ライフサイエンスコーパス: recycle

1 thout chromatography, and the enzymes can be recycled.

2 id gel exhibited consistent activity in five recycles.

3 rocyte homeostasis and are required for iron recycling.

4 ual steel demand and the scrap available for recycling.

5 alter net primary productivity and elemental recycling.

6 eparation as well as emulsifier and catalyst recycling.

7 reviously unidentified stage, termed here as recycling.

8 nd benzophenone, with the latter amenable to recycling.

9 rforms controlled heat extraction and energy recycling.

10 f LRRK2 kinase inhibition in promoting cargo recycling.

11 at the ejection process might delay ribosome recycling.

12 ng robustness and cost-effective storage and recycling.

13 mulated in terminals and facilitated vesicle recycling.

14 and NTPase HelD have been implicated in RNAP recycling.

15 emonstrated along with catalyst recovery and recycling.

16 a sequence-specific manner to regulate their recycling.

17 s truncated at the A site, allowing ribosome recycling.

18 nd SV protein levels and rescued impaired SV recycling.

19 hown to participate in synaptic vesicle (SV) recycling.

20 le ubiquitination predominantly inhibits SK2 recycling.

21 firming the role of deubiquitination in GCGR recycling.

22 ylation and mitochondrial H(+) and phosphate recycling.

23 irecting damaged proteins towards proteasome recycling.

24 ted by fungal saprotrophs involved in carbon recycling.

25 e proteins following defective exocytosis or recycling.

26 BP14 in the auxin response through ubiquitin recycling.

27 n and 2) secondary overprinting by microbial recycling.

28 bited during NMDAR-LTD to decrease endocytic recycling.

29 hing ratio <0.2%, indicating efficient NO(x) recycling.

30 gens, and metals, which pose problems during recycling.

31 le (lysosome in mammals) for degradation and recycling.

32 econdary organic aerosols and atmospheric OH recycling.

33 livers them to lysosomes for degradation and recycling.

34 consistent with a deficiency in chromophore recycling.

35 t epithelium (RPE)65 isomerase necessary for recycling 11-cis-retinal, the light-sensitive chromophor

36 tein and AA losses by ~6% (the proportion of recycled 15N divided by the sum of endogenous N and recy

37 d 15N divided by the sum of endogenous N and recycled 15N).

38 oat complex that has a function in endocytic recycling(4-6).

39 ity of the modified ortho-carborane guest by recycling a CB[7]-functionalized resin.

40 t stress relaxation, direct reprocessing and recycling abilities of a range of thiol-anhydride elasto

41 Catalyst recycling after pai-conjugated polymerization has previo

42 life and high plasma levels; similarly, FcRn recycles albumin and is the portal of entry for enteric

43 eceptor (FcRn) that mediates IgG and albumin recycling also participates in cellular responses to IgG

44 propose a novel role for this cocatalyst to recycle an allyl chloride byproduct generated in the cou

45 Synaptic vesicles need to be recycled and refilled rapidly to maintain high-frequency

46 n; accordingly, synaptic vesicles need to be recycled and refilled rapidly.

47 overed from waste streams, and how it can be recycled and used as a resource for new products.

48 55 and 94% of its initial activity after 10 recycles and 125 days storage at 25 degrees C, respectiv

49 function in regulating transmembrane protein recycling and BMP signaling.

50 always better than single-use plastics; (4) recycling and composting should be the highest priority;

51 ion tracers (BC and NO(x)) near 30% of metal recycling and concrete batch plant facilities within our

52 eading to futile cycles of SAM synthesis and recycling and explaining the necessity for MTHFR to be r

53 erase created a dual amplification by target-recycling and generation of an catalytic DNAzyme product

54 IL1RL1-deficient mice showed defective iron recycling and increased splenic iron deposition.

55 e damage with important implications to iron recycling and iron homeostasis.

56 impurities impede in many cases closed-loop recycling and require advanced pretreatment steps, incre

57 the lower atmosphere, which reduced moisture recycling and resulted in increased drought extent and s

58 ist-activation to facilitate Rab4a-dependent recycling and that USP33 and STAMBP activities are criti

59 natal Fc receptor (FcRn), which mediates IgG recycling and transcytosis in peripheral endothelium, wa

60 ing insights into the mechanisms of ribosome recycling and tRNA translocation.

61 duction of short-chain fatty acids, nitrogen recycling, and amino acid production.

62 ostatic interactions, can influence ribosome recycling, and could be particularly relevant to the syn

63 l trafficking hub where secretory, vacuolar, recycling, and endocytic pathways merge.

64 e trafficking pathways: anterograde traffic, recycling, and Golgi integrity.

65 autophagy in synaptic plasticity, endocytic recycling, and memory.

66 Pi uptake, metabolic recycling, and vacuolar sequestration were distinguished

67 e dynamics of insulin signaling and receptor recycling are more complex, is unknown.

68 , followed by retention and aggregation, and recycling associated with the large b-BSA-Gd-DTPA conjug

69 Decreased ATP production and NADH recycling, associated with mitochondrial uncoupling, wer

70 of the lung extracellular matrix, is rapidly recycled at sites of vessel injury and repair.

71 generation is discussed, as is the effect of recycling at end of life.

72 chemistry, with no indication of missing OH recycling at low nitrogen oxide concentrations.

73 ions, endocytosed AMPA receptors are rapidly recycled back to the plasma membrane.

74 rtion of the endocytic tracer FM4-64 is also recycled back to the PM after internalization.

75 0.03 pptv), indicating persistent I(y,part) recycling back to I(y,gas) as a result of active multiph

76 lso permitted a limited degree of phosphorus recycling back to the water column.

77 ating BCBM, and suggest that the recycleome, recycling-based control of the cell surface proteome, is

78 f autophagy and vacuole proteins involved in recycling but also result in the down-regulation of many

79 COPI vesicles mediate Golgi-to-ER recycling, but COPI vesicle arrival sites at the ER have

80 ed product (2-phosphoglycolate) that must be recycled by a series of biochemical reactions (photoresp

81 Hepcidin regulates iron absorption and recycling by inducing the internalization and degradatio

82 ation of external treadmilling and selective recycling by internal vesicular transport of cortex-boun

83 The molecular basis for ribosome recycling by RRF and EF-G remains unclear.

84 bination with a transition metal catalyst to recycle byproducts back into the catalytic cycle will pr

85 A minor role for retromer in Snc1 recycling can also be observed in single and double muta

86 ) is excreted in feces, indicating the large recycling capacity and high transport efficacy of ASBT-m

87 (CC), the combination of carbon capture and recycling (CCR) is an emerging area of research.

88 uld be initiated using lyophilized or spent (recycled) cells.

89 Autophagy is a conserved process that recycles cellular contents to promote survival.

90 ia formation and the polarization of MT1-MMP recycling compartments, required for invadopodia activit

91 translation reactivation by stabilizing the recycling-competent state of inactive ribosomes.

92 ether the material attributes recyclability, recycled content, compostability, and biobased, commonly

93 Recycled cooking oil (RCO) is widely used in many small

94 The energy requirements for recycling copper from end-of-life products already reach

95 d pretreatment steps, increasing the overall recycling cost.

96 pic variations-useful for tracing subducted, recycled crust-relate to high (3)He/(4)He and anomalous

97 phagy is a cellular degradation pathway that recycles cytoplasmic content.

98 vitrimer-like ability for being reshaped and recycled, despite their crosslinked structures.

99 ded DNA that we propose underlies polymerase recycling during lagging strand synthesis, in analogy to

100 Overall, the H(2)-recycling electrochemical cell allowed us to accomplish

101 sorption in a continuous system using a H(2)-recycling electrochemical cell.

102 he GTPase Rab11, generated in Rab11-positive recycling endosomal MVBs.

103 recently proposed that the tubular-vesicular recycling endosome membranes were a core platform on whi

104 n Grp1 being recruited preferentially to the recycling endosome rather than to the plasma membrane, o

105 ging two peripheral membrane proteins of the recycling endosome.

106 ignaling cascades are altered when early and recycling endosomes are disrupted by the expression of d

107 g DNM2 from autophagosome formation sites on recycling endosomes by causing increased binding to an a

108 ffects the dynamics of fusion and fission of recycling endosomes by controlling ubiquitination of the

109 ted and shows augmented trafficking to Rab4a recycling endosomes compared with the WT, thus affirming

110 ant negative (DN) that blocks trafficking at recycling endosomes enabled GCGR deubiquitination, where

111 Rab11A-containing recycling endosomes have been identified as a platform f

112 the release of autophagosome precursors from recycling endosomes is mediated by DNM2-dependent scissi

113 ed on our results, we propose that early and recycling endosomes provide a platform for the integrati

114 diated postendocytic sorting of nephrin from recycling endosomes to lysosomes for degradation.

115 uration, membrane sorting, pH homeostasis in recycling endosomes, and cargo trafficking, and they als

116 king through Rab5a early endosomes and Rab4a recycling endosomes, but also induced rapid deubiquitina

117 on pathway and instead enter Rab 11-positive recycling endosomes, where they are returned to the surf

118 mited contribution of vesicular transport in recycling endosomes.

119 pes of endosomes, including early, late, and recycling endosomes.

120 utamine, which diverts membrane flux through recycling endosomes.

121 sequently, BACE1 is endocytosed to early and recycling endosomes.

122 eton within the Rab11-related domain of slow recycling endosomes.

123 introduces the key factors in enterohepatic recycling, especially the mechanism of bile acid uptake

124 is result suggests that zooplankton nutrient recycling exceeds grazing pressure in nutrient-limited s

125 crease rates of reuse, waste collection, and recycling; expand safe disposal systems; and accelerate

126 Additionally, a recycling experiment demonstrated the stability of the c

127 urce separation of urine can enable nutrient recycling, facilitate wastewater management, and conserv

128 two essential translation factors, ribosome-recycling factor (RRF) and GTPase elongation factor G (E

129 characterize the biological role of ribosome recycling factor (RRF) in Escherichia coli.

130 elongation factor G (EF-G) and the ribosome recycling factor (RRF).

131 functional complexes with mt-mRNA, mt-tRNAs, recycling factor and additional trans factors.

132 The ability of AasS to recycle fatty acids may help pathogenic gram-negative ba

133 FcRn regulates IgG epithelial transport and recycling, Fc effector activities, such as antibody-depe

134 is the presence of the historical, but still recycled, flame-retardant, hexabromocyclododecane.

135 ct in recycling FM4-64 while snx4Delta cells recycle FM4-64 normally.

136 nt in ubiquitin binding, display a defect in recycling FM4-64 while snx4Delta cells recycle FM4-64 no

137 to leaching into solution phase, and may be recycled for reuse at least five times.

138 tion of the 100S complexes enabling ribosome recycling for participation in new rounds of translation

139 a subunit of the retromer complex mediating recycling from endosomes, in a subset of axons.

140 ing essential roles in RNA polymerase (RNAP) recycling, gene regulation, and genomic stability in mos

141 that are involved in RNA maturation and RNA recycling, govern gene expression in bacteria, and catal

142 The precise pathway of 100S ribosome recycling has been unclear.

143 Membrane filtration using recycled hemodialyzers allows water purification.

144 rients, one of which is to recover them from recycled human urine; once recovered, N and P can be red

145 initiatives, RRs above 55%, where 75-90% was recycled in a closed loop, were demonstrated.

146 hich cytoplasmic components are degraded and recycled in response to various stresses including starv

147 C10-AMS can be used to study fatty acid recycling in other bacteria as more AasS enzymes continu

148 nappropriate for describing phosphoglycolate recycling in these nonphotosynthetic autotrophs, we sugg

149 Previous studies have suggested a role for recycling in translational coupling within operons; if a

150 eveal a failure in post-termination ribosome recycling in UPF1 ATPase mutants.

151 ts between spatial locations in mammals are "recycled" in humans to represent a bidimensional multise

152 plastic exports in the EU, (iii) design-for-recycling initiatives, (iv) improved collection, and (v)

153 The bacterial ribosome is recycled into subunits by two conserved proteins, elonga

154 and limiting free enzyme pools, but how RNAP recycling into active states is achieved remains elusive

155 learing senescent red blood cells (RBCs) and recycling iron from hemoglobin.

156 Recycling is commonly included among the most viable opt

157 tion of energy via ribosomal hibernation and recycling is critical.

158 neuronal activity regulates synaptic vesicle recycling is largely unknown.

159 rical analysis of 48 metals shows that their recycling is mainly impeded by their low concentrations.

160 e low W and (4)He concentrations compared to recycled materials and are therefore highly susceptible

161 IFGEM uses recycled materials such as tire crumb and iron filings t

162 cation of these metals from natural sources, recycled materials, and industrial waste are inefficient

163 (206)Pb/(204)Pb-lacking strong signatures of recycled materials.

164 er regulates the matrix invasion activity by recycling matrix metalloprotease, MT1-MMP.

165 that (1) secretion delivers TM proteins and recycled membrane lipids to the same apical PM domain, a

166 tential strategies toward a sustainable ASSB recycling model.

167 he transmembrane domain but lacking both the recycling motif and all four STAT3-recruiting tyrosine r

168 This Rab6-dependent pool of recycled MR1, which is available for reloading with liga

169 other in matrix degradation via selectively recycling MT1-MMP but not MT2-MMP.

170 catalyst exhibits high stability and can be recycled multiple times without loss of activity.

171 albumin engagement with its cognate cellular recycling neonatal Fc receptor.

172 esults suggest that a composting system that recycles nutrients between cities and local farms has th

173 re important contributors to carbon cycling, recycling nutrients and organic material through host ly

174 ers a new approach toward a cleaner route to recycling nylons.

175 quisition of reading in humans relies on the recycling of a brain network evolved for other visual fu

176 actions can lead to changes in enterohepatic recycling of androgens.

177 it from the early endosome disrupts eventual recycling of beta1 integrins back to the cell surface, r

178 AmpD is cytoplasmic and plays a role in the recycling of cell wall muropeptides, with a link to anti

179 own to induce autophagy, the degradation and recycling of cellular components.

180 atic organelle dedicated to the disposal and recycling of cellular waste to a highly dynamic structur

181 Subduction focus the largest recycling of crustal carbonates and the most intense sei

182 that TSP-12 and TSP-14 are required for the recycling of DAF-4/BMPRII.

183 Subduction zones are pivotal for the recycling of Earth's outer layer into its interior.

184 s highlights the importance of intracellular recycling of ER-resident molecular chaperones for collag

185 Recycling of ESS is shown to reduce terrestrial acidific

186 lfields provides secure storage with limited recycling of gas; the injection of large amounts of wate

187 Our results identify Rab11b-mediated recycling of integrin beta1 as regulating BCBM, and sugg

188 ooperate with both SNX27 and retromer in the recycling of ligands encompassing the SBM, PDZ-binding m

189 Recurrent signal flow enables recycling of limited computational resources over time,

190 rmogenesis, and macrophages are required for recycling of lipids released by adipocytes.

191 gy and lysosome biogenesis for the efficient recycling of macromolecules.

192 ution to SOC were presumably due to enhanced recycling of microbial residues via increased activity o

193 ns p62 and NBR1 (neighbour of BRCA1) and the recycling of mitochondria (mitophagy), and peroxisomes (

194 s study demonstrates that Rab6 regulates the recycling of MR1 molecules from the cell surface through

195 proved to be economically promising, due to recycling of nutritious products, but also improves the

196 entral role for flotillin in the endocytotic recycling of Orai1 channels and that endocytosed wild ty

197 r, lithified deep biosphere that include the recycling of organic matter.

198 Recycling of organic waste (OW) as fertilizer on farmlan

199 The metabolic recycling of phosphoglycolate was extensively studied in

200 ght, thus completing a closed loop cycle for recycling of polyamides.

201 sights into the generation, recognition, and recycling of polyprenyl lipids.

202 Autophagic recycling of proteins, lipids, nucleic acids, carbohydra

203 arrestin-dependent ERK1/2 activation, faster recycling of receptors to the plasma membrane, and impai

204 ndocytic trafficking and/or the formation or recycling of signaling complexes during rhizobial and AM

205 Postendocytic recycling of Snc1 requires a phospholipid flippase (Drs2

206 by which EHD1 couples with SNX17 to regulate recycling of SNX17-interacting receptors.

207 Recycling of the 15N marker was determined to be ~11%, s

208 na) ARF-GEF GNOM, which is involved in polar recycling of the auxin transporter PIN-FORMED1.

209 Recycling of the contact lenses and their packaging amou

210 BP activities are critical for the endocytic recycling of the GCGR.

211 ation between the ubiquitination profile and recycling of the GCGR.

212 Here, we report that FCHSD2 loss impacts recycling of the RTKs, epidermal growth factor receptor

213 lasses of phosphine oxides, (ii) the one-pot recycling of TPPO generated from a Wittig reaction, and

214 essential elements to better comprehend the recycling of waste oyster shells.

215 I(y) amounts are indicative of active iodine recycling on ice in the upper troposphere (UT), support

216 view of the effects of the loss of ribosome recycling on protein synthesis in E. coli.

217 The methionine salvage pathway recycles one-carbon units lost to polyamine biosynthesis

218 In this process called "enterohepatic recycling", only 5% of the bile acid pool (~3 g in human

219 athrin-mediated endocytosis (CME), endosomal recycling, or degradation.

220 f the newly formed autophagic vesicle to the recycling organelle, the lysosome.

221 ously unsuspected state of binding (peptidyl/recycling, p/R) that is analogous to that seen during in

222 Autophagy is a highly conserved recycling pathway that promotes cell survival during per

223 ork demonstrates the involvement of distinct recycling pathways for the type I and type II BMP recept

224 the existence of three distinct and parallel recycling pathways mediated by Drs2/Rcy1/COPI, Snx4-Atg2

225 endosome via retrograde and plasma membrane recycling pathways.

226 ge form of nitrogen, released via endogenous recycling pathways.

227 protein (SBP) MppA, which is responsible for recycling peptidoglycan fragments in Escherichia coli, h

228 peritoneal injections of IL1B and intestinal recycling perfusion was measured; some mice were given d

229 Calvin cycle independent of light must also recycle phosphoglycolate.

230 Here, we analyse the role of photon recycling (PR) in assisting light extraction from perovs

231 D-Ia) leads to impaired hepatic autophagy, a recycling process important for cellular metabolism and

232 Autophagy, a catabolic recycling process, has been implicated as a critical pat

233 Autophagy, an integral part of the waste recycling process, plays an important role in cellular p

234 am a distillation/condensation system in the recycling processes for waste Hg-containing devices.

235 ies and final concentrations of dhurrin, the recycling products and free amino acids reached within t

236 to investigate accumulation of dhurrin, its recycling products and key general metabolites in four d

237 Little or no dhurrin or recycling products were present in the dry grain, but th

238 The dhurrin recycling products, however, were mainly located in the

239 ductase (GR), the enzyme responsible for GSH recycling, promoted ULBP2/5 surface expression.

240 Autophagy degrades and recycles proteins, macromolecules, and organelles for ce

241 t Rab11b controls the cell surface proteome, recycling proteins required for successful interaction w

242 Vps29, is a protein complex responsible for recycling proteins within the endolysosomal pathway.

243 sults suggest inhibition of phosphoinositide recycling provides a useful anti-angiogenic approach.

244 n; accordingly, synaptic vesicles need to be recycled rapidly to replenish the vesicle pool.

245 w that a further increase in the end-of-life recycling rate (EOL-RR) could contribute to minimizing t

246 le parameters (U.S. steel stocks per capita, recycling rate, product lifespan, and manufacturing yiel

247 Low recycling rates (RR, 13-20%) and dependence on virgin pl

248 tant ecosystem processes including elemental recycling rates and nutrient supply to living hosts.

249 However, the recycling rates of metals are still incomplete and, in p

250 mers and increase consumer-mediated nutrient recycling rates, potentially intensifying eutrophication

251 ocyst protein Sec15 and with endocytosis and recycling regulators Rab5, Rab7, and Rab11.

252 led to various receptors and regulates their recycling remains unknown.

253 Although this scrap is collected and recycled, remelting this scrap requires approximately 2

254 rin to proteolytic pathways, diminishing its recycling required for maintaining slit diaphragm integr

255 EC specific suppression of phosphoinositide recycling results in reduced tumor growth and tumor angi

256 e phosphatase implicated in synaptic vesicle recycling, results in PD.

257 or charging and operation, ease of component recycling/reuse, and reduced parts replacement is shown

258 translation because they are blocked by non-recycled ribosomes at stop codons.

259 chanism by which a helicase-like factor HelD recycles RNAP.

260 of an environmentally friendly approach for recycling smelting slag without generating any hazardous

261 x4Delta single mutants retain the ability to recycle Snc1, but a snx4Deltarcy1Delta mutant substantia

262 onship between Snx4, Drs2, Rcy1, and COPI in recycling Snc1 or FM4-64 is unclear.

263 Combined with recycling solutions, redox-active organic species could

264 The analytical data reveal increased recycling, some isolated imports of Islamic plant ash gl

265 During the recycling stage, post-terminational RNAPs one-dimensiona

266 They claim that reliance on narrow 'recycled' stimulus sets: object(s) centered on 'generic'

267 that entails extensive protein synthesis and recycling, structural remodeling, and considerable bioen

268 The peptidoglycan-recycling substrate binding protein (SBP) MppA, which is

269 the pH changes encountered during endocytic recycling, suggesting APOL1 forms a cytotoxic cation cha

270 Here we present evidence of recycled supra-subduction zone mantle wedge peridotite d

271 region 34 protein (Dom34)-dependent ribosome recycling system, which splits Lso2-containing, but not

272 pact of platinum-group element (PGE) mining, recycling techniques are being explored.

273 reviously unrecognized cross-talk with STING recycling that may have implications for STING agonism i

274 Additionally, we are able to recycle the catalysts from the isolated polymer chains.

275 lower decomposition, building up as the fuel recycles the components, and are a favored product of th

276 ite and avoid host detection, bacteria often recycle their peptidoglycan, transporting its components

277 embodiment exploits these same mechanisms by recycling them to support a different function altogethe

278 guanine exchange factor eIF2B to block eIF2 recycling, thereby halting translation initiation and re

279 of strumpellin with CAV1 stimulated integrin recycling, thereby promoting cell adhesion.

280 es the ability of the complex to efficiently recycle these proteins or to dynamically exchange them.

281 xides rapidly oxidized volatile Se products, recycling these compounds back to soluble forms.

282 ough 4-exo-trig radical cyclization could be recycled through an unprecedented triflation/fragmentati

283 tudy is an example of apple by-products (AP) recycling through a designed fermentation by selected au

284 scade expose the Cys-122-Cys-66 disulfide to recycling through thioredoxin.

285 onics and mantle dynamics necessitate mantle recycling throughout Earth's history, yet direct geochem

286 p but must be eliminated so that Scap can be recycled to bind and transport additional SREBPs.

287 The resulting poly(dihydrofuran) can be recycled to monomer via depolymerization with Grubbs cat

288 By coupling [4-(2)H]-NADH-recycling to an array of C=O, C=N, and C=C bond reductas

289 ephrocytes requires balanced endocytosis and recycling to maintain its structural integrity and that

290 ed Rab10 phosphorylation stalls vesicle fast recycling to promote PI3K-Akt immunological responses.

291 targeting endocytic trafficking and retromer recycling to the plasma membrane, we were able to reduce

292 n and releases endosome-derived vesicles for recycling to the plasma membrane.

293 of glycolytic substrates but, due to carbon recycling to the TCA cycle via enhanced anaplerosis, the

294 on of Rab10 potently blocks EHBP1L1-mediated recycling tubules and cargo turnover.

295 s findings that the type I receptor SMA-6 is recycled via the retromer complex, our work demonstrates

296 to advancing the understanding of endocytic recycling, we uncover a fundamentally different function

297 RNAP is recycled when, after releasing trapped nucleic acids, He

298 nction in allantoin degradation for nutrient recycling, whereas under stress, both genes may be invol

299 less likely to have been made by mixing and recycling, which has very important implications for the

300 the analyzed TM proteins, undergo endocytic recycling within a clearly defined subapical region.