ライフサイエンスコーパス: macaque monkey

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

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

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

4 scending brainstem pathways in the Old World macaque monkey.

5 ctrophysiological and imaging studies in the macaque monkey.

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

7 onses to tactile and auditory stimuli in the macaque monkey.

8 identified corticogeniculate neurons in the macaque monkey.

9 luorescence confocal microscopy in V1 of the macaque monkey.

10 12 finger pads of digits 2-5 (D2-D5) of the macaque monkey.

11 to areas middle temporal (MT), V3, and V2 of macaque monkey.

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

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

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

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

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

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

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

19 acellular recordings in acutely anesthetized macaque monkeys.

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

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

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

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

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

25 the primary visual cortex of awake behaving macaque monkeys.

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

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

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

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

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

31 ale modifications to the cortical network in macaque monkeys.

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

33 n multimodal sensorimotor areas of cortex in macaque monkeys.

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

35 guided manual and saccadic eye movements in macaque monkeys.

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

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

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

39 ion of milestones of neuronal development in macaque monkeys.

40 and lateral intraparietal area (LIP) of two macaque monkeys.

41 dorsal column lesions at cervical levels in macaque monkeys.

42 humans and chimpanzees, to the exclusion of macaque monkeys.

43 to volitionally controlled action in rhesus macaque monkeys.

44 9, 32, and 4 among humans, chimpanzees, and macaque monkeys.

45 vagus evoked potential (VEP) focus in Pf of macaque monkeys.

46 uts to CM by injecting retrograde tracers in macaque monkeys.

47 e cells are also found in PH of squirrel and macaque monkeys.

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

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

50 eurons recorded individually in anesthetized macaque monkeys.

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

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

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

54 ate functional magnetic resonance imaging in macaque monkeys.

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

56 scending auditory system of both rodents and macaque monkeys.

57 markedly inferior to that of chimpanzees and macaque monkeys.

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

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

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

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

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

63 which infects and induces disease in rhesus macaque monkeys.

64 ndary responses in V1 and V2 in anesthetized 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 Studies of macaque monkey ACC, in contrast, have failed to find con

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

69 Humans and macaque monkeys adjust their response time adaptively in

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

71 used an electrophysiological technique with macaque monkeys analogous to procedures for recording sc

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

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

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

75 onstrate the feasibility of using MEG in the macaque monkey and provide a non-human primate model for

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

77 Three macaque monkeys and 13 healthy human volunteers underwen

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

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

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

81 Herpes B virus (BV) naturally infects macaque monkeys and is a close relative of herpes simple

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

83 of New World monkeys with those of Old World macaque monkeys and prosimian galagos, we placed injecti

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

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

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

90 Here we show that when macaque monkeys are offered a water reward of variable m

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

92 Macaque monkeys are widely used in order to understand t

93 r neurons, located in the premotor cortex of macaque monkeys, are activated both by the performance a

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

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

96 Recent studies of macaque monkey auditory cortex have revealed convergent

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

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

99 d flash ERGs were recorded from anesthetized macaque monkeys before and after pharmacologic blockade

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

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

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 a mixed sex sample of perfusion-fixed adult macaque monkey brains to determine whether purported int

106 n galagos, together with those obtained from macaque monkeys by Graziano and coworkers, suggest that

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

108 ic analysis of striosomes was carried out in macaque monkeys by using immunocytochemistry for the Kv4

109 in different auditory cortical fields in the macaque monkey carry sufficient information to account f

110 e other New World Monkeys, but much like the macaque monkey, cebus monkeys possess a proprioceptive c

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

112 A new study has found that, when a macaque monkey chooses where to look, activity in pariet

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

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

115 An additional six macaque monkeys constituted an unoperated control group.

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

117 In macaque monkeys, cortical synaptogenesis peaks during ea

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

119 For both humans and macaque monkeys, digital brain atlases of many varieties

120 cal field potentials (LFPs) were recorded in macaque monkeys during a stop-signal task, which elicits

121 l geniculate nucleus (LGN) and pulvinar of 2 macaque monkeys during a visual illusion that induced th

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

123 2, V4, and inferotemporal (IT) cortex of two macaque monkeys during performance of a sensory discrimi

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

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

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

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

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

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

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

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

132 ructures of neurons in visual area V2 of the macaque monkey for encoding combinations of orientations

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

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

135 In both humans and macaque monkeys, functional magnetic resonance imaging (

136 sing targeted single-unit recording in alert macaque monkeys, guided by functional magnetic resonance

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

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

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

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

141 n of the connections of the CA3 field of the macaque monkey hippocampus.

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

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

144 and for choline acetyltransferase (ChAT) in macaque monkeys, in which most preganglionic motoneurons

145 Eleven macaque monkeys, including four controls and seven with

146 cterize three-dimensional shape responses in macaque monkey inferotemporal cortex (IT).

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

148 test this idea, we studied single neurons in macaque monkey intermediate visual (area V4) and somatos

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

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

151 sly that cholinergic modulation in V1 of the macaque monkey is strongly targeted toward GABAergic int

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

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

154 idea that the main function of the fornix in macaque monkeys is to support new learning about spatio-

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

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

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

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

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

160 e obtained in both eyes of four adult rhesus macaque monkeys (Macaca mulatta) during two baseline ses

161 Four sophisticated macaque monkeys (Macaca mulatta) learned 6 different, 15

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

163 th single cell recordings in V1 while rhesus macaque monkeys (Macaca mulatta) performed a task that d

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

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

166 d the social dominance hierarchy of juvenile macaque monkeys (Macaca mulatta) that received bilateral

167 using a virtual-reality system to translate macaque monkeys (Macaca mulatta) while they viewed motio

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

169 avenex, and D.G. Amaral (2006) reported that macaque monkeys (Macaca mulatta) with neonatal neurotoxi

170 e we show, by recording neurons in attending macaque monkeys (Macaca mulatta), that attention modulat

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

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

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

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

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

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

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

180 reversal learning by studying the effect, in macaque monkeys, of disconnecting PFC from IT by crossed

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

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

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

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

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

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

187 d neuronal activity in the hippocampus while macaque monkeys performed a visual recognition memory ta

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

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

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

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

192 ons in the prefrontal cortex and striatum of macaque monkeys performing a routine visuomotor task.

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

194 occurrence of conflict, errors and reward in macaque monkeys performing a saccade-countermanding task

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

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

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

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

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

200 d the activity of single neurons in CGp in 2 macaque monkeys performing simple tasks in which their b

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

202 Like humans, macaque monkeys possess a macula and develop age-related

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

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

205 icant fraction of the LFP time course in the macaque monkey primary visual cortex.

206 inuity in single-neuron responses from awake macaque monkeys' primary auditory cortex (A1).

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

208 To investigate such a role, six macaque monkeys received a bilateral transection of the

209 We asked how neurons in PRR of macaque monkeys reflect the decision process of selectin

210 mporal dynamics of cortical responses in the macaque monkey relative to the human.

211 Two macaque monkeys reported whether they perceived a circul

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

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

214 Here, we show in the macaque monkey retina in vitro that at photopic light le

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

216 d structure of parasol ganglion cells in the macaque monkey retina.

217 ON and OFF parasol retinal ganglion cells in macaque monkey retina.

218 in primary somatosensory cortex (area 3b) of macaque monkeys revealed an ipsilateral hand input undet

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

220 om recordings of single-cell activity in the macaque monkey's primary visual cortex (V1), we found th

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

222 d 44 in a sample of humans, chimpanzees, and macaque monkeys showed that regions involved in speciali

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

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

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

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

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 e dorsal lateral geniculate nucleus (LGN) of macaque monkeys that have chronically self-administered

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

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

234 m whole-cell recordings of photoreceptors in macaque monkey, that "blue-yellow" opponency is already

235 l, based on other experimental evidence from macaque monkeys, that PFC has a highly specific role in

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

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

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

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

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

241 dback pathways between the LGN and V1 in the macaque monkey to provide a lower bound on how quickly t

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

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

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

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

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

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

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

249 ly adapting), and PC (Pacinian) afferents of macaque monkeys to sinusoidal, diharmonic, and bandpass

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

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

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

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

254 In two macaque monkeys trained to perform center-out reaching m

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

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

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

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

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

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

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

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

263 ellothalamic projections was investigated in macaque monkeys using injections of retrograde tracers (

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

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

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

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

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

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

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

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

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

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

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

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

276 In the STN of trained macaque monkeys, we found neurons that showed a phasic c

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

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

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

280 Two macaque monkeys were anesthetized and received a unilate

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

282 To this end, V1 and V2 of macaque monkeys were immunofluorescently labelled for ga

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

287 Cynomolgus macaque monkeys were trained to perform memory-related t

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 neurons in the middle temporal area (MT) of macaque monkeys while presenting a variety of center-sur

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

293 ponses from individual neurons in area V4 of macaque monkeys while they performed a task that indepen

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

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 ields in cebus monkeys and distantly related macaque monkeys with similar manual abilities indicates

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

300 Macaque monkeys worked to collect rewards for themselves