ライフサイエンスコーパス: culture method

1 im broth was compared to the CDC-recommended culture method.

2 ly diverse subtype population than the solid culture method.

3 ty and 98.1% specificity versus those of the culture method.

4 n comparison to that of the semiquantitative culture method.

5 xcellent concordance with a more established culture method.

6 antigenemia assay and the conventional tube culture method.

7 as equivalent in sensitivity to our standard culture method.

8 th culture using a standard automated liquid culture method.

9 h is much faster than the conventional viral culture method.

10 ar to that of the hornworm by patterned cell culture method.

11 NoVs remains lacking due to a lack of a cell culture method.

12 30) of which were also negative based on the culture method.

13 xamined for NTM using a membrane filtration, culture method.

14 ensional (3D) Madin-Darby canine kidney cell culture method.

15 because it cannot be recovered using routine culture methods.

16 ine utilization of the relatively slow viral culture methods.

17 ng immunohistochemistry and 3D in-vitro cell culture methods.

18 numbers by standard clinical microbiological culture methods.

19 ecially difficult to identify using standard culture methods.

20 A and BDGO assays when they were compared to culture methods.

21 l epithelial cells cultured with organotypic culture methods.

22 lid fecal culture or automated liquid medium culture methods.

23 t our laboratory's contribution to promoting culture methods.

24 an mucosa for microbiological screening with culture methods.

25 olonization by lactobacilli were assessed by culture methods.

26 cellular products, remains essential to the culture methods.

27 Tissue banks should validate processes and culture methods.

28 direct plating or enrichment broth selective culture methods.

29 and susceptibility testing with traditional culture methods.

30 Each patient was screened by 32 culture methods.

31 is also cost-saving compared to conventional culture methods.

32 it (2-5% of the microbiota) of non-selective culture methods.

33 tudies using conventional in vitro bacterial culture methods.

34 ith pulmonary tuberculosis than conventional culture methods.

35 are unrecognized by conventional laboratory culture methods.

36 = MM-3) cell lines were grown using standard culture methods.

37 enhanced recovery characteristics of fungal culture methods.

38 an be detected by either autofluorescence or culture methods.

39 ked by conventional acid-fast bacillus (AFB) culture methods.

40 rched for such factors using newly developed culture methods.

41 versatile and compares well to C. difficile culture methods.

42 aginal swabs were used for the wet mount and culture methods.

43 ier using the BC-GP test compared to routine culture methods.

44 the results of standard smear microscopy and culture methods.

45 ing on-site for Campylobacter, 97% used only culture methods.

46 (54.7% [95% CI, 42.7%-66.2%]) compared with culture methods.

47 re assessed with respect to case finding and culture methods.

48 time of MTBC identification of gold standard culture methods.

49 colonization was determined by conventional culture methods.

50 incidence was reported when using automated culture methods.

51 bacterial pathogens that are undetectable by culture methods.

52 f the limits of current metagenomic and cell culturing methods.

53 or Shigella entero-pathogens in traditional culturing methods.

54 that HPIV-1 may be underdiagnosed by routine culturing methods.

55 Of 3,923 samples tested by both DFA and culture methods, 22 (3 by DFA testing and 21 by culture)

56 Of 1,426 samples tested by both DFA and culture methods, 48 (44 by DFA testing and 15 by culture

57 detected more true-positive results than the culture method (58 versus 55 swabs); however, this diffe

58 of 16s rRNA sequencing replacing traditional culture methods, a strong association between the presen

59 Compared to passive screening using culture methods, active screening resulted in discontinu

60 ed from investigations utilizing traditional culturing methods, advances in sequencing technologies h

61 nient tool that can be embedded into routine culture methods, allowing the culture of all sputum samp

62 This two-step culture method allows for the production of large number

63 was significantly more sensitive than either culture method alone and was also more sensitive than th

64 Primary tissue culture methods also are described, and their value in u

65 ct these growth components by comparing cell culture methods and identifying the benefits and pitfall

66 This approach is compared with conventional culture methods and PCR-based assay, as well as with imm

67 easured before and during gull control using culture methods and quantitative polymerase chain reacti

68 of the biopsy specimens was performed using culture methods and real-time polymerase chain reaction

69 etection sensitivity than conventional urine culture methods and resulted in typical colony growth at

70 tanding microalgal heterogeneity, optimizing culture methods and screening mutant microalgae.

71 the first attempts were made to develop mass culture methods and to formulate artificial diets that w

72 Diverse culturing methods and detection of various combinations

73 specimen collection in pregnancy, selective culture methods, and study sample size did not explain t

74 relationships within ecosystems, develop new culturing methods, and discover new products and process

75 Furthermore, the liquid culture method appeared to select for a more genotypical

76 l Africa was investigated with molecular and culture methods applied to preserved core samples.

77 Culture methods are not useful in characterisation of po

78 Standard culture methods are preferred for hospital diagnostic mi

79 Reliable, scalable and time-efficient culture methods are required to fully realize the clinic

80 in the United States, and traditional organ culture methods are still used in Europe.

81 Enriched culture methods are the current standard for prenatal GB

82 Conventional culture methods are time-consuming and associated with a

83 However, culture methods are time-consuming and need at least 24

84 Costly, genotype-dependent tissue culture methods are used in many crops, while seed-based

85 Three-dimensional cell culture methods are viable in vitro approaches that faci

86 ical utility of rapid detection (vs standard culture methods) are scant.

87 ble to those of standard and/or single rapid-culture methods as shown by parallel testing of 590 fres

88 nscription-PCR and was detected later by the culture method at the time of moribund necropsy.

89 the MS5 coculture system or a novel defined culture method based on pharmacological inhibition of bo

90 This clonal culture method can be scaled up to produce NSCs for diff

91 Whole-culture methods cannot produce a set of cells that refle

92 There is a need for cell culture methods capable of dissecting the intricate regu

93 The modified culture method could be utilized to improve screening fo

94 rom the same fecal samples suggests that the culture method could provide a "microbiological" bias an

95 The isolation and co-culture methods could provide a stable platform for crea

96 Overall, the standard culture methods detected Shigella spp., EPEC, ETEC, and

97 Using tissue culture methods developed to study high-risk HPV types,

98 sure drugs, whereas conventional bone marrow culture methods do not.

99 ouse gene-targeting protocol include ES cell culture methods, drug selection scheme, colony picking a

100 This may partly be due to the culturing methods employed in hospital laboratories, whi

101 This stable isotope labeling in cell culture method enables the unequivocal identification of

102 on of mycobacteria, but as with other liquid culture methods, ESP II should be used in combination wi

103 they were not detected by standard clinical culture methods, especially for low-prevalence or fastid

104 syndrome is often empirical because clinical culture methods fail to detect prostate-associated patho

105 onsiderably more sensitive than the standard culture method for detecting VRE directly from perianal

106 nostic Systems, Sparks, Md.), and a standard culture method for detection of group A streptococci (GA

107 late method combined with a broth enrichment culture method for detection of group B streptococcus co

108 Previous studies describe a unique culture method for the commitment of murine embryonic st

109 CSA) and a standard acid-fast bacillus (AFB) culture method for the isolation of nontuberculous mycob

110 (BCSA) has been recommended as an expedient culture method for the isolation of rapidly growing NTM

111 known, mainly due to the lack of a long-term culture method for this parasite.

112 were evaluated by comparison to traditional culture methods for detecting Chlamydia trachomatis and

113 t the MAGI assay is more sensitive than PBMC culture methods for detecting infectious virus in female

114 PCR-hybridization was compared to culture methods for evaluating suspected blood infection

115 results demonstrate the utility of rapid DC culture methods for high efficiency in vitro T cell sens

116 This paper establishes culture methods for immature sheep cardiomyocytes and re

117 We sought to develop culture methods for immature sheep cardiomyocytes in ord

118 remains difficult to study in the absence of culture methods for luxuriant growth.

119 With the recent FDA approval of culture methods for platelet bacterial testing and the p

120 WGS is a promising alternative to culture methods for resistance prediction in S. aureus a

121 Studies have demonstrated that large-volume culture methods for sterile body fluids other than blood

122 nsitivity as an exemplar to (i) develop cell culture methods for the detection of drug-specific B-cel

123 Current cell culture methods, however, cannot cost-effectively produc

124 A recently developed culture method identified glial cell line-derived neurot

125 specificity (96.7%) compared to those of the culture method in this multisite evaluation.

126 combined direct and broth-enriched toxigenic culture methods in a large, multicenter clinical trial.

127 and displayed similar diagnostic accuracy as culture methods in children with suspected tuberculosis.

128 re as sensitive and specific as conventional culture methods in detecting Salmonella spp. from feces.

129 ues during the development of general tissue culture methods in the 1950s to 1970s or from specimens

130 een numerous proposals suggesting that whole-culture methods - in which all cells in a growing cultur

131 The culture method included direct inoculation of a MacConke

132 However, most culture methods involve the use of animal serum to estab

133 and further validation of the proposed novel culture method is required.

134 ell purification techniques and quantitative culture methods, it was found that IFN-alpha directly in

135 Culture methods lack the capacity to detect VBNC cells,

136 Improvements in stem cell culture methods, materials and biophysical tools that as

137 Current culture methods may fail to detect non-O157 STEC.

138 ignals from relatively rare cells while cell culture methods may significantly alter cellular phenoty

139 remia (57 versus 37%; P = 0.004), making any culture method more likely to identify them.

140 Plant tissue culture methods need optimization and simplification for

141 We have developed a purification and cell culture method of BFCN in order to examine the regulatio

142 ome this limitation, we developed an ex vivo culture method of the mammary gland where the direct act

143 tobacco (Nicotiana tabacum L.) and in vitro culture methods optimised for their maturation to fully

144 significant difference (P > 0.1) between the culture methods or the ciprofloxacin concentrations in t

145 bility to be detected by standard laboratory culturing methods, or a lack of adherence and hence rapi

146 l (p < 0.001 and p = 0.012, respectively for culture methods; p = 0.012 and p = 0.034, respectively f

147 This time-efficient and simplified culture method paves the way for large-scale, high-throu

148 New in vitro cell culture methods permitted isolated mouse islet progenito

149 hese species remain recalcitrant to standard culture methods, prohibiting their use as sources of uni

150 This culture method provides a platform for studying the BCR

151 The described culture method provides quantitation of the cell produci

152 Typical sputum culture methods quantitate the relative amounts of each

153 l depend on enhancing the sensitivity of the culture method rather than increasing the volume of mate

154 g the combined direct and enriched toxigenic culture method (reference method), for a prevalence rate

155 When the PCR-hybridization and culture method results were compared, the positive and n

156 assessed by the IB method and the reference culture method (RM).

157 carried out days or even weeks before other culture methods, significantly reducing associated labor

158 The current gold standard based on culture methods takes up to 10 days to show positive res

159 We have developed a microfluidic cell culture method that allows for the formation of linear i

160 of Cell Stem Cell, Csaszar et al. develop a culture method that overcomes current limitations in ex

161 ity, and mortality emphasizes the need for a culture method that permits simultaneous isolation and d

162 In this study, we describe a novel culture method that uses human brain endothelial cells (

163 We describe here primary culture methods that allow C. elegans embryonic cells to

164 plication of hESC-derived cells will require culture methods that are low-cost, robust, scalable and

165 ial, however, depends on the availability of culture methods that are robust, scalable, and use chemi

166 developing both specific assays and new cell culture methods that enabled them to report, in the acco

167 e successfully analyzed by MALDI-TOF MS when culture methods that suppress pigment expression are use

168 s (49%) or from frozen feces (40%) than from culture methods that used HEp-2 adherence assays (13%) (

169 We demonstrate, using two culture methods, that EMT does not underlie the appearan

170 ribe here a novel selective and differential culture method, the Cdifftox plate assay, which combines

171 omogenic medium was compared to the standard culture method, the sensitivity and specificity, respect

172 For direct culture methods, the agreement between MS and CA was 98.

173 f NA function because, unlike available cell culture methods, the results of such assays are predicti

174 Compared to the results of traditional culture methods, the sensitivities of a rapid chromatogr

175 mental cues that are missing in conventional culturing method, this approach did not require any gene

176 Application of this culture method to a human iPS cell line also generated r

177 We developed an in vitro culture method to characterize the expression of bacteri

178 In the present study, we use a two-step culture method to demonstrate efficient generation of fu

179 ethod which combines a wet preparation and a culture method to detect Trichomonas vaginalis.

180 We used a novel microfluidic single-cell culture method to directly observe the differentiation c

181 rpose of this study was to use the two-layer culture method to improve donor-organ use from marginal

182 We used a high-throughput B-cell culture method to isolate neutralizing antibodies from a

183 ic bottle may be useful as a selective blood culture method to optimize the recovery of fungi and myc

184 We used a stroma-supported culture method to study the prevalence and growth charac

185 We developed a culture method to support the efficient activation and p

186 Cell culture methods to assess CMV drug resistance in vivo wi

187 We used continuous culture methods to avoid potential confounding variables

188 ds, PCR could serve as an adjunct to current culture methods to facilitate early detection of bloodst

189 een impeded by the inability of conventional culture methods to interrogate microenvironments of comp

190 Failure of current culture methods to mimic the physiologic temperature and

191 ation that researchers adopt serum-free cell culture methods to reduce animal use in this area.

192 red interest in using three-dimensional (3D) culture methods to study biology, model disease and pers

193 production of HAV antigen by standard tissue culture methods to the production of HAV antigen with th

194 le isotope labeling with amino acids in cell culture) method to monitor three conditions simultaneous

195 d from 80.6%, compared to the less sensitive culture method, to 97.0%, compared to PCR.

196 one and was also more sensitive than the two culture methods used in tandem (the tandem culture sensi

197 health problem in part because the standard culture methods used to determine the appropriate treatm

198 y up to 16 weeks), (iii) liquid-solid double culture method using modified 7H9 broth (8 weeks) follow

199 immunofluorescence assay and in vitro organ culture method using NHC were used.

200 Low-cost, robust, scalable culture methods using chemically defined materials need

201 compared to those from direct and extracted culture methods using Gram staining and a GAS-specific l

202 The sensitivities of culture methods using self- and clinician-collected spec

203 cant difference between the sensitivities of culture methods using self- and clinician-collected vagi

204 A culture method utilizing quantitative plating on antibio

205 A novel semisolid culture method was developed to support the formation of

206 A two-step culture method was devised to generate large numbers of

207 id antigen H (ipaH) gene by PCR and standard culture methods was used to identify Shigella species or

208 In order to improve the culture method, we investigated the effects of four cult

209 To identify the most optimal culturing method, we compared various techniques that co

210 compared to the combined direct and enriched culture method were 92.9% (131/141; 95% confidence inter

211 The sensitivities of five culture methods were determined for patients known to ha

212 y identified by conventional microbiological culture methods were identified to the species level by

213 nd Prevention guidelines that used selective culture methods were included in the analyses.

214 ficult to study because until recently blood culture methods were too insensitive to detect spirochet

215 Culture methods were used to isolate E. coli O157:H7 fro

216 Optimal clinical and culture methods were used to select 135 men with chronic

217 lysis in ascitic fluid is currently based on culture methods, which are time-consuming and laborious.

218 identification approaches include bacterial culturing method, which takes several days.

219 film-associated infections relies heavily on culturing methods, which fail to detect nonculturable ba

220 We believe that the new culture method will enable inquiries into the antimicrob

221 e of this study was to compare this standard culture method with the detection of GBS directly from a

222 We compared a rigorous culture method with the Gen-Probe AccuProbe Group B Stre

223 an effectively replace the traditional batch culture methods with nanoliter volumes of bacterial cult

224 dividual genera, PCR was as sensitive as the culture method, with the exception of Salmonella culture

225 Here we used a single air-liquid interface culture method without modification to engineer oncogeni