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1 ing that endothelial NOS likely explains the age difference.
2 ding to a 13.8 +/- 5.3 million year apparent age difference.
3 tch of potential transplant, and donor-donor age difference.
4 dative peak velocities showed no significant age differences.
5 eness and Conscientiousness paralleled human age differences.
6 nted tremendous obstacles due to species and age differences.
7 efficients were included to test for sex and age differences.
8 Glu3 receptor mRNA levels showed substantial age differences.
9 source of dysregulated Ca2+ should eliminate aging differences.
10 --but does this approach capture even coarse age differences?
11 Daughters of tea consumers had a later mean age (difference = 0.41 years at >/= 3 cups (0.7 liter)/d
12 males and four females in each group; median age difference: 1 year; age range: 29-63 for patients an
13 n the overall AMD cohort after adjusting for age (difference, -19.9% [95% CI, -25.6% to -12.7%], P <
14 CT cohort; P = .06) did not differ in either age (difference, 69.20 years; 95% CI, 62.84-72.07 years;
15 and five (8.3%) were aged 41-49 years: mean age difference 8.7 years (95% CI 6.8-10.6; p<0.0001).
16 ively associated with BMD and BMC at 20 y of age [differences: 8.6 mg/cm(2) (95% CI: 3.0, 14.1 mg/cm(
18 two experiments, one in which we manipulated age differences among nestlings within broods, and anoth
21 n but more salient during mental replay, and age differences at perception could not account for olde
25 tionwide Inpatient Sample, we calculated the age difference between patients with SLE and their race-
26 rther supported independently by the stellar age difference between quiescent and star-forming galaxi
27 s were found to only be significant when the age difference between siblings was less than 2 years.
32 Mother-daughter pairs and pairs with large age differences between members interacted and associate
34 characteristics (accuracy 69%) but not when age differences between the groups were taken into accou
37 uration (height, weight, body mass index for age, difference between current and expected adult heigh
39 ut recipient age, donor age, recipient-donor age difference, donor gender, donor type, or cold ischem
40 ings with the 56 women aged 25-40 years, the age difference dropped to 1.1 years (95% CI -0.6 to 2.8;
44 life, which resulted in a 2.98-cm height-for-age difference (HAD) between sexes in the village and a
48 present findings support the hypothesis that age differences in brain signal variability reflect agin
49 number of CRH-BP positive fibers revealed no age differences in CeA; however, with regards to CRH-pos
50 nths) demonstrated statistically significant age differences in cerebellum-dependent delay eyeblink c
51 , 50-64, and 65-75 years) and assess whether age differences in chemotherapy matched survival gains a
55 rences in EaI/E(LV)I during exercise, due to age differences in EaI, E(LV)I, or both, may help to exp
59 This cross-sectional study examined whether age differences in frontostriatal white matter integrity
61 lated to general task demands and to examine age differences in functional connectivity both within a
66 be performed within the focus of attention, age differences in interference control may be more easi
71 creased gray matter volume in these regions, age differences in motor distinctiveness remained signif
76 cline, we used functional MRI to investigate age differences in PFC activity during separate WM task
77 ondom during sex were associated with larger age differences in relationships of both men and women.
78 se "compensatory" activations simply reflect age differences in response to experimental task demands
79 tal white matter integrity could account for age differences in reward learning in a community life s
82 Of greater significance, however, are the age differences in the different conditioning paradigms.
83 captured by this pattern is associated with age differences in the differential encoding of unique m
84 ated the contributions of brain structure to age differences in the distinctiveness of motor represen
85 nces in GABAergic regulation of the LAT, and age differences in the mechanism for the effects of repe
90 e using neuroimaging methodology, identified age differences in trust and their neural underpinnings.
92 f this study were to characterize the normal age differences in white matter integrity in several bra
94 properties, inter-animal variability, animal age, differences in spike timing between the synaptic re
97 ity increased with age, and the magnitude of age differences increased beginning with the middle of t
98 the shift to reproductive status rather than age differences matched the pattern of changes in olfact
101 5; P = .07), trisomy 8 (HR = 2.26; P = .02), age (difference of 10 years, HR = 1.46; P = .01), and th
102 rida couples were Hispanic; there was a mean age difference of 18 years between perpetrators and vict
105 k was used to integrate 44 studies reporting age differences or changes in coping from infancy throug
106 timated to be "older," with a mean predicted age difference (PAD) between chronological and estimated
109 sults are often confounded by small numbers, age differences, severity of symptoms, comorbidity, use
110 of unconnected folds associated with higher age differences than bridged folds, but this difference
120 ncrease in male participant age, the average age difference with their partners increased by 0.26 yea
121 This study was successful in determining age differences within the empty cases, which to date, h
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