ライフサイエンスコーパス: macaque monkey

1 tage along the ventral visual pathway of the macaque monkey.

2 identified corticogeniculate neurons in the macaque monkey.

3 uit for eye movements has been identified in macaque monkey.

4 cribe resulting medial-frontal EEG on a male macaque monkey.

5 pulations in cortical areas V1 and V2 of the macaque monkey.

6 nd single-unit data in the same species, the macaque monkey.

7 in both the visual and motor systems of the macaque monkey.

8 in laminae II-III of the dorsal horn of the macaque monkey.

9 ago in the ventral premotor region F5 of the macaque monkey.

10 of the connectivity of their homologs in the macaque monkey.

11 scending brainstem pathways in the Old World macaque monkey.

12 ctrophysiological and imaging studies in the macaque monkey.

13 sual cortical areas V4 and IT) in the rhesus macaque monkey.

14 orilla, and chimpanzee great apes and in the macaque monkey.

15 onal segregation of this brain region in the macaque monkey.

16 rchitecture in the mouse, cat, marmoset, and macaque monkey.

17 athways during strength training in 2 female macaque monkeys.

18 lection and performed whole-brain imaging in macaque monkeys.

19 eurons recorded individually in anesthetized macaque monkeys.

20 atedly and non-invasively inactivate rmCD of macaque monkeys.

21 s within prefrontal and (pre)motor cortex of macaque monkeys.

22 ing-state functional MRI in 38 humans and 25 macaque monkeys.

23 ate functional magnetic resonance imaging in macaque monkeys.

24 g a high-level visual behavior of humans and macaque monkeys.

25 scending auditory system of both rodents and macaque monkeys.

26 markedly inferior to that of chimpanzees and macaque monkeys.

27 he primary somatosensory cortex (area 3b) of macaque monkeys.

28 ns interfere with a covert attention task in macaque monkeys.

29 h the inferior parietal cortex (area PFG) in macaque monkeys.

30 cial layers of V1 in anesthetized, paralyzed macaque monkeys.

31 ned electrical stimulation with fMRI in male macaque monkeys.

32 ons found in the superior temporal sulcus of macaque monkeys.

33 which infects and induces disease in rhesus macaque monkeys.

34 ndary responses in V1 and V2 in anesthetized macaque monkeys.

35 ntia nigra or striatum of wild-type mice and macaque monkeys.

36 no evidence for such a division of labor in macaque monkeys.

37 l structure to humans of either sex and male macaque monkeys.

38 pulations in areas V1 and V2 of anesthetized macaque monkeys.

39 acellular recordings in acutely anesthetized macaque monkeys.

40 y somatosensory cortex (area 1) in two awake macaque monkeys.

41 1) and dorsal premotor (PMd) cortex of three macaque monkeys.

42 the pyramidal tract were made in three adult macaque monkeys.

43 d area during the use of a tool by two adult macaque monkeys.

44 erformance of a slow finger movement task in macaque monkeys.

45 tures, urethane-anesthetized rats, and awake macaque monkeys.

46 lyzed in visual area 2 (V2) of form-deprived macaque monkeys.

47 n the visual posterior sylvian area (VPS) of macaque monkeys.

48 ys implanted in the primary visual cortex of macaque monkeys.

49 ale modifications to the cortical network in macaque monkeys.

50 ure surround suppression in area MT of alert macaque monkeys.

51 n multimodal sensorimotor areas of cortex in macaque monkeys.

52 y eye field and anterior cingulate cortex of macaque monkeys.

53 guided manual and saccadic eye movements in macaque monkeys.

54 levels (C3-5) 3-12 days after birth in five macaque monkeys.

55 ent cancellation in medial frontal cortex of macaque monkeys.

56 urround organization of V1 and V2 neurons in macaque monkeys.

57 pecies, including great and lesser apes, and macaque monkeys.

58 field potentials (LFP) in visual area MT of macaque monkeys.

59 Two cynomogulus macaque monkeys.

60 ecordings from V1 neurons of awake, fixating macaque monkeys.

61 in response to a DRL/DCL, much as it does in macaque monkeys.

62 uency, contrast, and size) in V1 of two male macaque monkeys.

63 es for long-term two-photon imaging in awake macaque monkeys.

64 the primary visual cortex of awake behaving macaque monkeys.

65 In PET imaging studies in rhesus macaque monkeys, [(18)F]1 demonstrated high quality card

66 d organization of sensory cortical fields in macaque monkeys, a species with a relatively small brain

67 alized on a sequential saccade task in which macaque monkeys acquired repetitive scanning sequences w

68 Humans and macaque monkeys adjust their response time adaptively in

69 we performed a stereological analysis of the macaque monkey amygdala in order to characterize the cel

70 enual (p32) and subgenual (s32) in human and macaque monkey and areas d32 and v32 in rat and mouse.

71 e nucleus (LGN) of the thalamus in the alert macaque monkey and compare these responses to those in t

72 the development of the parietal cerebrum in macaque monkey and found that, indeed, the oSVZ initiall

73 s because they possess a brain as large as a macaque monkey and have a similar life span.

74 ing from single neurons in the cortex of the macaque monkey and using computational models from mathe

75 Three macaque monkeys and 13 healthy human volunteers underwen

76 ells from SIV-infected and uninfected rhesus macaque monkeys and determined the make-up of the ILC su

77 We injected virus into SC or area MT of macaque monkeys and examined labeled cells in V1.

78 y precise eye tracking in three well trained macaque monkeys and found that even fleeting (~8 ms dura

79 Here, we show that macaque monkeys and humans exhibit the same posterior ER

80 memory-masking paradigm previously used with macaque monkeys and humans.

81 discuss how neurophysiological recordings in macaque monkeys and in humans can help us understand the

82 Herpes B virus (BV) naturally infects macaque monkeys and is genetically similar to herpes sim

83 In six macaque monkeys and three human subjects, the length of

84 gos, one New World owl monkey, one Old World macaque monkey, and one baboon.

85 des in the primary visual cortex of 2 female macaque monkeys, and also recorded electroencephalogram

86 ordings from medial premotor cortex (MPC) in macaque monkeys, and computational modeling, to establis

87 ing in primary visual cortex of anesthetized macaque monkeys, and how quickly responses recover after

88 non-neural tissues from humans, chimpanzees, macaque monkeys, and mice based on over 10,000 hydrophil

89 ement of four terminally anesthetized female macaque monkeys, and recorded recurrent IPSPs in respons

90 igh-density electrocortigraphy data from two macaque monkeys, and show that the informational "weakes

91 ulate the responses of neurons in area MT of macaque monkeys, and that these modulations generate neu

92 that MNs of the ventral premotor area F5 of macaque monkeys are particularly sensitive to HVF relati

93 ) and the anterior cingulate cortex (ACC) of macaque monkeys as they performed approach-avoidance (Ap

94 mporal responses in the entorhinal cortex of macaque monkeys as they viewed complex images.

95 somatosensory cortex could be identified in macaque monkeys as well as humans.

96 logous) scene-selective regions in the awake macaque monkey, based on direct comparison to human maps

97 onal correlations in area V4 of two behaving macaque monkeys before and after a V1 lesion while the m

98 activity in the lateral prefrontal cortex of macaque monkeys before and after the administration of s

99 activity in the lateral prefrontal cortex of macaque monkeys before and after the administration of s

100 ctures, we recorded CDh neuronal activity of macaque monkeys before and during unilateral SC inactiva

101 midget RGC circuit in the central retina of macaque monkey both structurally and functionally.

102 The ventral intraparietal area (VIP) of the macaque monkey brain is a multimodal area with visual, v

103 etics and electrical microstimulation in the macaque monkey brain to functionally map the koniocellul

104 In the macaque monkey brain, posterior inferior temporal (PIT)

105 neuronal morphology previously described in macaque monkeys [Briggs et al. (2016) Neuron, 90, 388].

106 We explored this possibility in macaque monkeys by injecting retrograde tracers into gra

107 By comparing human and macaque monkey cerebral cortex, we infer that the patter

108 Our experiments on three macaque monkeys clearly show that arm movements can be e

109 at delivered NIr (670 nm) to the midbrain of macaque monkeys, close to the substantia nigra of both s

110 ification (EVM) heart tracking method in the macaque monkey combined with wavelet transform.

111 urface models of the marmoset, capuchin, and macaque monkey cortex were registered using the software

112 In macaque monkeys, cortical synaptogenesis peaks during ea

113 Here, we report that in macaque monkeys, deep and superficial cortical white mat

114 lectrocorticographic recordings in two awake macaque monkeys demonstrated that repeated presentations

115 udy, we show that probability distortions in macaque monkeys differ significantly between sequences i

116 e morphology and transcriptome of L3PNs from macaque monkey DLPFC and posterior parietal cortex (PPC)

117 (FEF), and the lateral intraparietal area of macaque monkeys during a visuomotor decision-making task

118 we recorded from single otolith afferents in macaque monkeys during linear motion along the preferred

119 ials and multiunit activities from the IT of macaque monkeys during performance of an intermodal sele

120 corded the activity of neurons in area V1 of macaque monkeys during tasks requiring fast (exploratory

121 f the vestibulo-spinal circuitry of behaving macaque monkeys during temporally precise activation of

122 veloped and recorded human-comparable EEG in macaque monkeys during visual stimulation with colored d

123 medial septum and diagonal band of Broca) of macaque monkeys encodes a unique combination of informat

124 populations of frontal eye field neurons in macaque monkeys engaged in a memory-guided saccade task.

125 onically implanted electrode arrays from two macaque monkeys engaged in a shape-tracking task.

126 Here, we show that macaque monkeys exhibit perceptual crowding for target o

127 ed cells in the cerebral cortex of postnatal macaque monkeys exposed to either [(3)H]dT or BrdU as em

128 Brain specimens from 18 macaque monkeys exposed to haloperidol, olanzapine, or s

129 rent types of rhythmic orofacial behavior in macaque monkeys, finding that the perioral muscles inner

130 tal evidence that, under certain conditions, macaque monkeys follow an affect heuristic that can caus

131 litating their use in genetic engineering of macaque monkeys for basic and translational neuroscience

132 erefore, we investigated economic choices in macaque monkeys for evidence of probability distortion.

133 of an additional S-OFF midget circuit in the macaque monkey fovea with scanning block-face electron m

134 Recent work in macaque monkeys has identified six discrete face areas w

135 Electrophysiological evidence in macaque monkeys has revealed neural correlates of such i

136 Recent studies in the macaque monkey have revealed age-related changes in the

137 Macaque monkeys have become the predominant nonhuman pri

138 udies of prefrontal and premotor cortices of macaque monkeys have found neural signals associated wit

139 abstract rules by prefrontal neurons, while macaque monkeys held the rules in working memory before

140 The organization of projections from the macaque monkey hippocampus, subiculum, presubiculum, and

141 eurons was qualitatively similar to that for macaque monkeys (i.e., the RF center is surrounded by ex

142 To test this prediction, we trained two macaque monkeys in a coarse orientation discrimination t

143 We report a difference between humans and macaque monkeys in the functional organization of cortic

144 V4.(6-10) Here, we report on experiments in macaque monkeys in which we experimentally assessed the

145 Eleven macaque monkeys, including four controls and seven with

146 dial axis shape in high-level object cortex (macaque monkey inferotemporal cortex or IT).

147 Visual area V4 in the macaque monkey is a cortical area that is strongly invol

148 ition of connectivity data in humans and the macaque monkey is anchored by, at one end, regions servi

149 ion in the primary visual cortex (V1) of the macaque monkey is strongly targeted toward GABAergic int

150 nto-parietal areas during active behavior of macaque monkeys is highly complex.

151 oreactive to calbindin, whereas in primates (macaque monkey, lar gibbon and human) the highest propor

152 shows that one such communicative gesture in macaque monkeys, lip-smacking, has motor parallels with

153 o acquire displacement images in two healthy macaque monkeys (M fascicularis) which showed the FUS be

154 tinotopically corresponding sites within the macaque monkey (Macaca mulatta) brain.

155 igate whether rhythmic activity in V1 of the macaque monkey (macaca mulatta) is affected by top-down

156 in layer 6 of primary visual cortex in male macaque monkeys (Macaca fascicularis) to achromatic grat

157 In dual-tracer experiments undertaken in macaque monkeys (Macaca fascicularis), cMRF neurons labe

158 Using behavioural data from a group of moor macaque monkeys (Macaca maura), we used permutation-base

159 rtex (A1) under two conditions: while rhesus macaque monkeys (Macaca mulatta) actively performed a th

160 trodes in parallel in AIP and F5 while three macaque monkeys (Macaca mulatta) performed a delayed gra

161 single- and multi-unit activity in two male macaque monkeys (Macaca mulatta) performing an attention

162 chemical staining of tissue from a series of macaque monkeys (Macaca mulatta) showed that cells in th

163 ntribution of the LGN to visual functions of macaque monkeys (Macaca mulatta) with chronic V1 lesions

164 In two male rhesus macaque monkeys (Macaca mulatta), we found that lateral

165 from primary visual cortex of anaesthetized macaque monkeys (Macaca mulatta).

166 rimary visual cortex and V2 of six amblyopic macaque monkeys (Macaca nemestrina) and two visually nor

167 We studied macaque monkeys (Macaca nemestrina) for which we have de

168 onal groups in areas V1 and V2 of six female macaque monkeys (Macaca nemestrina) made amblyopic by ar

169 cell types between human and the cynomolgus macaque monkey, Macaca fascicularis.

170 astriate visual area of both male and female macaque monkeys (Maccaca mulatta).

171 We recorded from single OFC neurons while macaque monkeys made cost-benefit decisions.

172 ng on neurons encoding memorized rules while macaque monkeys made responses based on those rules.

173 We investigated how four macaque monkeys maintained representations of the value

174 for both professional baseball pitchers and macaque monkeys making reaching movements, motor variabi

175 l coherence tomography (OCTA) in cynomogulus macaque monkey model following increase in intraocular p

176 visuomotor tracking task, in which 2 female macaque monkeys moved their index finger against a resis

177 y applying caudate electrical stimulation in macaque monkeys (n = 3) to bias decision-making in a tas

178 ct portion of posterolateral thalamus of the macaque monkey, named the posterior part of the ventral

179 recorded from single hippocampal neurons in macaque monkeys navigating a virtual maze during a forag

180 d laterality of gene expression in human and macaque monkey neocortex.

181 nd noise images in V1 and V2 of anesthetized macaque monkeys of both sexes.

182 ocal lesions of posterior parietal area 5 in macaque monkeys on bimanual behavior performed with and

183 To explore their specializations, we trained macaque monkeys on two tasks: one required updating repr

184 tion of corticoreticular connections in five macaque monkeys (one male) using both intracellular and

185 ses of EEG recorded over the frontal lobe of macaque monkeys (one male, one female) performing a sacc

186 he inferior temporal cortex (IT) while naive macaque monkeys passively viewed images of letters, Engl

187 We first show that macaque monkeys perceive a size-distance illusion simila

188 l cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a delayed-match-to-sample targ

189 (V1)] and midlevel (V4) visual cortex while macaque monkeys performed a fine orientation discriminat

190 ion-selective neurons in V1 and V2 while two macaque monkeys performed a fine orientation discriminat

191 l cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a task that required them to f

192 ity from populations of neurons in PMd/M1 as macaque monkeys performed a visually guided reaching tas

193 Macaque monkeys performed an eight-alternative 3D orient

194 ical stimulations to areas 8Av and 45 of two macaque monkeys performing a concurrent goal-directed sa

195 Rs to persistent firing in the dlPFC of male macaque monkeys performing a delayed saccade to a memori

196 rom hundreds of units in prearcuate gyrus of macaque monkeys performing a direction discrimination ta

197 activity in small subregions of IT cortex of macaque monkeys performing a facial gender-discriminatio

198 ng this adaptive response time adjustment in macaque monkeys performing a saccade countermanding task

199 and primary somatosensory cortex (S1) in two macaque monkeys performing a vibrotactile detection task

200 and female human subjects as well as in male macaque monkeys performing a visual detection task.

201 auditory cortex in face/voice integration in macaque monkeys performing a vocal-detection task.

202 ltielectrodes from the striate cortex of two macaque monkeys performing an intermodal selective atten

203 uronal spike trains recorded in adult female macaque monkeys performing attention-demanding contrast-

204 eld potential and neural spiking activity in macaque monkeys performing memory-guided and pro- and an

205 in the striatum and motor-premotor cortex of macaque monkeys performing reaching tasks.

206 for behavior and predicts neural dynamics of macaque monkeys performing visual search for a target st

207 differentially encoded and maintained in the macaque monkey prefrontal (frontal eye fields) and parie

208 ibution of VGluT2-ir puncta in all layers of macaque monkey primary visual cortex (V1), and found a v

209 secondary (V2) visual areas were revealed in macaque monkeys ranging in age from 2 to 16 weeks by inj

210 ntion Paradigm (IAP) and use it to show that macaque monkeys readily learn to use auditory or visual

211 ighted MRI data before and after male rhesus macaque monkeys received extensive training to learn nov

212 prefrontal cortex (PFC; area 46) of two male macaque monkeys, recording >500 neurons simultaneously.

213 eurons in the middle temporal cortex (MT) of macaque monkeys represent overlapping random-dot stimuli

214 rdial tissue of female mice or female rhesus macaque monkeys, respectively.

215 e numerically dominant output pathway in the macaque monkey retina, the midget (parvocellular-project

216 y OFF-bipolar cells in slice preparations of macaque monkey retina, where the low (midget/parvocellul

217 his study, we address both questions for the macaque monkey retina.

218 In this rare case of a Rhesus macaque (monkey S), likely born without V1, the animal's

219 tivity in the face-processing regions of the macaque monkey's amygdala and inferior temporal (IT) cor

220 ol functions through coordinated firing when macaque monkeys select and monitor relevant stimuli for

221 previous experiments on squirrel monkeys and macaque monkeys showed that social isolation [2, 3], dea

222 breaks of viral hemorrhagic fever in captive macaque monkeys since the 1960s.

223 Two macaque monkeys sitting across a touch-sensitive table i

224 VIP are less medially displaced relative to macaque monkeys, so that human LIP paradoxically ends up

225 In humans and macaque monkeys, socially relevant face processing is ac

226 We show that this is the case in humans and macaque monkeys, suggesting that the reflex pathways tha

227 present retinal projections of ipRGCs in the macaque monkey, supporting previous retrograde tracer st

228 We report that macaque monkeys take into account the welfare of their p

229 ly discovered face-processing network of the macaque monkey that consists of six interconnected face-

230 We report a novel class of V4 neuron in the macaque monkey that responds selectively to equiluminant

231 ential (LFP) activity in cortical area V4 of macaque monkeys that is triggered by the execution of sa

232 k for new cells in the motor cortex of adult macaque monkeys that might form the cellular bases of im

233 We show in macaque monkeys that retinal ganglion cells (RGCs) that

234 rning set as a concept, and we show that, in macaque monkeys, the amygdala and medial prefrontal cort

235 n the middle temporal area (MT) of the alert macaque monkey; these responses are interpreted using a

236 unctional state of PMv neuronal ensembles in macaque monkeys through the process of passive viewing,

237 esults, we use single-unit recordings in the macaque monkey to determine where these computations--se

238 age of the large and slowly developing SP in macaque monkey to examine the origin, settling pattern,

239 vity in the middle temporal (MT) area of the macaque monkey to study the neural mechanisms that under

240 ueing are similarly intermediate, we trained macaque monkeys to detect changes in stimulus orientatio

241 We studied two groups of adult macaque monkeys to determine the time course of adult ne

242 We instructed male rhesus macaque monkeys to initiate saccade-free smooth pursuit

243 Here, we used fMRI in rhesus macaque monkeys to map the superior temporal sulcus (STS

244 ed voltage-sensitive-dye imaging in fixating macaque monkeys to measure V1 population responses to sp

245 ty of neurons in dorsal visual area V5/MT of macaque monkeys to relative disparity, using two superim

246 rcuit on visual perception by first training macaque monkeys to report their perceived eye direction,

247 We exposed naive macaque monkeys to such experimental conditions by intro

248 We trained macaque monkeys to trade speed for accuracy on cue durin

249 ammals, with a shift of the core of cats and macaque monkeys toward the less neuronally dense areas o

250 pulation of V1 neurons in alert and behaving macaque monkeys trained on an attention-demanding contra

251 Here we study prefrontal cortex activity in macaque monkeys trained to flexibly select and integrate

252 isualized in coronal brain sections from two macaque monkeys, two owl monkeys, two squirrel monkeys,

253 dial portion of posterior parietal area 5 in macaque monkeys; two areas that are part of a network in

254 PET studies were performed in a rhesus macaque monkey under control conditions or after intrave

255 esponses in the primary visual cortex of the macaque monkey using a novel variant of current source d

256 nal connections of the insular cortex of the macaque monkey using modern high-resolution methods, we

257 visual categories can be ordered serially by macaque monkeys using a behavioral paradigm that provide

258 d EEG event-related potentials (ERPs) in two macaque monkeys using a paradigm developed to evaluate h

259 nderstand this interaction, we tested 3 male macaque monkeys using both [(11)C]DASB and [(18)F]MPPF,

260 neurons in the nucleus prepositus of rhesus macaque monkeys using eight-channel linear microelectrod

261 In this study, we used two-photon imaging in macaque monkey V1 to demonstrate the three-dimensional c

262 analyzed shape tuning of recently described macaque monkey ventral pathway neurons that prefer scene

263 LGN) and primary visual cortex (V1) of alert macaque monkeys viewing stimuli known to produce strong

264 ze and quantify the internal dynamics of the macaque monkey vocal tract during lip-smacking (a rhythm

265 urons as a function of two factors: species (macaque monkey vs. rat) and morphology (chandelier vs. b

266 del of the primary visual cortex (V1) of the macaque monkey was constructed to reconcile the visual f

267 of neurons in the frontal eye field (FEF) of macaque monkeys was recorded during an object-based dela

268 thods to the neocortex and cerebellum of the macaque monkey, we found that its cerebellum was relativ

269 However, in motor cortex of the awake macaque monkey, we observe very different dynamics: mass

270 Within cortical visual area V5/MT of two macaque monkeys, we applied electrical stimulation at si

271 ain functional magnetic resonance imaging in macaque monkeys, we discovered a network centered in the

272 Using Pavlovian conditioning procedures in macaque monkeys, we examined the contribution of the sub

273 In six macaque monkeys, we examined the effects from focal stim

274 In cats, squirrel monkeys, and macaque monkeys, we found neurochemically defined subdiv

275 al mechanisms mediating the effects of OT in macaque monkeys, we investigated whether OT would modula

276 Using retrograde tracing in macaque monkeys, we quantified projection strength by co

277 Here, using multi-structure recordings in macaque monkeys, we show that the brainstem transiently

278 lectrode recordings from alert, task-engaged macaque monkeys, we showed previously that local electro

279 ng biplanar videoradiography (XROMM) of four macaque monkeys, we tested the extrinsic muscle shorteni

280 Whole orbits of two humans and one macaque monkey were serially sectioned at 10 mum thickne

281 Two macaque monkeys were anesthetized and received a unilate

282 cavity and face in somatosensory area 3b of macaque monkeys were identified with microelectrode reco

283 Five juvenile macaque monkeys were perfused with formalin for 5 weeks:

284 Whole orbits of two humans and five macaque monkeys were serially sectioned at 10-microm thi

285 Macaque monkeys were trained for a behavioral task desig

286 Macaque monkeys were trained for a behavioural task desi

287 Two female rhesus macaque monkeys were trained to grasp 4 different object

288 Macaque monkeys were trained to report their heading (le

289 ccessful surgery was performed in six rhesus macaque monkeys, which have a very similar choroidal blo

290 tones of varying modulation depths to awake macaque monkeys while measuring the responses of neurons

291 ivity from the primary visual cortex (V1) of macaque monkeys while they discriminated between n/u sha

292 y of 1215 neurons in the motor cortex of two macaque monkeys while they performed a center-out reachi

293 e used fMRI to monitor the brain activity of macaque monkeys while they viewed low- and high-level mo

294 Here, we used rER BOLD fMRI in macaque monkeys while viewing real-world images, and fou

295 e reticular formation of three anaesthetized macaque monkeys whilst TMS was performed over primary mo

296 o-photon imaging with genetic tools in awake macaque monkeys will enable fundamental advances in our

297 ments of entire white matter trajectories in macaque monkeys with diffusion MRI tractography of both

298 neration in sectioned archived retinae of 26 macaque monkeys with unilateral V1 ablation and post-sur

299 in the distal pads of all five digits in the macaque monkey (with hands similar to humans)?

300 Macaque monkeys worked to collect rewards for themselves