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1 PAV increased by 0.3% (p < 0.001), and 19.9% of subjects
2 PAV-TAS2R38 mRNA expression was measured in 18 of 22 het
3 V delivered with the Puritan-Bennett 7200ae, PAV is associated with more rapid improvements in some p
4 of the children of the AVI/AVI, PAV/AVI, and PAV/PAV genotypes differed from each other, and that the
5 eline) and was attenuated with hyperoxia and PAV (-18 +/- 1 and -17 +/- 2% baseline, P < 0.01, respec
6 iking scores of the children of the AVI/AVI, PAV/AVI, and PAV/PAV genotypes differed from each other,
7 ctors associated with MACE included baseline PAV (p < 0.0001), change in PAV (p = 0.002), smoking (p
9 A stronger correlation was observed between PAV and glycated hemoglobin (r = 0.22, p = 0.0003) than
11 3'TE in cis and capped mRNA lacking any BYDV-PAV sequence was inhibited specifically by added 3'TE RN
12 etitive hierarchy: the coinoculation of BYDV-PAV lowered CYDV-RPV infection rate, but the reverse was
15 e of the PAV barley yellow dwarf virus (BYDV-PAV) which stimulates translation from uncapped mRNA by
19 yed a positive correlation with the anti-cod PAV polyclonal antibody, but no correlation with the ant
20 ent, the mean increase of distance-corrected PAV for near vision was +0.25+/-0.64 D (P < 0.001) for d
21 ntly influence liking of accessions, despite PAV/PAV 'supertasters' scoring higher for this attribute
29 17.0% [95% CI, 10.4% to 23.6%]; P < .001 for PAV and 61.5% vs 48.9%; difference, 12.5% [95% CI, 5.9%
30 atorvastatin and 68.5% with rosuvastatin for PAV (P=0.07) and 64.7% and 71.3%, respectively, for TAV
35 o acid sequence) form do not; heterozygotes (PAV/AVI) show the widest range of bitter perception.
37 ncluded baseline PAV (p < 0.0001), change in PAV (p = 0.002), smoking (p = 0.0002) and hypertension (
38 parameters were prespecified: the change in PAV and the change in nominal atheroma volume in the 10-
42 seline characteristics showed an increase in PAV of 0.64% (95% CI, 0.23% to 1.05%) for glimepiride an
45 (21.1 +/- 3.7 months), greater increases in PAV, but not total atheroma volume, were observed in sub
48 erative adaptive optics assessment, the mean PAV increase at near was significantly higher (P < 0.05)
49 With medical therapy, the rate of change of PAV (0.7 +/- 0.6% vs. 0.7 +/- 0.5%, p = 0.92) and TAV (-
50 mine individual differences in expression of PAV-TAS2R38 messenger RNA (mRNA) among heterozygotes, to
53 DL-C was associated with less progression of PAV (+0.30%, 95% confidence interval [CI]: -0.17% to 0.7
54 n was associated with greater progression of PAV (+0.43 +/- 0.07% vs. +0.02 +/- 0.11%; p = 0.002).
55 was not associated with less progression of PAV (+0.51%, 95% CI: 0.04% to 0.99% vs. +0.61%, 95% CI:
57 participants who demonstrated regression of PAV (56.9% vs 48.9%; P = .08) and TAV (64.4% vs 57.5%; P
60 5 719 genes were affected by an SNP, CNV, or PAV across the panel, providing a firm foundation to ide
63 ine the correlation between the parvalbumin (PAV) contents and their corresponding immunoreactivity (
64 sease progression for the primary end point (PAV) but showed a favorable effect on the secondary end
65 e modified using proprietary polyallylamine (PAV) and coupled with macromolecular heparin conjugates
69 d paced atrioventricular (AV) intervals (SAV/PAV) accounted for 34.5% of all ventricular sensing epis
75 t time a statistical correlation between the PAV content and the immunoreactivity and allowed to rank
79 ty-one and 23 patients were entered into the PAV and PSV groups, respectively, and had similar diagno
80 translated region (UTR) of the genome of the PAV barley yellow dwarf virus (BYDV-PAV) which stimulate
84 stics for patients not completing the trial, PAV increased 0.25% (-0.04% to 0.55%) vs 0.57% (0.29% to
85 , defined as the pseudo-accommodation value (PAV = [1/reading distance {m}] - minimum addition [D]).
86 -CNVs) and 14 430 presence/absence variants (PAVs), affecting a total of 9979 genes, including two up
87 iation (CNV) and presence-absence variation (PAV) can lead to variation in the genome content of indi
88 vantages of proportional assist ventilation (PAV) has been the automatic synchrony between the end of
92 g sequences in the barley yellow dwarf virus PAV genome required for this programmed readthrough in v
93 stop codon of the barley yellow dwarf virus (PAV serotype) coat protein gene is read through at a low
94 two virus species, barley yellow dwarf virus-PAV (BYDV-PAV) and cereal yellow dwarf virus-RPV (CYDV-R
96 plaque in terms of percent atheroma volume (PAV) (33.9 +/- 10.2% vs. 37.8 +/- 10.3%, p < 0.001) and
97 onstrated a greater percent atheroma volume (PAV) (36.0 +/- 7.6% vs. 29.0 +/- 8.5%; p < 0.001) and to
98 onstrated a greater percent atheroma volume (PAV) (40.2 +/- 0.9% vs. 37.5 +/- 0.8%, p < 0.0001) and t
99 ts had a greater percentage atheroma volume (PAV) (45% vs. 34%, p < 0.001), total atheroma volume (TA
100 less progression in percent atheroma volume (PAV) (p < 0.001) and total atheroma volume (TAV) (p < 0.
101 changes in coronary percent atheroma volume (PAV) and CaI were measured across matched coronary segme
102 eline and change in percent atheroma volume (PAV) and total atheroma volume with incident major adver
105 e nominal change in percent atheroma volume (PAV) from baseline to week 78, measured by serial intrav
106 efficacy end point, percent atheroma volume (PAV), decreased by 0.99% (95% confidence interval [CI],
107 of regression using percent atheroma volume (PAV), the most rigorous IVUS measure of disease progress
108 meter was change in percent atheroma volume (PAV); the secondary efficacy parameter was change in nor
109 no-statin therapy (n = 224) associated with PAV progression (+0.8 +/- 0.1% and +1.0 +/- 0.1%; p < 0.
110 cteristics, HIST (n = 1,545) associated with PAV regression from baseline (-0.6 +/- 0.1%; p < 0.001),
112 We show that Polo kinase associates with PAV-KLP with which it shows an overlapping pattern of su
113 iciency were randomized to receive NPPV with PAV delivered using the Respironics Vision ventilator or
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