ライフサイエンスコーパス: culture technique

1 membrane substrate using a xeno-free explant culture technique.

2 diagnosed with Salmonella spp. by a routine culture technique.

3 14 days using a completely xeno-free explant culture technique.

4 e or duration, edge versus base sampling, or culture technique.

5 lant lines using a more time-consuming, cell culture technique.

6 h conventional and a novel, modified ex vivo culture technique.

7 complete, and it requires experience in cell culture techniques.

8 not currently reported using standard urine culture techniques.

9 a photoreceptor cell line (661w) using cell culture techniques.

10 ion in six of the twelve samples, but not by culture techniques.

11 on (LCR)-based assay and acid-fast stain and culture techniques.

12 from men and women was compared to standard culture techniques.

13 reaction (PCR), pyrosequencing, and standard culture techniques.

14 re examined using both the standard and EQUC culture techniques.

15 disease using specific but infrequently used culture techniques.

16 previously published values from macroscale culture techniques.

17 niae infection relies heavily on insensitive culture techniques.

18 Bacteria were recovered using standard culture techniques.

19 and researchers in algal identification and culture techniques.

20 a DETA SAM, a serum-free medium and refined culture techniques.

21 ium in environmental samples by conventional culture techniques.

22 female genital secretions by standard virus culture techniques.

23 i challenge, using both PCR and quantitative culture techniques.

24 een isolated from root canals using standard culture techniques.

25 nd plastic surfaces using established tissue culture techniques.

26 controlled growth conditions with continuous-culture techniques.

27 r conventional or lysis centrifugation blood culture techniques.

28 lication will increase with advances in cell-culturing techniques.

29 into is currently determined using standard culturing techniques.

30 using high-throughput dilution-to-extinction culturing techniques.

31 S south of Bermuda by using high-throughput culturing techniques.

32 Samples were analyzed using culturing techniques.

33 n what is currently demonstrated by standard culturing techniques.

34 ount for the loss of sensitivity compared to culturing techniques.

35 lacking resources for traditional anaerobic culturing techniques.

36 acterial pathogen, as determined by standard culture techniques; 107 (44%) Shigella isolates, 73 (30%

37 samples were tested by established clinical culture techniques: 3,179 DNA samples by the Universal B

38 ) throat culture using a two-plate selective culture technique, 4) optical immunoassay (OIA) followed

39 g diagnostic test properties of conventional culture techniques (aerobic and anaerobic agars and thio

40 Here, Golyshina et al. apply an enrichment culture technique and find that the ungapped genome of t

41 ration approaches demonstrated that both the culture technique and genetic background of donor plants

42 The use of a sensitive culture technique and the choice of the proper sampling

43 th minimal animal surgery skills, basic cell culture techniques and access to human breast tissue wil

44 ons in the intestines using both traditional culture techniques and bacterial tag-encoded FLX amplico

45 the bDNA assay was at least as sensitive as culture techniques and displayed a nearly 3 log10 dynami

46 by allowing a user to perform standard cell culture techniques and experimental manipulation outside

47 Special culture techniques and PCR may help to identify pathogen

48 4+ cells is more rapid and precise than cell culture techniques and results are available in time to

49 njury-stimulated neurogenesis, we used organ culture techniques and tested nine peptide growth factor

50 We used tissue culture techniques and transgenic mice expressing herpes

51 not overlap with those of conventional blood culture techniques and we are still learning how best to

52 he genus or species level, using appropriate culturing techniques and assays.

53 Lack of appropriate culturing techniques and documentation of infectious age

54 ls were cultivated using a xeno-free explant culture technique, and cultivated cells were transplante

55 Advances in cell isolation, in vitro culture techniques, and genetic manipulation of animal m

56 ivity similar to those of quantitative blood culture techniques, and it may prove useful for rapid sc

57 Changing epidemiology, advances in blood culture techniques, and new diagnostics guide the applic

58 Conventional culture techniques are limited in the ability to detect

59 n periodontally healthy individuals, because culturing techniques are not sufficiently sensitive.

60 24 h severely compromised the sensitivity of culture techniques but not that of PCR.

61 athogens, stool antigen assays, and improved culture techniques, but there is little penetration of s

62 This optimized cell culture technique can be used to culture and maintain ne

63 Current cell culture techniques commonly fail to adequately replicate

64 gingivitis was characterized by traditional culture techniques, comparative 16S rRNA gene sequencing

65 nal methods that rely on viral isolation and culture techniques continue to be the gold standards use

66 he reference method, which included standard culture techniques coupled with alternate PCR and sequen

67 udy validate the use of the semiquantitative culture technique for the evaluation of catheter-related

68 Culture techniques for detection and identification of f

69 t analysis (HRMA) was compared with standard culture techniques for diagnosis of SBP in 106 peritonea

70 Traditional diagnostics for SBP rely on culture techniques for proper diagnosis, although recent

71 accepted limitations associated with classic culture techniques for the diagnosis of invasive fungal

72 To evaluate culture techniques for the diagnosis of spontaneous bact

73 We have explored culture techniques for the in vitro selection and develo

74 By using microaerobic culture techniques, H. pullorum was isolated from the fe

75 The development of new tools and culture techniques has also enabled the factors that inf

76 As stem-cell mobilization and in vitro culture techniques have increased the feasibility of adm

77 ssay) were compared to results from standard culture techniques held for 6 weeks.

78 Using complementary grafting and explant culture techniques, however, we have now found that well

79 With conventional culturing techniques, however, cell proliferation and ul

80 Cell and explant culture techniques, immunohistochemistry, electrophysiol

81 AxSYM CMV IgM assay and compared it with CMV culture technique in a cohort of 40 liver transplant rec

82 imals were assessed first using conventional culture techniques in the small and large intestine.

83 iderable progress in the development of cell culture techniques, including the development of the ser

84 A comparison with classical "cell culture" techniques indicates that the biosensor provide

85 is of this process using genetics and simple culture techniques is becoming a powerful way of investi

86 to prolong allograft survival using in vitro culture techniques is possible, and provides a new thera

87 aceuticals are produced using mammalian cell culture techniques, it becomes increasingly important fo

88 lso seems to be a real possibility that cell culture techniques may finally produce clinically useful

89 Advances in tomato cell culturing techniques offer an economical tool for genera

90 hnique would be more sensitive than standard culture techniques or serology for diagnosis of R. equi

91 Our use of an in situ larval culturing technique overcomes the previous challenge of

92 a 2-year study of 100 children with CF using culture techniques sensitive for S. aureus SCVs, and eva

93 showed that the semiquantitative roll-plate culture technique (SQC) was as accurate as the sonicatio

94 agenomic analysis, combined with traditional culture techniques, tetrachloroethene (PCE) was identifi

95 ality of the Tbx1-/- mice, we used long-term culture techniques that allow the unharmed growth of inc

96 Through rapid culture techniques that prepared either mature, CD83+ DC

97 method incorporating established insect cell culture techniques that supports sustained growth of hon

98 accessible archaeal organisms require unique culturing techniques that present real challenges.

99 For conventional periprosthetic tissue culture techniques, the greatest accuracy was observed w

100 Here, we applied a three-dimensional (3D) culture technique to a liver progenitor cell line, HPPL,

101 Using a three-dimensional culture technique to grow MECs ex vivo, we found that th

102 intestinal tract than conditions using batch culture techniques to investigate adherence and biofilm

103 and the necessary modifications to existing culture techniques to prepare viable adult human sensory

104 logist of the early 20th century who devised culture techniques to visualize anaerobic bacteria, para

105 We used a simple ex vivo culturing technique to assess the suitability of Wolbach

106 have attempted to optimize our isolation and culturing techniques to produce a reliable, in vitro mod

107 were engineered by the air/liquid interface culture technique using human oral fibroblasts and kerat

108 Sensitivity using an enhanced culture technique was 99.4% (163 of 164).

109 differentiation regimen and a monolayer cell culture technique was combined with multielectrode array

110 ndosperm cell fates, a maize endosperm organ culture technique was established whereby the developing

111 compared with that of established anaerobic culturing techniques was similar and significantly bette

112 Using a novel thymic stromal culture technique, we evaluated the ability of a hairpin

113 Using directed microbial culture techniques, we discovered Clostridium immunis, a

114 acterial DNA compared with those of standard culture techniques were 100% (17/17) and 91.5% (85/89),

115 nonenrichment) rectoanal mucosal swab (RAMS) culture techniques were developed and compared to tradit

116 ther nitrate or nitrite, anaerobic chemostat culture techniques were employed using nrfA-lacZ and nir

117 of nitrate, nitrite, and formate, chemostat culture techniques were employed with fdnG-lacZ and fdhF

118 ell makes these two enzymes, continuous cell culture techniques were used to examine napF and narG ge

119 In the present study, selective culturing techniques were employed to localize ADP-ribos

120 The combination of traditional cell culture techniques with high-throughput screening approa

121 le Isotope Labeling with Amino acids in Cell culture) technique with interventional experiments (kina

122 report, we combine high-throughput anaerobic culturing techniques with gnotobiotic animal husbandry a

123 ce of bacteria in endodontic infections when culture techniques yield a negative result and can be us