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1 sensitivity remains suboptimum compared with culture tests.
2 e sol-gel TiO2 devices through in-vitro cell culture tests.
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
23 entation of the Verigene Gram-positive blood culture test led to reductions in time to acceptable ant
27 l admission consistently predicted increased culture testing, regardless of principal diagnosis or ag
30 1 to 2 days, and based on results from cell culture tests, the probe correctly detected the presence
32 ce of the MicroPhage KeyPath MRSA/MSSA blood culture test was compared to conventional identification
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