ライフサイエンスコーパス: recycle

1 creased the amount of aluminum available for recycle.

2 regenerated by heating and can therefore be recycled.

3 iverted from degradation in lysosomes and is recycled.

4 dge a system toward an appreciable degree of recycling.

5 n initiating early lagging-strand polymerase recycling.

6 also promising for waste glass and coal ash recycling.

7 ufacturing location and ensuring end of life recycling.

8 s allows imaging of integrin endocytosis and recycling.

9 moting intracellular catabolism and nutrient recycling.

10 le in translation re-initiation and ribosome recycling.

11 nd damaged organelles from the cytoplasm for recycling.

12 d rainfall, indicative of amplified moisture recycling.

13 tion of the holoenzyme to trigger polymerase recycling.

14 ended by the Australian Guidelines for Water Recycling.

15 ts role with respect to alpha6beta4 integrin recycling.

16 hich is critical for regulation of ubiquitin recycling.

17 V maturation through its role in DCV protein recycling.

18 naling by modulating IL-6R stabilization and recycling.

19 lipoprotein receptor (LDLR), preventing its recycling.

20 NA and polypeptide, ribosome disassembly and recycling.

21 ) signaling by enhancing their stability and recycling.

22 ent to endosomal membranes and GLUT1 surface recycling.

23 hibiting intestinal iron absorption and iron recycling.

24 fine the dynamical states of vesicles during recycling.

25 lay important roles in postsynaptic receptor recycling.

26 ded in landfills, with the rest utilized for recycling (26%) and energy recovery (36%) via combustion

27 WAP ice scouring may be recycling 80 000 tonnes of carbon yr(-1) .

28 Furthermore, the amount of recycled albumin in cell culture media corresponded to F

29 dynamic phosphorylation events and endocytic recycling, although the molecular mechanisms that contro

30 Given the importance of N recycling, an important but underestimated effect of NDE

31 alytic activity is maintained even after ten recycles and CEES is completely decontaminated in 3 mins

32 ntial for purine biosynthesis and methionine recycling and affects methylation of DNA, histones, and

33 ed cells illustrate that FcRn mediates basal recycling and bidirectional transcytosis of albumin and

34 e bacterial PG utilizing metabolic cell wall recycling and biosynthetic machineries.

35 Autophagy is a physiological process for the recycling and degradation of cellular materials.

36 Autophagy is an intracellular recycling and degradation pathway that depends on membra

37 ecialized vesicles called autophagosomes for recycling and degradation.

38 s complexes dedicated to opposing functions: recycling and degradation.

39 minal PDZ-binding motif was required for DAT recycling and exit from retromer.

40 his explains how a single Rab can coordinate recycling and fusion on endosomes.

41 graded by the lysosome but instead undergoes recycling and incorporation into fibrils, a process depe

42 g in a higher turnover rate due to decreased recycling and increased degradation.

43 ation at Ser-845, which is crucial for AMPAR recycling and is known to be dephosphorylated in the pre

44 n aid the design of better processes for kef recycling and low cost photovoltaics.

45 echanism that drives increased AMPA receptor recycling and LTP.

46 l the balance between GLP-1R plasma membrane recycling and lysosomal degradation and, in doing so, de

47 d a new function for Vps13 in early endosome recycling and Neo1 localization.

48 mbrane proteins, disrupting synaptic vesicle recycling and neurotransmission.

49 helial MV miR-17/221 promoted beta1 integrin recycling and presentation back onto the surface of macr

50 These results also associate glutamate recycling and sleep regulation, adding further complexit

51 has been implicated in regulating endosomal recycling and sorting of several important neuronal rece

52 cells (A-ICs) is regulated by apical vesicle recycling and stimulated by cAMP.

53 itter release preserve their identity during recycling and syt1 function in suppression of spontaneou

54 Metal recycling and technological change will contribute to su

55 ccounting for spatial variations in membrane recycling and tension.

56 damental mechanisms of intracellular albumin recycling and the possibility to tune albumin-based ther

57 stinct effects on the apical and basolateral recycling and transcytotic pathways, demonstrating that

58 BRI1 abundance is regulated by endosomal recycling and vacuolar targeting, but the role of vacuol

59 ultiple rounds of exo-endocytosis, involving recycling and/or degradation of synaptic proteins.

60 material transport/metabolism and amino acid recycling, and accordingly disfavored many genes with ot

61 number, changes in rates of internalization, recycling, and membrane delivery were investigated.

62 igment dephosphorylation, visual chromophore recycling, and ultimately photoreceptor dark adaptation.

63 s can be useful resources, offering a simple recycling approach for similar organic-inorganic solid w

64 gest that characteristic signatures of clast recycling are different in the two environments.

65 d as rainfall reaching the soil and directly recycled as transpiration increased to 100%.

66 titative confocal microscopy, and an albumin-recycling assay.

67 c activity, plasticity, and synaptic vesicle recycling at distinct developmental and activity stages.

68 tobleaching and endocytosis assays, integrin recycling between both sites requires the small GTPase A

69 t in facilitating continental-scale moisture recycling but are poorly understood at regional scales.

70 cycling factor, are known to be required for recycling, but there is controversy concerning whether t

71 sink, many wall polymers can be degraded and recycled by plant cells, either via direct re-incorporat

72 etion relies on urea transporter-driven urea recycling by the kidneys and on urea production by liver

73 defined here as cascades relying on cofactor recycling by the metabolism or on a metabolite from the

74 ination, the released bromide is reoxidized (recycled) by chlorine to HOBr, leading to further electr

75 anisms are cellular digestion processes that recycle cellular components and contribute to protein ho

76 effective and continued leaching of REEs by recycled citric acid, with up to 392 mg of Nd L(-1) and

77 ia have attracted much attention as hosts to recycle CO2 into valuable chemicals.

78 Using renewable energy to recycle CO2 provides an opportunity to both reduce net C

79 The plasma membrane and the endocytic recycling compartment (ERC) are both highly enriched in

80 argets to either degradation or an undefined recycling compartment.

81 PINK1 regulate the mitophagy pathway, which recycles damaged mitochondria following oxidative stress

82 Cargo release and vesicle recycling depend on the fate of the pore, which may rese

83 ane were previously shown to facilitate both recycling-dependent and -independent iron uptake.

84 GLUT4 leads to an arrest of synaptic vesicle recycling during sustained AP firing, similar to what is

85 The photon recycling efficiencies are revealed to be less than 0.5%

86 Using a H2 recycling electrochemical system (HRES) we achieved high

87 its dependence upon long product lifespans, recycling end-of-life products is expected to be the lea

88 imentin interacts with Jagged, impedes basal recycling endocytosis of ligands, but is required for ef

89 of the henipavirus fusion protein occurs in recycling endosomal compartments.

90 somal trafficking, leading to expansion of a recycling endosomal signaling compartment containing Sor

91 mbryos, Nuf/FIP3, a Rab11 effector, mediates recycling endosome (RE)-based vesicle delivery to the cy

92 results demonstrate a requirement for normal recycling endosome function in AMPAR-dependent synaptic

93 early endosome marker Rab5 and the long loop recycling endosome marker Rab11 and to a much lesser ext

94 of VAMP2 or NCS1, whereas recruitment of the recycling endosome marker VAMP3 was unaffected.

95 tenin/E-cadherin complexes to pericentriolar recycling endosomes (PCREs).

96 gments are transported via Rab11A-containing recycling endosomes (RE) and use both microtubules (MT)

97 itment corresponds to directed exocytosis of recycling endosomes (REs) containing these integrins and

98 endritic secretory pathway and accumulate in recycling endosomes (REs) located in dendrites and spine

99 both found to traffic through Rab11-positive recycling endosomes (REs), suggesting a model in which F

100 cally, we demonstrate that NHE9 localizes to recycling endosomes in hBMVECs where it raises the endos

101 LTP, kainate-receptor-dependent LTP recruits recycling endosomes to spines, enhances synaptic recycli

102 ecycling of SK2 channels from both early and recycling endosomes while filamin A probably aids the re

103 ded sensors between the surface membrane and recycling endosomes, and is presumably triggered by chan

104 s have not detected DAT targeting to classic recycling endosomes, suggesting that internalized DAT ta

105 zes with PD-L1 at the plasma membrane and in recycling endosomes, where it prevents PD-L1 from being

106 colocalizes with KSR1 and Rab11, a marker of recycling endosomes, whereas p-ERK associates predominan

107 a1 can be rapidly altered by Rab11A-positive recycling endosomes.

108 ably aids the recycling of SK2 channels from recycling endosomes.

109 sparing synapses that were large and lacked recycling endosomes.

110 the Golgi apparatus, presumably through the recycling endosomes.

111 he cotransmission, we targeted the glutamate-recycling enzyme glutaminase (gene Gls1).

112 on factors, elongation factor G and ribosome recycling factor, are known to be required for recycling

113 entified roles played by ribosome rescue and recycling factors in regulating ribosome homeostasis.

114 operate, consistent with the role of CpI in recycling Fdred that accumulates during fermentation.

115 Recycled fiber mill effluents, tested for the first time

116 llular mechanisms that mediate DAT endocytic recycling following constitutive and regulated internali

117 dissociate into subunits and are presumably recycled for new rounds of translation.

118 -bound respiratory syncytial virus G rapidly recycles from the membrane via clathrin-mediated endocyt

119 ion of iron absorption in the duodenum, iron recycling from erythrocytes, and iron mobilization from

120 ssociated with both endocytic and phagocytic recycling functions, confirming evolutionary and functio

121 romer and ESCRT that balance degradative and recycling functions.

122 s for stochastically scanning, rewiring, and recycling genetic information on an extraordinary scale.

123 The conversion from un-recycled glass to favorable materials is of great signif

124 reases kinetic competition between sRNAs and recycles Hfq from the sRNA-mRNA duplex.

125 e on PARD6B for apical, but not basolateral, recycling, implicating this cell polarity gene in assemb

126 llular and foreign material are degraded and recycled in eukaryotic cells.

127 ough hydrothermal liquefaction, and nutrient recycling in a laboratory-scale system.

128 ch is in accord with the established role of recycling in GPCR resensitization.

129 dence supporting the occurrence of cell-wall recycling in plants, make predictions regarding the deve

130 lorine assimilation provides key evidence of recycling in submarine samples, while bands of oxides bo

131 The efficiency of iron recycling in the equatorial Pacific implies the evolutio

132 protoporphyrin IX (SnPP) decreased heme-iron recycling in the liver and ameliorated anemia in the Th3

133 ration and repair, and their degradation and recycling in the lysosome is essential for cellular main

134 e propose that NHE9 regulates TfR-dependent, recycling-independent iron uptake in hBMVECs by fine-tun

135 recombination lifetime instead of the photon-recycling-induced photon propagation as the origin of th

136 a is not merely a toxic waste product but is recycled into central amino acid metabolism to maximize

137 used as an effective tracer of oceanic crust recycled into the mantle, as a diagnostic criterion by w

138 rts cell growth and survival autonomously by recycling intracellular proteins and/or organelles.

139 Unfortunately, their recycling is currently limited, and the conventional tec

140 Moreover, we found that KCC2 recycling is enhanced by protein kinase C-mediated phosp

141 Synaptic vesicle recycling is essential for maintaining normal synaptic f

142 Based on these results, we propose that recycled jute should be considered for fabrication of hi

143 If this recycled litter nitrogen is retained in ecosystem pools

144 These data suggested that LDLR-R410S recycles loaded with its LDL-cargo.

145 The production system contains a recycling loop leading to nonlinearities.

146 These results define the DAT recycling mechanism and provide a unifying explanation f

147 d find that it is associated with a moisture recycling mechanism, rather than the classic albedo-base

148 fragment or primer-primase complexes as the recycling mechanism.

149 ly or following evoked release share similar recycling mechanisms.

150 on-Bassham cycle activity may be involved in recycling metabolic CO2 Glandular trichomes cope with ox

151 ng the developmental processes to which wall recycling might contribute, and identify outstanding que

152 at intraseasonal timescales using a dynamic recycling model, based on a Lagrangian trajectory approa

153 This argues against recycling models and in favor of pulling models.

154 anation for this unusual requirement are (1) recycling models, in which the ligand must be endocytose

155 Livestock recycle more than 43.2 x 10(9) kg of human-inedible food

156 mplex called retriever that is essential for recycling numerous cell-surface cargoes from endosomes a

157 Renal proximal tubular cells constantly recycle nutrients to ensure minimal loss of vital substr

158 an often be met by flow cells operating with recycle of the reactant solution.

159 cling endosomes to spines, enhances synaptic recycling of AMPA receptors to increase their surface ex

160 developed an innovative method for the inner-recycling of biomass that could harvest the typical micr

161 ents of the retromer complex, which mediates recycling of cargo from endosomes to the Golgi.

162 nce of phage genes and genes involved in the recycling of cellular material.

163 ophagy is a protective mechanism that allows recycling of defective organelles and proteins to mainta

164 nsaminitis, revealing enhanced enterohepatic recycling of deglucuronidated tacrine in this subgroup,

165 hingolipids by both de novo biosynthesis and recycling of exogenous sphingolipids.

166 Lowered IIS thus elevates endosomal recycling of GJs in neurons and other cell types, pointi

167 Endosomal recycling of GJs was also stimulated in cultured human c

168 supply to the brain and for the reuptake and recycling of glutamate in the synapse.

169 This enzyme contributes to the cellular recycling of glycosphingolipids such as galabiosylcerami

170 This process supports the recycling of heavier N into the deep mantle in this sect

171 Recycling of hydrogen gas (H2) produced at the cathode t

172 by RAB4A, an essential regulator of the fast recycling of integrin beta3.

173 ynaptic AMPA receptors, mediated by enhanced recycling of internalized AMPA receptors back to the pos

174 nitrate consumption must be supported by the recycling of iron within surface waters.

175 stasis via tight control of partitioning and recycling of misfolded proteins.

176 interaction is key to the retromer-dependent recycling of mitochondrial DLP1 complex during mitochond

177 k the VPS35-DLP1 interaction and inhibit the recycling of mitochondrial DLP1 complexes.

178 by allowing indirect oxidation to Mn(IV) and recycling of Mn(II).

179 ents, as well as opportunities for efficient recycling of molecules from dead cells.

180 nosa catalyzes the first cytoplasmic step in recycling of muropeptides, cell-wall-derived natural pro

181 eration of ATP and reducing equivalents, and recycling of N and possibly CO2 through refixation.

182 rase (NAMPT) is a key enzyme involved in the recycling of nicotinamide to maintain adequate NAD level

183 osomal targeting can impact the activity and recycling of receptors.

184 t not retained efficiently, causing repeated recycling of retinol between plasma and tissues (541 com

185 he translation process that would favour the recycling of ribosomes.

186 alpha-Actinin2 facilitated recycling of SK2 channels from both early and recycling

187 endosomes while filamin A probably aids the recycling of SK2 channels from recycling endosomes.

188 via selective activation, concatenation, and recycling of specific subsequences; and (iii) enabling t

189 Efficient recycling of subducted sedimentary nitrogen (N) back to

190 Accordingly, these data elucidate the recycling of subsolidus material into voluminous rhyolit

191 per function of synapses relies on efficient recycling of synaptic vesicles.

192 We verify that Vps34 is required for recycling of the beta2-adrenoceptor (beta2AR), a prototy

193 By performing treatment and recycling of the bleed stream, its disposal decreases an

194 ibit superior catalytic properties following recycling of the catalysts.

195 emonstrated that Vps4, the key regulator for recycling of the ESCRT-III complex, is required for effi

196 and Neo1, have nonredundant functions in the recycling of the synaptobrevin-like v-SNARE Snc1 from ea

197 Further analyses showed that recycling of the TCR-CD3 complex was impaired, leading t

198 these cells by upregulating Rab27-dependent recycling of the transmembrane matrix metalloprotease, M

199 maintenance of photoreceptors, including the recycling of visual chromophore for the opsin visual pig

200 ring the last glacial period, with much less recycling of water and probably reduced plant transpirat

201 by inhibiting TORC1, leading to release and recycling of zinc from degraded proteins.

202 e for initiation by favoring either ribosome recycling on the same mRNA or de novo ribosome recruitme

203 ubiquitin itself to determine whether it is recycled or degraded in the vacuole.

204 tor internalization, down-regulation, direct recycling, or Smad signaling were unaffected by motif mu

205 d through complex food webs that extensively recycle organic material, but lose a fraction as particu

206 maximizes their collective metabolic rate by recycling organic carbon through complementary excretion

207 rubrisubalbicans up-regulates the methionine recycling pathway as well as phyto-siderophore synthesis

208 Gtr1 and Gtr2 control the recycling pathway independently of TORC1 regulation thro

209 It is thus evident that the canonical recycling pathway is under the regulation of mTORC1 and

210 could be partially affected by the ascorbate recycling pathway, as lines under-expressing monodehydro

211 RC6A is recycled via the Rab11-positive slow recycling pathway, which may be responsible for ensuring

212 igh albumin plasma levels through a cellular recycling pathway.

213 o deficient sorting into a retromer-mediated recycling pathway.

214 pontaneous and evoked vesicles use separable recycling pathways and then partially intermix during su

215 results suggest that spontaneous and evoked recycling pathways are segregated during the retrieval p

216 We examined synaptic vesicle recycling pathways at complexin null neuromuscular junct

217 delivery of GLP-1 gene through enterohepatic recycling pathways of bile acids.

218 transport function of myosin-5B in cellular recycling pathways.

219 of the endomembrane system in intracellular recycling pathways.

220 G did alter ENaC insertion from constitutive recycling pathways.

221 ts of intrinsic viscosity indicate that, the recycled PE comprises longer linear chains.

222 The observed delay in thermal events of recycled PE reflects different types of PE in the plasti

223 , and 188 kJ/mol to 268 kJ/mol, for neat and recycled PE, respectively, and the so-called compensatio

224 ion of NOx formed in thermal processes using recycled plastics such as polyethylene (PE).

225 enables reliable tracking of the spontaneous recycling pool.

226 omycin indicated that spontaneous and evoked recycling pools partially intermix during the release pr

227 aging assay, we further determined that KCC2 recycling primarily occurs within 1-2 h and that GluK2 p

228 These functions result, for example, in recycling processed pseudogenes into mRNAs or lncRNAs wi

229 byproduct yield improvement, and end-of-life recycling rate improvement.

230 ainfall levels are largely determined by the recycling rate of local moisture, regulated by planetary

231 Notch transport assays reveal that receptor recycling rates increase when GSK3beta activity is inhib

232 Internalization and recycling rates of the ACKR3 R142(3.50)A substitution in

233 Given plausible iron recycling rates, seasonal variability in nitrate concent

234 nsitive to waste composition, energy mix and recycling rates.

235 ation, either by starvation or by inhibitor, recycling receptors and plasma membrane lipids, such as

236 ion into internal vesicles while in parallel recycling receptors via tubular carriers back to the Gol

237 s governing synaptic vesicle dynamics during recycling remain poorly understood.

238 A complex link exists between cell-wall recycling/repair and the manifestation of resistance to

239 Here we report that endocytic recycling requires active mechanistic target of rapamyci

240 Bacterial ribosome recycling requires breakdown of the post-termination com

241 addition to their canonical role in protein recycling, REs also mediate forward secretory traffickin

242 ersee mRNA and nascent chain destruction and recycle ribosomal subunits.

243 We discovered that yeast has a recycling route from endosomes to the cell surface that

244 lore the impact of a recently discovered NOx recycling route, namely photolysis of particulate nitrat

245 paration units as well as to utilise CO2 and recycle side-products in the process are described in th

246 acuole for degradation, can also function as recycling signal to sort a SNARE into COPI vesicles in a

247 per initial product is crucial to make waste recycling simpler.

248 Furthermore, increasing the activity of the recycling small guanosine triphosphatases (GTPases) Rab4

249 ion was occasionally noted, association with recycling/sorting structures was not observed.

250 This study attempts to recycle spent Cu/Fe layered double hydroxide (Cu/Fe-LDH)

251 ts excellent water treatment performance and recycle stability, such a hybrid is promising for large

252 However, recycling strategies for future CM quantities in end-of-

253 ironmental and economic implications of such recycling strategies must be considered.

254 thod for an efficient, green, and economical recycling strategy for Sn with economic value added that

255 A new type of waste recycling strategy is described in which nitrogen oxides

256 Synaptic vesicle recycling studies suggested functional synaptic vesicle

257 ionarily conserved intracellular degradation/recycling system that is essential for cellular homeosta

258 a useful tool in this regard; its ability to recycle target DNA molecules results in markedly improve

259 wide range of further analytical methods and recycling tests.

260 t, and, especially, the need to separate and recycle the catalysts.

261 namide phosphoribosyltransferase enzyme that recycles the nicotinamide precursor, whereas the nicotin

262 In the presence of target DNA, the Exo III recycles the target DNA by selectively digesting the dye

263 y to initiate Fe/S cluster transfer to IRP1, recycling the cytosolic apo-IRP1 into holo-aconitase.

264 balance, producing NADPH for biosynthesis by recycling the two other primary redox carriers, NADH and

265 s, B cells did not degrade the complexes but recycled them in native form to the cell surface, enabli

266 e of their ligands by FcRn-mediated antibody recycling, thereby evading ligand renal clearance and re

267 suppresses autophagy and maintains endosomal recycling, thereby preventing endosomes and autophagosom

268 not adhere or blend, creating challenges for recycling these materials.

269 another SNX5 and SNX6 binding receptor that recycles through SNX-BAR heterodimers, but not via the r

270 vesicles with the plasma membrane, and then recycles through the endocytic pathway to the Golgi for

271 oximately 40% increase in the amount of KCC2 recycled to the membrane during this time period.

272 alf of the internalized GPR15 receptors were recycled to the plasma membrane.

273 The lagging-strand polymerase sometimes recycles to begin the synthesis of a new Okazaki fragmen

274 ows constitutive VE-cadherin endocytosis and recycling to contribute to adherens junction dynamics wi

275 e basic mechanism(s) governing sGC heme iron recycling to its NO-sensitive, reduced state remain poor

276 ological and metabolic contributions of wall recycling to plant growth and development are largely un

277 oglycosidase D under conditions that inhibit recycling to the ER, indicating that it normally reaches

278 cargo away from degradation, promoting cargo recycling to the Golgi.

279 R undergoes constitutive internalization and recycling to the plasma membrane with agonist binding in

280 sphate 5-kinase and Rab11 to facilitate hERG recycling to the plasma membrane.

281 und that the GluK2-mediated increase in KCC2 recycling to the surface membrane translates to a hyperp

282 ggesting that the incorporation of Neo1 into recycling tubules may influence their formation.

283 pt7 from cargo-bound CSC during formation of recycling tubules.

284 usly, the oxidant (IBX) and solvent could be recycled up to five times with only a slight loss in act

285 spirit drinks sector, counterfeiters often 'recycle' used genuine packaging, or employ good quality

286 physiology to monitor evoked and spontaneous recycling vesicle pools.

287 bability (0.7), from a single pool of slowly recycling vesicles, indicating that the distinct respons

288 id emissions from landfills, (v) waste being recycled, (vi) waste for energy recovery, (vii) total wa

289 onist-independent internalization, GPRC6A is recycled via the Rab11-positive slow recycling pathway,

290 However, N recycling via litter decomposition provides most of the

291 frastructure systems that use stormwater and recycled water to augment groundwater recharge through s

292 es, California, we illustrate how delivering recycled water to spreading basins could be optimally im

293 ntralized Hyperion system could deliver more recycled water to the Hansen Spreading Grounds, this sys

294 operation schedule for systems that deliver recycled water to underutilized stormwater spreading bas

295 ally, block copolymer synthesis and catalyst recycling were demonstrated.

296 ste glass end up in landfills without proper recycling, which aggravates the burden of waste disposal

297 titutive endocytosis, endocytic sorting, and recycling, which delivers nutrients to the lysosomes.

298 t ensure efficient proteolysis and ubiquitin recycling while preventing nonselective proteolysis, and

299 Following fusion, vesicles are retrieved and recycled within nerve terminals.

300 The catalyst is easily recycled without noticeable loss of catalytic activity.