ライフサイエンスコーパス: assimilation

1 ver, hormones affect also sulfate uptake and assimilation.

2 ty offers an example of Waddington's genetic assimilation.

3 olved in nitrogen metabolism, transport, and assimilation.

4 identified putative genes regulating nitrate assimilation.

5 its two daughters can evolve through genetic assimilation.

6 ation, providing strong evidence for genetic assimilation.

7 ults in the modulation of sulfate uptake and assimilation.

8 pe plants due to the suppression of ammonium assimilation.

9 stimulate chloroplast division and nitrogen assimilation.

10 ith the construction of tissues allowed by C assimilation.

11 070/2, with utility for EPA production and N-assimilation.

12 e (Rubisco) catalyzes primary carbon dioxide assimilation.

13 and citrate and severely suppressed ammonium assimilation.

14 nabling ligand substitution and/or substrate assimilation.

15 unction of nodules as an important site of S-assimilation.

16 esponse to optimise N utilisation for carbon assimilation.

17 t the cost of disrupting nitrogen uptake and assimilation.

18 ong interdependency between N-fixation and S-assimilation.

19 ns defining this water-saving mode of carbon assimilation.

20 btC help mediate ferrilegiobactin uptake and assimilation.

21 s offer insight into some aspects of crustal assimilation.

22 levels in their cells by a process of rapid assimilation.

23 lifestyle alongside with anaplerotic carbon assimilation.

24 , consistent with limited nighttime nitrogen assimilation.

25 emmerer & Berry (FvCB) representation of CO2 assimilation.

26 nal variation in eddy covariance-derived CO2 assimilation.

27 of the ethylmalonyl-CoA pathway for acetate assimilation.

28 ITRATE REDUCTASE (NR), an enzyme of nitrogen assimilation [5].

29 canopy level responses of photosynthetic CO2 assimilation (A) to key environmental variables: light,

30 s exchange analysis examined diel changes in assimilation (A), stomatal conductance (gs ) and transpi

31 ough stomatal pores in order to acquire CO2 (assimilation [A]) and control their carbon-for-water bal

32 er uses three forecasting machines: (i) data assimilation, a technique borrowed from atmospheric phys

33 seven European shrublands using indices of C assimilation (aboveground net primary production: aNPP)

34 Large scale assimilation absorbs the intrinsic variability of electr

35 s of warming and associated soil drying on C assimilation across an entire growing season.

36 igh gs at low Px, thereby maintaining carbon assimilation, albeit at the cost of loss of hydraulic co

37 wing that Gln-1;2 was essential for ammonium assimilation and amino acid synthesis.

38 nisms and contain special traits in nitrogen assimilation and associated processes.

39 his refines the current paradigm that canopy assimilation and below-ground respiration are tightly co

40 nsport with concomitant reductions in carbon assimilation and biomass production when effects on resp

41 em model along with 3-dimensional ocean data assimilation and by prescribing the external radiative f

42 expression of genes involved in nitrogen (N) assimilation and carbon (C) metabolism, which may redire

43 thways, leading to down-regulation of carbon assimilation and chlorophyll biosynthesis, and an increa

44 carbon dioxide are expected to affect carbon assimilation and evapotranspiration (ET), ultimately dri

45 e, it provides carbon backbones for nitrogen assimilation and evolves CO2 and thus impacts on plant c

46 s genes involved in urea metabolism, acetate assimilation and fermentation, acetoin production and gl

47 Furthermore, shade decreased C-assimilation and generated less mutualistic mycorrhizal

48 y in TBMs that utilize the FvCB model of CO2 assimilation and highlights the importance of incorporat

49 eaf-level Chl on canopy-scale photosynthetic assimilation and identify possible opportunities for imp

50 utrition in regulating stomatal opening, CO2 assimilation and ion channel activity.

51 trophic modes, proteins involved in nitrogen assimilation and light-independent chlorophyll synthesis

52 Despite the importance of nitrogen assimilation and NO signalling, it remains largely unkno

53 bolite contributes to coordination of carbon assimilation and partitioning during photosynthesis by a

54 In C4 photosynthesis CO2 assimilation and reduction are typically coordinated acr

55 thesis to cytoskeletal dynamics and cofactor assimilation and serve as models for uncovering strategi

56 nd NLP6&7-dependent up-regulation of nitrate assimilation and signaling genes and down-regulation of

57 ses to nitrate availability, linking nitrate assimilation and signaling with cell-cycle progression.

58 nge; oilseed varieties had higher net carbon assimilation and stomatal conductance relative to vegeta

59 asured response functions linking carbon (C) assimilation and temperature- and moisture-related micro

60 piration can be decoupled from recent canopy assimilation and that stored carbohydrates can be mobili

61 ed that elevated CO2 at night slowed NO3 (-) assimilation and thus decreased dark respiration in the

62 The newly described phenomena of epigenetic assimilation and tissue dedifferentiation may help us be

63 In the shoot, HY5 promotes carbon assimilation and translocation, whereas in the root, HY5

64 ppressed stomatal movements and affected CO2 assimilation and transpiration differentially between da

65 lecting individual variation in acquisition, assimilation and/or recycling of plasma proteins that pr

66 tive contributions of direct (through carbon assimilation) and indirect (via soil moisture savings du

67 ered genes directly related to N use (e.g. N assimilation) and to other shared biological processes i

68 regulator involved in sulfate transport and assimilation, and a high-affinity sulphate transporter a

69 into and growth within host cells, nutrient assimilation, and alterations in host ion flux.

70 We measured chlorophyll content, CO2 assimilation, and carbohydrate production under varying

71 ic sensitivity tests, enable pool-based data assimilation, and facilitate tracking and benchmarking o

72 nce, light response curves of carbon dioxide assimilation, and manual confirmation of canopy architec

73 ance (g) increases growth, nitrate (NO3 (-)) assimilation, and nitrogen (N) utilization at elevated C

74 e expression coincided with a drop in carbon assimilation, and only in the late stages with an increa

75 hydraulic conductance (k), canopy G, carbon assimilation, and productivity.

76 N, (15)N isotope fractionation, (15)NO3 (-) assimilation, and the ratio of shoot CO2 evolution to O2

77 ta establish that fatty acid and cholesterol assimilation are inexorably linked in Mtb and reveals a

78 These data reveal genetic assimilation as a potentially adaptive response of Trich

79 ypical LD acclimation of carbon and nitrogen assimilation as well as redox-related parameters was not

80 up-regulation of sulfate/selenate uptake and assimilation, associated with elevated concentrations of

81 ly, the highest and lowest potential for CO2 assimilation at both high and low chloroplastic CO2 conc

82 upt decline in quantum yield (QY) of net CO2 assimilation at low photosynthetic photon flux density (

83 ics in between the analysis cycles and/or by assimilation at the next analysis cycle.

84 ic algal CCM and its interaction with carbon assimilation, based largely on Chlamydomonas as a model,

85 del is able to quantify the evolution of the assimilation because it characterizes the fitness conseq

86 a Biolog assay determining the carbon source assimilation behavior of an xpp1 deletion strain.

87 alnutrition results from disordered nutrient assimilation but is also characterized by recurrent infe

88 t mixing between sediment and peridotite, or assimilation by arc crust sediment, unlikely to be the m

89 as associated with maintenance of net carbon assimilation by compensatory increases of leaf CO2 gradi

90 Nearly all algae enhance their carbon assimilation by operating a CO2-concentrating mechanism

91 between C and N in which external supply and assimilation by organisms are adjusted to maintain their

92 For example, riverine organic matter assimilation by the glacier-nesting seabirds Kittlitz's

93 s, suggesting that despite higher rates of C assimilation, C turnover was also very high and less C i

94 oreover, our theory predicts that net carbon assimilation can be maximized by means of a trade-off be

95 the intercanopy light environment and carbon assimilation capacity of canopies with wild type, a Chl-

96 d in Synechococcus sp. PCC 7002, the acetate assimilation capacity of the resulting strain was greate

97 WPL>1 (where the N load exceeds the basin's assimilation capacity), cover about 17% of the global la

98 ponsive aeration with changing environmental assimilation capacity.

99 ranscription factors, transporters, nitrogen assimilation, carbon/nitrogen metabolism, redox, signall

100 The increased carbon assimilation corresponds with greater starch accumulatio

101 d implications for water reuse because plant assimilation could be employed advantageously in enginee

102 Here, we explore data assimilation (DA) with the Ensemble Kalman filter to fus

103 pt abundances for genes involved in ammonium assimilation differed from the classical "enteric paradi

104 st, a response that influences shoot NO3 (-) assimilation during both day and night.

105 ng PCBs and Hg to determine dietary chemical assimilation efficiencies (AEs) and elimination coeffici

106 Mean assimilation efficiencies varied from 0.32 to 0.50 for B

107 udy, congener-specific estimates of net PBDE assimilation efficiencies were calculated from dietary e

108 Selenium assimilation efficiency (AE) averaged 63.2 +/- 8.8% from

109 The assimilation efficiency (AE) of TiO2 NPs by mussels from

110 Zinc assimilation efficiency (AE) varied from 28% for the Ani

111 Estimates of PBDE assimilation efficiency can be used in bioaccumulation m

112 Additional studies estimate dietary assimilation efficiency in several primary consumers ran

113 Laboratory experiments demonstrated that the assimilation efficiency of (137)Cs was 16% in polychaete

114 The assimilation efficiency of BDE49 was significantly great

115 Net assimilation efficiency represents the fraction of the c

116 Excluding BDE49, PBDE assimilation efficiency was not significantly related to

117 mulation in an organism depends on exposure, assimilation efficiency, and elimination/metabolism.

118 ding processes, including ingestion rate and assimilation efficiency, that affect the dietary uptake

119 We specifically examined Se assimilation efficiency, tissue distribution, efflux rat

120 es encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was similar in gr

121 rovides subsidiary carbon for photosynthetic assimilation, especially under drought conditions.

122 e boundary is associated with limited carbon assimilation even in average climatic conditions.

123 By altering host nutrient assimilation/excretion flexibility, parasites could play

124 lowest g had similar rates of shoot NO3 (-) assimilation following N deprivation at elevated CO2 con

125 carbohydrates can decouple respiration from assimilation for prolonged periods by mobilizing reserve

126 The data assimilation forecasts are empirically evaluated against

127 The evaluation suggests that the data assimilation forecasts compare well with specific glucos

128 ntrations, processed using the modelling and assimilation framework of the Copernicus Atmosphere Moni

129 how Crc affects the hierarchy of metabolite assimilation from complex mixtures.

130 tion of ammonia respiration genes and carbon assimilation genes.

131 ctions and is defined as the ratio of carbon assimilation (GPP) to evapotranspiration (ET).

132 eral rhizobial and plant genes involved in S-assimilation, highlight the function of nodules as an im

133 2 supplies and to perform photosynthetic CO2 assimilation in a cost-effective way.

134 stimation of the capacity for leaf-level CO2 assimilation in Arctic vegetation.

135 TnrA is a master regulator of nitrogen assimilation in Bacillus subtilis.

136 Ammonium assimilation in Escherichia coli is regulated by two par

137 genes and pathways responsible for nitrogen assimilation in M. tuberculosis.

138 the few available data demonstrating genetic assimilation in microbial photoautotrophs.

139 veals a potential for accelerated epigenetic assimilation in neurodegenerative disease.

140 GS1 (Gln synthetase) is central for ammonium assimilation in plants.

141 ive nitrogen in generalists but for nitrogen assimilation in specialists.

142 ratory pathway stimulates photosynthetic CO2 assimilation in the Calvin-Benson cycle.

143 effect of cooking conditions on meat protein assimilation in the elderly.

144 explore the metabolic networks for nitrogen assimilation in this bacterium, changes in gene expressi

145 to ecosystems through stimulation of carbon assimilation, increased root exudates to supply nitrogen

146 alysis and/or detergent absorbents, and A2AR assimilation into synthetic liposomes can be visualized

147 proportion of global CH4 emissions, but CH4 assimilation into the aquatic food web in arctic lakes i

148 the 7th century and in agreement with their assimilation into the Indian sub-continent's population

149 o toxicity, bioaccumulation, and degradation/assimilation into the natural carbon cycle.

150 les was inferred from calculations of (66)Zn assimilation into the snail's soft tissues.

151 Nitrogen assimilation is a highly regulated process requiring met

152 Genetic assimilation is an important evolutionary transition, bu

153 Mineral nutrient uptake and assimilation is closely coordinated with the production

154 Inter-individual epigenetic assimilation is concurrent with increasing similarity be

155 of observation locations where the effect of assimilation is most prominent.

156 intriguing link between hormones and sulfate assimilation is the fact that the main regulator of the

157 Passing Attributes between Networks for Data Assimilation) is a gene regulatory network inference met

158 mine synthetase, the key enzyme for nitrogen assimilation, is poorly understood.

159 se (GS), a key enzyme in biological nitrogen assimilation, is regulated in multiple ways in response

160 t change the empirical ATP cost of gross CO2 assimilation (JATP/GA).

161 In this work, we quantified the plant assimilation kinetics of MBT using Arabidopsis under hyd

162 The proposed data assimilation machine, the primary focus of the paper, us

163 irected to the de novo synthesis of nitrogen assimilation machinery, simultaneously, the photobiologi

164 conductance plasticity suggests that genetic assimilation may be ongoing.

165 consistently regulated, suggesting that food assimilation may have been affected.

166 ion dynamics, which we optimize using a data assimilation method and two observed data streams, mosqu

167 onjunction with surveillance data and a data assimilation method to forecast influenza activity.

168 er and ensemble square root filters are data assimilation methods used to combine high-dimensional, n

169 We combine modern data assimilation methods with Wikipedia access logs and CDC

170 Assimilation methods, meant to constrain divergence of m

171 observations of influenza incidence and data assimilation methods.

172 ions with climate reanalysis data, snow data assimilation model output, and satellite spectral data.

173 the anatomical features used to support the 'assimilation model' in Europe might not have been inheri

174 and ATP-ADP ratios led to increased nitrogen assimilation, NADP-malate dehydrogenase activation, and

175 Plant assimilation occurs at other times, potentially liberati

176 a match to any known genus, demonstrated the assimilation of (13)C-aniline.

177 tified bacterial sRNA regulating the primary assimilation of a macronutrient.

178 this pathway plays an important role in the assimilation of acetate for growth in one of those organ

179 ole-rock or zircon isotope studies, and that assimilation of altered roof material may represent a vi

180 ard mechanism in the placenta to enhance the assimilation of beta-carotene for proper embryogenesis.

181 The capture and assimilation of CO(2) delivered by the C(4) cycle was lo

182 Our results show partial re-assimilation of CO2 and H2 by n-butanol-producer C. beij

183 The photosynthetic assimilation of CO2 in C4 plants is potentially limited

184 tic productivity is limited by the enzymatic assimilation of CO2 into organic carbon compounds.

185 A complex intracellular pathway supports the assimilation of cobalamin into its active cofactor forms

186 ultural explanations such as exposure to and assimilation of culturally transmitted ideologies.

187 This processing step is critical for assimilation of dietary cobalamin into the active cofact

188 encodes a cell-surface protein required for assimilation of exogenous heme.

189 ough the feeding activity of the animals and assimilation of filtered particles in shellfish tissues.

190 ntrogression from closely-related strains or assimilation of further genetic diversity from parental

191 Assimilation of GOSAT SIF with DGVMs causes a redistribu

192 The acquisition and assimilation of inorganic carbon (Ci) represents the lar

193 molecular genetics approach to restrict the assimilation of inorganic nitrogen by knocking down nitr

194 rical basis for describing and understanding assimilation of limiting nutrients in the oceans.

195 samples, which might have resulted from the assimilation of local females during the initial settlem

196 ay help developing strategies to improve the assimilation of lutein in humans to avoid macular degene

197 The assimilation of magnetic nanoparticle synthesis into mam

198 ent work showed that the bioavailability and assimilation of meat amino acids in the elderly is lower

199 on observed electrical conductivity, better assimilation of meteorological data, and the use of unst

200 ese shocks are essentially eliminated by the assimilation of near-homogenous global Argo distribution

201 large B cell lymphoma (DLBCL) requires rapid assimilation of new biological data.

202 Assimilation of nitrate, the primary source of nitrogen

203 ate reductase, a key enzyme required for the assimilation of nitrate.

204 dy, we investigated the factors required for assimilation of phosphate from eDNA.

205 of (14)C carbon, suggesting Orf306-dependent assimilation of PNP in E. coli cells.

206 emiologists, and clinicians, an orchestrated assimilation of required resources, and a more systemati

207 Our data provide strong evidence that assimilation of sulphur into Martian magmas was a common

208 terotrophic values associated to mixotrophic assimilation of synthesis gas (H2, CO2 and CO).

209 Assimilation of the final lid subunit, Rpn12, triggers a

210 s, (13)CO2 labeling revealed enhanced carbon assimilation of the flag leaf from flowering to late gra

211 lization, which entails a fast and efficient assimilation of the products.

212 l modification, ring opening, and subsequent assimilation of these compounds into the tricarboxylic a

213 thousand, due to magma residence within, and assimilation of, local granite basement.

214 piration and the dependence of shoot NO3 (-) assimilation on photorespiration.

215 cose forecasts; (ii) model averaging of data assimilation output; and (iii) dynamical Gaussian proces

216 Passing Attributes between Networks for Data Assimilations (PANDA) to construct the gene regulatory n

217 rient uptake from the soil, plant carbon (C) assimilation, partitioning and release to the soils, and

218 N-assimilation pathway genes respond uniquely, apparently

219 The altered carbon assimilation pathway of crassulacean acid metabolism (CA

220 etabolize thiosulfate to sulfite in a sulfur assimilation pathway rather than in sulfide stress respo

221 Fe-containing enzymes of the plastid sulfur assimilation pathway were major targets of Fe deficiency

222 id metabolism (CAM), a photosynthetic carbon assimilation pathway with high water-use efficiency, and

223 uMP cycle was established as the main carbon assimilation pathway, and the classical methanol dehydro

224 pathway of serine biosynthesis, the ammonium assimilation pathway, or the metabolism of gamma-aminobu

225 se activity, the other enzyme in the cyanide assimilation pathway, suggesting that nitrilase activity

226 porate H2S efficiently as part of the sulfur assimilation pathway.

227 iosynthesis and is regulated by the nitrogen assimilation pathway.

228 flux than any naturally occurring one-carbon assimilation pathway.

229 teins involved in photosynthesis and nitrate assimilation pathways show opposite diurnal expression p

230 Additionally, increased rates of CO2 assimilation, photorespiration, and plant growth were ob

231 te feeding resulted in the inhibition of net assimilation, photosynthetic electron transport, and iso

232 we propose 'progressively inhibited crustal assimilation' (PICA) as a major cause of bimodality in c

233 dence are two major factors limiting the CO2 assimilation potential of plants.

234 species specific, they largely affected the assimilation potential of Rubisco from the different cro

235 Specifically, chlorine assimilation provides key evidence of recycling in subma

236 The net carbon assimilation rate (A) at high irradiance and saturating

237 p between mass-based stem photosynthetic CO2 assimilation rate (Amass ) and specific stem area (SSA;

238 The oscillations in net assimilation rate and isoprene emission in feedback-inhi

239 ying twofold increases in photosynthetic CO2-assimilation rate and plant growth were measured for tob

240 Depending on the individual assimilation rate of each plant, the (18) O-label was pa

241 s (for example, the relationship between net assimilation rate per area (Aa) and leaf mass per area (

242 f area index (LAI) and increasing leaf-level assimilation rate related to leaf demography), and alloc

243 tic parameters were derived from analysis of assimilation rate vs internal CO2 concentration curves (

244 ean and variance, while vein density (carbon assimilation rate) increased in mean, consistent with a

245 We studied isoprene emission, net assimilation rate, and chlorophyll fluorescence under di

246 ly inhibitory level (1973 mug/L) lowered the assimilation rate.

247 at the mutant stomata can bestow an improved assimilation rate.

248 ght, where provenances sustaining higher CO2 assimilation rates also revealed increased water-use eff

249 nhanced stomatal conductance, photosynthetic assimilation rates and, to a lesser extent, tree radial

250 odes, IE plants reached higher daily net CO2 assimilation rates compared with NE genotypes.

251 rations and reduced stomatal conductance and assimilation rates in our eight sample species.

252 Furthermore, whole-leaf CO2 assimilation rates of both ADGase and pPGI mutants were

253 a reduction in stomatal conductance and CO2 -assimilation rates of the transgenic plants.

254 iency, maintaining higher photosynthetic CO2 assimilation rates than the wild type under limiting nit

255 Stomatal responses to [CO2] shifts and CO2 assimilation rates were compared in Arabidopsis (Arabido

256 gop ), saturated (Asat ) and maximum (Amax ) assimilation rates were investigated for 18 extant taxa

257 approach a constant level at high ca because assimilation rates will reach a maximum and stomatal con

258 3 stress inhibited photosynthesis and carbon assimilation, sequential herbivory counteracted the init

259 sphorylation that senses carbon and nitrogen assimilation status.

260 The balance between carbon assimilation, storage and utilisation during photosynthe

261 anism (CCM) is a key component of the carbon assimilation strategy of aquatic microalgae.

262 Determining the temporal dynamics of carbon assimilation, subsequent transport into developing wood,

263 ovides insights into the complexity of the N assimilation system throughout development and identifie

264 Phu (Pseudomonas heme uptake) and Has (heme assimilation system) systems.

265 huR (Pseudomonas heme uptake) and HasR (heme assimilation system).

266 int) SM/ST dataset prepared from a land data assimilation system, as part of a national monsoon missi

267 nsporters but found no evidence of a nitrate assimilation system, in agreement with the N preference

268 servations in two different ocean models and assimilation systems, that such shocks are generated in

269 ransmission models using Bayesian data-model assimilation techniques to baseline and follow-up infect

270 were identified by employing biochemical and assimilation test procedures and using CHROMagar Candida

271 crops, leading to a reduction of land carbon assimilation that, consequently, influences the land sin

272 howed delayed senescence and enhanced carbon assimilation that, ultimately, increased the number of f

273 selection can favor the evolution of genetic assimilation, the process by which the expression of a t

274 e chloroplast and inhibit photosynthetic CO2 assimilation through disruption of photosystem II.

275 ontrol of the nitrate/nitrogen transport and assimilation to adapt nutrition to growth.

276 enhance the efficiency of Pi acquisition and assimilation to avoid nutrient starvation.

277 coordinates protein translation and nitrogen assimilation to optimize cell growth in different enviro

278 ter-use efficiency (Wi; the ratio of net CO2 assimilation to stomatal conductance for water vapor) of

279 contributions of ammonium versus amino acid assimilation to the cellular nitrogen pool.

280 s spectrometry for precise quantification of assimilation, translocation, and molecular reallocation

281 sponse of the system and the expected carbon assimilation under constant and periodically forced envi

282 es showed considerable increases in nodule N assimilation, ureide synthesis, and metabolite levels.

283 glutamine pool and thus [Formula: see text] assimilation via GS.

284 plement channel resistance by limiting toxin assimilation via the digestive process.

285 Phaeodactylum tricornutum In NR-KO cells, N-assimilation was abolished although NO3(-) transport rem

286 Maximum quantum yield for light-limited CO2 assimilation was also high relative to other C3 species.

287 Daily C assimilation was greater at elevated [CO2 ] in both cult

288 benefit to modeled net assimilation, whereas assimilation was sensitive to either wetter or drier con

289 cellular and genetic basis of diatom NO3(-) assimilation, we generated a knockout in the nitrate red

290 The activities of the enzymes for N assimilation were also coordinated to a certain degree,

291 and AQP for N uptake and GOGAT and GS for N assimilation were the key genes, validated by RT-qPCR, w

292 ons should lead to increased rates of carbon assimilation when water and nutrients are not limiting.

293 ded relatively little benefit to modeled net assimilation, whereas assimilation was sensitive to eith

294 ect on the processes most limiting to carbon assimilation, which differ by plant type.

295 mbe possesses an unexpected pathway for heme assimilation, which may also serve as a source of iron f

296 It is further extended to multiscale data assimilation, which provides the large-scale estimation

297 Plants optimize carbon assimilation while limiting water loss by adjusting stom

298 -bisphosphate leads to photosynthetic carbon assimilation, while the oxygenation reaction competes wi

299 rsion of parameters extracted from different assimilation windows was studied.

300 ility of electrophysiological data over wide assimilation windows.