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 is also feeds back to regulate the circadian oscillator.
2 ve at the native behaviour of the cell cycle oscillator.
3 gene expression from the mammalian circadian oscillator.
4 oplasm drives a self-organized standing wave oscillator.
5 vely coupling it with a Josephson parametric oscillator.
6 the 'repressilator', a three-node synthetic oscillator.
7 sugar sensor, HEXOKINASE1, or the circadian oscillator.
8 th Si3 being part of the primary half-center oscillator.
9 perated in dynamic mode within a closed loop oscillator.
10 scillator genes in vivo that may entrain the oscillator.
11 cillator is different from the average plant oscillator.
12 of the effects of ethylene on the circadian oscillator.
13 re very large numbers of nanoscale nonlinear oscillators.
14 approach can be applied to other biological oscillators.
15 es, and wireless transmitters clocked by the oscillators.
16 itro and a lack of known molecular ultradian oscillators.
17 ed femtosecond degenerate optical parametric oscillators.
18 roscopic level, cells must synchronize their oscillators.
19 dual cells can behave as autonomous cellular oscillators.
20 ze alternatives to conventional quartz-based oscillators.
21 ies between aperiodic fluctuations and noisy oscillators.
22 ular molecular connections between these two oscillators.
23 ted circuits based on exciton-polariton Rabi oscillators.
24 matic changes to the dynamics of interacting oscillators.
25 inct patterns of interactions between neural oscillators.
26 est, such as magnetic memory and spin torque oscillators.
27 ermines the intrinsic (natural) frequency of oscillators.
28 r aspects of physiology involving biological oscillators.
29 a compromise between AIS and somatodendritic oscillators.
30 stigate a network of coupled micromechanical oscillators.
31 artmentalised chemical networks and designed oscillators.
32 el, on-chip computation based on networks of oscillators.
33 e potentials and budded more slowly than non-oscillators.
34 synchronization in ensembles of interacting oscillators.
35 w experimentally that a nanoscale spintronic oscillator (a magnetic tunnel junction) can be used to a
36 -maintenance midbandwidth optical parametric oscillator, a few second measurement should yield nearly
37 es, including memristive and superconducting oscillators, a proof of concept of neuromorphic computin
38 knock-in cells NF-kappaB behaves as a damped oscillator able to synchronize to a variety of periodic
39 adian clocks and the connections between the oscillator and circadian-regulated processes such as met
40 cells compared with the "average" whole-leaf oscillator and examined gene expression and stomatal ape
41 structure of the cyanobacterial clock as an oscillator and explored the physiological relevance of t
43 identified TF, is a central circadian clock oscillator and is required not only for the daily oscill
44 s mediate metabolic signals to the circadian oscillator and that sucrose directly affects PIF binding
46 ock and cell cycle as interdependent coupled oscillators and identify DNA replication as a critical p
47 lying numerical techniques to control linear oscillators and pave the way for utilizing their large H
49 transistors to fabricate GHz self-sustained oscillators and synchronized oscillator arrays that prov
50 ical systems, including linear and nonlinear oscillators and the chaotic Lorenz system, to the fluid
51 ranslates to large networks of type-II phase oscillators and, hence, crucially impacts on the overall
52 arger than previously achieved in a harmonic oscillator, and create complex multi-component superposi
53 urcations associated with a noisy biological oscillator, and demonstrate a general strategy for bifur
54 models (e.g., the fluctuating charge, Drude oscillator, and the induced dipole models), the angular
55 ation and characteristics of inverters, ring oscillators, and NAND gates based on complementary-like
59 ead as the only driving force, these fluidic oscillator arrays realize a wide range of periods (0.4 s
60 self-sustained oscillators and synchronized oscillator arrays that provide RF references, and wirele
61 effects of intrinsic noise on the Hes1/miR-9 oscillator as a consequence of low molecular numbers of
64 ) neurons of primates behave as synchronized oscillators as was found for rodents using intracellular
66 Here we demonstrate a coupled relaxation oscillator based dynamical system that exploits insulato
68 mote the entrainment of CA3-autonomous gamma oscillators bilaterally, synchronizing lateralized gamma
69 ian rhythmicity controlled by the core clock oscillator BMAL1 and AKT/glycogen synthase kinase 3beta
72 ently, networks of mutually injected optical oscillators, called coherent Ising machines, have been d
75 our technique, even low-frequency mechanical oscillators can in principle be cooled arbitrarily close
76 on of whether a complex network of nonlinear oscillators can maintain its synchronization stability a
78 hing-related motor pattern, a brainstem core oscillator circuit projects to a population of premotor
80 uprachiasmatic nucleus (SCN), noisy cellular oscillators communicate within a neuronal network to gen
82 hip in mRNA oscillations was altered between oscillator components in the circadian pacemaker system
83 ripts (NATs) to transcripts encoding central oscillator components were proposed as modulators of cor
86 urons into a Melibe-like primary half-center oscillator configuration, indicating that the connectivi
91 discover that an independent RhoA pacemaking oscillator controls this instability, generating a pulsa
92 trength of coupling between individual actin oscillators controls cell polarization and directional m
93 pears already at weak connectivity, with the oscillators converging to one common oscillation frequen
94 response pathways and the internal circadian oscillator coordinate physiological processes with predi
95 e how an ensemble of these noisy spontaneous oscillators could be entrained to efficiently detect sig
96 Here the authors demonstrate a spin torque oscillator device driven by pure spin current arising fr
98 ns-morning oscillators (M cells) and evening oscillators (E cells)-are largely responsible for these
99 ar behaviors, we show that two complementary oscillators emerge from i) mechanical stretch with calci
100 s in silicon-based monolithic optomechanical oscillators, enabled by the strong and coupled nonlinear
102 the Dual Oscillator Model, that a glycolytic oscillator endogenous to islet beta-cells drives pulsati
103 hing spatiotemporal structures in biological oscillator ensembles is a challenging task that requires
106 lates the strength of coupling between actin oscillators for efficient polarity and directional migra
107 del based on a broadly coupled set of neural oscillators for PD, but a more finely tuned set of oscil
108 ex networks of VO2 oscillators, or any other oscillators, for more complex tasks have been challengin
109 nstrate that an inhibition-coupled intrinsic oscillator framework, pyramidal resonance interneuron ne
112 LE (CLK-CYC) heterodimers initiate circadian oscillator function by activating per and tim transcript
114 Moreover, the differences in guard cell oscillator function may be important for the correct reg
116 s (Arabidopsis thaliana) plants in which the oscillator gene CIRCADIAN CLOCK ASSOCIATED1 (CCA1) was o
117 sed large-scale qRT-PCR to compare circadian oscillator gene expression in guard cells compared with
119 IF binding to the promoters of key circadian oscillator genes in vivo that may entrain the oscillator
121 g biochemical answers to why this remarkable oscillator has such a long time constant and how it can
123 rly coupled to dissipative baths of harmonic oscillators, has become the workhorse of this field.
124 d genes, indicating that the circadian clock oscillators have been reset, was independent of its pres
125 xperimental realizations of globally coupled oscillators have proven to be invaluable in settings as
127 y of a large population of discrete chemical oscillators, here we report on the unexpected discovery
128 owave signals generated by spin orbit torque oscillators hinders practical applications of these magn
131 o, by coupling the sensory input to a neural oscillator in continuous time, we show that the mechanis
133 ons of limiting nutritional carbon; the core oscillator in the prd-1 mutant strain runs with a long p
134 idual neurons oscillate or from a population oscillator in which individual neurons fire sparsely and
135 e the structurally and dynamically identical oscillators in a coupled networked system spontaneously
138 ral desynchrony between autonomous circadian oscillators in different regions, with different consequ
139 ed on enhanced or reduced interactions among oscillators in different spatial groups, to explain why
142 genous cell-autonomous human skeletal muscle oscillators in regulating lipid metabolism independent o
144 ral clock in the SCN is dampened, peripheral oscillators in the hippocampus and olfactory bulb become
146 m, we have focused on the cardio-respiratory oscillators in the medulla oblongata that modulate heart
148 e this array of all-to-all coupled nonlinear oscillators in the presence of stochasticity and demonst
149 can be used to generate entanglement between oscillators in the quantum regime.Coupled mechanical res
150 the hypothalamus and it regulates circadian oscillators in tissues throughout the body to prevent in
153 igh-dimensional data from various biological oscillators increases, ZeitZeiger should enhance efforts
154 d mechanism: that of a stochastic population oscillator independent of the dynamics of individual neu
155 ics theory that describes how weakly coupled oscillators influence each other's phase relations.
156 omplementary shear-driven and stretch-driven oscillators interact, either may dominate, producing a r
158 ed CCA1 Our results show that the guard cell oscillator is different from the average plant oscillato
159 KaiC phosphomimetic, KaiC-pST, in which the oscillator is locked in the most active output state, ph
161 tion of a room-temperature AFM THz-frequency oscillator is similar to that of a cryogenic JJ oscillat
162 display a WT period when the core circadian oscillator is tracked using a frq-luciferase transcripti
163 The synchronization of stochastic coupled oscillators is a central problem in physics and an emerg
164 eriod and phase that-unlike other biological oscillators-is maintained over a wide range of condition
165 ct coherent states in a single-mode harmonic oscillator, known as "cat states," have been an elegant
166 o distinct clusters of clock neurons-morning oscillators (M cells) and evening oscillators (E cells)-
167 Even wider ramifications of the Hechtian oscillator may implicate AGPs in osmosensing or gravisen
168 o cortical rhythms and suggest that thalamic oscillators may be subject to both local and global cont
169 a dispersed network of dissociable circadian oscillators may provide greater flexibility when faced w
170 (ING) oscillations may arise from a coupled oscillator mechanism in which individual neurons oscilla
175 analytical methods are applied to a coupled oscillator model implemented in inhomogeneous networks.
176 en critical for developing the neuronal dual oscillator model in which clock gene expression in key c
178 nchronized regime, the stochastic population oscillator model is often characterized by sparse firing
179 When comparing the AI with the harmonic oscillator model of AI, the latter is found to exaggerat
180 emical shielding surfaces (ICSSzz), harmonic oscillator model of aromaticity (HOMA), MCBO, Shannon ar
182 demonstrate with a static model and a neural oscillator model that recurrent excitation in the thalam
183 behavior is explained by the damped harmonic oscillator model with temperature dependent coefficients
184 tion, and here we review the classical Drude oscillator model, in which electronic degrees of freedom
185 support for the main hypothesis of the Dual Oscillator Model, that a glycolytic oscillator endogenou
191 tostatin (SST) is considered to be a primary oscillator of the GH axis, we examined its acute effects
193 trinsic environmental cues and the intrinsic oscillators of immune cells, which together optimize imm
195 self-organizes into a cell-pole to cell-pole oscillator on the membrane to prevent divisions at the c
196 hythms in the fetal SCN begin with few noisy oscillators on E14.5, followed by widespread oscillation
199 perations, but using complex networks of VO2 oscillators, or any other oscillators, for more complex
200 imple estimation indicates that to fit 10(8) oscillators organized in a two-dimensional array inside
201 ircadian system is a hierarchical network of oscillators organized to optimally coordinate behavior a
202 where a lab-built 500 Hz optical parametric oscillator outputting nanosecond optical pulses at a wav
203 anoscale resonators for their use to improve oscillator performance and probe the frontiers of fundam
204 since no cross correlation is necessary, RF oscillator phase noise can be directly suppressed via fe
205 s inspiration, and can reset the respiratory oscillator phase, we hypothesized that synaptic inhibiti
206 that the palatable meal-inducible circadian oscillator (PICO) and wheel-inducible circadian oscillat
207 which are well described by a simple coupled oscillator picture that assumes the vibrational coupling
209 se extreme periodicities, we reveal that the oscillator progresses as a sequence of distinct stages.
210 that Suc affects the stability of circadian oscillator proteins and can mask the effects of ethylene
212 hich contribute to a network of bio-chemical oscillators responsible for the slime mould's distribute
213 A simple mathematical model of coupled actin oscillators reveals the importance of appropriate coupli
214 hronized but then show monotonic decrease in oscillator rhythm amplitude and synchrony with time.
216 s we show that the newly identified shear-NO oscillator shares similarities with the well-known Van d
218 An important property of spin-torque nano-oscillators (STNOs) is their ability to produce a freque
222 relative to pure CsPbBr3 indicates enhanced oscillator strength consistent with earlier published at
223 ystems with low exchange energy, substantial oscillator strength is sustained at the singlet-triplet
224 ime, together with the combination of modest oscillator strength of atoms and low collection efficien
225 ture is not identified probably due to lower oscillator strength of plasmon compared to the coronene.
226 bits approximately 8-fold greater absorptive oscillator strength over the 380-700 nm range relative t
227 mitting characteristics and enormous exciton oscillator strength, however, their low charge carrier m
228 ular architecture (M-(PM')n-M), wherein high-oscillator-strength NIR absorptivity up to 850 nm, near-
229 explored the physiological relevance of the oscillator structure for accurately timed rhythmicity in
231 However, in complex systems with interacting oscillators such as the brain, amplitude and frequency a
232 s a simple, miniaturized, voltage-controlled oscillator suitable for a variety of practical applicati
233 me with mutual coupling between a mechanical oscillator supporting the mirror of a laser and the opti
237 en tube tip growth based on a novel Hechtian oscillator that integrates a periplasmic arabinogalactan
243 iological clocks are autonomous anticipatory oscillators that play a critical role in the organizatio
244 e SCN, interconnected individual neurons are oscillators that, as an ensemble, function to send a coh
245 es, and later vertebrae, relies on a genetic oscillator (the segmentation clock) driving the rhythmic
247 Here we revisit the first synthetic genetic oscillator, the repressilator, and modify it using princ
249 l qubits or larger dimensional modes such as oscillators, the individual elements in realistic device
250 result from the interaction of two distinct oscillators: the preBotzinger Complex (preBotC) driving
251 g effect in a high-Q coherent optomechanical oscillator to dramatically enhance the sensing resolutio
252 nsing of sugars to feedback to the circadian oscillator to dynamically adjust the timing of starch tu
253 , this circuit potentially functioning as an oscillator to integrate the effects of these two hormone
256 r dynamic response of microelectromechanical oscillators to couple two different vibrational modes th
257 s exhibiting complex dynamics-from inorganic oscillators to gene regulatory networks-have been long k
258 me-multiplexed degenerate optical parametric oscillators to implement maximum cut problems on arbitra
259 combined with the ability of the spintronic oscillators to interact with each other, and their long
260 Metabolic compensation allows circadian oscillators to run with a constant speed at different su
261 etwork model of loosely-coupled Wilson-Cowan oscillators to simulate a patch of cortical sheet, we de
262 The ability of a large population of coupled oscillators to synchronize constitutes an important mech
263 lized Bogoliubov modes of the two mechanical oscillators to the cavity modes via beam-splitter-like i
264 ported a decrease in the period of torsional oscillators (TO) containing samples of solid (4)He, as t
265 a phosphorylation-based protein modification oscillator, together with its accompanying push-pull rea
268 ies that are fractions of the basic harmonic oscillator trap quantum and have spatially separated gro
272 cular properties of alpha-cell and beta-cell oscillators using a mouse model expressing three reporte
273 rformance complementary carbon nanotube ring oscillators using fully manufacturable processes, with a
274 nguish molecular characteristics of the core oscillator we compared preBotC neurons derived from Dbx1
275 genetic requirements of this stress response oscillator, we hypothesize that such oscillatory behavio
276 ncodes a critical component of the circadian oscillator, we showed that dper codon usage is important
278 To understand the interactions between these oscillators, we independently altered their excitability
280 0% of all active neurons were self-sustained oscillators when disconnected, each with its own natural
281 synchronization principles of weakly coupled oscillators, where input drive determines the intrinsic
282 ibility is that the preBotzinger inspiration oscillator, which paces whisking, can selectively lock w
283 Neurons in the brain behave as nonlinear oscillators, which develop rhythmic activity and interac
284 from phase coherence in a system of coupled oscillators, which is consistent with the notion of "coh
285 t dopaminergic neurons function as a coupled oscillator whose frequency of discharge results from a c
287 illator (PICO) and wheel-inducible circadian oscillator (WICO) are generated by non-canonical circadi
289 eckers may be modeled in terms of a harmonic oscillator with an impulsive forcing, and this hypothesi
290 We here consider an adaptive network of oscillators with a stochastic, fitness-based, rule of co
293 show that networks of coupled heterogeneous oscillators with different structures capture well the g
295 ted and sustained in nanocontact spin-torque oscillators with perpendicular magnetic anisotropy free
296 sically realistic network of micromechanical oscillators with silicon-based fabrication process can b
297 ve photonic signal, supplied by a Gunn diode oscillator, with coherent acoustic waves of frequency ~1
298 illator is similar to that of a cryogenic JJ oscillator, with the energy of the easy-plane magnetic a
299 rrays of flames that act as master and slave oscillators, with groups of candles numbering greater th
300 erns in ensembles of heterogeneous nonlinear oscillators without using state feedback information.
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。