ライフサイエンスコーパス: sequestration

1 is important for radioactive Cs removal and sequestration.

2 is of particular interest for carbon dioxide sequestration.

3 terification is a common means of carotenoid sequestration.

4 regulates both root function and soil carbon sequestration.

5 are an important sink for terrestrial carbon sequestration.

6 ibuting significantly to carbon and nitrogen sequestration.

7 cluding land-atmosphere feedbacks and carbon sequestration.

8 he benefits of tree planting for ecosystem C sequestration.

9 us aureus to calprotectin-mediated manganese sequestration.

10 rming the immune-antagonistic nature of this sequestration.

11 tant as these are hotspots of genuine carbon sequestration.

12 importance of N-rich residues for greater C sequestration.

13 llagen expression, which was increased by BA sequestration.

14 ut were less effective than MOF for NH(3)(g) sequestration.

15 a sink of CO(2) exchange and helps in carbon sequestration.

16 een undertaken investigating EV anthelmintic sequestration.

17 of biochar production and atmospheric carbon sequestration.

18 respond to an offset of 30% of the net CO(2) sequestration.

19 s the prevailing explanation for this carbon sequestration.

20 d serum, both of which are important in iron sequestration.

21 ssor that inactivates the phage repressor by sequestration.

22 E1A causes YAP/TAZ cytoplasmic sequestration.

23 istance and consequent parasite clearance by sequestration.

24 l regulator of ocean productivity and carbon sequestration.

25 ing ecological effects and impacts on carbon sequestration.

26 ognised as an important ecosystem for carbon sequestration.

27 stem services including high rates of carbon sequestration.

28 of globally programmed phase separation and sequestration.

29 hore carbon cycling and (potentially) carbon sequestration.

30 negatively regulates YAP through cytoplasmic sequestration.

31 +9.4 million Canadian dollars (CA$)], carbon sequestration (+2.2 million CA$), and ecotourism (+42.0

32 nthocyanins, participating in their vacuolar sequestration, a function conserved across the flowering

33 uitination abrogates p62 oligomerization and sequestration activity and negatively regulates the Keap

34 cucurbiturils, and pillararenes) as in vivo sequestration agents for neuromuscular blockers, drugs o

35 ng and delivery applications, and as in vivo sequestration agents.

36 Esterification promotes the sequestration and accumulation of carotenoids, thereby e

37 l rainforests play important roles in carbon sequestration and are hot spots for biodiversity.

38 of environmental outcomes in terms of carbon sequestration and biodiversity conservation and social e

39 Results highlight the synergy between carbon sequestration and biodiversity conservation under altern

40 key ecosystems supporting fisheries, carbon sequestration and coastal protection, are globally threa

41 ks will improve models of terrestrial carbon sequestration and ecosystem services.

42 A similar sequestration and elimination process occurs for the cor

43 spase-1 cysteine 397 that leads to caspase-1 sequestration and inactivation.

44 by achieving a win-win outcome of enhanced C sequestration and increased crop yield.

45 Consequently, GLUT4 intracellular sequestration and mobilization by insulin is achieved, i

46 in suggests it plays a role in the premature sequestration and phagocytosis of RBCs in the spleen.

47 gastrointestinal pathology is impeded by the sequestration and replication of T. cruzi in host tissue

48 raphy simulation predicted sinus of Valsalva sequestration and resultant coronary obstruction during

49 of antimalarial treatment, ongoing parasite sequestration and schizogony both affect initial changes

50 ity, long-term ecosystem carbon and nutrient sequestration and sustainable agriculture.

51 tanding of plant root effects on soil carbon sequestration and the sensitivity of SOC stocks to clima

52 best management practices to maximize carbon sequestration and to minimize soil CO(2) emissions durin

53 This facilitated p62-mediated Keap1 sequestration and ultimately increased Nrf2-mediated tra

54 CLC/Gal-10 functions as a carrier for the sequestration and vesicular transport of the potent eosi

55 the BCP can significantly alter ocean carbon sequestration and, thus, atmospheric CO(2) and climate,

56 UCNR1) inhibition abrogated PMN priming, PMN sequestration, and ARDS.

57 ntial applications in molecular sieving, gas sequestration, and catalysis.

58 proteins that regulate synthesis, transport, sequestration, and degradation of these molecules and th

59 tion and structural optimization for in vivo sequestration applications.

60 arctic because productivity and ecosystem C sequestration are not synonymous.

61 In C. elegans, iron uptake and sequestration are regulated by HIF-1.

62 This work implicates CP-mediated Fe(II) sequestration as a component of nutritional immunity in

63 mmunity and iron availability, and show iron sequestration as a component of the innate immune respon

64 rbon uptake did not lead to increased carbon sequestration at the ecosystem level.

65 at could enhance our understanding of carbon sequestration at the whole plant level and provide futur

66 valuate its use in energy recovery and CO(2) sequestration based on the premise that it could signifi

67 ing the lifecycle from crop establishment to sequestration below ground in geological formations.

68 We highlighted differences in pollutant sequestration between urban areas and between species, s

69 The mechanisms linking sequestration, brain swelling and death remain poorly un

70 o days, illustrating efficient autophagosome sequestration but delayed lysosomal fusion or acidificat

71 ecules involved in DNA looping, resulting in sequestration but not inactivation of RcopLS20.

72 understanding of microbial responses to iron sequestration by CP and highlight the importance of heme

73 Results indicate that in situ carbon sequestration by greenery varied moderately across citie

74 Growth factor sequestration by IGFBP-3-Fc enhances the activity of EGF

75 which can release carbon stocks, and, carbon sequestration by in situ vegetation.

76 , we reveal a molecular link between calcium sequestration by melanin inside the phagosome and induct

77 ly in embryos and larval tissues, with CBP-1 sequestration by MRG-1 having a major role in differenti

78 Carbon sequestration by sediments and vegetated marine systems

79 The efficiency of carbon sequestration by the biological pump could decline in th

80 y, and there is potential to increase carbon sequestration capacity by ~20% (-187.7 million metric to

81 ncrease in this century and continue their C sequestration capacity in all climate change scenarios,

82 ctivity which could negatively affect carbon sequestration capacity of Northern Hemisphere (NH) fores

83 missions and the potential to enhance carbon sequestration capacity on productive forestland.

84 The soil C(org) sequestration capacity prevailed in shallow and deep veg

85 Gln4p depletion reduces this sequestration capacity, allowing uncharged tRNAGln to in

86 Advancing the scale of carbon capture and sequestration (CCS) will require both technological adva

87 In geologic carbon sequestration, CO(2) is injected into geologic reservoir

88 ssments that forest regrowth and peak carbon sequestration coincided with European arrival.

89 ese results suggest that inhibiting LSD1 via sequestration contributes to tau-mediated neurodegenerat

90 l profiles in the root, but only vacuolar Pi sequestration corresponded with steady-state cytosolic P

91 Carbon sequestration could further increase under moderate (+1

92 Enhanced soil carbon sequestration could offset only a small part of the high

93 ed CO(2) costs from this sector for geologic sequestration could reach as low as $22/tCO(2).

94 etaCyD is shown to result from a sequence of sequestration-dependent reactions that occur in commonly

95 Here, we study protein sequestration during glucose deprivation-induced ATP dec

96 athophysiological mechanisms related to iron sequestration during infection and regulation of TfR1 ex

97 pBiomas 3.1 and recently refined IPCC carbon sequestration estimates, we mapped the age and extent of

98 st choice because of its affinity for Ra-226 sequestration even in the presence of very high total di

99 ation of plasma membrane is required for the sequestration event, preventing the inheritance of long-

100 st National Laboratory led a geologic carbon sequestration field demonstration where ~1000 tonnes of

101 er production is an option to achieve carbon sequestration for cities relying on biomass-fuelled dist

102 and the critical ecosystem service of carbon sequestration for mitigating climate change.

103 ed aquaculture to provide sufficient CO(2)eq sequestration for several climate change mitigation scen

104 ime zero' landscapes but also a solution for sequestration [Formula: see text] into soils.

105 Heavy metal sequestration from industrial wastes and agricultural so

106 the potential to efficiently enhance carbon sequestration from the atmosphere with a rate as high as

107 tes that CHC22 traffic initiates human GLUT4 sequestration from the ERGIC and defines a role for CHC2

108 Furthermore, there is a considerable sequestration gap (71 Mt of CO(2)e.y(-1) of unaccounted

109 omic conditions, and when accounting for the sequestration gap, carbon stored annually in HWPs is <1%

110 Sub-surface activity such as geologic carbon sequestration (GCS) has the potential to contaminate gro

111 on to increase plant productivity and thus C sequestration has been suggested.

112 variance with climate as well as ecosystem C sequestrations have yet to be fully quantified.

113 SF with a haptoglobin-affinity column or its sequestration in a soluble hemoglobin-haptoglobin comple

114 n at other nearby sites, we find that carbon sequestration in above-ground biomass may have offset ro

115 pointing out that the role of FSa in carbon sequestration in agricultural soils at a global scale ma

116 metabolites prime PMNs and induce pulmonary sequestration in an animal model of ARDS.

117 enabled the enzyme to evolve improved CO(2) sequestration in an oxygen-rich atmosphere and may guide

118 isms highlight the impact of GR phases on As sequestration in anoxic subsurface environments.

119 n be challenging due to their degradation or sequestration in cell culture media prior to analysis.

120 ytic recapture, enhancing pathways for GLUT4 sequestration in humans relative to mice, which lack CHC

121 logy utilizes multiple strategies, including sequestration in lipid vesicles, to raise the rate and s

122 tershed land management, that aims at carbon sequestration in mitigating climate change while maintai

123 However, direct evidence of Sb sequestration in natural peat samples is lacking.

124 udies show that the potential for carbon (C) sequestration in no-till farming sometimes is not realiz

125 by a high parasite load, leading to parasite sequestration in organs and consequent excessive inflamm

126 function as specialized structures for Na(+) sequestration in P. vaginatum, illustrating a possible p

127 relevant mineral substrate for arsenic (As) sequestration in reduced, subsurface environments.

128 s are disproportionately important to carbon sequestration in semiarid climates where low elevations

129 ween bioenergy production and biochar carbon sequestration in Stockholm's context is dominated by the

130 Conversely, T-cell sequestration in the bone marrow was not governed throug

131 sts that CM results from infected RBC (iRBC) sequestration in the brain microvasculature and resultin

132 on for the drier site is a net decrease in C sequestration in the coming decades to centuries.

133 eroding, promoted by the conjunction of mud sequestration in the delta plain driven by expansion of

134 Intravenous (IV) succinate-induced PMN sequestration in the lung, a first event, and followed b

135 tivity causes gamma aminobutyric acid (GABA) sequestration in the mitochondria, reducing GABAergic si

136 as well as the linear dose-dependent ammonia sequestration in the peritoneal space provide a strong b

137 ree control, demonstrating efficient ammonia sequestration in the peritoneal space.

138 to efficient chemical weathering and carbon sequestration in the Southeast Asian islands.

139 d resistance mechanisms, including herbicide sequestration in the vacuole, a rapid cell death respons

140 properties that govern the kinetics of water sequestration in this class of materials as well as inve

141 the effects of N on vegetation or increase C sequestration in this system.

142 to combat climate change through carbon (C) sequestration in tree biomass.

143 ain process for long-term atmospheric carbon sequestration in vegetation.

144 lack of accommodation space and that carbon sequestration increases according to the vertical and la

145 specifically to CsgG and that its subsequent sequestration induces a marked transition in the conform

146 ited to depolarized mitochondria followed by sequestration into autophagosomes.

147 ization of a target protein, followed by its sequestration into cellular foci and subsequent degradat

148 n such neurons under AD pathology due to the sequestration into cytoplasmic amyloid beta (Abeta) aggr

149 lowing determination of ponatinib uptake and sequestration into lysosomes during the development of a

150 o found that methionine is required for GSK3 sequestration into multivesicular bodies through microau

151 Iron sequestration is a recognized innate immune mechanism ag

152 basic C-terminal residues, and this membrane sequestration is disrupted in EHEC that expresses consti

153 ighlight that the major potential for carbon sequestration is in cropland soils, especially those wit

154 We propose that sequestration is mechanistically related to the Repeat-A

155 Notably, this sequestration leads to reduced levels of the encoded pro

156 nced by CM status (CM+ > CM-, P = 0.004) and sequestration level (Seqhi > Seqlo, P = 0.010).

157 glyphosate translocation and tissue-specific sequestration may be the basis of reduced plant sensitiv

158 These data suggest that sequestration may regulate amounts of individual Rpt sub

159 The implementation of soil carbon sequestration measures requires a diverse set of options

160 salinity increase, soil organic carbon (SOC) sequestration mechanisms in estuarine wetlands remain po

161 t due to nucleocytoplasmic transport protein sequestration, nor blockade of the phenylalanine-glycine

162 Sequestration occurs during stressed conditions, for exa

163 l reforestation projects could safeguard the sequestration of 6.7 Gt CO(2) over the next 20 years.

164 mpartmentalized DSB repair pathway choice by sequestration of a fatty acylated repair factor at the i

165 This sequestration of a-BTA leads to short, stable species co

166 formed by a-BTA is controlled by competitive sequestration of a-BTA monomers by Nle-BTA, while the ob

167 The biomaterial-assisted sequestration of adenosine leverages the transient surge

168 Sequestration of air pollutants is one of the main ecosy

169 es are decoupled because of the preferential sequestration of anions into solvating TMP domains aroun

170 a vaccine candidate with the aim of reducing sequestration of asexual "blood-stage" parasites in the

171 eolar hemorrhages, extensive alveolar septal sequestration of bacteria and neutrophils, diffuse desta

172 We have proposed that sequestration of beta-catenin destruction complex compon

173 and affects class I Ag presentation through sequestration of beta2M inside endoplasmic reticulum, wh

174 The sequestration of biologically relevant macromolecules ca

175 e oceanic biological pump, which impacts the sequestration of carbon and resupply of nutrients in the

176 nd Tropical Atlantic Ocean (TAO), leading to sequestration of carbon dioxide.

177 ive contributions of these reservoirs to the sequestration of carbon in the deep mantle(1).

178 ns of different algal glycans to cycling and sequestration of carbon remain unknown, partly because o

179 secretion and decreased protein turnover by sequestration of chaperones and proteases or formation o

180 roughly $38/tCO(2) remains for the geologic sequestration of CO(2) and $56/tCO(2) for CO(2)-EOR (bef

181 to advance technologies for the capture and sequestration of CO(2), the transformation of emitted CO

182 These results reveal that the sequestration of cytoplasmic molecular chaperones by tau

183 gy is the fundamental mechanism that ensures sequestration of cytosolic material and its subsequent d

184 oA) demonstrated that activity was driven by sequestration of divalent metal cations, a mechanism whi

185 that A-to-I editing impedes MDA5 sensing and sequestration of dsRNAs encoding membrane proteins, whic

186 ingredients (in terms of shared enzymes and sequestration of enzymes) to generate bistability and os

187 ice and was accompanied by increased splenic sequestration of erythrocytes and fewer erythropoietic e

188 cell contact triggers secretion of ExsE and sequestration of ExsD by ExsC to cause the release of Ex

189 n of two PI(4)P kinases, Stt4p and Pik1p; or sequestration of free PI(4)P via expression of a PI(4)P-

190 ower acetylation state, permitting increased sequestration of Galpha(s) in lipid-raft domains, where

191 neral reaction conditions that allow for the sequestration of halide ions through simple precipitatio

192 Our results indicate that sequestration of HdrR is likely to be the only mechanism

193 Membrane sequestration of HdrR prevents the positive feedback aut

194 ound that ESAT-6:beta2M interaction leads to sequestration of HFE in endoplasmic reticulum, causing p

195 Sequestration of HSPCs in bone marrow after SCI is linke

196 IFITM proteins have been associated with the sequestration of incoming virions in endosomes (target c

197 Sequestration of industrial carbon dioxide (CO(2)) in de

198 ical bone remodeling, which in turn leads to sequestration of infectious foci from innate immune effe

199 stimulating the recognition and proteolytic sequestration of insoluble ubiquitinated protein aggrega

200 DAF-2B, that modulates insulin signaling by sequestration of insulin peptides.

201 Sequestration of intestinal BAs by in vivo delivery of s

202 ntributes to I/R injury, and CaMKII promotes sequestration of KATP from myocardial cell membranes.

203 Endosomal sequestration of lipid-based nanoparticles (LNPs) remain

204 The sequestration of MBNL1 results in RNA-splicing defects t

205 critical factor in efficacy is Lactobacillus sequestration of metronidazole, and efficacy decreases w

206 ghly expressed during Pi starvation, and the sequestration of miR399 molecules protects PHO2 mRNA fro

207 Using live-cell imaging, we find that sequestration of misfolded proteins and nascent polypept

208 strategy in neural progeny cells to promote sequestration of misfolded proteins into protective incl

209 The chaperone-mediated sequestration of misfolded proteins into specialized qua

210 This also induced increased lysosomal sequestration of mitochondria and enhanced the competiti

211 we present a chemical approach for on-device sequestration of more than 96 per cent of lead leakage c

212 n of dehydration-associated transcripts, the sequestration of mRNAs in ribonucleoprotein partials pri

213 son@Man-Se/Man-Se NPs also induced autophagy sequestration of Mtb, evolving into lysosome-associated

214 this can only be explained by a preferential sequestration of Nb relative to Ta in a hidden (unsample

215 ally injured patients leads to the pulmonary sequestration of neutrophils (PMNs), which serves as the

216 We show that ICP22 results in (i) nuclear sequestration of nonnative proteins, (ii) reduction of c

217 1031-1047) reveal that sequestration of nonstoichiometric subunits into aggrega

218 Especially, the sequestration of OM (rich in carboxyl, aromatic, and/or

219 However, sequestration of OXPHOS components in cristae membranes

220 ly suggest that there is no significant skin sequestration of P. falciparum gametocytes.

221 oses to bacteremia, which is associated with sequestration of parasitized red blood cells and increas

222 Sequestration of Plasmodium falciparum-infected erythroc

223 Intrahepatic sequestration of platelets was significantly higher in t

224 l for applications such as catalysis and the sequestration of precious materials.

225 on of the extracellular microenvironment and sequestration of pro-angiogenic signaling, may connect A

226 These results support a general mechanism of sequestration of pro-apoptotic BCL-2 proteins into fiber

227 erties of MCL1 revolve around inhibiting its sequestration of proapoptotic factors.

228 Sequestration of proteins into distinct compartments dur

229 Our findings indicate that nucleolar sequestration of RAG1 is a negative regulatory mechanism

230 Splenic sequestration of red blood cells, the appearance of circ

231 Observed photochemically induced sequestration of REEs into sediments can explain a signi

232 two alternative mechanisms, degradation and sequestration of Rpt subunits, may help control the onse

233 owever, the molecular mechanisms involved in sequestration of senescent erythrocytes, their recogniti

234 n may be the primary process controlling the sequestration of sinking organic carbon.

235 Herein, biomaterial-assisted sequestration of small molecules is described to localiz

236 Ptch1 and Ptch2 functionally overlap in the sequestration of Smo, the spatiotemporal expression of B

237 Sequestration of such segments by protein partners, howe

238 lt F. hepatica have a biological role in the sequestration of TCBZ and additional toxic xenobiotic me

239 This is associated with cytoplasmic sequestration of TFEB, preventing induction of the lysos

240 In cultured cells, TMG promoted sequestration of the cap-binding protein eIF4E (eukaryot

241 g protein 1 (4E-BP1), is O-GlcNAcylated, and sequestration of the cap-binding protein eukaryotic tran

242 uding substrate-consuming side reactions and sequestration of the catalyst as an inactive species.

243 hese studies suggest a role for Vps13 in the sequestration of the ER into autophagosomes at late endo

244 m of innate immune signaling which relies on sequestration of the NF-kappaB subunit p65 to a biomolec

245 ilar to RNA exosome mutants due to nucleolar sequestration of the poly(A)-binding protein (PABP) Nab2

246 TDP-43, we confirmed the increased cytosolic sequestration of the poly-ubiquitinated and aggregated f

247 so provides a mechanism for the preferential sequestration of the respiratory chain complex mRNAs by

248 complex, facilitates end protection through sequestration of the terminal telomere repeat sequence w

249 and nuclear localized E-cadherin, increases sequestration of these proteins in cell membranes, disru

250 S disease aetiologies, and explains how aaRS sequestration of uncharged tRNAs can prevent GCN4 activa

251 ver, VMA21 deficiency triggers ER stress and sequestration of unesterified cholesterol in lysosomes,

252 Efficient PfEMP1-dependent IE sequestration often depends on soluble serum proteins, i

253 ing increase in carbon capture-to-storage-to-sequestration on the seafloor.

254 lly enhanced oil recovery (EOR) and geologic sequestration opportunities.

255 OP resistance often involves sequestration or hydrolysis of OPs by carboxylesterases.

256 ed absorption or translocation and increased sequestration or metabolic degradation.

257 en-fixing trees could either mitigate (CO(2) sequestration outweighs soil N(2)O emissions) or exacerb

258 eagrass) sustain the highest rates of carbon sequestration per unit area of all natural systems(1,2),

259 tem services, including potential for carbon sequestration, pollination potential and groundwater rec

260 ative and the FAO's Global assessment of SOC sequestration potential (GSOCseq) programme.

261 Sequestration potential of novel mangrove forests should

262 It was calculated that only ~3% of the CO(2) sequestration potential of the >30 Mt slag heap has been

263 fset in Europe provides an estimate of CO(2) sequestration potential to 2030.

264 rease in the estimated global biochar carbon sequestration potential to over 2.6 Gt CO(2)-C(eq) yr(-1

265 ing natural form of carbon storage with high sequestration potential.

266 proving estimates of secondary forest carbon sequestration potential.

267 har production can increase biochar's carbon sequestration potential; by up to 45% in this study.

268 s, crop yield gap, and the associated carbon-sequestration potentials, as well as the provision of in

269 Sustainable soil carbon sequestration practices need to be rapidly scaled up and

270 Sequestration protects substrates from further uncontrol

271 which is roughly equivalent to the seagrass sequestration rate for GHG inventory accounting but lowe

272 rained by elemental budgets, indicated CO(2) sequestration rates of 2-4 t CO(2) /ha, 1-5 years after

273 omposition was monitored to determine carbon sequestration rates.

274 How is cargo sequestration regulated under nonselective and selective

275 gies (GGRTs); one such GGRT uses soil carbon sequestration (SCS) in agricultural land.

276 we explore two CDR technologies: soil carbon sequestration (SCS), and carbon capture and storage (CCS

277 ped by clinical diagnosis (CM+ or CM-), iRBC sequestration (Seqhi, Seqlo, Seq0) and HIV status (HIV+

278 s: delivery to and injection within reliable sequestration sites, and delivery and injection for the

279 biophysically unique and the site of carbon sequestration, the benthos, faces less anthropogenic dis

280 s pelagic ecology, biogeochemistry and CO(2) sequestration, the projected increase in the geographica

281 , and releases Beclin-1 from LRPPRC-mediated sequestration, thereby enabling the initialization of do

282 erate natural geological processes of carbon sequestration through application of crushed silicate ro

283 Pi uptake, metabolic recycling, and vacuolar sequestration to cytosolic Pi homeostasis in Arabidopsis

284 This phenomenon is due to LC3-I sequestration to p62 aggregates, which accumulate when a

285 discusses the energy cost of vacuolar Na(+) sequestration, under different scenarios.

286 a reveal that respiratory chain complex mRNA sequestration underlies the mitochondrial defects charac

287 elated with LRP5/6 and FZD10, and miR-153-3p sequestration via a plasmid-based miR inhibitor system a

288 Pi uptake, metabolic recycling, and vacuolar sequestration were distinguished in each zone by using c

289 ounds, both macrophage polarization and iron sequestration were impaired.

290 parasite development and vascular and tissue sequestration, which is responsible for disease symptoms

291 -expressing phagocytes to promote local iron sequestration, which regulated the microbiota and conseq

292 that the trajectory of this region's carbon sequestration will be sensitive to reduced or delayed su

293 that decadal semiarid montane forest carbon sequestration will remain relatively stable in the absen

294 tions between cells by extracellular calcium sequestration with Ethylenediaminetetraacetic acid (EDTA

295 tional C losses in drained soils and limit C sequestration with reflooding.

296 Lymphocyte sequestration with sphingosine-1-phosphate receptor 1 an

297 he model to explore the potential for soil C sequestration with sugarcane biochar in Sao Paulo State,

298 d States to extrapolate the status of carbon sequestration within a framework of projected warming an

299 ive (Rab 5(+)) vesicles and targeting it for sequestration within the trans- Golgi network (TGN).

300 and significantly (p < 0.001) increased SOC sequestration without having significant (p > 0.05) effe