ライフサイエンスコーパス: decline(s|d|ing) with

1 biquitination revealed KCNQ1 surface-density declined with a 3.5 hr t1/2 by impaired forward traffi

2 ing a Ca spark, which peaked at 8+/-3 pA and declined with a half time of 7+/-2 ms.

3 the noncaffeine end, [Ca(2+)](SR) gradually declined with a similar tau, until [Ca(2+)](SR) througho

4 uably rate-limiting enzyme of the TCA cycle, declines with AD, but the mechanism of inactivation and

5 al education and fair/poor self-rated health declined with advancing age (age 50-64 years: adjusted o

6 GABA levels more rapidly declined with advancing age in the schizophrenia compare

7 a-cells, which requires islet proliferation, declined with advancing age; however, mice lacking p16IN

8 ay to dietary protein (i.e., meal threshold) declines with advancing age or reduced physical activity

9 The efficiency of this process declines with advancing age, which may play a critical r

10 The efficacy of various transmitter systems declines with advancing age.

11 Episodic memory declines with advancing age.

12 ADCC activity declines with advancing infection, and yet the underlyin

13 ted eggs to activate following fertilisation declines with advancing maternal age.

14 The prevalence of sexual activity declined with age (73% among respondents who were 57 to

15 ize and survival improved with body mass and declined with age (c. 4-5 years).

16 The scale-invariant correlations at 1.5-8 h declined with age (P = 0.01) and were significantly redu

17 AD67- and somatostatin-positive interneurons declined with age across multiple fields of the hippocam

18 lence of 14 high-risk HPV genotypes (HR-HPV) declined with age among women with <5 lifetime sex partn

19 of a breast cancer diagnosis with mortality declined with age among women with advanced disease [cor

20 eric preparations of Abeta1-42 in particular declined with age and advancing AD.

21 r SCs converted into HCs, but such responses declined with age and ceased by P16.

22 Use of adjuvant therapy declined with age and comorbidity.

23 ough the percentage of CD56(bright) NK cells declined with age and the percentage of CD56(dim) NK cel

24 h of the association per 20 mm Hg higher SBP declined with age and with increasing body mass index.

25 Both global mean BMO-MRW and RNFLT declined with age at a rate of -1.34 mum/year and -0.21

26 the NADH regenerating capacity continuously declined with age beginning at 2 months.

27 However, growth rates declined with age for whites but not for blacks (P = 0.0

28 The number of yawns observed declined with age from 28 weeks gestation, whereas simpl

29 In bone marrow MSCs, FOXP1 expression levels declined with age in an inverse manner with those of the

30 f NK cells responding to exogenous cytokines declined with age in line with a decreased proportion of

31 Volumes of these subregions declined with age in the TS group but not in controls, s

32 NKG2A expression declined with age on both NK cells and T cells.

33 gnitude of the acute T cell response to LCMV declined with age though this age-dependent decline was

34 ger ages (20.9% of those aged <30 years) and declined with age to 3.6% among women aged 60 years or m

35 HIV-positive women aged 25-34 years and then declined with age to 37.5% in those >or=55 years old (Pt

36 Cognitive performance declined with age, and more rapidly with increasing age,

37 Strike selectivity declined with age, and no selectivity was observed after

38 Expression of endoglin in NCSCs declined with age, coinciding with a reduction in both s

39 Binocular summation of contrast signals declined with age, independent of interocular difference

40 ll, transitions between both breeding states declined with age, suggesting that males that breed tend

41 For all risk factors, proportional effects declined with age, were generally consistent by sex, and

42 Performance on all cognitive measures declined with age, with the most rapid rate of change po

43 CVHS was low at baseline and declined with age.

44 cohort was higher for women than for men and declined with age.

45 2-mediated expression of p27(Kip1) gradually declined with age.

46 eatment with the GLP-1 analog exendin-4 also declined with age.

47 proportion of high to low sensitivity efflux declined with age.

48 rrelations showed that all cognitive domains declined with age.

49 had a transient calbindin-expression, which declined with age.

50 Moreover, pupillary reward sensitivity declined with age.

51 t a Pavlovian attraction to potential reward declined with age.

52 A(A) alpha3 was relatively high at birth but declined with age; and (3) GABA(A) alpha2 remained relat

53 DNA repair declines with age and correlates with longevity in many

54 Notably, nuclear YAP progressively declines with age and correlates with proliferative pote

55 Immune function declines with age and has been associated with reduced v

56 Understanding why BubR1 declines with age and how to slow this process is theref

57 Exercise capacity declines with age and improves with exercise training.

58 nse breast tissue area to total breast area, declines with age and is a strong risk factor for breast

59 We found that FGF21 expression in thymus declines with age and is induced by CR.

60 and the capacity of beta-cells to regenerate declines with age and is regulated by the Bmi1/p16(Ink4a

61 dentate gyrus (DG) throughout adulthood but declines with age and stress.

62 Episodic memory (EM) declines with age and the rate of decline is variable ac

63 ent peptic ulcer bleeding, although the risk declines with age because of death being the competing c

64 Bone mass declines with age but the mechanisms responsible remain

65 ir is essential for life, yet its efficiency declines with age for reasons that are unclear.

66 ge, and endothelium-dependent vasodilatation declines with age in coronary resistance arterioles.

67 e response to vaccines and infectious agents declines with age in humans and animal models.

68 onal selection in germinal centers (GCs) and declines with age in mice and humans.

69 Consistent with this, stem cell function declines with age in numerous tissues as a result of gat

70 Immune responsiveness declines with age in part due to the development of CD8(

71 vo in the steady state, and their proportion declines with age in secondary lymphoid organs.

72 There are declines with age in speed of processing, working memory

73 arget of rapamycin (mTOR) complex 2 (mTORC2) declines with age in the brain of both fruit flies and r

74 Tissue homeostasis declines with age partly because stem/progenitor cells f

75 scovered that the function of the MOC system declines with age prior to OHC degeneration, as measured

76 re, only the two tasks that show performance declines with age show age-related decreases in task-pos

77 ak postnatal proliferation but progressively declines with age thereafter.

78 However, HSF1 activity declines with age, a change that may open the door to pr

79 cell replication in juvenile mice and humans declines with age, and elucidating the basis for this de

80 B lymphopoiesis declines with age, and in rabbits this occurs by 8 wk of

81 Cardiorespiratory fitness also declines with age, and the independent and linked associ

82 Spatial and episodic memory performance declines with age, and the neural basis for this decline

83 B lymphopoiesis declines with age, and this decline correlates with incr

84 he regenerative potential of skeletal muscle declines with age, and this impairment is associated wit

85 reperfusion, so eligibility for reperfusion declines with age, and yet elderly patients are less lik

86 Memory performance typically declines with age, as does cortical structural integrity

87 Heart function declines with age, but the genetic factors underlying su

88 Regeneration capacity declines with age, but why juvenile organisms show enhan

89 We show maximum velocity declines with age, correlates well with longevity, accur

90 Contrast sensitivity declines with age, high myopia, and astigmatism.

91 Skeletal muscle regenerative potential declines with age, in part due to deficiencies in reside

92 As the regular function of the thymus declines with age, it is of fundamental and clinical rel

93 Because the production of T cells declines with age, naive T cells must be long-lived.

94 The CD4:CD8 ratio of RTEs declines with age, partly because of a striking decrease

95 Self-renewal capacity declines with age, partly because of increasing expressi

96 Although LV filling reserve declines with age, relaxation reserve does not.

97 The hematopoietic system declines with age, resulting in decreased hematopoietic

98 Dopaminergic neuromodulation declines with age, suggesting that incentive processing

99 although the ability make optimal decisions declines with age, there is still much individual variab

100 e determined that the proportion of B1 cells declines with age, which may contribute to disease susce

101 function of adult tissue-specific stem cells declines with age, which may contribute to the physiolog

102 The ability of injured axons to regenerate declines with age, yet the mechanisms that regulate axon

103 tinuity between the proximal and distal ends declines with age.

104 Experience-dependent cortical plasticity declines with age.

105 ve capacity of the peripheral nervous system declines with age.

106 The regenerative capacity of skeletal muscle declines with age.

107 The hematopoietic system declines with age.

108 oduction from bone marrow in mice and humans declines with age.

109 1 as a circulating factor in young mice that declines with age.

110 uman immune system to respond to vaccination declines with age.

111 e rate at which leaf photosynthetic capacity declines with age.

112 t studies to date, however, suggest that PPI declines with age.

113 fetal neural stem cells but that expression declines with age.

114 ble for prevention of shingles, its efficacy declines with age.

115 bstrates by the hydrolysis of triglycerides, declines with age.

116 Pot1a is highly expressed in young HSCs, but declines with age.

117 T cell function declines with age.

118 on in various situations, and its expression declines with age.

119 ency of central nervous system remyelination declines with age.

120 well known that the peripheral visual system declines with age: the yellowing of the lens causes a se

121 defining the temporal patterns of functional declines with ageing, identifying the underlying mechani

122 ndrial respiration transiently increased and declined with aging along with higher muscle reactive ox

123 umbers and diversity of naive CD8(+) T cells declined with aging, surviving cells underwent faster ra

124 l tests [1, 2], and recall performance often declines with aging [3].

125 1b), a small protein that regulates calcium, declines with aging in the hippocampus, a brain region i

126 In humans, recognition memory declines with aging, and this impairment is characterize

127 Functional status declines with aging, thus impeding autonomy.

128 These results show that human islet function declines with aging, which can reduce insulin action and

129 Density normally declines with aging.

130 ssess an efficient ER adaptive response that declines with aging.

131 d in learning and memory throughout life but declines with aging.

132 re dose-proportional, increased rapidly, and declined with an apparent terminal half-life of 42 hours

133 year; 95% CI, -0.4 to 0.9), after which they declined with an EAPC of -3.07% per year (95% CI, -3.5 t

134 CI, 1.2 to 1.3), whereas the absolute rates declined with an estimated annual percentage change near

135 Antibody responses to tetanus declined with an estimated half-life of 14 years (95% co

136 onses to diphtheria were more long-lived and declined with an estimated half-life of 27 years (18-51

137 Dosage-balanced retention declines with antiquity of duplication: 24.1% of alpha-d

138 c-Kit expression declines with apparent migration, and CXCR4 expression d

139 The OR significantly declined with attained age for breast cancer overall (P

140 D-dimer declined with ATV/r and DRV/r and was unchanged with RAL

141 the 96 weeks of follow-up as follows: hsCRP declined with ATV/r and RAL, IL-6 declined only with RAL

142 B) leprosy, and the rate of positive results declined with bacterial burden.

143 elial cells, Suv39H1 and Suv39H2 mRNA levels declined with cAMP induction of SP-A.

144 ith apparent migration, and CXCR4 expression declines with canalization of new vessels.

145 hness of endemic savanna woody plant species declines with carbon storage both at the local scale, as

146 Telomere length in proliferative tissues declines with cell replication and the effect can be acc

147 en the associations were strong at birth but declined with child aging.

148 Bariatric surgery mortality has steadily declined with current rates of less than 0.5%.

149 on site footprint and thus distribution cost declines with decreasing permeability for a given reserv

150 apacity peaks just after summer solstice and declines with decreasing photoperiod, before air tempera

151 UES pressure progressively declined with deeper stages of sleep.

152 (3) Although UES pressure progressively declines with deeper stages of sleep, it can still refle

153 cordings and show that direction selectivity declines with depth in the SC.

154 eas the magnitude of the NMDAR-mediated EPSC declines with development and is associated with changes

155 ises prior to diagnosis of diabetes and then declines with diabetes duration.

156 tistical power to detect a recombination QTL declined with diminishing QTL effect, genome target size

157 The presence of early active plaques rapidly declined with disease duration.

158 on of neuron-specific endophilin-B1 isoforms declined with disease progression.

159 ude was initially constant and then steadily declined with distance from the soma.

160 014 were elevated near mining activities and declined with distance from the source region, whereas N

161 We also show that cross-shelf coral cover declines with distance from the coast (R(2) = 0.596).

162 is high, whereas the interregion similarity declines with distance.

163 mpeting species, species diversity generally declined with disturbance.

164 nd xylem to quantify how canopy water supply declines with drought and ceases by hydraulic failure.

165 nt examples of the same texture, performance declined with duration, a paradoxical result given that

166 The consistency of these declines with existing estimates of the relative risk of

167 s but that their contribution to performance declines with experience.

168 pected, we found that lifespan significantly declined with exposure to males.

169 asting or prolonged calorie restriction, and declined with feeding.

170 The SMR declined with follow-up but was still 3-fold higher than

171 However, fertility of P2rx2(-/-) males declines with frequent mating over days, suggesting that

172 r unique variants; (4) error rates generally declined with genotype quality (GQ) score, but in a nonl

173 R: 1.19; 95% CI: 1.15, 1.23; P < 0.0001) and declined with greater fruit intake (per pieces/d; RR: 0.

174 rginal increase in attractiveness eventually declined with greater penis size (i.e., quadratic select

175 to the age of the head of the household, but declined with gross annual income.

176 IIV recipients, explained in part by faster declines with higher peak postvaccination titer.

177 on index, beta-cell function relative to IS, declined with IL infusion in AA and C youth, with a sign

178 s before October 2007 (P=0.50 for trend) but declined with implementation of the bundle, from 1.64 in

179 Population growth rates declined with increased elevation and more modestly with

180 sample volume and treatment time, however it declined with increased gas flow.

181 risk of suicide for rural females aged >30 y declined with increased values of the drought index.

182 ion with which each orientation was recalled declined with increases in total memory load, but also d

183 known risk factors, endometrial cancer risk declined with increasing age at last birth (P(trend) < 0

184 were not affected by age in T1D subjects but declined with increasing age in control subjects.

185 Kaplan-Meier survival curves rapidly declined with increasing age in patients with BRAF V600E

186 R increased from ages 6 to 60 years and then declined with increasing age.

187 ARI frequency generally declined with increasing age.

188 Cone production has declined with increasing annual temperatures, and these

189 years, pH at a north-temperate coastal site declined with increasing atmospheric CO(2) levels and va

190 The strength of the association declined with increasing body mass index and age.

191 rate for which thresholds could be obtained declined with increasing carrier frequency for all liste

192 y and temporally: per capita predation rates declined with increasing cat density.

193 AIDS-related mortality declined with increasing CD4:CD8 ratio and decreasing CD

194 Outcome rates declined with increasing coffee intake: 11.1/100 person-

195 in (DM-MBP), the rate of folding in solution declined with increasing concentration, and the folding

196 In SNHs, densities of bumblebees declined with increasing cover of MFCs but densities of

197 e found that preference for the risky option declined with increasing delay between sequential choice

198 Similarly, densities of L. tumana declined with increasing distance from stream source.

199 to simulated control lesions (p = 0.002) and declined with increasing distance from the microbleed (p

200 t in the band adjacent to the ventricles and declined with increasing distance from the ventricles.

201 Crane vigilance declined with increasing distance from wildlife tourists

202 Air CO2 Enrichment site showing that the CFE declined with increasing drought stress.

203 effective population sizes and gene flow all declined with increasing elevation, resulting in substan

204 found that variance in reproductive success declined with increasing environmental quality (temporal

205 ial reef diving was high amongst novices and declined with increasing experience.

206 and resilience (return to prefire condition) declined with increasing fire severity.

207 Nectar production declined with increasing flower height on average, but t

208 The strength of the association declined with increasing follow-up time.

209 Microbial substrate use efficiency (SUE) declined with increasing incubation temperature in both,

210 Estimates of excess odds ratio per pack-year declined with increasing intensity, suggesting greater r

211 ll species were highest at Lizard Island and declined with increasing latitude, corresponding with di

212 Multidiversity declined with increasing LUI among grasslands, particula

213 at which the multidiversity of rare species declined with increasing LUI.

214 al scale, soil organic C concentrations also declined with increasing MAT and decreasing MAP.

215 Live-birth rates declined with increasing maternal age and increasing cyc

216 -8 levels in MDSCs of breast cancer patients declined with increasing MDSC frequency, implicating IRF

217 we found perennial grass cover in grasslands declined with increasing mean annual temperature in the

218 e adult survival was density independent but declined with increasing prevalence of diseased individu

219 We found that plant diversity significantly declined with increasing richness of introduced earthwor

220 ment T of 25 degrees C (Vcmax(25) ) linearly declined with increasing Tgrowth , linked to a concomita

221 reign-born population overall, TB case rates declined with increasing time since US entry, but remain

222 herapeutic efficacy of both (90)Y and (131)I declined with increasing tumor burden.

223 amin E supplement use (231 cases), ALS rates declined with increasing years of use (P-trend=0.01).

224 Ghrelin expression declines with increasing age in spleen and T cells and e

225 anisotropy of T2 also interacts with age and declines with increasing age.

226 In tissue in which (18)F-FDG uptake declines with increasing blood glucose, correction for b

227 traight forward, whereas heading sensitivity declines with increasing eccentricity of the reference d

228 ghly predictable, but predictability rapidly declines with increasing group size because of a lack of

229 nchrony; instead most focus on how synchrony declines with increasing linear distance between locatio

230 Growth sharply declines with increasing sea-ice blockage of light from

231 e revealed that the E/I ratio systematically declines with increasing stimulus contrast or size.

232 e with increasing TMP, and RSF substantially declines with increasing TMP.

233 Results suggest that foraging efficiency declines with increasing traffic noise levels due to aco

234 Cosegregation information also declines with increasing training data size, and its per

235 Weight loss in both groups generally declined with longer follow-up (12-24 months).

236 le distribution) with the endovascular group declined with longer time from symptom onset to arterial

237 rception of dust-borne P ("canopy trapping") declines with lower plant biomass and leaf area, limitin

238 KSHV DNA copy number in PBMC and in plasma declined with lymphoma-directed cytotoxic chemotherapy i

239 ctivation associated with reward expectation declined with more severe disease, whereas activation fo

240 as also only partial for the CNBH as flavans declined with nitrogen but saponins increased.

241 sodium balance, renin activity progressively declined with older age, whereas serum and urinary aldos

242 Furthermore, VOCC-mediated Ca(2+) influx declined with OPC differentiation, indicating that VOCCs

243 IgG(+) cells within viable progeny generally declined with PGE(2) supplementation.

244 We found that LD declined with physical distance approximately five times

245 ymic stromal cells and that their expression declines with physiological aging.

246 6% and 15% +/- 3% change, respectively), but declined with placebo (-5.0% +/- 6% and -2.0% +/- 3% cha

247 Since the anomalous current declines with postnatal age, PIEZO2 may contribute to ha

248 hypothesis that the sGC response to NO also declines with pressure-overload stress and assessed the

249 cury concentrations in clams and snails also declined with productivity, and consumer concentrations

250 Mst1 levels declined with progression from clinically localized to h

251 owing RA treatment, its expression gradually declined with prolonged RA treatment.

252 absent from bone marrow-derived macrophages, declines with prolonged culture of macrophages, and requ

253 mpared with healthy children, and the levels declined with remission-inducing therapy in the individu

254 multiple tests per building, concentrations declined with repeated measurements over time.

255 and overall group conflict deaths (G), have declined with respect to growing populations, implying t

256 Instead, abundances of all species declined with rising daily minimum temperatures, suggest

257 Preferential allocation declined with shading, as A. vineale allocated 25% of la

258 Pax3/7 progenitor cells, the extent of which declines with size and age.

259 FGFR2 (odds ratio [OR] = 2.1, P = 0.004) and declined with SNPs in EDN1 (OR = 0.5, P = 0.007).

260 0.005) and COL1A1 (OR = 2.1, P = 0.008) and declined with SNPs in TBX5 (OR = 0.5, P = 0.014).

261 ot toward everyone alike: generosity usually declines with social distance between individuals, a phe

262 The biodiversity surplus (extinction debt) declines with some delay through the process of relaxati

263 The relative abundance of T21 declined with storage time but differences were found as

264 ental lower-bound on recall precision, which declines with storage duration and number of stored item

265 hypothesis that contaminant bioaccumulation declines with stream primary production via the mechanis

266 e overall SHS exposure in nonsmoking workers declined with substantial drops in food preparation/serv

267 The model predicts that community similarity declines with terragenetic distance, and that local ende

268 ADCC activity declined with the 2-wk IgG half-life but was boosted at

269 ee reliance on mycorrhizae as tip production declined with the addition of nitrogen as has been shown

270 The incidence of PCME has declined with the advent of modern surgical techniques.

271 The average number of viral genomes declined with the age of the donor.

272 ear period with both belatacept regimens but declined with the cyclosporine regimen.

273 Visual sensitivity in the transition zone declined with the decrease in ONL thickness.

274 Shear force values were also declined with the increase of post-mortem aging showing

275 Following a meal, patients' CAP values declined with the peak value at 60 min, contrasting with

276 one concentrations (from 1489 fecal samples) declined with the ratio of elk to wolves.

277 C3a and the C3a/C3 ratio declined with the start of IA treatment, and this declin

278 rates at which specific antibiotics are used declines with the frequency of resistance to these drugs

279 common or very rare, and when female fitness declines with the number of other females choosing the s

280 tension than men, but this sexual dimorphism declines with the onset of menopause.

281 Retrieval speed from memory declines with the probed object's distance from the curr

282 our concern for the welfare of future people declines with their distance from us in time--are at the

283 we could account for 83% of the variation in declines with these two variables alone.

284 Emotional memories declined with time after ICU discharge, particularly pan

285 y of C-degradation microbial genes generally declined with time during the incubation in all treatmen

286 oncentrations of CVX-4164 determined in situ declined with time, with C(max) approximately 1 muM and

287 time, while INF-gamma single-positive cells declined with time.

288 sepsis, although its influence on mortality declined with time.

289 Diffusion capacity declines with time after exposure to pulmonary-toxic the

290 regenerate at early stages in a manner that declines with time.

291 ided into 2 groups: those in whom BDG levels declined with treatment and those in whom BDG remained e

292 injury, even though markers of inflammation declined with treatment.

293 the other, Queens (New York City), most taxa declined with warming, perhaps due to habitat loss that

294 because overwintering larvae, whose survival declined with warming, were disproportionately important

295 In addition, growth declines with warming above the temperature optima were

296 te models indicate that annual mean snowfall declines with warming in most regions but increases in r

297 Walking is decreased in obesity and declines with weight gain.

298 evated influenza-associated mortality, which declines with widespread HAART introduction but does not

299 RV strain declined with worse functional class, shorter 6-minute w

300 As expected, preference values declined with worsening visual function.