ライフサイエンスコーパス: growth rate

1 osomes, at the expense of lower steady-state growth rate.

2 follow-up echocardiography to assess aortic growth rate.

3 ult in a reduced standard metabolic rate and growth rate.

4 e of assembly negatively impacts the network growth rate.

5 re still inherently limited by the bacterial growth rate.

6 mited advantages for maximizing steady-state growth rate.

7 rent degradation is slower than the cellular growth rate.

8 id at baseline were associated with a higher growth rate.

9 aling strongly influences both cell size and growth rate.

10 t permits time-varying carrying capacity and growth rate.

11 breeding and wintering grounds on population growth rate.

12 The analysis revealed a bimodal growth rate.

13 ncentration could be correlated with crystal growth rate.

14 Geographic atrophy incidence and growth rate.

15 lytic efficiency had little if any effect on growth rate.

16 tio and pH were found to affect the particle growth rate.

17 iances along the apical-to-basal gradient in growth rate.

18 of prey type on standard metabolic rate and growth rate.

19 asymptotic limit determined by the wild pool growth rate.

20 heir yeast orthologs with minimal effects on growth rate.

21 aves of the rosette and correlated with leaf growth rate.

22 thway changes, including an 80% reduction in growth rate.

23 bserved wall stress relaxation and expansive growth rate.

24 sponse to nutrient availability and cellular growth rate.

25 the importance of high potential population growth rate.

26 es where we could precisely control the cell growth-rate.

27 for the maintenance of genetic diversity on growth rates.

28 cing daughter cells with different sizes and growth rates.

29 ced responsiveness to estradiol, and reduced growth rates.

30 inetics, diffusion could support normal cell growth rates.

31 "year effects" strongly influence population growth rates.

32 Cells grown on urea showed the highest growth rates.

33 and monomer proteins consistently decreased growth rates.

34 es at division, and fluctuations in cellular growth rates.

35 y culture conditions that support suboptimal growth rates.

36 le differences among genotypes in population growth rates.

37 candidate significantly enhanced VZV plaque growth rates.

38 ing discussion of how to measure and compare growth rates.

39 reas others (E46K, A30P, and G51D) decreased growth rates.

40 ific to germination and only weakly affected growth rates.

41 st of the evolutionary changes in population growth rates.

42 s (DP=22n -1) with significantly accelerated growth rates.

43 hunting has led to high wild boar population growth rates.

44 c strategies (LDM) for tumors with different growth rates.

45 roteins and chaperones measured at different growth rates.

46 ter-taxa interaction strengths and intrinsic growth rates.

47 he main factor contributing to the divergent growth rates.

48 fibril accumulation through increased fibril growth rates.

49 th weight of 1200 g, who achieved near-fetal growth rates.

50 n of deterministic and stochastic population growth rates.

51 lability, which is consistent with increased growth rates.

52 than eyes treated with bevacizumab (adjusted growth rate, 0.38 vs. 0.28 mm/year; P = 0.009).

53 ity, it exhibited smaller plaques, a reduced growth rate, a change in monoclonal antibody footprint,

54 predicted growth rates that are higher than growth rates achieved by only considering exchange of me

55 the need to impose a time-averaged constant growth rate across all members for a community to ensure

56 y in cell division placement and exponential growth rate across individual cells in a population rela

57 However, similar population growth rates across generations suggest that different l

58 However, correlations in the per capita growth rate affected productivity only shortly following

59 Increasing Gross Domestic Product (GDP) growth rates alone cannot restore absolute mobility to t

60 ly identified as having the fastest measured growth rate among cyanobacteria.

61 e making sensitive genome-wide fitness (i.e. growth rate) analysis available for most transposons and

62 n tubes grown in vitro exhibited an enhanced growth rate and a decreased thickness of the tip cell wa

63 nstrates that fatty-acid availability limits growth rate and cell envelope capacity, revealing that f

64 Together, the data suggest a model in which growth rate and cell size are mechanistically linked by

65 We found that ATP supported a similar growth rate and cell yield as L1 medium and observed DIP

66 commissural axons are seen to decrease their growth rate and cones increase in size.

67 y demographic properties, such as population growth rate and demographic resilience, but also has imp

68 s size phenotype is associated with a faster growth rate and larger cell size and is not simply due t

69 wo distinct steps due to alterations in both growth rate and lifetime.

70 ness of cultured tumor cells, as well as the growth rate and metastatic efficiency of xenografted tum

71 -AS from the leaf surface increased M. sexta growth rate and plant fungal susceptibility.

72 he assayed species showed differences in the growth rate and produced mycelia, which should be consid

73 R037 and MDR045, colonisation also increased growth rate and reproductive success of S. avenae on the

74 rmation also coincides with the reduction in growth rate and termination of cell division of the unde

75 nsects, body size variation is determined by growth rate and the mechanisms that stop growth at the e

76 factors responsible for the decrease in the growth rate and the onset of the stationary phase.

77 icals, thereby strongly influencing particle growth rate and the resulting particle morphology.

78 s an explicit relationship between expansive growth rate and the wall's mechanical properties.

79 geneous across the brain but the exponential growth rate and time of half maximal Abeta concentration

80 Tumor growth rate and uptake varied among the different PDXs a

81 -450 degrees C within a restricted domain of growth rate and V/III flux ratio.

82 ther USPIO-enhanced MRI can predict aneurysm growth rates and clinical outcomes.

83 rapeutic schedules for tumors with different growth rates and develops quantitative tools to optimize

84 For both species, potential mean annual growth rates and duration of bloom seasons significantly

85 been significant increases in the potential growth rates and duration of these HAB events.

86 r incorporating experimental measurements of growth rates and extracellular fluxes from a set of pert

87 oth the inhibitors significantly reduced the growth rates and final virus yields of viruses without i

88 However, the growth rates and glucose uptake rates of the mutant WX-z

89 d how climatic variation affected population growth rates and how these relationships varied with res

90 d concurrently, at three to six times higher growth rates and independently of said receptors.

91 trength of evidence was very low quality for growth rates and low quality for rupture rates.

92 d map for halophyte growers to attain better growth rates and nutritional value of Salicornia and Sar

93 hese synergistic effects for controlling the growth rates and particle morphologies at the nanoscale.

94 ymbionts that can increase or decrease aphid growth rates and reproduction, but the reason by which t

95 they find that any amount of mixture propels growth rates and spread of introduced populations.

96 Growth rates and steady-state cell concentrations decrea

97 ayers destabilize archaeal chromatin, reduce growth rate, and impair transcription regulation, confir

98 m in the context of its population dynamics, growth rate, and light adaptation, and the size and macr

99 er-population differences in effective size, growth rate, and timing or amount of gene flow.

100 egions where seasonal conditions permit high growth rates, and only a few areas around the Scotia Sea

101 gy budget; thus, standard metabolic rate and growth rate are two measures frequently used as an indic

102 esults in spurious negative growth trends if growth rates are calculated in fixed size classes, as 'f

103 Expansive growth rates are calculated using the calculated Pi valu

104 mortality and the associated changes in tree growth rates are still limited.

105 Scenario modeling shows that, where growth rates are suppressed outside PAs, extinction rate

106 ifferent prey on standard metabolic rate and growth rate as well as the effects that early prey speci

107 ementation of cyanobacteria is their limited growth rates as compared to industrial mainstays.

108 DL female mice exhibit similar latencies and growth rates as Muc4(wt)/NDL animals.

109 information allows estimation of population growth rate, as well as projection of future population

110 removal, total nitrogen removal, and biomass growth rates at each scale were statistically different.

111 Low growth rates at high elevations appear primarily driven

112 ing mechanisms of population persistence and growth rates at range edges.

113 of the between-year variation in population growth rate, because it strongly influenced reproductive

114 g 36 species), and compared early and recent growth rates between trees that died and those that surv

115 dilution of Lac enzymes due to an increased growth rate beyond the saturation point.

116 s, we evaluated covariates that could affect growth rates; body size, diet, and year have significant

117 High salinity inhibited the cell growth rate but increased the viability and bacterial me

118 and wild-type E. faecalis results in reduced growth rate but provides resistance to a key immune defe

119 rsely proportional to the variation in their growth rates but increases with the frequency and severi

120 reparatory response, observed for decreasing growth rates, but with limited advantages for maximizing

121 hat would otherwise have an average negative growth rate by increasing the duration of favorable envi

122 in homologs all directly enhance microtubule growth rate by several-fold in vitro.

123 volution (ALE), the knockouts increase their growth rate by up to 3.6-fold.

124 TraDis, HiTS, IN-Seq) and includes fitness (growth rate) calculations, sliding window analysis, bott

125 crease-or alternatively the total population growth rate can decrease.

126 sed expression of mcr-1 results in decreased growth rate, cell viability, competitive ability and sig

127 to occur, and (ii) poorly constrained zircon growth rates combined with the assumption of continuous

128 ty of the whole NRs exhibiting a 4.2% higher growth rate compared with lands not declared as NRs over

129 that a trade-off between swimming speed and growth rate constrains the evolution of faster migration

130 We assembled growth rate data from throughout the West Atlantic for g

131 DeltakhpA mutations reduce growth rate, decrease cell size, minimally affect shape

132 Further, this fraction increases as growth rate decreases and these excess ribosomal protein

133 or the origin of overflow metabolism and the growth rate dependence of fermentation and respiration,

134 rbation, (iii) how this balancing determines growth rate dependence on temperature and is achieved th

135 They also demonstrate that this growth-rate dependent control occurs through the express

136 Organs are made from cells whose individual growth rates differ, yet the final shape of organs is hi

137 ghtforward mechanism of generating sustained growth rate differences at subinhibitory antibiotic conc

138 y aspects of global shape depend on regional growth rate differences generated by the coordinated act

139 are still necessary to recover the observed growth rate distribution in SD medium.

140 omics constraints necessary to reproduce the growth rate distributions seen experimentally.

141 pecified isotropic growth, can reproduce the growth rate distributions that generate thallus shape gi

142 s did not propagate to affect the population growth rate due to the small effect of body mass on vita

143 bolic and physiological analyses showed that growth rates during log phase were not controlled primar

144 nts grown under fluctuating light had a slow growth rate early in development, likely due to the fact

145 characterized for their optical properties, growth rate, elemental composition, iron content, and ox

146 found to be well represented by those in the growth rate estimated by the BJ index.

147 Population growth rate, estimated from a Leslie-Lefkovitch stage-cl

148 higher dispersal ability and lower intrinsic growth rates evolve at the expansion edge compared with

149 nd easily measured experimental data such as growth rates, extracellular fluxes, transcriptomics and

150 We measured traits such as leaf area, growth rate, flowering time, main stem branching, rosett

151 nalysis tools which accurately calculate the growth rate for each disrupted gene in the genome to ena

152 is characteristic of nucleation and particle growth; rates for these processes followed expected depe

153 and the environmental variance in population growth rate, [Formula: see text] Allowing these paramete

154 a turtle hatchlings to elevate metabolic and growth rates - had evolved 54 million years ago.

155 Our work shows that growth rate heterogeneity is the primary shape determina

156 , was the most critical stage for population growth rate; however, the survival of younger crocodiles

157 sphorus content for the rapid growth in the "growth rate hypothesis" may underline its potential role

158 volumes that will give rise to rapid plaque growth rates if left untreated.

159 ined methods in the prediction of infarction growth rate (IGR) with reasonable accuracy, over wide ti

160 antly decreases disease penetrance and tumor growth rate in a MYCN-driven transgenic zebrafish model

161 undity has very limited impact on population growth rate in American crocodiles.

162 o events contributed to a lower decadal mean growth rate in atmospheric CH4 concentrations throughout

163 tween baseline T/E ratio and aortic diameter growth rate in BAVnon-dil patients (r=0.66, P<0.001).

164 positive influence of some mutations on the growth rate in contrast to their in vitro action, reflec

165 PRMT5 decreased intracranial tumour size and growth rate in mice implanted with both primary tumour-d

166 ind that it is possible to detect changes in growth rate in response to each of nine antibiotics that

167 We demonstrate that wave growth rate in shallow estuaries is a function of wind f

168 By contrast, loss of Pten or Nf1 increases growth rate in vivo, and reduces survival following cisp

169 ism in the presence of oxygen occurs at fast growth rates in a wide range of organisms including bact

170 owever, for all conditions tested, the daily growth rates in batch cultures decreased steadily over t

171 ctor responsible for the gradual decrease of growth rates in batch cultures during log phase, culmina

172 S-linked PFN1 mutants, increased microtubule growth rates in cells.

173 s and pathways, we have measured competitive growth rates in mice of 2,578 barcoded Plasmodium berghe

174 genus Ulva increase their photosynthesis and growth rates in response to elevated pCO2 the most, wher

175 climate processes did not affect population growth rates in the predicted direction based on range p

176 es and compares nitrogen removal and biomass growth rates in treatment systems that utilize an algae-

177 mbers of mutations correlated with increased growth rates in vitro, indicating that the viruses evolv

178 th, this decreases with declining increasing growth rates, in favour of a higher elasticity of the ju

179 The oxide growth rate initiated rapidly, with rates comparable to

180 ding demographic model to project population growth rates into the next century.

181 in plant longevity, reproductive output and growth rate is fundamental to effective predictions of v

182 The lateral ordering improves as the growth rate is increased and can be explained by more sp

183 bacterial growth in many environments where growth rate is limited by the availability of nutrients.

184 ore tenet of this hypothesis-that population growth rate is more strongly affected by species interac

185 orldwide - as measured by in situ population growth rate, its temporal variation and extinction risk

186 rovide justification for our use of absolute growth rate, justification for not using instantaneous g

187 g demographic rates contribute to population growth rate (lambda) is key to understanding how animal

188 ons of estimates of deterministic population growth rate, lambda, and demographic variance, sigmad2,

189 estimates of both the low-density intrinsic growth rate, lambda, and the carrying capacity density,

190 Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative.

191 opulations to simulate stochastic population growth rates (log lambdas ) under different temporal aut

192 sh maintaining a standard metabolic rate and growth rate lower than expected when fed on a diet diffe

193 medium, the calculated broad distribution of growth rates matches experimental observations from sing

194 ws governing cell size and its dependence on growth rate may arise as byproducts of a regulatory mech

195 ical cases will likely match this population growth rate meaning there will be many more surgeons tra

196 e adjustments under the repealed Substantial Growth Rate model.

197 irometric assays, estimated maximum specific growth rate (mumax), nitrite half saturation coefficient

198 Hindlimb weight, linear growth rate, muscle protein accretion rate and fractiona

199 stage-class model, showed a positive annual growth rate of 4% over the study period.

200 Here we quantify the growth rate of a Martian volcano by (40)Ar/(39)Ar and co

201 Of 26 studies, 5, 10, and 8 described the growth rate of aneurysms 3 mm and smaller, 5 mm and smal

202 Large interannual variations in the measured growth rate of atmospheric carbon dioxide (CO2) originat

203 ow precipitation over the tropics, while the growth rate of atmospheric carbon dioxide (CO2) was the

204 Although correlations between the growth rate of atmospheric CO2 concentrations and the El

205 To estimate the incidence, size, and growth rate of geographic atrophy (GA) during 5 years of

206 The relative growth rate of HDPCs of modified groups were higher than

207 onstrate that profilin directly enhances the growth rate of microtubules.

208 er with 30 mL L(-1) (3%) CO2 accelerated the growth rate of the control strain (CS) 4-fold, whereas D

209 tive for aminoacylation quality control, the growth rate of the ileS(T233P) strain was not significan

210 While the growth rate of the mmpL11 mutant is similar to that of w

211 hat higher temperatures increase the natural growth rate of the population as more females are produc

212 temperatures near lethal levels, the natural growth rate of the population decreases and the long-ter

213 ons is studied based on the energy dependent growth rate of the track diameter to understand the intr

214 with canopy and root growth rates the woody growth rate of these forests is a poor proxy for their o

215 ative information on the number, volume, and growth rate of voids, and the EM parameter of DZ*.

216 hat the Pi parameter is central to expansive growth rate of walled cells.

217 eomagnetic Polarity Time Scale 2012, implies growth rates of 4.82 mm/Ma, 4.95 mm/Ma, 4.48 mm/Ma and 1

218 st time, we provide experimental evidence of growth rates of Ag nanoparticles in the presence of Pt i

219 Annual growth rates of all species were highest at Lizard Islan

220 n a marine assemblage, with near doubling of growth rates of Antarctic seabed life.

221 The growth rates of bacteria must be coordinated with major

222 ted tumor-initiating frequencies, as well as growth rates of BCSC-derived tumor xenografts in immunod

223 xposed to 0, 0.2, or 1 Gy of X-rays, and the growth rates of cell populations were assessed by measur

224 f water limitation, we observed intra-annual growth rates of four conifer species using point dendrom

225 Elevated pCO2 significantly increased the growth rates of Gracilaria and Ulva and yielded signific

226 strong correlations between annualized mean growth rates of green turtles and both sea surface tempe

227 The growth rates of influenza at postal area level were rela

228 e multiplicative, as in returns on assets or growth rates of populations.

229 ther variability and seasonal influenza, and growth rates of seasonal influenza epidemics among diffe

230 nts of CO2 uptake resulted in a ratio of the growth rates of Synechococcus 2973 to Synechococcus 7942

231 oncentration of 10 mug/ml did not affect the growth rates of these two strains, nor did we observe th

232 rds (1982 to 2016) and temperature-dependent growth rates of two algae that produce potent biotoxins,

233 n that flagellar assembly is affected by the growth-rate of the cell.

234 e that motility is intimately coupled to the growth-rate of the cell.

235 els, and low early reproductive rates, group growth rates, offspring mass and offspring eclosion succ

236 Here, we investigated the effect of growth rate on flagellar assembly in Escherichia coli us

237 ulation of respiratory pathways and enhanced growth rates on glycolytic substrates of E. coli, coinci

238 tion so as to maximize its own instantaneous growth rate, only to achieve a lower final growth rate t

239 ons between resource preferences and maximal growth rate or biomass composition.

240 der such conditions, no effect on organismal growth rate or loss of the reddish colony phenotype due

241 No significant difference in growth rate or maximum size of the bubbles was measured

242 cannot make ceramides fail to modulate their growth rate or size in response to changes in nutrients.

243 e, justification for not using instantaneous growth rate (or a measure of growth in proportion to pre

244 f context-dependent fluctuating selection on growth rates over time in a long-lived species.

245 The elevated growth rates parallel increases in circulating CD71-posi

246 in the West Atlantic for years of declining growth rates (r = -.94) and the Multivariate ENSO Index

247 2.03, which nearly recapitulates the in vivo growth rate ratio of 2.13.

248 nged duration of growth also compensates for growth rate reduction caused by abiotic stresses.

249 H2 inhibition with a concomitant increase in growth rate relative to cells without FHL.

250 By averaging the growth rate response to an antibiotic over many individu

251 common phenotypic changes including delayed growth rate, retarded swarming motility, and pyocyanin o

252 ometry and associated explanatory variables (growth rate, RNA:DNA, and energy storage molecules).

253 teria to vertebrates, is proportional to the growth rate set by nutrient availability, but the underl

254 risk factors were used to estimate adjusted growth rates, standard errors (SEs), and 95% confidence

255 ta-exhibited similar significant declines in growth rates starting in 1997 in the West Atlantic, base

256 CHIR99021 reduced the growth rate, stem/progenitor cell marker content and clo

257 rlier compared to slow growers and thus fast growth rates tend to have earlier calendar dates.

258 t 2 years of the clinical trial had a higher growth rate than eyes treated with bevacizumab (adjusted

259 s growth rate, only to achieve a lower final growth rate than had it not manipulated.

260 ewborn care, had larger health care spending growth rates than other conditions.

261 ve high rates of minorities and high natural growth rates than would be expected by chance (p = 0.074

262 otypes give rise to an evolutionarily stable growth rate that stands in stark contrast with that obse

263 f exchange metabolites resulted in predicted growth rates that are higher than growth rates achieved

264 live under strong energy limitation and have growth rates that are orders of magnitude slower than la

265 opulation studies can obscure low population growth rates that should cause management concern.

266 find that (iv) compared with canopy and root growth rates the woody growth rate of these forests is a

267 on, we estimated asymptotic growth, relative growth rate, the timing of inflection point and duration

268 n is thought to contribute to their elevated growth rate through their activation of the mitogen-acti

269 ween individuals can contribute to improving growth rates through more efficient breeding schemes.

270 and here we use an empirical relationship of growth rate to assess seasonal spatial variability.

271 The predicted growth rate under nitrogen-replete and -deplete conditio

272 associated with warming by 1 degrees C, with growth rates up to doubled in some species.

273 ancer model, we have observed a reduction in growth rate upon withdrawal of folate.

274 . jejuni physiology were studied at constant growth rate using carbon (serine)-limited continuous che

275 crofluidic chip and monitor their individual growth rates using microscopy.

276 s (QDs) has been quantified as a function of growth rate, using the Hopkins-Skellam index (HSI).

277 study finds that, in an ancient land plant, growth rate variation patterned by meristematic cells pr

278 alls along the elongation zone, but plots of growth rate versus wall compliances were strikingly nonl

279 e show that nutrients modulate cell size and growth rate via the TORC2 signaling network in budding y

280 The overall GA growth rate was 0.33 mm/year (SE, 0.02 mm/year).

281 74-cells, and their overall intramacrophagic growth rate was comparable to that of B. inopinata BO1 a

282 The annualized growth rate was less than 3% in all but 1 study for all

283 tes from a Martian volcano and find that its growth rate was much slower than analogous volcanoes on

284 We found that growth rate was not altered by exposure of P. gingivalis

285 ecause only one gene was mutated and because growth rate was unaffected, thereby allowing us to query

286 ynamics influence the evolution of bacterial growth rates, we couple a model of flow-biofilm interact

287 m to conclude that our observed increases in growth rate were in fact much lower and in accordance wi

288 set of mice in which subject-specific tumor growth rates were accurately predicted.

289 These growth rates were correlated with OCTA morphologic featu

290 Despite this, stem growth rates were similar to today.

291 coexistence theory, we developed a metric of growth rate when rare, Deltari , to identify and quantif

292 ate that flagellar abundance correlates with growth rate, where faster growing cells produce more fla

293 tions (i.e. H50Q and A53T) greatly increased growth rates, whereas others (E46K, A30P, and G51D) decr

294 is explored as a function of temperature and growth rate which provides the first detailed report of

295 a novel environment can increase population growth rates, which also promotes spread.

296 he graphitic substrates enable high nanowire growth rates, which is favourable for cost-effective dev

297 epopulation using the gradually accelerating growth rate with tumor shrinkage.

298 to an increase by 10 degrees C; doubling of growth rates with a 1 degrees C change gives Q10s around

299 Sensitivity analysis shows that growth rates within PAs have to be high if they are to c

300 ligomers with tailored structures and a high growth rate would greatly facilitate research into the s