ライフサイエンスコーパス: feedback

1 rom poor controllability and lack of sensory feedback.

2 performance did not benefit from information feedback.

3 ity between several options before receiving feedback.

4 ary amplification conferred by late positive feedback.

5 rection and strength of permafrost C-climate feedback.

6 nabling accurate force calibration and force feedback.

7 tracortically controlled closed-loop sensory feedback.

8 while exposed to abnormal (delayed) auditory feedback.

9 not hold in the presence of measurement and feedback.

10 ry circuit characterized by a high degree of feedback.

11 ex in healthy motor control better than sham feedback.

12 ng stochastic transcriptional pulses without feedback.

13 siderations, and temperature measurement and feedback.

14 e/decrease activity in SMA without receiving feedback.

15 hampering long-term predictions of climate C-feedbacks.

16 ections of ecosystem functioning and climate feedbacks.

17 rtant to predict future climate-carbon cycle feedbacks.

18 ojecting future climate and carbon (C) cycle feedbacks.

19 ned in a more standardized manner, providing feedback about which cases would benefit most from more

20 ategorization is possible with somatosensory feedback alone, with an accuracy that is similar to the

21 This wind-albedo-wind feedback also leads to an increase in the frequency of h

22 on the silty clay arose from a net negative feedback among exp(H), species turnover, and soil water

23 Thus, pDCs act as positive feedback amplifiers of neutrophil effector activity agai

24 tions in this system give rise to a positive feedback and bistable collective switching of Rab5.

25 greater frontal theta, an index of negative feedback and emotion regulation.

26 sponse to threats relies on a combination of feedback and feedforward circuits.

27 to deep layers), suggesting that long-range feedback and intracolumnar signaling are important.

28 al the discriminatory role of early negative feedback and necessary amplification conferred by late p

29 mination abilities may rely more on auditory feedback and thus may be less adept at updating their st

30 otic implications, including land-atmosphere feedbacks and carbon sequestration.

31 ) collaborative analysis, (iii) constructive feedback, and (iv) action planning.

32 nic connectivity between projection neurons, feedback, and lateral inhibition of these axons by a lar

33 APs may play an important role in inhibitory feedback, and may have implications for understanding th

34 Vegetation-fire feedbacks are important for determining the distribution

35 If positive density-dependent feedbacks are not transient, the diversity of tropical w

36 nal remapping crucially depended on top-down feedback as chemogenetic silencing of lateral OFC neuron

37 te the role of social-network plasticity and feedback as key adaptive mechanisms for refining individ

38 ramework of Stepwise Generalized Equilibrium Feedback Assessment (SGEFA) and machine learning techniq

39 We show that positive feedback at the level of the GATA3-BMP4 axis induces fas

40 d and is followed by accelerative allosteric feedback autoactivation.

41 e propose an active polar fluid model with a feedback between cell polarization and tissue flow.

42 The feedback between dyke and sill intrusions and the evolut

43 deling framework was developed that set up a feedback between hydraulic controls over carbon allocati

44 d to require vertical proprioception through feedback between sensing stem weight and responding with

45 may acquire different fates depending on the feedback between SHR's availability and the state of the

46 ll further our understanding of the cyclical feedback between sleep and opioid use.

47 TiFoSi allows to model feedbacks between cellular mechanics and gene expression

48 ogy and tissue engineering are the result of feedbacks between gene expression and cell biomechanics.

49 ved mechanistic understanding of the complex feedbacks between plants and microbes during, and partic

50 amical behaviours, such as autoregulation or feedback by microRNAs, is unknown.

51 ose that the engagement of these homeostatic feedback circuits by internal and external cues forms th

52 vides a proof-of-concept that the plant-soil feedback concept can be applied to steer soil microbiome

53 Although feedback connections are ubiquitous in the cortex, it is

54 ated by the network's own, context-modulated feedback connections.

55 With feedback control based on recordings of acoustic emissio

56 Feedback control is a universal feature of cell signalin

57 was dependent on APC/C(CDC20), indicating a feedback control of APC/C to SAC during prolonged mitoti

58 For example, high-bandwidth feedback control of frequency combs is used in optical-f

59 duction is required to maintain the negative feedback control of macrophage activation in response to

60 urnover, the linchpin of cell equilibrium is feedback control of the epidermal growth factor (EGF) pr

61 e thermodynamics of continuous, time-delayed feedback control using the motion of an optically levita

62 ing the predictive role of the cerebellum in feedback control.

63 e NO donor doped silicone rubber films using feedback-controlled photolysis.

64 We further demonstrate the acceleration-feedback-controlled power application, and prove that th

65 We show that top-down feedback controls the neural responses to Kanizsa illusi

66 ealed that reward led to both an increase in feedback correction in the middle of the movement and a

67 e laminar patterns of direct feedforward and feedback cortico-cortical projections.

68 ith the ensuing interruption of the positive feedback cycle of LTP serving as a possible critical ear

69 This feedback cycle operated historically at within-reef scal

70 e quality of narrative operative performance feedback delivered with these tools compares.

71 oach provides insights into eco-evolutionary feedbacks determining the structure, functioning and sta

72 op an alternative model of scaling driven by feedback downregulation of Dpp receptors and co-receptor

73 sive feedforward process and a fast-reactive feedback-driven process.

74 n the analysis of speech and nonspeech vocal feedback driving adaptation of these responses.

75 nt of aggression regulation following social feedback during childhood, while this is an important pe

76 adaptation of movements to perturbed sensory feedback) emphasize the role of automatic, implicit corr

77 ion gate for feedforward (telencephalic) and feedback (entorhinal-hippocampal) signal propagation.SIG

78 of early visual cortex develops for auditory feedback, even in the lifelong absence of vision.

79 al changes, the stage at which this cortical feedback first occurs is not known.

80 on during compressions, rhythm check timing, feedback for CPR quality, alternative techniques, public

81 We find that DANs compare convergent feedback from aversive and appetitive systems, which ena

82 sensations and can be used to convey sensory feedback from brain-controlled bionic hands.

83 This way, the CE incorporated interoceptive feedback from IC to improve discrimination of CS valence

84 The aim of this study was to obtain feedback from key stakeholders and end users to identify

85 se results confirm the importance of sensory feedback from movements in driving activity in sensorimo

86 -loop methodology automatically incorporates feedback from past experiments to inform future decision

87 We demonstrate that feedback from the autocorrelation function of the order

88 that this misaligned contribution likely is feedback from the downstream areas.

89 developed the recommendations, and solicited feedback from the larger clinical community.

90 sodium and chloride induces tubuloglomerular feedback from the macula densa to increase GFR.

91 Feedback from the pilot resulted in establishment of a f

92 barrel activity was attributable to sensory feedback from whisker movements.

93 on the sandy loam was reinforced by positive feedbacks from aboveground net primary productivity and

94 esults indicate that vegetation-dust climate feedbacks from Sahara drying may have been the catalyst

95 Biological feedbacks generated through patterns of disturbance are

96 Recently, feedback has been suggested as a tool to induce phase tr

97 eraction between intentionality and valenced feedback has not been systematically examined.

98 s attempts to model carbon-phosphorus-oxygen feedbacks have neglected key parameters that could shape

99 ssive locomotor muscle group III/IV afferent feedback; however, this has never been investigated in h

100 sess the effect of differential baroreceptor feedback (i.e. aortic-carotid g-gradient).

101 that locomotor muscle group III/IV afferent feedback in patients with HFrEF leads to increased syste

102 paired in rLG, confirming the role of reflex feedback in regulating force duration in intact muscle.

103 d that bistability also arises from positive feedback in the regulation of the Cdk1-counteracting pho

104 ndent of canonical LPS-induced intercellular feedback in the tumor necrosis factor (TNF) response.

105 This may fundamentally alter feedbacks in the relationships between parrotfishes and

106 Activation of feedback increased spontaneous activity and decreased st

107 Moreover, we showed that increasing feedback information induced a switch from absolute to r

108 The mechanism of feedback inhibition and its role in pathogenesis are unc

109 ons require different strength and timing of feedback inhibition for optimal processing.

110 onal AgR gene on one allele, with subsequent feedback inhibition of V(D)J recombination on the other

111 R-3085-3p, but in this instance, it exerts a feedback inhibition on signaling with SMAD3 and SMAD4 sh

112 Additionally, net feedback inhibition shows frequency-dependent facilitati

113 levates Vbeta rearrangement frequency before feedback inhibition, dramatically increasing the frequen

114 of IMPDH2 makes the enzyme less sensitive to feedback inhibition, explaining why assembly occurs unde

115 ng the levels of folding factors removed the feedback inhibition.

116 also upregulated ZEB1, which could act as a feedback inhibitor of FOXM1, and caused the transition o

117 Feedback inhibitory motifs are thought to be important f

118 Interestingly, feedback inputs often outnumber feedforward inputs.

119 region of yeast MTHFR to create a series of feedback-insensitive, deregulated mutants.

120 vidence for a circuit of local recurrent and feedback interactions that mediate rapid brain plasticit

121 e randomly assigned ICUs to either audit and feedback (intervention group) or participation to a nati

122 H could be used to develop novel prospective feedback interventions designed to avert hospital outbre

123 that transform the monosynaptic Ia afferent feedback into task-dependent co-contraction of antagonis

124 inner edge of the habitable zone, through a feedback involving decreasing ocean coverage and increas

125 from an unanticipated RANKL immunoregulatory feedback, involving the induction of Tregs and a host re

126 ochlear inhibition, suggesting that efferent feedback is important for long-term maintenance of inner

127 Our results also indicate that feedback is more relevant under uncertainty, and its eff

128 This feedback is predicted to be chromosome autonomous, but t

129 d 4.16 uJ cm(-2) is achieved and distributed feedback lasers are also demonstrated.

130 most research has focused on striatal-based feedback learning, open questions remain regarding the r

131 Finally, while antibody feedback limited responses to the PfCSP repeat region in

132 lock consists of a transcription-translation feedback loop (TTFL) composed of CLOCK-BMAL1 transcripti

133 ining transcriptional-translational negative feedback loop (TTFL) in which the negative regulators Pe

134 malformations-3), participate in a negative feedback loop among RhoA and its cytoskeletal effectors

135 A feedback loop between Amazonian BVOCs and the trends of

136 These results revealed a negative feedback loop between appressorium formation and cell cy

137 In our model, contraction mediates a feedback loop between myosin-induced flow and advection-

138 that early-life stress initiates a positive feedback loop between peripheral inflammatory cells and

139 We and others previously reported a feedback loop between PROX1 and vascular endothelial gro

140 otential pathogenic mechanism that acts as a feedback loop contributing to the progression of IIM.

141 The recurrent feedback loop effectively carried frequencies up to 100

142 sm offers robustness to a dynamic epigenetic feedback loop ensuring long-term centromere inheritance.

143 el activity, thereby establishing a positive feedback loop for PI(4,5)P(2) microdomain compartmentali

144 The feedback loop further enables prolonged production of Bi

145 can be generated by a time-delayed negative feedback loop in which Plk4 inactivates the interaction

146 We describe an optical feedback loop involving both partners of the association

147 wn, our results suggest the possibility of a feedback loop involving these two genes, with the CTNNB1

148 actor in spatially coordinating the negative feedback loop of its own genetic circuit.

149 nce mediated by FOXM1-Nedd4-VDAC2/3 negative feedback loop provides an initial framework for creating

150 Social interaction can be seen as a dynamic feedback loop that couples action, reaction, and interna

151 ncer cell signaling through a self-enforcing feedback loop that expands the glycocalyx and furthers c

152 Their combination constitutes a positive feedback loop that exponentially amplifies their antimic

153 revealing a MUS81-triggered and ATR-mediated feedback loop that fine-tunes MUS81 activity at replicat

154 These mutants thus appear to lack a negative feedback loop that inhibits DSB formation when homologs

155 ult C. elegans males employ a neuroendocrine feedback loop that integrates food detection and genetic

156 s FBP1 and PRC2 are part of a novel negative feedback loop that is deregulated in liver and kidney ca

157 ity, suggesting that Zta may contribute to a feedback loop that would limit its own expression, thus

158 lling and experimental data demonstrated the feedback loop to act as a scalable converter of unimodal

159 e proof-of-concept illustrated here, using a feedback loop to couple in situ material characterizatio

160 tivity, demonstrating an unexpected positive feedback loop to persistently promote pain.

161 ed glucocorticoid secretion, demonstrating a feedback loop whereby stressful stimuli activate RFRP ne

162 egative arm of the transcription/translation feedback loop without affecting period length.

163 hat microRNA-144 targets Dicer in a negative feedback loop, affecting global canonical microRNA expre

164 e propose a model based on a double-negative feedback loop, vertically transmitted via the entero-mam

165 d investigated the JNK-AP-1-RUNX1 regulatory feedback loop, which can be modulated by VEGF.

166 a inside the tumor mass, creating a positive feedback loop.

167 in cells overlying LRP, creating a negative feedback loop.

168 tionally conserved transcription-translation feedback loop.

169 between voltage and Ca2+, forming a delayed feedback loop.

170 s apoptosis in part by blocking the MDM2-p53 feedback loop.

171 via PP2A inhibition, and thereby rescues the feedback loop.

172 put owing to disruption of the MDM2-negative feedback loop.

173 trol neuronal firing frequency in a negative feedback loop.

174 ytoskeletal structures through a biophysical feedback loop.

175 strocytic Ca(2+) and resulting in a positive-feedback loop.

176 gulates IL-12 secretion by DCs in a positive feedback loop.

177 ulates PDLSCs activities by fine-tuning this feedback loop.

178 ated mechanism relies on the inhibition of a feedback-loop in the JNK-pathway by the immune effector

179 ll-autonomous, transcriptional/translational feedback loops (TTFLs), active in all tissues.

180 y regulate endocytic trafficking by creating feedback loops in cells to enhance tumor progression.

181 ities in the active cytoskeleton network and feedback loops in the biochemical network of activators

182 nt interpretation could be altered by adding feedback loops or morphogen cascades to receiver cell re

183 ted by interlocked transcription-translation feedback loops that establish cell-autonomous biological

184 provides a temporal compartmentalization of feedback loops, enabling duration-dependent desensitizat

185 hanical load regimes and altered dynamics of feedback loops, illustrate that the waiting time distrib

186 clocks keep time via ~ 24 h transcriptional feedback loops.

187 that AN may arise from pathological positive feedback loops: voluntary food restriction activates SIR

188 This feedback makes the ecosystem more prone to coral collaps

189 Eco-evolutionary feedbacks may help to understand changes in the adaptive

190 nly in recently divided cells, pointing to a feedback mechanism between the cell cycle, cytoskeleton,

191 cer silencing as a cell-intrinsic epigenetic feedback mechanism by which the duration of the transcri

192 versus wild-type mice, suggesting a negative feedback mechanism for TAAR1 in sensing tyramine levels.

193 ogramming includes a positive autoregulatory feedback mechanism in which ectopic PHF7 overcomes its o

194 e sarcoplasmic reticulum (SR) via a positive feedback mechanism in which fluxed Ca(2+) activates near

195 stimulated to 61-71% of wild-type level by a feedback mechanism increasing translation initiation.

196 This feedback mechanism may act to stabilize translaminar pre

197 suggest that this microglia-driven negative feedback mechanism operates similarly to inhibitory neur

198 dependent inactivation (CDI) is a regulatory feedback mechanism that reduces GluN2A-type NMDA recepto

199 mulation, which may be considered a negative feedback mechanism to limit their uncontrolled expansion

200 at transcriptional regulation incorporates a feedback mechanism whereby transcribed RNAs initially st

201 ng mutations in disrupting an autoregulatory feedback mechanism, thereby deregulating HNRNPH1 protein

202 heoretical model to elucidate how a negative feedback mechanism, tied to the distance between the int

203 murine P19 cells using an intricate negative feedback mechanism.

204 T activity and the relatively unexplored BAT feedback mechanisms on neuronal regulation.

205 hypoactive platelets resulting from negative feedback mechanisms, including upregulation of Csk homol

206 This behaviour results from total-flux feedback mediated by cAMP-Crp signalling but also requir

207 equences were sustained by a set of positive feedbacks, mediated by the oxygen and sulfur cycles, tha

208 phenomenon referred to as mechanoelectrical feedback (MEF), via stretch-activated channels.

209 e that this non-corrupting choice-correlated feedback might be related to learning or reinforcing sen

210 We propose a dynamic feedback model of vestibular and podokinetic adaptation

211 e of LOC, supporting a functionally relevant feedback modulation from LOC to EVC for scaling size inf

212 To test for the potential contributions of feedback modulations on size representations in EVC, we

213 ational modeling reveals that the discovered feedback motifs increase model flexibility and performan

214 In all, Ca(2+) feedback of Ca(V) channels depends exquisitely on a sing

215 rs (GEF) to effectors, generating a positive feedback of GTPase activation and membrane recruitment.

216 The negative feedback of marine P cycle to terrestrial P input would

217 rsatility, a virtual environment with haptic feedback of the force is ideally suited to investigating

218 y nonspeech like, involving distorted visual feedback of tongue shape.

219 retreat) losses generate a valuable negative feedback on climate change.

220 effect (CFE)] sustains an important negative feedback on climate warming, but the temporal dynamics o

221 transporters (MCTs), resulting in a negative feedback on glycolytic rate.

222 reviewer provided diagnostic and management feedback on patients' cervical images, which were review

223 studies investigating the impact of valenced feedback on skill learning have only considered unintent

224 bonate rocks can exert an important positive feedback on strain localization and fluid channelization

225 mospheric CO(2) implies a weakening negative feedback on the climatic system and increased societal d

226 rol the material reaction based on real-time feedback on the system chemistry from in situ X-ray abso

227 changes in biogeochemical cycles and climate feedbacks on Earth.

228 position on Earth's surface leads to adverse feedbacks on ecosystems and humans.

229 atic observational analysis of soil moisture feedbacks on propagating MCSs anywhere in the world and

230 f the outer retina, which provide inhibitory feedback onto photoreceptors and contribute to image pro

231 to the membrane composition, thus providing feedback onto the function of the P4-ATPases.

232 ding non-olfactory inputs and memory-related feedback onto third-order olfactory neurons.

233 not rely on persistent activity, excitatory feedback, or synaptic plasticity for storage.

234 We show that this weathering feedback ought to produce a log-linear relationship betw

235 is a central component of all electrosensory feedback pathways to the electrosensory lateral line lob

236 we examined whether the content of response feedback plays a critical role for the acquisition and l

237 recall responses were inhibited by antibody feedback, potentially via epitope masking of the immunod

238 implemented a post-prescription review with feedback (PPRF) in November 2015 with mandatory infectio

239 reveal moreover that the damage initiates a feedback process where initial ice shelf weakening trigg

240 cated in cortical layers that receive strong feedback projections and are absent in the main input la

241 higher-level areas but are also modulated by feedback projections from these same areas.

242 uare and hexagonal GKP code states through a feedback protocol that incorporates non-destructive meas

243 n of microcombs requires complex startup and feedback protocols that necessitate difficult-to-integra

244 degrees of the target for at least 1 s, with feedback provided by the sizes of the rings.

245 Interestingly, the feedback regulation of DBL-1/BMP signaling by collagens

246 We now identify feedback regulation of DBL-1/BMP through analysis of fou

247 The type of feedback regulation of DGKepsilon by PA depends on the p

248 Negative feedback regulation, that is the ability of a gene to re

249 of COPD status, possibly reflecting negative feedback regulation.

250 Our work reveals TiPARP as a negative-feedback regulator for multiple oncogenic transcription

251 ein directly interacts with IR to serve as a feedback regulator of insulin action in control of liver

252 ole of the lncRNA LUCAT1 as a post-induction feedback regulator which functions to restrain the immun

253 Taken together, our results have revealed a feedback regulatory circuit connecting RPW8.1 and the et

254 REGgamma activity in HCC, forming a positive feedback regulatory loop.

255 d to the disruption of proprioceptive facial feedback reinforcing negative emotions.

256 High levels of skeletal muscle sensory feedback related to peripheral fatigue development are t

257 h soil microbiota, with strongly contrasting feedback responses among some plant lineages.

258 This paper focuses on uncovering the feedbacks responsible for the WPS.

259 High levels of muscle sensory feedback restrict motor unit activation and limit exerci

260 These interactions are often seen as social feedback rules, whereby individuals copy the decisions t

261 ort" (BS, n = 48), "Brief Support + Shopping Feedback" (SF, n = 48) or "Control" (n = 17).

262 Differentiated columella cells provide a feedback signal via secretion of the peptide CLAVATA3/ES

263 Particularly, if feedback signals from LOC to EVC are crucial for generat

264 t that V1 LPZ responses reflect task-related feedback signals rather than reorganized feedforward vis

265 , suggesting the involvement of task-related feedback signals.

266 nties in polar regions while the water vapor feedback spread explains uncertainties elsewhere.

267 We show that the ice-albedo feedback spread explains uncertainties in polar regions

268 ation strategy emphasizing communication and feedback, standardized processes, coordination, distribu

269 sm may allow for a physiological homeostatic feedback system.

270 omponents and cytoskeleton-mediated positive feedback that reinforces these nanodomains into polarize

271 primary producers, inducing disease-mediated feedbacks that alter net primary productivity and elemen

272 Optimizing the feedbacks that shape chemical interaction networks in th

273 During the transition, feedbacks that stabilize the new regime are still weak,

274 rogress in resolving mechanisms of CaM-Ca(V) feedback, the stoichiometry of CaM interaction with Ca(V

275 Combined with simple optical or electrical feedback, the structure is suitable for precise electrop

276 These mediate inhibitory olivocochlear feedback through the activation of associated calcium-ga

277 The feedback time constant is shown to determine the relaxat

278 state of the environment, which may in turn feedback to change the incentive structure of strategic

279 advances our capacity to predict terrestrial feedback to climate change under projected warming scena

280 creating a potentially substantial positive feedback to climate change.

281 between individual chromosomes provides the feedback to down-regulate Spo11 activity, thereby reveal

282 The same feedback to early visual cortex might support visual per

283 al imagery is not a prerequisite of auditory feedback to early visual cortex.

284 ng processes with implications of a positive feedback to global climate and emphasize the close linka

285 Osteocytes provide negative feedback to PDLSCs and inhibit their activities through

286 d system) provide deterministic and rigorous feedback to researchers who submit sequences with unexpe

287 also depends on deep-layer neurons providing feedback to superficial layers (not to deep layers), sug

288 canal during screw placement provides manual feedback to the surgeon, indicating an impending breach

289 ng CO(2) concentrations, generating negative feedbacks to climate change.

290 However, its feedbacks to climate warming and underlying microbial me

291 rient supply rates on infectious disease and feedbacks to ecosystem carbon and nutrient cycling.

292 We confirm that feedback via a trained reinforcement learning agent can

293 cialized plasma membrane domains in cellular feedback via the Hippo pathway.

294 binocular rivalry, which includes asymmetric feedback, visual saliency, or a combination of both (Ske

295 Feedback was recorded and discussed among development te

296 These positive density-dependent feedbacks were not associated with a decrease in abovegr

297 ystem function with consequences for climate feedbacks, wildlife and human communities.

298 symmetry and its reinforcement by mechanical feedback within the inner cell walls, not the outer epid

299 ons that are amplified by nonlinear positive feedbacks within the internal iron and sulfur cycling of

300 gested that a single CaM sufficed for Ca(2+) feedback, yet biochemical, FRET, and structural studies