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1                                                    Although we did not observe a clear age trend for infants, BDCIPP leve
2 posed that leaf expansion and movement are causally linked, we did not observe a consistent temporal relationship between
3    In an analysis of data from the Nurses' Health Study II, we did not observe a convincing association between PPI use a
4 pite serial reversal of latency over 1 month of VOR dosing, we did not observe a measurable decrease (>0.3 log10) in the
5              After progression while receiving bevacizumab, we did not observe a negative rebound effect (ie, shorter sur
6                                                In contrast, we did not observe a significant down-regulation of Cldn-1 in
7                 Despite a large variation in wheel running, we did not observe a significant relationship between the amo
8                                                    However, we did not observe a similar protective effect in SIV-infecte
9                                                    However, we did not observe a survival advantage associated with total
10 , despite these bidirectional changes in PSD-95 clustering, we did not observe an alteration in basal electrophysiologica
11                        Despite the extensive tissue damage, we did not observe an impact on longevity, suggesting a remar
12                              Similar to the original study, we did not observe an impact on mouse body weight with DOX an
13                                                    Finally, we did not observe any C5aR1 expression in naive or activated
14                        Unlike in previous studies, however, we did not observe any clear differences in the quantities of
15 ngth) and reliability: in more than 8,000,000 recorded APs, we did not observe any conduction or branch-point failures.
16                                              Interestingly, we did not observe any correlation between intracellular H2O2
17                                           Most importantly, we did not observe any correlation between PMP22 messenger RN
18                                                    Notably, we did not observe any correlation between the dose level and
19                                              In these mice, we did not observe any defects in B cell signaling and B cell
20 raft function, respectively, both at 1 and 5 years, whereas we did not observe any difference among patients with a score
21 ion defects were limited to these morphological changes, as we did not observe any differences in epigenetic profiles.
22                                        In the dosing study, we did not observe any evidence of microembolization after ca
23                                                In addition, we did not observe any impact on stomatal aperture following
24 n the 161 persons with sporadic congenital scoliosis (11%); we did not observe any null mutations in TBX6 in 166 controls
25                                   In a cohort of 582 cases, we did not observe any pathogenic mutations indicating that m
26                                               Surprisingly, we did not observe any relevant changes in the vascular endot
27                                                In addition, we did not observe cannibalism.
28                                                Furthermore, we did not observe changes in the activity of glucose-6-phosp
29                                                    However, we did not observe co-immunoprecipitation between Nedd4L and
30 g a catalytic mutant form of RAG1 to prevent recombination, we did not observe cooperation between RAG1 and RAG2 in their
31  control fibroblast cell lines, but in our restricted study we did not observe correlations between disease status and au
32       Using Chromatin Immunoprecipitation-qPCR (ChIP-qPCR), we did not observe direct binding of p53 to MIR182, MIR203, M
33     When connections within the peri-infarct were isolated, we did not observe equal down-scaling of responses after stro
34 er according to age in individuals of European descent, but we did not observe evidence of statistically significant gene
35                                                    Further, we did not observe expected cross-pathway inhibition in betwe
36 lysis of criteria used in histopathologic diagnosis of LGD, we did not observe improvement in level of agreement among ex
37 ypes display particularly large increases in apoptosis that we did not observe in older animals.
38                                                    Although we did not observe it with direct methods, a functional dimer
39       However, in our immunoprecipitation (IP) experiments, we did not observe myoferlin binding with IL-6R.
40 fficacy of the 2 drugs in Human Embryonic Kidney 293 cells, we did not observe rescue of the electrophysiological phenoty
41                                              In this study, we did not observe short-term changes in behavior associated
42                                                    Finally, we did not observe significant association between total diet
43                                               Additionally, we did not observe significant differences in response to gem
44                                                In contrast, we did not observe significant differences in the Autism Brai
45 actions between the phase-forming polymers and the enzymes, we did not observe significant rate enhancements from colocal
46  adjusted for age, smoking, region, and population density, we did not observe statistically significant associations bet
47 f enrollment, the study was closed because of the futility; we did not observe sufficient events to evaluate the primary
48      However, in four direct replication attempts (n = 64), we did not observe the critical impairment effect that has pr
49                                                 Critically, we did not observe the expected second peak in decoding perfo
50 ndrial membrane potential was diminished by PINK1 deletion, we did not observe the predicted increases in mitochondrial d

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