ライフサイエンスコーパス: colony-forming

1 d 6-phosphogluconate was carefully poured on colonies, forming a second semi-solid layer.

2 mpletely blocks their invasive and soft agar colony-forming abilities, but it spares nontransformed c

3 effective against GBM-SCs and retained their colony-forming abilities.

4 However, colony forming ability and leukemogenicity are abrogated

5 adiation led to a prolonged loss of in vitro colony forming ability by airway epithelial progenitor c

6 y require RNase E activity to form colonies (colony-forming ability [CFA]).

7 ation bias, evident from increased erythroid colony-forming ability and decreased megakaryocyte outpu

8 or cells following TKI exposure, maintaining colony-forming ability and engraftment potential in immu

9 ilencing of LZK caused near-complete loss of colony-forming ability in cells harboring 3q gain.

10 gression, leading to less cell viability and colony-forming ability in vitro and to reduced tumor gro

11 hagy significantly reduced the viability and colony-forming ability of HDACi-treated AML cells.

12 16(Ink4a) and p19(Arf) rescues the defective colony-forming ability of HIF1alpha(-/-) LSCs.

13 ly, have been linked to the self-renewal and colony-forming ability of murine hematopoietic stem cell

14 ptase knockdown suppressed proliferation and colony-forming ability of neoplastic B cells in culture

15 erfering RNA (siRNA) selectively reduced the colony-forming ability of VHL-deficient CC-RCC, thus mim

16 is in vivo and decreases their viability and colony-forming ability, while transiently delaying cell-

17 nd microRNA-196b inhibited in vitro leukemic colony forming activity and depleted in vivo leukemia-in

18 MLL(DNMT1 CXXC)-AF9 shows robust in vitro colony forming activity and in vivo leukemogenesis, simi

19 ficient to abrogate the observed increase in colony forming activity implying a direct role for strom

20 iferation of Itpkb(-/-) HSC without rescuing colony forming activity.

21 Itpkb(-/-) HSC showed reduced colony-forming activity and increased stem-cell-factor a

22 ed several defects in hematopoiesis, reduced colony-forming activity in vitro, decreased expression o

23 and a unique mouse Runx1bEx6e showed higher colony-forming activity than the full-length Runx1b (Run

24 Reduced definitive erythroid colony-forming activity was found in the bloodstream of

25 ineage differentiation capacity, and possess colony-forming activity, despite constituting a small fr

26 the fetal liver, as demonstrated by in vitro colony-forming and immunophenotypic as well as in vivo l

27 progenitors and basal MaSCs, reducing their colony-forming and regenerative potentials in a cell-aut

28 cycline or infrared light was evaluated by a colony-forming assay and DNA probe analysis at different

29 t progenitors in a mouse embryonic stem cell colony-forming assay and in embryonic day 10.5 aorta-gon

30 We have used a colony-forming assay to reliably determine chondroprogen

31 By using colony-forming assay, we found that IFNgamma enhanced th

32 Hematopoietic colony forming assays confirmed the CD34+ population stu

33 performed fate-tracing studies combined with colony-forming assays and crosstransplantation studies.

34 Colony-forming assays and hematopoietic reconstitution s

35 Colony-forming assays in MLL-AF9(+) leukemic cells expre

36 Intrathymic transplantation and in vitro colony-forming assays reveal that the engraftment and pr

37 ytokine arrays combined with flow cytometry, colony-forming assays, and competitive transplant assays

38 In colony-forming assays, EoP from blood of severe asthmati

39 In colony-forming assays, MSCs overexpressing TERT and MYOC

40 lesions displayed self-renewal capability in colony-forming assays.

41 SR-1 as quantified by standard hematopoietic colony-forming assays.

42 in melanoma cells reduced proliferation and colony-forming capability, induced apoptosis, and inhibi

43 patient DNMT3A-mutant AML samples, reducing colony-forming capacity (CFC) and inducing terminal diff

44 TgPKR mice have reduced colony-forming capacity and the colonies also are more s

45 had self-renewal capacity as demonstrated by colony-forming capacity in limiting dilution and by tran

46 BTK-targeted RNAi knockdown reduced colony-forming capacity of primary AML blasts and prolif

47 which contains the bulk of the megakaryocyte colony-forming capacity of the bone marrow, including bi

48 ncluding bipotential megakaryocyte-erythroid colony-forming capacity, and can generate both erythrocy

49 CVB3-infected mice showed a markedly reduced colony-forming capacity, consonant with the observed los

50 with healthy DPSCs, IP-DPSCs expressed lower colony-forming capacity, population-doubling rate, cell

51 ession in NB4 cells was sufficient to reduce colony-forming capacity, proliferation, and survival.

52 ium and blood precursors with multipotential colony-forming capacity.

53 , significantly decreased cell viability and colony forming cell (CFC) potential.

54 in colony-forming unit Hill and endothelial-colony forming cell functional assays (P=0.033 and P=0.0

55 We used endothelial colony forming cell-derived EC and lentiviral vectors to

56 IL-6) negatively correlated with endothelial colony-forming cell colony maximum in the BM of patients

57 wed a dose-dependent decrease in endothelial colony-forming cell colony outgrowth in the presence of

58 and the more ancestral Kit(+) Sca1(+) blast colony-forming cell fraction.

59 hematopoietic progenitors are compromised in colony-forming cell serial replating in vitro and long-t

60 LH1) and MutS homologue 2 (MSH2) in HPCs and colony-forming cell-derived clones (CFCs) from human don

61 ogrammed into human MPPs (rEC-hMPPs) acquire colony-forming-cell potential and durably engraft into i

62 Here we investigated whether endothelial colony forming cells (ECFC) and mesenchymal progenitor c

63 Circulating endothelial colony forming cells (ECFCs) contribute to vascular repa

64 to support the proliferation of endothelial colony forming cells (ECFCs) in 2D cultures and the form

65 ion of endothelial monolayers by endothelial colony forming cells (ECFCs).

66 pulations and were enriched in hemangioblast colony-forming cells (Bl-CFC).

67 ls with properties of cord-blood endothelial colony-forming cells (CB-ECFCs) may enable the derivatio

68 Endothelial colony-forming cells (ECFCs) are a subpopulation of endo

69 Endothelial colony-forming cells (ECFCs) are endothelial precursor c

70 Endothelial colony-forming cells (ECFCs) are endothelial precursors

71 Endothelial colony-forming cells (ECFCs) are promising candidates fo

72 otential of highly proliferative endothelial colony-forming cells (ECFCs) can be explained by the abs

73 senchymal stem cells (hMSCs) and endothelial colony-forming cells (ECFCs) encapsulated in a patterned

74 previous studies determined that endothelial colony-forming cells (ECFCs) from neonates exposed to GD

75 ibute to blood vessel formation, endothelial colony-forming cells (ECFCs) have received widespread at

76 impaired angiogenic activity of endothelial colony-forming cells (ECFCs) in this condition.

77 on and activity in human CD34(+) endothelial colony-forming cells (ECFCs) isolated from PBs in a dose

78 Endothelial colony-forming cells (ECFCs) represent a subset of circu

79 el, we examined the potential of endothelial colony-forming cells (ECFCs) transfusion on vascular deg

80 ion, cells expressing markers of endothelial colony-forming cells (ECFCs) were the most abundant EPC

81 long-term HSCs in the marrow, a decrease in colony-forming cells and a reduction in circulating prog

82 oduced by multipotential hematopoietic blast colony-forming cells and show that basophils and mast ce

83 embryonic day (E) 8.5 all megakaryocyte (MK) colony-forming cells belong to the conventional hematopo

84 pondin 1, a wingless-int agonist, Ring/Dense colony-forming cells can be expanded more than 100,000-f

85 an mesenchymal stromal cells and endothelial colony-forming cells implanted subcutaneously into immun

86 , highly neurogenic in vivo, and enriched in colony-forming cells in vitro.

87 ll phenotype and are enriched in sphere- and colony-forming cells in vitro.

88 assumption that the hematopoietic progenitor/colony-forming cells of the embryonic yolk sac (YS), whi

89 de molecular and functional studies in blast colony-forming cells to gain insight into the function o

90 In clonal cultures, up to 64% of blast colony-forming cells were able to generate mast cells wh

91 otease-8, were also produced by 50% of blast colony-forming cells with a strong concordance in the pr

92 by vascular cells, specifically endothelial colony-forming cells, pericytes, and vascular smooth mus

93 ietic cells and progenitor cells to generate colony-forming cells.

94 ction of both cell types by individual blast colony-forming cells.

95 d recovery of Brca1(-/-) hormone-independent colony-forming cells.

96 onditions, we study here the response of the colony-forming choanoflagellate Salpingoeca rosetta to o

97 and serially replatable myeloid and lymphoid colony-forming cultures could be established from BCR-AB

98 g, propensity to form spheres, and increased colony forming efficacy compared with the primary cells.

99 s as effective in inhibiting AGC kinases and colony forming efficiency of melanoma with Pten wild-typ

100 ubsequently increases cell proliferation and colony forming efficiency of mESCs.

101 xyuridine labeling for a long time, and have colony-forming efficiency (CFE) in vitro.

102 Similar to DPSCs, I-DPSCs were capable of colony-forming efficiency and adipogenic and osteo/denti

103 cells and normal fibroblasts, increased the colony-forming efficiency of cancer cells, and reduced t

104 The colony-forming efficiency of cells from these cultures i

105 found a significant (P = 0.038) reduction in colony-forming efficiency of stem/progenitor cells harve

106 In DMEM, cells from TZ showed higher colony-forming efficiency than LL, BM, and HP.

107 type by reducing proliferation and secondary colony-forming efficiency, and by accelerating senescenc

108 e adult mouse kidney that displays long-term colony-forming efficiency, clonogenicity, immunosuppress

109 Lrig1+ keratinocytes and 3.8-fold increased colony-forming efficiency.

110 Botryococcus braunii race B is a colony-forming, green algae that accumulates triterpene

111 t only increased the number of the long-term colony forming HSCs, but also enhanced their repopulatio

112 n FLK1 mesoderm that were enriched for blast colony forming potential, whereas the P/-8-kb enhancer t

113 ition promoted chemosensitization, decreased colony-forming potential in clonogenic assays, and delay

114 alpha knockdown attenuates proliferation and colony-forming potential in Pten-null hepatocytes.

115 Treatment with 10 also resulted in decreased colony-forming potential in rhabdoid and NSCLC tumor cel

116 tly enhanced inhibition of proliferation and colony-forming potential of CML stem and progenitor cell

117 type selectively reduced both the number and colony-forming potential of mammary luminal epithelial p

118 affecting cell growth, migration, invasion, colony-forming potential, and apoptosis.

119 pleted HSPCs displayed a significant loss of colony-forming potential, as well as short- and long-ter

120 dent changes in cell migration, invasion and colony-forming potential.

121 wn of KLF5 in human CD34(+) cells suppressed colony-forming potential.

122 Colony forming/replating and bone marrow transplantation

123 Through in vitro colony-forming/replating assays and in vivo bone marrow

124 ersibly toggle between the fluffy and smooth colony-forming states.

125 t the intrinsic radiosensitivity of unsorted colony-forming tumor cells, in combination with the frac

126 ng Lin(-)Sca-1(+)cKit(+) (LSK) cells, and by colony forming unit (CFU) assay.

127 systematic centrifugation and comparison of colony forming unit (CFU) counting and optical density (

128 per 10(6) nucleated cells), proliferation by colony forming unit (CFU) counts, and differentiation by

129 blood may contain as little as one bacterial colony forming unit (cfu).

130 lactis (Bb12) (final dose verified at 10(5) colony forming unit (cfu)/g diet, comparable to human co

131 r achieved a limit of detection (LOD) of 150 colony forming unit (CFU)mL(-1) of C. jejuni in solution

132 l results are validated against conventional colony forming unit assays.

133 nsor for Listeria was found to be 2.17x10(2) colony forming unit/ml (CFU/ml).

134 iving rise to erythroid burst- and erythroid colony-forming unit (BFU-E and CFU-E) colonies, the clon

135 By colony-forming unit (CFU) assay and confocal microscopy,

136 d a novel dual-detection functional in vitro colony-forming unit (CFU) assay for single cells that di

137 After 2 months of treatment, lung colony-forming unit (CFU) counts were similar in mice re

138 E. coli in milk at an initial count of >/=1 colony-forming unit (cfu)/mL after an 8-h infection.

139 hment technique for major blood lineages and colony-forming unit assays for hematopoietic progenitors

140 Colony-forming unit assays further demonstrate decreased

141 lineages than did WT progenitors in myeloid colony-forming unit assays, supporting a cell-intrinsic

142 ples using both bioluminescence and standard colony-forming unit assays.

143 mitted myeloid progenitors, as determined by colony-forming unit assays.

144 udying the instantaneous cell viability, the colony-forming unit count, the concentration of free end

145 biofilms, with an improved sensitivity over colony-forming unit counting in a stressed biofilm model

146 of vital cells was found when compared with colony-forming unit counting, highlighting the sensitivi

147 ey were assessed for bacterial viability and colony-forming unit counting.

148 The DMADDM groups reduced the colony-forming unit counts significantly (P < 0.05) and

149 The colony-forming unit counts, scanning electron microscope

150 n and bacterial growth were analyzed through colony-forming unit enumeration and electron microscopy.

151 er erythroid colonies derived from the later colony-forming unit erythroid progenitor erythropoietin

152 table with erythropoietin (Epo), because the colony-forming unit erythroid progenitors (CFU-Es) that

153 nd CD51, are marked by LepR-Cre, and exhibit colony-forming unit fibroblast activity and tri-lineage

154 ranulocyte-macrophage progenitors, increased colony-forming unit granulocyte activity in BM, and acce

155 and in those with faster BMC growth rates in colony-forming unit Hill and endothelial-colony forming

156 ythropoiesis in CD34(+) cells, but increased colony-forming unit MK cell numbers twofold vs control i

157 Erythroid burst-forming unit and colony-forming unit numbers are greatly reduced, indicat

158 Colony-forming unit numbers, host myeloid cell counts, c

159 The number of colony-forming unit osteoblasts (CFU-Os), a surrogate ma

160 imilar levels, based on quantitative PCR and colony-forming unit progenitor analysis.

161 Aortic macrophage colony-forming unit progenitors coexpressed stem cell an

162 nt, minocycline was more effective (>2 log10 colony-forming unit reduction) than light treatment (P <

163 rotein correlated positively with BM-derived colony-forming unit-endothelial colony maximum (estimate

164 subsequent increase in the total numbers of colony-forming unit-erythroid (CFU-E) progenitors and er

165 opoiesis at the burst-forming unit-erythroid/colony-forming unit-erythroid transition, but without af

166 ause they can be easily expanded to generate colony-forming unit-fibroblasts (CFU-Fs) on plastic and

167 bone marrow cells were analyzed in vitro: 1) colony-forming unit-fibroblasts and 2) hematopoietic ste

168 In ARDSp, colony-forming unit-fibroblasts count was higher but not

169 In ARDSexp, irregular colony-forming unit-fibroblasts morphology with disperse

170 with a decrease in the number of clonogenic colony-forming unit-fibroblasts within the BM of Meflin-

171 eg-IFNalpha 2a), significantly decreased MPN colony-forming unit-granulocyte macrophage and burst-for

172 (-) cells and all classes of assayable HPCs (colony-forming unit-megakaryocyte [CFU-MK], CFU-granuloc

173 sed burst-forming unit-erythroid and reduced colony-forming unit-megakaryocyte colony formation drive

174 spectively, had E. coli concentrations of <1 colony-forming unit/100 mL.

175 CR-based method that could reliably detect 1 colony-forming unit/mL of Salmonella Typhi.

176 to germination solution triggered ~1 log(10) colony forming units (CFU) of spores to germinate, and h

177 l recommended national criterion value of 61 colony forming units (CFU) per 100 mL every year in Camp

178 en the inoculum shows a dramatic decrease in Colony Forming Units (CFU) upon soil inoculation but thi

179 otal fungi colonies during 20 years were 507 colony forming units (CFU)/5 plate every year.

180 shing a median lethal dose (LD(50)) of 2,772 colony forming units (cfu)/animal, we tested the ability

181 sensitivity (bacteria concentration of 10(2) colony forming units (CFU)/mL and -88.1+/-6.3mV/pH over

182 ne samples, with a limit of detection of 300 colony forming units (CFU)/mL for C. trachomatis and 150

183 After exposure of the LPG-ISAM to 10(2) colony forming units (CFU)/ml of MR S. aureus (MRSA) for

184 cteria at concentrations starting from 10(1) colony forming units (CFU)mL(-1) in KCl and from 10(2) C

185 challenge route, challenge-killing interval, colony forming units (CFUs) in mouse spleen, and CFU red

186 All samples were analyzed for colony forming units (CFUs) of E. coli, and households w

187 ricidal activity--defined as the decrease in colony forming units (CFUs) of Mycobacterium tuberculosi

188 and 5.0 g/L of nZVI caused the reduction in colony forming units (CFUs) substantially for almost 3 o

189 ory tract (intranasal challenge of 1 x 10(7) colony forming units [CFU] per mouse), intravenous (1 x

190 s included high-level bacteriuria (>/=50 000 colony forming units [CFU]/mL) with any uropathogen, hig

191 groups have equivalent peritoneal bacterial colony forming units and recruitment of phagocytes.

192 in vitro, resulting in a 4 log reduction in colony forming units following compound exposure.

193 rface types (carpet and laminate) with 10(6) colony forming units of B. atrophaeus spores deposited p

194 cultures of B. cereus was found to be 10(0) colony forming units per milliliter (CFU/mL) with a dete

195 d viable plate counting recorded in terms of colony forming units per milliliter and flow cytometry.

196 r each of the strains detected at just 10(1) colony forming units per mL (CFU/mL).

197 dose averaged a CSF clearance rate of -0.37 colony forming units per mL per day (95% CI -0.41 to -0.

198 disease model, where a 4.5-log reduction in colony forming units versus control was demonstrated.

199 The numbers of colony forming units were reduced by up to ~400 fold fro

200 cle value against the bacterial number (log (colony forming units) per milliliter) via linear regress

201 e) and 1.7 x 10(4) (sedimentation pond) cfu (colony forming units)/100 mL.

202 nto infected lungs, by reducing pneumococcal colony forming units, and by elevation of chemokine CXCL

203 of pathogens for concentrations as low as 10 colony forming units/milliliter (CFU/ml), in less than 2

204 on of pathogens, for concentrations of 10(3) colony forming units/milliliter, in less than 20 min.

205 al concentrations of 10(4), 10(6), and 10(8) colony forming units/ml (CFU/ml).

206 ococcus sanguinis bacterial broth (1 x 10(8) colony forming units/mL) for 48 hours.

207 uced fungal growth on day 2 by a mean of 3.5 colony-forming units (95% CI, -6.19 to 13.20 colony-form

208 Good correlations between bioluminescence, colony-forming units (CFU) count and fluorescence were o

209 tic cell count was higher than 6.5 and 7 log colony-forming units (CFU) g(-1) of cheese at the 1st an

210 threshold with CNIR800 is approximately 100 colony-forming units (CFU) in vitro and <1000 CFU in the

211 ontamination with more than 0 and 10 or more colony-forming units (CFU) of aerobic bacterial growth o

212 We observed that <100 colony-forming units (CFU) of B. bronchiseptica efficien

213 s, with a positive predictive value of 10(2) colony-forming units (CFU) per milliliter of 93% (Spearm

214 of the multiplex PMA-qPCR assay achieved two colony-forming units (CFU) per reaction for L. pneumophi

215 ation produced higher numbers of Metarhizium colony-forming units (cfu) than corn or alfalfa.

216 CXCR4 gene ablation increased the number of colony-forming units (CFU), CFU-positive for alkaline ph

217 Viable bacteria were quantified by colony-forming units (CFU).

218 ntitative bacterial culture and expressed as colony-forming units (CFU).

219 microbiome components that were 2-3-log(10) colony-forming units (CFU)/g lower.

220 ey-based formula containing a total of 10(7) colony-forming units (CFU)/g of Bifidobacterium bifidum,

221 etection were 0.5ng/ml of genomic DNA and 10 colony-forming units (CFU)/ml of bacterial cells with dy

222 rom cultures containing 1000 E. coli O157:H7 colony-forming units (cfu)/mL, or approximately 500 E. c

223 ulation, which possesses higher fibroblastic colony-forming units (CFUs) and mesensphere capacity, cr

224 BCR-ABL expression levels in persisting MMR colony-forming units (CFUs) compared with CML CFUs from

225 Colony-forming units (CFUs) have been previously shown t

226 rains allowed us to detect, on average, five colony-forming units (CFUs) of this strain in 1 L of wat

227 airborne A. fumigatus conidia levels were 0 colony-forming units (CFUs) per cubic meter, and no case

228 rees C for 48 hours, and the total number of colony-forming units (CFUs) was counted and statisticall

229 ng by the criterion that they do not grow as colony-forming units (cfus) when plated on agar.

230 fections composed of as few as 10(5) E. coli colony-forming units (CFUs), and can identify drug resis

231 ls, and severity of infection as measured by colony-forming units (CFUs).

232 itro, single-dose phage therapy killed 7 log colony-forming units (CFUs)/g of fibrin clots in 6 hours

233 plemented with concentrations from <1 to 100 colony-forming units (CFUs)/mL for 5 different Candida s

234 analyzed by flow cytometry, endothelial cell colony-forming units (EC-CFU), paracrine measures, blood

235 Few cells expressing markers of EC colony-forming units (EC-CFUs) were detected.

236 nal correlation between (18)F-FDG uptake and colony-forming units (r = 0.63) but a much better correl

237 nt at 1 of 2 dose levels (group 1: 1-5 x 103 colony-forming units [CFU] and group 2: 0.5-1 x 103 CFU)

238 arance from cerebrospinal fluid (-0.42 log10 colony-forming units [CFU] per milliliter per day vs. -0

239 ures showed a mean log10 C. difficile count (colony-forming units [CFU]) of 6.7 +/- 2.0 at study entr

240 ral dose of vaccine (approximately 5 x 10(8) colony-forming units [CFU]) or placebo in double-blind f

241 acterial loads in both the host (up to 10(5) colony-forming units [CFU]/ml) and vector (more than 10(

242 ificantly by treatment strategy (-0.32 log10 colony-forming units [CFU]/mL/day+/-0.20 intervention an

243 s: Presence of bacteriuria (ie, at least 105 colony-forming units [CFUs] per milliliter of 1 or 2 mic

244 of forming multilineage progenitor colonies (colony-forming units [CFUs]) increased from 4% of all CF

245 eceived intra-amniotic injections with 10(7) colony-forming units C.albicans or saline at 3 or 5 days

246 Median (IQR) endothelial cell colony-forming units count per well at baseline and mont

247 cacy study outcomes and measures were fungal colony-forming units from inoculated vials of optisol-GS

248 in tubing cultures demonstrated more than 50 colony-forming units in 19% (8/43) of control drains ver

249 E. coli colony-forming units in bronchoalveolar lavage were redu

250 li), the signal was linear with 5-13 x 10(8) colony-forming units in measuring buffer.

251 itors (CMPs), erythroid burst-forming units, colony-forming units in spleen, and more differentiated

252 In a treatment study, the colony-forming units in the bladder could be reduced by

253 ewal and differentiation of adult Ring/Dense colony-forming units in vitro and suggest an approach to

254 saturable was 2.45 x 10(6) +/- 6.84 x 10(5) colony-forming units of bacteria per gram of tissue (CFU

255 On day 3, subjects drank 1 x 109 colony-forming units of colonization factor I (CFA/I)-ET

256 an acidified milk drink containing >/=10(9) colony-forming units of L. casei 431 (n = 553) or placeb

257 biotic group (n = 55) ingested daily 9 log10 colony-forming units of L. salivarius PS2 from approxima

258 We recently demonstrated that colony-forming units of M. tuberculosis in cough-generat

259 iversity students were inoculated with 10(4) colony-forming units of N. lactamica or were sham-inocul

260 mice by oral inoculation 9 times with 10(9) colony-forming units of Porphyromonas gingivalis A7436 t

261 CDG-3 can detect 10 colony-forming units of the attenuated Mycobacterium bov

262 were injected intra-amniotically with 10(7) colony-forming units of Ureaplasma parvum or saline (con

263 door environments, and the culturable fungal colony-forming units per cubic metre of air samples in t

264 on (measured as the geometric mean number of colony-forming units per gram) by the E. faecium clades

265 Bacterial burden was quantified using both colony-forming units per milliliter (CFU/mL) and time to

266 owing higher maternal challenge of MS (>4500 colony-forming units per milliliter of saliva [CFU/mL])

267 nd adjusted to concentrations of 1.5 x 10(4) colony-forming units per milliliter.

268 in the incidence of UTIs with 10(3) or more colony-forming units per mL of vaccine-serotype E coli w

269 UTIs with higher bacterial counts (>/=10(5) colony-forming units per mL), the number of vaccine sero

270 At inoculum concentrations as low as 8 colony-forming units per plate, 4 different bacterial sp

271 hrombopoietin, and bone marrow megakaryocyte colony-forming units remained unchanged.

272 The study of hematopoietic colony-forming units using semisolid culture media has g

273 At death, as many as 10(10) colony-forming units were found in the lungs, spleen, an

274 ly infected with Candida albicans (1 x 10(6) colony-forming units) and sterile stool.

275 Two dose levels (10(3) or 10(4) colony-forming units) were required to achieve the prima

276 hallenged with Staphylococcus aureus (7 x 10 colony-forming units).

277 identified as approximately 2000 and 150 000 colony-forming units, respectively; credible interval es

278 cell imaging and post-experiment counting of colony-forming units, these results provide evidence tha

279 acterial burden was evaluated by enumerating colony-forming units.

280 ted for their capacity to form hematopoietic colony-forming units.

281 nique predilection for generating macrophage colony-forming units.

282 ilar methods can be used to study pancreatic colony-forming units.

283 ither a probiotic (2 capsules/d, 1.5 billion colony-forming units/capsule) or placebo during spring a

284 B. animalis subsp. lactis at a dose of 10(9) colony-forming units/d (intervention group, n = 362) onc

285 ity of A. lwoffii and A. baumannii by >10(3) colony-forming units/mL at 5-8 times MIC.

286 fluid (CSF) fungal burden (OR, 1.4 per log10 colony-forming units/mL increase; 95% CI, 1.0-1.8), olde

287 ltures were positive with a growth of >10(4) colony-forming units/mL of E. coli were included in the

288 0.176, 0.168, 0.167, 0.265, and 0.261 log10 colony-forming units/ml sputum in the 10, 20, 25, 30, an

289 UTI, defined as 10 or more bacterial colony-forming units/mL urine, developed in 247 (21%) of

290 The limit of detection was low (10 colony-forming units/ml) for both toxigenic V. cholerae

291 containing pneumonia panel bacteria (>10(4) colony-forming units/ml) from five patients (15%) (4 Sta

292 of bacterial infection (defined as >/=10(4) colony-forming units/mL) was compared between BAL HAdV(+

293 However, after inoculating PS with 10 colony-forming units/mL, only a cefazolin concentration

294 had lower fungal burdens (10 400 vs 390 000 colony-forming units/mL; P < .001), higher cerebrospinal

295 in (with a 30-fold increase in the number of colony-forming units/mL; P < .01) as compared to infecti

296 /-) mice were infected with C. jejuni (10(9) colony-forming units/mouse) 24 hours after a 7-day cours

297 Changes in inoculum size (10(2)-10(5) colony-forming units/spot) or cation concentrations of c

298 colony-forming units (95% CI, -6.19 to 13.20 colony-forming units; P = .34), a 77.8% decline compared

299 s of age pigs were inoculated with 2 x 10(4) colony-forming-units LGG+EcN to initiate colonization.

300 f E. coli in synthetic urine was 1.2 x 10(2) colony-forming-units per mL (CFU/mL), which is well belo