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1 is patients by reverse transcription-PCR and restriction fragment length polymorphism analysis.
2 d sequencing, and for RSTs by nested PCR and restriction fragment length polymorphism analysis.
3 s using group-specific LGV real-time PCR and restriction fragment length polymorphism analysis.
4 ic PCR, followed by species-specific PCR and restriction fragment length polymorphism analysis.
5 Isolates underwent IS6110-based restriction fragment length polymorphism analysis.
6 s determined by direct PCR amplification and restriction fragment length polymorphism analysis.
7 olymerase chain reaction (PCR), or PCR-based restriction fragment length polymorphism analysis.
8 s the source of T. gondii infection based on restriction fragment length polymorphism analysis.
9 med by conventional methods and confirmed by restriction fragment length polymorphism analysis.
10 le nucleotide polymorphisms were detected by restriction fragment length polymorphism analysis.
11 were identified by polymerase chain reaction-restriction fragment length polymorphism analysis.
12 (38 of 59) of the IS6110 copies predicted by restriction fragment length polymorphism analysis.
13 ned by polymerase chain reaction followed by restriction fragment length polymorphism analysis.
14 ed to identify individuals with this gene by restriction fragment length polymorphism analysis.
15 acterization using nucleotide sequencing and restriction fragment length polymorphism analysis.
16 and genotyped by arbitrarily primed PCR and restriction fragment length polymorphism analysis.
17 stent with those from an independent method, restriction fragment length polymorphism analysis.
18 rs and polymerase chain reaction followed by restriction fragment length polymorphism analysis.
19 e genotypes obtained by conventional PCR and restriction fragment length polymorphism analysis.
20 The bacterial species was confirmed by PCR-restriction fragment length polymorphism analysis.
21 OWP and TRAP-C1 genes can be detected by PCR-restriction fragment length polymorphism analysis.
22 COMT genotypes were determined by restriction fragment length polymorphism analysis.
23 encapsulated vaccine serotypes by using PCR-restriction fragment length polymorphism analysis.
24 ing techniques of both direct sequencing and restriction fragment length polymorphism analysis.
25 typed with the polymerase chain reaction and restriction fragment length polymorphism analysis.
26 in the YMDD motif of the polymerase gene by restriction fragment-length polymorphism analysis.
27 G, by means of polymerase chain reaction and restriction fragment--length polymorphism analysis.
28 ment was verified by cytogenetic analysis or restriction-fragment--length polymorphism analysis.
29 terest in previous studies, were analyzed by restriction fragment length polymorphism analysis after
30 The PCR-restriction fragment length polymorphism analysis allowe
31 subtyped with a small subunit rRNA-based PCR-restriction fragment length polymorphism analysis and a
32 sinase gene correction was also confirmed by restriction fragment length polymorphism analysis and DN
33 patterns, and indistinguishable patterns on restriction fragment length polymorphism analysis and ka
34 e point, HCV genotype was determined by both restriction fragment length polymorphism analysis and ph
35 mmunity composition was assessed by terminal restriction fragment length polymorphism analysis and py
37 k of diarrhea in France were analyzed by PCR-restriction fragment length polymorphism analysis and se
39 Limatin was mapped to mouse Chromosome 19 by restriction fragment length polymorphism analysis and to
41 files, monoclonal antibody binding patterns, restriction fragment length polymorphism analysis, and k
43 mbrane protein A (ompA) gene sequencing, and restriction fragment length polymorphism analysis are cu
45 the mutant fibrinogen A alpha chain gene by restriction fragment length polymorphism analysis based
46 zed by restriction endonuclease analysis and restriction fragment length polymorphism analysis by usi
47 petitive units (MIRU-VNTR), and IS6110-based restriction fragment length polymorphism analysis cumula
48 range of diversity exists among the E genes, restriction fragment length polymorphism analysis demons
49 morphism analysis, and sequencing as well as restriction fragment length polymorphism analysis for id
50 was assessed by ribosomal DNA (rDNA) spacer restriction fragment length polymorphism analysis, genom
51 -based assays or a polymerase chain reaction-restriction fragment length polymorphism analysis in 160
52 were genotyped by polymerase chain reaction-restriction fragment length polymorphism analysis in 58
53 be homoplasmic by polymerase chain reaction/restriction fragment length polymorphism analysis in all
54 morphisms by using polymerase chain reaction-restriction fragment-length polymorphism analysis in 134
55 y detectable level of gene conversion by the restriction fragment length polymorphism analysis, indic
56 validated by polymerase chain reaction (PCR)-restriction fragment length polymorphism analysis of 60
62 igh rate of dissemination), according to PCR-restriction fragment length polymorphism analysis of int
63 tate tuberculosis transmission, we performed restriction fragment length polymorphism analysis of M.
65 strains suggests that flagellin gene typing (restriction fragment length polymorphism analysis of PCR
67 o sequence-tagged virus easily identified by restriction fragment length polymorphism analysis of rev
69 s and performed DNA sequencing and PCR-based restriction fragment length polymorphism analysis of sev
71 f Mycobacterium tuberculosis are produced by restriction fragment length polymorphism analysis of the
72 s/genotype of isolates was determined by PCR restriction fragment length polymorphism analysis of the
73 p1a locus in the TIGR4 genetic background by restriction fragment length polymorphism analysis of the
74 It was confirmed to be genotype 1 by PCR-restriction fragment length polymorphism analysis of the
76 polymerase chain reaction amplification and restriction fragment length polymorphism analysis of the
78 2-kb region of variable chloroplast DNA, and restriction fragment length polymorphism analysis of the
80 s achieved by preformed enzyme analysis, PCR-restriction fragment length polymorphism analysis of the
81 acter jejuni and Campylobacter coli based on restriction fragment length polymorphism analysis of the
84 cribed sequence (ITS) and mitochondrial cox1 Restriction fragment-length polymorphism analysis of ITS
85 On the basis of a polymerase chain reaction-restriction fragment-length polymorphism analysis of the
88 ing differentiation without the necessity of restriction fragment length polymorphism analysis or seq
89 ymes were used for polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-R
90 ining the complete rib43a coding region, and restriction fragment length polymorphism analysis placed
91 PCR and restriction fragment length polymorphism analysis reconf
92 om 15 dogs and 27 cats were typed using URA5 restriction fragment length polymorphism analysis (RFLP)
93 typing and biotyping) and molecular methods (restriction fragment length polymorphism analysis, ribot
94 tions disrupted a Taq I restriction site and restriction fragment length polymorphism analysis showed
95 PCR products were subjected to restriction fragment length polymorphism analysis, singl
96 as developed by using commercially available restriction fragment length polymorphism analysis softwa
97 , chromosome painting, Southern blotting and restriction fragment length polymorphism analysis, subcl
98 Restriction fragment-length polymorphism analysis sugges
99 olates underwent insertion sequence (IS)6110 restriction-fragment-length polymorphism analysis, targe
100 By use of a polymerase chain reaction-based restriction fragment-length polymorphism analysis techni
101 nts map exclusively to centromere regions by restriction fragment length polymorphism analysis, the d
102 and subfamily-specific primers, followed by restriction fragment length polymorphism analysis, to co
103 of Listeria monocytogenes by serotyping and restriction fragment length polymorphism analysis using
104 Subsequent restriction fragment length polymorphism analysis, using
108 n among 18 of the 20 biotype 1 isolates in a restriction fragment length polymorphism analysis with a
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