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1 tch of potential transplant, and donor-donor age difference.
2 ing that endothelial NOS likely explains the age difference.
3 ding to a 13.8 +/- 5.3 million year apparent age difference.
4 chieve equal self-reported sex and a minimal age difference.
5 is now difficult to reconcile with a >11-My age difference.
6 asured by gestational age at birth and PedBE age difference.
7 were numerically higher after adjusting for age difference.
8 eness and Conscientiousness paralleled human age differences.
9 nted tremendous obstacles due to species and age differences.
10 efficients were included to test for sex and age differences.
11 Glu3 receptor mRNA levels showed substantial age differences.
12 were observed, alongside large and variable age differences.
13 her samples cannot be explained by income or age differences.
14 ver time in TMD symptoms and possible sex or age differences.
15 of anxiety disorders, this study identified age differences.
16 dative peak velocities showed no significant age differences.
17 source of dysregulated Ca2+ should eliminate aging differences.
18 --but does this approach capture even coarse age differences?
19 Daughters of tea consumers had a later mean age (difference = 0.41 years at >/= 3 cups (0.7 liter)/d
20 [95% CI, -39.53 to 14.24] g) and gestational age (difference, -0.09 [95% CI, -0.16 to -0.03] weeks),
21 males and four females in each group; median age difference: 1 year; age range: 29-63 for patients an
22 n the overall AMD cohort after adjusting for age (difference, -19.9% [95% CI, -25.6% to -12.7%], P <
23 min D deficiency was associated with younger age (difference, -5.0; 95% CI, -7.2 to -2.8), Black race
24 CT cohort; P = .06) did not differ in either age (difference, 69.20 years; 95% CI, 62.84-72.07 years;
25 and five (8.3%) were aged 41-49 years: mean age difference 8.7 years (95% CI 6.8-10.6; p<0.0001).
26 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(
28 a (weighted odds ratio [OR], 1.95 per 5-year age difference; 95%, CI, 1.77-2.14) and MCI (OR, 1.17 pe
30 roductivity and NIH funding not explained by age differences alone warrant additional investigation.
31 two experiments, one in which we manipulated age differences among nestlings within broods, and anoth
36 n but more salient during mental replay, and age differences at perception could not account for olde
37 our study uncovers hitherto unknown sex and age differences at the level of proteins and protein net
42 tionwide Inpatient Sample, we calculated the age difference between patients with SLE and their race-
43 rther supported independently by the stellar age difference between quiescent and star-forming galaxi
44 antibody response were older age (mean [SE] age difference between responders and nonresponders, 3.9
45 s were found to only be significant when the age difference between siblings was less than 2 years.
46 ease, allowing the alignment of the ~30-year age difference between the cohorts on a clinically meani
47 provides further protection according to the age difference between the index child and the sibling.
54 Mother-daughter pairs and pairs with large age differences between members interacted and associate
56 cial effect of smoking on outcomes is due to age differences between smokers and non-smokers and is t
58 characteristics (accuracy 69%) but not when age differences between the groups were taken into accou
62 uration (height, weight, body mass index for age, difference between current and expected adult heigh
64 Here, we evaluated whether brain-predicted age difference (brain-PAD) was sensitive to the presence
66 the model, we calculated the brain-predicted age difference (brain-PAD: predicted age-chronological a
70 ated at a whole brain level as the predicted age difference defined using T1-weighted images, and at
71 statistically insignificant, confirming that age differences did not influence the observed refractiv
72 contextualizes prior findings that regional age differences do progress along an S-A axis at a group
73 ut recipient age, donor age, recipient-donor age difference, donor gender, donor type, or cold ischem
74 ings with the 56 women aged 25-40 years, the age difference dropped to 1.1 years (95% CI -0.6 to 2.8;
76 ion in ventral visual cortex, whether or not age differences exist at the item level was a matter of
79 DA, PFNA) were observed, showing larger mean age differences for the combined puberty indicator in th
82 Conclusions were identical if we examined a) age difference from one's own age, and b) a dataset limi
83 life, which resulted in a 2.98-cm height-for-age difference (HAD) between sexes in the village and a
84 site for AL scoring incorporating gender and age differences, high quartile approach, clinical refere
85 ld BMI emerged from age 4 and increased with age (difference in BMI z score comparing low with high e
86 U, with the most marked difference at 1 y of age (difference in means -0.71 kg/m(2), 95% confidence i
88 e breastfed group during FU from 1 to 5 y of age (differences in means from 0.59 to 0.96 kg/m(2), res
89 ationships among dyads were common (>=5-year age difference in 67% of dyads), including 3/6 dyads inv
90 nt work has suggested that one cause of this age difference in exploration is a reduction in the exte
98 dult and pubertal mice were pair-housed, the age differences in both peripheral cytokine concentratio
99 present findings support the hypothesis that age differences in brain signal variability reflect agin
100 number of CRH-BP positive fibers revealed no age differences in CeA; however, with regards to CRH-pos
101 nths) demonstrated statistically significant age differences in cerebellum-dependent delay eyeblink c
102 , 50-64, and 65-75 years) and assess whether age differences in chemotherapy matched survival gains a
106 rences in EaI/E(LV)I during exercise, due to age differences in EaI, E(LV)I, or both, may help to exp
111 This cross-sectional study examined whether age differences in frontostriatal white matter integrity
113 lated to general task demands and to examine age differences in functional connectivity both within a
117 ward-guided behavioral model that quantifies age differences in impulsive actions in adult and adoles
120 be performed within the focus of attention, age differences in interference control may be more easi
125 creased gray matter volume in these regions, age differences in motor distinctiveness remained signif
127 ght pattern similarity analyses to elucidate age differences in neural distinctiveness at both catego
136 cline, we used functional MRI to investigate age differences in PFC activity during separate WM task
137 ondom during sex were associated with larger age differences in relationships of both men and women.
138 se "compensatory" activations simply reflect age differences in response to experimental task demands
139 tal white matter integrity could account for age differences in reward learning in a community life s
141 While this identifies a substrate underlying age differences in social drive, we then determined that
144 Of greater significance, however, are the age differences in the different conditioning paradigms.
145 captured by this pattern is associated with age differences in the differential encoding of unique m
146 ated the contributions of brain structure to age differences in the distinctiveness of motor represen
147 dhood along with more subtle region-specific age differences in the effects of task switching on rule
148 orcement learning work that has investigated age differences in the effects of uncertainty and sugges
149 11-30 years, to allow for the exploration of age differences in the impact of online social evaluativ
150 dy assessed the neural mechanisms underlying age differences in the integration of auditory and visua
151 nces in GABAergic regulation of the LAT, and age differences in the mechanism for the effects of repe
153 nation across age groups, with evidence that age differences in the nature of representations emerges
156 gue-mimicking condition, potentially masking age differences in the sensitivity of the cross-bridge t
157 ts, the present study measured the extent of age differences in the specificity of memory representat
160 e using neuroimaging methodology, identified age differences in trust and their neural underpinnings.
163 f this study were to characterize the normal age differences in white matter integrity in several bra
165 properties, inter-animal variability, animal age, differences in spike timing between the synaptic re
166 ducted in separate cohorts, models examining age-differences in association, and in RQR models examin
167 eal that the OFC-DMS pathway is critical for age-differences in reward-guided impulsive actions and p
172 ity increased with age, and the magnitude of age differences increased beginning with the middle of t
173 treatment strategies rarely consider patient age differences, leading to variable therapeutic efficac
174 the shift to reproductive status rather than age differences matched the pattern of changes in olfact
177 large interjurisdictional variation in this age difference (odds ratio 0.05; 95% PI 0.01 to 0.19).
178 antial interjurisdictional variation in this age difference (odds ratio [OR] 0.38; 95% PI 0.20-0.73).
179 5; P = .07), trisomy 8 (HR = 2.26; P = .02), age (difference of 10 years, HR = 1.46; P = .01), and th
180 rida couples were Hispanic; there was a mean age difference of 18 years between perpetrators and vict
181 6.1 +/- 11.1 and 36.7 +/- 12.3 years, a mean age difference of 19.3 +/- 5.2 years (P < .0001); accele
182 nd that among children in the same grade, an age difference of a few months was associated with the f
184 ions, but previous studies mostly focused on age differences of categorical information representatio
186 k was used to integrate 44 studies reporting age differences or changes in coping from infancy throug
187 timated to be "older," with a mean predicted age difference (PAD) between chronological and estimated
188 of cognitive reserve and the predicted brain age difference (PAD) on the risk of being diagnosed with
189 msTBI) is associated with a higher predicted age difference (PAD), but the progression of PAD over ti
194 sults are often confounded by small numbers, age differences, severity of symptoms, comorbidity, use
197 of unconnected folds associated with higher age differences than bridged folds, but this difference
198 These findings suggest that, despite the age difference, the clinical phenotype of BP is not affe
203 To understand the etiology of biological age differences, we also examined DNA methylation predic
206 treatment RESULTS: No clinical parameters or age differences were found between males and females, al
212 ger compared to younger participants, but no age differences were seen in brain responses to emotiona
217 ncrease in male participant age, the average age difference with their partners increased by 0.26 yea
219 ulation, reaching almost 26%; (2) gender and age differences, with the largest prevalence of isolatio
220 This study was successful in determining age differences within the empty cases, which to date, h