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1 s restriction fragment length polymorphisms (DNA fingerprints).
2 bacteria matched the monkey input strain in DNA fingerprint.
3 ut bacterial vaginosis, none shared the same DNA fingerprint.
4 tuberculosis isolates with identical IS6110 DNA fingerprints.
5 he 3 patient-workers' isolates had different DNA fingerprints.
6 parated on analytical agarose gels to create DNA fingerprints.
7 seven M. tuberculosis isolates had matching DNA fingerprints.
8 s, the method provided a set of reproducible DNA fingerprints.
9 ncrease or decrease in the band intensity of DNA fingerprints.
10 ical technique utilized in the production of DNA fingerprints.
11 overed during periodic videogastroscopy were DNA fingerprinted.
12 repeats used for over 20 years in humans for DNA fingerprinting.
13 sis isolates from the study period underwent DNA fingerprinting.
14 their pigs at birth were analyzed by genomic DNA fingerprinting.
15 s of Mycobacterium avium could be matched by DNA fingerprinting.
16 or observations attributed to reinfection by DNA fingerprinting.
17 and pulsed-field gel electrophoresis (PFGE) DNA fingerprinting.
18 epetitive-sequence polymerase chain reaction DNA fingerprinting.
28 25%) of 104 clustered patients shared both a DNA fingerprint and strong antecedent epidemiologic link
31 ability in the colonic mucosa as measured by DNA fingerprinting and fluorescent in situ hybridization
32 identified by randomly amplified polymorphic DNA fingerprinting and gene sequencing: one group from s
33 cin (Gm phenotype), all of which had similar DNA fingerprints and all of which were collected during
34 e of their usefulness as genomic markers and DNA fingerprints and more recently as their role in huma
36 premise that tuberculosis cases that share a DNA fingerprint are epidemiologically related while case
38 able repetitive-sequence-based PCR (rep-PCR) DNA fingerprinting assay adapted to an automated format,
41 agment length polymorphism analysis and were DNA fingerprinted by random amplification of polymorphic
46 S. mutans were examined based on chromosomal DNA fingerprints (CDF), a hypervariable region (HVR) of
48 4%) of the remaining 168 isolates were in 15 DNA fingerprinting clusters, which ranged in size from 2
53 ins inferred to be clonally related based on DNA fingerprinting) detected, one, lineage C, dominated
57 e 301 patients with completed interviews and DNA fingerprints fell into 20 different clusters of 2 to
58 n of (IS6110) can be harnessed to generate a DNA fingerprint for each strain, by digesting the genome
59 The study findings do not support the use of DNA fingerprinting for nosocomial tuberculosis surveilla
61 oach for the computational identification of DNA fingerprints for design of microarray-based pathogen
63 and analysis of approximately 150 in silico DNA fingerprints for Yersinia pestis and 250 fingerprint
67 ogy developed for optical mapping to acquire DNA fingerprints from single genomes for the purpose of
68 the diversity of Mycobacterium tuberculosis DNA fingerprints from three geographically separate stat
69 a constant enzyme buffer, and the intrinsic DNA fingerprints, from which amplicons may be quantitati
70 Only 20 (24%) of 84 cases with clustered DNA fingerprints had epidemiologic evidence of recent co
72 have unlocked new opportunities to identify 'DNA fingerprints', i.e. oligonucleotide sequences that u
74 F with this approach, the finding of altered DNA fingerprints in these microscopic lesions suggests t
76 identifying victims in a mass disaster using DNA fingerprints involves a scale of computation that re
77 the molecular epidemiology of tuberculosis, DNA fingerprinting is used to estimate the fraction of i
79 sequencing and repetitive element PCR-based DNA fingerprinting, it was found that H. aurati represen
80 e used as controls to create a rep-PCR-based DNA fingerprint library with the DiversiLab software.
85 North and South America and used a ribosomal DNA-fingerprinting method to compare bacterial community
86 e detection of mRNA expression, and numerous DNA fingerprinting methods have also proved valuable, be
87 ng two polymerase chain reaction (PCR)-based DNA fingerprinting methods, arbitrarily primed PCR and i
88 idlands from 2001-05 (n=20) were assessed by DNA fingerprinting (MIRU-VNTR and spoligotyping), with a
89 ude qualitative detection, sub-species-level DNA fingerprinting, molecular resistance testing and gen
94 of relapse and reinfection, distinguished by DNA fingerprinting of Mycobacterium tuberculosis strains
95 plays during tumor development, we compared DNA fingerprints of 44 aberrant crypt foci (ACF; the ear
97 based PCR (rep-PCR) is useful for generating DNA fingerprints of diverse bacterial and fungal species
99 s are illustrated by an analysis of standard DNA fingerprints of Mycobacterium tuberculosis in San Fr
101 with positive cultures) were identified; the DNA fingerprints of the 13 isolates available for testin
104 rent clinical laboratories revealed that the DNA fingerprint pattern of each case isolate was indisti
109 terspersed nuclear elements (SINEs) detected DNA fingerprint patterns in 14 species of salmonid fishe
112 Compared with strains having unique genomic DNA fingerprint patterns, the S. aureus clonotypes occur
113 e analysis to the 275 isolates with distinct DNA fingerprint patterns, we observed the same associati
114 r, recent analyses of the URA5 sequences and DNA fingerprinting patterns suggest significant genetic
115 as defined by insertion sequence (IS) IS6110 DNA fingerprinting, polymorphic GC-rich repetitive seque
116 es, and Southern blot hybridization with the DNA fingerprinting probe Ca3 combined with computer-assi
118 microevolutionary changes identified by the DNA fingerprinting probe Cg6 and does not involve tandem
119 Molecular fingerprinting with Ca3, a complex DNA fingerprinting probe specific for C. albicans, and C
120 pecific for C. albicans, and Cd25, a complex DNA fingerprinting probe specific for C. dubliniensis, p
122 rable for some applications than traditional DNA fingerprinting probes that detect tandemly repeated
124 for antibiotic susceptibility, O:H serotype, DNA fingerprinting, pulsed-field gel electrophoretic pat
129 is, mapping studies, human identity testing (DNA fingerprinting), sequence homology and population st
130 m var. Copenhagen strains) but that had AFLP DNA fingerprints similar or identical to those of strain
131 polymorphism (AFLP) analysis, which revealed DNA fingerprint similarities that correlated with both r
132 We provide a quantifiable definition of a DNA fingerprint stated both from a computational as well
134 h a setting, we performed a population-based DNA fingerprinting study among TB patients in Botswana.
135 identified by computer-assisted analysis of DNA fingerprints submitted during 1996 and 1997 by diffe
136 e patients had indistinguishable profiles by DNA fingerprinting, suggesting common-source exposure.
139 n site PCR (IRS-PCR) is a recently described DNA fingerprinting technique based on selective amplific
143 c microbes works by genotyping isolates with DNA fingerprinting techniques and then using these genot
144 opulation from an undisturbed site, and (iv) DNA fingerprinting techniques can be exploited to unders
146 We present the use of short tandem repeat DNA "fingerprinting" technology as a method of early, de
149 study of sufficient size and duration using DNA fingerprinting to investigate tuberculosis relapse a
151 the value of MLST relative to those of other DNA fingerprinting tools for discriminating among strain
152 modification of PCR that generates a genomic DNA fingerprint using a single, arbitrarily chosen prime
153 ycobacterium tuberculosis isolates underwent DNA fingerprinting using IS6110 restriction fragment len
154 within the species that had been selected by DNA fingerprinting using probes linked to mating type.
155 e mutation model to describe the dynamics of DNA fingerprint variation in Mycobacterium tuberculosis.
165 f clinical E. coli mastitis were compared by DNA fingerprinting with enterobacterial repetitive inter
166 Candida albicans isolates were selected for DNA fingerprinting with the complex DNA fingerprinting p
168 urrent infections was assessed by sequential DNA fingerprinting with the following three probes: the
172 tical or differed by at most one band, while DNA fingerprints with < or =5 bands were considered clus
173 Bacillus strains and quantitatively compare DNA fingerprints with the known taxonomy of the genus.
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