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1 h conventional and a novel, modified ex vivo culture technique.
2 membrane substrate using a xeno-free explant culture technique.
3 diagnosed with Salmonella spp. by a routine culture technique.
4 14 days using a completely xeno-free explant culture technique.
5 e or duration, edge versus base sampling, or culture technique.
6 lant lines using a more time-consuming, cell culture technique.
7 een isolated from root canals using standard culture techniques.
8 nd plastic surfaces using established tissue culture techniques.
9 controlled growth conditions with continuous-culture techniques.
10 r conventional or lysis centrifugation blood culture techniques.
11 a photoreceptor cell line (661w) using cell culture techniques.
12 ion in six of the twelve samples, but not by culture techniques.
13 on (LCR)-based assay and acid-fast stain and culture techniques.
14 from men and women was compared to standard culture techniques.
15 complete, and it requires experience in cell culture techniques.
16 and other agricultural products through cell culture techniques.
17 d and requires experience with aseptic cell culture techniques.
18 ocol requires proficiency in basic stem cell culture techniques.
19 morphogenic regulators and advancing tissue culture techniques.
20 not currently reported using standard urine culture techniques.
21 reaction (PCR), pyrosequencing, and standard culture techniques.
22 re examined using both the standard and EQUC culture techniques.
23 disease using specific but infrequently used culture techniques.
24 to model PCE using animals and current cell culture techniques.
25 previously published values from macroscale culture techniques.
26 niae infection relies heavily on insensitive culture techniques.
27 Bacteria were recovered using standard culture techniques.
28 and researchers in algal identification and culture techniques.
29 a DETA SAM, a serum-free medium and refined culture techniques.
30 ium in environmental samples by conventional culture techniques.
31 ibed and is derived largely from insensitive culture techniques.
32 female genital secretions by standard virus culture techniques.
33 i challenge, using both PCR and quantitative culture techniques.
34 lacking resources for traditional anaerobic culturing techniques.
35 between polyp subtypes using sequencing and culturing techniques.
36 Samples were analyzed using culturing techniques.
37 lication will increase with advances in cell-culturing techniques.
38 into is currently determined using standard culturing techniques.
39 using high-throughput dilution-to-extinction culturing techniques.
40 S south of Bermuda by using high-throughput culturing techniques.
41 n what is currently demonstrated by standard culturing techniques.
42 ount for the loss of sensitivity compared to culturing techniques.
43 acterial pathogen, as determined by standard culture techniques; 107 (44%) Shigella isolates, 73 (30%
44 samples were tested by established clinical culture techniques: 3,179 DNA samples by the Universal B
45 ) throat culture using a two-plate selective culture technique, 4) optical immunoassay (OIA) followed
46 g diagnostic test properties of conventional culture techniques (aerobic and anaerobic agars and thio
47 Here, Golyshina et al. apply an enrichment culture technique and find that the ungapped genome of t
48 ration approaches demonstrated that both the culture technique and genetic background of donor plants
50 edure requires a proficiency in aseptic cell culture techniques and a basic understanding of T cell b
51 th minimal animal surgery skills, basic cell culture techniques and access to human breast tissue wil
52 ons in the intestines using both traditional culture techniques and bacterial tag-encoded FLX amplico
53 the bDNA assay was at least as sensitive as culture techniques and displayed a nearly 3 log10 dynami
54 by allowing a user to perform standard cell culture techniques and experimental manipulation outside
55 e of origin, diversity in isolation methods, culture techniques and model systems of MSCs, together w
57 4+ cells is more rapid and precise than cell culture techniques and results are available in time to
58 njury-stimulated neurogenesis, we used organ culture techniques and tested nine peptide growth factor
60 not overlap with those of conventional blood culture techniques and we are still learning how best to
64 ls were cultivated using a xeno-free explant culture technique, and cultivated cells were transplante
65 VM/AST patient samples, RNA-sequencing, cell culture techniques, and a xenograft mouse model, we inve
67 ivity similar to those of quantitative blood culture techniques, and it may prove useful for rapid sc
68 Changing epidemiology, advances in blood culture techniques, and new diagnostics guide the applic
69 osis poses many challenges, and conventional culture techniques are frequently supplemented by non-cu
73 n periodontally healthy individuals, because culturing techniques are not sufficiently sensitive.
74 tidisciplinary project will utilize in vitro culture techniques, bioimaging, microbiological tests, m
76 athogens, stool antigen assays, and improved culture techniques, but there is little penetration of s
79 gingivitis was characterized by traditional culture techniques, comparative 16S rRNA gene sequencing
80 nal methods that rely on viral isolation and culture techniques continue to be the gold standards use
81 he reference method, which included standard culture techniques coupled with alternate PCR and sequen
82 With ongoing progress in gene editing and culture techniques, engineered stem cells and their appl
83 Here we report and benchmark a suspension culture technique for cancer organoids which allows for
85 eder-free, long-term, three-dimensional (3D) culture technique for hAT2 cells derived from primary hu
86 udy validate the use of the semiquantitative culture technique for the evaluation of catheter-related
88 t analysis (HRMA) was compared with standard culture techniques for diagnosis of SBP in 106 peritonea
90 accepted limitations associated with classic culture techniques for the diagnosis of invasive fungal
92 Here, we describe our development of cell culture techniques for the enrichment of functional HSPC
102 Using complementary grafting and explant culture techniques, however, we have now found that well
105 AxSYM CMV IgM assay and compared it with CMV culture technique in a cohort of 40 liver transplant rec
106 imals were assessed first using conventional culture techniques in the small and large intestine.
107 ative medicine, ongoing advancements in cell culture techniques, including isolation, expansion, bank
108 iderable progress in the development of cell culture techniques, including the development of the ser
110 is of this process using genetics and simple culture techniques is becoming a powerful way of investi
111 inguishing 3D bioprinting from other 3D cell culture techniques is its precise control over created s
112 to prolong allograft survival using in vitro culture techniques is possible, and provides a new thera
113 an be performed by anyone familiar with cell culture techniques, is conducted in serum-free condition
114 aceuticals are produced using mammalian cell culture techniques, it becomes increasingly important fo
115 lso seems to be a real possibility that cell culture techniques may finally produce clinically useful
116 m innovations in scaffold design, multi-cell culture techniques, neural engineering, and biofabricati
117 combines free-floating and scaffold-based 3D-culture techniques of liver cancer cells and fibroblasts
119 hnique would be more sensitive than standard culture techniques or serology for diagnosis of R. equi
122 a 2-year study of 100 children with CF using culture techniques sensitive for S. aureus SCVs, and eva
125 showed that the semiquantitative roll-plate culture technique (SQC) was as accurate as the sonicatio
126 agenomic analysis, combined with traditional culture techniques, tetrachloroethene (PCE) was identifi
127 Somatic embryogenesis is an important tissue culture technique that sometimes leads to phenotypic var
128 ality of the Tbx1-/- mice, we used long-term culture techniques that allow the unharmed growth of inc
130 method incorporating established insect cell culture techniques that supports sustained growth of hon
133 Here, we applied a three-dimensional (3D) culture technique to a liver progenitor cell line, HPPL,
134 is study reports the use of a simple explant culture technique to derive progenitor cell populations
136 intestinal tract than conditions using batch culture techniques to investigate adherence and biofilm
137 and the necessary modifications to existing culture techniques to prepare viable adult human sensory
138 logist of the early 20th century who devised culture techniques to visualize anaerobic bacteria, para
140 have attempted to optimize our isolation and culturing techniques to produce a reliable, in vitro mod
141 by conditional reprogramming culture, a cell culture technique used to grow large numbers of patient-
142 were engineered by the air/liquid interface culture technique using human oral fibroblasts and kerat
145 differentiation regimen and a monolayer cell culture technique was combined with multielectrode array
146 ndosperm cell fates, a maize endosperm organ culture technique was established whereby the developing
147 compared with that of established anaerobic culturing techniques was similar and significantly bette
151 acterial DNA compared with those of standard culture techniques were 100% (17/17) and 91.5% (85/89),
152 nonenrichment) rectoanal mucosal swab (RAMS) culture techniques were developed and compared to tradit
153 ther nitrate or nitrite, anaerobic chemostat culture techniques were employed using nrfA-lacZ and nir
154 of nitrate, nitrite, and formate, chemostat culture techniques were employed with fdnG-lacZ and fdhF
155 ell makes these two enzymes, continuous cell culture techniques were used to examine napF and narG ge
157 acerbated by limitations of traditional cell culture techniques, which fail to recapitulate mechanobi
158 contamination is detected using conventional culturing techniques, which are highly dependent on expe
161 le Isotope Labeling with Amino acids in Cell culture) technique with interventional experiments (kina
162 report, we combine high-throughput anaerobic culturing techniques with gnotobiotic animal husbandry a
163 we outline the value of modern in vitro cell culture techniques, with a focus on their current applic
164 ce of bacteria in endodontic infections when culture techniques yield a negative result and can be us