ライフサイエンスコーパス: receptive

1 ll as on researcher-administered measures of receptive (1.30, -0.48 to 3.08) and expressive language

2 ) on the MACI, but higher caregiver-reported receptive (37.17, 95% CI 10.59 to 63.75) and expressive

3 Hence, men who practice receptive AI may need additional strategies to detect an

4 havioural responses of the presumed, magneto-receptive American lobster and the electro-sensitive Lit

5 primary syphilis if they reported practising receptive anal intercourse (adjusted odds ratio 3.90, p<

6 primary syphilis if they reported practicing receptive anal intercourse (adjusted odds ratio 3.90; P

7 reduce onward transmission.Men who practiced receptive anal intercourse (AI) were more likely to pres

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

9 M with primary syphilis who did not practise receptive anal intercourse almost always (92%) had their

10 M with primary syphilis who did not practice receptive anal intercourse almost always (92%) had their

11 reased alpha diversity, which is linked with receptive anal intercourse in both males and females.

12 The finding that MSM who practiced receptive anal intercourse more commonly presented with

13 The finding that MSM who practised receptive anal intercourse more commonly presented with

14 en who have sex with men (MSM) who practised receptive anal intercourse were more likely to present w

15 We hypothesized that MSM who practiced receptive anal intercourse were more likely to present w

16 philis, compared to MSM who did not practise receptive anal intercourse.

17 philis, compared to MSM who did not practice receptive anal intercourse.

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

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

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

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

22 134 (24%) men reported not practising receptive anal sex.

23 these, 134 (24%) men reported not practicing receptive anal sex.

24 ntiretroviral therapy have increased odds of receptive and expressive language delays at 2 years of a

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

26 ting, more injections in the past month, and receptive cooker sharing were associated with increased

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

28 appy voices exhibiting posterior activity in receptive emotion areas and angry voices displaying acti

29 th specific features of tissue renewal and a receptive endometrium.

30 havior: concurrent animals were mated with a receptive female immediately after each session, while n

31 ections are essential for sexual behavior in receptive females.

32 ctiveness of their urinary scent to sexually receptive females.

33 teraction between signals from the classical receptive field (CRF) and the extra-classical receptive

34 eceptive field (CRF) and the extra-classical receptive field (eCRF) in primary visual cortex (V1) neu

35 The stimulation of this feedback receptive field (fbRF) elicits responses that are slower

36 rd pathways define the classical feedforward receptive field (ffRF), the area in space in which visua

37 Crucially, the neuron's receptive field (i.e., its response to presynaptic stimu

38 a standard linear-nonlinear spectro-temporal receptive field (LN) model and variants that incorporate

39 the visual system, using fMRI and population receptive field (pRF) mapping in 20 human females with m

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

41 esonance imaging (fMRI) and population-based receptive field (prf) mapping.

42 sage with an example application: population receptive field (pRF) methods for functional MRI data.

43 We used fMRI and population receptive field (pRF) modeling to measure the responses

44 ial spread can be estimated by measuring the receptive field (RF) and multiplying by the cortical mag

45 We found that RGC photopic receptive field (RF) center size and whole-field RGC fir

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

47 The noninvasive estimation of neuronal receptive field (RF) properties in vivo allows a detaile

48 Receptive field (RF) size and preferred spatial frequenc

49 FP) responses to stimuli detected inside the receptive field (RF) strengthen.

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

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

52 a span of time-delays in a spectro-temporal receptive field (STRF).

53 rly visual cortex despite the lack of direct receptive field activation.

54 simultaneously with one stimulus inside the receptive field and a second, competing stimulus outside

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

56 ze, where responses to stimuli exceeding the receptive field can be suppressed (surround suppression)

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

58 the S-OFF midget RGCs have a center-surround receptive field consistent with a role in spatial vision

59 ortical visual areas are enhanced when their receptive field contains a stimulus sharing target objec

60 We thus confirm that a neuron's receptive field does not follow directly from the weight

61 our findings and predicts a spatio-chromatic receptive field for fly photoreceptor outputs, with a co

62 gnificantly greater when the stimulus in the receptive field had been fixated previously in the trial

63 ertebrate retina, the location of a neuron's receptive field in visual space closely corresponds to t

64 ons may reduce their firing rates when their receptive field input can be predicted by spatial contex

65 nt linear functions enables a locally linear receptive field interpretation of the neural network.

66 e retina, estimated subunits partitioned the receptive field into compact regions, likely representin

67 efinement, through which the size of sensory receptive field is reduced.

68 cording to their response properties such as receptive field location and feature selectivity.

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

70 the dangers that uncorrected stimuli pose to receptive field mapping experiments.

71 Using functional neuroimaging and population receptive field mapping, we find that chromosome dosage

72 First, using single-cell receptive field mapping, we revealed the presence of coa

73 We used a novel population receptive field mapping-based approach to resolve the sp

74 The receptive field maps of hair cells undergoing efferent a

75 We present optical recordings, receptive field maps, and sensitivity curves that show a

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

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

78 Population receptive field models have been successful in character

79 nventional single-layer linear and nonlinear receptive field networks that capture the overall featur

80 Attention toward the stimulus in the receptive field of recorded neurons significantly facili

81 spatial cue deploying attention towards the receptive field of the recorded neural population.

82 Shifting spatial attention into the receptive field of visual neurons has been shown to diff

83 the temporal evolution of the spatiotemporal receptive field of visual neurons in the middle temporal

84 a multicell model to explore the effects of receptive field offset on the precision of edge-location

85 connectivity of these RGCs can explain their receptive field offset, and we use a multicell model to

86 natural image statistics, and resembled the receptive field only when nearby, same-type cells were i

87 ells were spatially independent, with little receptive field overlap.

88 bthreshold membrane responses induced by the receptive field plasticity and the increased input-outpu

89 Further, this receptive field plasticity was accompanied by increases

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

91 al thalamus but are essential for sharpening receptive field properties and improving contrast-gain o

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

93 known about feature detectors, including how receptive field properties differ from the motion pathwa

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

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

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

97 We investigated the receptive field properties of the S-OFF midget circuit w

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

99 We first modeled receptive field properties of voxels in SC, deriving a d

100 Their receptive field properties suggest that they could serve

101 t whether feedback circuits regulate spatial receptive field properties versus temporal responses amo

102 edforward pathways carry information such as receptive field properties via glutamatergic class 1 syn

103 ited for the transfer of information such as receptive field properties, suggesting the importance of

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

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

106 ion between V1 and SC.SIGNIFICANCE STATEMENT Receptive field refinement in superior colliculus differ

107 stitute for visual experience in maintaining receptive field refinement into adulthood, and that this

108 city, TrkB signaling plays a crucial role in receptive field refinement.

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

110 nterpreted as a link between crowding zones, receptive field scaling, and our perceptual experience.

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

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

113 ural sampling by retinal ganglion cells with receptive field size and spacing that increases with ecc

114 Its population-receptive field size, however, suggests that this ventra

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

116 The receptive field size, sensitivity to surround illuminati

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

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

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

120 pendent representations captured by neurons' receptive field sizes and sampling density that change w

121 howed distinct light response properties and receptive field sizes.

122 is more consistent with the S-OFF midget RGC receptive field structure and studies of hue perception.

123 revealed that these cells exhibit irregular receptive field structure composed of spatially segregat

124 recordings of T5 neurons and found a similar receptive field structure: fast depolarization and persi

125 ouse primary visual cortex generate a second receptive field that is driven by stimuli outside the ff

126 Longitudinal imaging of receptive field tuning (e.g., orientation selectivity) o

127 s in the primary visual cortex sharpen their receptive field tuning properties.

128 nsory cortex (S1) sharing the same cutaneous receptive field while monkeys judged the presence or abs

129 rts visual input to different regions of its receptive field with distinct action potential waveforms

130 ginally viewed as a part of the fundamental "receptive field" characteristic of neurons.

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

132 ell (RGC) is often summarized by its spatial receptive field, but in principle also depends on the re

133 acrine cell (AC), exhibits a spatially tuned receptive field, composed of an excitatory center and an

134 rons are suppressed by stimuli outside their receptive field, is an example of this integration takin

135 timuli lying in the null space of the linear receptive field, revealed stronger nonlinearities in OFF

136 ion of inflammatory mediators to their dural receptive field, sensitize their responses to stimulatio

137 interactions of local stimulation across the receptive field, we found no amplifying responses, only

138 ns are stronger with multiple stimuli in the receptive field, whereas feature attention modulations a

139 presented at locations outside the neuron's receptive field, which suggests a contribution of multip

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

141 ion where test compounds were applied to the receptive field.

142 trength of L, M, and S cone input across the receptive field.

143 were contained within or extended beyond the receptive field.

144 odulated by stimuli outside of the classical receptive field.

145 as the stimulus crosses the ganglion cell's receptive field.

146 ic stimulus attributes intersecting with the receptive field.

147 by stimuli that extend beyond the classical receptive field.

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

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

150 ample and the second on the spectro-temporal receptive field.

151 hibition before or after reaching the cell's receptive field: the response is weaker in the former th

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

153 optic lobe, particularly in ON-pathway (T4) receptive-field circuits, in concert with physiological

154 A spectral receptive-field model incorporating broadband inhibition

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

156 system, we use two-photon imaging to measure receptive fields (RFs) and size-tuning in primary visual

157 sufficient for spatial refinement of visual receptive fields (RFs) in superior colliculus (SC) and v

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

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

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

161 Receptive fields (RFs) of SDs are organized concentrical

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

163 C contains neurons with spatially-restricted receptive fields (RFs) that form an azimuthal topographi

164 rse correlation to estimate spectro-temporal receptive fields (STRFs) implied by the learned GFs.

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

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

167 ragranular-layer neurons by sharpening their receptive fields and frequency tuning, as well as increa

168 etworks that consist of neurons with similar receptive fields and increased connectivity relative to

169 thermore, apical dendrite inputs have larger receptive fields and longer response latencies than basa

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

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

172 rons and endow neural populations with broad receptive fields and sharp frequency tuning.

173 They have small receptive fields and strong antagonistic surrounds.

174 hought to preserve the spatial resolution of receptive fields and to enable connections for the ocula

175 Receptive fields and tuning curves of sensory neurons re

176 nal cord and that their cutaneous and muscle receptive fields are found around the ears, occipital sk

177 s view was later challenged by evidence that receptive fields are modulated by stimuli outside of the

178 can only reach healthy performance levels if receptive fields are still plastic, in line with finding

179 functional taxonomy of cells with vectorial receptive fields as reported in experiments and proposed

180 prevents the normal development of binocular receptive fields by impairing the maturation of ipsilate

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

182 shed within ~10 ms after response onset, and receptive fields dynamically sharpen while suppression s

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

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

185 hway and comprehensively identify inputs and receptive fields for T5.

186 neurons in Drosophila and to extract calcium receptive fields from cortical neurons in mammals.

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

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

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

190 The temporal resolution of these receptive fields has traditionally been limited by image

191 Receptive fields in both cell types have a center-surrou

192 mporal area and to the estimated size of the receptive fields in human depth-sensitive cortical regio

193 elative to seen spatial frequencies and that receptive fields in imagined space are larger than in vi

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

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

196 d it demonstrated a diversity of suppressive receptive fields in the RGC population.

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

198 uencies, as well as the location and size of receptive fields in visual and imagined space.

199 Consistent with spatially coarse receptive fields in vLGN, visually evoked changes in spi

200 from V1 to LL, along with the quality of the receptive fields inferred through reverse correlation.

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

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

203 ry inputs onto a single neuron, to study how receptive fields may change on short and long time scale

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

205 Our computational analyses reveal that the receptive fields of human midget and parasol ganglion ce

206 initial studies identifying the overlapping receptive fields of multisensory neurons, to subsequent

207 We recorded the receptive fields of multiunit clusters in male macaques

208 emory processes may underlie linear temporal receptive fields of neurons beyond 25 ms.

209 The spatial receptive fields of neurons in medial entorhinal cortex

210 Here, we measured the spatial receptive fields of neurons in primary auditory cortex (

211 R neurons (also known as ring neurons); the receptive fields of R neurons tile visual space(5).

212 velopmental changes in linear spatiotemporal receptive fields of simple cells, implying alterations i

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

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

215 The anatomical receptive fields of these two mechanoreceptor subtypes h

216 on due to synergistic interactions even when receptive fields overlap and shared noise between cells

217 This contrasts with dragonfly TSDNs, where receptive fields possess a sharp midline boundary, confi

218 It identified multiple receptive fields reflecting the main excitatory and supp

219 puts from higher visual areas have scattered receptive fields relative to their putative targets in t

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

221 The development of sensory receptive fields requires the coordinated spatial patter

222 sign choice whereby neurons with overlapping receptive fields sample environmental stimuli to convey

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

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

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

226 This data can be used to map receptive fields that describe neural associations with

227 ng, requiring scales at least as small as V1 receptive fields to generate metamers.

228 ble with past, qualitative descriptions, the receptive fields we quantified in vLGN were larger than

229 Receptive fields were mapped in the superior colliculus

230 tream model when information was averaged in receptive fields with a scaling of about half their reti

231 frequency adaptation, to apparent changes in receptive fields with changes in stimulus statistics, to

232 redicts that-after learning-the granule-cell receptive fields with respect to sensory and with respec

233 es the timing of neural measurements to find receptive fields with temporal resolutions higher than t

234 tudies show that such responses (i.e., their receptive fields) depend on context.

235 eld maps: estimated linear filters (temporal receptive fields) systematically differ across and withi

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

237 Here, we investigated processing by receptive fields, a fundamental property of neurons in t

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

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

240 neurons (TSDNs) with matching frontal visual receptive fields, anatomically and functionally homologo

241 rsus dLGN had wider dendritic arbors, larger receptive fields, and fired with lower temporal precisio

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

243 and distinguished their distinct ON and OFF receptive fields, and it demonstrated a diversity of sup

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

245 the power and flexibility of our approach on receptive fields, ion channels, and Hodgkin-Huxley model

246 stimuli were spatially separated within the receptive fields, the contrast dominance was abolished.

247 ance the selectivity and expand the range of receptive fields, therefore potentially sharpening the p

248 and independently within individual neurons' receptive fields, which segregate sensitive and selectiv

249 rive two neural populations with overlapping receptive fields.

250 stabilize the lateral inhibition that shapes receptive fields.

251 the classic center-surround model of retinal receptive fields.

252 excitatory and suppressive components of RGC receptive fields.

253 V4 neural sites, even those with overlapping receptive fields.

254 ion, despite comparable stimulation of their receptive fields.

255 group tuning displayed view-point selective receptive fields.

256 et-specific contrast preferences and spatial receptive fields.

257 he spatial arrangement of current and future receptive fields.

258 ching in the superficial epidermis and large receptive fields.

259 the balance of inputs that generate neuronal receptive fields.

260 generate orientation-selective cue-invariant receptive fields.

261 are rapidly changing outside their classical receptive fields.

262 amatic context-dependent changes of neurons' receptive fields.

263 vides a first mechanistic model for flexible receptive fields.

264 in tonal (TRFs) and spectrotemporal (STRFs) receptive fields.

265 ility among neurons in macaque area V4 whose receptive-fields lie at the attended location.

266 cycle, while other species are the opposite, receptive for mere hours out of their several-week cycle

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

268 CVID+AIC subjects provided efficient help to receptive healthy donor B cells but not unresponsive CVI

269 ve (effect size 0.52 SD [95% CI 0.21-0.83]), receptive language (0.42 SD [0.08-0.77]), and socioemoti

270 children scored lower than HIV-unexposed for receptive language (adjusted mean difference -1.03 [95%

271 her than those of HIV-unexposed children for receptive language (adjusted odds ratio 1.96 [95% CI 1.0

272 = -0.74; 95% CI -1.46 to -0.03, p = 0.042], receptive language [beta = -1.10; 95% CI -1.70 to -0.49,

273 left perisylvian surface area, particularly receptive language centers.

274 domains (369 [50.5%] cognition, 402 [55.6%] receptive language, 389 [55.4%] expressive language, 169

275 unity practitioners, especially if there are receptive local palliative and hospice care champions.

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

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

278 icide will increase the length of the female receptive period, emphasizing the possible importance of

279 size, each influence the length of females' receptive periods.

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

281 e-scale approach at characterising molecular receptive ranges (MRRs) of glomeruli in the dorsal olfac

282 pered by incomplete knowledge about chemical receptive ranges of primary receptors.

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

284 ematic spatial offset between the ON and OFF receptive subfields in F-mini-ON retinal ganglion cells

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

286 HR, 1.45 [95% CI, 1.01-2.08]; P = .042), and receptive syringe sharing (aHR, 1.43 [95% CI, 1.33-1.53]

287 ploma (GED) (aPR, 1.17 [95% CI, 1.03-1.33]), receptive syringe sharing (aPR, 1.37 [95% CI, 1.21-1.56]

288 ly to report injecting more than once a day, receptive syringe sharing, sharing of other injection eq

289 ecute effective courtship behaviors toward a receptive target sex, which is female.

290 ived payoffs, with some followers being more receptive than others to such leadership tactics.

291 I (KL), VGN firing patterns may become more receptive to extrinsic control.

292 neurons, maintaining them in a state that is receptive to future sensory stimuli.

293 me primate species are like humans, sexually receptive to mating throughout their entire estrus cycle

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

295 However, officials are most receptive to refugees whom they perceive as a strong eco

296 alpha range (8-12 Hz) of neural populations receptive to target visual stimuli may be part of the me

297 Patients were receptive to the inclusion of out-of-pocket cost as rele

298 able for support, and patients are generally receptive to this type of discussion with their physicia

299 ion between the competent blastocyst and the receptive uterus.

300 Thus, these experimentally defined "temporal receptive windows" are longest in cortical regions that