ライフサイエンスコーパス: be released from

1 The bound coronene was released from 1 upon addition of benzene, and both t

2 ntaining nucleic acid and protein cargo that are released from a multitude of cell types and have gai

3 Peptide neuromodulators are released from a unique organelle: the dense-core ves

4 o-sized membrane vesicles (50-120 nm), which are released from a wide variety of cells.

5 As GLUC can also be released from a reporter construct by internal signal

6 small amount of the studied metal oxides NPs was released from abrasion of the textiles coated by the

7 Soluble CD206 is released from activated LPMs and increased concentrat

8 Polyphosphate (polyP) is released from activated platelets and mediates FXII a

9 In this work we obtained material that was released from aged paint containing nano-TiO2, chara

10 Urinary extracellular vesicles (uEVs) are released from all regions of the kidney's nephron an

11 the body's principal hyperglycaemic hormone, is released from alpha-cells of the pancreatic islet.

12 ollectively these results suggest that ABCF1 is released from and binds to shed POSs in an autocrine

13 essary and sufficient for suppressed buds to be released from apical dominance.

14 ABCF1 was released from apoptotic cells and selectively bound

15 inhibit itch and show that dynorphin, which is released from B5-I neurons, is a key neuromodulator o

16 ILPs are released from BAGs themselves in an activity-depende

17 Volatile organic compounds (VOCs) are released from biogenic sources in a temperature-depe

18 is important for autoinhibition and needs to be released from both kinases that form the dimer.

19 , 9.4 GBq of (240)Pu and 29.7 GBq of (241)Am were released from both fire events corresponding to a s

20 A great number of compounds were released from bread matrices in mastication, and th

21 FGF22 is released from CA3 pyramidal neurons and organizes the

22 s consisting of endogenous and exogenous Tau are released from cells and demonstrate their potential

23 the non-vesicular extracellular compartment are released from cells as full-length precursors and ar

24 Exosomes are released from cells both in vitro and in vivo, and h

25 data suggest that the different sgp130 forms are released from cells into their immediate surrounding

26 ) and some members of the Enterovirus genus, are released from cells nonlytically in membranous vesic

27 In addition, components can be released from cells as secretory molecules, enzymes,

28 These miRNAs may be released from cells in extracellular vesicles that ar

29 detected in plasma and therefore proposed to be released from cells in whole blood.

30 The intracellular protein HMGB1 is released from cells and acts as a damage-associated m

31 DAs are released from centrosomes in mitosis by an undefined

32 calize with Kv2.1 clusters in live cells and are released from channels activated by voltage stimuli.

33 turn assembles with the large subunit as it is released from chaperonins.

34 The mechanism whereby gaseous protein ions are released from charged solvent droplets during electr

35 ngs provide molecular insights into how PCNA is released from chromatin to finalize DNA replication/r

36 they demonstrate in HeLa cells that once RNA is released from chromatin, the modifications are surpri

37 has undergone splicing, but before the mRNA is released from chromatin.

38 h mediated by Scc1-cohesin, which in mitosis is released from chromosomes by Wapl and separase.

39 Endotrophin is released from COL VI and promotes pleiotropic pro-fib

40 ations can be explained if ACh and glutamate are released from common vesicles onto spatially segrega

41 oxygenase products thromboxane and PGF2alpha are released from coronary artery PVAT from pigs.

42 Upon ETI induction, CKIs are released from CPR5 to cause overactivation of anothe

43 The delivered substrates could be released from CPS into the cytosol through desthiobio

44 "danger signal" adenosine triphosphate (ATP) is released from damaged cells and promotes proliferatio

45 In TPA-induced skin inflammation, MIF is released from damaged keratinocytes and then triggers

46 Here, we show that dsRNA, which is released from damaged skin, activates Toll-Like Recep

47 d even by non-CpG DNA and by self-DNA, which is released from dead cells and complexes with antimicro

48 geting tyrosine kinase inhibitor, masitinib, was released from degradable polymer microspheres delive

49 itical microRNAs that regulate inflammation, are released from dendritic cells within exosomes and ar

50 We further tested if ATP is released from dental pulp upon dentin mechanical or t

51 ation is the process in which mature oocytes are released from developmental arrest and gain competen

52 experiments (170 L/batch) proved vanadium to be released from diatomite (Kieselguhr), increasing its

53 CCK is released from DMH neurons in response to repeated pos

54 tamate is a second synchronizing signal that is released from DN1s and perceived in LNvs via the meta

55 nner dependent on PDS5 proteins, or until it is released from DNA by WAPL.

56 Finally, let-7b can be released from DRG neurons by neuronal activation, and

57 holog of the primary human adipokine leptin, is released from Drosophila fat cells.

58 nt probes whose signals become quenched upon being released from drug carriers.

59 s reveal that numerous proteolytic fragments are released from dying tumor cells.

60 Endothelial microparticles (EMPs) are released from dysfunctional endothelial cells.

61 a closed state at AUG codons, from which Pi is released from eIF2 . GDP . Pi.

62 Post-storage, hLMSC were released from encapsulation, and viability-assessed

63 de the first direct evidence that Zn(2+) can be released from endolysosomal vesicles to the cytosol i

64 Taken together, the results show that eRNA is released from endothelial cells in response to shear

65 Although adiponectin is released from epicardial adipose tissue (EpAT), it is

66 e to environmental changes, TEs are known to be released from epigenetic repression and to become tra

67 ATP is released from erythrocytes and platelets, and purinoc

68 Cell-free hemoglobin that is released from erythrocytes into the cerebrospinal flu

69 Being released from Escherichia coli, it contains mainly

70 tion showed that ~89-100% of As in porewater was released from exchangeable and specifically adsorbed

71 1,500 farmed bullfrogs and in the water that is released from farms into the environment.

72 by the bioaffinity mechanism; 26% of the IgG were released from films embedded with pAG(MG) after fiv

73 roximately 1 mum (particulate matter, PM(1)) are released from fossil fuel combustion into the air, t

74 the heterotrimeric G-protein complex that is being released from G-protein-coupled receptors on vagal

75 Epitaxial films may be released from growth substrates and transferred to st

76 GLP-2) are proglucagon derived peptides that are released from gut endocrine cells in response to nut

77 Specifically, formaldehyde is released from H(2)C(OSiPh(3))(2) upon treatment with

78 plete RBCs and by SNO-Hb itself, whereby SNO is released from Hb and RBCs during deoxygenation, in pr

79 Exosomes are extracellular vesicles which are released from healthy and tumor cells into blood cir

80 ulating form of the MIF receptor, CD74, that is released from hepatic stellate cells and that binds M

81 ns, is unique in that it is hepatotropic and is released from hepatocytes without lysis in small vesi

82 on rhizobial fitness (i.e. how many rhizobia are released from host nodules) and strain-specific effe

83 enzyme Cajal body-associated protein, TCAB1, was released from hTR in mitotic cells coincident with T

84 endogenous oils have a higher propensity to be released from hypertrophied visceral fat in MUO indiv

85 At low fat level more aroma compounds were released from ice creams with lower protein content

86 More than 600,000 prisoners are released from incarceration each year in the United

87 throcytes, producing progeny merozoites that are released from infected cells via a poorly understood

88 cated to 1.4-fold higher titers (P = 0.004), were released from infected cells 4.2-fold more efficien

89 s become necrotic immediately after rhizobia are released from infection threads into symbiotic cells

90 corticotropin-releasing hormone (CRH), which is released from inflamed tissues by cellular stress sig

91 PCs are released from insect eggs, and they induce salicylic

92 We found that K17 was released from intermediate filaments and translocate

93 ients with chronic spontaneous urticaria and was released from isolated basophils following either an

94 s separate from the rest of the root cap and are released from its edge as a layer of living cells.

95 ting that under harsh shear conditions FVIII is released from its carrier protein.

96 udy shows that a conserved bioactive peptide is released from its cytoplasmic precursor upon wounding

97 is maintained if the slower-growing species is released from its dependence on the other, but if the

98 opsis is regulated by a peptide hormone that is released from its precursor by a network of redundant

99 We found that small amounts of UDP-sugars were released from keratinocytes and that UDP-glucose (U

100 These allergens are released from kiwi seeds after oral and gastric dige

101 maging we show that dynamic lipid structures are released from L. monocytogenes during infection.

102 g alternative ribosomes when M. tuberculosis is released from macrophages, to allow survival in the e

103 e-1, oligomeric NLRP3 inflammasome particles were released from macrophages.

104 Cytokines are released from many tissues, including skeletal muscl

105 The capsid-associated tegument protein pp150 is released from maturing endosomes and migrates to the

106 Previous work showed that Mad2 is released from MCC by the joint action of the TRIP13 A

107 The mechanisms by which PS-ASOs are released from membrane-enclosed endocytotic organell

108 zed via a number of endocytotic pathways and are released from membrane-enclosed endocytotic organell

109 study, shaving experiments showed that Shu1 is released from membrane preparations when spheroplast

110 PKCdelta is released from membranes as a Tyr(313)-phosphorylated

111 hniques, (1) showing that clean hydrogen can be released from Mg(BH4)2 under mild conditions and (2)

112 P-aglycone, whereas only the superficial ORP was released from microparticles.

113 uced, conformationally destabilized proteins are released from mitochondria in a size-limited manner.

114 cytochrome c, a proapoptotic peroxidase that is released from mitochondria during sustained oxidative

115 Exosomes are released from multivesicular bodies via an exocytic

116 rylation events allow ubiquitylated Vac17 to be released from Myo2 and Vac8.

117 8 complex, Vac17 is degraded and the vacuole is released from Myo2.

118 Isl1 is released from nascent motor neuron enhancers and recr

119 Neuronal transmitters are released from nerve terminals via the fusion of syna

120 hysiological settings, the persulfide sulfur is released from NFS1 and transferred to a scaffold prot

121 Eggs were released from nine different known spawning grounds

122 NR is released from NR@MOP2 within HeLa cancer cells.

123 Strikingly, we found that nucleoporins can be released from nuclear bodies and reintegrated into ex

124 We further demonstrate that mESCs must be released from Oct4-maintained pluripotency prior to e

125 inner plexiform layer (IPL), where glutamate is released from ON and OFF bipolar cell terminals in se

126 on electron microscopy revealed that virions were released from or associated with the apical membran

127 nge the direction of EE transport, kinesin-3 is released from organelles, and dynein binds subsequent

128 ow for the first time that parenchymal cells are released from organs under non-proliferative patholo

129 detecting the alarmin S100A11 protein, which is released from parasite-infected cells via caspase-1-d

130 demonstrated that intracellular HMGB1 could be released from PHCCA cells and induce invasion and ang

131 In conclusion, intracellular HMGB1 could be released from PHCCA cells and promote angiogenesis vi

132 gging the question of how tightly bound cAMP is released from PKA to reset its signaling state to res

133 ecular machinery by which effector molecules are released from platelets.

134 Short-chain polyphosphate (polyP) is released from platelets upon platelet activation, but

135 uring the process of blood coagulation, BDNF is released from platelets, which has led to its extensi

136 Phl p 12 and Phl p 1 are released from pollen simultaneously and in similar a

137 More nanoclay particles were released from PP-clay films (0.15 mg L(-1)) than fr

138 tures, and auditory brainstem, synaptic zinc is released from presynaptic terminals to modulate neuro

139 More than 30 million people are released from prison worldwide every year, who inclu

140 tive study a cohort of 4,357 individuals who were released from prison via an amnesty on July 16, 200

141 tion of ENM are entering an in-use stock and are released from products over time (i.e., have a lag p

142 Participants were released from protocol treatment at 2 years and exa

143 uman bone samples during aging when TGFbeta1 is released from resorbing bone.

144 Receptors can be released from retention in the TGN by coexpression of

145 In vitro, terminated transcripts are released from RNA polymerase after synthesis.

146 Upon dephosphorylation, UVRAG is released from RUBICON to interact with the HOPS compl

147 rate that PKA-dependent phosphorylated HDAC4 is released from Runx2 bound to the MMP-13 promoter in t

148 A small proportion of lipid was released from ruptured cells on fractured surfaces o

149 Finally, we identified proteins that are released from Samba and newly discovered Tupanvirus

150 es indicated that the addition of CS - which was released from scaffolds quickly - significantly upre

151 tier brine, but also revealed that chemicals are released from sea ice at variable rates.

152 Arsenic is released from sediments when iron-oxide minerals, ont

153 virtually unknown how transmembrane proteins are released from senescent cancer cells.

154 th intercellular adhesion molecule 1 (ICAM1) is released from senescent cells by microvesicles indepe

155 food context with the diacetyl odor, FLP-34 is released from serotonergic neurons and signals throug

156 ary to exponential phase (outgrowth), 6S RNA is released from sigma(70)-RNAP, resulting in a fast inc

157 sent on infectious virions of ZIKV when they are released from specific cell types, and enhances viru

158 t with IFN-gamma, an antiviral cytokine that is released from stimulated immune cells.

159 Upon DNA damage, p53 mRNA is released from stress granules and associates with pol

160 Epidermal growth factor is released from stressed cells and signals to activate

161 Our data suggest that PDI is released from subcellular compartments to the cytosol

162 measurements revealed that Sucnr1(-/-) mice were released from succinate-induced inhibition of lipol

163 ATP is released from such cells.

164 8 colocalize across the AML genome, and each is released from super-enhancer regions upon chemical in

165 Zn(2+) is released from synaptic vesicles of certain nerve term

166 studies demonstrated that some gut peptides are released from taste buds by prolonged application of

167 In a lithium-ion battery, electrons are released from the anode and go through an external e

168 Particles are released from the apical and basolateral surfaces an

169 We predict that more ions are released from the cell with increasing basal area, r

170 mes, mitochondrion-containing autophagosomes are released from the cell.

171 of the energy metabolism, such as l-lactate, are released from the cell.

172 eptide (FCAP) and cerebral peptide-2 (CP-2)] are released from the cholinergic command-like neuron ce

173 They are released from the contractile ring as it disassemble

174 Only native polypeptides are released from the endoplasmic reticulum (ER) to be t

175 y mediators, such as nitric oxide (NO), that are released from the endothelium in response to fluid s

176 atory factors such as nitric oxide (NO) that are released from the endothelium under the influence of

177 Consequently, Myrf N-terminal fragments are released from the ER only as homo-trimers.

178 ER, where mRNAs that encode signal sequences are released from the ER to the cytosol.

179 Correctly folded proteins are released from the ER, and poorly folded proteins are

180 Elastin-derived peptides are released from the extracellular matrix remodeling by

181 ged due to the presence of CN(-) ions, which are released from the ferri/ferrocyanide redox probe.

182 Volatile organic compounds (VOCs) are released from the food matrix and then reach the rec

183 hotoproduct-containing oligonucleotides that are released from the genome during excision repair.

184 temporary adhesive secretory vesicles (TASV) are released from the gland cells into the antennule via

185 AT1R-enriched exosomes are released from the heart under conditions of in vivo

186 vironmental conditions after virus particles are released from the host cells.

187 Cytochrome c and other apoptotic factors are released from the intermembrane space through these

188 stroke, various damage-associated molecules are released from the ischemic core and diffuse to the i

189 the ultrasmall water-soluble gold particles are released from the micelle and readily dispersed.

190 y, we show that significant amounts of lipid are released from the nanodiscs upon insertion of larger

191 A fraction of the major histones are released from the nuclear opening and degraded in th

192 The cations are released from the organic structures by digestion wi

193 .3 x 10(10) moles of carbon dioxide per year are released from the slab beneath the forearc, and thus

194 ear, branched, and dendritic structures that are released from the solid support by addition of TEV p

195 s virus (VSV), newly assembled VSV particles are released from the surface of infected cells.

196 of broken, PM "bubbles" with exposed PS that are released from the surface of the otherwise intact ce

197 A key question is how both heads are released from the surface to approach actin and prod

198 proteins were functionally active and could be released from the bacterial surface by specific prote

199 The conjugated rapamycin can be released from the bioconjugate and prevent immune res

200 e C. elegans demonstrated that ectosomes can be released from the cilium and can mediate the intercel

201 DISC, phosphorylated caspase-8 is unable to be released from the complex; this inhibits further cycl

202 not as tightly bound and are predisposed to be released from the filament.

203 h aspect ratios (>10(4)); such nanowires can be released from the glass matrix and show relatively hi

204 at which the hyperpolarized gas mixture can be released from the hyperpolarizer (with negligible amo

205 teins (vRNPs) that carry the RNA genome must be released from the incoming particle before they can e

206 ed, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the

207 -PCL nanoparticles simultaneously, and could be released from the micelles in an extended period in v

208 Interestingly, GSK3beta can be released from the multienzyme complex in response to

209 Bacteriorhodopsin can be released from the octylglucoside-micelle efficiently

210 stR that promote the KstR-DNA interaction to be released from the operator, retaining its dimeric sta

211 licated in many physiological processes, can be released from the persulfide product of the MPST reac

212 s fibers in which dopamine and glutamate can be released from the same axons, but are not normally re

213 compression allows hydrophobic surfactant to be released from the vesicle.

214 the kinase inhibitor Hexim1 once P-TEFb has been released from the 7SK snRNP.

215 n persist long after the nascent protein has been released from the ribosome, and that a sufficient l

216 nt fluids attempting to migrate upward after being released from the downgoing plate.

217 The rates at which C is being released from the permafrost zone at different soi

218 We found that L13a is released from the 60S ribosomal subunit in response t

219 The mechanisms whereby SpA is released from the bacterial surface to access the hos

220 ATP is released from the bladder epithelium, also termed the

221 at the targeting site, the CPP modified drug is released from the blockage by a second triggering age

222 xide is produced, and in the lungs, where it is released from the blood.

223 considerably change, and much of the peptide is released from the cargo.

224 tact in the IL-37D20A mice once the cytokine is released from the cell and binds to its receptor.

225 Full-length uPAR is released from the cell surface, but the mechanism and

226 r cells convert glutamine to glutamate which is released from the cell through the system Xc- antipor

227 replication is complete and the mature virus is released from the cells.

228 drophobic core in the intermediate state but is released from the core in the fully activated state,

229 n, and completely native and soluble insulin is released from the depot in a well behaved, first orde

230 acterial endotoxin, lipopolysaccharide, that is released from the gastrointestinal tract through the

231 and immunoproteasome inhibition, doxorubicin is released from the immunoproteasome inhibitor through

232 Insulin is released from the islets of Langerhans in discrete pu

233 in which the cellular ribosomal protein L13a is released from the large ribosomal subunit soon after

234 tic exocytosis whereby the cryptococcal cell is released from the macrophage into the extracellular e

235 y, wherein the soluble catalytic sector, V1, is released from the membrane and its MgATPase activity

236 in contains a transcriptional regulator that is released from the membrane when engagement of the cog

237 Sec18 is released from the membrane when PA is hydrolyzed to d

238 How cytochrome C is released from the mitochondria to the cytosol via Bax

239 poptosis, XIAP is antagonized by SMAC, which is released from the mitochondria upon caspase-mediated

240 Considerable amount of protein drug is released from the nanoparticles (NPs) in the gastroin

241 ly localizes to the nuclear envelope, but it is released from the nuclear envelope into the nucleopla

242 On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cad

243 uclear receptor retinoic acid receptor gamma is released from the nucleus to disrupt TNF initiated ce

244 We demonstrate that RARgamma is released from the nucleus to orchestrate the formatio

245 Insulin is released from the pancreas in pulses with a period of

246 Insulin is released from the pancreas with variable dynamics, ye

247 Corticotropin-releasing factor (CRF) that is released from the paraventricular nucleus (PVN) of th

248 The CuDox complex is released from the particle by elevated temperature; h

249 -linker fimbrin before the endocytic vesicle is released from the plasma membrane.

250 Upon injection, donor DNA (1 to 5 kb) is released from the plasmid by Cas9.

251 ed cleavage of thioketal linker, doxorubicin is released from the polyprodrug.

252 a soluble form of NRX-1's ectodomain, which is released from the post-synaptic membrane by the SUP-1

253 to the initial ring radius if either myosin is released from the ring during contraction and actin f

254 or, both in solution after the DNA-initiator is released from the solid support as well as directly o

255 des in the nucleus until after the viral DNA is released from the transport vesicle.

256 n protein (Mat), and then the Mat-bound gRNA is released from the viral capsid and somehow crosses th

257 llowing laser treatment, hydrophilic AMD3100 was released from the aqueous liposome chamber and then

258 potential (Deltapsimito) depolarized; Ca(2+) was released from the endoplasmic reticulum (ER), increa

259 was recruited near the RARb RARE by RA, but was released from the Fgf8 RARE by RA.

260 ine-inducing, fully reduced isoform of HMGB1 was released from the ischemic brain in the hyperacute p

261 only 70% of the more hydrophobic doxorubicin was released from the material, whereas the more hydroph

262 Furthermore, the rate at which the drug was released from the nanoparticles could be controlled

263 DEX, a powerful ameliorator of inflammation, was released from the polymer by external application of

264 The peptide or protein was released from the resin by addition of a hydroxylami

265 SP was released from the sensory neurons, MNECs, and HNECs

266 x 10(14) and 2.5 x 10(15) g of black carbon was released from the target and ejected into the atmosp

267 Ferulic acid was released from the wheat bran during degradation but

268 or bevacizumab and to 1 of 3 dosing regimens were released from the clinical trial protocol after 2 y

269 After 2 years, patients were released from the clinical trial protocol.

270 Mono- and dichlorinated PCBs were released from the colorant at a faster rate than th

271 Ultimately, viral particles were released from the compartment and the cell lysed.

272 ective capture, the purified MC-LR molecules were released from the extractor nanoparticles within 5m

273 Early-discharge patients were released from the hospital at the completion of che

274 water, we find that vibrational bonds of C2 were released from the molecule containing carbon-carbon

275 Therefore, in mDCs, fewer progeny capsids were released from the nuclei into the cytosol, and fewe

276 total fluorine per square meter (mug F/m(2)) were released from the PA and PES/CO fabrics, respective

277 , genes and a putative enhancer in LADs that were released from the periphery during T-cell activatio

278 Young adults that were released from the program also appeared more anxiou

279 netics, we found that dopamine and glutamate were released from the same mesoaccumbens fibers.

280 ydrogen, electrostatic and covalently bonds, were released from the sandwiches after dissolving in di

281 The captured drug and catabolites were released from the streptavidin-coated magnetic bead

282 This study shows that CA are released from these regions to the cerebrospinal flu

283 Piceatannol could be released from these lignins upon derivatization follo

284 Leaching tests confirmed that PCB 11 could be released from these materials into water.

285 Approximately 80% of arsenic is released from these foodstuffs, potentially becoming

286 Ca(2+) is released from these organelles through a channel, ino

287 gnificant proportion of the total U (20-57%) was released from these three shales after reaction with

288 capture support, the purified DNA sequences were released from this support upon treatment with tetr

289 Recently, lipids have been identified that are released from tissues and act locally or systemicall

290 incarcerated, and more than 11 million have been released from U.S. correctional facilities.

291 Whereas TLR9 and TLR3 are released from UNC93B1, TLR7 does not dissociate from

292 ments, but they clearly demonstrated that MC are released from underwater munitions to the water colu

293 receptors also sense endogenous ligands that are released from uninfected dying cells, thereby activa

294 We also find that Mon1 is released from vacuoles during the fusion reaction and

295 junctions, the synapses, where transmitters are released from vesicles in a Ca(2+)-dependent fashion

296 These results suggest that Vpx is released from virions without a need for uncoating of

297 ast Vo The structure indicated that, when V1 is released from Vo, the N-terminal cytoplasmic domain o

298 Regardless of encapsulation, more phenolics were released from W and P than F.

299 not all polyphenolic compounds were able to be released from WPM, stronger interactions, possibly by

300 Therefore, much more THY was released from zein-THY/gamma-CD-IC-NF (2:1) than zei