ライフサイエンスコーパス: monkey

1 d saccadic eye movement response (humans and monkeys).

2 ng the ventral visual pathway of the macaque monkey.

3 ions affected the reward received by another monkey.

4 (IVI) of saline was given in one eye of each monkey.

5 al prefrontal cortex (dlPFC) of unrestrained monkey.

6 he self, a partner, both monkeys, or neither monkey.

7 sulting medial-frontal EEG on a male macaque monkey.

8 ctivity via hM3Dq within minutes in mice and monkeys.

9 ssory basal [AB]) in six Macaca fascicularis monkeys.

10 not differ between control and parkinsonian monkeys.

11 the VApc and CM of MPTP-treated parkinsonian monkeys.

12 gurable 3D spatial setting with unrestrained monkeys.

13 acodynamic study was conducted in cynomolgus monkeys.

14 ellation in medial frontal cortex of macaque monkeys.

15 otion that can be observed in awake behaving monkeys.

16 one of the short vaccine regimens in rhesus monkeys.

17 performance when given systemically to aged monkeys.

18 otentials (LFP) in visual area MT of macaque monkeys.

19 lation of two Mamu-A*01 (+) RRV-naive rhesus monkeys.

20 lactic dose-dependent efficacy in hemophilic monkeys.

21 led with (11)C and studied in vivo in rhesus monkeys.

22 ontrol over a group of inhibitory neurons in monkeys.

23 ol of disjunctive saccades in trained rhesus monkeys.

24 leus (LGN) and cortical area MT, in marmoset monkeys.

25 luD1 immunoreactivity (GluD1-IR) in mice and monkeys.

26 Two cynomogulus macaque monkeys.

27 ues when compared to Old World and New World monkeys.

28 ts against SARS-CoV-2 are observed in rhesus monkeys.

29 B in PK studies conducted in mice, dogs, and monkeys.

30 cal microstimulation (ICMS) in male squirrel monkeys.

31 bloodstream infections of Aotus and Saimiri monkeys.

32 Subjects were 10 adult titi monkeys.

33 netic marker for Saimiri and other New World monkeys.

34 ure to humans of either sex and male macaque monkeys.

35 al lobe white matter in humans compared with monkeys.

36 during strength training in 2 female macaque monkeys.

37 -8), which displayed favorable properties in monkeys.

38 responses to the same electrical stimuli in monkeys.

39 trical stimulation with fMRI in male macaque monkeys.

40 n the DCP was 68.8% and 78.6% of baseline in monkey 1 and monkey 2, respectively.

41 asks and brain regions consistently across 4 monkeys (1 female and 1 male Macaca mulatta; and 2 male

42 ere compared in 12 healthy young male rhesus monkeys (~1-2 y old, ~3 +/- 1 kg).

43 [12, 13], single-unit and lesion studies in monkey [14-20], and computational modeling [21] suggests

44 68.8% and 78.6% of baseline in monkey 1 and monkey 2, respectively.

45 rom 28 healthy humans, 10 baboons, 12 rhesus monkeys, 20 Yorkshire pigs, 20 Sprague-Dawley rats, 10 N

46 resonance imaging scans from tufted capuchin monkeys (5 male, 15 female).

47 D keeps track of rapid eye movements, and in monkeys, a circuit carrying this CD extends from midbrai

48 In monkeys, a circuit from superior colliculus (SC) through

49 on hippocampal OXTR in male and female titi monkeys, a pair-bonding primate species that exhibits bi

50 ied by compound 52, in an in vivo cynomolgus monkey acute adrenocorticotropic hormone (ACTH) challeng

51 aneous stimuli in the area 3b hand cortex of monkeys after dorsal column lesions (DCLs) in the cervic

52 Currently, the African green monkey (AGM) best mimics human henipavirus-induced disea

53 in 2-6 hours of fever onset in African green monkeys (AGM).

54 A model was developed in African green monkeys (AGMs) after challenge with a lethal dose of Y.

55 two cases of ARDS in two aged African green monkeys (AGMs) infected with SARS-CoV-2 that had patholo

56 We show that African green monkeys (AGMs) support robust SARS-CoV-2 replication and

57 ivered by the aerosol route in African green monkeys (AGMs) used the Malaysia strain (NiVM), which ha

58 n lung CYP2A protein levels in African green monkeys (AGMs).

59 Using monkey and human electrophysiology data, we show here th

60 an anti-CD22 monoclonal antibody spiked into monkey and human serum, where lower limits of quantifica

61 es in timing and distribution across rodent, monkey and human studies.

62 ACE2 of human/rhesus monkey and rat/mouse exhibited the highest and lowest re

63 oma (microbead occlusion in rat and squirrel monkey and the genetic DBA/2 J mouse model) with distinc

64 nce suggests that platyrrhine (or New World) monkeys and caviomorph rodents of the Western Hemisphere

65 es; however, behavioural studies in lesioned monkeys and data from neuropsychological examinations of

66 m SIV-infected and uninfected rhesus macaque monkeys and determined the make-up of the ILC subpopulat

67 Capuchin monkeys and especially rhesus macaques persisted to tria

68 ADx-001 was well tolerated in rats and monkeys and exhibited the slow clearance from circulatio

69 e eye tracking in three well trained macaque monkeys and found that even fleeting (~8 ms duration) st

70 d with the strength of serial biases in both monkeys and humans, as predicted by a computational mode

71 In monkeys and humans, one such CD keeps track of rapid eye

72 facilitates the comparison of the circuit in monkeys and humans, particularly for comparison of the l

73 plicated in learning and memory processes in monkeys and humans.

74 son of the location of the thalamic relay in monkeys and in humans.

75 ontrast, type II is well-tolerated in normal monkeys and shows both acute and prophylactic dose-depen

76 e consistent with optical imaging studies in monkeys and support the notion that arousal increases pr

77 al frequencies, LGN sensitivity exceeded the monkeys' and approached the upper bound set by cone phot

78 tor 21 (FGF21) induces weight loss in mouse, monkey, and human studies.

79 he primary visual cortex of 2 female macaque monkeys, and also recorded electroencephalogram (EEG), w

80 gamma power in LFP versus ECoG in up to four monkeys, and found them to be surprisingly similar.

81 enetically-encoded glutamate sensor in awake monkeys, and map the excitatory synaptic inputs on dendr

82 d a spatial selective detection paradigm for monkeys, and recorded activity in primary auditory corte

83 four terminally anesthetized female macaque monkeys, and recorded recurrent IPSPs in response to ant

84 rk of Marr (1982) across research in humans, monkeys, and rodents to propose that information process

85 Using monkey, ape and human auditory functional fields and dif

86 vestibular morphology of extant anthropoids (monkeys, apes and humans) and two extinct apes (Oreopith

87 cular inputs to the entorhinal cortex in the monkey are organized similar to those described in nonpr

88 border the forest while tamarin and capuchin monkeys are also common to edge habitats, creating oppor

89 These results indicate that, in principle, monkeys are capable of forming internal models linking s

90 he visual system and we show that neurons in monkey area V1 use knowledge of eye torsion to compensat

91 In cynomolgus monkeys, ARGX-117 dose-dependently reduces free C2 level

92 omparable peak immune responses in 30 rhesus monkeys as in humans and resulted in an 83% (95% CI 38.7

93 esponses in the entorhinal cortex of macaque monkeys as they viewed complex images.

94 ADx-001 toxicity was evaluated in rats and monkeys at doses up to 0.30 mmol Gd/kg.

95 rapolated to populations, was similar to the monkeys' at low temporal frequencies.

96 restingly, AC also encoded the choice of the monkey before dlPFC and around the time of BLA.

97 we recorded CDh neuronal activity of macaque monkeys before and during unilateral SC inactivation in

98 visual cue presentation, was correlated with monkeys' behavior and showed uncorrelated spiking activi

99 matter samples from the corpus callosum of a monkey brain reveal that blood vessels, cells, and vacuo

100 is well documented in haplorrhines (apes and monkeys) but not in strepsirrhines (lemurs and lorises).

101 Monkeys can learn the implied ranking of pairs of images

102 sed in the striosomes than the matrix in the monkey caudate nucleus, the opposite was found in the mo

103 the striosome and matrix compartments of the monkey caudate nucleus, with the exception of a small am

104 ance of sequential movements, we trained two monkeys (Cebus apella) to perform two sequential reachin

105 archival formalin-fixed lungs of cynomolgus monkeys challenged with the fully virulent B. anthracis

106 n (EVM) heart tracking method in the macaque monkey combined with wavelet transform.

107 Two rhesus monkeys conducted instructed walk-and-reach movements to

108 eased when the number of dots was increased, monkeys continued to preferentially select the middle do

109 , GBM and neuroblastoma cells, as well as in monkey COS-7 cells.

110 vity in SMA and primary motor cortex (M1) as monkeys cycled various distances through a virtual envir

111 In the delayed match-to-category (DMC) task, monkeys decided whether sequentially presented stimuli w

112 Previously we showed that monkeys' decisions on a direction-discrimination task wi

113 ate sites during motion viewing affected the monkeys' decisions.

114 Here, we report that in macaque monkeys, deep and superficial cortical white matter neur

115 le for IL-31 in allergic pruritus of humans, monkeys, dogs, and mice was acknowledged.

116 ral responses in the visual cortex of rhesus monkeys during a motion direction change detection task.

117 nstrates high specificity of base editing in monkey embryos.

118 Neurophysiological studies in monkeys engaged in passive fixation and behavioral tasks

119 the different layers and subdivisions of the monkey entorhinal cortex (Eo, Er, Elr, Ei, Elc, Ec, Ecl)

120 Eighteen rhesus monkeys euthanized between 3 and 8 days post-infection,

121 Here, we show that macaque monkeys exhibit perceptual crowding for target orientati

122 gyrus of the medial prefrontal cortex while monkeys expressed context-dependent positive or negative

123 y induced spatial working memory deficits in monkeys expressing hM4Di in the prefrontal cortex.

124 Preparatory activity evolves in the monkey FEF(SEM) during fixation in parallel with an obje

125 l rebound in chronically SIV-infected rhesus monkeys following ART discontinuation.

126 -suppressed, chronically SIV-infected rhesus monkeys following ART discontinuation.

127 er tracts within the spinal cord of squirrel monkeys following traumatic injuries, and their relation

128 as a tool to track HR of the awake behaving monkey, for ethological, behavioural, neuroscience or we

129 the anterior cingulate cortex (ACC) prevents monkeys from learning what actions are prosocial but doe

130 recording single-neuron activity in behaving monkeys from the amygdala, dorsolateral prefrontal corte

131 s-species comparisons with mouse, cynomolgus monkey gastrulae, and post-implantation human embryos, w

132 ST-2 of its natural host, greater spot-nosed monkey (GSN).

133 During learning, but not when the monkey had learned the association, the simple spike res

134 The depressive-like monkeys had characteristic disturbances of the phylum Fi

135 s of the novel options were unknown, and the monkeys had to explore them to see if they were better t

136 ization of the M1 forelimb representation in monkeys have focused on inputs and outputs.

137 However, numerous studies in monkeys have reported that gustatory cortical neurons ar

138 organization of projections from the macaque monkey hippocampus, subiculum, presubiculum, and parasub

139 Whether a monkey homolog exists is controversial and the nature of

140 YFV was detected in October 2017 in Aloutta monkeys in an Atlantic Forest area.

141 0) Here, we report on experiments in macaque monkeys in which we experimentally assessed the presence

142 time PCR revealed levels similar to those in monkeys infected with recombinant gL(+) RRV.

143 We further show through brain PET scans of monkeys injected with radiolabeled recombinant human LCN

144 odeficiency virus (SHIV) infection of rhesus monkeys is an important preclinical model for human immu

145 e to calbindin, whereas in primates (macaque monkey, lar gibbon and human) the highest proportion of

146 -cells) in the mid-lateral cerebellum as the monkey learned to associate one arbitrary symbol with th

147 ateral intraparietal area LIP) neurons while monkeys learned 7-item transitive inference (TI) lists w

148 allowed us to study population coding while monkeys learned choices between actions or objects.

149 As the monkeys learned the association, the magnitude of this r

150 nistic and neuroimaging work in young rhesus monkeys linked the central nucleus of the amygdala to AT

151 In contrast, spiking patterns measured in monkey M1 are clearly distinct.

152 r 6 of primary visual cortex in male macaque monkeys (Macaca fascicularis) to achromatic grating stim

153 Here we address whether rhesus monkeys (Macaca mulatta) can learn the abstract concept

154 social cognition is causal by testing rhesus monkeys (Macaca mulatta) on a vicarious reinforcement ta

155 In two male rhesus macaque monkeys (Macaca mulatta), we found that lateral MD neuro

156 erminals to (inputs) the ACC of adult rhesus monkeys (Macaca mulatta).

157 ments using electrical stimulation in rhesus monkeys (Macaca mulatta).

158 pes between human and the cynomolgus macaque monkey, Macaca fascicularis.

159 corded from single OFC neurons while macaque monkeys made cost-benefit decisions.

160 Monkeys maintained a preference to choose the middle dot

161 n activity in primary motor cortex (M1) when monkeys make reaching movements.

162 In monkeys making saccadic decisions based on motion cues a

163 We explored this problem by training 2 monkeys (male, Macaca mulatta) in a postural perturbatio

164 nce tomography (OCTA) in cynomogulus macaque monkey model following increase in intraocular pressure

165 tor tracking task, in which 2 female macaque monkeys moved their index finger against a resisting mot

166 Similar to human data, we validated that monkey muscle activity also exhibited low-pass filtered

167 Humans and monkeys navigated to a remembered goal location in a vir

168 d from single hippocampal neurons in macaque monkeys navigating a virtual maze during a foraging task

169 Monkeys needed to track a moving target with a joystick-

170 to the other monkey ("Other"), or to neither monkey ("Neither").

171 However, compared with vehicle-treated monkeys, neurons from EV-treated monkeys showed lower fi

172 healthy mice by oral gavage or to cynomolgus monkeys (nonhuman primates) by colonic spray increased c

173 of preclinical species, rats and cynomolgus monkeys [nonhuman primates (NHPs)], to predict the human

174 from humans, several OWMs, and two New World monkeys (NWMs).

175 a divergence time between apes and Old World monkeys of 65 million years, too old to be consistent wi

176 In rhesus monkeys of both sexes, we investigated how these functio

177 The snake caught the juvenile monkey on the ground during a terrestrial play session.

178 corticoreticular connections in five macaque monkeys (one male) using both intracellular and extracel

179 EG recorded over the frontal lobe of macaque monkeys (one male, one female) performing a saccade coun

180 reward delivery to the self, a partner, both monkeys, or neither monkey.

181 ard outcomes: to self ("Self"), to the other monkey ("Other"), or to neither monkey ("Neither").

182 reference genome assemblies for 3 Old World monkey (OWM) species: Colobus angolensis ssp. palliatus

183 ior temporal cortex (IT) while naive macaque monkeys passively viewed images of letters, English word

184 h muscle cells) in the murine and cynomolgus monkey pelvis-kidney junction.

185 atal cholinergic interneurons (critic) while monkeys performed a classical conditioning task.

186 primary motor and somatosensory cortices as monkeys performed a reaching task, for up to 2 years.

187 ld [FEF], and prefrontal cortex [PFC]) while monkeys performed a task that modulated visual stimulus

188 orbitofrontal cortex (OFC) while three male monkeys performed a three-armed bandit learning task.

189 frontal cortex (dlPFC; 768 electrodes) while monkeys performed a two-armed bandit reinforcement learn

190 Macaque monkeys performed an eight-alternative 3D orientation di

191 nd simultaneously measured IT activity while monkeys performed object discrimination tasks.

192 GABA in regulating delay activity in rhesus monkeys performing a delayed decision task requiring wor

193 ding cellular activity in PFC of male rhesus monkeys performing a delayed decision task requiring wor

194 rsistent firing in the dlPFC of male macaque monkeys performing a delayed saccade to a memorized spat

195 and ventrolateral anterior nucleus [VLa]) in monkeys performing a reaching task.

196 , we characterized neural representations in monkeys performing a task described by different hidden

197 frontal and anterior cingulate cortex of two monkeys performing a valuation task.

198 le human subjects as well as in male macaque monkeys performing a visual detection task.

199 re established during neuronal recordings in monkeys performing direction discriminations, but also b

200 Finally, modeling data in two monkeys performing saccades demonstrated the generalizat

201 neural spiking patterns recorded in two male monkeys performing the identical task.

202 Modeling data in two monkeys performing three-dimensional reach and grasp tas

203 he ability to generate a switching signal in monkey PFo when a strategy is changed.

204 of CSF and brain Abeta(40) levels in rat and monkey pharmacodynamic models.

205 ia hand presses on a newly designed device ("monkey piano").

206 We recorded neural activity in male monkeys playing a variant of the game 'chicken' in which

207 We then record from neuronal populations in monkey primary visual cortex (V1).

208 These bumps were present in monkeys raised without seeing faces and that lack face p

209 the one-interval categorization task (OIC), monkeys rapidly reported their decisions with a saccade.

210 d how features of neural activity changed as monkeys reached to targets in two workspaces.

211 Hamsters and African green monkeys received a primary intranasal infection with RSV

212 ctional connectivity is altered after rhesus monkeys received extensive training to learn novel visuo

213 RI data before and after male rhesus macaque monkeys received extensive training to learn novel visuo

214 After the well-trained monkeys received fornix transection, they were impaired

215 Here, however, in awake monkey recording experiments, we found that roughly half

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

217 g iontophoresis of antagonists in the PFC of monkeys remembering the location of a visual stimulus fo

218 Both monkeys responded with an anti-RRV antibody response, an

219 from both spinal and motor cortical cells in monkeys responding to index finger perturbations.

220 response modalities, and in both humans and monkeys, response times were faster when the target was

221 After surgery, all monkeys retained the social preferences they had demonst

222 tion-competent, recombinant strain of rhesus monkey rhadinovirus (RRV) expressing the Gag protein of

223 The related rhesus monkey rhadinovirus (RRV) has shown potential as a vecto

224 virus (VSV), adenovirus type 5 (Ad5), rhesus monkey rhadinovirus (RRV), and DNA again.

225 Four rhesus monkeys self-administered i.v. infusions of fentanyl (0.

226 To minimize the work required for a reward, monkeys should have always persisted for at least 1 s, b

227 Monkeys showed a pro-variance bias (PVB): a preference t

228 cle-treated monkeys, neurons from EV-treated monkeys showed lower firing rates, greater spike frequen

229 ts of the decision process that mimicked the monkeys' similarly coordinated voluntary strategies for

230 We provide behavioral evidence using monkey smooth pursuit eye movements for four principles

231 In humans and macaque monkeys, socially relevant face processing is accomplish

232 We review studies in marmoset monkeys, songbirds, and other vertebrates.

233 rain white matter in humans and 48% in three monkey species: vervets (Chlorocebus aethiops), rhesus m

234 enuates heroin self-administration in rhesus monkeys, suggesting it could be an effective treatment f

235 that this is the case in humans and macaque monkeys, suggesting that the reflex pathways that regula

236 es in humans and single-neuron recordings in monkeys suggests a pivotal role for the prefrontal corte

237 ve approach, we assessed capuchin and rhesus monkeys' susceptibility to sunk costs in a psychomotor t

238 of a moving object during self-motion, while monkeys switched, from trial to trial, between reporting

239 and deschloroclozapine, in four male rhesus monkeys tested in a spatial delayed response task before

240 us and less defined receptor assembly in the monkey than in rodent brain.

241 Rhesus macaque is an Old World monkey that shared a common ancestor with human ~25 Myr

242 We recently reported in monkeys that following a combined cervical dorsal root/d

243 In African green monkeys that received a primary infection with RSV, a bo

244 We recently showed, in aged female rhesus monkeys, that systemic administration of MSC-EVs enhance

245 Here, we provide evidence that, in marmoset monkeys, the size of a domestication phenotype-a white f

246 Monkeys then completed 50 trials with weights progressiv

247 ab, the virus that naturally infects sabaeus monkeys, through different strategies: administration of

248 and their more rudimentary underpinnings in monkeys to circuit-level and cell-type-specific instanti

249 performed a pool competition study in rhesus monkeys to define the optimal variant for each SHIV prio

250 To fill these gaps, we trained monkeys to discriminate the frequency of ICMS pulse trai

251 t-dependent timing task requiring humans and monkeys to flexibly produce different time intervals wit

252 oscopy and RNA sequencing in 47 young rhesus monkeys to investigate AT's molecular underpinnings by f

253 o address these questions, we trained rhesus monkeys to perform a novel decision-making task with bot

254 modulate strategy, we trained 2 male rhesus monkeys to perform a novel perceptual decision-making ta

255 We trained rhesus monkeys to perform a two-stage decision task designed to

256 disrupted in schizophrenia, we trained male monkeys to perform a variant of the AX continuous perfor

257 We probed the ability of humans and monkeys to perform overt and covert target selection in

258 on model (dorsal root/dorsal column) in male monkeys to remove sensory input from just the opposing d

259 First, we trained monkeys to select the middle dot in a horizontal series

260 se longitudinal data from wild Phayre's leaf monkeys to test the hypothesis that fluctuations in repr

261 o did a parallel preclinical study in rhesus monkeys to test the protective efficacy of the shortened

262 In monkeys trained to detect faint visual targets, the timi

263 In normal monkeys, type I causes many adverse effects including an

264 Adult female African green monkeys underwent right C5/6 lateral hemisection with ev

265 aging of (89)Zr-labeled antibodies in rhesus monkeys up to 30 d after injection.

266 neurons (NPNs) in the BNC of the baboon and monkey using the Golgi technique.

267 Such responses have been studied in monkeys using optical imaging with a limited field of vi

268 We show that in awake monkey V1, there exists a distinct cell type (>>30% of n

269 we model a worst-case scenario using rhesus monkeys vaccinated or unvaccinated with the rVSV-ZEBOV v

270 could be reliably elicited in V1 and V4 when monkeys viewed a visual contour illusion and showed phas

271 igh affinity to mouse, human, and cynomolgus monkey VISTA.

272 rded spiking activity of >100 neurons in the monkey visual and prefrontal cortices is comparable with

273 responses of neurons in different levels of monkey visual cortex.

274 n of GABA(A) receptor subunits in the rhesus monkey was highly heterogeneous indicating a high number

275 ife after BIVV001 administration in mice and monkeys was 25 to 31 hours and 33 to 34 hours, respectiv

276 ce of "As" terminals in VApc of parkinsonian monkeys was 51.4% lower than in controls.

277 Dose-related drug exposure in monkeys was established and renal transplants were then

278 boutons in both VApc and CM of parkinsonian monkeys was significantly larger than in controls, but t

279 The vervet monkeys we study were not provided with a trained model;

280 the neocortex and cerebellum of the macaque monkey, we found that its cerebellum was relatively much

281 tained from spleen-intact and splenectomized monkeys, we identified 67 P. vivax genes whose expressio

282 using multi-structure recordings in macaque monkeys, we show that the brainstem transiently modulate

283 nar videoradiography (XROMM) of four macaque monkeys, we tested the extrinsic muscle shortening hypot

284 Two monkeys were impaired after 0.1 mg/kg olanzapine and two

285 ty using a strategy task in which two rhesus monkeys were instructed by a visual cue either to repeat

286 In contrast, spiking patterns in monkeys were quite distinct for both fingers and directi

287 Macaque monkeys were trained for a behavioural task designed to

288 on of frontal lobe connections compared with monkeys, when normalized by total brain white matter vol

289 roportionally larger in humans compared with monkeys, whereas other tracts associated with emotional

290 duced marked weight loss in obese cynomolgus monkeys while elevating serum adiponectin and the adipos

291 ent levels of visual cortex of 2 male rhesus monkeys while the animals did a visual discrimination ta

292 Here, we used rER BOLD fMRI in macaque monkeys while viewing real-world images, and found visua

293 white matter of the auditory system of aged monkeys, while thalamocortical FA was lower only in visu

294 d S2 terminals in VApc or CM of MPTP-treated monkeys, while the prevalence of "As" terminals in VApc

295 ue samples from a NiV-infected African green monkey with viral loads as low as 52 genome copies/mg.

296 cues, but this preference was reduced in the monkeys with ACC lesions.

297 has shown potential as a vector to immunize monkeys with antigens from simian immunodeficiency virus

298 In addition, daily treatment of lean monkeys with rh-LCN2 decreases food intake by 21%, witho

299 In monkeys with short-term recoveries, the area 3b hand neu

300 Next, we asked whether monkeys would generalize the middle concept to a 7 dot s