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1 C administration in HI mouse brains produced identical results.
2 cells with purified recombinant hUG yielded identical results.
3 ng standard operating procedures with almost identical results.
4 umulative coal dust exposure produced almost identical results.
5 to depolymerize the tubulin network yielded identical results.
6 The two data sets yielded nearly identical results.
7 gle-step and seminested PCR methods produced identical results.
8 7% recovery) and reutilized once with almost identical results.
9 se steps proceed in the absence of gold with identical results.
10 ction and variance component estimation with identical results.
11 process PET scans showed correlated but not identical results.
12 eed and memory usage, while achieving nearly identical results.
13 under the same reaction conditions to afford identical results.
14 ls as exfoliated cells (Part 1) yield nearly identical results.
15 e input and output interface while producing identical results.
16 he matched propensity-score analyses yielded identical results.
17 te Carlo simulations while leading to nearly identical results.
18 sing acutely dissociated neurons, which gave identical results.
19 model selection approaches gave essentially identical results.
20 lly functional alternative splicing produced identical results.
21 onte Carlo algorithms have given rise to the identical results.
22 samples analysed from the same patient gave identical results.
23 se, but the two species produced essentially identical results.
24 a coli ADP-Glc PPase and both assays yielded identical results.
25 Both techniques yielded nearly identical results.
26 The 3 methods gave similar but not identical results.
27 ve fibers, labeled only for NADPH-d, yielded identical results.
28 acted at least one additional time; all gave identical results.
29 susceptibility studies of A. fumigatus with identical results.
30 in reward rates can produce similar, but not identical, results.
31 nditional power produces similar, though not identical, results.
33 uman as well as rat LADA pancreases provided identical results, allowing the conclusion that LADA is
34 results (r = 0.77; 728 strains) showed 55.4% identical results and agreement of 99.7% +/- one log2 di
36 the algebraic and differential methods yield identical results and neither shows drift in computed pa
37 substituted (E)- and (Z)-alkenes give nearly identical results, and a trisubstituted alkene substrate
38 rocess in well-mixed populations, but almost identical results are found for the Wright-Fisher and Pa
43 The comparisons show SLAM to produce almost identical results as BFM for NH3, but higher concentrati
44 ng the HSP receptor CD40 with CD40L produced identical results as extracellular riHSP70, and, moreove
45 des was no more difficult and yielded nearly identical results as the analysis of the same sample usi
47 ined in a previous study, the PEPIS returned identical results at each analysis step with the origina
49 l methylation estimates and can be run, with identical results, either on a single computer, in an HP
50 e experiments done with C57BL/6 mice yielded identical results, even though only the early phase of g
51 ADPH-d) histochemistry, which yielded almost identical results except for the primary olfactory proje
52 n spectroscopic (XAS) studies gave virtually identical results for all NcAA9C variants, showing that
53 ffer complementary computing advantages with identical results for genomic prediction of breeding val
56 ctrometry; each technique produced virtually identical results for the neutral desialylated glycans.
60 Quantitative arteriosclerosis studies showed identical results in both apoCIII transgenic/apoE0 and a
61 differentiation of the temporalis and found identical results in both control and mutant mice before
63 We also show that the assay gives nearly identical results in trial screening to those obtained b
64 t to experimental uncertainties and produces identical results irrespective of the type of mobility c
65 GDP-[U-(14)C]Fuc as substrate gave virtually identical results: K(m) = 54.3 +/- 4.6 microM and k(cat)
68 -cohort analyses generating similar, but not identical results, particularly for non-European ancestr
69 rence preparations tested by MAPREC produced identical results, suggesting that the method could take
78 s were not cell type or species specific, as identical results were observed for both HPV-11 URR-lacZ
79 y the Ser allele from heterozygous patients (identical results were observed in a pair-matched normal
82 These effects were directly mediated since identical results were observed in single-cell assays.
87 lls in STAT5b-CA vs littermate control mice; identical results were observed when crossing STAT5b-CA
88 to the amine.HCl salt catalyzed process and identical results were observed, indicating that the tru
100 ot due to insufficient amounts of S-HDAg, as identical results were obtained in a cell line that stab
102 the form of factor V present in plasma since identical results were obtained in an appropriately reco
110 e experiments were performed in C2C12 cells, identical results were obtained using mouse skeletal mus
126 neopterin had the same effect, and virtually identical results were obtained with RFL-6 fibroblasts,
127 n-denaturing immunoprecipitation method, and identical results were obtained with two detergents belo
133 Prothrombin and prethrombin-2 gave nearly identical results while meizothrombin in some regions mo
134 ratified analysis of summary scores produced identical results, while weighted analysis showed some d
138 ed to birth weight, our method showed nearly identical results with those obtained using individual-l
139 cy-compounded CCK-8 produce similar, but not identical, results with close correlation between them w
140 e-destabilizing drug, vinblastine, led to an identical result, with complete blockade of EC sprouting