1 We repeated analyses for Alzheimer disease and accounting for
2 To compare with pharmacological inhibition of eNOS,
we repeated both tests in the presence of l-NAME.
3 We repeated our analyses after stratifying hospitals into qui
4 In a sensitivity analysis,
we repeated our analysis from the perspective of Medicare.
5 might indicate abnormal weakening of response gain control,
we repeated our measurements at low contrast, where the effec
6 We repeated our observations using rabbit serum containing an
7 We repeated our study with an improved vector containing Tol2
8 18 months after VISHRAM was enacted,
we repeated sampling methods to select a separate population
9 Here,
we repeated similar experiments to test for complementarity o
10 o test whether these results were specific to stick insect,
we repeated some of these experiments in cockroach (Periplane
11 To verify these associations,
we repeated the analyses with an independent set of behaviora
12 We repeated the analysis for the subset of patients with infe
13 To simulate data limitations,
we repeated the analysis using a single criterion at a time (
14 Our findings were similar when
we repeated the analysis using data from later years.
15 ta suitable for comparison with data of denatured proteins,
we repeated the assignment in 7 M urea (pH 2.3) and in DMSO.
16 We repeated the behavioral portions of these studies in wild-
17 Second,
we repeated the coprecipitation assays.
18 We repeated the experiment from three homing sites using mult
19 Second,
we repeated the experiments by substituting phosphatidylserin
20 In this study,
we repeated the experiments to ensure that the high variance
21 When
we repeated the experiments with C3-deficient mice, we observ
22 r ischemia affects the systemic immune response to antigen,
we repeated the immunization experiment using mice deficient
23 We repeated the original experiments separately in three diff
24 Finally,
we repeated the pretraining and pretesting experiments with t
25 Supporting this finding,
we repeated the primary analysis in a cohort of patients not
26 We repeated the process for those with >/=2 samples within 28
27 For additional controls,
we repeated the same experiments with herpes simplex virus (H
28 When
we repeated the same visual stimulus, we found that the same
29 We repeated the sensitivity analysis with Xpert MTB/RIF as th
30 tion types from the tropics to the northern high-latitudes,
we repeated the site and global simulations using two reanaly
31 We repeated the study by identifying and removing several ext
32 xplore these puzzling effects and their mechanisms further,
we repeated the tests for RI associated with diet-specific gu
33 We repeated these analyses among networks offered in the same
34 We repeated these analyses stratifying by age.
35 We repeated these analyses using TV-viewing time instead of d
36 We repeated these assessments at 24 and 48 weeks.
37 l effects in the presence of significant amyloid pathology,
we repeated these experiments in older APP/PS1 mice with sign
38 To assess the reproducibility of the diagnosis,
we repeated these measurements after 4 weeks.
39 We repeated these studies in mice, and find that injections o
40 might be achieved across a variable population of animals,
we repeated this analysis across six sets of maximal conducta
41 We repeated this analysis after adjustment with both small si
42 We repeated this analysis for ICD subtypes: single chamber, d
43 enome sequencing and evolutionary convergence analysis, and
we repeated this analysis in an independent validation cohort
44 We repeated this analysis, adding the peak TnT measurement du
45 We repeated this analysis, adding the peak TnT measurement du
46 To prevent DA activation of D4 receptors,
we repeated this experiment in LHb slices from DA-depleted ra
47 We repeated this process on 22 colorectal cell lines and foun
48 To verify these important observations,
we repeated this study in our laboratory.
49 Here, using a superior 5-HTT tracer, (11)C-DASB,
we repeated this study with a prospective design with 8 wk of
50 oxygenation prolonged exercise time only in severe hypoxia,
we repeated this trial and assessed peripheral fatigue follow