts was cultured in vitro and then implanted around the femo

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

136 FU/ml of a laboratory strain of B. pertussis was cultured in vitro, ACT production was detected in 60

137 sely related to pHo when primary macrophages were cultured in 21% oxygen, 4% oxygen, or with LPS at e

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

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

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

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

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

143 Cardiomyocytes were cultured in a novel microfluidic cardiac cell cultu

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

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

146 the DBPCFC, and peripheral mononuclear cells were cultured in an 18-h ELISpot assay with casein, alph

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

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

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

150 from an immortalized astrocyte line (C8-D1A) were cultured in direct contact with the porous membrane

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

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

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

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

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

156 ts of VfrB on hla transcription when strains were cultured in liquid media, the level of hla transcri

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

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

159 RECs were cultured in M131 medium supplemented with growth fa

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

161 cells and, alternatively, fetal liver cells were cultured in media containing M-CSF for 7-10 d, resu

162 Cells were cultured in media containing TGF-beta1 at concentra

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

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

165 iremis and amphipod Leptocheirus plumulosus--were cultured in oxic to anoxic sediments with SEM[Ni]-A

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

167 Similar findings were observed when cells were cultured in reduced glucose concentrations.

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

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

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

171 Spheroids of HT-29 human carcinoma cells were cultured in the microsystem for four weeks.

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

173 y in the primitive endoderm, embryoid bodies were cultured in the presence of a small molecule inhibi

174 ripheral blood monocytes from healthy donors were cultured in the presence of cord blood-derived norm

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 Further, bone marrow-derived DCs were cultured in the presence of NP and showed similar c

179 One day postinjury, PP mixed cells were cultured in the presence of plate-bound anti-CD3/so

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

181 Mouse myoblasts (C2C12 cell line) were cultured in the presence of type 1 or type 2 IFNs a

182 ARPE-19 and primary mouse RPE cells were cultured in the presence or absence of varying conc

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

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

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

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

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

188 Cells were cultured in vitro with four phthalate metabolites a

189 nitis (AR), or healthy control (HC) subjects were cultured in vitro with IL-25 or IL-33.

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

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

192 When tumor cells were cultured in vitro, TAg transcription increased near

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

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

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

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

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

198 In this approach, cells are cultured on a thin polymer membrane that serves as a

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

200 hway is significantly up-regulated when VICs are cultured on stiff gels or tissue culture polystyrene

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

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

203 a of the limbus, the limbal epithelial cells were cultured on a denuded human amniotic membrane subst

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

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

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

207 repression of expression when the host cells were cultured on low stiffness substrate.

208 Samples were cultured on Lowenstein Jensen media and the BACTEC

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

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

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

212 ddress this, human podocytes and human GEnCs were cultured on opposite sides of porous inserts and th

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

214 Hippocampal neurons were cultured on polydimethylsiloxane substrates fabrica

215 Cells were cultured on profibrotic conditions including stiff

216 Fibroblasts were cultured on soft elastic hydrogels embedded with fl

217 Human and rabbit corneal fibroblasts were cultured on surfaces of varying substrate complianc

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

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

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

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

222 Rat calvarial osteogenic cells were cultured on Ti disks with the surfaces mentioned ab

223 Osteogenic MC3T3-E1 cells were cultured on titanium disks on which the carbon conc

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

225 Cells were cultured onto plastic substrates containing selecti

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

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

228 LGR5(+) stem cells can now be cultured over long periods in vitro as epithelial org

229 Peripheral blood mononuclear cells were cultured overnight with and without phorbol 12-myri

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

231 Stool specimens were cultured selectively for ciprofloxacin-resistant gr

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

233 RT-qPCR-positive specimens were cultured, sequenced, and phenotypically tested for

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

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

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

237 icipants' nares, axillae, and inguinal folds were cultured to detect S aureus colonization.

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

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

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

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

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

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

244 Sterechinus neumayeri was cultured under the combined environmental stressors

245 0 generation, subsequent generations (F1-F5) were cultured under arsenite-free conditions.

246 Human primary keratinocytes were cultured under differentiation-promoting conditions

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

248 ENS cells were cultured under proliferation conditions leading to

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

250 Cord blood mononuclear cells were cultured unstimulated or after stimulation with lip

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

252 When cardiomyocytes are cultured upon those nanotubes, the cell membrane not

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

254 Blood was cultured using the automated Bactec incubator system

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

256 Specimens were cultured using Bactec MGIT liquid medium and Middle

257 ecimens from March 25, 2002 to July 11, 2012 were cultured using both membrane filter system and bloo

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

259 Cells were cultured using standard approaches.

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

261 mean age of patients from whom C. difficile was cultured was 58 years, with only 4/21 patients aged

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

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

264 When whole marrow was cultured with PTH+1,25D3, more TRAP(+) MNCs were see

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

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

267 -2B and A549) and human primary airway cells were cultured with CCL17 or various other cytokines, and

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

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

270 ; these limitations were overcome when cells were cultured with dimethyl sulfoxide.

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

272 Peripheral blood mononuclear cells (PBMCs) were cultured with gp120 and infectious or inactivated H

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

274 'not-yet' sensitized or sensitized children were cultured with highly purified allergens.

275 Monocytes from healthy controls were cultured with IFN-gamma and IL-4, agonists of M1 an

276 NK cells or sorted peripheral blood NK cells were cultured with IL-15 for 7 d with inhibitory or acti

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

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

279 Among other stimuli, basophils were cultured with IL-3 alone.

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

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

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

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

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

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

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

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

288 an umbilical vein endothelial cells (HUVECs) were cultured with or without Mn(2+) supplementation and

289 upported osteoclastogenesis, confluent BMSCs were cultured with parathyroid hormone (PTH), 1,25-dihyd

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

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

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

293 The fragments were cultured with RAW 264.7 macrophage cell line for 9

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

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

296 oplasm (intracellular), and S. flexneri that were cultured with, but did not invade, Henle cells (ext

297 ntation years, 2,353 and 2,302 CSF specimens were cultured, with 49 and 99 patients having positive c

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

299 nels where tumor cells and endothelial cells are cultured within extracellular matrix under perfusion

300 A total of 183 eyes were cultured, yielding 225 isolates.