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1 amydia trachomatis such as the plasmid-based ligase chain-reaction and polymerase chain-reaction test
2 dia trachomatis and Neisseria gonorrhoeae by ligase chain reaction as well as to determine the preval
4 tis infection detected in urine specimens by ligase chain reaction assay and leukocyturia detected by
7 ucleic acid amplification tests, such as the ligase chain reaction assay, provides new opportunities
8 or gonococcal or chlamydial infection by the ligase chain reaction assay; secondary outcome measure w
9 populations was determined using urine-based ligase chain reaction DNA amplification assays (DAAs).
11 e specimens from both cohorts were tested by ligase chain reaction for Chlamydia trachomatis or Neiss
12 s by using COBAS PCR (Roche Diagnostics) and ligase chain reaction LCR (Abbott laboratories) and comp
14 bott Laboratories, Abbott Park, Ill.) uses a ligase chain reaction (LCR) amplification in the LCx pro
16 tability of this enzyme are exploited in the ligase chain reaction (LCR) and ligase detection reactio
18 women, we compared the results of commercial ligase chain reaction (LCR) and PCR tests performed on c
21 cation of the standard Chlamydia trachomatis ligase chain reaction (LCR) detection assay resulted in
22 of a Mycobacterium tuberculosis-specific gap ligase chain reaction (LCR) DNA amplification assay as w
23 f the sensitivity and specificity of PCR and ligase chain reaction (LCR) for detecting Chlamydia trac
24 nt-antibody assay (DFA), commercial PCR, and ligase chain reaction (LCR) for the verification of EIA
25 of nucleic acid amplification tests such as ligase chain reaction (LCR) have the potential to simpli
29 gonorrhoeae; evaluated the agreement between ligase chain reaction (LCR) performed on PreservCyt and
33 rrhoeae infection in pooled urine samples by ligase chain reaction (LCR) was examined in three popula
35 e no laboratory routinely used NAAT in 1995, ligase chain reaction (LCR) was used in 23% of laborator
38 er mycobacterial infections were tested by a ligase chain reaction (LCR)-based assay and acid-fast st
39 lified and typed from 60 of 126 samples from ligase chain reaction (LCR)-positive women and 3 samples
44 le (October 1996 to October 1999) were used (ligase chain reaction [LCx Probe System; Abbott Laborato
45 ireframe nanoassemblies using the isothermal ligase chain reaction lesion-induced DNA amplification (
47 py, all animals were positive for culture or ligase chain reaction (or both), and laparoscopy demonst
48 ithromycin-treated monkeys (P<.01); cervical ligase chain reaction remained positive in 15 placebo-,
49 s work reveals the suitability of isothermal ligase chain reactions such as LIDA to self-replicate co
50 Neisseria gonorrhoeae (n=884), using a urine ligase chain reaction test to determine prevalence and p
52 screening and treatment were initiated after ligase chain reaction testing became available midstudy,
53 s were invited to provide a urine sample for ligase chain reaction testing for C trachomatis infectio
54 rom BAL specimen cell pellets, and PCR-based ligase chain reaction was performed for mutations in the
55 e for gonococcal and chlamydial infection by ligase chain reaction, weighted to reflect variations in