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1 No evidence of an association was observed for NO2 or NOx.
3 There was minimal evidence of abuse, and no evidence of dependence or opioid withdrawal by AEs or obje
4 T cells with highly cytotoxic and proliferative states and no evidence of regulatory T cell depletion.
5 earlier studies with N-(hydroxymethyl)benzamide compounds, no evidence for mechanistic variation based upon the nature o
6 support an origin of the Arabian horse in the Middle East, no evidence for reduced global genetic diversity across the b
7 atient microbiota are linked with inflammation, but we find no evidence for a distinct microbial diagnostic signature, pr
9 ce acquisition and ingestion rates in >500 species, we find no evidence of a trade-off across species.
10 patient mortality in nonobstetrical care settings, 15 found no evidence of an association with liability risk and 5 found
11 Thermoplasmatota genomes/MAGs found no evidence of mcrA homologues outside of the Methanomassilii
15 Using chimeric Fls2/Fls3 proteins, we found no evidence that a single receptor domain is responsible for
16 When compared to control periods, we found no evidence that colony-wide escape (i.e., flight) behaviour
17 Community composition differed among locations but we found no evidence that primary remnants provide critical habitat to
19 She had no relevant medical or surgical history; no evidence of recent pregnancy, abortion, or breastfeeding;
22 en subjected to CRISPR/Cas9-mediated gene editing, there is no evidence of success in genetic alteration of Ag-experience
24 ard care for mechanically ventilated patients, but there is no evidence, using nonvolitional, objective measurements, tha
25 Groups with evidence of disease activity (EDA) or no evidence of disease activity (NEDA; occurrence of relapses
26 rombin-2, consistent with an E*-E equilibrium and providing no evidence that free thrombin is zymogen-like.
27 yi overlap in the Indo-West Pacific, yet their bindins show no evidence of positive selection, possibly because the two s
28 hoto-identification and telemetry studies, our results show no evidence of population structure (non-significant F(ST) <
29 Multidisciplinary evaluation of our national cohort showed no evidence for a severe, clinically relevant systemic immuno
30 hort interval between membrane rupture and delivery) showed no evidence of association with atopic dermatitis.
31 , ultrastructural examination by electron microscopy showed no evidence of viral particles in the biopsy samples.
32 group (10 per 10 000 person-years), adjusted results showed no evidence of any association between the use of glitazones
36 action in these mice, however, was unaltered, and there was no evidence for reduced pH-buffering capacity in the skeletal
39 In the intention-to-treat analysis, there was no evidence of a difference in the proportion of participants
41 clinically significant age-related cataracts, but there was no evidence of early onset of age-related cataracts in DS.
48 collagen II immunostaining in undamaged DDH cartilage, with no evidence of augmented cell death by activation of caspase
49 Twenty-nine samples from individuals with no evidence of TB infection by TST and no known exposure to T
50 els of Kv3.1 and Kv3.3 mRNA and protein were measured, with no evidence of compensation by Kv3.2 or Kv3.4 in the respecti