ライフサイエンスコーパス: receptive

1 daily, or RG-TFV rectal gel before and after receptive anal intercourse (RAI; or at least twice weekl

2 east annual rectal screening of men who have receptive anal intercourse for Neisseria gonorrhoeae (GC

3 women were more likely to report condomless receptive anal sex in the prior 12 months (OR 2.44, 95%

4 eeting criteria for screening nor history of receptive anal sex was significantly associated with HSI

5 When adjusted for age, condomless receptive anal sex, depression, interpersonal stigma, la

6 nd the interaction of gender with condomless receptive anal sex, the odds of HIV infection for transg

7 ieved that she had been doing well with both receptive and expressive language since she had received

8 from 17 healthy fertile-aged women from pre-receptive and receptive phase within one menstrual cycle

9 nes on 164 endometrial samples (76 from 'pre-receptive' and 88 from mid-secretory, 'receptive' phase

10 (ii) left superior-/middle-temporal gyri and receptive aphasia; (iii) widespread temporal/frontal lob

11 imported from outside the region into highly receptive areas, vector control must be maintained withi

12 be the underlying mechanism - pointing to a receptive class-related difference of sodium channel equ

13 the steady state it accumulates in a ligand-receptive conformation within the endoplasmic reticulum.

14 port a role of TAPBPR in stabilizing peptide-receptive conformation(s) of MHC-I, permitting peptide e

15 hat excitability of genetically isolated CRF-receptive (CRFR1) neurons in the CeA is potently enhance

16 cally to a glial microdomain surrounding AFD receptive ending microvilli, where it regulates K(+) and

17 world or from other neurons through neuronal receptive endings (NREs).

18 on) is fundamental to the establishment of a receptive endometrial microenvironment which can support

19 ggests that PAPPA is essential to maintain a receptive endometrium by up-regulating N-fucosylation, w

20 insulin resistance through the creation of a receptive environment at the plasma membrane for the ass

21 reported in vivo We used fMRI and population receptive field (pRF) mapping to demonstrate that the fi

22 of these deficits using fMRI and population receptive field (pRF) mapping to infer properties of vis

23 Further, we found that with maturation receptive field (RF) center sizes decrease, spike-trigge

24 for correlations among curvature preference, receptive field (RF) end-stopping, and RF eccentricity i

25 When light falls within a neuronal visual receptive field (RF) the resulting activity is referred

26 ity of stimuli in the surround of a neuron's receptive field (RF) to modulate (typically suppress) th

27 red with responses to distractor bars in the receptive field (RF).

28 Spectrotemporal receptive field (STRF) mapping describes the neural resp

29 ive cells, the second-order component of the receptive field aligned with stimulus preference, wherea

30 related modulation across both the classical receptive field and the surround.

31 We modeled each eye's receptive field at each cortical site using a difference

32 ation that will be brought into the neuron's receptive field by the saccade (the future receptive fie

33 em, the response to a stimulus in a neuron's receptive field can be modulated by stimulus context, an

34 ng sensory cells in which stimulation of the receptive field center excites the cell whereas stimulat

35 evation along with a concomitant decrease in receptive field center size for OFF RGCs.

36 e we use natural speech stimuli and advanced receptive field characterization methods to show that sp

37 maintained as the animal develops to ensure receptive field coverage.

38 cal and thalamic neurons, the weight of each receptive field element depends on the pattern of sound

39 A computational model shows that this receptive field expansion is consistent with the propaga

40 l statistics can account for many aspects of receptive field formation across models and sensory moda

41 The receptive field has an excitatory ON center, flanked by

42 The most common receptive field in rodent thalamus, however, is center-s

43 reas DALcl2 neurons share a large excitatory receptive field in the contralateral hemifield.

44 o measure BOLD activity at precisely defined receptive field locations in visual cortex (V1) of human

45 Using visual receptive field mapping, glutamate uncaging, two-photon

46 es on the activity of a recently-proposed V1 receptive field model and a deep convolutional neural ne

47 nction of stimulus location using population receptive field modeling to isolate each voxel's overlap

48 l experimental task and nonlinear population receptive field modeling, we map and characterize the to

49 Here we show that auditory cortex receptive field models benefit from a nonlinear preproce

50 Population receptive field models have been successful in character

51 ward network models expands on simple linear receptive field models in a manner that yields substanti

52 ng properties of neurons will likely improve receptive field models in other sensory modalities too.

53 icantly beyond that of simple, mostly linear receptive field models.

54 rine cell type, in which the extra-classical receptive field of ON parasol cells is formed by recipro

55 As the spatiotemporal receptive field of T5 in Drosophila is common to the sim

56 induced visual sensations is matched to the receptive field of the cortical site measured with broad

57 Most qualitative receptive field parameters were found to be unchanged be

58 ented cells, the second-order subunit of the receptive field predicted the preferred angle.

59 k, the spatiotemporal organization of the T5 receptive field predicts the activity of T5 in response

60 d by less than 10 mum shared similar spatial receptive field properties and exhibited a distance-depe

61 cally either concentrated on tuning curve or receptive field properties and remained agnostic as to t

62 gulating experience-dependent plasticity and receptive field properties develop late, like their inhi

63 pines defined by dimensionality reduction of receptive field properties exhibited non-random dendriti

64 Overall, however, receptive field properties in the anesthetized animal re

65 there have been few comprehensive studies of receptive field properties in the awake mouse, especiall

66 ly mature neural organization and adult-like receptive field properties in very young infants.

67 Spatial receptive field properties of dendritic spines were stri

68 nce is necessary for the development of some receptive field properties of neurons in primary sensory

69 e primary auditory cortex (A1) can shape the receptive field properties of neurons in the ventral div

70 The non-canonical receptive field properties of the OND RGC-integration of

71 s known about how feedforward pathways shape receptive field properties of visual neurons, relatively

72 Their receptive field properties suggest that they could serve

73 mouse, called the ON delayed (OND) RGC, with receptive field properties that deviate from center-surr

74 Thus, despite the absence of barrels, most receptive field properties were similar to those reporte

75 led stream differences in the development of receptive field properties.

76 ion in controlling both temporal and spatial receptive field properties.

77 lassical surround suppression is a prominent receptive field property of neurons in the lateral genic

78 anges exhibit properties similar to those of receptive field remapping, a phenomenon in which individ

79 map in V4 matches many of the properties of receptive field remapping.

80 he course of functional recovery, we tracked receptive field reorganization, spontaneous activity, an

81 The network receptive field reveals separate excitatory and inhibito

82 bbian learning is applied to natural images, receptive field shapes were strongly constrained by the

83 nd to the presaccadic enhancement [9-11] and receptive field shifts reported in neurophysiological st

84 This produces firing rate modulations and receptive field shifts.

85 ng-surround receptive field, which varied in receptive field size and degree of ON-OFF asymmetry with

86 ver, functional pairs exhibit asymmetries in receptive field size and response kinetics.

87 ive effects that are automatically scaled to receptive field size in any given area.

88 , biased competition automatically scaled to receptive field size) and receptive field structure (shi

89 ghtly tuned than predictions based simply on receptive field size, indicating that correlated activit

90 pike-timing precision, and reduced classical receptive field size.

91 (1) dendritic field size, which approximate receptive field size; (2) dendritic complexity, which af

92 rences exist between the species in terms or receptive field sizes and orientation map organization,

93 Here the authors show that the receptive field sizes of reticular neurons are small eno

94 atically scaled to receptive field size) and receptive field structure (shifts and resizing of recept

95 in the evolutionarily advantageous nature of receptive field structure in visual systems and suggests

96 For example, in rodent, thalamic receptive field structure is markedly diverse, and many

97 nglion cell in the retina and shows that the receptive field structure is remarkably similar to that

98 Thus, receptive field structure supersedes size per se for for

99 w sampling scheme motivated by physiological receptive field structure, localized random sampling, wh

100 l connectivity, or imposing simple-cell-like receptive field structure, no study has exploited the fa

101 tical columns exhibit an invariant aggregate receptive field structure: an OFF-dominated central regi

102 er, although it is well established that the receptive field surround is strongest when ambient or ba

103 Thus, Wave neurons match their receptive field to appropriate motor programs by partici

104 ion of visual space across which the current receptive field will be swept by the saccade.

105 Accounting for this change in effective receptive field with spectrotemporal context improves pr

106 nlinear feedforward network model (a network receptive field) to cortical responses to natural sounds

107 s receptive field by the saccade (the future receptive field), even before saccade begins.

108 Furthermore, the network receptive field, a parsimonious network consisting of 1-

109 e excited by a probe stimulus in the current receptive field, and also simultaneously by a probe stim

110 lying vibrotactile stimulation to the unit's receptive field, and unit-type perceptual reports are an

111 iven primarily by the visual stimulus in the receptive field, but by the broader context that stimulu

112 res in a region of visual space known as the receptive field, but can be modulated by stimuli outside

113 neurons are commonly characterized using the receptive field, the linear dependence of their response

114 ll characterized RGC with a comparably small receptive field, the local edge detector, in response to

115 osities with a small-center, strong-surround receptive field, which varied in receptive field size an

116 wo Bayesian population-decoding methods (one receptive field-based, and the other not), we systematic

117 by stimuli that extend beyond the classical receptive field.

118 y a surprising bias in inhibition within the receptive field.

119 on emanating from the centre of the neuron's receptive field.

120 implemented in different sub-regions of the receptive field.

121 citation and suppression associated with the receptive field.

122 ptic inputs, which generate a color-opponent receptive field.

123 t can be modulated by stimuli outside of the receptive field.

124 he increase of preferred contrast inside the receptive field.

125 y patterns presented over an unusually large receptive field: could this cell be a (de)focus detector

126 hree high-definition (HD) RGCs possess small receptive-field centers and strong surround suppression.

127 e three "high-definition" RGCs share certain receptive-field properties, they also have distinct tuni

128 logical recordings of their light responses, receptive-field size and structure, and synaptic mechani

129 Yet how attention interacts with the receptive-field structure of cortical neurons remains un

130 Notably, the receptive-field-free decoding method was found to be wel

131 We map spatial receptive fields (RFs) for SCN neurons and find that onl

132 Spatial receptive fields (RFs) mapped using melanopsin-isolating

133 We mapped the visual receptive fields (RFs) of neurons recorded at the same e

134 city of thalamocortical connectivity and the receptive fields (RFs) of postsynaptic cortical neurons.

135 cted LGN-V1 pairs were only found when their receptive fields (RFs) overlapped, and the probability o

136 are not influenced by stimuli outside their receptive fields (RFs), dynamics of the high-dimensional

137 s and integrating visual inputs across their receptive fields (RFs).

138 y altering the encoding properties of single receptive fields (RFs).

139 ave pronounced effects on the spatiotemporal receptive fields (STRFs) of neurons.

140 e use fMRI to relate changes in single voxel receptive fields (vRFs) to changes in population-level r

141 ling is vital to the maintenance of cortical receptive fields [2]; however, it is unclear how this fi

142 rround organization of retinal ganglion cell receptive fields [5], and biasing of competitive local n

143 non in which individual neurons change their receptive fields according to the metrics of each saccad

144 lls (HCs) to cones generates center-surround receptive fields and color opponency in the retina.

145 s) to photoreceptors creates center-surround receptive fields and color-opponent interactions.

146 standard (non-OMS) DS cells by their smaller receptive fields and different organization of preferred

147 he role of different circuits in shaping RGC receptive fields and establish a foundation for continue

148 Next we mapped receptive fields and found surprisingly precise micro-re

149 optimize response sensitivity across distant receptive fields and preclude any bias toward local ligh

150 cat, most retinal cells have center-surround receptive fields and push-pull excitation and inhibition

151 Cortical neurons remap their receptive fields and rescale sensitivity to spared perip

152 on of extra neurons, suggesting the neurons' receptive fields are not optimised for recognising abstr

153 ain accomplishes this is by remapping visual receptive fields around the time of a saccade.

154 tive field structure (shifts and resizing of receptive fields both spatially and in complex feature s

155 ity is not limited to the current and future receptive fields but encompasses the entire region of vi

156 opulation of V1 neurons with locally diverse receptive fields can be described with surprisingly limi

157 In all examples, receptive fields can be predicted a priori by reformulat

158 ecoding performance occurred for voxels with receptive fields closer to the fovea and overlapping wit

159 ained activation of the STG, spectrotemporal receptive fields could be reconstructed from vigorous re

160 aracterized by one or more linearly weighted receptive fields describing sensitivity in sensory space

161 However, receptive fields do not capture the fact that the respon

162 d orientation is decodable from voxels whose receptive fields do not overlap with the stimulus edges,

163 patial separation across multiple peripheral receptive fields ensures the composite stimulus timecour

164 hat neurons with protracted resting temporal receptive fields exhibit stronger chosen value correlate

165 onses in these areas increases, and neuronal receptive fields expand and shift towards the remembered

166 es display topographic organization, whereby receptive fields follow a characteristic pattern, from t

167 nse rates, as adaptations of spectrotemporal receptive fields following stimulation by temporally coh

168 vidual ring neurons inherit simple-cell-like receptive fields from their upstream partners.

169 Paradoxically, these highly variable receptive fields go alongside and are in fact required f

170 eading to a deep dynamic reshaping of neural receptive fields going far beyond simple surround suppre

171 murine cells with classical center-surround receptive fields had a "push-pull" structure of excitati

172 The development of sensory receptive fields has been modeled in the past by a varie

173 ractions create antagonistic centre-surround receptive fields important for detecting edges and gener

174 systems is typically addressed by measuring receptive fields in a fixed, sensor-based coordinate fra

175 d two-photon calcium imaging, have described receptive fields in anesthetized animals.

176 used to study contextual effects on auditory receptive fields in animal models.

177 We have performed a comparative survey of receptive fields in dLGN, lateral posterior nucleus, and

178 d space remains undefined: classical spatial receptive fields in head-fixed subjects can be explained

179 Our results show that the diversity of receptive fields in L2/3 is likely due to diversity in t

180 ere we revisited the spatial organization of receptive fields in mouse primary visual cortex by measu

181 regions, a structure similar to simple cell receptive fields in primary visual cortex.

182 ly moving subjects; here we recorded spatial receptive fields in the auditory cortex of freely moving

183 g with descriptions of random, discontinuous receptive fields in the central olfactory neurons in mam

184 ests participation of neurons with localized receptive fields in the comparison process.

185 location, implicating neurons with localized receptive fields in the comparison process.

186 We map voxel population receptive fields in V1 and evaluate orientation decoding

187 al waves are critical for the development of receptive fields in visual thalamus (LGN) and cortex (VC

188 ntre and surround components of bipolar cell receptive fields interact to decorrelate bipolar cell ou

189 Yet a full characterization of receptive fields is still incomplete, especially with re

190 Meanwhile, the VT2-3 cells have motion receptive fields matched to the lift axis.

191 sent novel cell types that have local motion receptive fields matched to translation self-motion, the

192 ad-out strategy that emphasized neurons with receptive fields near the stimulus center.

193 ction of neurons in early visual cortex with receptive fields not selective for orientation that have

194 miR-132/212 deletion affects development of receptive fields of cortical neurons determining a speci

195 Here we assessed one-dimensional spatial receptive fields of individual dendritic spines within i

196 plained by neurons having different temporal receptive fields of integration, indexed by examining ne

197 ON-OFF convergence visualized by mapping the receptive fields of layer 2/3 neurons in the tree shrew

198 The spatial receptive fields of neurons in medial entorhinal cortex

199 ending on where those stimuli lie within the receptive fields of neurons.

200 been used as the canonical model to describe receptive fields of retinal ganglion cells (RGCs) for de

201 that inhibition is evoked broadly across the receptive fields of simple cells, and we identify a surp

202 Characterizing the receptive fields of such neurons is difficult with stand

203 Moreover, we show that the receptive fields of the newly discovered speed neurons c

204 Recently the receptive fields of these neurons have been mapped, allo

205 Computational modeling of these receptive fields predicts responses to motion and reveal

206 ying stimuli, whereas the spatial aspects of receptive fields remain comparatively unchanged.

207 However, the relationship between these receptive fields remains unclear.

208 neural mechanism to construct such versatile receptive fields remains unclear.

209 ased stimulus selectivity and expanded their receptive fields significantly.

210 We introduce a new method for estimating receptive fields simultaneously for a population of V1 n

211 whether cells in the reticular nucleus have receptive fields small enough to provide localized feedb

212 in motion-sensitive neurons that have larger receptive fields than those found in V1, giving the pote

213 rons in early visual cortex have specialized receptive fields that allow them to selectively respond

214 that central auditory neurons have composite receptive fields that can arise through a combination of

215 ntribute most to classifier performance have receptive fields that cluster in cortical regions corres

216 a parsimonious network consisting of 1-7 sub-receptive fields that interact nonlinearly, consistently

217 s of inputs received from neurons in MT with receptive fields that resemble basis vectors recovered w

218 serine-treated animals, tectal neuron visual receptive fields were expanded, suggesting a failure to

219 Receptive fields were mapped in the superior colliculus

220 The data showed that receptive fields were offset in position by the ocular d

221 Both symmetrical and asymmetrical receptive fields were present.

222 mes completely fill available space in their receptive fields with evenly spaced dendrites to uniform

223 We then show that receptive fields with similar characteristics can be rep

224 cost function, AMA returns the filters (i.e. receptive fields) that extract the most useful stimulus

225 Early surveys of visual response properties (receptive fields) were performed in anesthetized animals

226 These cells exhibit center-surround receptive fields, a prototype of lateral inhibition betw

227 lly antagonistic surround to individual cone receptive fields, a signature inherited by downstream ne

228 CG neurons had simple, orientation-selective receptive fields, and generated sustained responses to s

229 ignal correlations, associated with neuronal receptive fields, and noise correlations, associated wit

230 ion drove the eyes accurately to the site of receptive fields, as in normal animals.

231 ervated volumes of muscle sheet, presumptive receptive fields, averaging 0.1 mm(3) .

232 well as modifying the structure and size of receptive fields, both in topological and feature space.

233 responses to mechanical stimulation of their receptive fields, compared to control animals.

234 /-) OFF bipolar cells showed enlarged visual receptive fields, demonstrating that expanded dendritic

235 ort-tailed opossum S1 exhibited multiwhisker receptive fields, including a single best whisker (BW) a

236 an be characterized by their spectrotemporal receptive fields, the spectral and temporal features of

237 ignals are characterised by relatively large receptive fields, this is likely to be due to an increas

238 fically center-surround, temporally biphasic receptive fields, to the generation of direction selecti

239 ay might be pooled to generate cue-invariant receptive fields, we recorded visual responses from sing

240 e small ipsilateral, retinotopically ordered receptive fields, whereas DALcl2 neurons share a large e

241 that S1 neurons had multimodal (tactile/IR) receptive fields, with clear preferences for those stimu

242 ction inhibition, on opposing sides of their receptive fields.

243 enerate orientation-selective, cue-invariant receptive fields.

244 ponses to auditory stimuli than the standard receptive fields.

245 fferent locations within and around neuronal receptive fields.

246 only 10 cells of two types with overlapping receptive fields.

247 an is seen in their standard spectrotemporal receptive fields.

248 hysical environments via regularly repeating receptive fields.

249 developing realistic, orientation-selective receptive fields.

250 via which ACh may mediate its effects on AC receptive fields.

251 e necessary for the development of localized receptive fields.

252 i-body-part responses and sexually dimorphic receptive fields.

253 he spatial arrangement of current and future receptive fields.

254 g neurons with the smallest (highest acuity) receptive fields.

255 et-specific contrast preferences and spatial receptive fields.

256 the balance of inputs that generate neuronal receptive fields.

257 generate orientation-selective cue-invariant receptive fields.

258 lls plays important roles to determine their receptive function to blastocysts.

259 a potential useful biomarker to evaluate the receptive functions of the endometrium.

260 ell state and that concomitant exposure to a receptive growth factor might result in the expansion of

261 teracting with the parent, and an expressive-receptive language composite.

262 system and special senses, conduct disorder, receptive language disorder, chronic serous otitis media

263 Receptive language scores were higher for the LNS-LNS gr

264 wherein the redox probe is contained in the receptive layer) mainly aiming dengue diagnosis in phosp

265 es peptide optimisation by promoting peptide-receptive MHC class I molecules to associate with the pe

266 romotes the association of UGT1 with peptide-receptive MHC class I molecules.

267 However, the instability of peptide-receptive MHC molecules has hindered characterization of

268 We compared the resultant peptide-receptive MHC molecules with non-hydrolyzed peptide-load

269 egated by the addition of peptide to peptide-receptive MHC molecules.

270 exchange between peptide-loaded and peptide-receptive molecules that were negated by the addition of

271 in females in the presence of vinegar become receptive more rapidly to courting males, while male cou

272 arity of luminal epithelial cells during the receptive period.

273 hy fertile-aged women from pre-receptive and receptive phase within one menstrual cycle.

274 during the transition from pre-receptive to receptive phase.

275 'pre-receptive' and 88 from mid-secretory, 'receptive' phase endometria) using a robust rank aggrega

276 , especially of nociceptors, correlates with receptive properties.

277 g should be prioritized among men who report receptive rectal sex.

278 rtex deprives thalamocortical axons of their receptive "sensory field" in layer IV, which normally pr

279 en and 175 women reporting a history of anal receptive sexual intercourse.

280 rus transitions from the prereceptive to the receptive stage is complex, involving an intricate inter

281 This structure captures a peptide-receptive state of MHC I and provides insights into the

282 onstrain the cognate receptor in an IL-1RAcP-receptive state.

283 uires that the uterus differentiate into the receptive state.

284 ultimately leads to the degeneration of the receptive synergid and PT rupture, releasing the sperm c

285 underpinning this process - the death of the receptive synergid cell and the coincident bursting of t

286 r, our findings reveal that the death of the receptive synergid cell is essential for maintenance of

287 LLATA3, interact to control the death of the receptive synergid cell.

288 ication between the pollen tube cell and the receptive synergid, culminating in the lysis of both int

289 In mice, the uterus becomes receptive to blastocyst implantation on day 4, but is re

290 shed light on why pluripotent cells are only receptive to differentiation signals during G1, that is,

291 These cells remain receptive to extracellular cues after gastrulation and c

292 ion, and thus the columnar dipole moment, is receptive to geometric frustration if the columns aggreg

293 gnaling causes immature T1 B cells to become receptive to Notch ligands via Taok3-mediated surface ex

294 zed structural flexibility makes MHC class I receptive to parasite-derived ligands that exhibit uniqu

295 ation changes during the transition from pre-receptive to receptive phase.

296 environment could allow them to be uniquely receptive to signals from local neurons, glia, and vascu

297 st F. tularensisin vivo requires macrophages receptive to stimulation.

298 der language processing posits that temporal receptive windows in the dorsal auditory stream provide

299 ictive coding architecture assuming temporal receptive windows of increasing length from auditory to

300 ion across different timescales via temporal receptive windows, which increase in length from lower t