ライフサイエンスコーパス: decoding

1 scale snapshots of transcriptional activity (decoding).

2 ecoding constrains less reliable lower-level decoding.

3 ity does not substantially drive orientation decoding.

4 NAs that elucidate the mechanism of accurate decoding.

5 ghts into the dynamics of high-fidelity tRNA decoding.

6 sed to explain the observed features of UAGN decoding.

7 on genetic code expansion through quadruplet decoding.

8 required for a detectable efficiency in UAGN decoding.

9 a default state interrupted by encoding and decoding.

10 ase modulates rapid and accurate information decoding.

11 to the stimulus edges underlies orientation decoding.

12 vity is likely not necessary for orientation decoding.

13 tions may contribute importantly to accurate decoding.

14 rating a previously unknown aspect of Bicoid decoding.

15 tions can have distinguishable influences on decoding.

16 mingled and each set can support orientation decoding.

17 cate pleiotropic mechanisms of action beyond decoding.

18 wledge of correlational structure matter for decoding?

19 mbinant hybrid ribosomes carrying eukaryotic decoding A site cassettes.

20 uated for selective binding to the ribosomal decoding A-Site sequence.

21 n and leishmanial ribosome structures at the decoding A-site sheds light on how the bacterial ribosom

22 parietal cortex (PPC) exhibited chance-level decoding according to both.

23 ls, motor brain areas exhibited above-chance decoding according to the original movement direction an

24 nd visual brain areas exhibited above-chance decoding according to the rotated visual target location

25 Furthermore, we detected slightly different decoding accuracies, depending on the task's visual cond

26 d not find any image features that predicted decoding accuracy differences between both interventions

27 ha oscillations (8-10 Hz), while the highest decoding accuracy for the apparent motion task (ISI = 12

28 The highest decoding accuracy for the two-flash fusion task (ISI = 4

29 tes can be decoded from activity in OFC, and decoding accuracy is related to task performance and the

30 l cortex, but there was no difference in the decoding accuracy of task-related information between sw

31 stimulus discriminability and ensures robust decoding across membrane states in a regime of highly co

32 he hypothesis of a functional role of MNs in decoding actions and understanding motor intentions.

33 le-shot error correction to develop a simple decoding algorithm for the gauge color code, and we nume

34 's control scheme ("encoding model") and the decoding algorithm's parameters.

35 Decoding analyses indicate that cortical odor representa

36 Multivariate decoding analyses indicated that neural markers of error

37 Moreover, multivariate decoding analyses revealed that amisulpride changed the

38 Source and decoding analyses revealed that perceptual maintenance r

39 Finally, a multivariate decoding analysis showed that activity patterns in the a

40 Here, we use multivariate decoding and analyses of spontaneous correlations to sho

41 an be devoted to other functions like visual decoding and endogenous attention.

42 ensure that the mRNA is held tightly during decoding and essential for the helicase activity at the

43 r a broad range of research efforts aimed at decoding and eventually manipulating YAP1 biology in can

44 outline various modes of alternative genetic decoding and expand existing terminology to accommodate

45 locational states, but also eEF1A-containing decoding and termination/recycling complexes.

46 expected relationship between aminoacyl-tRNA decoding and translocation suggests that miscoding antib

47 protein synthesis including aminoacylation, decoding and translocation.

48 modification in yeast tRNA(Lys) affects mRNA decoding and tRNA-mRNA translocation.

49 Using a whole-brain searchlight decoding approach we show that D2-receptor blockade enha

50 an assumption-free, whole-brain searchlight decoding approach, we identified for the first time regi

51 However, typical decoding approaches provide little insight into the natu

52 While the networks underlying this signal decoding are diverse, many are built around a common mot

53 processes of sensory encoding and perceptual decoding are matched and optimized based on identical as

54 genomic features and their dominant roles in decoding AS patterns, highlighting the necessity of incl

55 opography could provide a starting point for decoding at a very early stage in development, it may be

56 ribonucleases that cleave RNAs essential for decoding at the ribosomal A-site.

57 te unnatural anticodons, and their efficient decoding at the ribosome to direct the site-specific inc

58 participation of the unnatural base pair in decoding at the ribosome.

59 produced intermingled tectal responses, and decoding based on map topography yielded an accuracy of

60 -analysis was then analyzed using functional decoding based on ~7500 fMRI experiments in the BrainMap

61 Consistently, the accuracy of decoding behavior from SPN ensemble patterns was directl

62 rietal sulcus (IPS), but robust multivariate decoding being reported in occipital cortex.

63 rsible conformations of a DNA nanoswitch and decoding by gel electrophoresis.

64 top codon in bacteria results from increased decoding by near-cognate tRNAs (miscoding) rather than f

65 CaMKII plays a critical role in decoding calcium (Ca(2+)) signals to initiate long-lasti

66 However, the mechanism for decoding calcium signatures is unknown.

67 The mechanism for decoding calcium signatures to control expression of pla

68 ally that finite temperature maximum entropy decoding can give slightly better bit-error-rates than t

69 w protein densities were discovered near the decoding center and the peptidyl transferase center, res

70 the 30S subunit and aids the assembly of the decoding center but also binds the mature 30S subunit wi

71 to interact simultaneously with EF-4 and the decoding center of the ribosome.

72 tor exploits the plasticity of the ribosomal decoding center to differentially remodel ribosomal prot

73 nisms for communicating information from the decoding center to each GTPase.

74 e movement together of critical bases at the decoding center, and movements of the peptide tunnel lin

75 915 (Psi1915), which lies near the ribosomal decoding center.

76 like pseudoknot I (PKI) of the IRES from the decoding center.

77 states of tRNA engagement with the ribosomal decoding center.

78 inding to the canonical eukaryotic ribosomal decoding center.

79 from the RNAP active center to the ribosome decoding center.

80 Decoding-center rearrangements are coupled with the step

81 uces conformational changes in the ribosomal decoding centre that are similar to those seen in other

82 elix, initiating step-wise 'latching' of the decoding centre.

83 A transient conformation of decoding-centre nucleotide G530 stabilizes the cognate c

84 memory, and that more reliable higher-level decoding constrains less reliable lower-level decoding.

85 nucleobases, and the mechanisms of ribosomal decoding contributed to the position-dependent effects.

86 Only activity of neurons reflecting encoding/decoding correlated with changes in gamma burst rate.

87 Despite recent advances in decoding cortical activity for motor control, the develo

88 om 2 to 8; in the same parameter regime, the decoding delay decreased 2-5.2 times.

89 Population decoding demonstrated a high-accuracy progress code.

90 ficiency is largely thought of as the sum of decoding efficiencies for individual codons.

91 anisotropy/homogeneity improved encoding and decoding efficiency by reducing the number of neurons ne

92 RNA mutants with significantly improved UAGN decoding efficiency, which will augment the current effo

93 Previous decoding efforts have focused on classifying brain activ

94 ination was semi-automatically quantified by decoding electroencephalography responses to frequently

95 , subunit association, correlated evolution, decoding, energy-driven translocation, and surface prote

96 ncoding and show how they predict population decoding errors consistent with perceptual biases.

97 is essential for developmental progression, decoding extracellular cAMP pulses during early developm

98 Comparative analyses reveal that each decoding factor exploits the plasticity of the ribosomal

99 re selectively recognized by the appropriate decoding factorGTPase complex to ensure translational fi

100 tures of the mammalian ribosome engaged with decoding factorGTPase complexes representing intermediat

101 hanges that choreograph the accommodation of decoding factors into the peptidyl transferase center.

102 ranslational GTPases that pair with specific decoding factors to decipher the mRNA code on ribosomes.

103 ry cortex of ferrets and found that: (1) the decoding filters of auditory neurons resemble the filter

104 n is less clear, and most models assume that decoding follows the same low- to high-level hierarchy o

105 encoding techniques, synthesis methods, and decoding for applications including bio-detection, imagi

106 ologies have shown the feasibility of neural decoding for both users' gait intent and continuous kine

107 is of specific interest for applications in decoding for communication.

108 his objective by introducing a probabilistic decoding framework based on a novel topic model-Generali

109 To attain maximal utility, a decoding framework must be open-ended, systematic, and c

110 When decoding from AIP, F5, and M1 combined, the mean accurac

111 ion transmission across cortical states i.e. decoding from different states is less state dependent i

112 d controversy over the source of orientation decoding from fMRI responses in human V1.

113 that noise correlations enhance multivariate decoding from heterogeneous neural populations.

114 is study shows for the first time hand-shape decoding from human PPC.

115 When decoding from individual arrays, objects and grip types

116 edge-related activity" underlies orientation decoding from patterns of BOLD response in human V1.

117 Decoding from unselected populations enables a read-out

118 However, decoding functional RNA-regulatory features remains a li

119 S) has become a widely accepted strategy for decoding genotype-phenotype associations in many species

120 nly important in monitoring, estimating, and decoding H2O2 relevant physiological pathways but also v

121 uring columns, need to be accounted for when decoding haemodynamic signals.

122 Traditionally, cross-validated decoding has been used as a reliability measure, but it

123 We probed decoding hierarchy by comparing absolute judgments of si

124 der how working-memory properties may affect decoding hierarchy.

125 ations for understanding neural encoding and decoding in a broad class of fundamental sensory-percept

126 ned, we examined shape-based object category decoding in occipitotemporal and parietal regions.

127 We addressed the dynamics of auditory decoding in speech comprehension by challenging syllable

128 the serine 33 and serine 70 residues in UGA decoding in vivo.

129 Decoding individual trials of adaptation-affected activi

130 rior parietal cortex are valid for correctly decoding information relevant for grasping.

131 and without the need for complex time-gated decoding instrumentation.Luminescent materials that are

132 tion efficiency and codon use is that slower decoding is coupled to reduced mRNA stability.

133 Maintenance of triplet decoding is crucial for the expression of functional pro

134 Genetic decoding is not 'frozen' as was earlier thought, but dyn

135 ndent in the adaptive threshold case, if the decoding is performed in reference to the timing of the

136 from a theory combining optimal encoding and decoding, is well supported by a wide range of reported

137 emporal patterning of the calcium signal and decoding it by multiple, tunable, and often strategicall

138 a, we derived and validated a characteristic decoding map that relates morphogen input to the positio

139 Functional decoding mapped the left putamen to cognitive aspects of

140 nsor, and FHSS pattern analysis based sensor decoding may help establishing cost-effective, energy-ef

141 of the underlying dynamics, and instead the decoding mechanism acts as a simple low-pass filter.

142 s approach can be applied to identifying the decoding mechanisms of other plant calcium signalling pa

143 -to-trial variability and explored potential decoding mechanisms that can mimic mouse performance whe

144 ngstanding puzzle about extracellular signal decoding mechanisms.

145 Here, we introduce an analytical decoding method based on Biot's incremental stress model

146 Notably, the receptive-field-free decoding method was found to be well-tuned for hippocamp

147 Based upon two Bayesian population-decoding methods (one receptive field-based, and the oth

148 ough activation space, as measured using MEG decoding methods, correlates with reaction times for vis

149 Multivariate decoding methods, such as multivoxel pattern analysis (M

150 ing model of similar complexity; and (3) the decoding model accounts for the accuracy with which the

151 poorly reflects selectivity of neurons, the decoding model can account for the strong nonlinearities

152 rom the statistics of speech sounds; (2) the decoding model captures the dynamics of responses better

153 We demonstrated that this novel Bayesian decoding model is better at capturing the dynamic respon

154 ex have led to the development of methods of decoding movement information to restore coordinated arm

155 shes the life-sustaining tasks of faithfully decoding mRNA and catalyzing peptide bond formation at t

156 complex, 2.5 MDa nanomachine responsible for decoding mRNA and synthesizing proteins.

157 ge affects the efficiency/stringency of mRNA decoding, mRNA biogenesis/stability, and protein secreti

158 tion to people with neurological deficits by decoding neural activity into control signals for guidin

159 rrors and response variability as results of decoding noisy neural activity, and can account for the

160 ain and validate a Bayes classifier used for decoding objects and grip types.

161 We show that this problem can be resolved by decoding odor identity from a subpopulation of concentra

162 res that compromise ribosome fidelity during decoding of a heptanucleotide 'slippery' sequence.

163 can be estimated reasonably well by a linear decoding of a population of MT neurons with response gai

164 severely restricted, either by near-optimal decoding of a population with information-limiting corre

165 We discuss an example in which the decoding of a turbo code, which has been demonstrated to

166 iments or high-throughput screens enable the decoding of binary interactions, the building of large-s

167 We observed nearly equal decoding of both histidine codons, CAU and CAC, by an en

168 that the neuronal population allows reliable decoding of both stimulus properties.

169 Decoding of calcium signatures occurs via nonlinear inte

170 underlying low-frequency rhythm, permitting decoding of categorical information using the phase at w

171 d the technique has been instrumental in the decoding of cis-regulatory elements and the identificati

172 Our results suggest that optimal linear decoding of early sensory information is not a general d

173 We used multivariate decoding of electroencephalography (EEG) data to investi

174 r and nonlinear components contribute to the decoding of EMG of major muscles used in the task.

175 ss control systems that linked online neural decoding of extension and flexion motor states with stim

176 We propose that the brain prioritizes decoding of higher-level features because they are more

177 Our decoding of histone methylarginine at key genes supports

178 after stimulus onset, 100 ms later than peak decoding of intact objects.

179 ing, decisions about integrated percepts and decoding of integrated percepts are impaired in tandem,

180 In the present study, we used multivariate decoding of magneto-encephalography (MEG) data to track

181 Here we used multivariate decoding of magnetoencephalogaphy data to characterize t

182 terns in this visuomotor network enabled the decoding of manipulable versus non-manipulable object pi

183 We investigated the decoding of many grip types using spiking activity from

184 ively stronger security against unauthorized decoding of messages contained in communication transmis

185 dditional products occurs prominently in the decoding of mobile chromosomal element and viral genomes

186 Gene translation depends on accurate decoding of mRNA, the structural mechanism of which rema

187 t achieves interaction strength analysis and decoding of networks with nonlinear interactions by incl

188 ception and are potentially relevant for the decoding of ongoing pain sensitivity and pain management

189 ding may pave the way for further structural decoding of other 2D vdW superstructure systems with mor

190 ing with genetically encoded sensors enables decoding of regional activity and connectivity in anesth

191 h we show that D2-receptor blockade enhances decoding of reward signals in the medial orbitofrontal c

192 This suggests that optimal linear decoding of sensory signals is not generally a good pred

193 bi and Viterbi A* are used for inference and decoding of sequences.

194 -resolution microscopy based on the encoding/decoding of spatial information through manipulation of

195 A major such program involves enhanced decoding of specific mRNAs that are depleted in terminal

196 represent a proof of concept study for basic decoding of speech imagery, and delineate a number of ke

197 In contrast, maximum likelihood decoding of stimulus location based on the statistics of

198 onset, multivariate pattern analysis (MVPA) decoding of task in occipital-parietal sources remained

199 synchronization and supported more accurate decoding of temporal sound features in the inferior coll

200 Further, AIS allowed decoding of the cued category on a trial-by-trial basis.

201 sufficiently reliable to enable brain-based decoding of the participant's memory state at the single

202 To determine this, decoding of the salicylic acid (SA)-mediated plant immun

203 Here, we describe results of IgG-epitome decoding of three proteins from high-risk (HR-) oncogeni

204 emodulate these signals to recover the known decoding of touch as a function of vibrissa position in

205 Similarly, superior IPS exhibited consistent decoding of VSTM content across all distractor manipulat

206 However, occipital decoding of VSTM content was substantially modulated by

207 ly-circumscribed topics that enable flexible decoding of whole-brain images.

208 Encoding/decoding off-axis points with discrete orbital angular m

209 ction, transfer RNA (tRNA) charging and mRNA decoding on the ribosome.

210 e release of the selenocysteinyl-tRNA during decoding on the ribosome.

211 lds, without invoking suboptimal encoding or decoding or internal sources of variability such as stoc

212 e to incorporate these encoding changes, the decoding, or perception, of subsequent stimuli is biased

213 ed above chance for almost 1 s, and the task-decoding pattern interacted with task outcome.

214 ) are main effectors of messenger RNA (mRNA) decoding, peptide-bond formation, and ribosome dynamics

215 put) allowed for comparable levels of object-decoding performance and that removing a large fraction

216 eptive fields in V1 and evaluate orientation decoding performance as a function of stimulus location

217 did not observe the expected second peak in decoding performance at the outer stimulus edge as predi

218 ion procedure demonstrated that near-maximum decoding performance could be achieved using a relativel

219 utcome prediction was based on the change of decoding performance from hypothermia to normothermia.

220 nals from the different electrodes increased decoding performance in the high frequencies by up to ap

221 Specifically, decoding performance is enhanced when voxels with high v

222 decodable across the stimulus; however, peak decoding performance occurred for voxels with receptive

223 rrelations by trial shuffling did not impact decoding performance or bias.

224 in the developing zebrafish that topographic decoding performs very poorly compared with methods that

225 Recently discovered examples of decoding plasticity are particularly spectacular.

226 ew proteins, and expand our knowledge of the decoding potential of the ribosome.

227 a programmable annealer for the information decoding problem which we simulate as a random Ising mod

228 Whether the decoding process is bounded by the capacity of theta rhy

229 The numerical nonlinear decoding process of CS shares strong connections with po

230 adapt to syllabic rate, but by an endogenous decoding process.

231 ilar to those seen in other protein-involved decoding processes.

232 Notably, the neural decoding properties, including its autocorrelation struc

233 on are focused on reassigning termination or decoding quadruplet codons.

234 Together with previous studies on decoding reach trajectories from the medial posterior pa

235 e global-areal-map account, fMRI orientation decoding relies exclusively on fMRI voxels in V1 exhibit

236 erall perception, suggesting that perceptual decoding requires working memory, yet few models conside

237 nfection in the 21st century: new hints from decoding resolution mediators and mechanisms.

238 MEG decoding results revealed that scene-based facilitation

239 aining the classifier on baseline trials and decoding rotated trials, motor brain areas exhibited abo

240 ms, and certain genes are known to alter the decoding rules in a site-specific manner.

241 eveloped simple predictions to differentiate decoding schemes without needing measures of noise corre

242 eveloped simple predictions to differentiate decoding schemes, and found support for optimal linear r

243 n particular, whether they are necessary for decoding sensory stimuli is unknown.

244 this "topography" of wiring is essential for decoding sensory stimuli.

245 fMRI decoding showed that the multivariate representation of

246 canning model of translation initiation, the decoding site and latch of the 40S subunit must open to

247 factors regulate mRNA accommodation into the decoding site have not yet been elucidated.

248 By binding to the decoding site of helix44 of the small subunit RNA of the

249 1782) are N(6)-dimethylated by Dim1 near the decoding site, and one guanosine (G1575) is N(7)-methyla

250 ncorporated into the bacterial ribosomal RNA decoding site, fluorescently reports antibiotic binding

251 anticodon/codon interaction in the ribosomal decoding site.

252 state of full accommodation of mRNA into the decoding site.

253 Although decoding skills are clearly human-unique, given they are

254 isition of letter-sound relationships (i.e., decoding skills) and the ability to visually recognize w

255 task space and establish the feasibility of decoding state representations in humans using non-invas

256 e bacterial class I release factors (RFs) in decoding stop codons has evolved beyond a simple tripept

257 f early sensory information is not a general decoding strategy used by the brain.

258 Although topography is a useful initial decoding strategy, we suggest it may be replaced by bett

259 long been recognized that both the user and decoding system can adapt to increase the accuracy of th

260 The decoding techniques for each encoding technique are diff

261 coding techniques, synthesis strategies, and decoding techniques need to be considered.

262 gnetoencephalography (MEG) with multivariate decoding techniques to probe the representational conten

263 Using multivariate decoding techniques, we delineated three distinct proces

264 table giving task together with multivariate decoding techniques, we identified three distinct psycho

265 mory-related neural patterns and foil memory decoding technology, placing a significant boundary cond

266 ation-limiting correlations or by suboptimal decoding that is blind to correlations.

267 r the fate of mATG8s and will be valuable in decoding the biological functions of the individual LC3/

268 ides an efficiently systematic framework for decoding the co-expression gene modules in multiple tiss

269 Specifically, decoding the complex behavior of single molecules enable

270 de in identifying CD1-restricted T cells and decoding the diverse immunological functions of distinct

271 t study provides key insights for eventually decoding the earliest fossil record.

272 Decoding the effect of the electrical signals on the cel

273 that is, the chromatin codes, is crucial for decoding the epigenetic state of the cell.

274 ectural protein CTCF plays a complex role in decoding the functional output of the genome.

275 However, decoding the functions of the millions of putative regul

276 periods in brain development is essential to decoding the long-term impact of widespread, poorly defi

277 Decoding the mechanisms that instruct dB1 circuit format

278 by a load-related decline in the accuracy of decoding the memory stimuli (colors) from left superior

279 fungi, and we suggest future directions for decoding the molecular basis of the underground dance be

280 Decoding the molecular mechanisms that regulate nucleic

281 roscience initiatives are making progress in decoding the neural nature of such feelings in animal br

282 Although perception depends upon decoding the pattern of activity across a neuronal popul

283 putations that are optimal for combining and decoding the responses into estimates of speed.

284 y requires the development of techniques for decoding the spike times of the recorded neurons from th

285 support of an alternative approach, based on decoding the stimulus from the neural response.

286 the thousands of known protein structures, "decoding" them is challenging because of the complexity

287 Comprehensively decoding these regulatory mechanisms holds promise in ge

288 An increase in encoding and decoding time of 30% and 55% represents an additional pe

289 Here we use population decoding to better characterize three of these face patc

290 This fMRI study used multivariate pattern decoding to characterize the computational principles th

291 genetic variation as a powerful approach for decoding transcription factor combinations that play dom

292 The proposed method for decoding transport history from particle shape provides

293 Cross-linked reads originating from AAA-decoding tRNA(Lys)(UUU) were 10-fold enriched over its c

294 d the impact of correlations on encoding and decoding, typically denoted by Ishuffle and Idiag respec

295 by challenging syllable tracking and speech decoding using comprehensible and incomprehensible time-

296 olution) and are further confirmed by direct decoding using phase model analysis.

297 , a significant boundary condition on memory decoding validity may be the deployment of "countermeasu

298 Using single-trial decoding, we quantified the relation between prestimulus

299 nd searchlight-based fMRI multivoxel pattern decoding, we sought brain regions in human cortex that m

300 oximate marginalization by linear population decoding, we tested the hypothesis that vestibular signa