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1 sensitivity remains suboptimum compared with culture tests.
2 e sol-gel TiO2 devices through in-vitro cell culture tests.
3                    Of 370 isolates and stock cultures tested, 327 (88%) were given species names by t
4                      While using semi-annual culture test and culling of low and high shedders with a
5 certainty analysis showed that, using annual culture test and culling of only high shedders or cullin
6 ion, empirical therapy for UTI without urine culture testing and overdiagnosis of UTI were common and
7 n the same sputum specimen was compared with culture tests and drug susceptibility testing as referen
8 98 significantly reduced Sox9 transcripts in cultured testes and increased Sox9 levels in ovaries.
9 he Gen-Probe AccuProbe Group B Streptococcus Culture Test (APGB) and the BD GeneOhm StrepB assay (GOS
10 on of the rapid Verigene Gram-negative blood culture test (BC-GN), a microarray that detects 9 genus/
11 ificity) of the Verigene Gram-Positive Blood Culture Test (BC-GP) test to identify 12 Gram-positive b
12 inistic cell cycle IBM model fails the batch culture test, because it has an abrupt drop in cell quot
13 chastic IBM model fails the steady chemostat culture test, because it produces excessive numerical ra
14 tumor cell cultures, and normal ectocervical cultures tested, but no IGF-1 transcripts were detected.
15 ta revealed that the KeyPath MRSA/MSSA blood culture test delivered results a median of 30 h sooner t
16 tandard methods, the KeyPath MRSA/MSSA blood culture test demonstrated a sensitivity, specificity, po
17 xamine the incidence of urinalysis and urine culture testing for select diagnoses and patient factors
18 ual microwell AMPLICOR (Roche) (MWA), and by culture; testing for N. gonorrhoeae was done by CA and c
19                                              Culture testing identified the organism in 12 of the 23
20                                For the 1,389 cultures tested in phase 1, conducted to evaluate cutoff
21                Simulated body fluid and cell culture tests indicated favorable bioactivity and biocom
22  and has the possibility to impact how blood culture testing is performed.
23 entation of the Verigene Gram-positive blood culture test led to reductions in time to acceptable ant
24                                   Of the 314 cultures tested, multiplex, real-time PCR produced congr
25  by the reference standard method with rapid culture testing on saliva or urine.
26                                  Of 77 blood cultures tested, only 7 yielded results inconsistent wit
27 l admission consistently predicted increased culture testing, regardless of principal diagnosis or ag
28 f septic arthritis before the Gram stain and culture test results are known.
29                                   Of the 244 cultures tested retrospectively, 226 (92.6%) had concord
30  1 to 2 days, and based on results from cell culture tests, the probe correctly detected the presence
31                                        Urine culture testing varied by principal diagnosis.
32 ce of the MicroPhage KeyPath MRSA/MSSA blood culture test was compared to conventional identification
33           The most accurate catheter segment culture test was quantitative culture (Q* = 0.87 [CI, 0.
34                                              Culture tests were positive for tuberculosis in 12% (420
35 of tuberculosis underwent sputum testing and culture testing (when available).
36  of low shedding animals (based on the fecal culture test) will be necessary.

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