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1 pair with the therapeutic copper isotope (67)Cu.
2 arget location was cued than when it was not cued.
3 ided optic flow but lacked explicit position cues.
4 ited USV production in the absence of social cues.
5 the division site based on cellular polarity cues.
6 their membranes in response to environmental cues.
7 ociation of rewarding outcomes with relevant cues.
8 hways are regulated by external and internal cues.
9 ehavior without relying on the environmental cues.
10 s courtship or aggression promoted by female cues.
11 avior, possibly in response to environmental cues.
12 ing unpleasant, compared to pleasant context cues.
13 rotein in response to appropriate regulatory cues.
14 challenging version that nullifies intramaze cues.
15 ally manifested in response to environmental cues.
16  must rely on incidental visual and auditory cues.
17 L(-1)) and mothers of full-term (Fe = 0.733, Cu = 0.234, Zn = 2.91 and I = 0.255 mg L(-1)) infants.
18 s varied in mothers of pre-term (Fe = 0.997, Cu = 0.506, Zn = 4.15 and I = 0.458 mg L(-1)) and mother
19 is formed on the as-prepared Cu surface with Cu(0) which inhibits hydrocarbon formation.
20 atalyst with improved OER performance, Y(1.8)Cu(0.2)Ru(2)O(7-delta), and provides general guidelines
21 y of (Fe(3+) (2.15)Fe(2+) (1.59)Ni(2+) (0.17)Cu(+) (0.04))(Sigma) (=) (3.95)O(5) We further suggest a
22 n pairs formed by the V(O) defect, including Cu(1+) -Ti(4+) , Ti(3+) -Ti(4+) and Ti(3+) -Ti(3+) , are
23 n the 3D tumor model, governed by the Cu(+2)/Cu(+1) redox potential.
24 manipulation on a sodium chloride bilayer on Cu(111) at 5 K, and imaged by high-resolution atomic for
25  selectivity of a well-defined CeO(2)/Cu(2)O/Cu(111) catalyst from carbon monoxide and carbon dioxide
26 ing the selectivity of a well-defined CeO(2)/Cu(2)O/Cu(111) catalyst from carbon monoxide and carbon
27 tide-MBP chimeras corroborated the extent of Cu(2+) binding among the peptides.
28  lipid in lipid monolayers, while Mg(2+) and Cu(2+) did not.
29 of bioinformatics-based structure modelling, Cu(2+) ion docking, and MD simulations of peptide-MBP ch
30 on both lithium metal and copper (and Cu(+), Cu(2+) reduction).
31 used to measure diffusion constants of K(+), Cu(2+), and Cl(-) diffusing through loblolly pine (Pinus
32 e antiferromagnets exist, typically based on Cu(2+), d(9) compounds, though they feature structural i
33 -crystal X-ray analyses on MOF-1 showed that Cu(+2) ion was 6-coordinated.
34 icacy in the 3D tumor model, governed by the Cu(+2)/Cu(+1) redox potential.
35                       Herein, a Cu-Sn (e.g., Cu(3) Sn) intermetallic coating layer (ICL) is rationall
36 erromagnetic charge transfer insulator YBa(2)Cu(3)O(6.1) revealed rapid demagnetization within 90 fs
37            Meanwhile, the ultrasmall size of Cu(5.4)O USNPs enables rapid renal clearance of the nano
38 otective effect and good biocompatibility of Cu(5.4)O USNPs will facilitate clinical treatment of ROS
39 opy, and Raman techniques, we found that the Cu(68)Ag(32) nanowires underwent an irreversible structu
40 cluster with 81 copper atoms, formulated as [Cu(81)(PhS)(46)((t)BuNH(2))(10)(H)(32)](3+) (Cu(81)), wa
41 Cu(81)(PhS)(46)((t)BuNH(2))(10)(H)(32)](3+) (Cu(81)), was successfully synthesized and fully studied
42 te Cu(Z), the binuclear electron entry point Cu(A) is also utilized in other enzymes, including cytoc
43 nd A tensors that resemble axially perturbed Cu(A).
44 pment inside the host in response to sensory cues, a process called activation.
45 ing task, in which visual and proprioceptive cues about hand posture were incongruent.
46        These cells consistently responded to cues across multiple environments.
47 age reverses the localization of directional cues across venular walls, thus causing neutrophils enga
48                                     Guidance cues act during development to guide growth cones to the
49 Herein, it is demonstrated that mixed-valent Cu acts as an effective dopant to modulate the oxygen va
50 ng back once they became sensitized to these cues after midline crossing.
51 e bulk chemistry reconstructed from the FeNi(Cu) alloy, we propose that it formed by decomposition of
52  population, along with a high prevalence of CUD among current cannabis users, an urgent need exists
53  diagnostic and therapeutic potential of (64)Cu and (67)Cu, respectively, offers the possibility of u
54 te CO(2) to methanol on catalysts containing Cu and ZrO(2).
55   We found that frontal RFs require spectral cues and lateral RFs require ILDs.
56 lar coordinate system that represents visual cues and self-motion signals.
57 erated by the interaction between contextual cues and subtle emotional faces, such that participants'
58 ally, informed by the spatial correspondence cues and the inferred causal structure the frontal eye f
59 corticostriatal transfer of movement-related cues and their striatal integration with movement sequen
60 , insensitive to RORgamma-inducing bacterial cues and to IL6, and showed evidence of higher TCR-trans
61 ties, which rely on chemosensory and tactile cues and, to a lesser degree, on vision.
62 er, which blocks the long-range migration of Cu(+) and produces a drastic reduction of Cu(+) ion migr
63  measured manganese (Mn), lead (Pb), copper (Cu), and chromium (Cr) in hair, blood, urine, nails, and
64       In secondary analyses, saliva Mn, hair Cu, and saliva Cr were selected as the biomarkers most s
65 gh the perception of different environmental cues, and respond by changing their developmental gene e
66  extracts a diversity of naturalistic motion cues, and the retinorecipient pretectum organizes these
67 ution of incentive salience to reward-paired cues, and underscore the consequences of potential diffe
68  French coastal site contaminated by diffuse Cu anthropogenic sources.
69 ether dopamine neurons encode differences in cued approach behaviors and incentive salience.
70         While aerobic oxidations with Fe and Cu are well precedented, Ni-based oxidations are frequen
71 s inherent in peripheral mechanics, and wind cues are brought into the same circular coordinate syste
72 brain, it is unclear how visual and auditory cues are combined to improve speech perception.
73                        Second, reward-paired cues are powerful motivators and they can evoke pursuit
74 c field to guide their flight, but how these cues are processed and integrated into the brain to driv
75 amework for understanding how innate sensory cues are processed to elicit adaptive behavioral respons
76  fluid, synthetic membranes, while mitogenic cues are released slowly from the microrods.
77 he retinorecipient pretectum organizes these cues around the elements of behavior.
78 ings also support further investigation into Cu as both beneficial and toxic for neurobehavioral outc
79 rupted rats' ability to discriminate between cues associated with either a high or a low probability
80 troscopy both in the presence and absence of Cu at a common interface.
81  in the self-generated pressure and velocity cues at the sensitive mechanosensory antennae.
82 actors" to precisely confine multiple Fe and Cu atoms for NRR electrocatalysis is reported.
83 vo, as well as to evaluate the change in (64)Cu-ATSM signal after redox-active drug treatment.
84 sed to evaluate the relationship between (64)Cu-ATSM signal and levels of reducing molecules in vivo,
85 th beta-lapachone, there was a change in (64)Cu-ATSM signal in xenograft tumors smaller than 50 mg bu
86 e intrinsic activity and space time yield of Cu based heterogeneous methanol synthesis catalysts thro
87                   Despite recent research on Cu-based catalysts for the CO(2) and CO reduction reacti
88                          The precipitated Zn/Cu-bearing solids contained 33.6% Zn and 21.7% Cu, where
89  immune signaling and brain activity to food cues between depressed participants experiencing increas
90  revealed that the active-site structure and Cu binding of SOD5 strongly deviate from those of Cu/Zn-
91 neering of C(3) N(4) layers with single-atom Cu bonded with compositional N (Cu N(x) ) is demonstrate
92 sing M = Ti, Zr members of the Delta,Lambda-[Cu(bpy)(2)(H(2)O)](2)[MF(6)](2).3H(2)O (M = Ti, Zr, Hf;
93 uctivity of 10(-4) S cm(-1) , whereas here a Cu-Br congener, (EA)(2) CuBr(4) (EA=ethylammonium), exhi
94 y using not only grammatical and statistical cues but also their prior knowledge of the form of langu
95 ech sounds is affected by low-level acoustic cues, but also by their linguistic function.
96 are easily segregated, even without binaural cues, but the neural mechanisms underlying this ability
97 the neuronal gene expression associated with CUD by using RNA sequencing of dorsal-lateral prefrontal
98        The magnitude of reaction to predator cues by salmon group followed the gradient of previous p
99 roaches to study the representation of these cues by the perceptual system.
100                                          (64)Cu-CA003 and (64)Cu-CA005 showed high internalization ra
101                         (64)Cu-CA003 and (64)Cu-CA005 showed high internalization ratios (34.6% +/- 2
102                                              Cues can also promote dysfunctional reward-seeking behav
103 ersion of CO(2) to C(2+) products requires a Cu catalyst with a high density of defect sites that pro
104 ochemical CO(2) reduction mechanism over the Cu catalysts with various oxidation states was studied b
105 adily available via an improved protocol for Cu-catalyzed 1,3-dipolar cycloaddition.
106                          Herein, we report a Cu-catalyzed enantioselective allylic alkylation using a
107                                            A Cu-catalyzed regio-, diastereo-, and enantioselective ca
108                                      Linear [Cu(Cbz)((Dipp)CAArC)] (2) has been found to be an except
109 elements (K, Na, Mg, Ca, Fe, Zn, Hg, Se, As, Cu, Cd, Mn, Ni, Cr, Pb and Co) were determined in dorsal
110                                      Layered Cu-Cl perovskites require pressures >50 GPa to show a co
111 pyrochlores Y(1.8)M(0.2)Ru(2)O(7-delta) (M = Cu, Co, Ni, Fe, Y) controls the concentration of surface
112           Little is known about how spectral cues contribute to the neural encoding of auditory space
113                            The developmental cues controlling the differentiation of committed progen
114 mation on both lithium metal and copper (and Cu(+), Cu(2+) reduction).
115 de mice compared with the acid-mediated [(64)Cu]Cu-c[E(4)W(5)C] tracer.
116                                         [(64)Cu]Cu-c[R(4)W(5)C] demonstrated significantly reduced up
117  mice that received the highest dose of [(67)Cu]Cu-MeCOSar-Tz in a fractionated manner exhibited impr
118                This study suggests that [(64)Cu]Cu-pHLIC is a valuable tool to noninvasively assess a
119 says were performed for the novel tracer (64)Cu-CuCB-bicyclam.
120 Conclusion: This study demonstrates that (67)Cu-CuSarTATE is well tolerated in BALB/c nude mice and h
121 ndrial respiration and Fe accumulation, both Cu-dependent processes.
122                              Conclusion: (64)Cu-DOTATATE PET/CT is a safe imaging technique that prov
123 ospectively determine the lowest dose of (64)Cu-DOTATATE that facilitates diagnostic-quality scans an
124 I activity was modulated by visual attention cues during feature-based learning.
125 ly simple function of a single environmental cues (e.g. a linear function of one cue), which facilita
126 ed between copper (Cu) nanoparticles and the Cu-electrode beneath.
127 f the near-surface region of polycrystalline Cu electrodes under in situ conditions through a combina
128 the neuronal response to conditioned context cues evolves over time in the medial prefrontal cortex,
129 posed by 10% of ZrO(2) supported over 90% of Cu exhibits the highest mass-specific methanol formation
130 es in responsiveness to innate environmental cues, FcRgamma(-) NK cells responded robustly to adaptiv
131 ped for further determination of Al, Ca, Cr, Cu, Fe, K, Mn, Mo and Ni in rice samples by ICP OES.
132 x grain seed to expand throughout the entire Cu foil.
133  that anodic halogenation of electropolished Cu foils in aqueous solutions of KCl, KBr, or KI creates
134 h may alter their transcriptomes and provide cues for spatial reconstruction.
135 entiation of the AII ACs is not dependent on cues from BCs.
136  (25 and 28 degrees C) with/without predator cues from climbing perch (Anabas testudineus) for 11 gen
137 how these pathways are fine-tuned by diverse cues from commensal bacteria is not well understood.
138               However, to what extent innate cues from DCs dictate transcriptional changes in T cells
139 opmental decision of metamorphosis relies on cues from environmental bacteria.
140 extract continuously-varying spectrotemporal cues from the acoustic signal to perceive discrete phone
141 hese findings demonstrate that subtle timing cues fundamentally shape the experience of watching join
142  the insertion of an ester or amide into the Cu-H bond.
143 nd crystallographic characterization of rare Cu-hemiacetalate and Cu-hemiaminalate moieties from the
144 haracterization of rare Cu-hemiacetalate and Cu-hemiaminalate moieties from the insertion of an ester
145 riod and low temperature, the major seasonal cues heralding winter, suppress branching by simultaneou
146 p in the current block is the formation of a Cu-histidine coordination complex.
147                                             [Cu(I) (TPMA(PYR) )](+) exhibited the highest reported ac
148               This allows the doubly reduced Cu(I) 4H-imidazolate complex to be stored after photoche
149  are thiol-rich reducing molecules with high Cu(I) affinity, they are potential competitors for a cop
150 ate oxidation based on redox cycling between Cu(I) and Cu(II) , as well as their resistance to dissoc
151 with Cu(I) ions, which are present as mobile Cu(I) diamine complexes [Cu(I)(NH(3))(2)](+).
152 mperature NH(3)-SCR, oxygen only reacts with Cu(I) ions, which are present as mobile Cu(I) diamine co
153 r fulvic acid (SRFA) on Cu(II) reduction and Cu(I) oxidation kinetics at pH 8.2.
154 e present as mobile Cu(I) diamine complexes [Cu(I)(NH(3))(2)](+).
155 O results in an almost complete reduction to Cu(I), under the formation of N(2).
156 ction with reduced Hypocrea jecorina LPMO9A (Cu(I)-HjLPMO9A) is demonstrated to be 1,000-fold faster
157 the Glaser coupling product ArC=C-C=CAr and [Cu(I)](solvent).
158 ion based on redox cycling between Cu(I) and Cu(II) , as well as their resistance to dissociation or
159                The overall structure of NfoR-Cu(II) complex is a dimer that covalently binds with FMN
160                       We then identified two Cu(II) coordination geometries: in the type 1 coordinati
161 e 19-fold CO(2) uptake for CTH-12 containing Cu(II) dinuclear paddle-wheels.
162 , R154, and Q171 and bank vole recPrP, where Cu(II) is coordinated by three residues and by one water
163 (-) and Suwannee River fulvic acid (SRFA) on Cu(II) reduction and Cu(I) oxidation kinetics at pH 8.2.
164 a radical scavenger, the spin-coupled hidden Cu(II) was observed by EPR spectroscopy.
165 ellular prion protein interacts with copper, Cu(II), through octarepeat and nonoctarepeat (non-OR) bi
166 s a dimer that covalently binds with FMN and Cu(II)-binding pocket is located at the interface of the
167 imer, tetramer, and hexamer that precede the Cu(II)-induced amyloid assembly process, results which a
168 nd, the three-coordinate copper(II) alkynyl [Cu(II)]-C=CAr (Ar = 2,6-Cl(2)C(6)H(3)) forms upon reacti
169                                             [Cu(II)]-C=CAr also captures the trityl radical Ph(3)C. t
170                           In solution, this [Cu(II)]-C=CAr species cleanly transforms to the Glaser c
171 r with the copper(II) tert-butoxide complex [Cu(II)]-O(t)Bu.
172 alculations, redox disproportionation forms [Cu(III)](C=CAr)(R) species that reductively eliminate R-
173 e relationship between the two main forms of Cu in wine and their impact on the rate of oxygen consum
174                   These moths can use visual cues in combination with the geomagnetic field to guide
175 amically recalls memories to detect relevant cues in complex sensory scenes.
176  population activity strongly tracked visual cues in one environment, whereas responses were almost c
177 rs a mechanism for integrating environmental cues into BR signaling to shape growth.
178 concurrent transposition of retinal guidance cues into the superior colliculus providing positional i
179 utritionally-relevant stimuli including food cues, intragastric nutrients, cholecystokinin and ghreli
180 of Cu(+) and produces a drastic reduction of Cu(+) ion migration by nearly two orders of magnitude.
181                          The accumulation of Cu(+) ions via an ionic capacitive effect at the Schottk
182 ucleus accumbens evoked by reward-predictive cues is accompanied by a rapid suppression of glutamate
183 ond to dynamic variations in differentiation cues is not well characterized.
184 ellular fates are triggered by environmental cues is poorly understood.
185 cent (compared to about 66 per cent for pure Cu) is achieved at a current density of 400 milliamperes
186 this new biomonitoring tool, we investigated Cu isotope variations of two bivalves-the oyster Crassos
187  when the boundary is formed by flat surface cues, its physiological basis is not well understood.
188  of 22 elements (As, Ba, Be, Bi, Cd, Co, Cr, Cu, K, Mn, Mo, Na, Ni, P, Pb, Th, Tl, Sb, U, V, Y and Zn
189  in situ soft X-ray absorption spectroscopy (Cu L-edge), and online gas chromatography measurements.
190                          Conclusion: The (64)Cu-labeled PSMA ligands are promising agents to target P
191  avoidance in rats well trained on different cued lever-press avoidance tasks.
192 europhysiological mechanisms encode temporal cues like voice-onset time (VOT), which distinguishes so
193  that BCP may be useful for the treatment of CUD, likely by stimulation of PPARalpha and PPARgamma in
194  between the lipopolysaccharide dose and (64)Cu-LLP2A uptake, as quantified by in vivo PET (R = 0.69,
195          A DeltamntR strain had an increased Cu load and decreased growth in the presence of Cu, whic
196 find that attention spreads from a spatially cued location to the underlying object, and enhances all
197  valid and invalid trials (target at cued/un-cued location, respectively), pre- or post-cueing endoge
198 igation of cell contact dynamics as guidance cues may yield new insights into the regulation of innat
199 ods, we analysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harvested and commercially available term
200  single-atom Cu bonded with compositional N (Cu N(x) ) is demonstrated to address this challenge.
201 o those with callous-unemotional traits (DBD+CU, N=198) and without callous-unemotional traits (DBD o
202  through nanocavities formed between copper (Cu) nanoparticles and the Cu-electrode beneath.
203 carbon (M(1)/CN, M = Pt, Ir, Pd, Ru, Mo, Ga, Cu, Ni, Mn).
204 er active site for the formation of a stable Cu-O(2) intermediate.
205 solated Cu particles or atomically dispersed Cu-O-Zr sites only catalyze the reverse water-gas shift
206 protected carboxylic acid substituents, with Cu(OAc)(2) .
207  damaged leaves or those exposed to volatile cues of damage.
208 that manipulate food availability and social cues of density (frequency of territorial vocalizations)
209 indicate that increases in social (acoustic) cues of density in the absence of additional food can in
210 uction and well-stabilized chemical state of Cu on the catalyst surface under the working CO(2)RR con
211 attend (and learn about) only one of several cues on each trial.
212  estimate the influence of six environmental cues on germination proportion, mean germination time an
213                              On a track with cues on left and right sides, most cue cells only respon
214 ight sides, most cue cells only responded to cues on one side.
215                      Previous studies of the Cu-only enzyme SOD5 from the opportunistic fungal pathog
216 nt proteins, we found that, similar to SOD5, Cu-only SOD4 can react with superoxide at rates approach
217 se of Cu/Zn-SODs in its animal hosts, making Cu-only SODs a possible target for future antifungal dru
218        Mammalian sperm cells must respond to cues originating from along the female reproductive trac
219 assisted leaving group could be activated by Cu(OTf)(2) and avoided the use of harsh Lewis acids.
220                                         The [Cu(OTf)](2) .benzene catalyst that has been standard in
221             Materials consisting of isolated Cu particles or atomically dispersed Cu-O-Zr sites only
222  placebo) on reactivity to reward-predicting cues (Pavlovian-to-instrumental transfer) and flexibilit
223  cues.SIGNIFICANCE STATEMENT Drug-associated cues precipitate relapse, which is correlated with trans
224      In Pavlovian conditioning models, where cues predict reinforcer delivery at a different goal loc
225 osure in the river with and without predator cues present to measure their reaction to a predator.
226 tective immunity in barrier tissues, but the cues promoting Trm cell generation are poorly understood
227  The velocity of actions made in response to cues prospectively triggered by STN beta bursts was slow
228 onstrate this method across diverse systems: cued reaching in nonhuman primates, motor sequence produ
229                                   Mechanical cues regulate the function of a broad range of stem cell
230 e biomaterials that respond to environmental cues represents a significant step forward in the develo
231  and therapeutic potential of (64)Cu and (67)Cu, respectively, offers the possibility of using a sing
232 g rates and can be accessed directly without cued retrieval.
233 s also were sorted along other environmental cues, showing multidimensional adaptive trait syndromes.
234 ced during reinstated cocaine by drug-paired cues.SIGNIFICANCE STATEMENT Drug-associated cues precipi
235                                    Herein, a Cu-Sn (e.g., Cu(3) Sn) intermetallic coating layer (ICL)
236 d via stereodefined boron-stabilized allylic Cu species formed by an enantioselective transmetalation
237 artial oxidation of methane to methanol over Cu-SSZ-13 in a continuous-flow reactor.
238 ickly and accurately as possible to visually cued stimuli representing single-limb or combined upper
239 ments where social partners may change their cuing strategy or become untrustworthy.
240                    When they detect predator cues such as bat echolocation calls, males typically sto
241 tely controlled by site-specific directional cues such as chemokines.
242 nal inputs modulate entrainment to nonphotic cues such as time-restricted feeding.
243 tively filtering out noise and fast temporal cues such as voicing periodicity, that are not directly
244                                  Biophysical cues, such as electrical stimulus, mechanical feature, a
245 ly includes inputs from external signals and cues, such as quorum sensing and chitin availability.
246 ) requires the integration of a multitude of cues, such as wind speed and solar elevation, and the pr
247 n of the downstream effectors of directional cues suggests that different external signals regulate a
248 the VTA encode both predictive and incentive cues, support an important role for dopamine neurons in
249  reveal that lowering *CO(2) coverage on the Cu surface decreases the coverage of the *CO intermediat
250  with the initial degree of oxidation of the Cu surface prior to the exposure to negative potentials.
251 CO (CO(bridge)) is formed on the as-prepared Cu surface with Cu(0) which inhibits hydrocarbon formati
252 , surface speciation of the various types of Cu surfaces under reaction conditions remains a topic of
253 fication of physostigmine determination with Cu-SWCNT-Pc 3D/GCE were found to be 53 and 177 nM in the
254 n and electrochemical sensor features of the Cu-SWCNT-Pc hybrid towards to physostigmine pesticide we
255                                   The rGO@3D-Cu symmetric cells and half-cells achieve state-of-the-a
256                         The immiscible alloy Cu-Ta has the potential for enhanced mechanical performa
257 purpose-dependent nature and consequences of cued temporal expectations on brain and behavior in male
258  ~20 ms earlier when the target location was cued than when it was not cued.
259 ce of chemotropic proliferation and guidance cues that are commonly implicated in dorsal (cortical) p
260  new cell class ('cue cell') encoding visual cues that could be used to correct errors in path integr
261  along the myeloid lineage triggers cellular cues that drive reactivation.
262 sis [1-6], which are thought to act as local cues that pattern cortical Galphai, LGN, and nuclear mit
263    We exposed human participants to auditory cues that predicted the likely direction of visual movin
264  triggered by developmental and reproductive cues that repress the activity of proteostasis-related p
265 for spatially and temporally stable gradient cues that specifically indicate the location of the nata
266  provided missing speech and spatial hearing cues through haptic stimulation to augment the electrica
267                           hGrx1 can transfer Cu to the metallochaperone Atox1 and to the MBDs 5-6 of
268 n neuroimaging scans, in which subjects were cued to increase/decrease activity in SMA without receiv
269 he olfactory system can assign related odour cues to common and yet personalized percepts.
270 about the circuits that integrate these time cues to drive a coherent circadian output(1-3).
271  Therefore, by permitting unfiltered sensory cues to enter information processing and activate sensor
272 uggests that species reliant on chemosensory cues to locate their prey may be at an increased risk of
273 nterfering with the transmission of parental cues to offspring.
274 l gene programs in response to environmental cues to regulate cell fate and maintain normal homeostas
275 s unclear if EAAT2 responds to environmental cues to specifically shape action control.
276           Elevations on callous-unemotional (CU) traits designate a subgroup of youth with conduct di
277  etiology between aggression and these three CU-traits.
278 vity for valid and invalid trials (target at cued/un-cued location, respectively), pre- or post-cuein
279  in leaf reflectance may have altered visual cues used by the cabbage root flies in their host plant
280 ted in a fully aquatic animal, where sensory cues used for orientation may differ dramatically from t
281 ly induced in tendon by means of biophysical cues using a woven and electrospun patch.
282 wer oil enriched with curcuminoid compounds (CUs) was gelled by adding 5% (w/w) saturated monoglyceri
283                     In many studies, DSF and Cu were delivered in two separate formulations.
284     During the third breeding season, social cues were experimentally added at 10 formerly unoccupied
285              Developmental and environmental cues were shown to regulate CAM expression in stems, whe
286 -bearing solids contained 33.6% Zn and 21.7% Cu, whereas the Fe content was less than 0.2%.
287        Inside the scanner, participants were cued which task to perform and then sequentially identif
288 load and decreased growth in the presence of Cu, which was abrogated by the introduction of mntA::Tn.
289 aining 23.5 g/L Fe, 4.45 g/L Zn and 2.81 g/L Cu, which was subjected to hydrothermal treatment with t
290 mune homeostasis and respond to local tissue cues, which control their stability and function.
291 teinaceous environment control reactivity of Cu with O(2).
292 terials and showed that smooth topographical cues with proper period and orientation can efficiently
293                       Coupling topographical cues with the profibrotic agonist, TGFbeta (transforming
294 oteins are evolutionarily conserved polarity cues, yet Wnt mutants display variable PCP defects; thus
295 her than its unique tetranuclear active site Cu(Z), the binuclear electron entry point Cu(A) is also
296 of serum and 12 elements (Mg, S, Mn, Fe, Co, Cu, Zn Se, Br, Rb, Mo, and Cs) in less than 250 000 cell
297 transition metal ions M(II) (M = Mn, Co, Ni, Cu, Zn, Pd, and Cd) under mild conditions.
298 lements (Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb, Sr, Mo, I, Cs, and Ba) in 10 muL of
299 nding of SOD5 strongly deviate from those of Cu/Zn-SODs in its animal hosts, making Cu-only SODs a po
300 imes higher than the activity of traditional Cu/ZrO(2) catalysts (159 g(MeOH)kg(cat)(-1)h(-1)).

 
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