ライフサイエンスコーパス: nutrient

1 aceae for acquiring iron, an essential metal nutrient.

2 of environmental contaminants and biological nutrients.

3 pact the cycles of other elements, including nutrients.

4 e competition with other species for limited nutrients.

5 s complex carbohydrates as a major source of nutrients.

6 king cytosolic Ac-CoA in cells with abundant nutrients.

7 nsequence of decreased intake of antioxidant nutrients.

8 nd development with the available energy and nutrients.

9 een alga, rich with bioactive components and nutrients.

10 , where each community takes turns consuming nutrients.

11 converting plant-based feeds into accessible nutrients.

12 iota utilizes complex carbohydrates as major nutrients.

13 polar constituents and its macro- and micro- nutrients.

14 plex organic polymers are used as sources of nutrients.

15 intestine plays a central role in digestion, nutrient absorption and metabolism, with individual regi

16 RagA alters mTORC1-driven growth in times of nutrient abundance or scarcity.

17 Nutrient acquisition and energy storage are critical par

18 (PGPR) can improve plant health via enhanced nutrient acquisition and priming of the plant immune sys

19 3, and may reflect pathogen manipulation for nutrient acquisition and/or unsuccessful defence respons

20 l amoeba kills bacteria via phagocytosis for nutrient acquisition at its single-cell stage and for an

21 buscular mycorrhizal fungi, which facilitate nutrient acquisition from the soil.

22 mates the value of root traits for water and nutrient acquisition in environments and plant species.

23 AM fungi enhanced plant nutrient acquisition with both lower and more variable w

24 s morphologies to increase the efficiency of nutrient acquisition.

25 nt root and is critical for plant health and nutrient acquisition.

26 r every additional species consumed, dietary nutrient adequacy increased by 0.03 (P < 0.001).

27 h promotion was explained by slow release of nutrients, although a mechanistic understanding of nutri

28 sion, which has substantial implications for nutrient and carbon cycling, land productivity and in tu

29 f which could double or offset all projected nutrient and electricity use through newly installed san

30 events that occur in the setting of altered nutrient and energy exposures and offer a historical per

31 nd country-level resource recovery to impact nutrient and household electricity use through 2030.

32 ntrols to regulate metabolism in response to nutrient and signaling inputs.

33 nicipal wastewaters, their ability to remove nutrient and their biomass composition for downstream bi

34 ek bottle incubations amended with inorganic nutrients and carbon substrates (a mix of substrates, gl

35 ethal antibiotic doses once bacteria consume nutrients and enter stationary growth phase.

36 terized by extremely low levels of water and nutrients and exhibit highly heterogeneous distribution

37 timately depend upon interactions among soil nutrients and foliar microbes, yet this has never been t

38 Nutrients and growth factor stimuli converge on the cons

39 abolism with environmental inputs, including nutrients and growth factors.

40 ts are influenced by the altered profiles of nutrients and metabolic by-products that distinguish the

41 stinal tract, which is influenced by enteral nutrients and microbial activity.

42 and heterotrophs compete for the same scarce nutrients and niche space, and instead suggest that thes

43 They can be sources of nutrients and pathogen pollution and have been linked to

44 here to their advantage by secreting various nutrients and secondary metabolites.

45 ess, increasing the acquisition of essential nutrients and secreting conserved proteins of unknown fu

46 upper water column growth conditions (light, nutrient, and temperature).

47 ation is variable, and predicting how water, nutrients, and chronic disturbances interact to determin

48 lates tissue-fluid homeostasis, transport of nutrients, and migration of blood cells across the barri

49 ed interactions between dietary ingredients, nutrients, and the microbiota in specific pathogen-free

50 y the impact of prolonged frying on potatoes nutrients, and the potential alterations resulting from

51 ersity, reducing soil erosion, and improving nutrient- and water-use efficiency.

52 Nutrients-and by extension biosynthetic capacity-positiv

53 e transition from growth to development when nutrients are abundant.

54 Nutrients are necessary for life, as they are a crucial

55 trapment of useful extracellular enzymes and nutrients, as well as opportunities for efficient recycl

56 Consumption of 10 foods/nutrients associated with cardiometabolic diseases: frui

57 Three nutrient associations had highly suggestive evidence and

58 t to bacterial colonization and by supplying nutrients at the NAPL/water interface.

59 genes) coordinately regulated in response to nutrient availability and cellular growth rate.

60 Ecosystem-level adaptations to low soil nutrient availability and long-term low levels of distur

61 munities subject to the dual stresses of low nutrient availability and reduced access to organic mate

62 ory mechanism enables cellular adaptation to nutrient availability and supports the energy-demanding

63 Atmospheric CO2 concentrations and nutrient availability are two key variables that can aff

64 ke of As, the kinetics of Si dissolution and nutrient availability can also affect As uptake and toxi

65 both the metabolic state of immune cells and nutrient availability can alter immune responses.

66 nutrient uptake occurs during drought, high nutrient availability can increase water use efficiency

67 . neoformans experiences a drastic change in nutrient availability during host infection, ultimately

68 better isolate molecular adaptations to low nutrient availability during lactation.

69 High nutrient availability may play a detrimental role in dro

70 interactions that influence mortality risk, nutrient availability, and pathogen burden shape energy

71 temperature, redox chemistry, irradiance and nutrient availability.

72 ynthesis and secretion are closely linked to nutrient availability.

73 ivers of productivity, including climate and nutrient availability.

74 Identifying nutrients available in the environment and utilizing the

75 in adult bovine serum, which better reflects nutrients available to cells in vivo, exhibit decreased

76 The major nutrients available to human colonic Bacteroides species

77 Glycans are major nutrients available to the human gut microbiota.

78 association studies under varied spatial and nutrient backgrounds may help to understand the complex

79 mizing negative feedbacks between carbon and nutrient balance.

80 an (i.e., root nodule) where the exchange of nutrients between host and endosymbiont occurs.

81 ere showed evidence for symbiotic sharing of nutrients between the plant and the fungi, Laccaria bico

82 ehold actions in influencing urban watershed nutrient budgets.

83 nge photosynthetically fixed carbon for soil nutrients, but occasionally nonphotosynthetic plants obt

84 These data reveal how a widely consumed nutrient can paradoxically sustain brain starvation sign

85 ocon to the host membrane, where they form a nutrient channel.

86 r growth, Topt , is a saturating function of nutrient concentration.

87 rfect homeostasis-a condition where internal nutrient concentrations are completely independent of ex

88 tions are completely independent of external nutrient concentrations for all external nutrient concen

89 Stormwater nutrient concentrations were highly variable across wate

90 ncreasing elevation did not affect tree leaf nutrient concentrations, but did reduce ground-layer com

91 ced north to south gradients in salinity and nutrient concentrations.

92 nal nutrient concentrations for all external nutrient concentrations.

93 e water column, influence stratification and nutrient condition, and can affect local productivity an

94 t to fully restore chemoresistance under low nutrient conditions.

95 ne signaling tunes behavior appropriately to nutrient conditions.SIGNIFICANCE STATEMENT Animals adjus

96 technologies can be applied to improving the nutrient content and stability in these cereal grains ar

97 In the first, the nutrient content of foods and beverages was adjusted to

98 cies, we found that tissue stoichiometry and nutrient content were more plastic than has been describ

99 cycles, as well as modeling and forecasting nutrient controls over carbon-climate feedbacks.

100 The nutrient-coupled Ca(2+) signalling network integrates tr

101 Nutrient cross-feeding can stabilize microbial mutualism

102 mes activated at the lysosome in response to nutrient cues.

103 important parasites of primary producers and nutrient cyclers in aquatic ecosystems.

104 and consequences of N limitation in coupled nutrient cycles, as well as modeling and forecasting nut

105 rtant roles in ecosystem functioning, global nutrient cycling and climate regulation, but are declini

106 nt productivity, which can negatively impact nutrient cycling and food production, upon which future

107 These large changes in C and nutrient cycling could not have been predicted from the

108 s, possessing a suite of stress response and nutrient cycling genes to fix carbon under the fluctuati

109 rus-host dynamics and the role of viruses in nutrient cycling would benefit from direct observations

110 ncluding zooplankton community structure and nutrient cycling.

111 e to environmental stressors, toxicants, and nutrient deficiencies can affect DNA in several ways.

112 on high temperatures, UV-light, drought, and nutrient deficiencies, and may contribute to tolerance t

113 breast cancer cells adopted in response to a nutrient-deficient microenvironment.

114 We find that a nutrient-dependent decrease in Snf2 leads to an increase

115 The principle of nutrient-dependent fitness costs has implications for th

116 lts reveal a potential function of mTORC1 in nutrient-dependent regulation of glucagon secretion and

117 Rpc82, and Ret1, are particularly prominent nutrient-dependent SUMO targets.

118 PM emissions, as well as impacts on acid and nutrient deposition, are discussed.

119 ntal conditions within tumor masses, such as nutrient deprivation, oxygen limitation, high metabolic

120 he severe growth limitations associated with nutrient deprivation.

121 Nutrient-driven O-GlcNAcylation is strikingly abundant i

122 Forest mycorrhizal type mediates nutrient dynamics, which in turn can influence forest co

123 it and sugar-sweetened beverages (SSBs)] and nutrients (e.g., total calories and sodium).Regardless o

124 as a simple and rapid method for analysis of nutrient elements in seed kernels of cucurbits.

125 had little effect on other trace- and macro-nutrient elements in the rice bran.

126 at chromatin marks are not established until nutrient/energy contingencies are satisfied.

127 cter strain Ruegeria pomeroyi DSS-3, both in nutrient-enriched and natural oligotrophic seawater.

128 Respiration rates increased under nutrient-enriched conditions on leaves (1.32x) and wood

129 wing Populus tremulodes seedlings on a thin, nutrient-enriched Phytagel matrix that allows pixel to p

130 in headwater streams, where most carbon and nutrients enter river networks, has hindered effective m

131 te host endoreduplication and development of nutrient exchange/feeding sites include manipulation cen

132 we provide the first geographic footprint of nutrient excretion by freshwater fishes across the Unite

133 Toxin delivery and nutrient extraction occur in a contact-dependent manner,

134 Besides nutrients, flavan-3-ols (i.e., epicatechin and B-type pr

135 To study such a nutrient flow, a new application of Fourier transform in

136 of a monocarboxylate transporter involved in nutrient flux and hepatic lipid metabolism.

137 tion of organic carbon that could serve as a nutrient for OPs.

138 to lactate, which is itself also a potential nutrient for tissues and tumours.

139 us, which is thought to be a major source of nutrients for E. coli in the gut.

140 ale mosquitoes take a blood meal and use the nutrients for egg maturation.

141 liver autophagy, which is thought to provide nutrients for use by other organs and thereby maintain w

142 r pathogen must increase host cell uptake of nutrients from plasma.

143 itter removal may lead to AM fungi obtaining nutrients from recalcitrant organic or mineral sources i

144 in leaves and the availability of water and nutrients from roots.

145 s that facilitate their growth by liberating nutrients from the environment.

146 Globally, potential nutrient gains are an order of magnitude larger than ele

147 ional (3D) architecture, cell heterogeneity, nutrient gradients and the interaction between cells and

148 imuli; intra- and extravascular transport of nutrients, growth factors and drugs; and cell proliferat

149 e potential contributions of these essential nutrients in biology.

150 Nutrients in freshwater ecosystems are highly variable i

151 takes of energy, macronutrients, and several nutrients in fruits and vegetables, such as carotenoids.

152 y an important role in the redistribution of nutrients in rainforests.

153 reas the angiosperm forests distributed more nutrients in stems.

154 is the key link between the availability of nutrients in the environment and the control of most ana

155 etabolism is dictated by the availability of nutrients in the tsetse fly vector.

156 to pixel measurement of the distribution of nutrients, in particular, nitrate, in the rhizosphere.

157 In conclusion, RPE cells consume multiple nutrients, including glucose and taurine, but prefer pro

158 ly, this rewiring may render certain outside nutrients indispensable.

159 c pH, including epithelial water absorption, nutrient inflow, and luminal buffering capacity, and gen

160 l is essential for the incretin effect after nutrient ingestion and is critical for the actions of di

161 are experiencing high rates of anthropogenic nutrient inputs.

162 urinary recovery biomarkers in representing nutrient intake variation in a feeding study, and thus a

163 In disease models with energy and 1 or more nutrient intakes, predicted bias in estimated nutrient r

164 ncludes a new formulation of the temperature-nutrient interaction and test a novel prediction: that a

165 Our findings of frequent plant-microbe-nutrient interactions are novel and suggest that these i

166 milk powder was enriched with some essential nutrients (Inulin, DHA & EPA, vitamins B6, K1, and D3) a

167 rporated into contemporary diets and how the nutrient landscapes of these staples vary as a function

168 Significant changes occurred in metal nutrients level due to excess Pi supply.

169 ulation of transporter synthesis by internal nutrient levels can create a system that mitigates the s

170 temperature increases tempered by increased nutrient levels resulting from changing demographics and

171 substrates, possibly due to higher residual nutrient levels upon TOrC exposure.

172 l membrane is the locus for sensing cellular nutrient levels, which are transduced to mTORC1 via the

173 endocrine disease; cognitive function; serum nutrient levels; and others (total of 139 AMD and non-AM

174 y be important for survival under starvation/nutrient limitation conditions.

175 Nutrient limitation of oceanic primary production exerts

176 We examined the effects of nutrient limitation within a mutualism using theoretical

177 Plant functional type-based nutrient limitation, underpinned by a core SDGVM hypothe

178 , which can promote PDAC cell survival under nutrient limited conditions, and that collagen-derived p

179 luding those important for carbon cycling in nutrient-limited anaerobic environments.

180 m abrogated type VI secretion activity under nutrient-limited conditions, indicating a previously unr

181 PknG mutant displayed minimal growth in nutrient-limited conditions, suggesting its role in modu

182 bout the utility of secreted proteins during nutrient-limited growth.

183 ortance of growth-independent metabolism for nutrient-limited mutualistic communities.

184 e by Pseudomonas aeruginosa, under different nutrient-limiting conditions.

185 heavy load of nitrogenous compounds reflects nutrient loss and influences water quality in large rive

186 and nutrient storage, or whether fire-driven nutrient losses limit plant productivity.

187 To inform more ecologically based landscape nutrient management, we compared watershed inputs, outpu

188 Our results demonstrate that seabird-derived nutrients not only spread across the terrestrial ecosyst

189 The attractive nutrients of teff include protein, dietary fiber, polyph

190 d survival, since they are key for uptake of nutrients on the one hand, and for defence against endog

191 to overcome the pressures of reduced oxygen, nutrients or chemically induced cell death, but the mech

192 ss, the variety of processes contributing to nutrient patchiness, and the wide range of spatial and t

193 the major bioavailable form of the essential nutrient phosphorus.

194 e in the abundance of biologically important nutrients phosphorus and nickel across the Archean-Prote

195 the transport and fate of sediment, carbon, nutrients, pollutants, pathogens and manufactured nanopa

196 ontribute to a diet that is energy dense but nutrient poor and increase risk of developing obesity, c

197 tivity and higher accumulation of biomass in nutrient-poor forests compared to nutrient-richer forest

198 mortality, aboveground wood productivity) of nutrient-poor tropical forests.

199 lth and disease is in part a function of the nutrient processing and release of metabolites.

200 are key structural determinants of food and nutrient production that need to be considered in plans

201 ferences in regional oxygen distribution and nutrient provision by the host.

202 This work aims at evaluating the main nutrients (proximate, minerals), their contribution for

203 Here we show that nutrient pulses from decomposing Atlantic salmon (Salmo

204 t and implementation of guidelines regarding nutrient recommendations and estimation of vitamin C int

205 g 12 treatment technologies on emissions and nutrient recovery were further explored through scenario

206 n and is therefore an interesting source for nutrient recovery.

207 e IUGR at birth because of moderate maternal nutrient reduction.

208 Genetic ablation of SIN3A abolishes nutrient regulation of glucokinase without affecting oth

209 utrient intakes, predicted bias in estimated nutrient relative risks was reduced on average, but bias

210 ed for the characteristics and mechanisms of nutrient release from CRFs.

211 d application of energy-efficient biological nutrient removal processes through effective Nitrospira

212 a fine control of nutrient uptake even under nutrient-replete conditions.

213 Although phosphorus is an essential nutrient required for multiple physiological functions,

214 pre-existing vasculature, in order to obtain nutrients required for continued growth and proliferatio

215 derstanding of how M. tuberculosis meets its nutrient requirements under hypoxic conditions.

216 that PDAC extracellular matrix represents a nutrient reservoir for tumour cells highlighting the met

217 ustments to increase acquisition of limiting nutrient resources, but they may also result in construc

218 nce and the presence of a continuous flow of nutrients, respectively.

219 KEY POINTS: Maternal nutrient restriction induces intrauterine growth restric

220 ABSTRACT: Maternal nutrient restriction induces intrauterine growth restric

221 tergenerational in utero parental energy and nutrient restriction on offspring growth in rural Gambia

222 rtant for oceanic uptake of carbon and heat, nutrient resupply for sustaining oceanic biological prod

223 effects on plant and fungal productivity and nutrient retention, but no effect on CO2 efflux.

224 Under nutrient-rich conditions, PP2A-B55(Pab1) dephosphorylate

225 In nutrient-rich fat cells, GRASP clusters in close proximi

226 n urban runoff, which includes deposition of nutrient-rich leaf litter onto streets connected to stor

227 Here we identify a complex, nutrient-rich organic coating on co-composted biochar th

228 3)C in CO2) indicate that upwelling of cold, nutrient-rich water from near the seafloor accompanies m

229 biomass in nutrient-poor forests compared to nutrient-richer forests.

230 However, based on modeling results, nutrients seem efficiently retained in actively feeding

231 essential role in GATOR- and SESN-dependent nutrient sensing and mTORC1 regulation.

232 lated diverse biological processes including nutrient sensing and the DNA damage response, and implic

233 heme turnover, inflammation, and oxygen and nutrient sensing have been discovered for organelles tha

234 role of the hyperosmotic-response pathway in nutrient sensing may indicate that cells use osmolarity

235 The indifference of HSC to nutrient sensing through RagA contributes to their molec

236 verall, these findings reveal a key parasite nutrient-sensing mechanism that is critical for modulati

237 neurogenesis and highlight the role of this nutrient-sensing pathway in developmental plasticity and

238 g and give an overview of the involvement of nutrient-sensing pathways in controlling both reproducti

239 reveal a novel regulatory connection between nutrient-sensitive glycosylation and NRF2 signaling and

240 ices, such as nursery grounds for fisheries, nutrient sequestration, and ecotourism.

241 ding to the anti-incretin theory, intestinal nutrients should also cause a reduction of insulin sensi

242 mmon signaling pathway translates a specific nutrient signal into physiological activities, and the i

243 Nutrients signal via the Rag guanosine triphosphatases (

244 n by beta cells, whether it directly engages nutrient signaling pathways in skeletal muscle to mainta

245 et of rapamycin complex 1 (TORC1) integrates nutrient signals to control cell growth and organismal h

246 sponding not only to hormones but also to FA nutrient signals to modulate food-directed behavior.

247 In particular, macropinocytosis can be a nutrient source for pancreatic cancer cells, but it is n

248 ntaining dissolved organic matter (DOM) as a nutrient source supporting eutrophication in N-sensitive

249 oundwater upwelling had a major influence on nutrient spatial patterns.

250 mation of autophagosomes under conditions of nutrient starvation and that the mature Red Blood Cells

251 tic target of rapamycin inhibition by either nutrient starvation or use of an active site inhibitor r

252 Nutrient starvation usually halts cell growth rather tha

253 PD2 and GPD3 GPDH isoforms are important for nutrient starvation-induced TAG accumulation but have di

254 tion of triacylglycerol (TAG) in response to nutrient starvation.

255 Adipocytes sense systemic nutrient status and systemically communicate this inform

256 regate, these findings provide evidence that nutrient stoichiometry is a strong predictor of bacteria

257 rize that mangrove encroachment may increase nutrient storage and improve storm protection, but cause

258 nts, although a mechanistic understanding of nutrient storage in biochar is missing.

259 Nutrient storage in consumer biomass may be especially i

260 long-term effects of fire on soil carbon and nutrient storage, or whether fire-driven nutrient losses

261 tive stress induced by hydrogen peroxide and nutrient stresses caused by amino acid or glucose withdr

262 nutrition (MAM) are treated with lipid-based nutrient supplement (LNS) or corn-soy blend (CSB).

263 pment of home fortification with lipid-based nutrient supplements (LNSs) for mothers and/or children

264 ntrolled trial of small-quantity lipid-based nutrient supplements (SQ-LNS) fortified with 23 micronut

265 As for nutrient supply, we emphasize how consumers enhance prim

266 nnected to that of their host, primarily for nutrient supply.

267 ight into the extracellular battle for metal nutrients that occurs during infection.

268 Lipids are important nutrients that proliferating cells require to maintain e

269 Nutrients that regulate methylation processes may modify

270 u dep ), based on the retention of deposited nutrients, their allocation within plants, and C:N and C

271 hange the release kinetics of the fertilizer nutrients through an abatement strategy to offset these

272 productivity is sustained by the cycling of nutrients through decomposing organic matter.

273 sms that live in environments that lack this nutrient; thus, unusual enzyme reactions have also evolv

274 ations of genes involved in the transport of nutrients to developing seeds and the mobilization of ca

275 al proximal tubular cells constantly recycle nutrients to ensure minimal loss of vital substrates int

276 Dust provides ecosystem-sustaining nutrients to landscapes underlain by intensively weather

277 Gymnosperm forests tended to allocate more nutrients to leaves as compared with angiosperm forests,

278 Mammalian tissues rely on a variety of nutrients to support their physiological functions.

279 cytic sorting, and recycling, which delivers nutrients to the lysosomes.

280 late tectonics started and how the supply of nutrients to the oceans changed through time.

281 receptor-RPE complex that provides essential nutrients to the photoreceptors and in turn helps patien

282 consumers, potentially affecting energy and nutrient transfer rates in soil food webs of cold ecosys

283 and hypoxia-response signaling and decreased nutrient transport and metabolism.

284 novel mTOR-dependent regulatory network for nutrient transport in renal proximal tubular cells.

285 nsing in trophoblast cells matches placental nutrient transport, and therefore fetal growth, to folat

286 and climatic impacts on hydrology that drive nutrient transport.

287 odulation of cell cycle, meiosis-related and nutrient transporter genes, suggesting a fine control of

288 Plants with high nutrient uptake capacities and the ability to efficientl

289 nsporter genes, suggesting a fine control of nutrient uptake even under nutrient-replete conditions.

290 When nutrient uptake occurs during drought, high nutrient ava

291 coupling of stream ecosystem metabolism and nutrient uptake responded to a realistic warming scenari

292 ay crucial role in signaling, ion transport, nutrient uptake, as well as in maintaining the dynamic e

293 ibutes to both invasion and channel-mediated nutrient uptake.

294 robiomes-i.e., those enhancing plant growth, nutrient use efficiency, abiotic stress tolerance, and d

295 The goal of increasing crop productivity and nutrient-use efficiency is being addressed by a number o

296 and the primary organs for water uptake and nutrients, we sought to use root hairs as a single-cell

297 ss, as genes involved in scavenging of these nutrients were being actively transcribed.

298 rent model systems, particularly the flow of nutrients, when performing anti-biofilm efficacy evaluat

299 ent, 3) carnitine, a conditionally essential nutrient with an important role in the carnitine shuttle

300 rural disparities and spatial colocation of nutrients with agricultural needs.