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1 pectively, with the conventional broth micro-dilution method).
2 obtained by the gold standard stable isotope dilution method.
3 two methods, the modern-dead and the isotope dilution method.
4 ass spectrometry (GC-MS), using the isotopic dilution method.
5  age with the dose-to-mother deuterium oxide dilution method.
6 ffusion, disc volatilisation and micro broth dilution method.
7 ry Standards Institute) recommends the broth dilution method.
8 was consistent with the results of the broth dilution method.
9 stigated at various oil loads by the 10-fold dilution method.
10 onfirm the results by using a CLSI reference dilution method.
11 assay involves the use of the stable isotope dilution method.
12 ibility testing was performed using the agar dilution method.
13 was measured using the [U-13C]glucose tracer dilution method.
14 ow been found to be a trimer using a His-tag dilution method.
15 cose turnover was measured using the isotope dilution method.
16 r H2S precursors non-detectable by the brine dilution method.
17 2 dilutions of the MICs observed by the agar dilution method.
18 ult was validated with a traditional isotope dilution method.
19 e tool as a substitute to the classical agar dilution method.
20  significantly depending upon dispensing and dilution methods.
21 uents were quantified using standard isotope dilution methods.
22  the dissociation constant using traditional dilution methods.
23 elation between broth microdilution and agar dilution methods.
24 stituted into proteoliposomes by a detergent dilution method (1).
25 re compared to those from the reference agar dilution method, 191 (95.5%) and 183 (91.5%) of strains
26 in) were determined using the reference agar dilution method according to Clinical and Laboratory Sta
27 soil Zn forms were determined using isotopic dilution methods, alongside conventional agronomic soil
28 eloped by simultaneously using the H2[(18)O] dilution method and BI in 12 infants with a gestational
29 O measurement compared well with the lithium dilution method and can be considered an accurate techni
30 o measure MM using the D(3)creatine (D(3)Cr) dilution method and determine its relationship with stre
31 ibility to six antimicrobials using the agar dilution method and genotyped using two high-resolution
32 rotaxanes were obtained using the UV-vis-NIR dilution method and the [2]pseudorotaxanes were characte
33   Tissue AEA was quantified using an isotope-dilution method and UPLC-ESI-MS/MS giving intra- and int
34 mendments (CLIA)-approved CLSI standard agar dilution method and, separately, by the Etest according
35 formed only by using labor-intensive, manual dilution methods and lies outside the capacity of most c
36                                    This agar dilution methods appears to highly correlate with NCCLS
37 red by our method and by traditional isotope dilution method are in excellent agreement, with the dis
38               IAA was measured by an isotope dilution method as the pentaflurobenzyl ester.
39 s, who received T cells produced by limiting dilution methods, but persisted 5 to 9 weeks in the next
40 termined from the standard CLSI M27-A2 broth dilution method by balanced-weight regression analysis.
41                     A double-spiking isotope dilution method capable of correcting and quantifying th
42                        The nonlinear isotope dilution method could, in principle, be applied to corre
43  counting) to total body water (TBW; isotope dilution) methods (ECW(TBK-TBW)) in an ethnically mixed
44                            The presented D2O dilution method enables such direct and quick quantifica
45 tory Standards Institute (CLSI) M38-A2 broth dilution method for amphotericin B (AMB), itraconazole (
46 as sensitive and quantitative as the isotope-dilution method for measuring blood-retinal barrier brea
47 f the Etest compared with the reference agar dilution method for penicillin, tetracycline, ciprofloxa
48 adapted as a safe alternative to the isotope-dilution method for quantitating blood-retinal barrier b
49 s spectrometry coupled with a stable isotope dilution method for rigorous quantitation of DPCs formed
50 ve, simple alternative to the reference agar dilution method for the direct quantification of N. gono
51 p is used in conjunction with an exponential dilution method for the gradient separation of peptides
52 those of the eosin-maleimide labeled protein dilution method for the limiting cases; the analysis ind
53  LC-MS/MS/MS coupled with the stable isotope-dilution method for the sensitive and accurate quantific
54 pecific, sensitive, and rapid stable isotope dilution method for the simultaneous detection of the or
55  size using the deuterated creatine (D(3)Cr) dilution method, for their associations to strength.
56  tear film in vivo--were determined by a dye-dilution method from the fluorescence of Texas red-dextr
57 cessible fraction (E) derived by the isotope dilution method (IDM) ranged from 0.28 to 0.89 and was s
58 ctrometry (SPE-UPLC-MS/MS) using the isotope dilution method in the colostrums of 21 women who had co
59 ere lower than with the previous pseudo-high-dilution method, indicating ineffective templation in th
60 uid secretion process, was measured by a dye dilution method involving fluid collections using a seco
61                                  The lithium dilution method is at least as accurate as bolus thermod
62                                   The D(3)Cr dilution method may provide a biomarker of disease progr
63 ility was lowered to </=1 microg/ml for agar dilution methods, more CoNS isolates with oxacillin resi
64 thodologies, including use of stable-isotope dilution methods, now allows for an accurate determinati
65 od with those obtained by the reference agar dilution method of the National Committee for Clinical L
66 ntionally performed by either a serial broth dilution method or with the commercially available Etest
67 e second study, we use a stable iron isotope dilution method over a 6-month period to demonstrate tha
68 m computed tomography (EBCT)-based indicator-dilution methods provide an estimate of intramyocardial
69                The non-invasive D(3)creatine dilution method provides novel data on whole body functi
70 ns were measured with the deuterated-retinol-dilution method; serum retinol and carotenoid concentrat
71  blank contamination; therefore, the isotope dilution method should be used with caution when the var
72 e- to fivefold dilutions lower than the agar dilution method susceptibilities but only with ampicilli
73                                 In this agar dilution method, susceptible Candida albicans colonies a
74 by the carboxyfluorescein succinimidyl ester dilution method that allogeneic mature AdTGF-beta1 Rh MD
75 eptibility testing automatically via a broth dilution method to accurately determine the minimum inhi
76                        We used the deuterium dilution method to determine FFMI and FMI and %FFM and %
77 thod that couples MALDI-TOF-MS with a simple dilution method to quantify curcumin in food condiments
78 y (LC-MS/MS) coupled with the stable isotope-dilution method to quantify DNA-protein cross-link (DPC)
79                             We present a D2O dilution method to quantify submicroliter volumes of aqu
80 ngal activity was assessed by the microbroth dilution method using four common human pathogenic fungi
81  Aqueous humor flow (Fa) was determined by a dilution method using rhodamine-dextran.
82  by LC-MS/MS under MRM condition and isotope dilution method, using d(2)-labelled internal standards
83  equivalence of the SGE method with the agar dilution method was assessed with a wide variety of anae
84                 A sensitive LC-MS/MS isotope dilution method was developed to simultaneously quantify
85 robial susceptibility testing using the agar dilution method was performed for anaerobic gram-negativ
86                                The indicator dilution method was used to measure the single-pass maxi
87 ass spectrometry (LC-MS/MS) with the isotope dilution method, we assessed quantitatively the formatio
88         In contrast, the results of the agar dilution method were in least agreement (93.2%) with the
89                    MICs obtained by the agar dilution method were within 1 dilution of MECs for 85% o
90                               Agar and broth dilution methods were in concordance with PCR detection
91                Standard addition and isotope dilution methods were used for quantifications in select
92                          RSA and NCCLS broth dilution methods were used to determine the MICs of amph
93                                    Indicator dilution methods were used to measure single pass hydrol
94                           The Etest and agar dilution methods were well correlated.
95 atory Standards Institute (CLSI) M38-A broth dilution method with itraconazole (ITR), posaconazole (P
96  humor production (F(a)) was measured by the dilution method with rhodamine-dextran.