ライフサイエンスコーパス: recycling

1 rocyte homeostasis and are required for iron recycling.

2 eparation as well as emulsifier and catalyst recycling.

3 nd benzophenone, with the latter amenable to recycling.

4 reviously unidentified stage, termed here as recycling.

5 ng robustness and cost-effective storage and recycling.

6 rforms controlled heat extraction and energy recycling.

7 f LRRK2 kinase inhibition in promoting cargo recycling.

8 at the ejection process might delay ribosome recycling.

9 mulated in terminals and facilitated vesicle recycling.

10 and NTPase HelD have been implicated in RNAP recycling.

11 emonstrated along with catalyst recovery and recycling.

12 a sequence-specific manner to regulate their recycling.

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

14 nd SV protein levels and rescued impaired SV recycling.

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

16 le ubiquitination predominantly inhibits SK2 recycling.

17 firming the role of deubiquitination in GCGR recycling.

18 ted by fungal saprotrophs involved in carbon recycling.

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

20 irecting damaged proteins towards proteasome recycling.

21 1 to bind to cargo proteins to promote their recycling.

22 e proteins following defective exocytosis or recycling.

23 ects in vesicle endocytosis, exocytosis, and recycling.

24 er, within the scope of Germany, a leader in recycling.

25 and AP2A1/2 as the adaptor for slower IGF1R recycling.

26 oth oligopeptide transport and peptidoglycan recycling.

27 BP14 in the auxin response through ubiquitin recycling.

28 n and 2) secondary overprinting by microbial recycling.

29 bited during NMDAR-LTD to decrease endocytic recycling.

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

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

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

33 econdary organic aerosols and atmospheric OH recycling.

34 livers them to lysosomes for degradation and recycling.

35 consistent with a deficiency in chromophore recycling.

36 ual steel demand and the scrap available for recycling.

37 alter net primary productivity and elemental recycling.

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

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

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

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

42 Catalyst recycling after pai-conjugated polymerization has previo

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

44 implicates Flot-1 as the adaptor for faster recycling and AP2A1/2 as the adaptor for slower IGF1R re

45 function in regulating transmembrane protein recycling and BMP signaling.

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

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

48 unctions with EARP to control both endocytic recycling and DCV maturation.

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

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

51 the cell periphery and thereby late endosome recycling and had a major impact on YAP signaling.

52 uces low-density lipoprotein receptor (LDLR) recycling and hence cholesterol uptake.

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

54 geodynamic context of crustal subduction and recycling and informs on survival of other early-formed

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 While recycling and reuse of fluoropolymers is performed on so

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

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

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

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

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

64 With variations in input electricity source, recycling, and efficiency, the life cycle global warming

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

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

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

68 ation, driving vacuolar remodeling, receptor recycling, and resolution of the organelles.

69 ective contributions of Pi uptake, metabolic recycling, and vacuolar sequestration to cytosolic Pi ho

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

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

72 al FcRn inhibitors selectively targeting IgG recycling are now moving rapidly toward clinical practic

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

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

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

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

77 0.03 pptv), indicating persistent I(y,part) recycling back to I(y,gas) as a result of active multiph

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

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

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

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

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

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

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

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

86 y raises the question of the extent to which recycling can be conducted without losing its mitigating

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

88 tom-efficient integrated cofactor/co-product recycling cascade employing cycloalkylamines as multifac

89 nts to support the NH(3) production and NADH recycling catalyzed by nitrogenase and diaphorase.

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

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

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

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

94 d pretreatment steps, increasing the overall recycling cost.

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

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

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

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

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

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

101 rtant for viral assembly, such as Golgi- and recycling endosome-derived membranes.

102 ging two peripheral membrane proteins of the recycling endosome.

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

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

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

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

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

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

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

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

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

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

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

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

115 mited contribution of vesicular transport in recycling endosomes.

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

117 utamine, which diverts membrane flux through recycling endosomes.

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

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

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

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

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

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

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

125 37 flame retardants at three Quebec e-waste recycling facilities.

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

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

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

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

130 by the conserved eukaryotic hibernation and recycling factor Lso2.

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

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

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

134 te, there are only limited options for their recycling from consumer articles.

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

136 free inositol from de novo biosynthesis and recycling from inositol polyphosphates and participates

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

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

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

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

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

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

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

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

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

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

147 Recycling is commonly included among the most viable opt

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

149 Finally, autophagy-dependent plastid recycling is induced in uninfected host cells.

150 neuronal activity regulates synaptic vesicle recycling is largely unknown.

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

152 electively degraded by autophagy, a cellular recycling machinery implicated in surveillance and quali

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

154 f Kif19a by inhibiting autophagy, a cellular recycling mechanism for damaged proteins and organelles.

155 llizable (Fc) receptor (FcRn) functions as a recycling mechanism to prevent degradation and extend th

156 tential strategies toward a sustainable ASSB recycling model.

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

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

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

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

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

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

163 xyalkanoates as carbon-storage molecules and recycling of amino acids to produce compounds that can p

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

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

166 This, in turn, further decreased anoxic recycling of bioavailable phosphorus to the water column

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

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

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

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

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

172 iomass-derived feedstocks would allow carbon recycling of distributed, energy-poor resources in the a

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

174 pyrimidine salvage pathways that enables the recycling of endogenous or exogenous-supplied pyrimidine

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

176 Recycling of ESS is shown to reduce terrestrial acidific

177 cretion of cell wall material with endocytic recycling of excess material incorporated into the plasm

178 iting molecular cues and is required for the recycling of focal adhesions.

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

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

181 Endocytic recycling of internalized transmembrane proteins is esse

182 complete processing of 18S rRNA and retarded recycling of late-acting ribosome biogenesis factors, re

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

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

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

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

187 stically, we find that PCSK9 can disrupt the recycling of MHC I to the cell surface by associating wi

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

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

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

191 g enzymes, it is consumed, necessitating the recycling of NAD(+) consumption products (i.e., nicotina

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

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

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

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

196 Our data indicate that COPI vesicle-mediated recycling of PAM from the cis-Golgi to the endoplasmic r

197 The metabolic recycling of phosphoglycolate was extensively studied in

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

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

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

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

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

203 of a retromer subunit completely eliminates recycling of Snc1 in the triple mutant (snx4Deltarcy1Del

204 Postendocytic recycling of Snc1 requires a phospholipid flippase (Drs2

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

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

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

208 Recycling of the contact lenses and their packaging amou

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

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

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

212 tion, and live cell imaging reveals aberrant recycling of the WNT ligand-binding protein WLS and mis-

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

218 Endosomal trafficking and subsequent recycling or degradation of these receptors is controlle

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 Our findings identify the late endosome recycling pathway as a key mechanism that controls YAP a

223 Inhibition of autophagy, the major cellular recycling pathway in mammalian cells, is a promising str

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

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

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

227 hetase is an essential enzyme of de novo and recycling pathways of NAD(+) biosynthesis in Mycobacteri

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

229 endosome via retrograde and plasma membrane recycling pathways.

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

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

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

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

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

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

236 As a mechanism, internal recycling processes during mycelial growth and an overal

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

238 nsight into rhizome development and nutrient recycling, processes critical for sustainable biomass ac

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

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

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

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

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

244 recently identified the endosome-associated recycling protein (EARP) complex and the EARP-interactin

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

246 enomenon was specific to GLUT4 because other recycling proteins were unaffected.

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

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

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

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

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

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

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

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

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

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

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

258 and spleen, the sites of iron absorption and recycling, respectively.

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

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

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

262 easing RNA product at intrinsic termination, recycling RNAP diffuses on the DNA template for reinitia

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

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

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

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

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

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

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

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

271 elation between hFcRn expression and albumin recycling supports hFcRn-mediated diversion of albumin f

272 acrophages of the CNS, with key functions in recycling synapses and maintaining the local environment

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

274 ual scenarios, insufficient to meet existing recycling targets.

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

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

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

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

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

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

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

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

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

287 ytosis is facilitated by PKA activation, SK2 recycling to synaptic membranes after TBS is inhibited b

288 t blockade of CAR ubiquitination induces CAR recycling to the cell surface, leading to increased CAR

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

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

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

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

293 We find that the axonal traffic of recycling vesicles is not supported by ubiquitous microt

294 When 60S recycling was inhibited, disomes accumulated at stop cod

295 elated processes, such as glutamate receptor recycling, we also identified altered synthesis of prote

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

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

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

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

300 x3 is crucial for NT closure via its role in recycling WLS in order to control levels of WNT signalin