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1 still controversial whether gliotransmitters are released from a cytosolic pool or by Ca(2+)-dependen
2                      Peptide neuromodulators are released from a unique organelle: the dense-core ves
3 o-sized membrane vesicles (50-120 nm), which are released from a wide variety of cells.
4                             As GLUC can also be released from a reporter construct by internal signal
5 rsion of the inverted task and when the rats were released from a novel start point.
6 small amount of the studied metal oxides NPs was released from abrasion of the textiles coated by the
7      On cellular activation or injury, HMGB1 is released from activated immune cells or necrotic tiss
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            Here, we present evidence that XO is released from and active in intestinal tissues and fl
13 ollectively these results suggest that ABCF1 is released from and binds to shed POSs in an autocrine
14 essary and sufficient for suppressed buds to be released from apical dominance.
15                                        ABCF1 was released from apoptotic cells and selectively bound
16  The canonical TGFbeta pathway, whose ligand is released from ASI, regulates satiety quiescence.
17                      Endogenous ligands that are released from astrocytes in an in vitro wounding ass
18 ted by ambient D-serine, whereas glycine may be released from astrocytes in response to afferent impu
19  inhibit itch and show that dynorphin, which is released from B5-I neurons, is a key neuromodulator o
20 capture the toxin efficiently once the toxin is released from BiP.
21 is important for autoinhibition and needs to be released from both kinases that form the dimer.
22 , 9.4 GBq of (240)Pu and 29.7 GBq of (241)Am were released from both fire events corresponding to a s
23                                        FGF22 is released from CA3 pyramidal neurons and organizes the
24 tion assays show that in solution zebularine is released from CDA (k(off) > 0.14 s(-1)) much more rap
25 iments in vitro suggest that 2-aminoacrylate is released from CdsH following cysteine desulfhydration
26            Our data indicate that vasostatin is released from cell-surface CRT and impairs differenti
27 s consisting of endogenous and exogenous Tau are released from cells and demonstrate their potential
28                                     Exosomes are released from cells both in vitro and in vivo, and h
29 data suggest that the different sgp130 forms are released from cells into their immediate surrounding
30 ) and some members of the Enterovirus genus, are released from cells nonlytically in membranous vesic
31 s, small endocytically derived vesicles that are released from cells.
32                  In addition, components can be released from cells as secretory molecules, enzymes,
33                           These vesicles can be released from cells, are packed with information incl
34 ibe three basic mechanisms by which GLUC can be released from cells: first, classical secretion by vi
35              The intracellular protein HMGB1 is released from cells and acts as a damage-associated m
36                                     TGF-beta is released from cells in a latent complex consisting of
37        In addition, the virus particles that were released from cells had reduced specific infectivit
38 calize with Kv2.1 clusters in live cells and are released from channels activated by voltage stimuli.
39  turn assembles with the large subunit as it is released from chaperonins.
40   The mechanism whereby gaseous protein ions are released from charged solvent droplets during electr
41 they demonstrate in HeLa cells that once RNA is released from chromatin, the modifications are surpri
42                                  Endotrophin is released from COL VI and promotes pleiotropic pro-fib
43 ts using a series of sodiated N-glycans that were released from commercially available glycoproteins
44 ations can be explained if ACh and glutamate are released from common vesicles onto spatially segrega
45 nt studies suggest that interleukin 6 (IL-6) is released from contracting skeletal muscles; however,
46 oxygenase products thromboxane and PGF2alpha are released from coronary artery PVAT from pigs.
47                     Upon ETI induction, CKIs are released from CPR5 to cause overactivation of anothe
48                         We conclude that sap is released from cucurbit phloem upon wounding but contr
49 diates proteasomal degradation of slGFP that is released from cytosolic protein handling centers.
50 "danger signal" adenosine triphosphate (ATP) is released from damaged cells and promotes proliferatio
51        In TPA-induced skin inflammation, MIF is released from damaged keratinocytes and then triggers
52 e proinflammatory danger signal IL-33, which is released from damaged or dying cells, achieves its ef
53              Here, we show that dsRNA, which is released from damaged skin, activates Toll-Like Recep
54 d even by non-CpG DNA and by self-DNA, which is released from dead cells and complexes with antimicro
55 geting tyrosine kinase inhibitor, masitinib, was released from degradable polymer microspheres delive
56 itical microRNAs that regulate inflammation, are released from dendritic cells within exosomes and ar
57                     We further tested if ATP is released from dental pulp upon dentin mechanical or t
58 n the bones of mice suggests that (89)Zr(4+) is released from DFO in vivo.
59                                          CCK is released from DMH neurons in response to repeated pos
60 tamate is a second synchronizing signal that is released from DN1s and perceived in LNvs via the meta
61 nner dependent on PDS5 proteins, or until it is released from DNA by WAPL.
62                          Finally, let-7b can be released from DRG neurons by neuronal activation, and
63 holog of the primary human adipokine leptin, is released from Drosophila fat cells.
64 nt probes whose signals become quenched upon being released from drug carriers.
65 s reveal that numerous proteolytic fragments are released from dying tumor cells.
66            Endothelial microparticles (EMPs) are released from dysfunctional endothelial cells.
67  a closed state at AUG codons, from which Pi is released from eIF2 . GDP . Pi.
68                                        CRAMP is released from emigrated neutrophils and then transpor
69                         Although adiponectin is released from epicardial adipose tissue (EpAT), it is
70 e to environmental changes, TEs are known to be released from epigenetic repression and to become tra
71                                          ATP is released from erythrocytes and platelets, and purinoc
72                                              Being released from Escherichia coli, it contains mainly
73 tion showed that ~89-100% of As in porewater was released from exchangeable and specifically adsorbed
74 by the bioaffinity mechanism; 26% of the IgG were released from films embedded with pAG(MG) after fiv
75 the heterotrimeric G-protein complex that is being released from G-protein-coupled receptors on vagal
76 ulating form of the MIF receptor, CD74, that is released from hepatic stellate cells and that binds M
77 the very low density lipoprotein pathway and are released from hepatocytes as entities varying in the
78 enzyme Cajal body-associated protein, TCAB1, was released from hTR in mitotic cells coincident with T
79  endogenous oils have a higher propensity to be released from hypertrophied visceral fat in MUO indiv
80        At low fat level more aroma compounds were released from ice creams with lower protein content
81                  More than 600,000 prisoners are released from incarceration each year in the United
82 throcytes, producing progeny merozoites that are released from infected cells via a poorly understood
83    HIV transactivator of transcription (Tat) is released from infected cells and has the ability to r
84 cated to 1.4-fold higher titers (P = 0.004), were released from infected cells 4.2-fold more efficien
85 s become necrotic immediately after rhizobia are released from infection threads into symbiotic cells
86 corticotropin-releasing hormone (CRH), which is released from inflamed tissues by cellular stress sig
87 nt in the extracellular space, but that PEPD is released from injured cells and tissues and that such
88                            We found that K17 was released from intermediate filaments and translocate
89 is signal is conveyed by a neuropeptide that is released from intestinal cells and acutely depolarize
90      Vasoactive intestinal polypeptide (VIP) is released from intracardiac neurons during vagal stimu
91 hed E. coli and 8% of attached Ent. faecalis were released from IOCS columns during draining and rewe
92 ients with chronic spontaneous urticaria and was released from isolated basophils following either an
93 e cell wall, as opposed to the fraction that is released from it.
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    We found that small amounts of UDP-sugars were released from keratinocytes and that UDP-glucose (U
97                              These allergens are released from kiwi seeds after oral and gastric dige
98                                   Hemoglobin is released from lysed RBCs in numerous clinical setting
99        This finding is consistent with SCMAS being released from lysosomes, an event known as lysosom
100 g alternative ribosomes when M. tuberculosis is released from macrophages, to allow survival in the e
101 e-1, oligomeric NLRP3 inflammasome particles were released from macrophages.
102                                    Cytokines are released from many tissues, including skeletal muscl
103 yme and its citrullinated substrate proteins are released from mast cells on activation with ATP.
104       The appetite-regulating hormone leptin is released from mature adipocytes, and its production m
105               Previous work showed that Mad2 is released from MCC by the joint action of the TRIP13 A
106 zed via a number of endocytotic pathways and are released from membrane-enclosed endocytotic organell
107              The mechanisms by which PS-ASOs are released from membrane-enclosed endocytotic organell
108  study, shaving experiments showed that Shu1 is released from membrane preparations when spheroplast
109                                     PKCdelta is released from membranes as a Tyr(313)-phosphorylated
110 hniques, (1) showing that clean hydrogen can be released from Mg(BH4)2 under mild conditions and (2)
111 uced, conformationally destabilized proteins are released from mitochondria in a size-limited manner.
112                                     Exosomes are released from multivesicular bodies via an exocytic
113                                         Isl1 is released from nascent motor neuron enhancers and recr
114                        Neuronal transmitters are released from nerve terminals via the fusion of syna
115 hysiological settings, the persulfide sulfur is released from NFS1 and transferred to a scaffold prot
116                                         Eggs were released from nine different known spawning grounds
117                                           NR is released from NR@MOP2 within HeLa cancer cells.
118   Strikingly, we found that nucleoporins can be released from nuclear bodies and reintegrated into ex
119       We further demonstrate that mESCs must be released from Oct4-maintained pluripotency prior to e
120 inner plexiform layer (IPL), where glutamate is released from ON and OFF bipolar cell terminals in se
121 nge the direction of EE transport, kinesin-3 is released from organelles, and dynein binds subsequent
122              Furthermore, NAADP was found to be released from pancreatic islets upon stimulation by h
123 gging the question of how tightly bound cAMP is released from PKA to reset its signaling state to res
124 ecular machinery by which effector molecules are released from platelets.
125            Short-chain polyphosphate (polyP) is released from platelets upon platelet activation, but
126 uring the process of blood coagulation, BDNF is released from platelets, which has led to its extensi
127                         Phl p 12 and Phl p 1 are released from pollen simultaneously and in similar a
128 n the observation that fluorescent reporters being released from polymeric drug delivery systems poss
129                                       PSD-95 is released from postsynaptic membranes in response to C
130                      More nanoclay particles were released from PP-clay films (0.15 mg L(-1)) than fr
131                  More than 30 million people are released from prison worldwide every year, who inclu
132 tive study a cohort of 4,357 individuals who were released from prison via an amnesty on July 16, 200
133 tion of ENM are entering an in-use stock and are released from products over time (i.e., have a lag p
134  cells during the host immune response, iron is released from proteins and can act as a catalyst for
135                                 Participants were released from protocol treatment at 2 years and exa
136                                Receptors can be released from retention in the TGN by coexpression of
137             In vitro, terminated transcripts are released from RNA polymerase after synthesis.
138                Upon dephosphorylation, UVRAG is released from RUBICON to interact with the HOPS compl
139 rate that PKA-dependent phosphorylated HDAC4 is released from Runx2 bound to the MMP-13 promoter in t
140                  A small proportion of lipid was released from ruptured cells on fractured surfaces o
141 es indicated that the addition of CS - which was released from scaffolds quickly - significantly upre
142                Importantly, we show that ACs are released from SCs and induce axonal degeneration.
143                                      Arsenic is released from sediments when iron-oxide minerals, ont
144 virtually unknown how transmembrane proteins are released from senescent cancer cells.
145 th intercellular adhesion molecule 1 (ICAM1) is released from senescent cells by microvesicles indepe
146 ary to exponential phase (outgrowth), 6S RNA is released from sigma(70)-RNAP, resulting in a fast inc
147                                          ATP is released from skeletal muscle by contractile activity
148 ead emergence when fungal spores develop and are released from sori formed at kernel positions.
149 t with IFN-gamma, an antiviral cytokine that is released from stimulated immune cells.
150                    Upon DNA damage, p53 mRNA is released from stress granules and associates with pol
151                      Epidermal growth factor is released from stressed cells and signals to activate
152                    Our data suggest that PDI is released from subcellular compartments to the cytosol
153  measurements revealed that Sucnr1(-/-) mice were released from succinate-induced inhibition of lipol
154                                          ATP is released from such cells.
155 8 colocalize across the AML genome, and each is released from super-enhancer regions upon chemical in
156                                       Zn(2+) is released from synaptic vesicles of certain nerve term
157  In conclusion, our data indicate that CD154 is released from T-cells by ADAM10 and ADAM17 upon CD40
158  studies demonstrated that some gut peptides are released from taste buds by prolonged application of
159                             It is assumed DA is released from terminals innervating from the ventral
160          In a lithium-ion battery, electrons are released from the anode and go through an external e
161                                    Particles are released from the apical and basolateral surfaces an
162 uses, which preferentially enter through and are released from the apical surface of polarized human
163 me of the Cfl1 proteins undergo shedding and are released from the cell wall.
164 mes, mitochondrion-containing autophagosomes are released from the cell.
165 eptide (FCAP) and cerebral peptide-2 (CP-2)] are released from the cholinergic command-like neuron ce
166 technique is typically applied, the peptides are released from the chromatography column by the gradu
167                                         They are released from the contractile ring as it disassemble
168                     Only native polypeptides are released from the endoplasmic reticulum (ER) to be t
169 y mediators, such as nitric oxide (NO), that are released from the endothelium in response to fluid s
170 atory factors such as nitric oxide (NO) that are released from the endothelium under the influence of
171      Consequently, Myrf N-terminal fragments are released from the ER only as homo-trimers.
172 ER, where mRNAs that encode signal sequences are released from the ER to the cytosol.
173                    Correctly folded proteins are released from the ER, and poorly folded proteins are
174 ged due to the presence of CN(-) ions, which are released from the ferri/ferrocyanide redox probe.
175            Volatile organic compounds (VOCs) are released from the food matrix and then reach the rec
176 hotoproduct-containing oligonucleotides that are released from the genome during excision repair.
177 temporary adhesive secretory vesicles (TASV) are released from the gland cells into the antennule via
178                       AT1R-enriched exosomes are released from the heart under conditions of in vivo
179 vironmental conditions after virus particles are released from the host cells.
180                       As a result, the cells are released from the hydrogel.
181     Cytochrome c and other apoptotic factors are released from the intermembrane space through these
182  stroke, various damage-associated molecules are released from the ischemic core and diffuse to the i
183                   Exosomes are vesicles that are released from the kidney into urine.
184 y, we show that significant amounts of lipid are released from the nanodiscs upon insertion of larger
185             A fraction of the major histones are released from the nuclear opening and degraded in th
186 vanov et al. report that chromatin fragments are released from the nuclei of senescent cells and are
187 amers representative of the native topology, are released from the precursor upon SID, significantly
188  of an inflammatory response, ions/particles are released from the surface of the implant into the bi
189 of broken, PM "bubbles" with exposed PS that are released from the surface of the otherwise intact ce
190 re extra U residues, the nascent transcripts are released from the transcription initiation complex,
191 e C. elegans demonstrated that ectosomes can be released from the cilium and can mediate the intercel
192  DISC, phosphorylated caspase-8 is unable to be released from the complex; this inhibits further cycl
193  not as tightly bound and are predisposed to be released from the filament.
194  favoring the production of a PAH, which can be released from the framework under acidic conditions i
195 h aspect ratios (>10(4)); such nanowires can be released from the glass matrix and show relatively hi
196 -PCL nanoparticles simultaneously, and could be released from the micelles in an extended period in v
197    In vitro release assays showed heparin to be released from the microparticles over 8-12 h and for
198                  Interestingly, GSK3beta can be released from the multienzyme complex in response to
199                        Bacteriorhodopsin can be released from the octylglucoside-micelle efficiently
200 stR that promote the KstR-DNA interaction to be released from the operator, retaining its dimeric sta
201 s fibers in which dopamine and glutamate can be released from the same axons, but are not normally re
202 ith visible light, the ruthenium complex can be released from the surface of the nanoparticles by sel
203  the kinase inhibitor Hexim1 once P-TEFb has been released from the 7SK snRNP.
204 n persist long after the nascent protein has been released from the ribosome, and that a sufficient l
205 and responding to endosomal acidification by being released from the complex and inserting into and d
206                      The rates at which C is being released from the permafrost zone at different soi
207                           We found that L13a is released from the 60S ribosomal subunit in response t
208  between PcpB and PcpD can occur before TCBQ is released from the active site of PcpB.
209  how the ATP that provides the amplification is released from the attacked cells.
210                   The mechanisms whereby SpA is released from the bacterial surface to access the hos
211                                          ATP is released from the bladder epithelium, also termed the
212 at the targeting site, the CPP modified drug is released from the blockage by a second triggering age
213 ntrol subjects, suggesting that, in MS, ET-1 is released from the brain to the cerebral circulation.
214 considerably change, and much of the peptide is released from the cargo.
215 e, elucidating the mechanisms by which CD154 is released from the cell surface following its interact
216                             Full-length uPAR is released from the cell surface, but the mechanism and
217 r cells convert glutamine to glutamate which is released from the cell through the system Xc- antipor
218   Finally, we report that the excised 30-mer is released from the chromatin in complex with the repai
219 n is phosphorylated at the N-terminus, c-Jun is released from the complex and cannot be ubiquitinated
220 r of normal nuclear import cargoes, HIV-1 IN is released from the complex with TRN-SR2 by RanGTP.
221 drophobic core in the intermediate state but is released from the core in the fully activated state,
222 rtex of cells in both embryos and larvae and is released from the cortex in a Wnt-responsive manner.
223 n, and completely native and soluble insulin is released from the depot in a well behaved, first orde
224  peptide 1 (GLP-1) is a peptide hormone that is released from the gut in response to nutrient ingesti
225                                      Insulin is released from the islets of Langerhans in discrete pu
226 in which the cellular ribosomal protein L13a is released from the large ribosomal subunit soon after
227 tic exocytosis whereby the cryptococcal cell is released from the macrophage into the extracellular e
228 y, wherein the soluble catalytic sector, V1, is released from the membrane and its MgATPase activity
229 in contains a transcriptional regulator that is released from the membrane when engagement of the cog
230                               Further, SPE-8 is released from the membrane when the activation signal
231                             How cytochrome C is released from the mitochondria to the cytosol via Bax
232 poptosis, XIAP is antagonized by SMAC, which is released from the mitochondria upon caspase-mediated
233          Considerable amount of protein drug is released from the nanoparticles (NPs) in the gastroin
234                       On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cad
235 uclear receptor retinoic acid receptor gamma is released from the nucleus to disrupt TNF initiated ce
236                 We demonstrate that RARgamma is released from the nucleus to orchestrate the formatio
237                                      Insulin is released from the pancreas in pulses with a period of
238                            The CuDox complex is released from the particle by elevated temperature; h
239 The mechanism through which soluble endoglin is released from the placenta is currently unknown; howe
240 -linker fimbrin before the endocytic vesicle is released from the plasma membrane.
241 t, throughout seedling development, a factor is released from the plastid to the cytoplasm that indic
242  a soluble form of NRX-1's ectodomain, which is released from the post-synaptic membrane by the SUP-1
243  central nervous system, (S)-glutamate (Glu) is released from the presynaptic neuron where it activat
244 omain immediately before the nascent protein is released from the ribosome and decrease its chances o
245 ive structure before the full-length protein is released from the ribosome.
246  to the initial ring radius if either myosin is released from the ring during contraction and actin f
247 , except when the duplicated terminus region is released from the septum and recoils to the center of
248 or, both in solution after the DNA-initiator is released from the solid support as well as directly o
249                                       Ca(2+) is released from the SR to the MS based on the voltage a
250 des in the nucleus until after the viral DNA is released from the transport vesicle.
251  receptor on the cell surface but before RNA is released from the virus capsid.
252 llowing laser treatment, hydrophilic AMD3100 was released from the aqueous liposome chamber and then
253 sical adsorption loading, while less than 1% was released from the covalently loaded particles.
254 potential (Deltapsimito) depolarized; Ca(2+) was released from the endoplasmic reticulum (ER), increa
255  was recruited near the RARb RARE by RA, but was released from the Fgf8 RARE by RA.
256 ine-inducing, fully reduced isoform of HMGB1 was released from the ischemic brain in the hyperacute p
257 only 70% of the more hydrophobic doxorubicin was released from the material, whereas the more hydroph
258      Furthermore, the rate at which the drug was released from the nanoparticles could be controlled
259                     The cellular debris that was released from the OSE into the lumen of the nasal ai
260 , EFA6R lacking the CC domain (EFA6RDeltaCC) was released from the PM into the cytosol upon PIP2 depl
261 DEX, a powerful ameliorator of inflammation, was released from the polymer by external application of
262 OH acids occupied), and the absorbed peptide was released from the polymer for >2 weeks in a controll
263                       The peptide or protein was released from the resin by addition of a hydroxylami
264                                           SP was released from the sensory neurons, MNECs, and HNECs
265                 Greater than 80% of the drug was released from the SND in less than 30 min, with sust
266                                 Ferulic acid was released from the wheat bran during degradation but
267                      After 2 years, patients were released from the clinical trial protocol.
268  extraction of recombinant virions, peptides were released from the coat protein by chemical cleavage
269                  Ultimately, viral particles were released from the compartment and the cell lysed.
270 ective capture, the purified MC-LR molecules were released from the extractor nanoparticles within 5m
271                     Early-discharge patients were released from the hospital at the completion of che
272      After thermal processing, nanoparticles were released from the KCl matrix and transferred in an
273  water, we find that vibrational bonds of C2 were released from the molecule containing carbon-carbon
274 , genes and a putative enhancer in LADs that were released from the periphery during T-cell activatio
275            Energetically speaking, the MWNTs were released from the primary energy minimum when the b
276                            Young adults that were released from the program also appeared more anxiou
277 netics, we found that dopamine and glutamate were released from the same mesoaccumbens fibers.
278 ydrogen, electrostatic and covalently bonds, were released from the sandwiches after dissolving in di
279     During intermittent flow, fewer bacteria were released from the saturated column compared to the
280 o postinfection, suggesting that these cells were released from the spleen to other tissues.
281            The captured drug and catabolites were released from the streptavidin-coated magnetic bead
282                 We demonstrate that GABA can be released from these cells and modulate mossy fiber ex
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  capture support, the purified DNA sequences were released from this support upon treatment with tetr
287   Recently, lipids have been identified that are released from tissues and act locally or systemicall
288  incarcerated, and more than 11 million have been released from U.S. correctional facilities.
289 rms of two substrate proteins, but while BiP is released from unfolded substrates in the presence of
290 receptors also sense endogenous ligands that are released from uninfected dying cells, thereby activa
291                       We also find that Mon1 is released from vacuoles during the fusion reaction and
292  junctions, the synapses, where transmitters are released from vesicles in a Ca(2+)-dependent fashion
293               These results suggest that Vpx is released from virions without a need for uncoating of
294 ast Vo The structure indicated that, when V1 is released from Vo, the N-terminal cytoplasmic domain o
295  Regardless of encapsulation, more phenolics were released from W and P than F.
296  induces hepatic influx of fatty acids which are released from WATs.
297 s a highly toxic priority pollutant that can be released from wetlands as a result of biogeochemical
298  not all polyphenolic compounds were able to be released from WPM, stronger interactions, possibly by
299 6 h, whereas larger peptides (1050-1800 kDa) were released from WPs in the first 3 h.
300                     Therefore, much more THY was released from zein-THY/gamma-CD-IC-NF (2:1) than zei

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