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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 epetitive-sequence polymerase chain reaction DNA fingerprinting.
13 repeats used for over 20 years in humans for DNA fingerprinting.
14 sis isolates from the study period underwent DNA fingerprinting.
15 their pigs at birth were analyzed by genomic DNA fingerprinting.
16 or observations attributed to reinfection by DNA fingerprinting.
17 s of Mycobacterium avium could be matched by DNA fingerprinting.
18 and pulsed-field gel electrophoresis (PFGE) 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
34 cin (Gm phenotype), all of which had similar DNA fingerprints and all of which were collected during
35 e of their usefulness as genomic markers and DNA fingerprints and more recently as their role in huma
37 premise that tuberculosis cases that share a DNA fingerprint are epidemiologically related while case
39 able repetitive-sequence-based PCR (rep-PCR) DNA fingerprinting assay adapted to an automated format,
43 agment length polymorphism analysis and were DNA fingerprinted by random amplification of polymorphic
48 S. mutans were examined based on chromosomal DNA fingerprints (CDF), a hypervariable region (HVR) of
50 4%) of the remaining 168 isolates were in 15 DNA fingerprinting clusters, which ranged in size from 2
55 ins inferred to be clonally related based on DNA fingerprinting) detected, one, lineage C, dominated
59 e 301 patients with completed interviews and DNA fingerprints fell into 20 different clusters of 2 to
60 n of (IS6110) can be harnessed to generate a DNA fingerprint for each strain, by digesting the genome
61 The study findings do not support the use of DNA fingerprinting for nosocomial tuberculosis surveilla
63 oach for the computational identification of DNA fingerprints for design of microarray-based pathogen
65 and analysis of approximately 150 in silico DNA fingerprints for Yersinia pestis and 250 fingerprint
69 ogy developed for optical mapping to acquire DNA fingerprints from single genomes for the purpose of
70 the diversity of Mycobacterium tuberculosis DNA fingerprints from three geographically separate stat
71 a constant enzyme buffer, and the intrinsic DNA fingerprints, from which amplicons may be quantitati
72 Only 20 (24%) of 84 cases with clustered DNA fingerprints had epidemiologic evidence of recent co
74 have unlocked new opportunities to identify 'DNA fingerprints', i.e. oligonucleotide sequences that u
76 F with this approach, the finding of altered DNA fingerprints in these microscopic lesions suggests t
78 identifying victims in a mass disaster using DNA fingerprints involves a scale of computation that re
79 the molecular epidemiology of tuberculosis, DNA fingerprinting is used to estimate the fraction of i
81 sequencing and repetitive element PCR-based DNA fingerprinting, it was found that H. aurati represen
82 e used as controls to create a rep-PCR-based DNA fingerprint library with the DiversiLab software.
87 North and South America and used a ribosomal DNA-fingerprinting method to compare bacterial community
88 e detection of mRNA expression, and numerous DNA fingerprinting methods have also proved valuable, be
89 ng two polymerase chain reaction (PCR)-based DNA fingerprinting methods, arbitrarily primed PCR and i
90 idlands from 2001-05 (n=20) were assessed by DNA fingerprinting (MIRU-VNTR and spoligotyping), with a
91 ude qualitative detection, sub-species-level DNA fingerprinting, molecular resistance testing and gen
96 of relapse and reinfection, distinguished by DNA fingerprinting of Mycobacterium tuberculosis strains
97 plays during tumor development, we compared DNA fingerprints of 44 aberrant crypt foci (ACF; the ear
99 based PCR (rep-PCR) is useful for generating DNA fingerprints of diverse bacterial and fungal species
101 s are illustrated by an analysis of standard DNA fingerprints of Mycobacterium tuberculosis in San Fr
103 with positive cultures) were identified; the DNA fingerprints of the 13 isolates available for testin
106 rent clinical laboratories revealed that the DNA fingerprint pattern of each case isolate was indisti
111 terspersed nuclear elements (SINEs) detected DNA fingerprint patterns in 14 species of salmonid fishe
114 Compared with strains having unique genomic DNA fingerprint patterns, the S. aureus clonotypes occur
115 e analysis to the 275 isolates with distinct DNA fingerprint patterns, we observed the same associati
116 r, recent analyses of the URA5 sequences and DNA fingerprinting patterns suggest significant genetic
117 as defined by insertion sequence (IS) IS6110 DNA fingerprinting, polymorphic GC-rich repetitive seque
118 es, and Southern blot hybridization with the DNA fingerprinting probe Ca3 combined with computer-assi
120 microevolutionary changes identified by the DNA fingerprinting probe Cg6 and does not involve tandem
121 Molecular fingerprinting with Ca3, a complex DNA fingerprinting probe specific for C. albicans, and C
122 pecific for C. albicans, and Cd25, a complex DNA fingerprinting probe specific for C. dubliniensis, p
124 rable for some applications than traditional DNA fingerprinting probes that detect tandemly repeated
126 for antibiotic susceptibility, O:H serotype, DNA fingerprinting, pulsed-field gel electrophoretic pat
131 is, mapping studies, human identity testing (DNA fingerprinting), sequence homology and population st
132 m var. Copenhagen strains) but that had AFLP DNA fingerprints similar or identical to those of strain
133 polymorphism (AFLP) analysis, which revealed DNA fingerprint similarities that correlated with both r
134 We provide a quantifiable definition of a DNA fingerprint stated both from a computational as well
136 h a setting, we performed a population-based DNA fingerprinting study among TB patients in Botswana.
137 identified by computer-assisted analysis of DNA fingerprints submitted during 1996 and 1997 by diffe
138 e patients had indistinguishable profiles by DNA fingerprinting, suggesting common-source exposure.
141 n site PCR (IRS-PCR) is a recently described DNA fingerprinting technique based on selective amplific
145 c microbes works by genotyping isolates with DNA fingerprinting techniques and then using these genot
146 opulation from an undisturbed site, and (iv) DNA fingerprinting techniques can be exploited to unders
148 We present the use of short tandem repeat DNA "fingerprinting" technology as a method of early, de
152 study of sufficient size and duration using DNA fingerprinting to investigate tuberculosis relapse a
154 the value of MLST relative to those of other DNA fingerprinting tools for discriminating among strain
155 modification of PCR that generates a genomic DNA fingerprint using a single, arbitrarily chosen prime
156 ycobacterium tuberculosis isolates underwent DNA fingerprinting using IS6110 restriction fragment len
157 within the species that had been selected by DNA fingerprinting using probes linked to mating type.
158 e mutation model to describe the dynamics of DNA fingerprint variation in Mycobacterium tuberculosis.
168 f clinical E. coli mastitis were compared by DNA fingerprinting with enterobacterial repetitive inter
169 Candida albicans isolates were selected for DNA fingerprinting with the complex DNA fingerprinting p
171 urrent infections was assessed by sequential DNA fingerprinting with the following three probes: the
175 tical or differed by at most one band, while DNA fingerprints with < or =5 bands were considered clus
176 Bacillus strains and quantitatively compare DNA fingerprints with the known taxonomy of the genus.