ライフサイエンスコーパス: recycling

1 n initiating early lagging-strand polymerase recycling.

2 ufacturing location and ensuring end of life recycling.

3 s allows imaging of integrin endocytosis and recycling.

4 also promising for waste glass and coal ash recycling.

5 moting intracellular catabolism and nutrient recycling.

6 le in translation re-initiation and ribosome recycling.

7 nd damaged organelles from the cytoplasm for recycling.

8 d rainfall, indicative of amplified moisture recycling.

9 tion of the holoenzyme to trigger polymerase recycling.

10 ended by the Australian Guidelines for Water Recycling.

11 ts role with respect to alpha6beta4 integrin recycling.

12 hich is critical for regulation of ubiquitin recycling.

13 V maturation through its role in DCV protein recycling.

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

15 lipoprotein receptor (LDLR), preventing its recycling.

16 iever complexes critical for endosomal cargo recycling.

17 suggesting roles in endocytosis and vesicle recycling.

18 atalyst, polymer purification and by-product recycling.

19 pid membrane fission during synaptic vesicle recycling.

20 product purification and the transfer agent recycling.

21 NA and polypeptide, ribosome disassembly and recycling.

22 ) signaling by enhancing their stability and recycling.

23 ent to endosomal membranes and GLUT1 surface recycling.

24 hibiting intestinal iron absorption and iron recycling.

25 fine the dynamical states of vesicles during recycling.

26 lay important roles in postsynaptic receptor recycling.

27 dge a system toward an appreciable degree of recycling.

28 ds is giving rise to new approaches in waste recycling(17), industrial fermentation(18), bioremediati

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

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

31 olic mechanism for macromolecule and protein recycling, allows the maintenance of amino acid pools an

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

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

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

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

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

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

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

39 ecialized vesicles called autophagosomes for recycling and degradation.

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

41 iple studies have demonstrated DAT endocytic recycling and enhanced surface delivery in response to v

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

43 bay in the Baltic Sea, thereby inhibiting P recycling and further eutrophication (B).

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

45 howed convergent disruptive effects on AMPAR recycling and glutamate uncaging-induced structural and

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

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

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

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

50 echanism that drives increased AMPA receptor recycling and LTP.

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

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

53 mbrane proteins, disrupting synaptic vesicle recycling and neurotransmission.

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

55 ts into a dual role for ABCE1 in translation recycling and reinitiation and revisits the interpretati

56 s define the vesicle dynamical states during recycling and reveal their activity-dependent modulation

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

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

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

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

61 Metal recycling and technological change will contribute to su

62 ccounting for spatial variations in membrane recycling and tension.

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

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

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

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

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

68 ellular material to lysosomes for degrading, recycling, and generating molecules that fuel cellular m

69 uced faster receptor internalization, slower recycling, and longer intracellular sojourn of ACKR3 tha

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

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

72 massive lysosome swelling, disrupts membrane recycling, and, in macrophages, blocks phagosome maturat

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

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

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

76 Correct identification of recycling at basaltic vents will improve (lower) estimat

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

78 ng being a key regulator of synaptic vesicle recycling at nerve terminals.

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

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

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

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

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

84 inds K63-linked polyubiquitin, disrupts Snc1 recycling causing aberrant accumulation in internal comp

85 otherapy.Autophagy is a cellular process for recycling cell constituents, and is essential for T cell

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

87 argets to either degradation or an undefined recycling compartment.

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

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

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

91 wever, it remains unclear whether the photon recycling effect is significant enough to improve solar

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

93 nd re-emission processes to determine photon recycling efficiency in hybrid perovskite with its singl

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

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

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

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

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

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

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

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

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

103 om the endosome, we find that disrupting the recycling endosome reduces ciliary polycystin-2 and caus

104 ycystin-2 and causes its accumulation in the recycling endosome.

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

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

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

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

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

110 ssessed the transport of BACE1 from early to recycling endosomes and have identified essential roles

111 mimetic S498D BACE1 mutant was trafficked to recycling endosomes at a faster rate compared with wild-

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

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

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

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

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

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

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

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

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

121 sparing synapses that were large and lacked recycling endosomes.

122 the Golgi apparatus, presumably through the recycling endosomes.

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

124 red for Golgi trans-Golgi network 46 (TGN46) recycling, exhibited Ca(2+)-stimulated interactions with

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

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

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

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

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

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

131 romer and ESCRT that balance degradative and recycling functions.

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

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

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

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

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

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

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

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

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

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

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

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

144 Although endosome-to-plasma membrane recycling is critical for many cellular processes, much

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

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

147 Synaptic vesicle recycling is essential for maintaining normal synaptic f

148 actor by reducing thiosulfate to sulfide and recycling it.

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

150 and several components of vesicle fusion and recycling machinery as essential for the maintenance of

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

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

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

154 ly or following evoked release share similar recycling mechanisms.

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

156 ted OS, as well as providing a mechanism for recycling metabolic intermediates back to the outer reti

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

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

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

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

161 s, catabolizing extracellular peptides while recycling nitrate to nitrite.

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

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

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

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

166 organelles responsible for the breakdown and recycling of cellular machinery.

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

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

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

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

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

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

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

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

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

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

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

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

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

180 d and RNAP, allowing efficient targeting and recycling of Mfd and expedient conflict resolution.

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

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

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

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

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

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

187 Recycling of N and P by Noctiluca may supply substantial

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

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

190 ariation in acquisition, assimilation and/or recycling of plasma proteins that predicted overwinter s

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

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

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

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

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

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

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

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

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

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

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

202 ibit superior catalytic properties following recycling of the catalysts.

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

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

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

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

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

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

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

210 es (initiation, elongation, termination, and recycling) of the translation mechanism.

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

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

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

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

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

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

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

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

219 igh albumin plasma levels through a cellular recycling pathway.

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

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

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

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

224 tosed cell surface membrane proteins rely on recycling pathways for their return to the plasma membra

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

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

227 of the endomembrane system in intracellular recycling pathways.

228 G did alter ENaC insertion from constitutive recycling pathways.

229 enables reliable tracking of the spontaneous recycling pool.

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

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

232 e experiments employing a six-electron photo-recycling process that modify the terminal group of a se

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

234 oles of the two cytoskeletal proteins on the recycling processes of SK2 channels from endosomes.

235 in turn modulates macrophage beta1 integrin recycling, promoting macrophage recruitment and ultimate

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

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

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

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

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

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

242 alf-life is the ability to interact with the recycling receptor, FcRn, in a pH-dependent manner.

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

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

245 ent intracellular sorting for degradation or recycling regulates the strength and specificity of down

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

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

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

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

250 Vps35 knockdown revealed that DAT endocytic recycling requires intact retromer.

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

252 We further show that the early-endosome recycling route and its control though the Vam6>Gtr1/Gtr

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

254 Only a model with this novel NOx recycling route reproduces levels of gaseous nitrous aci

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

256 novo biosynthesis pathways and by salvage or recycling routes.

257 tussis and Bordetella parapertussis have the recycling/salvage pathway genes pncA and pncB, for use o

258 The novel phospholipid-recycling scheme opens new avenues for metabolic enginee

259 can be used at least 10 times in a pH-based recycling scheme that enables the catch and release of o

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

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

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

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

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

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

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

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

268 Synaptic vesicle recycling studies suggested functional synaptic vesicle

269 roteins involved in thylakoid membrane lipid recycling suggested more abrupt repartitioning of carbon

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

271 wide range of further analytical methods and recycling tests.

272 Photon recycling, that is, iterative self-absorption and re-emi

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

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

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

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

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

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

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

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

281 n DA action, and provides for presynaptic DA recycling to replenish neurotransmitter pools.

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

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

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

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

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

287 This GluK2-mediated increase in surface recycling translated to a significant increase in KCC2 e

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

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

290 physiology to monitor evoked and spontaneous recycling vesicle pools.

291 We found that the total number of recycling vesicles was equal to those retrieved through

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

293 ould be explained by a single pool of slowly recycling vesicles.

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

295 different physiological function other than recycling vitamin K.

296 clusively follows this pathway revealed that recycling was subject to metabolic control through the R

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

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

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

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