戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 s greater cell viability over ZnO due to MZO releasing 4-times lower Zn(2+) density in the cell mediu
2 purred administrators to respond directly by releasing 400 datasets in one week.
3 +) binding to C2A enables lipid transport by releasing a charge-based autoinhibitory interaction betw
4 ctors in one group could help a recipient by releasing a food box, but the same action for another gr
5                                       We are releasing a tool to allow users to identify areas of the
6 one-third of the wells may leak, potentially releasing a total of 3-17 kt of methane per year into th
7  calculations reveals similar sigma-electron-releasing abilities for all of them; however, their pi-a
8  fine-tuned by variations in the pi-electron releasing/accepting nature of the basal ligand.
9  by elevating presynaptic choline uptake and releasing acetylcholine is attenuated in sign-trackers.
10 nism that amplified and dispersed stimuli by releasing activated kinases from receptors lacking intri
11 ic lung strips responded to tensile force by releasing active TGF-beta1 from latent stores with subse
12      Recent studies showed that the fluoride-releasing activity of conventional GICs is inadequate fo
13 systemically communicate this information by releasing adipokines.
14 be, the photocurrent signal decreased due to releasing adsorbed Ru(NH3)6(3+) on aptamer and preventin
15          Here, the connectivity between GABA-releasing AgRP neurons and POMC neurons was examined in
16 ing floods scour away overwintering grazers, releasing algae from spring and early summer grazing.
17 -lactams can be designed that are capable of releasing alternatively reactive species.
18                         Here we show that by releasing an additional tailored escort electron beam at
19 omotes E-Syt1-mediated membrane tethering by releasing an inhibition that prevents C2E from interacti
20 ssociated t-SNAREs, a zippering-like process releasing approximately 65 kT per SNAREpin.
21                  Here we show that glutamate-releasing ARC neurons expressing oxytocin receptor, unli
22 e may undergo reductive dissolution, thereby releasing As, Sb, and Fe(2+) coincident with a rise in p
23  the resting tone of the cerebral vessels by releasing ATP and COX-1 derivatives.
24                                       A slow-releasing ATRA formulation inhibits solid tumors such as
25 ng Pin1, with a better potency than the slow-releasing ATRA formulation, consistent with its improved
26 nd 4-fold higher Cmax and AUC over the slow-releasing ATRA formulation.
27                               Moreover, slow-releasing ATRA potently and dose-dependently inhibited H
28    Further, we show that application of BMP4-releasing beads in one place in an organoid can break th
29                                              Releasing beta-lapachone first from the CARNs selectivel
30 re also required for the ciliary function of releasing bioactive EVs, and TTLL-11 is itself a novel E
31           Plants respond to insect attack by releasing blends of volatile chemicals that attract thei
32 tal mice motoneurons excite Renshaw cells by releasing both acetylcholine (ACh) and glutamate.
33                               In addition to releasing bradykinin from HK, Kal directly activated mon
34 Bik reduces hyperplastic epithelial cells by releasing calcium from endoplasmic reticulum stores and
35 the effectiveness of BAG in neutralizing and releasing calcium ions in acidic conditions.
36 r potential mucolipin 1 (TRPML1) is a Ca(2+)-releasing cation channel that mediates the calcium signa
37                                        In EV-releasing cephalic male (CEM) cilia, TTLL-11 and the deg
38 the "template-cladded" strategy succeeded in releasing channel space of up to approximately 24% of th
39 c of substituents on ArH, with more electron-releasing character favoring ArF-ArH interactions, and (
40 res, occur in these solids: (i) the electron-releasing characteristic of substituents on ArH, with mo
41 tracellular matrix (ECM) in conjunction with releasing chemoattractive signals increases cellularity
42  poplar trees, that rapidly metabolizes TCE, releasing chloride ion.
43 mune defense and can respond to infection by releasing chromatin in the form of neutrophil extracellu
44 ed that RAG1/2 causes aberrant insertions by releasing cleaved antibody gene fragments that subsequen
45 environment via detection of thiols and then releasing CO when triggered with visible light and O2.
46 s from substrate/ion-loaded into a substrate-releasing conformer.
47 fer protection from tumors and infections by releasing cytotoxic granules and pro-inflammatory cytoki
48 e, this represents the first long-term, drug-releasing depot that can be administered as a traditiona
49 e within the brain, neutrophils degranulate, releasing destructive molecules that may exacerbate brai
50 hin MoS2-graphene heterostructure and strain-releasing device designs.
51 ation of organic matter is the major pathway releasing DFe throughout the water column in the open oc
52 d anti-inflammatory activity of the H2S slow-releasing donor GYY4137 on enveloped RNA viruses from Or
53 ong these changes are alterations of neurons releasing dopamine in the ventral and dorsal territories
54 ture drug release in blood circulation while releasing drug on-demand at tumor site have profound imp
55 llate ATTM represents a new class of sulfide-releasing drugs.
56 egulation of Id3 in B cells is essential for releasing E2A and E2-2, which in a redundant manner are
57 ernal surface of the vacuole membrane before releasing efferent molecules, vacuole membrane proteins
58 bination of the stored hydrogen with oxygen, releasing energy and reforming water.
59 and proof-of-concept devices for storing and releasing energy with defects are discussed.
60                     Cells can also signal by releasing exosomes - extracellular vesicles containing b
61                        CD8 Tregs suppress by releasing exosomes that carry preassembled NOX2 membrane
62        The stress neuropeptide corticotropin releasing factor (CRF) and its receptors (CRF-R1, CRF-R2
63                            The corticotropin-releasing factor (CRF) family of peptides includes CRF a
64 e self-administration, reduced corticotropin-releasing factor (CRF) immunodensity in the paraventricu
65                                Corticotropin-releasing factor (CRF) mediates anxiogenic responses by
66 d activates a subpopulation of corticotropin-releasing factor (CRF) neurons in the bed nucleus of the
67 of an intravenous injection of corticotropin-releasing factor (CRF) on fructose malabsorption and the
68                                Corticotropin-releasing factor (CRF) orchestrates the stress response,
69                                Corticotropin-releasing factor (CRF) signaling at the CRF1 receptor (C
70                            The corticotropin releasing factor (CRF) system in the central amygdala (C
71 this, the CEA highly expresses corticotropin-releasing factor (CRF), an important modulator of stress
72  is thought to communicate via corticotropin-releasing factor (CRF), but studies have yet to examine
73  that produce the neuropeptide corticotropin-releasing factor (CRF).
74  al. provide a causal link between histamine-releasing factor (HRF) interactions with IgE and food al
75 de), D2R agonist (quinpirole), corticotropin-releasing factor 1 (CRF1) antagonist (antalarmin), and a
76 ene (Ras protein-specific guanine nucleotide-releasing factor 2) with all clinical events except stro
77  neuropeptides vasopressin and corticotropin-releasing factor facilitate, while serotonin inhibits, a
78 cting to vasopressinergic and corticotrophin releasing factor neurons in the paraventricular nucleus,
79 ior hypothalamus that may gate corticotropin-releasing factor output from the amygdala to the anterio
80 g the efficacy of GSK561679, a corticotropin-releasing factor receptor 1 (CRF1 receptor) antagonist i
81                    Blockade of corticotropin-releasing factor receptor 1 (CRF1) suppresses stress-ind
82 ed significant upregulation of corticotropin releasing factor receptor 2 (CrfR2) in the amygdala of m
83 ed interactions of the class B corticotropin-releasing factor receptor type 1 (CRF1R) with two peptid
84 bserved abnormal expression of corticotropin-releasing factor receptor type 2 (CRFR2) to be associate
85                                Corticotropin-releasing factor receptors (CRFRs), class B G protein-co
86 ion-like protein (RepA-WH1) into the E. coli releasing factor RF1 promotes its aggregation and enable
87                  We found that corticotropin-releasing factor type 1 receptor within the paraventricu
88 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
89 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
90 l axis, including signaling by corticotropin-releasing factor, in the pathophysiology of PTSD.
91 counteracting the functions of corticotropin-releasing factor, the primary stress-mediating neuropept
92 mone 44 (DH44), an ortholog of corticotropin-releasing factor.
93 buting ions, removing neurotransmitters, and releasing factors to influence blood flow and neuronal a
94 erials into the Costa Rican subduction zone, releasing fluids with lighter N isotope signatures.
95 onic acid containing phospholipid substrates releasing free arachidonic acid and lysophospholipids an
96  of the somata of the neuroendocrine neurons releasing GnRH and controlling reproduction are located.
97  extraordinary ability to respond rapidly by releasing granule-stored and newly made mediators underp
98 and stronger acids cleave the metal-O bonds, releasing H2O2.
99 orming sulphur salt Na2S as well as the slow-releasing H2S-liberating compound GYY4137 increased tran
100 egrade in an appropriate time period without releasing harmful substances, not exerting a pathologica
101 and 3 respiration with diabetic mitochondria releasing higher amounts of ROS.
102        TIB64 mast cells responded to cold by releasing histamine and IL-4, and this medium stimulated
103 luster express a reporter for corticotrophin-releasing hormone (Bar(CRH) ).
104 sh with transgenically labeled corticotropin-releasing hormone (CRH) cells, which represent a major r
105 l-genetic approaches to reduce corticotropin-releasing hormone (Crh) expression in the central nucleu
106 xiety-related behaviours, and corticotrophin releasing hormone (crh) neurons, key regulators of the s
107 ansmit signals to hypothalamic corticotropin-releasing hormone (CRH) neurons, which control stress ho
108 atory synaptic strength in PVN corticotropin-releasing hormone (CRH) neurons, with GLP-1R activation
109 u receptor 2 and signaling via corticotropin releasing hormone (Crh) receptor 1.
110 adigm posits that hypothalamic corticotropin-releasing hormone (CRH) regulates neuroendocrine functio
111                                Corticotropin-releasing hormone (CRH) released from the paraventricula
112 XT neurons that co-express the corticotropin-releasing hormone (CRH).
113 th inadequate compensation by Growth hormone-releasing hormone (GHRH) and Growth hormone (GH), undera
114 fects of agonistic analogs of growth hormone-releasing hormone (GHRH) and their mechanism of action w
115                               Growth hormone-releasing hormone (GHRH) is a hypothalamic neuropeptide
116        It has been shown that growth hormone-releasing hormone (GHRH) reduces cardiomyocyte (CM) apop
117 nthetic nonapeptide analogue of gonadotropin-releasing hormone (GnRH or LHRH), is the active pharmace
118                                 Gonadotropin-releasing hormone (GnRH) agonists (e.g., triptorelin) ar
119 the synthesis and/or release of gonadotropin-releasing hormone (GnRH) and gonadotropins.
120 diol (E2) regulating release of gonadotropin releasing hormone (GnRH) and luteinizing hormone (LH) ar
121  Elagolix, an oral, nonpeptide, gonadotropin-releasing hormone (GnRH) antagonist, produced partial to
122                                 Gonadotropin-releasing hormone (GnRH) is a trophic peptide hormone sy
123    Estradiol feedback regulates gonadotropin-releasing hormone (GnRH) neurons and subsequent luteiniz
124                                 Gonadotropin-releasing hormone (GnRH) neurons are the final common pa
125                                 Gonadotropin-releasing hormone (GnRH) neurons produce the central out
126 erminal Ca(2+) is controlled in gonadotropin-releasing hormone (GnRH) neurons via action potentials a
127 drive the pulsatile activity of gonadotropin-releasing hormone (GnRH) neurons.
128 ain regulates fertility through gonadotropin-releasing hormone (GnRH) neurons.
129 ion by brain-secreted pulses of gonadotropin-releasing hormone (GnRH) represents a longstanding puzzl
130 ropin hormones are regulated by gonadotropin-releasing hormone (GnRH) via MAPK signaling pathways tha
131 duction in mammals by secreting gonadotropin-releasing hormone (GnRH).
132                   In vertebrates thyrotropin-releasing hormone (TRH) is a highly conserved neuropepti
133  transcriptionally regulated by gonadotropin-releasing hormone 1 (GNRH).
134 astration and those who receive gonadotropin-releasing hormone agonist (GnRHa) therapy.
135 rchiectomy or receipt of luteinising hormone-releasing hormone agonist or antagonist therapy started
136 rogression and continued luteinising hormone-releasing hormone agonist therapy.
137 rian suppression induced by the gonadotropin-releasing hormone agonist, leuprolide acetate; leuprolid
138                                 Gonadotropin-releasing hormone agonists (GnRHa) have been suggested a
139 ticotrophin-releasing hormone or thyrotropin-releasing hormone and do not express arginine vasopressi
140  rs28365143 variant within the corticotropin-releasing hormone binding protein (CRHBP) gene predicted
141                            The corticotropin-releasing hormone family mediates functional responses i
142 aging in the nerve terminals of gonadotropin-releasing hormone neurons.
143 these neurons largely express corticotrophin-releasing hormone or thyrotropin-releasing hormone and d
144 duction relies on hypothalamic gonadotrophin-releasing hormone output, and most cells producing repro
145  stimulates transcription of the thyrotropin-releasing hormone receptor (TRHR) by negative modulation
146 icant three-way interaction on corticotropin-releasing hormone receptor-1 (Crhr1) gene expression, in
147  gold nanorods (gGNRs) promotes gonadotropin releasing hormone receptor-mediated internalization and
148 responses by binding to type 2 corticotropin-releasing hormone receptors.
149 eptors, and by the hypothalamic gonadotropin-releasing hormone through activation of PKA.
150  prohormone processing of proinsulin, pro-GH-releasing hormone, and proghrelin in association with re
151 mitters such as glutamate, GABA, thyrotropin releasing hormone, and substance P encoded by the Tachyk
152 tide markers (cholecystokinin, corticotropin-releasing hormone, and tachykinin 1) label sleep-promoti
153 de homologous to the vertebrate gonadotropin-releasing hormone, is downregulated as workers become ga
154                        Using a corticotropin releasing hormone-cre driver X tdTomato reporter mouse,
155 lective C-C and C-N bond formations, thereby releasing hydrogen and water.
156 Oral epithelial cells interact with HMOBs by releasing IFN-gamma to regulate RANKL expression and con
157                                         Drug-releasing implants exhibited no significant difference i
158 di-GMP hydrolysis by phosphodiesterase BifA, releasing inhibition of protease LapG by the c-di-GMP ef
159  roles of Syt1 and Syt2 at two types of fast-releasing inhibitory connections in the mammalian CNS: t
160 -mediated copper transfer activates ATP7B by releasing inhibitory constraints through increased freed
161 nctionally relevant Ca(2+) sensor(s) at fast-releasing inhibitory synapses and shows that two major S
162 functionally important Ca(2+) sensor at fast-releasing inhibitory synapses, and show that Syt1 and Sy
163 localizes to lysosomal membranes of neurons, releasing intracellular Ca(2+) to trigger vesicle exocyt
164  necrosis, with the dying cell rupturing and releasing intracellular components that can trigger an i
165 e microbes associated with the plant biomass releasing intracellular proteins that contaminate the me
166 es a major absorption peak at 422 nm without releasing iron or sulfide from the clusters.
167  tourniquet prior to vein identification and releasing it after sample tubes are filled may result in
168 TGF-beta and activating its growth factor by releasing it from the latency imposed by its surrounding
169  delivery system that is not only capable of releasing its cargo when stimulated by light but also pr
170 eme conditions, pb10 protects the phage from releasing its genome.
171 anisidine then reacted preferentially with 3 releasing its guest.
172 ilable hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-as
173  In this work, a liquid-infused nitric oxide-releasing (LINORel) material is created by incorporating
174 ng membrane proteins to the cell surface and releasing material into the extracellular space.
175 ides several key advantages over previous NO-releasing materials, including decreased leaching of NO
176 ible signal molecules delivered through drug-releasing microparticles.
177 D on the membrane when the ratio is high and releasing MinD from the membrane when the ratio is low.
178              We introduce a biocompatible CO-releasing molecule (CORM, A) as Mn(I) tricarbonyl comple
179   In this work, a visible light-sensitive CO-releasing molecule (photoCORM) derived from manganese(I)
180 cally driven, sense-of-logic carbon monoxide-releasing molecule (SL-photoCORM).
181                         CO-applied as the CO-releasing molecule, CORM-2-prolonged the APs and induced
182                              Carbon monoxide-releasing molecules (CORMs) are chemical agents used to
183                              Carbon monoxide-releasing molecules (CORMs) suppress inflammation by red
184         Applicability of phototherapeutic CO-releasing molecules (photoCORMs) is limited because they
185 -molecular framework advance the field of CO-releasing molecules by providing feedback on the diversi
186 ve than Detroit water in short-term testing, releasing more iron, which is a key Legionella nutrient,
187  while also maintaining a common trigger for releasing multiple biomarkers.
188 developed thermally controllable, antibiotic-releasing nanofibrous sheets.
189 ypocretin and GABA (gamma-aminobutyric-acid)-releasing neurons of the lateral hypothalamus, which pro
190                Here we report that glutamate-releasing neurons of the supramammillary region (SuM(vgl
191 lin code in the ciliary specialization of EV-releasing neurons using genetics, fluorescence microscop
192 taining glutamate-, acetylcholine-, and GABA-releasing neurons with connections to basal ganglia and
193 cifically regulates PKD-2 localization in EV-releasing neurons.
194 iary functions of extracellular vesicle (EV)-releasing neurons.
195 ration of GABAergic (gamma-aminobutyric-acid-releasing) neurons from ventral to dorsal forebrain and
196 ing in size and increasing the likelihood of releasing neurotransmitter.
197 mainly involving apoptosis and cell death by releasing neutrophil extracellular traps (NETs) (NETosis
198 ils could increase VTE in cancer patients by releasing neutrophil extracellular traps whereas monocyt
199 te and ends, 48 hours later, with a schizont releasing newly formed merozoites, all committed to eith
200 oducing moieties and the functional entities releasing NO are spatially separated from each other.
201 c constant is found to depend on the binding/releasing nucleotide, and it is smaller for ADP than for
202  is probably attributed to the formation and releasing of ABTS(2+) which has a much greater reactivit
203 ponse, new methods involving the rearing and releasing of large numbers of mosquitoes to eliminate or
204 - 0.8 to approximately 7.6 +/- 0.5 ns) after releasing of pressure from 11 GPa.
205 utrality in the GONR which is compensated by releasing *OH functional groups.
206 riphosphorylated compound into a nucleoside, releasing one molecule of inorganic phosphate at a time.
207                              Strong electron releasing or electron withdrawing substituents lead almo
208  only in the presence of moderately electron-releasing or moderately electron-withdrawing groups on t
209 e interaction of p73 and mutant-p53, thereby releasing p73 from sequestration and allowing it to be t
210 al and hematopoietic stem cells, and insulin-releasing pancreatic beta cells through a signaling path
211 ole in establishing this microenvironment by releasing paracrine factors that control the functions o
212  that acute and selective activation of GABA-releasing parafacial zone (PZ(Vgat)) neurons in behaving
213 ater surface is still a major route of loss, releasing PCBs from the lake into the air.
214 NuRD complex for binding to Pdcd1 enhancers, releasing Pdcd1 expression from Satb1-mediated repressio
215  that contribute to these processes: gastrin-releasing peptide (GRP) and the small conductance, calci
216      Previous studies suggested that gastrin-releasing peptide (GRP) is an itch-specific neurotransmi
217                                      Gastrin-releasing peptide (GRP) receptors (GRPr) are frequently
218 t of spinal interneurons, labeled by gastrin-releasing peptide (Grp), that receive direct synaptic in
219 for biomarker determination using ProGastrin Releasing Peptide (ProGRP), a highly sensitive biomarker
220    We recently introduced the potent gastrin-releasing peptide receptor (GRPR) antagonist (68)Ga-SB3
221        Because overexpression of the gastrin-releasing peptide receptor (GRPR) has been reported on v
222 owing body of evidence suggests that gastrin-releasing peptide receptor (GRPR) might be a valuable ta
223                          Ablation of gastrin-releasing peptide receptor (GRPR) or GRPR neurons in the
224 sin receptor antagonist that targets gastrin-releasing peptide receptor (GRPr).
225       Azapeptide analogues of growth hormone releasing peptide-6 (GHRP-6) exhibit promising affinity,
226 le moths compete to arrive first at a female releasing pheromone.
227 n of greater than two as a glucose acceptor, releasing phosphate from glucose 1-phosphate.
228 ort the development of small interfering RNA-releasing poly(amine-co-ester) nanoparticles, distinguis
229                 The resulting photoactive CO-releasing polymer (photoCORP-1) incorporates 1 such that
230                          This photoactive CO-releasing polymer could find use in delivering controlle
231 ge of reports utilizing periadventitial drug-releasing polymer platforms, most commonly bioresorbable
232 d Ra2535) were identified as endoglucanases, releasing predominantly cellobiose and cellotriose.
233 rowed band gap is partially retainable after releasing pressure, promoting its optoelectronic applica
234 r modulators of hemostasis by expressing and releasing pro- and anticoagulant mediators into the circ
235 sorbing excessive Ca(2+), or kill neurons by releasing proapoptotic factors.
236 a handy mobile phone to remotely control the releasing process and its application in delivering an a
237 , a large influx of astrocytes and microglia releasing proinflammatory cytokines leads to dramatic in
238 nd to nonimmunodominant gliadin fragments by releasing proinflammatory mediators.
239 on of iminothioethers (ITEs), exhibiting H2S-releasing properties and producing vasorelaxing effects
240 aser with particularly pronounced serotonin- releasing properties, has unique subjective effects that
241  B1 cells express only Ras guanyl nucleotide-releasing protein (RasGRP) 1, whereas B2 cells express m
242                                          The releasing rate of molecules can be accurately controlled
243                       The rate law of the H2 releasing reaction indicates that diazene binding occurs
244           They kill endocytosed pathogens by releasing reactive oxygen species in the phagosome and r
245 neralization induced by the experimental ion-releasing resin-based materials.
246  a filler-free (RESIN) or 2 experimental ion-releasing resins (BAG or BAG-F) and immersed in artifici
247 ate the remineralization induced by such ion-releasing resins before and after AS immersion.
248 imens in contact with a filler-free or 2 ion-releasing resins containing micrometer-sized particles o
249 yers after multiple cycles of stretching and releasing revealed that the soft skin layer enabled dyna
250 orus spp. larvae, in addition to potentially releasing sediment methane bubbles twice a day by enteri
251 put facilitate primary nociceptive output by releasing short neuropeptide F, the Drosophila neuropept
252 rocapsules that communicate by producing and releasing signaling molecules.
253  factor receptor signalling in Drosophila by releasing signalling ligands from their transmembrane te
254 se silylcarbynes undergo C-C bond formation, releasing silylated C2O1 fragments and demonstrating tha
255 l semiconductors, there is great interest in releasing single crystal thin films and fabricating flex
256 opioid receptor genes and OT genes at the OT-releasing sites in the human brain.
257 brain structures are in vicinity to tyramine releasing sites, a specific tyramine antibody was applie
258 sion allowed considerable SL biosynthesis by releasing SL biosynthetic genes from an SL-dependent neg
259  activation, WASP limits nucleation rates by releasing slowly from nascent branches.
260 ibutes to the suppression of tumor growth by releasing soluble factors that promote neuroblast differ
261 sses of projection neurons-glutamate/GABA co-releasing somatostatin neurons, glutamatergic parvalbumi
262 cement of the LSL was predicted to result in releasing spikes with significantly high concentrations
263      On this basis, RanGTP is ineffective at releasing standalone Kapbeta1 from NPCs.
264 es at lure-baited traps while simultaneously releasing sterile males) is increasing the ratio of ster
265 n spinning could be directly responsible for releasing stray fibers.
266          Results highlight the importance of releasing substantive updates at regular intervals durin
267 een surface defects and adsorbed O2 and H2O, releasing sulfoxy species (e.g., S2O3(2-), SO4(2-)) and
268                                              Releasing syntaphilin is also activated in the early pat
269 oteasomes, but not standard 26S proteasomes, releasing the 20S catalytic immunoproteasome.
270 tic macrophage secretion of IGFBP-3, thereby releasing the brake and enhancing palmitate-induced IL-8
271 t metal-ion-dependent cleavage, resulting in releasing the cleaved product containing a fluorophore.
272 imal nucleotides control Cas3 recruitment by releasing the Cse1 subunit.
273 alow power (<2 mW), controllably and rapidly releasing the encapsulated contents in less than 5 s.
274 a key intermediate in translocation, thereby releasing the essential assembly factor Dim1 from pre-40
275 n the conformational impact of recruiting or releasing the Mg(2+) cofactor highlights two loop region
276 of this mutant suggests it has difficulty in releasing the N-terminal membrane targeting sequences (M
277 e it is cleaved by Golgi-resident proteases, releasing the N-terminal product, which traffics to the
278 l where IcsA and N-WASP form a tight complex releasing the N-WASP VCA domain to recruit the host cell
279 on contact with skin interstitial fluid thus releasing the nanoparticles into the skin.
280 mino acid conjugates may easily deconjugate, releasing the parent molecule.
281            The recovery process consisted of releasing the particle-bound aluminum from primary sludg
282 celles migrating into the capillary, thereby releasing the peptides that were bound to these micelles
283 ve set off a revolution in cancer therapy by releasing the power of the immune system.
284 rominent, with both MassIVE and PeptideAtlas releasing the results of reprocessed data sets.
285 on of the receptive synergid and PT rupture, releasing the sperm cells for double fertilization.
286 ubiquitin are required to activate parkin by releasing the UBL domain, forming an extended structure
287 n of the HSV-1 pUL25 protein is required for releasing the viral genome from capsids docked at nuclea
288 e unstable at elevated SNARE concentrations, releasing their content after fusion had occurred, recon
289 rt a method of protecting these proteins and releasing them in a controlled manner via a heparin-base
290 ath around the proteins and then tracelessly releasing them in the cytosol.
291 reds of fish (roach, Rutilus rutilus) before releasing them into their lake of origin, thereby exposi
292                                       We are releasing this highly sampled, individual-focused datase
293 s can subsequently act as secondary sources, releasing U back to the aquifer.
294  into PCU, functions as a bioactive porogen, releasing upon contact with blood to interact with endot
295 nal testosterone cream (IVT) or an estradiol-releasing vaginal ring (7.5 mug/d) in patients with earl
296               We found that both the rapidly releasing vesicle pool and the releasable vesicle pool o
297 on the synaptic ribbon replenish the rapidly releasing vesicle pool; and at any given time, there are
298                                   The energy-releasing, VHF-to-DHA, ring closures also occur in a ste
299  pUL25 capsid protein has a critical role in releasing viral DNA from NPC-bound capsids.IMPORTANCE He
300 acemic alcohol precursors in up to >97 % ee, releasing water as the only byproduct.

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top